| Description |
chromosome 1 open reading frame 94 |
docking protein 6 |
| Image |
No pdb structure |
No pdb structure |
| GO Annotations |
Cellular Component |
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| Molecular Function |
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| Biological Process |
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| Pathways |
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| Drugs |
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| Diseases |
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| GWAS |
- Generalized epilepsy ( 22949513)
- Lateral ventricle temporal horn volume ( 31530798)
- Pediatric nonalcoholic steatohepatitis ( 28918882)
- Sleep duration (short sleep) ( 30846698)
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- Bone fracture in osteoporosis ( 28580392)
- Caudate activity during reward ( 28927378)
- Mean platelet volume ( 31194788)
- Neonatal total 25-hydroxyvitamin D levels (maternal genetic effect) ( 32047095)
- Osteoporosis-related phenotypes ( 20548944)
- Platelet distribution width ( 32888494)
- Pursuit maintenance gain ( 29064472)
- Response to cytidine analogues (gemcitabine) ( 24483146)
- Skin aging (microtopography measurement) ( 28502801)
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| Interacting Genes |
89 interacting genes:
ACTN3
AKAP9
ATRIP
ATXN1
ATXN1L
BANP
BOLA1
BOLA2
BOLA2B
BOLL
BYSL
C1orf109
CAMK2A
CARD9
CCHCR1
CCNJL
CDKN2D
CFAP206
CHERP
CLK1
CRK
CRYBA4
DAB1
DAZAP2
DGCR6
DMRTB1
DOK6
DTX2
FAM168A
FHL3
GCC1
GORASP2
GRB2
GSE1
HGS
HNRNPF
HSF2BP
INTS11
IPO11
KLHL32
KRTAP6-2
KRTAP7-1
KRTAP8-1
LCE2C
LMO2
MAGED1
MAPK1IP1L
MAPK9
MEIS2
MVP
NFKBID
NGB
NR3C1
OAZ3
OIP5
PITX1
PLA2G10
PLEKHB2
PRKAG1
PROP1
PRR20A
PRR20B
PRR20C
PRR20D
PRR20E
R3HDM2
RAD51D
RBFOX1
RBFOX2
RBM47
RBPMS
RFX2
RHOXF2
ROR2
SMAP2
SS18L1
TBX6
TENT5D
TLE5
TNPO2
TNS2
TSC1
TXNDC9
UBQLN2
UBQLN4
USO1
VENTX
VPS37C
YES1
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21 interacting genes:
ABHD11
ARID5A
C1orf94
CD226
CRYBB3
EGFR
ERBB2
FAM86C1P
LASP1
LGALS14
METTL27
NTRK3
PRR22
RBPMS
RET
RUSC1
SLC30A6
TBX15
TLE5
USP54
YPEL3
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| Entrez ID |
84970 |
220164 |
| HPRD ID |
11310 |
13244 |
| Ensembl ID |
ENSG00000142698
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ENSG00000206052
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| Uniprot IDs |
Q6P1W5
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Q6PKX4
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| PDB IDs |
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| Enriched GO Terms of Interacting Partners? |
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| Tagcloud ? |
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| Tagcloud (Difference) ? |
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| Tagcloud (Intersection) ? |
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