RUNDC3B |
DYNC1I1 |
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---|---|---|---|
Gene Name | RUN domain containing 3B | dynein, cytoplasmic 1, intermediate chain 1 | |
Image | No pdb structure | No pdb structure | |
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 3 interactors: CSNK1G1 CSNK1G2 DYNC1I1 | 31 interactors: ANXA7 BICD1 C2orf44 CADM4 CDKN1A DNM2 DYNLL1 DYNLL2 DYNLRB1 DYNLT1 DYNLT3 EMILIN1 FAM110A FAM83D FBP1 GRB7 GSK3B KAT7 MCC NAGK NUDT21 PIN1 RAP1GAP RCC1 RUNDC3B SMN1 STAU1 TAOK1 TK1 TRIM58 UBC | |
Entrez ID | 154661 | 1780 | |
HPRD ID | 15274 | 04798 | |
Ensembl ID | ENSG00000105784 | ENSG00000158560 | |
Uniprot IDs | Q96NL0 | A4D1I7 B4DME3 F5H050 G5E9K1 O14576 Q8N542 Q8TBF7 | |
PDB IDs | |||
Enriched GO Terms of Interacting Partners? |
|
||
Tagcloud ? | 10q24
17p13
cgh
cnvs
congenital
deletions
dlx5
duplications
eexons
encompassing
enhancer
enhancers
exonic
exons
families
foot
fourth
hearing
hs1642
kb
malformation
microdeletions
shfm
shfm1
split
syndromic
telomeric
tp63
unrelated
|
||
Tagcloud (Difference) ? | 10q24
17p13
cgh
cnvs
congenital
deletions
dlx5
duplications
eexons
encompassing
enhancer
enhancers
exonic
exons
families
foot
fourth
hearing
hs1642
kb
malformation
microdeletions
shfm
shfm1
split
syndromic
telomeric
tp63
unrelated
|
||
Tagcloud (Intersection) ? |