C1d Gene Search Result

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10 records found for search term C1d

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RGD ID	Symbol	Name	Description	Chr	Start	Stop	Species	Annotations	Match	Type
1607075	C1D	C1D nuclear receptor corepressor	The protein encoded by this gene is a DNA binding and apoptosis-inducing protein and is localized in the nucleus. It is also a Rac3-interacting protein which acts as a corepressor for the thyroid hormone receptor. This protein is thought to regulate TRAX/Translin complex formation. Alternate splicin ... (more) g results in multiple transcript variants that encode the same protein. Multiple pseudogenes of this gene are found on chromosome 10.[provided by RefSeq, Jun 2010]	2	68041130	68063004	Human	89	symbol , old_gene_name , COSMIC , name , Human Proteome Map , old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
1604328	WDR93	WD repeat domain 93	Predicted to be involved in electron transport chain. Predicted to be part of respiratory chain complex I. [provided by Alliance of Genome Resources, Jul 2025]	15	89690348	89743638	Human	24	old_gene_symbol	gene, protein-coding, VALIDATED [RefSeq]
3362449	C1DP1	C1D nuclear receptor corepressor pseudogene 1		10	32510628	32511796	Human		symbol , COSMIC , name , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]
3129877	C1DP2	C1D nuclear receptor corepressor pseudogene 2		10	80031610	80032449	Human		symbol , COSMIC , name , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]
3129884	C1DP3	C1D nuclear receptor corepressor pseudogene 3	INTERACTS WITH butanal	10	80024379	80025218	Human	1	symbol , old_gene_name , COSMIC , name , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]
2816606	C1DP4	C1D nuclear receptor corepressor pseudogene 4		10	80040264	80041098	Human		symbol , COSMIC , name , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]
10399213	C1DP5	C1D nuclear receptor corepressor pseudogene 5		11	83111035	83111501	Human		symbol , COSMIC , name , Human Proteome Map	gene, pseudo, INFERRED [RefSeq]
1320809	RBM8A	RNA binding motif protein 8A	This gene encodes a protein with a conserved RNA-binding motif. The protein is found predominantly in the nucleus, although it is also present in the cytoplasm. It is preferentially associated with mRNAs produced by splicing, including both nuclear mRNAs and newly exported cytoplasmic mRNAs. It is t ... (more) hought that the protein remains associated with spliced mRNAs as a tag to indicate where introns had been present, thus coupling pre- and post-mRNA splicing events. Previously, it was thought that two genes encode this protein, RBM8A and RBM8B; it is now thought that the RBM8B locus is a pseudogene. There are two alternate translation start codons with this gene, which result in two forms of the protein. An allele mutation and a low-frequency noncoding single-nucleotide polymorphism (SNP) in this gene cause thrombocytopenia-absent radius (TAR) syndrome. [provided by RefSeq, Jul 2013]	1	145921556	145927484	Human	292	old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
69144	NFIA	nuclear factor I A	This gene encodes a member of the NF1 (nuclear factor 1) family of transcription factors. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Sep 2011]	1	61077227	61462788	Human	297	old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]
1346592	ZBTB18	zinc finger and BTB domain containing 18	This gene encodes a C2H2-type zinc finger protein which acts a transcriptional repressor of genes involved in neuronal development. The encoded protein recognizes a specific sequence motif and recruits components of chromatin to target genes. Alternative splicing results in multiple transcript varia ... (more) nts. [provided by RefSeq, May 2013]	1	244048491	244057476	Human	198	old_gene_symbol	gene, protein-coding, REVIEWED [RefSeq]