symbol withdrawn MRX21

Preferred Label : symbol withdrawn MRX21;

Obsolete resource : true;

Approved symbol HGNC : MRX21;

Chromosome HGNC : Xp22.3-p21.1;

Locus type HGNC : phenotype;

Détails

Origin ID

HGNC:7251;

Automatic exact mappings (from CISMeF team)
- Intellectual developmental disorder, X-linked 21 [OMIM Phenotype]
Replaced by
- interleukin 1 receptor accessory protein like 1 [HGNC gene]

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