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RP21 retinitis pigmentosa 21 [ Homo sapiens (human) ]

Gene ID: 8020, discontinued on 17-Nov-2010
Official Symbol
RP21provided by HGNC
Official Full Name
retinitis pigmentosa 21provided by HGNC
Primary source
HGNC:HGNC:13434
See related
MIM:500004
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
RPD1

GeneRIFs: Gene References Into FunctionsWhat's a GeneRIF?

Associated conditions

Description Tests
retinitis pigmentosa 21
GeneReviews: Not available

Other Names

  • Retinitis pigmentosa-deafness syndrome, autosomal dominant

Property

  • phenotype only
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