symbol withdrawn SMCR

Preferred Label : symbol withdrawn SMCR;

Obsolete resource : true;

Approved symbol HGNC : SMCR;

Alias symbols HGNC : SMS;

Chromosome HGNC : 17p11.2;

Locus type HGNC : other;

Détails

Origin ID

HGNC:11113;

Automatic exact mappings (from CISMeF team)
- Smith-magenis syndrome [OMIM Phenotype]
- Spermine synthase [OMIM gene]
Replaced by
- retinoic acid induced 1 [HGNC gene]

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