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EFEMP2 and TLX3
Data Source:
BioGRID
(two hybrid)
EFEMP2
TLX3
Description
EGF containing fibulin extracellular matrix protein 2
T cell leukemia homeobox 3
Image
No pdb structure
GO Annotations
Cellular Component
Microfibril
Extracellular Region
Basement Membrane
Extracellular Matrix
Collagen-containing Extracellular Matrix
Extracellular Exosome
Elastic Fiber
Extracellular Vesicle
Chromatin
Nucleus
Nucleoplasm
Molecular Function
Extracellular Matrix Structural Constituent
Calcium Ion Binding
Protein Binding
Heparin Binding
Protein Homodimerization Activity
RNA Polymerase II Cis-regulatory Region Sequence-specific DNA Binding
DNA-binding Transcription Factor Activity, RNA Polymerase II-specific
Protein Binding
Sequence-specific Double-stranded DNA Binding
Biological Process
Aorta Development
Elastic Fiber Assembly
Aorta Smooth Muscle Tissue Morphogenesis
Vascular Associated Smooth Muscle Cell Development
Regulation Of Collagen Fibril Organization
Positive Regulation Of Collagen Fibril Organization
Negative Regulation Of Vascular Associated Smooth Muscle Cell Proliferation
Positive Regulation Of Aortic Smooth Muscle Cell Differentiation
Positive Regulation Of Smooth Muscle Cell-matrix Adhesion
Neuron Migration
Regulation Of Respiratory Gaseous Exchange By Nervous System Process
Regulation Of Transcription By RNA Polymerase II
Central Nervous System Development
Respiratory Gaseous Exchange By Respiratory System
Negative Regulation Of Neuron Differentiation
Animal Organ Development
Neuron Fate Specification
Pathways
Molecules associated with elastic fibres
Molecules associated with elastic fibres
Drugs
Diseases
Cutis laxa, including: Autosomal dominant cutis laxa (ADCL); Autosomal recessive cutis laxa I (ARCL1); Autosomal recessive cutis laxa II (ARCL2); X-linked recessive cutis laxa (XRCL); Wrinkly skin syndrome
Acute lymphoblastic leukemia (ALL) (precursor T lymphoblastic leukemia)
GWAS
Acne (severe) (
24927181
)
Adult body size (
32376654
)
Birth weight (
31043758
)
Body size at age 10 (
32376654
)
Retinal detachment or retinal break (
31816047
)
Body size at age 10 (
32376654
)
Interacting Genes
130 interacting genes:
ADAMTSL4
AMMECR1
ANAPC11
AP1M1
APEX2
AQP1
ARRDC3
ATN1
ATXN1
ATXN7
BAG6
C3
C5orf24
CACNA1A
CATSPER1
CCDC33
CCND3
CCNK
CDPF1
CLPP
CNNM3
COL8A1
CREB5
CXCL5
CYSRT1
DGCR6
DOK7
FAM107A
FAM110A
FAM124B
FAM74A4
FAM90A1
FBXW5
FTO
GFI1B
GLRX3
HDAC4
HHEX
HHIPL1
HOXA1
HPCAL1
HSD3B7
HSPA12B
HSPBP1
IGFBP6
IL16
INCA1
ITGB5
KLF1
KRTAP10-8
KRTAP11-1
KRTAP12-2
KRTAP13-3
KRTAP19-5
KRTAP26-1
KRTAP3-2
LBX1
LCE1A
LCE1C
LCE1E
LCE2C
LCE2D
LCE3A
LCE3C
LCE3D
LCE3E
LINGO1
LNX1
MDFI
MEOX2
MRPL12
MXI1
NEDD4L
NOS3
NR1D2
NTM
NUFIP2
OTX1
P2RX7
PIDD1
PITX1
PLSCR1
PLSCR4
PROP1
PRPF31
PRR32
PTGER3
RAB40B
RBAK
RBP3
RBPMS
RERE
RHOXF2
RHPN1
RIBC2
RNF138
SGTA
SGTB
SLC16A5
SLC23A1
SLC25A48
SPACA9
SPATA24
SPATA3
SPATA8
SPRY4
STK16
TCAF1
THAP7
TLE5
TLX3
TP53
TRIB3
TRIM42
UBQLN1
UBQLN4
USP21
ZNF263
ZNF345
ZNF426
ZNF558
ZNF57
ZNF581
ZNF587
ZNF638
ZNF670
ZNF699
ZNF768
ZNF774
ZNF837
106 interacting genes:
ACY1
AKAP9
ANKRD10
ANKRD33
AOC1
APBB1IP
ARMC5
ASB12
ATP6V0D1
B9D2
BPIFA1
C11orf1
C11orf45
C19orf54
C2orf42
CEACAM6
CRX
CSNK2B
CTNNA3
DENND4A
EFEMP2
ERAS
FAM166B
FAM168B
FCSK
FNTB
FOSB
FOXH1
GGTLC2
GOLGA6L9
GTF2A1L
H2BC11
HNRNPUL1
HOPX
HSPB2
HSPB2-C11orf52
HYI
IGFL2
ING4
INTS11
IRF9
ITIH6
KRT34
KRTAP11-1
KRTAP13-3
KRTAP19-1
KRTAP19-7
KRTAP3-1
KRTAP6-1
KRTAP6-2
KRTAP6-3
KRTAP7-1
KRTAP8-1
LASP1
LMO2
MAGED1
MEIS1
METTL27
MORN5
MSX2
NDUFAB1
NHLRC4
NICN1
OIP5
PLA2G10
PLAAT1
POU2AF1
POU6F2
PPP1CC
PQBP1
PRR20A
PRR20B
PRR20C
PRR20D
PRR20E
PSMB11
REL
ROR2
RSKR
SERPINE1
SLC15A2
SMU1
SNTA1
SP1
SPATA46
SPRYD7
STH
SYNGAP1
TBX22
TCIRG1
TEKT5
TEX37
THTPA
TLE1
TLE2
TMEM42
TOX2
TP53BP1
TRIM42
UFSP1
WDR83
YPEL3
ZBTB32
ZNF34
ZNF41
ZNF44
Entrez ID
30008
30012
HPRD ID
05221
06868
Ensembl ID
ENSG00000172638
ENSG00000164438
Uniprot IDs
A0A024R5G1
O95967
Q9H3D5
O43711
PDB IDs
2KL7
Enriched GO Terms of Interacting Partners
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Tagcloud (Intersection)
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