RBM19

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RBM19
Protein RBM19 PDB 2cpf.png
Available structures
PDB Ortholog search: PDBe RCSB
Identifiers
Aliases RBM19
External IDs MGI: 1921361 HomoloGene: 7158 GeneCards: RBM19
Genetically Related Diseases
amyotrophic lateral sclerosis[1]
RNA expression pattern
PBB GE RBM19 206019 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001146698
NM_001146699
NM_016196

NM_028762

RefSeq (protein)

NP_001140170
NP_001140171
NP_057280

NP_083038.1
NP_083038

Location (UCSC) Chr 12: 113.82 – 113.97 Mb Chr 5: 120.12 – 120.2 Mb
PubMed search [2] [3]
Wikidata
View/Edit Human View/Edit Mouse

Probable RNA-binding protein 19 is a protein that in humans is encoded by the RBM19 gene.[4][5][6]


References[edit]

  1. ^ "Diseases that are genetically associated with RBM19 view/edit references on wikidata". 
  2. ^ "Human PubMed Reference:". 
  3. ^ "Mouse PubMed Reference:". 
  4. ^ Ishikawa K, Nagase T, Suyama M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O (Dec 1998). "Prediction of the coding sequences of unidentified human genes. X. The complete sequences of 100 new cDNA clones from brain which can code for large proteins in vitro". DNA Res. 5 (3): 169–76. doi:10.1093/dnares/5.3.169. PMID 9734811. 
  5. ^ Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Bocher M, Blocker H, Bauersachs S, Blum H, Lauber J, Dusterhoft A, Beyer A, Kohrer K, Strack N, Mewes HW, Ottenwalder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A (Mar 2001). "Toward a Catalog of Human Genes and Proteins: Sequencing and Analysis of 500 Novel Complete Protein Coding Human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072Freely accessible. PMID 11230166. 
  6. ^ "Entrez Gene: RBM19 RNA binding motif protein 19". 

Further reading[edit]