0421	SAMHD1	ENSG00000101347	72.2	SAM domain and HD domain 1	1001	http://gfp-cdna.embl.de/loc-html/Q9Y3Z3.html	This gene may play a role in regulation of the innate immune response. The encoded protein is upregulated in response to viral infection and may be involved in mediation of tumor necrosis factor-alpha proinflammatory responses. Mutations in this gene have been associated with Aicardi-Goutieres syndrome. [provided by RefSeq, Mar 2010]
0528	TFIP11	ENSG00000100109	96.8	tuftelin interacting protein 11	1011	http://gfp-cdna.embl.de/loc-html/Q9UBB9.html	TFIP11 is a nuclear speckle-localized protein that may play a role in spliceosome disassembly in Cajal bodies (Stanek et al., 2008 [PubMed 18367544]).[supplied by OMIM, Apr 2009]
0592	RBM22	ENSG00000086589	46.9	RNA binding motif protein 22	2011	http://gfp-cdna.embl.de/loc-html/Q9NW64.html	This gene encodes an RNA binding protein. The encoded protein may play a role in cell division and may be involved in pre-mRNA splicing. Related pseudogenes exist on chromosomes 6, 7, 9, 13, 16, 18, and X. [provided by RefSeq, Mar 2009]
0739	SYF2	ENSG00000117614	28.7	SYF2 homolog, RNA splicing factor (S. cerevisiae)	1010	http://gfp-cdna.embl.de/loc-html/O95926.html	This gene encodes a nuclear protein that interacts with cyclin D-type binding-protein 1, which is thought to be a cell cycle regulator at the G1/S transition. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. [provided by RefSeq, Jul 2008]
0775	HORMAD1	ENSG00000143452	45.2	HORMA domain containing 1	2000	http://gfp-cdna.embl.de/loc-html/Q9H0K8.html	This gene encodes a HORMA domain-containing protein. HORMA domains are involved in chromatin binding and play a role in cell cycle regulation. The encoded protein may play a role in meiosis, and expression of this gene is a potential marker for cancer. A pseudogene of this gene is located on the long arm of chromosome 6. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2010]
0827	TARDBP	ENSG00000120948	44.7	TAR DNA binding protein	1010		HIV-1, the causative agent of acquired immunodeficiency syndrome (AIDS), contains an RNA genome that produces a chromosomally integrated DNA during the replicative cycle. Activation of HIV-1 gene expression by the transactivator Tat is dependent on an RNA regulatory element (TAR) located downstream of the transcription initiation site. The protein encoded by this gene is a transcriptional repressor that binds to chromosomally integrated TAR DNA and represses HIV-1 transcription. In addition, this protein regulates alternate splicing of the CFTR gene. A similar pseudogene is present on chromosome 20. [provided by RefSeq, Jul 2008]
0921	LHX6	ENSG00000106852	43.1	LIM homeobox 6	2000	http://gfp-cdna.embl.de/loc-html/Q9UPM6.html	This gene encodes a member of a large protein family that contains the LIM domain, a unique cysteine-rich zinc-binding domain. The encoded protein may function as a transcriptional regulator and may be involved in the control of differentiation and development of neural and lymphoid cells. Two alternatively spliced transcript variants encoding distinct isoforms have been described for this gene. Alternatively spliced transcript variants have been identified, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
1099	ZFP82	ENSG00000181007	62.5	zinc finger protein 82 homolog	2110	http://gfp-cdna.embl.de/loc-html/Q8N141.html	N/A
1115	UTP3	ENSG00000132467	54.6	UTP3, small subunit (SSU) processome component, homolog (S. cerevisiae)	1210	http://gfp-cdna.embl.de/loc-html/Q9NQZ2.html	N/A
1153	ZC3H13	ENSG00000123200	196.6	zinc finger CCCH-type containing 13	1010	http://gfp-cdna.embl.de/loc-html/Q9H0L6.html	N/A
1238	KIF22	ENSG00000079616	73.3	kinesin family member 22	2100	http://gfp-cdna.embl.de/loc-html/Q14807.html	The protein encoded by this gene is a member of the kinesin-like protein family. The family members are microtubule-dependent molecular motors that transport organelles within cells and move chromosomes during cell division. The C-terminal half of this protein has been shown to bind DNA. Studies with the Xenopus homolog suggests its essential role in metaphase chromosome alignment and maintenance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jan 2012]
1246	USP1	ENSG00000162607	88.2	ubiquitin specific peptidase 1	1000	http://gfp-cdna.embl.de/loc-html/O94782.html	This gene encodes a member of the ubiquitin-specific processing (UBP) family of proteases that is a deubiquitinating enzyme (DUB) with His and Cys domains. This protein is located in the cytoplasm and cleaves the ubiquitin moiety from ubiquitin-fused precursors and ubiquitinylated proteins. The protein specifically deubiquitinates a protein in the Fanconi anemia (FA) DNA repair pathway. Alternate transcriptional splice variants have been characterized. [provided by RefSeq, Jul 2008]
1291	DDX24	ENSG00000089737	96.3	DEAD (Asp-Glu-Ala-Asp) box polypeptide 24	1200	http://gfp-cdna.embl.de/loc-html/Q9GZR7.html	DEAD box proteins, characterized by the conserved motif Asp-Glu-Ala-Asp (DEAD), are putative RNA helicases. They are implicated in a number of cellular processes involving alteration of RNA secondary structure such as translation initiation, nuclear and mitochondrial splicing, and ribosome and spliceosome assembly. Based on their distribution patterns, some members of this family are believed to be involved in embryogenesis, spermatogenesis, and cellular growth and division. This gene encodes a DEAD box protein, which shows little similarity to any of the other known human DEAD box proteins, but shows a high similarity to mouse Ddx24 at the amino acid level. [provided by RefSeq, Jul 2008]
1353	SAP130	ENSG00000136715	110.3	Sin3A-associated protein, 130kDa	1010	http://gfp-cdna.embl.de/loc-html/Q9H0E3.html	SAP130 is a subunit of the histone deacetylase (see HDAC1; MIM 601241)-dependent SIN3A (MIM 607776) corepressor complex (Fleischer et al., 2003 [PubMed 12724404]).[supplied by OMIM, Mar 2008]
1368	KIAA1967	ENSG00000158941	102.9	KIAA1967	1000	http://gfp-cdna.embl.de/loc-html/Q8N3G7.html	N/A
1376	RPL36	ENSG00000130255	12.3	ribosomal protein L36	1201	http://gfp-cdna.embl.de/loc-html/Q9Y3U8.html	Ribosomes, the organelles that catalyze protein synthesis, consist of a small 40S subunit and a large 60S subunit. Together these subunits are composed of 4 RNA species and approximately 80 structurally distinct proteins. This gene encodes a ribosomal protein that is a component of the 60S subunit. The protein belongs to the L36E family of ribosomal proteins. It is located in the cytoplasm. Transcript variants derived from alternative splicing exist; they encode the same protein. As is typical for genes encoding ribosomal proteins, there are multiple processed pseudogenes of this gene dispersed through the genome. [provided by RefSeq, Jul 2008]
1383	ZBTB20	ENSG00000181722	81.1	zinc finger and BTB domain containing 20	2001	http://gfp-cdna.embl.de/loc-html/Q9Y410.html	N/A
1431	MED23	ENSG00000112282	156.5	mediator complex subunit 23	1000	http://gfp-cdna.embl.de/loc-html/Q9ULK4.html	The activation of gene transcription is a multistep process that is triggered by factors that recognize transcriptional enhancer sites in DNA. These factors work with co-activators to direct transcriptional initiation by the RNA polymerase II apparatus. The protein encoded by this gene is a subunit of the CRSP (cofactor required for SP1 activation) complex, which, along with TFIID, is required for efficient activation by SP1. This protein is also a component of other multisubunit complexes e.g. thyroid hormone receptor-(TR-) associated proteins which interact with TR and facilitate TR function on DNA templates in conjunction with initiation factors and cofactors. This protein also acts as a metastasis suppressor. Two alternatively spliced transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008]
1499	PNMAL1	ENSG00000182013	48.2	paraneoplastic Ma antigen family-like 1	1200	http://gfp-cdna.embl.de/loc-html/Q8N3H4.html	N/A
1750	APOLD1	ENSG00000178878	30.5	apolipoprotein L domain containing 1	1200	http://gfp-cdna.embl.de/loc-html/Q9H0S4.html	APOLD1 is an endothelial cell early response protein that may play a role in regulation of endothelial cell signaling and vascular function (Regard et al., 2004 [PubMed 15102925]).[supplied by OMIM, Dec 2008]
1838	RPL10	ENSG00000147403	24.6	ribosomal protein L10	1201	http://gfp-cdna.embl.de/loc-html/P27635.html	N/A
1882	H2AFB2	ENSG00000185978	12.7	H2A histone family, member B3	2100	http://gfp-cdna.embl.de/loc-html/akxq28c161063.html	Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene encodes a member of the histone H2A family. This gene is part of a region that is repeated three times on chromosome X, once in intron 22 of the F8 gene and twice closer to the Xq telomere. This record represents the middle copy. [provided by RefSeq, Jul 2008]
1909	DMAP1	ENSG00000178028	53.0	DNA methyltransferase 1 associated protein 1	2101	http://gfp-cdna.embl.de/loc-html/Q9NPF5.html	This gene encodes a subunit of several, distinct complexes involved in the repression or activation of transcription. The encoded protein can independently repress transcription and is targeted to replication foci throughout S phase by interacting directly with the N-terminus of DNA methyltransferase 1. During late S phase, histone deacetylase 2 is added to this complex, providing a means to deacetylate histones in transcriptionally inactive heterochromatin following replication. The encoded protein is also a component of the nucleosome acetyltransferase of H4 complex and interacts with the transcriptional corepressor tumor susceptibility gene 101 and the pro-apoptotic death-associated protein 6, among others. Alternatively spliced transcript variants encoding the same protein have been described. [provided by RefSeq, Jul 2008]
1947	SMARCE1	ENSG00000073584	46.6	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1	1000	http://gfp-cdna.embl.de/loc-html/Q969G3.html	The protein encoded by this gene is part of the large ATP-dependent chromatin remodeling complex SWI/SNF, which is required for transcriptional activation of genes normally repressed by chromatin. The encoded protein, either alone or when in the SWI/SNF complex, can bind to 4-way junction DNA, which is thought to mimic the topology of DNA as it enters or exits the nucleosome. The protein contains a DNA-binding HMG domain, but disruption of this domain does not abolish the DNA-binding or nucleosome-displacement activities of the SWI/SNF complex. Unlike most of the SWI/SNF complex proteins, this protein has no yeast counterpart. [provided by RefSeq, Jul 2008]
1988	PDZD4	ENSG00000067840	86.2	PDZ domain containing 4	1200	http://gfp-cdna.embl.de/loc-html/Q9BUH9.html	N/A
2002	DKC1	ENSG00000130826	57.7	dyskeratosis congenita 1, dyskerin	1001	http://gfp-cdna.embl.de/loc-html/O60832.html	Biosynthesis of stable cellular RNAs such as tRNAs, rRNAs, snRNAs, and snoRNAs is aided by covalent nucleotide modification after transcription. The modified nucleotides are involved in correct RNA folding, establishment of correct RNA-RNA and RNA-protein interactions, and in the correct function of mature RNAs. The RNA encoded by this gene is thought to mediate the pseudouridylation of residue U1664 of 28S rRNA. [provided by RefSeq, Feb 2009]
2018	FAM50A 	ENSG00000071859	40.2	family with sequence similarity 50, member A	1000	http://gfp-cdna.embl.de/loc-html/Q14320.html	This gene belongs to the FAM50 family. The encoded protein is highly conserved in length and sequence across different species. It is a basic protein containing a nuclear localization signal, and may function as a DNA-binding protein or a transcriptional factor. [provided by RefSeq, Sep 2009]
2093	MECP2	ENSG00000169057	52.4	methyl CpG binding protein 2 (Rett syndrome)	2000	http://gfp-cdna.embl.de/loc-html/P51608.html	DNA methylation is the major modification of eukaryotic genomes and plays an essential role in mammalian development. Human proteins MECP2, MBD1, MBD2, MBD3, and MBD4 comprise a family of nuclear proteins related by the presence in each of a methyl-CpG binding domain (MBD). Each of these proteins, with the exception of MBD3, is capable of binding specifically to methylated DNA. MECP2, MBD1 and MBD2 can also repress transcription from methylated gene promoters. In contrast to other MBD family members, MECP2 is X-linked and subject to X inactivation. MECP2 is dispensible in stem cells, but is essential for embryonic development. MECP2 gene mutations are the cause of most cases of Rett syndrome, a progressive neurologic developmental disorder and one of the most common causes of mental retardation in females. [provided by RefSeq, Jul 2009]
2148	HP1BP3	ENSG00000127483	61.2	heterochromatin protein 1, binding protein 3	2110	http://gfp-cdna.embl.de/loc-html/Q8NDF0.html	N/A
2176	PMF1	ENSG00000160783	23.3	polyamine-modulated factor 1	1200	http://gfp-cdna.embl.de/loc-html/Q69YZ9.html	This locus represents naturally occurring read-through transcription between the neighboring PMF1 (polyamine-modulated factor 1) and BGLAP (bone gamma-carboxyglutamate Gla protein) genes on chromosome 1. Alternative splicing results in multiple transcript variants encoding isoforms that share sequence identity with the upstream gene product, but they contain distinct C-termini due to frameshifts versus the downstream gene coding sequence. [provided by RefSeq, Dec 2010]
2214	NEIL2	ENSG00000154328	36.8	nei endonuclease VIII-like 2 (E. coli)	1001	http://gfp-cdna.embl.de/loc-html/Q7Z3Q7.html	NEIL2 belongs to a class of DNA glycosylases homologous to the bacterial Fpg/Nei family. These glycosylases initiate the first step in base excision repair by cleaving bases damaged by reactive oxygen species and introducing a DNA strand break via the associated lyase reaction (Bandaru et al., 2002 [PubMed 12509226])[supplied by OMIM, Mar 2008]
2256	HOXA9	ENSG00000078399	30.2	homeobox A9	2000	http://gfp-cdna.embl.de/loc-html/P31269.html	In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is highly similar to the abdominal-B (Abd-B) gene of Drosophila. A specific translocation event which causes a fusion between this gene and the NUP98 gene has been associated with myeloid leukemogenesis. Read-through transcription exists between this gene and the upstream homeobox A10 (HOXA10) gene.[provided by RefSeq, Mar 2011]
2318	ZSCAN22	ENSG00000182318	54.6	zinc finger and SCAN domain containing 22	2000	http://gfp-cdna.embl.de/loc-html/Q7Z3L8.html	N/A
2432	CGGBP1	ENSG00000163320	18.8	CGG triplet repeat binding protein 1	1100	http://gfp-cdna.embl.de/loc-html/Q9UFW8.html	CGGBP1 influences expression of the FMR1 gene (MIM 309550), which is associated with the fragile X mental retardation syndrome (MIM 300624), by specifically interacting with the 5-prime (CGG)n-3-prime repeat in its 5-prime UTR.[supplied by OMIM, Mar 2008]
2444	RFX7	ENSG00000181827	157.3	regulatory factor X, 7	1001	http://gfp-cdna.embl.de/loc-html/Q8N3J0.html	RFX7 is a member of the regulatory factor X (RFX) family of transcription factors (see RFX1, MIM 600006) (Aftab et al., 2008 [PubMed 18673564]).[supplied by OMIM, Mar 2009]
2464	TCF12	ENSG00000140262	73.0	 transcription factor 12	2000	http://gfp-cdna.embl.de/loc-html/Q86TC1.html	The protein encoded by this gene is a member of the basic helix-loop-helix (bHLH) E-protein family that recognizes the consensus binding site (E-box) CANNTG. This encoded protein is expressed in many tissues, among them skeletal muscle, thymus, B- and T-cells, and may participate in regulating lineage-specific gene expression through the formation of heterodimers with other bHLH E-proteins. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some of these variants has not been determined. [provided by RefSeq, Jul 2008]
2542	USP37	ENSG00000135913	110.2	ubiquitin specific peptidase 37	1001	http://gfp-cdna.embl.de/loc-html/Q86T82.html	N/A
2672	UTP15	ENSG00000164338	58.4	UTP15, U3 small nucleolar ribonucleoprotein, homolog (S. cerevisiae)	1201	http://gfp-cdna.embl.de/loc-html/Q8TED0.html	N/A
2692	H3F3B	ENSG00000132475	15.3	H3 histone, family 3B (H3.3B)	2000	http://gfp-cdna.embl.de/loc-html/CAD97621.html	Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene contains introns and its mRNA is poyadenylated, unlike most histone genes. The protein encoded is a member of the histone H3 family. [provided by RefSeq, Jul 2008]
2851	AC004381.6	ENSG00000005189	89.9	Putative RNA exonuclease NEF-sp	1201	http://gfp-cdna.embl.de/loc-html/Q96IC2.html	N/A
2960	F8A2	ENSG00000198444	39.1	coagulation factor VIII-associated 2	1001	http://gfp-cdna.embl.de/loc-html/Q8IXP3.html	This gene is part of a region that is repeated three times on chromosome X, once in intron 22 of the F8 gene and twice closer to the Xq telomere. This record represents the most telomeric copy. Although its function is unknown, the observation that this gene is conserved in the mouse implies it has some function. Unlike factor VIII, this gene is transcribed abundantly in a wide variety of cell types. [provided by RefSeq, Jul 2008]
3033	SENP3	ENSG00000161956	64.9	SUMO1/sentrin/SMT3 specific peptidase 3	2200	http://gfp-cdna.embl.de/loc-html/Q9H4L4.html	The reversible posttranslational modification of proteins by the addition of small ubiquitin-like SUMO proteins (see SUMO1; MIM 601912) is required for numerous biologic processes. SUMO-specific proteases, such as SENP3, are responsible for the initial processing of SUMO precursors to generate a C-terminal diglycine motif required for the conjugation reaction. They also have isopeptidase activity for the removal of SUMO from high molecular mass SUMO conjugates (Di Bacco et al., 2006 [PubMed 16738315]).[supplied by OMIM, Jun 2009]
3099	SF3B5	ENSG00000169976	10.1	splicing factor 3b, subunit 5, 10kDa	2001	http://gfp-cdna.embl.de/loc-html/Q9BWJ5.html	N/A
3140	XBP1	ENSG00000100219	28.7	X-box binding protein 1	2001	http://gfp-cdna.embl.de/loc-html/P17861.html	This gene encodes a transcription factor that regulates MHC class II genes by binding to a promoter element referred to as an X box. This gene product is a bZIP protein, which was also identified as a cellular transcription factor that binds to an enhancer in the promoter of the T cell leukemia virus type 1 promoter. It may increase expression of viral proteins by acting as the DNA binding partner of a viral transactivator. It has been found that upon accumulation of unfolded proteins in the endoplasmic reticulum (ER), the mRNA of this gene is processed to an active form by an unconventional splicing mechanism that is mediated by the endonuclease inositol-requiring enzyme 1 (IRE1). The resulting loss of 26 nt from the spliced mRNA causes a frame-shift and an isoform XBP1(S), which is the functionally active transcription factor. The isoform encoded by the unspliced mRNA, XBP1(U), is constitutively expressed, and thought to function as a negative feedback regulator of XBP1(S), which shuts off transcription of target genes during the recovery phase of ER stress. A pseudogene of XBP1 has been identified and localized to chromosome 5. [provided by RefSeq, Jul 2008]
3155	GATA3	ENSG00000107485	47.9	GATA binding protein 3	2000	http://gfp-cdna.embl.de/loc-html/P23771.html	This gene encodes a protein which belongs to the GATA family of transcription factors. The protein contains two GATA-type zinc fingers and is an important regulator of T-cell development and plays an important role in endothelial cell biology. Defects in this gene are the cause of hypoparathyroidism with sensorineural deafness and renal dysplasia. [provided by RefSeq, Nov 2009]
3163	GADD45A	ENSG00000116717	18.3	growth arrest and DNA-damage-inducible, alpha	1001	http://gfp-cdna.embl.de/loc-html/P24522.html	This gene is a member of a group of genes whose transcript levels are increased following stressful growth arrest conditions and treatment with DNA-damaging agents. The protein encoded by this gene responds to environmental stresses by mediating activation of the p38/JNK pathway via MTK1/MEKK4 kinase. The DNA damage-induced transcription of this gene is mediated by both p53-dependent and -independent mechanisms. Alternatively spliced transcript variants encoding distinct isoforms have been found for this gene.[provided by RefSeq, Dec 2010]
CENPAC07	CENPA	ENSG00000115163	16.0	centromere protein A	2100	http://gfp-cdna.embl.de/loc-html/P49450.html	Centromeres are the differentiated chromosomal domains that specify the mitotic behavior of chromosomes. CENPA encodes a centromere protein which contains a histone H3 related histone fold domain that is required for targeting to the centromere. CENPA is proposed to be a component of a modified nucleosome or nucleosome-like structure in which it replaces 1 or both copies of conventional histone H3 in the (H3-H4)2 tetrameric core of the nucleosome particle. Alternative splicing results in multiple transcript variants encoding distinct isoforms. [provided by RefSeq, Jul 2008]
DDIT3G06	DDIT3	ENSG00000175197	19.2	DNA-damage-inducible transcript 3	1000	http://gfp-cdna.embl.de/loc-html/P35638.html	This gene encodes a member of the CCAAT/enhancer-binding protein (C/EBP) family of transcription factors. The protein functions as a dominant-negative inhibitor by forming heterodimers with other C/EBP members, such as C/EBP and LAP (liver activator protein), and preventing their DNA binding activity. The protein is implicated in adipogenesis and erythropoiesis, is activated by endoplasmic reticulum stress, and promotes apoptosis. Fusion of this gene and FUS on chromosome 16 or EWSR1 on chromosome 22 induced by translocation generates chimeric proteins in myxoid liposarcomas or Ewing sarcoma. Multiple alternatively spliced transcript variants encoding two isoforms with different length have been identified. [provided by RefSeq, Aug 2010]
H2A	HIST3H2A	ENSG00000181218	14.1	histone cluster 3, H2A	2000	N/A	Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Nucleosomes consist of approximately 146 bp of DNA wrapped around a histone octamer composed of pairs of each of the four core histones (H2A, H2B, H3, and H4). The chromatin fiber is further compacted through the interaction of a linker histone, H1, with the DNA between the nucleosomes to form higher order chromatin structures. This gene is intronless and encodes a member of the histone H2A family. Transcripts from this gene contain a palindromic termination element. [provided by RefSeq, Jul 2008]
HP1	CBX5	ENSG00000094916	22.2	chromobox homolog 5, heterochromatin protein 1 isoform alpha	2000	N/A	This gene encodes a highly conserved nonhistone protein, which is a member of the heterochromatin protein family. The protein is enriched in the heterochromatin and associated with centromeres. The protein has a single N-terminal chromodomain which can bind to histone proteins via methylated lysine residues, and a C-terminal chromo shadow-domain (CSD) which is responsible for the homodimerization and interaction with a number of chromatin-associated nonhistone proteins. The encoded product is involved in the formation of functional kinetochore through interaction with essential kinetochore proteins. The gene has a pseudogene located on chromosome 3. Multiple alternatively spliced variants, encoding the same protein, have been identified. [provided by RefSeq, Jul 2008]
ZNF339D10	OVOL2	ENSG00000125850	30.4	ovo-like 2 (Drosophila)	2200	http://gfp-cdna.embl.de/loc-html/Q9BRP0.html	N/A
ZNF183104	RNF113A	ENSG00000125352	38.8	ring finger protein 113A	1000	http://gfp-cdna.embl.de/loc-html/O15541.html	This intronless gene encodes a protein which contains a C3H1-type zinc finger domain and a C3HC4 Ring-type (Really Interesting New Gene-type) zinc finger domain. The Ring-type zinc finger domain is identified in various tumor suppressors, DNA repair genes and cytokine receptor-associated molecules, and is probably involved in mediating protein-protein interactions. [provided by RefSeq, May 2010]
EYFP	EYFP	UNKNOWN	0.0	enhanced yellow fluorescent protein	1101	N/A	N/A
