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EBP and GJB2
Data Source:
BioGRID
(two hybrid)
EBP
GJB2
Description
EBP cholestenol delta-isomerase
gap junction protein beta 2
Image
GO Annotations
Cellular Component
Nuclear Envelope
Endoplasmic Reticulum
Endoplasmic Reticulum Membrane
Integral Component Of Plasma Membrane
Cytoplasmic Vesicle
Endoplasmic Reticulum-Golgi Intermediate Compartment
Cytosol
Plasma Membrane
Integral Component Of Plasma Membrane
Gap Junction
Connexin Complex
Lateral Plasma Membrane
Cell Body
Perinuclear Region Of Cytoplasm
Astrocyte Projection
Molecular Function
C-8 Sterol Isomerase Activity
Steroid Delta-isomerase Activity
Transmembrane Signaling Receptor Activity
Protein Binding
Identical Protein Binding
Xenobiotic Transmembrane Transporter Activity
Cholestenol Delta-isomerase Activity
Gap Junction Channel Activity
Calcium Ion Binding
Protein Binding
Identical Protein Binding
Gap Junction Channel Activity Involved In Cell Communication By Electrical Coupling
Biological Process
Skeletal System Development
Cholesterol Biosynthetic Process
Cholesterol Metabolic Process
Sterol Biosynthetic Process
Cholesterol Biosynthetic Process Via Desmosterol
Cholesterol Biosynthetic Process Via Lathosterol
Xenobiotic Transport
Response To Ischemia
Cell-cell Signaling
Aging
Sensory Perception Of Sound
Cell Communication By Electrical Coupling
Gap Junction Assembly
Response To Estradiol
Response To Lipopolysaccharide
Response To Retinoic Acid
Response To Progesterone
Cellular Response To Oxidative Stress
Response To Human Chorionic Gonadotropin
Response To Antibiotic
Decidualization
Inner Ear Development
Transmembrane Transport
Cellular Response To Glucagon Stimulus
Cellular Response To Dexamethasone Stimulus
Epididymis Development
Gap Junction-mediated Intercellular Transport
Pathways
Cholesterol biosynthesis via desmosterol
Cholesterol biosynthesis via lathosterol
Oligomerization of connexins into connexons
Transport of connexins along the secretory pathway
Gap junction assembly
Transport of connexons to the plasma membrane
Drugs
Tamoxifen
Diseases
Keratitis-ichthyosis-deafness syndrome
Palmoplantar keratoderma with deafness
Deafness, autosomal dominant
Deafness, autosomal recessive
Vohwinkel syndrome, including: Vohwinkel syndrome (VS); Vohwinkel syndrome with ichthyosis
GWAS
Facial emotion recognition (happy faces) (
28608620
)
Interacting Genes
171 interacting genes:
ABHD16A
ANKRD46
APP
AQP6
ARL13B
ARL6IP6
ARV1
ATP13A1
BMP10
BNIP3
BTN2A2
C2
C2CD2L
C4orf3
C5
C5orf46
CCDC167
CCL4L2
CD40
CD69
CD81
CDIPT
CHODL
CLDND2
CREB3
CREB3L1
CYB561
CYB5B
CYP4F2
DEFB103A
DEFB103B
DEFB127
DNAJC30
EBPL
EMC6
EMP1
ERG28
ERGIC3
ESRRG
FA2H
FAM209A
FAXDC2
FCER1G
FETUB
FIS1
FKBP8
FUNDC2
FXYD3
FXYD6
GIMAP1
GIMAP5
GJB2
GJB6
GLP1R
GOSR2
GPR152
HMOX2
HSD17B13
IER3IP1
INSIG2
JAGN1
LDLRAD1
LEMD1
LPCAT2
LRP10
LRRC59
LTC4S
MFSD6
MITF
MMP14
MS4A13
MTNR1B
NAT8
NDUFA3
NDUFB11
NEU1
NINJ1
NINJ2
NKG7
ODF4
ORMDL1
ORMDL2
ORMDL3
OTOP3
PLLP
PLP2
PLPP6
PMP22
PNLIPRP1
PTPN9
PVR
RNF152
RTP2
RUSF1
SACM1L
SCAMP4
SEC22B
SERP1
SERP2
SFXN5
SLC35G1
SLC3A2
SLC41A2
SMAGP
SMCO4
SMIM1
SMIM3
SNORC
STX12
STX1B
STX5
STX6
STX7
STX8
SYNGR1
SYNJ2BP
SYS1
TBC1D20
THBD
TIMM23
TLCD1
TLCD4
TMBIM6
TMEM100
TMEM11
TMEM120B
TMEM140
TMEM147
TMEM14B
TMEM14C
TMEM167B
TMEM199
TMEM203
TMEM208
TMEM218
TMEM222
TMEM229B
TMEM239
TMEM242
TMEM243
TMEM254
TMEM31
TMEM42
TMEM51
TMEM60
TMEM65
TMEM86A
TMEM86B
TMEM97
TMIE
TRARG1
TREX1
TSNARE1
TSPO2
UBE2J1
UBIAD1
UNC50
UNC93B1
USE1
VAMP1
VAMP2
VAMP3
VAMP4
VAPA
VAPB
YIF1A
YIPF1
YIPF4
YIPF6
ZDHHC24
ZFPL1
43 interacting genes:
AMIGO1
APLNR
AQP6
ARL13B
CAV1
CD14
CNST
CREB3
EBP
ERGIC3
FAM209A
FFAR2
GJA5
GJA8
GJB1
GJB6
GPR152
GPR42
HSD17B13
KCNK5
KLRC1
LHFPL5
LMNA
LRRC4C
MFSD6
MS4A6E
PEX12
PLEKHB2
SAR1A
SHISAL1
SLC18A1
SLC30A2
SSMEM1
TBXA2R
TEX29
TIMMDC1
TLCD4
TM2D2
TMEM106A
TMEM237
TMEM31
TMX2
TRHR
Entrez ID
10682
2706
HPRD ID
02192
00413
Ensembl ID
ENSG00000147155
ENSG00000165474
Uniprot IDs
A0A024QYX0
Q15125
H9U1J4
P29033
PDB IDs
6OHT
6OHU
1XIR
2ZW3
3IZ1
3IZ2
5ER7
5ERA
5KJ3
5KJG
6UVR
6UVS
6UVT
Enriched GO Terms of Interacting Partners
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