| Name |
flotillin 1 |
calpain 10 |
| Structure |
|
No pdb structure
|
| GO Annotations |
Cellular Component |
|
|
| Molecular Function |
|
|
| Biological Process |
|
|
| Pathways |
|
|
| Diseases |
None
|
|
| GWAS |
- Autism spectrum disorder or schizophrenia ( 28540026
)
- Cutaneous lupus erythematosus ( 25827949
)
- Decreased fine motor function in Charcot-Marie-Tooth disease 1A (eating with utensils) ( 30958311
)
- General cognitive ability ( 29844566
)
- Handedness (non-right-handed vs right-handed) ( 31504236
)
- Hip circumference adjusted for BMI ( 34021172
)
- Schizophrenia ( 30285260
)
- Sleep duration ( 25469926
)
- Ulcerative colitis ( 20848476
)
|
No GWAS studies recorded
|
| Interacting Genes |
26 interacting genes:
ANXA1
APP
ARG1
AURKB
BANP
CAPN10
CBL
CCDC102B
COX5B
FAM90A1
FLOT2
FYN
GOLM1
HGS
INCENP
NGB
NME7
PSMD4
RSPH1
SHBG
SORBS1
SORBS2
SORBS3
SRPK1
UBC
VHL
|
5 interacting genes:
EFNB1
FANCC
FLOT1
PSMA7
SHD
|
| Entrez ID |
10211 |
11132 |
| HPRD ID |
06105
|
05595
|
| Ensembl ID |
ENSG00000137312
|
ENSG00000142330
|
| Uniprot IDs |
O75955
Q5ST80
|
Q9HC96
|
| PDB IDs |
9BQ2
|
Not available
|
| GO Terms Enriched among Interactors |
|
None
|