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RSS Russell Silver syndrome [ Homo sapiens (human) ]

Gene ID: 140821, discontinued on 24-Sep-2024

Summary

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Official Symbol
RSSprovided by HGNC
Official Full Name
Russell Silver syndromeprovided by HGNC
Primary source
MIM:180860
Gene type
unknown
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as
SRS

Genomic context

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Location:
17q25

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
Russell Silver syndrome
OMIM: 180860GeneReviews: Not available

General gene information

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Other Names

  • Russell-Silver dwarfism

Property

  • phenotype only

Gene LinkOut

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