EGLN1 - Gene browser

EGLN1

egl-9 family hypoxia inducible factor 1

HCNC Approved Symbol: EGLN1 (HGNC:1232)
Genomic Coordinates: 1:231,363,756 - 231,422,287 (1q42.2)
Synonyms: SM-20, PHD2, ZMYND6, HIFPH2, C1orf12
Disease Associations: This gene is associated with the following 2 diseases in OMIM.

0Patient

There are no patients diagnosed with a variant in the EGLN1 gene.

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

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