Gene Name |
survival of motor neuron 2, centromeric |
small nuclear ribonucleoprotein polypeptides B and B1 |
Image |
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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 |
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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48 interactors:
ASCC2
BANP
C14orf1
CALCOCO2
CD2BP2
CDKN2A
CEP55
CLNS1A
COIL
CTDP1
DAB1
DDX20
DHX9
FNBP4
GEMIN4
GEMIN5
GEMIN6
GEMIN7
GIGYF2
GOLGA2
IL7R
KRT40
L3MBTL3
LSM11
LSM2
LSM8
PNMA1
PRMT5
PRMT7
PSMA3
RBPMS
RFX6
SKIV2L
SMN1
SMN2
SMNDC1
SNRPD1
SNRPD3
SNUPN
SS18L1
STRAP
STXBP2
STXBP3
TFIP11
TOP3B
TRIM23
WBP4
WDR77
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Entrez ID |
6607 |
6628 |
HPRD ID |
09036 |
01655 |
Ensembl ID |
ENSG00000205571
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ENSG00000125835
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Uniprot IDs |
B4DP61
Q16637
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P14678
Q66K91
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PDB IDs |
1G5V
1MHN
2LEH
3S6N
4A4E
4A4G
4GLI
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1D3B
2Y9A
2Y9B
2Y9C
2Y9D
3CW1
3PGW
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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
|
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Tagcloud (Intersection) ? |
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