13q12.11-CRYL1 Copy Number Variation - CNVPathwayAtlas

13q12.11-CRYL1 Copy Number Variation

Description

Deletion or duplication of the CRYL1 gene located at chromosome 13q12 is a risk factor for psychiatric disorders as reported by (Kirov et al., 2014).

Genomic location

Assembly:

Coordinates:

Disorder Information from Orphanet

This CNV is not yet linked to an OrphaCode.

Molecular pathway

View on WikiPathways

Gene Information

HGNC Gene Name NCBI Ensembl UniProt
CRYL1 crystallin lambda 1 51084 ENSG00000165475 Q9Y2S2

Evidence