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RP22 retinitis pigmentosa 22 (autosomal recessive) [ Homo sapiens (human) ]

Gene ID: 6114, updated on 31-Aug-2024

Summary

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Official Symbol
RP22provided by HGNC
Official Full Name
retinitis pigmentosa 22 (autosomal recessive)provided by HGNC
Primary source
MIM:602594
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo

Genomic context

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Location:
16p12.3-p12.1

Bibliography

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Related articles in PubMed

  1. Homozygosity mapping of autosomal recessive retinitis pigmentosa locus (RP22) on chromosome 16p12.1-p12.3. Finckh U, et al. Genomics, 1998 Mar 15. PMID 9545639

GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
retinitis pigmentosa 22 (autosomal recessive)
OMIM: 602594GeneReviews: Not available

General gene information

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Markers

Property

  • phenotype only

Gene LinkOut

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