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HPE1 holoprosencephaly 1, alobar [ Homo sapiens (human) ]

Gene ID: 3244, updated on 2-Oct-2019

Summary

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Gene symbol
HPE1
Gene description
holoprosencephaly 1, alobar
Primary source
MIM:236100
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
HPEC

Genomic context

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Location:
21q22.3

Bibliography

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Related articles in PubMed

  1. Physical mapping of the holoprosencephaly critical region in 21q22.3, exclusion of SIM2 as a candidate gene for holoprosencephaly, and mapping of SIM2 to a region of chromosome 21 important for Down syndrome. Muenke M, et al. Am J Hum Genet, 1995 Nov. PMID 7485157, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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holoprosencephaly 1, alobar

General gene information

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Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases