Description |
SET and MYND domain containing 1 |
family with sequence similarity 86 member C1, pseudogene |
Image |
No pdb structure |
No pdb structure |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
- Night sleep phenotypes ( 27126917)
- Retinal detachment or retinal break ( 31816047)
|
|
Interacting Genes |
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
|
22 interacting genes:
ANKS1A
BCAS2
C1orf109
CDKN2D
CDR2L
COL8A1
CRACR2A
CSNK2B
CTTNBP2
DOK6
GPSM3
HNRNPF
KRT26
KYNU
MAGED4B
PCSK5
POU4F2
SAT1
SMYD1
SPG21
TRAF1
VENTX
|
Entrez ID |
150572 |
55199 |
HPRD ID |
06025 |
13337 |
Ensembl ID |
ENSG00000115593
|
|
Uniprot IDs |
E9PHG3
Q5HYE8
Q8NB12
|
Q9NVL1
|
PDB IDs |
|
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
|
|
Tagcloud (Difference) ? |
|
|
Tagcloud (Intersection) ? |
|