RBM12

RNA-binding protein 12 is a protein that in humans is encoded by the RBM12 gene.[4][5]

RBM12
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesRBM12, HRIHFB2091, SWAN, RNA binding motif protein 12, SCZD19
External IDsOMIM: 607179 MGI: 1922960 HomoloGene: 34993 GeneCards: RBM12
Gene location (Human)
Chr.Chromosome 20 (human)[1]
Band20q11.22Start35,648,925 bp[1]
End35,664,956 bp[1]
Orthologs
SpeciesHumanMouse
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 Mbn/a
PubMed search[2][3]
Wikidata
View/Edit HumanView/Edit Mouse

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.[5]

References

  1. GRCh38: Ensembl release 89: ENSG00000244462 - Ensembl, May 2017
  2. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. 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. S2CID 20555964.
  5. "Entrez Gene: RBM12 RNA binding motif protein 12".

Further reading


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