Protein Ercc5

URN urn:agi-llid:2073
Connectivity 12
Name Ercc5
Description excision repair cross-complementing rodent repair deficiency, complementation group 5
Notes Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum, complementation group G) is involved in excision repair of UV-induced DNA damage. Mutations cause Cockayne syndrome, which is characterized by severe growth defects, mental retardation, and cachexia. Multiple alternatively spliced transcript variants encoding distinct isoforms have been described, but the biological validity of all variants has not been determined. [provided by RefSeq]

Pathway nucleotide excision repair pathway

GO Molecular Function catalytic activity
hydrolase activity
protein N-terminus binding
DNA binding
protein homodimerization activity
double-stranded DNA binding
single-stranded DNA binding
bubble DNA binding
metal ion binding
magnesium ion binding
nuclease activity
endonuclease activity
endodeoxyribonuclease activity

GO Cellular Component nucleoplasm
DNA-directed RNA polymerase II, holoenzyme
holo TFIIH complex
nucleus

GO Biological Process multicellular organism growth
determination of adult lifespan
negative regulation of apoptosis
DNA repair
nucleotide-excision repair, DNA incision, 3'-to lesion
nucleotide-excision repair
nucleotide-excision repair, DNA damage removal
transcription-coupled nucleotide-excision repair
response to DNA damage stimulus
response to UV
UV protection
response to UV-C

Ariadne Ontology DNA repair

Group DNA repair
catalytic activity
multicellular organism growth
determination of adult lifespan
negative regulation of apoptosis
DNA repair
nucleotide-excision repair, DNA incision, 3'-to lesion
nucleotide-excision repair
nucleotide-excision repair, DNA damage removal
transcription-coupled nucleotide-excision repair
response to DNA damage stimulus
response to UV
UV protection
response to UV-C
hydrolase activity
protein N-terminus binding
DNA binding
protein homodimerization activity
double-stranded DNA binding
single-stranded DNA binding
bubble DNA binding
metal ion binding
magnesium ion binding
nuclease activity
endonuclease activity
endodeoxyribonuclease activity
nucleoplasm
DNA-directed RNA polymerase II, holoenzyme
holo TFIIH complex
nucleus

MedScan ID 2073

Hugo ID 3437

Human chromosome position 13q33

LocusLink ID 2073
22592
301382

Alias XPG
UVDR
XPGC
COFS3
ERCM2
RP11-484I6.5
DNA repair protein complementing XP-G cells
excision repair protein
XPG-complementing protein
DNA excision repair protein ERCC-5
xeroderma pigmentosum, complementation group G
xeroderma pigmentosum group G-complementing protein
xeroderma pigmentosum complementation group G protein
MGC176031
DNA repair protein complementing XP-G cells homolog
OTTMUSP00000023812
xeroderma pigmentosum group G-complementing protein homolog
excision repair cross-complementing rodent repair deficiency, complementation group 5
complementation group 5
complementation group V
DNA excision repair protein ERCC V
DNA repair XPGC
DNA-repair protein complementing XP-G cells
ERCC5
Excision repair cross-complementing rodent repair deficiency, complementation group 5 (xeroderma pigmentosum complementation group G (Cockayne syndrome))
OTTHUMP00000064902
xeroderma pigmentosum complementing group G
Xeroderma pigmentosum group G complementing protein
XPG_HUMAN

Organism Homo sapiens
Mus musculus
Rattus norvegicus

GenBank ID NC_000013
NM_000123
NP_000114
NT_009952
NW_001838084
NW_925517
NG_007146
AC_000145
AC_000056
AF255433
AAF89177
AAF89178
AAF89179
AF255436
AF550128
AAN46091
AL157769
CAI14529
CAI14530
CAI14531
CH471085
EAX09071
EAX09072
X71341
CAA50481
X71342
AF462447
AAP97715
AK294708
BAG57863
AK299758
BAG61647
AK303558
BAG64582
BC031522
AAH31522
BQ707436
BX647399
D16305
BAA03812
L20046
AAC37533
X69978
CAA49598
P28715
Q9HD60
Q9NR54
DQ891818
ABM82744
DQ895006
ABM85932
NC_000067
NM_011729
NP_035859
NT_039170
NW_001030671
AC_000023
AC123800
CH466589
EDK96888
U39892
AAB17885
U39893
U39894
U39895
U39896
U40073
U40431
U40432
U40668
U40669
U40670
U40792
U40793
U40794
U40795
AK038822
BAC30139
AK047192
AK137563
BAE23409
AK140825
AK160581
BAE35888
AK160645
BAE35937
AK164205
BAE37682
BC033413
BC053034
BC060659
AAH60659
BC092235
BC141070
AAI41071
D16306
BAA03813
U40796
AAA91039
P35689
Q3TPQ3
Q3TUN4
Q3TUT3
Q3UV64
Q6P9Q0
Q8CAG2
NC_005108
NM_001106910
NW_047814
NW_001084882
AC_000077
CH473965
EDL99134

OMIM ID 133530
214150
278780

Mouse chromosome position 1 26.6 cM

GO ID 0003677
0000405
0003690
0004520
0004519
0016787
0046872
0047485
0042803
0003697
0009650
0008340
0035264
0043066
0000718
0006295
0009411
0010225
0006283
0016591
0005675
0005654
0005634
0003824
0004518
0006281
0006289
0006974
0000287

Rat chromosome position 9q22

Swiss-Prot Accession P28715
Q9HD60
Q9NR54
Q3UV64
P35689
Q3TPQ3
Q3TUN4
Q3TUT3
Q6P9Q0
Q8CAG2
A6NGT4
Q5JUS4
Q5JUS5
Q7Z2V3
Q8IZL6
Q8N1B7
Q9HD59

PIR ID I58009
S35993

Unigene ID Hs.258429
Mm.2213
Rn.208330

KEGG ID hsa:2073
mmu:22592
rno:301382

EC Number 3.1.-.-

Swiss-Prot ID ERCC5_HUMAN
Q3UV64_MOUSE

Cell Localization Nucleus

IPI ID IPI00477535
IPI00640241
IPI00875692
IPI00848102
IPI00005267
IPI00552845
IPI00310463
IPI00460333
IPI00408780
IPI00357888
IPI00777181
IPI00763212

Homologene ID 37265

RGD ID 1586176

MGI ID 103582