SMN2 |
SNRPD2 |
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Gene Name | survival of motor neuron 2, centromeric | small nuclear ribonucleoprotein D2 polypeptide 16.5kDa | |
Image | |||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS |
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Protein-Protein Interactions | 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 | 25 interactors: CEP70 CLNS1A DDX20 DMTN EEF1G EGFR GEMIN2 GEMIN4 GEMIN5 GEMIN6 GEMIN7 IL7R KAT5 LSM2 LSM6 OS9 SMN1 SMN2 SNRPD1 SNRPF STRAP STXBP2 STXBP3 WDR77 ZCCHC10 | |
Entrez ID | 6607 | 6633 | |
HPRD ID | 09036 | 03038 | |
Ensembl ID | ENSG00000205571 | ENSG00000125743 | |
Uniprot IDs | B4DP61 Q16637 | P62316 | |
PDB IDs | 1G5V 1MHN 2LEH 3S6N 4A4E 4A4G 4GLI | 1B34 1VU2 1VU3 2Y9A 2Y9B 2Y9C 2Y9D 3CW1 3PGW 3S6N 4F77 | |
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
|
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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) ? |