RCC1 |
DYNC1I1 |
||
---|---|---|---|
Gene Name | regulator of chromosome condensation 1 | dynein, cytoplasmic 1, intermediate chain 1 | |
Image | No pdb structure | ||
Gene Ontology Annotations | Cellular Component | ||
Molecular Function | |||
Biological Process | |||
Pathways | |||
Drugs | |||
Diseases | |||
GWAS | |||
Protein-Protein Interactions | 50 interactors: ACTB APLP1 BAG6 CCT7 CDK1 CDK2AP2 CHGB CHKA CSAD CSNK1A1 DDAH2 DYNC1I1 FAF1 FLAD1 GNB2 HADHB HIST1H3A HIST1H4A HIST2H2AA3 HIST2H2AC HIST2H2BE HMGA1 HOXD8 KMT2B KPNA3 KPNA4 KPNB1 LRIF1 NGFR NTMT1 NUDT21 NUP98 PDHB PKM PTMA RAN RANBP1 RANBP3 RPA1 SDF4 SPRED1 TLE1 TP53 TRMT2A TUBB3 UNC119 USP4 WIZ XPO1 ZNF135 | 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 | 1104 | 1780 | |
HPRD ID | 01559 | 04798 | |
Ensembl ID | ENSG00000180198 | ENSG00000158560 | |
Uniprot IDs | P18754 Q5T081 | A4D1I7 B4DME3 F5H050 G5E9K1 O14576 Q8N542 Q8TBF7 | |
PDB IDs | 1A12 1I2M | ||
Enriched GO Terms of Interacting Partners? |
|
|
|
Tagcloud ? | almost
cellulose
chromosome
column
condensation
consistently
cytoplasm
digestion
dispersed
dnase
eluted
encode
kd
located
locates
maturation
mitotic
nacl
nuclei
onset
p45
prepared
presumably
putative
regulating
regulator
released
sequential
synthetic
|
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) ? | almost
cellulose
chromosome
column
condensation
consistently
cytoplasm
digestion
dispersed
dnase
eluted
encode
kd
located
locates
maturation
mitotic
nacl
nuclei
onset
p45
prepared
presumably
putative
regulating
regulator
released
sequential
synthetic
|
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) ? |