Incidental Mutation 'IGL00427:Xrcc1'
| ID |
5306 |
| Institutional Source |
Australian Phenomics Network
(link to record)
|
| Gene Symbol |
Xrcc1
|
| Ensembl Gene |
ENSMUSG00000051768 |
| Gene Name |
X-ray repair complementing defective repair in Chinese hamster cells 1 |
| Synonyms |
Xrcc-1 |
| Accession Numbers |
|
| Essential gene? |
Essential
(E-score: 1.000)
|
| Stock # |
IGL00427
|
| Quality Score |
|
|
Status
|
|
| Chromosome |
7 |
| Chromosomal Location |
24246124-24272863 bp(+) (GRCm39) |
| Type of Mutation |
critical splice donor site (2 bp from exon) |
| DNA Base Change (assembly) |
T to A
at 24247309 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000146105
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000011776]
[ENSMUST00000063249]
[ENSMUST00000205573]
|
| AlphaFold |
Q60596 |
| Predicted Effect |
probably benign
Transcript: ENSMUST00000011776
|
| SMART Domains |
Protein: ENSMUSP00000011776
Gene: ENSMUSG00000011632
| Domain | Start | End | E-Value | Type |
|---|
|
signal peptide
|
1 |
24 |
N/A |
INTRINSIC |
|
LU
|
27 |
123 |
9.63e-2 |
SMART |
|
Pfam:UPAR_LY6
|
126 |
191 |
1.3e-8 |
PFAM |
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000063249
|
| SMART Domains |
Protein: ENSMUSP00000070995
Gene: ENSMUSG00000051768
| Domain | Start | End | E-Value | Type |
|---|
|
Pfam:XRCC1_N
|
1 |
151 |
6.9e-66 |
PFAM |
|
low complexity region
|
212 |
238 |
N/A |
INTRINSIC |
|
low complexity region
|
278 |
294 |
N/A |
INTRINSIC |
|
BRCT
|
317 |
393 |
8e-19 |
SMART |
|
low complexity region
|
407 |
424 |
N/A |
INTRINSIC |
|
low complexity region
|
444 |
459 |
N/A |
INTRINSIC |
|
BRCT
|
538 |
617 |
5.5e-9 |
SMART |
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000205561
|
| Predicted Effect |
probably null
Transcript: ENSMUST00000205573
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000206067
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000206620
|
| Predicted Effect |
noncoding transcript
Transcript: ENSMUST00000206889
|
| Coding Region Coverage |
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] The protein encoded by this gene is involved in the efficient repair of DNA single-strand breaks formed by exposure to ionizing radiation and alkylating agents. This protein interacts with DNA ligase III, polymerase beta and poly (ADP-ribose) polymerase to participate in the base excision repair pathway. It may play a role in DNA processing during meiogenesis and recombination in germ cells. A rare microsatellite polymorphism in this gene is associated with cancer in patients of varying radiosensitivity. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous null mutants accumulate unrepaired DNA strand breaks in the egg cylinder, show increased cell death in epiblast, developmental arrest at embryonic day 6.5, morphological anomalies in visceral embryonic endoderm by day 7.5 and die by day 8.5. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 42 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adcy3 |
A |
G |
12: 4,244,357 (GRCm39) |
D289G |
probably damaging |
Het |
| Adnp |
C |
T |
2: 168,024,482 (GRCm39) |
D938N |
probably benign |
Het |
| Arpin |
T |
A |
7: 79,577,423 (GRCm39) |
N208I |
probably benign |
Het |
| Cby3 |
A |
G |
11: 50,248,638 (GRCm39) |
|
probably benign |
Het |
| Cmklr2 |
A |
T |
1: 63,222,497 (GRCm39) |
I246N |
probably damaging |
Het |
| Cnih4 |
T |
A |
1: 180,981,312 (GRCm39) |
S28T |
probably damaging |
Het |
| D130052B06Rik |
G |
T |
11: 33,573,558 (GRCm39) |
V97L |
possibly damaging |
Het |
| Dchs1 |
T |
C |
7: 105,407,631 (GRCm39) |
E2067G |
probably damaging |
Het |
| Dennd6a |
C |
T |
14: 26,329,768 (GRCm39) |
T113I |
probably damaging |
Het |
| Dock4 |
T |
A |
12: 40,882,305 (GRCm39) |
F1590L |
possibly damaging |
Het |
| Dop1a |
G |
T |
9: 86,403,553 (GRCm39) |
Q1582H |
probably benign |
Het |
| Dop1a |
A |
T |
9: 86,403,552 (GRCm39) |
Q1582L |
probably damaging |
Het |
| Dop1a |
C |
A |
9: 86,403,551 (GRCm39) |
Q1582K |
possibly damaging |
Het |
| Ebna1bp2 |
A |
T |
4: 118,483,018 (GRCm39) |
K291M |
probably damaging |
Het |
| Evpl |
G |
T |
11: 116,125,331 (GRCm39) |
Q73K |
probably benign |
Het |
| Fam131b |
G |
T |
6: 42,295,895 (GRCm39) |
T139K |
probably damaging |
Het |
| Golga3 |
A |
G |
5: 110,368,753 (GRCm39) |
T1358A |
probably damaging |
Het |
| Hgf |
G |
A |
5: 16,783,484 (GRCm39) |
D265N |
probably benign |
Het |
| Homer1 |
A |
G |
13: 93,538,622 (GRCm39) |
N333S |
probably benign |
Het |
| Igkv17-134 |
A |
T |
6: 67,697,968 (GRCm39) |
|
probably benign |
Het |
| Il16 |
T |
C |
7: 83,301,666 (GRCm39) |
D152G |
probably benign |
Het |
| Ireb2 |
T |
C |
9: 54,806,766 (GRCm39) |
|
probably benign |
Het |
| Itgb2 |
C |
T |
10: 77,393,790 (GRCm39) |
T410I |
probably benign |
Het |
| Kctd14 |
C |
A |
7: 97,106,919 (GRCm39) |
A111E |
possibly damaging |
Het |
| Lmod3 |
A |
C |
6: 97,229,258 (GRCm39) |
V92G |
probably damaging |
Het |
| Lmtk2 |
A |
G |
5: 144,070,973 (GRCm39) |
D83G |
probably damaging |
Het |
| Myh1 |
A |
G |
11: 67,111,691 (GRCm39) |
E1682G |
probably damaging |
Het |
| Myo9a |
T |
A |
9: 59,750,342 (GRCm39) |
|
probably benign |
Het |
| Nlrc4 |
T |
C |
17: 74,754,087 (GRCm39) |
N99D |
probably benign |
Het |
| P2rx3 |
A |
G |
2: 84,865,616 (GRCm39) |
Y10H |
probably damaging |
Het |
| Pcsk7 |
C |
A |
9: 45,838,958 (GRCm39) |
D623E |
probably benign |
Het |
| Plxna1 |
A |
G |
6: 89,297,980 (GRCm39) |
I1766T |
probably damaging |
Het |
| Ptk7 |
T |
C |
17: 46,885,353 (GRCm39) |
Y691C |
probably damaging |
Het |
| Rec8 |
A |
T |
14: 55,856,108 (GRCm39) |
T17S |
probably damaging |
Het |
| Rtraf-ps |
A |
C |
3: 88,484,230 (GRCm39) |
|
probably benign |
Het |
| Ryr1 |
T |
C |
7: 28,804,162 (GRCm39) |
|
probably benign |
Het |
| Scg3 |
T |
G |
9: 75,570,519 (GRCm39) |
K345T |
probably damaging |
Het |
| Serpina3b |
A |
T |
12: 104,099,200 (GRCm39) |
K238N |
probably benign |
Het |
| Slc38a9 |
T |
A |
13: 112,838,152 (GRCm39) |
S306T |
probably damaging |
Het |
| Txndc16 |
A |
G |
14: 45,382,547 (GRCm39) |
|
probably benign |
Het |
| Vmn1r238 |
T |
A |
18: 3,123,243 (GRCm39) |
Y57F |
probably benign |
Het |
| Vmn2r104 |
A |
T |
17: 20,258,501 (GRCm39) |
S548T |
probably damaging |
Het |
|
| Other mutations in Xrcc1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01830:Xrcc1
|
APN |
7 |
24,272,767 (GRCm39) |
utr 3 prime |
probably benign |
|
|
IGL02349:Xrcc1
|
APN |
7 |
24,266,467 (GRCm39) |
nonsense |
probably null |
|
|
IGL02433:Xrcc1
|
APN |
7 |
24,264,979 (GRCm39) |
missense |
possibly damaging |
0.96 |
|
IGL03131:Xrcc1
|
APN |
7 |
24,272,719 (GRCm39) |
nonsense |
probably null |
|
|
Bilberry
|
UTSW |
7 |
24,269,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R0090:Xrcc1
|
UTSW |
7 |
24,269,642 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R0517:Xrcc1
|
UTSW |
7 |
24,269,744 (GRCm39) |
splice site |
probably benign |
|
|
R0612:Xrcc1
|
UTSW |
7 |
24,269,744 (GRCm39) |
splice site |
probably benign |
|
|
R1234:Xrcc1
|
UTSW |
7 |
24,267,270 (GRCm39) |
missense |
possibly damaging |
0.71 |
|
R1577:Xrcc1
|
UTSW |
7 |
24,265,052 (GRCm39) |
nonsense |
probably null |
|
|
R1796:Xrcc1
|
UTSW |
7 |
24,247,252 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1863:Xrcc1
|
UTSW |
7 |
24,270,000 (GRCm39) |
missense |
possibly damaging |
0.65 |
|
R3788:Xrcc1
|
UTSW |
7 |
24,266,333 (GRCm39) |
missense |
probably benign |
0.08 |
|
R3794:Xrcc1
|
UTSW |
7 |
24,269,985 (GRCm39) |
missense |
probably benign |
0.05 |
|
R4806:Xrcc1
|
UTSW |
7 |
24,269,905 (GRCm39) |
missense |
probably benign |
0.14 |
|
R5206:Xrcc1
|
UTSW |
7 |
24,266,988 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5414:Xrcc1
|
UTSW |
7 |
24,269,643 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R5532:Xrcc1
|
UTSW |
7 |
24,267,353 (GRCm39) |
critical splice donor site |
probably null |
|
|
R5624:Xrcc1
|
UTSW |
7 |
24,259,270 (GRCm39) |
missense |
possibly damaging |
0.57 |
|
R5990:Xrcc1
|
UTSW |
7 |
24,267,293 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6603:Xrcc1
|
UTSW |
7 |
24,270,459 (GRCm39) |
nonsense |
probably null |
|
|
R6669:Xrcc1
|
UTSW |
7 |
24,246,762 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R6716:Xrcc1
|
UTSW |
7 |
24,266,571 (GRCm39) |
critical splice donor site |
probably null |
|
|
R6881:Xrcc1
|
UTSW |
7 |
24,246,776 (GRCm39) |
nonsense |
probably null |
|
|
R7227:Xrcc1
|
UTSW |
7 |
24,246,757 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8204:Xrcc1
|
UTSW |
7 |
24,271,709 (GRCm39) |
missense |
possibly damaging |
0.88 |
|
R8284:Xrcc1
|
UTSW |
7 |
24,271,703 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8285:Xrcc1
|
UTSW |
7 |
24,271,703 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8287:Xrcc1
|
UTSW |
7 |
24,271,703 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R9015:Xrcc1
|
UTSW |
7 |
24,271,642 (GRCm39) |
missense |
probably benign |
0.05 |
|
R9607:Xrcc1
|
UTSW |
7 |
24,265,690 (GRCm39) |
missense |
probably benign |
0.17 |
|
X0019:Xrcc1
|
UTSW |
7 |
24,272,553 (GRCm39) |
missense |
probably damaging |
1.00 |
|
X0024:Xrcc1
|
UTSW |
7 |
24,272,504 (GRCm39) |
missense |
probably damaging |
1.00 |
|
Z1176:Xrcc1
|
UTSW |
7 |
24,247,264 (GRCm39) |
missense |
probably benign |
0.31 |
|
| Posted On |
2012-04-20 |
Incidental Mutation