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ICR1 ichthyosis congenita I, erythromatous lamellar ichthyosis, ichthyosiform erythroderma [ Homo sapiens (human) ]

Gene ID: 3388, discontinued on 2-Oct-2019
  • This record was withdrawn by the HUGO Gene Nomenclature Committee (HGNC).

Summary

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Official Symbol
ICR1provided by HGNC
Official Full Name
ichthyosis congenita I, erythromatous lamellar ichthyosis, ichthyosiform erythrodermaprovided by HGNC
Primary source
HGNC:HGNC:5352
Gene type
unknown
RefSeq status
WITHDRAWN
Organism
Homo sapiens
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Summary
DISCONTINUED: This record was withdrawn by the HUGO Gene Nomenclature Committee (HGNC).

Bibliography

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GeneRIFs: Gene References Into Functions

Phenotypes

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Associated conditions

Description Tests
ichthyosis congenita I, erythromatous lamellar ichthyosis, ichthyosiform erythroderma
GeneReviews: Not available

General gene information

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Property

  • phenotype only

Gene LinkOut

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