HNRNPUL1 |
SMN2 |
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Gene Name | heterogeneous nuclear ribonucleoprotein U-like 1 | survival of motor neuron 2, centromeric | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
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 | 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 | |
Entrez ID | 11100 | 6607 | |
HPRD ID | 10428 | 09036 | |
Ensembl ID | ENSG00000105323 | ENSG00000205571 | |
Uniprot IDs | B7Z4B8 Q9BUJ2 | B4DP61 Q16637 | |
PDB IDs | 1G5V 1MHN 2LEH 3S6N 4A4E 4A4G 4GLI | ||
Enriched GO Terms of Interacting Partners? |
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Tagcloud ? | 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) ? |