Description |
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1 |
coiled-coil domain containing 136 |
Image |
No pdb structure |
No pdb structure |
GO Annotations |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
|
- Reading disability or specific language impairment (pleiotropy) ( 25065397)
- Reading disability or specific language impairment adjusted for intelligence quotient (pleiotropy) ( 25065397)
|
Interacting Genes |
64 interacting genes:
AMOTL2
AR
ARID2
BAZ1B
BRAP
BRMS1
CCDC136
CCDC172
CDR2
CEP170P1
CEP63
CEP70
DISC1
EPS8
ESR1
ESR2
EXOC7
GATA1
GOLGA2
ING5
ITCH
JAKMIP2
KIFC3
KLF1
KRT15
KRT31
KRT40
KRTAP10-9
MDM2
MED4
MEOX2
MIPOL1
MRFAP1L1
MTUS2
NBPF22P
NCOA1
NCOA2
NCOA3
NOTCH2NLA
NR0B2
NR3C1
NUP62
PGR
PRMT5
RALBP1
RARB
RCOR1
RELB
RINT1
SIN3A
SIN3B
SMAD1
SMARCA4
SPAG5
SRC
STX11
SYCE1
TFE3
TFIP11
TNIK
TRIM54
TRIP10
TXLNA
USHBP1
|
64 interacting genes:
ABT1
AQP1
ATP5PO
ATXN1
BARD1
BLOC1S6
BYSL
C1orf216
CBX8
CCDC146
CCHCR1
CDC5L
CDK2AP1
CEP57L1
COIL
CWF19L2
DISC1
ENKD1
FAM107A
FAM161A
GFI1B
HAUS1
HDAC4
HGS
HMG20A
HMG20B
JMY
KANSL1
KAT5
KIFC3
LENG1
MAGEB4
MOS
NDN
NEBL
PDLIM5
PKN2
PPP1R18
PRPF31
PSMD9
RAB33A
SHFL
SMARCE1
TBRG1
TCEA2
TNNT1
TXLNA
UBQLN4
USP2
WT1
ZBTB38
ZC2HC1C
ZNF20
ZNF230
ZNF250
ZNF408
ZNF417
ZNF490
ZNF564
ZNF572
ZNF581
ZNF587
ZNF688
ZSCAN26
|
Entrez ID |
6605 |
64753 |
HPRD ID |
04382 |
10887 |
Ensembl ID |
ENSG00000073584
|
ENSG00000128596
|
Uniprot IDs |
A0A024R1S7
Q969G3
|
A0A024R758
Q96JN2
|
PDB IDs |
|
|
Enriched GO Terms of Interacting Partners? |
|
|
Tagcloud ? |
|
|
Tagcloud (Difference) ? |
|
|
Tagcloud (Intersection) ? |
|