HIVEP3 |
FHL1 |
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Gene Name | human immunodeficiency virus type I enhancer binding protein 3 | four and a half LIM domains 1 | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process |
|
||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 5 interactors: FHL1 RUNX2 TNFRSF1B TRAF1 TRAF2 | 19 interactors: AKAP12 CBX4 DBN1 DEAF1 EED FHL2 HES1 HIVEP3 MYBPC1 PDE4DIP PRNP RBPJ RING1 SRF SRPK1 TTN TXNIP UBE2E2 USP15 | |
Entrez ID | 59269 | 2273 | |
HPRD ID | 09442 | 02157 | |
Ensembl ID | ENSG00000127124 | ENSG00000022267 | |
Uniprot IDs | Q5T1R4 | B7Z9A1 Q13642 | |
PDB IDs | 1X63 2CUP 2CUR 2EGQ | ||
Enriched GO Terms of Interacting Partners? |
|
|
|
Tagcloud ? | alterations
attracted
candidates
cdh13
chip
coincided
correlations
date
displaying
disturbance
epigenome
explain
h3k4me3
hpse2
il4r
immunological
inverse
mcns
microarray
mononuclear
nephrology
nephrotic
prkd2
probes
q
qrt
trimethylation
validate
variations
|
764g
atrophy
biopsy
bodies
boy
cardiomyopathy
distal
dreifuss
dystrophy
echocardiogram
emery
exon
hemizygous
hypertrophic
linked
missense
muscle
muscular
myopathy
occurring
pathology
postural
predominantly
reducing
scapuloperoneal
sequencing
vacuolar
wasting
weakness
|
|
Tagcloud (Difference) ? | alterations
attracted
candidates
cdh13
chip
coincided
correlations
date
displaying
disturbance
epigenome
explain
h3k4me3
hpse2
il4r
immunological
inverse
mcns
microarray
mononuclear
nephrology
nephrotic
prkd2
probes
q
qrt
trimethylation
validate
variations
|
764g
atrophy
biopsy
bodies
boy
cardiomyopathy
distal
dreifuss
dystrophy
echocardiogram
emery
exon
hemizygous
hypertrophic
linked
missense
muscle
muscular
myopathy
occurring
pathology
postural
predominantly
reducing
scapuloperoneal
sequencing
vacuolar
wasting
weakness
|
|
Tagcloud (Intersection) ? |