RBM12

RNA-binding protein 12 is a protein that in humans is encoded by the RBM12 gene.^[5][6]

RBM12
Available structures PDB Ortholog search: PDBe RCSB List of PDB id codes 1WEL, 2CPY, 2DNN, 2EK1, 2EK6
Identifiers
Aliases	RBM12, HRIHFB2091, SWAN, RNA binding motif protein 12, SCZD19
External IDs	OMIM: 607179; MGI: 1922960; HomoloGene: 34993; GeneCards: RBM12; OMA:RBM12 - orthologs
Gene location (Human) Chr. Chromosome 20 (human)[1] Band 20q11.22 Start 35,648,925 bp[1] End 35,664,956 bp[1]
Gene location (Mouse) Chr. Chromosome 2 (mouse)[2] Band 2|2 H1 Start 155,933,878 bp[2] End 155,953,898 bp[2]
RNA expression pattern Bgee Human Mouse (ortholog) Top expressed in Achilles tendon epithelium of colon secondary oocyte bone marrow cell embryo ganglionic eminence islet of Langerhans amniotic fluid ventricular zone cartilage tissue Top expressed in primitive streak tail of embryo genital tubercle abdominal wall aortic valve mandibular prominence maxillary prominence ureter hair follicle somite More reference expression data BioGPS n/a
Orthologs Species Human Mouse Entrez 10137 75710 Ensembl ENSG00000244462 ENSMUSG00000089824 UniProt Q9NTZ6 Q8R4X3 RefSeq (mRNA) NM_152838 NM_001198838 NM_001198840 NM_006047 NM_029397 NM_170598 RefSeq (protein) NP_001185767 NP_001185769 NP_006038 NP_690051 NP_083673 NP_733486 Location (UCSC) Chr 20: 35.65 – 35.66 Mb Chr 2: 155.93 – 155.95 Mb PubMed search [3] [4]
Wikidata
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This gene encodes a protein that contains several RNA-binding motifs, potential transmembrane domains, and proline-rich regions. This gene and the gene for copine I overlap at map location 20q11.21. Alternative splicing in the 5' UTR results in two transcript variants. Both variants encode the same protein.^[6]