ANKFY1

Ankyrin repeat and FYVE domain containing 1
Identifiers
Symbols ANKFY1; ANKHZN; DKFZp686M19106; KIAA1255; ZFYVE14
External IDs OMIM607927 MGI1337008 HomoloGene9491 GeneCards: ANKFY1 Gene
RNA expression pattern
More reference expression data
Orthologs
Species Human Mouse
Entrez 51479 11736
Ensembl ENSG00000185722 ENSMUSG00000020790
UniProt Q9P2R3 Q5SPW9
RefSeq (mRNA) NM_016376.3 NM_009671.5
RefSeq (protein) NP_057460.3 NP_033801.4
Location (UCSC) Chr 17:
4.07 – 4.17 Mb
Chr 11:
72.5 – 72.59 Mb
PubMed search [1] [2]

Ankyrin repeat and FYVE domain-containing protein 1 is a protein that in humans is encoded by the ANKFY1 gene.[1][2][3]

This gene encodes a cytoplasmic protein that contains a coiled-coil structure and a BTB/POZ domain at its N-terminus, ankyrin repeats in the middle portion, and a FYVE-finger motif at its C-terminus. This protein belongs to a subgroup of double zinc finger proteins which may be involved in vesicle or protein transport. Alternative splicing has been observed at this locus and two variants, each encoding a distinct isoform, have been identified.[3]

References

  1. ^ Kuriyama H, Asakawa S, Minoshima S, Maruyama H, Ishii N, Ito K, Gejyo F, Arakawa M, Shimizu N, Kuwano R (Oct 2000). "Characterization and chromosomal mapping of a novel human gene, ANKHZN". Gene 253 (2): 151–60. doi:10.1016/S0378-1119(00)00247-X. PMID 10940552. 
  2. ^ Bouslam N, Bouhouche A, Benomar A, Hanein S, Klebe S, Azzedine H, Di Giandomenico S, Boland-Auge A, Santorelli FM, Durr A, Brice A, Yahyaoui M, Stevanin G (Apr 2007). "A novel locus for autosomal recessive spastic ataxia on chromosome 17p". Hum Genet 121 (3–4): 413–20. doi:10.1007/s00439-007-0328-0. PMID 17273843. 
  3. ^ a b "Entrez Gene: ANKFY1 ankyrin repeat and FYVE domain containing 1". http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=51479. 

Further reading