AHI1

Gene Information
  • Official Symbol: AHI1
  • Official Name: Abelson helper integration site 1
  • Aliases and Previous Symbols: N/A
  • Entrez ID: 54806
  • UniProt: Q8N157
  • Interactions: BioGRID
  • PubMed articles: Open PubMed
  • OMIM: Open OMIM
Function Summary
  • Entrez Summary: This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified. [provided by RefSeq, Oct 2008].
  • UniProt Summary: N/A

Pfam Domains GO Terms


CRISPR Data

Compound Hit Most Correlated Genes in Chemogenomics Tissues where Essential in the Avana Dataset (DepMap 20Q1)

Essentiality in NALM6
  • Essentiality Rank: 18319
  • Expression level (log2 read counts): 6.29

Expression Distribution

  • Last modified: 2026/01/07 22:36
  • by 127.0.0.1