RBM12 gene

RNA binding motif protein 12

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

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 four transcript variants. All variants encode the same protein. [provided by RefSeq, Nov 2010]

From NCBI Gene:

  • SCHIZOPHRENIA 19

From UniProt:

Genetic variants in RBM12 may be a cause of susceptibility to psychotic disorders. Psychotic disorders are characterized by a gross impairment in reality testing with delusions or prominent hallucinations.

Cytogenetic Location: 20q11.22, which is the long (q) arm of chromosome 20 at position 11.22

Molecular Location: base pairs 35,648,925 to 35,664,956 on chromosome 20 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 20q11.22, which is the long (q) arm of chromosome 20 at position 11.22
  • HRIHFB2091
  • SCZD19
  • SWAN