symbol withdrawn MRT5

Preferred Label : symbol withdrawn MRT5;

Obsolete resource : true;

Approved symbol HGNC : MRT5;

Chromosome HGNC : 5p15-p14;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:39146;

Automatic exact mappings (from CISMeF team)
- Intellectual developmental disorder, autosomal recessive 5 [OMIM Phenotype]
Replaced by
- NOP2/Sun RNA methyltransferase 2 [HGNC gene]

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