BHLHA9

Basic helix-loop-helix family, member a9 is a protein in humans that is encoded by the BHLHA9 gene.[5]

BHLHA9
Identifiers
AliasesBHLHA9, BHLHF42, basic helix-loop-helix family member a9, CCSPD
External IDsOMIM: 615416 MGI: 2444198 HomoloGene: 82363 GeneCards: BHLHA9
Gene location (Human)
Chr.Chromosome 17 (human)[1]
Band17p13.3Start1,270,559 bp[1]
End1,271,460 bp[1]
Orthologs
SpeciesHumanMouse
Entrez

727857

320522

Ensembl

ENSG00000205899

ENSMUSG00000044243

UniProt

Q7RTU4

Q5RJB0

RefSeq (mRNA)

NM_001164405

NM_177182

RefSeq (protein)

NP_001157877

NP_796156

Location (UCSC)Chr 17: 1.27 – 1.27 MbChr 11: 76.67 – 76.67 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

References

  1. GRCh38: Ensembl release 89: ENSG00000205899 - Ensembl, May 2017
  2. GRCm38: Ensembl release 89: ENSMUSG00000044243 - Ensembl, May 2017
  3. "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. "Entrez Gene: Basic helix-loop-helix family, member a9". Retrieved 2012-04-26.

Further reading


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