RBM12

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RBM12
Protein RBM12 PDB 1wel.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases RBM12, HRIHFB2091, SWAN, RNA binding motif protein 12, SCZD19
External IDs MGI: 1922960 HomoloGene: 34993 GeneCards: RBM12
Gene location (Human)
Chromosome 20 (human)
Chr. Chromosome 20 (human)[1]
Chromosome 20 (human)
Genomic location for RBM12
Genomic location for RBM12
Band 20q11.22 Start 35,648,925 bp[1]
End 35,664,956 bp[1]
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
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: 156.09 – 156.11 Mb
PubMed search [3] [4]
Wikidata
View/Edit Human View/Edit Mouse

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

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]

References[edit]

  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000244462 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000089824 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". 
  4. ^ "Mouse PubMed Reference:". 
  5. ^ Stover C, Gradl G, Jentsch I, Speicher MR, Wieser R, Schwaeble W (Jul 2001). "cDNA cloning, chromosome assignment, and genomic structure of a human gene encoding a novel member of the RBM family". Cytogenet Cell Genet. 92 (3-4): 225–30. doi:10.1159/000056908. PMID 11435693. 
  6. ^ a b "Entrez Gene: RBM12 RNA binding motif protein 12". 

Further reading[edit]

External links[edit]