FEZF1

FEZF1
Identifiers
Aliases FEZF1, FEZ, ZNF312B, HH22, FEZ family zinc finger 1
External IDs MGI: 1920441 HomoloGene: 19252 GeneCards: FEZF1
Orthologs
Species Human Mouse
Entrez

389549

73191

Ensembl

ENSG00000128610

ENSMUSG00000029697

UniProt

A0PJY2

Q0VDQ9

RefSeq (mRNA)

NM_001024613
NM_001160264

NM_028462

RefSeq (protein)

NP_001019784.2
NP_001153736.1

NP_082738.1

Location (UCSC) Chr 7: 122.3 – 122.31 Mb Chr 6: 23.25 – 23.25 Mb
PubMed search [1] [2]
Wikidata
View/Edit HumanView/Edit Mouse

FEZ family zinc finger 1 is a protein that in humans is encoded by the FEZF1 gene. [3]

Clinical significance

Mutations in FEZF1 cause Kallmann Syndrome .[4]

References

  1. "Human PubMed Reference:".
  2. "Mouse PubMed Reference:".
  3. "Entrez Gene: FEZ family zinc finger 1". Retrieved 2014-09-09.
  4. Kotan, L. D.; Hutchins, B. I.; Ozkan, Y; Demirel, F; Stoner, H; Cheng, P. J.; Esen, I; Gurbuz, F; Bicakci, Y. K.; Mengen, E; Yuksel, B; Wray, S; Topaloglu, A. K. (2014). "Mutations in FEZF1 Cause Kallmann Syndrome". The American Journal of Human Genetics. 95 (3): 326–31. doi:10.1016/j.ajhg.2014.08.006. PMID 25192046.

Further reading


This article is issued from Wikipedia - version of the 5/20/2016. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.