Gene Name |
small nuclear ribonucleoprotein D2 polypeptide 16.5kDa |
survival of motor neuron 2, centromeric |
Image |
|
|
Gene Ontology Annotations |
Cellular Component |
|
|
Molecular Function |
|
|
Biological Process |
|
|
Pathways |
|
|
Drugs |
|
|
Diseases |
|
|
GWAS |
|
|
Protein-Protein Interactions |
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
|
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 |
6633 |
6607 |
HPRD ID |
03038 |
09036 |
Ensembl ID |
ENSG00000125743
|
ENSG00000205571
|
Uniprot IDs |
P62316
|
B4DP61
Q16637
|
PDB IDs |
1B34
1VU2
1VU3
2Y9A
2Y9B
2Y9C
2Y9D
3CW1
3PGW
3S6N
4F77
|
1G5V
1MHN
2LEH
3S6N
4A4E
4A4G
4GLI
|
Enriched GO Terms of Interacting Partners? |
|
|
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) ? |
|