| Description |
DiGeorge syndrome critical region gene 6 |
chromosome 1 open reading frame 94 |
| 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 |
- High light scatter reticulocyte count ( 32888494)
- High light scatter reticulocyte percentage of red cells ( 32888494)
- Metabolite levels ( 23823483)
- Plasma free amino acid levels ( 30659259)
- Plasma free amino acid levels (adjusted for twenty other PFAAs) ( 30659259)
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- Generalized epilepsy ( 22949513)
- Lateral ventricle temporal horn volume ( 31530798)
- Pediatric nonalcoholic steatohepatitis ( 28918882)
- Sleep duration (short sleep) ( 30846698)
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| Interacting Genes |
66 interacting genes:
ADAMTSL4
AGTRAP
AKAP8L
APP
ARNT2
C1orf94
C3orf62
CBLL1
CBY2
CCDC33
CEP126
CTBP1
DEUP1
DLGAP2
DLX2
DNPEP
DOCK8
EFEMP2
EFHC2
ENKD1
ESS2
FBF1
FH
GOLGA2
GSE1
HGS
HOMEZ
IHO1
IKZF3
INIP
KLHL12
KRTAP12-2
LZTS2
MBIP
MEIS2
MEOX2
MIA2
MID2
MIPOL1
NAB2
NECAB2
NOTCH2NLA
NQO2
NUP54
NUP62
PDLIM7
PRDM14
RABGEF1
REL
RFX6
RIMBP3
SPRY2
SS18L1
TCF12
TCF4
TFIP11
TLE5
TRAF1
TRAF2
TRIM27
TUBGCP4
VCP
ZBED1
ZC4H2
ZNF398
ZNF446
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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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| Entrez ID |
8214 |
84970 |
| HPRD ID |
03177 |
11310 |
| Ensembl ID |
ENSG00000183628
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ENSG00000142698
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| Uniprot IDs |
Q14129
X5D7D2
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Q6P1W5
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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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