Gene Name |
heterogeneous nuclear ribonucleoprotein U-like 1 |
survival of motor neuron 2, centromeric |
Image |
No pdb structure |
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Gene Ontology 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 |
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Protein-Protein Interactions |
46 interactors:
BRD7
C14orf1
CRMP1
DZIP3
EP300
ERG
EWSR1
GIT2
HNRNPF
HNRNPH2
HNRNPH3
IL7R
ITCH
MAPK1IP1L
MARS
MED31
NEDD4
NXF1
NXF2
NXF3
PIAS4
PPIL1
PRMT1
PRMT2
PRPF40A
RBM22
RBM4
RBM4B
ROPN1
RPA1
RPA2
SF1
SF3B4
SMN1
SMN2
SNRPB2
SNRPC
SORBS3
SRSF9
TGM2
TLX3
TP53
TP53BP2
VPS37C
WWP2
ZNF207
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24 interactors:
BLOC1S6
BYSL
CHTOP
DDX20
DHX9
FAM9B
FBL
GAR1
GEMIN2
HNRNPUL1
POLR1C
POLR2A
PPIG
SMN1
SNRPB
SNRPB2
SNRPD1
SNRPD2
SNRPD3
SNRPE
SNRPF
SNRPG
TIAL1
VPS28
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Entrez ID |
11100 |
6607 |
HPRD ID |
10428 |
09036 |
Ensembl ID |
ENSG00000105323
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ENSG00000205571
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Uniprot IDs |
B7Z4B8
Q9BUJ2
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B4DP61
Q16637
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PDB IDs |
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1G5V
1MHN
2LEH
3S6N
4A4E
4A4G
4GLI
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Enriched GO Terms of Interacting Partners? |
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Tagcloud ? |
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atrophy
centromeric
compensate
copies
copy
degeneration
deletions
detectable
display
donor
easily
exon
fails
fatal
harbor
hindering
homozygous
infant
intragenic
italian
modifier
muscular
null
predictable
sma
smn1
splice
unusually
weakness
|
Tagcloud (Difference) ? |
|
atrophy
centromeric
compensate
copies
copy
degeneration
deletions
detectable
display
donor
easily
exon
fails
fatal
harbor
hindering
homozygous
infant
intragenic
italian
modifier
muscular
null
predictable
sma
smn1
splice
unusually
weakness
|
Tagcloud (Intersection) ? |
|