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PTLAH patella aplasia-hypoplasia [ Homo sapiens (human) ]

Gene ID: 8830, updated on 2-Oct-2019

Summary

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Gene symbol
PTLAH
Gene description
patella aplasia-hypoplasia
Primary source
MIM:168860
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
FPAH

Genomic context

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Location:
17q

Bibliography

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Related articles in PubMed

  1. Localization of a gene for familial patella aplasia-hypoplasia (PTLAH) to chromosome 17q21-22. Mangino M, et al. Am J Hum Genet, 1999 Aug. PMID 10417287, Free PMC Article

GeneRIFs: Gene References Into Functions

Phenotypes

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patella aplasia-hypoplasia

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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Molecular Biology Databases