Description |
chromosome 1 open reading frame 94 |
family with sequence similarity 168 member A |
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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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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76 interacting genes:
ALKBH4
ATXN1
ATXN1L
BOLL
C10orf55
C1orf94
CALCOCO2
CAMK2A
DAB1
DAZAP2
DCUN1D1
DTX2
EPN2
EPN3
FAM168B
FBXW5
HGS
HIP1
HR
KLHL42
KRTAP19-1
KRTAP19-5
KRTAP19-7
KRTAP3-1
KRTAP3-3
KRTAP6-2
KRTAP7-1
KRTAP8-1
LASP1
MEIS2
NAF1
NFYC
OTUB2
OTULIN
PATZ1
PDE2A
PEF1
PITX1
PLEKHB2
PROP1
PRR20A
PRR20B
PRR20C
PRR20D
PRR20E
PSORS1C1
R3HDM2
RBFOX1
RBPMS
RBPMS2
RHOXF2
RNF216
RPS27A
SECISBP2
SF1
SMAP2
SNRPC
SS18L1
TAX1BP1
TFAP2D
TFG
TIAL1
TNIP1
TNK1
TOLLIP
UBA52
UBAC1
UBASH3B
UBC
UBE2V1
UBQLN2
UBXN6
UBXN7
VPS37C
YOD1
YTHDF1
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Entrez ID |
84970 |
23201 |
HPRD ID |
11310 |
13792 |
Ensembl ID |
ENSG00000142698
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ENSG00000054965
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Uniprot IDs |
Q6P1W5
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Q92567
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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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