Description |
family with sequence similarity 168 member A |
defective in cullin neddylation 1 domain containing 1 |
Image |
No pdb structure |
|
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
|
|
Interacting Genes |
75 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
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
|
33 interacting genes:
ABRAXAS2
ARIH1
ARIH2
ARRDC3
AURKB
CALM1
CAND1
CDIP1
CUL5
DAZAP2
DVL2
FAM168A
GMPPA
LAPTM5
LZTS2
MAP3K1
NEDD4
PLEKHB2
RHOA
RNF11
SMAD2
SUSD6
TLE5
TMEM239
TP53BP2
TRIM39
TRIM54
TRIM8
UBC
UBE2D3
UBE2F
UBE2M
VPS37B
|
Entrez ID |
23201 |
54165 |
HPRD ID |
13792 |
12067 |
Ensembl ID |
ENSG00000054965
|
ENSG00000043093
|
Uniprot IDs |
Q92567
|
B4DM76
C9JVE2
Q96GG9
|
PDB IDs |
|
3TDU
3TDZ
4P5O
5UFI
5V83
5V86
5V88
6B5Q
6BG3
6BG5
6P5V
6P5W
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
|
|
Tagcloud (Difference) ? |
|
|
Tagcloud (Intersection) ? |
|