CDH9 (cadherin 9)

2014-11-01  

Identity

HGNC
LOCATION
5p14.1
LOCUSID
ALIAS
-

Other Information

Locus ID:

NCBI: 1007
MIM: 609974
HGNC: 1768
Ensembl: ENSG00000113100

Variants:

dbSNP: 1007
ClinVar: 1007
TCGA: ENSG00000113100
COSMIC: CDH9

RNA/Proteins

Gene IDTranscript IDUniprot
ENSG00000113100ENST00000231021Q9ULB4
ENSG00000113100ENST00000511822D6RBT9
ENSG00000113100ENST00000513289E7EPN0

Expression (GTEx)

0
1
2
3
4
5
6
7

Pathways

PathwaySourceExternal ID
Cell-Cell communicationREACTOMER-HSA-1500931
Cell junction organizationREACTOMER-HSA-446728
Cell-cell junction organizationREACTOMER-HSA-421270
Adherens junctions interactionsREACTOMER-HSA-418990

Protein levels (Protein atlas)

Not detected
Low
Medium
High

References

Pubmed IDYearTitleCitations
194042562009Common genetic variants on 5p14.1 associate with autism spectrum disorders.389
210796072011A genome-wide association study on common SNPs and rare CNVs in anorexia nervosa.67
176680452007Cadherin-9 is a novel cell surface marker for the heterogeneous pool of renal fibroblasts.8
228469072012Analysis of four genes involved in the neurodevelopment shows association of rs4307059 polymorphism in the cadherin 9/10 region with completed suicide.3

Citation

Dessen P

CDH9 (cadherin 9)

Atlas Genet Cytogenet Oncol Haematol. 2014-11-01

Online version: http://atlasgeneticsoncology.org/gene/61649/cdh9