Protein Rbbp8

URN urn:agi-llid:5932
Total Entities 0
Connectivity 66
Name Rbbp8
Description retinoblastoma binding protein 8
Notes The protein encoded by this gene is a ubiquitously expressed nuclear protein. It is found among several proteins that bind directly to retinoblastoma protein, which regulates cell proliferation. This protein complexes with transcriptional co-repressor CTBP. It is also associated with BRCA1 and is thought to modulate the functions of BRCA1 in transcriptional regulation, DNA repair, and/or cell cycle checkpoint control. It is suggested that this gene may itself be a tumor suppressor acting in the same pathway as BRCA1. Three transcript variants encoding two different isoforms have been found for this gene. More transcript variants exist, but their full-length natures have not been determined. [provided by RefSeq, Jul 2008]

GO Molecular Function RNA polymerase II repressing transcription factor binding
DNA binding
damaged DNA binding
hydrolase activity
nuclease activity
endonuclease activity
single-stranded DNA specific endodeoxyribonuclease activity
RNA polymerase II transcription corepressor activity

GO Cellular Component transcriptional repressor complex
nucleus

GO Biological Process cell division
cell cycle
G1-S transition of mitotic cell cycle
cell cycle checkpoint
G2-M transition DNA damage checkpoint
mitosis
meiosis
negative regulation of transcription from RNA polymerase II promoter
regulation of transcription from RNA polymerase II promoter
DNA double-strand break processing involved in repair via single-strand annealing
nucleic acid phosphodiester bond hydrolysis
DNA repair
double-strand break repair via homologous recombination
response to DNA damage stimulus
blastocyst hatching

Pathway Double Strand DNA Homologous Repair
ataxia telangiectasia-mutated (ATM) signaling pathway
homologous recombination pathway of double-strand break repair

Group cell division
cell cycle
G1-S transition of mitotic cell cycle
cell cycle checkpoint
G2-M transition DNA damage checkpoint
mitosis
meiosis
negative regulation of transcription from RNA polymerase II promoter
regulation of transcription from RNA polymerase II promoter
DNA double-strand break processing involved in repair via single-strand annealing
nucleic acid phosphodiester bond hydrolysis
DNA repair
double-strand break repair via homologous recombination
response to DNA damage stimulus
blastocyst hatching
RNA polymerase II repressing transcription factor binding
DNA binding
damaged DNA binding
hydrolase activity
nuclease activity
endonuclease activity
single-stranded DNA specific endodeoxyribonuclease activity
RNA polymerase II transcription corepressor activity
transcriptional repressor complex
nucleus

MedScan ID 5932
347729

Hugo ID 9891

Human chromosome position 18q11.2

GenBank ID NC_000018
NM_002894
NP_002885
NM_203292
NP_976037
NM_203291
NP_976036
NG_012121
NC_018929
AC_000150
AC091147
AC106033
CH471088
EAX01143
EAX01144
EAX01145
EAX01146
AF043431
AAC34368
AK292481
BAF85170
BC001170
BC030590
AAH30590
BG723261
BU187672
BX648221
U72066
AAC14371
Q99708
DQ890956
ABM81882
DQ894119
ABM85045
NC_000084
NM_001252495
NP_001239424
NR_045527
NM_001081223
NP_001074692
NR_045526
AC_000040
NW_001035533
AC090479
AC115894
AK037049
AK041384
AK047433
AK048254
AK077614
AK087007
AK163908
BC019665
AAH19665
BC027367
AAH27367
BC050849
AAH50849
CD352622
CX567593
Q80YR6
NC_005117
NM_001134417
NP_001127889
AC_000086
CH474073
EDL86683
BC162012
AAI62012
FQ209715
FQ230337
B1WC58

LocusLink ID 5932
225182
291787
347729

Alias RIM
CTIP
JWDS
SAE2
SCKL2
DNA endonuclease RBBP8
RBBP-8
CTBP-interacting protein
sporulation in the absence of SPO11 protein 2 homolog
9930104E21Rik
retinoblastoma-binding protein 8
RGD1308872
rCG_41266
CTBP-interactive protein CtIP
Retinoblastoma-interactive protein and myosin-like
retinoblastoma-interactive myosin-like
Retinoblastoma-interacting protein and myosin-like
retinoblastoma-interacting myosin-like
retinoblastoma binding protein VIII
retinoblastoma binding protein 8
CtBP interacting protein
HGCN
RBBP8
CtBP interactive protein
CTBP-interacting protein CtIP
OTTHUMP00000162575
9930104E21
Seckel syndrome 2

Organism Homo sapiens
Mus musculus
Rattus norvegicus

OMIM ID 604124
251255
606744

Unigene ID Hs.546282
Mm.154275
Rn.128724

KEGG ID hsa:5932
mmu:225182
rno:291787

Swiss-Prot Accession Q99708
A6NKN2
Q80YR6
B1WC58
A8K8W6
E7ETY1
O75371
Q8NHQ3

EC Number 3.1.-.-

GO ID 0001103
0001106
0003684
0000014
0010792
0006281
0000082
0031572
0001835
0000075
0051301
0000724
0007126
0007067
0000122
0006357
0005634
0017053
0003677
0004519
0016787
0004518
0007049
0090305
0006974

Swiss-Prot ID COM1_MOUSE
COM1_RAT
COM1_HUMAN

Cell Localization Nucleus

IPI ID IPI00342157
IPI00363470
IPI00480111

Mouse chromosome position 18

Rat chromosome position 18p13

Homologene ID 28546

MGI ID 2442995

RGD ID 1308872