Description |
keratin 35 |
SET and MYND domain containing 1 |
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 |
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- Night sleep phenotypes ( 27126917)
- Retinal detachment or retinal break ( 31816047)
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Interacting Genes |
87 interacting genes:
ABI3
ATG9A
BCAS2
C1orf109
C21orf58
CCDC120
CCDC185
CCDC196
CCHCR1
CD33
CTSZ
DMRT3
DTNB
EFCAB3
ENKD1
EXOSC5
FAM221B
FRS3
HAPLN2
HCK
HDAC4
HGS
HOXA1
HOXC8
KCTD9
KDM1A
KIFC3
KLHL38
KRT1
KRT2
KRT3
KRT4
KRT5
KRT6A
KRT6B
KRT6C
KRT71
KRT72
KRT74
KRT75
KRT77
KRT78
KRT79
KRT8
KRT80
KRT81
KRT82
KRT83
KRT85
KRT86
LENG1
LGALS14
LONRF1
MAPKBP1
MCRS1
MYO15B
OIP5
OTX1
PKN1
POU4F2
PRPF18
PRPF31
PRR35
RUNX1T1
SCNM1
SHC3
SLC43A2
SMARCE1
SMYD1
TAPBPL
TBC1D21
TBC1D30
TBC1D7
TCEANC
TCHP
TEKT4
TEPSIN
TLE5
TRIM29
TSG101
TXLNA
TXLNB
UBASH3A
USP2
VPS9D1
ZNF417
ZNF446
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44 interacting genes:
ARID5A
BACH2
BHLHE40
C11orf1
C11orf16
C11orf53
CCDC113
CCDC33
DISC1
DVL1
FAM166A
FAM204A
FAM83A
FAM86C1P
H3-5
HDAC2
HDAC3
HDHD3
HMG20A
HOMEZ
KIF16B
KRT35
LENG8
MDFI
MEOX2
MYH7B
NACA
NEFL
OGDHL
PATZ1
POU6F2
PRR22
RBM4B
RSPH6A
RUSC1
SNX11
SPAG8
TBRG1
TTC33
USP54
UTP14A
WDR77
ZBTB3
ZBTB44
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Entrez ID |
3886 |
150572 |
HPRD ID |
04138 |
06025 |
Ensembl ID |
ENSG00000197079
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ENSG00000115593
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Uniprot IDs |
Q92764
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E9PHG3
Q5HYE8
Q8NB12
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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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