AIM1

AIM1
Available structures
PDBHuman UniProt search: PDBe RCSB
Identifiers
Aliases AIM1, CRYBG1, ST4, absent in melanoma 1
External IDs MGI: 109544 HomoloGene: 18168 GeneCards: AIM1
Genetically Related Diseases
stroke[1]
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez

202

11630

Ensembl

ENSG00000112297

ENSMUSG00000019866

UniProt

Q9Y4K1
Q96QW7

n/a

RefSeq (mRNA)

NM_001624

NM_172393

RefSeq (protein)

NP_001615.2

n/a

Location (UCSC) Chr 6: 106.36 – 106.57 Mb Chr 10: 43.95 – 44.15 Mb
PubMed search [2] [3]
Wikidata
View/Edit HumanView/Edit Mouse

Absent in melanoma 1 protein is a protein that in humans is encoded by the AIM1 gene.[4][5][6]

References

  1. "Diseases that are genetically associated with AIM1 view/edit references on wikidata".
  2. "Human PubMed Reference:".
  3. "Mouse PubMed Reference:".
  4. Millikin D, Meese E, Vogelstein B, Witkowski C, Trent J (Nov 1991). "Loss of heterozygosity for loci on the long arm of chromosome 6 in human malignant melanoma". Cancer Res. 51 (20): 5449–53. PMID 1680551.
  5. Rajini B, Graham C, Wistow G, Sharma Y (Apr 2003). "Stability, homodimerization, and calcium-binding properties of a single, variant betagamma-crystallin domain of the protein absent in melanoma 1 (AIM1)". Biochemistry. 42 (15): 4552–9. doi:10.1021/bi027384l. PMID 12693952.
  6. "Entrez Gene: AIM1 absent in melanoma 1".

External links

Further reading


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