symbol withdrawn SCKL2

Preferred Label : symbol withdrawn SCKL2;

Obsolete resource : true;

Approved symbol HGNC : SCKL2;

Chromosome HGNC : 18p11.31-q11.2;

Locus type HGNC : phenotype;

Details

Origin ID

HGNC:20805;

Automatic exact mappings (from CISMeF team)
- Seckel syndrome 2 [OMIM Phenotype]
Replaced by
- RB binding protein 8, endonuclease [HGNC gene]

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