G2Cdb::Gene report
- Gene id
- G00002207
- Gene symbol
- CTTN (HGNC)
- Species
- Homo sapiens
- Description
- cortactin
- Orthologue
- G00000958 (Mus musculus)
Diseases (3)
| Disease |
Nervous effect |
Mutations Found |
Literature |
Mutations Type |
Genetic association? |
| D00000220: Hearing impairment (autosomal recessive nonsyndromic) |
Y |
Y |
(17211611) |
No mutation found (N) |
N |
| D00000021: Colon cancer |
N |
Y |
(17192196) |
Splice variant (SpVar) |
Y |
| D00000015: Oesophageal squamous cell carcinoma |
N |
Y |
(17178864) |
Copy Number Polymorphism (CNP) |
Y |
References
Literature (118)
Pubmed - human_disease
Pubmed - other
Gene lists (5)
| Gene List |
Source |
Species |
Name |
Description |
Gene count |
| L00000009 |
G2C |
Homo sapiens |
Human PSD |
Human orthologues of mouse PSD adapted from Collins et al (2006) |
1080 |
| L00000015 |
G2C |
Homo sapiens |
Human NRC |
Human orthologues of mouse NRC adapted from Collins et al (2006) |
186 |
| L00000016 |
G2C |
Homo sapiens |
Human PSP |
Human orthologues of mouse PSP adapted from Collins et al (2006) |
1121 |
| L00000034 |
G2C |
Homo sapiens |
Pocklington H3 |
Human orthologues of cluster 3 (mouse) from Pocklington et al (2006) |
30 |
| L00000071 |
G2C |
Homo sapiens |
BAYES-COLLINS-MOUSE-PSD-FULL |
Mouse cortex PSD full list (ortho) |
1556 |
