Incidental Mutation 'R6766:Parp1'
| ID |
531902 |
| Institutional Source |
Beutler Lab
|
| Gene Symbol |
Parp1
|
| Ensembl Gene |
ENSMUSG00000026496 |
| Gene Name |
poly (ADP-ribose) polymerase family, member 1 |
| Synonyms |
5830444G22Rik, sPARP-1, PARP, Adprt1, parp-1, Adprp |
| MMRRC Submission |
044882-MU
|
| Accession Numbers |
|
| Essential gene? |
Probably essential
(E-score: 0.813)
|
| Stock # |
R6766 (G1)
|
| Quality Score |
225.009 |
|
Status
|
Not validated
|
| Chromosome |
1 |
| Chromosomal Location |
180396456-180428564 bp(+) (GRCm39) |
| Type of Mutation |
missense |
| DNA Base Change (assembly) |
T to A
at 180425927 bp (GRCm39)
|
| Zygosity |
Heterozygous |
| Amino Acid Change |
Valine to Glutamic Acid
at position 886
(V886E)
|
| Ref Sequence |
ENSEMBL: ENSMUSP00000027777
(fasta)
|
| Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000027777]
|
| AlphaFold |
no structure available at present |
| Predicted Effect |
probably damaging
Transcript: ENSMUST00000027777
AA Change: V886E
PolyPhen 2
Score 0.997 (Sensitivity: 0.41; Specificity: 0.98)
|
| SMART Domains |
Protein: ENSMUSP00000027777
Gene: ENSMUSG00000026496
AA Change: V886E
| Domain | Start | End | E-Value | Type |
|---|
|
zf-PARP
|
12 |
90 |
4.73e-36 |
SMART |
|
zf-PARP
|
116 |
200 |
3.99e-34 |
SMART |
|
low complexity region
|
221 |
234 |
N/A |
INTRINSIC |
|
PADR1
|
280 |
333 |
1.48e-28 |
SMART |
|
low complexity region
|
359 |
378 |
N/A |
INTRINSIC |
|
BRCT
|
388 |
467 |
9.62e-7 |
SMART |
|
low complexity region
|
494 |
512 |
N/A |
INTRINSIC |
|
WGR
|
553 |
633 |
2.36e-31 |
SMART |
|
Pfam:PARP_reg
|
663 |
794 |
4e-54 |
PFAM |
|
Pfam:PARP
|
797 |
1007 |
6.4e-79 |
PFAM |
|
| Predicted Effect |
probably benign
Transcript: ENSMUST00000195560
|
| Coding Region Coverage |
- 1x: 99.9%
- 3x: 99.8%
- 10x: 98.8%
- 20x: 96.7%
|
| Validation Efficiency |
|
| MGI Phenotype |
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] This gene encodes a chromatin-associated enzyme, poly(ADP-ribosyl)transferase, which modifies various nuclear proteins by poly(ADP-ribosyl)ation. The modification is dependent on DNA and is involved in the regulation of various important cellular processes such as differentiation, proliferation, and tumor transformation and also in the regulation of the molecular events involved in the recovery of cell from DNA damage. In addition, this enzyme may be the site of mutation in Fanconi anemia, and may participate in the pathophysiology of type I diabetes. [provided by RefSeq, Jul 2008]
PHENOTYPE: Homozygous ablation of this gene may lead to skin hyperplasia, extreme sensitivity to radiation and alkylating agents, abnormal response to xenobiotics and endogenous compounds, reduced noise-induced hearing loss, altered susceptibility to neurotoxicity,or protection against renal ischemic injury. [provided by MGI curators]
|
| Allele List at MGI |
|
| Other mutations in this stock |
Total: 56 list
| Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
|---|
| Adam32 |
G |
A |
8: 25,362,646 (GRCm39) |
S17L |
probably damaging |
Het |
| Akt3 |
A |
T |
1: 176,877,756 (GRCm39) |
Y337* |
probably null |
Het |
| Ankrd34c |
A |
G |
9: 89,611,381 (GRCm39) |
V320A |
probably benign |
Het |
| Aox1 |
C |
A |
1: 58,388,227 (GRCm39) |
L1112I |
possibly damaging |
Het |
| Arap2 |
A |
C |
5: 62,834,443 (GRCm39) |
|
probably null |
Het |
| Atm |
A |
T |
9: 53,401,582 (GRCm39) |
I1429N |
probably damaging |
Het |
| Ccdc68 |
A |
G |
18: 70,099,861 (GRCm39) |
N290D |
probably damaging |
Het |
| Chst1 |
T |
C |
2: 92,443,542 (GRCm39) |
W5R |
probably damaging |
Het |
| Clip1 |
G |
T |
5: 123,752,827 (GRCm39) |
|
probably benign |
Het |
| Crebbp |
T |
C |
16: 3,935,364 (GRCm39) |
T842A |
probably damaging |
Het |
| Cyp2b13 |
T |
C |
7: 25,781,236 (GRCm39) |
|
probably null |
Het |
| Dnah8 |
G |
A |
17: 30,967,542 (GRCm39) |
D2585N |
probably benign |
Het |
| Dock1 |
T |
A |
7: 134,358,522 (GRCm39) |
|
probably null |
Het |
| Dst |
A |
G |
1: 34,333,564 (GRCm39) |
I4800V |
probably damaging |
Het |
| Efcab7 |
CAAGTAAAGTAA |
CAAGTAA |
4: 99,735,161 (GRCm39) |
|
probably null |
Het |
| Epb41l2 |
C |
T |
10: 25,348,990 (GRCm39) |
Q382* |
probably null |
Het |
| Fam83e |
A |
G |
7: 45,376,070 (GRCm39) |
D261G |
probably damaging |
Het |
| Ifnk |
T |
G |
4: 35,152,134 (GRCm39) |
S21A |
possibly damaging |
Het |
| Ift122 |
A |
G |
6: 115,903,204 (GRCm39) |
H1157R |
probably benign |
Het |
| Ighv1-67 |
T |
C |
12: 115,567,654 (GRCm39) |
K67R |
possibly damaging |
Het |
| Inpp4a |
C |
A |
1: 37,411,422 (GRCm39) |
A97D |
probably damaging |
Het |
| Insm1 |
T |
A |
2: 146,065,346 (GRCm39) |
Y387* |
probably null |
Het |
| Irgm1 |
T |
C |
11: 48,756,928 (GRCm39) |
I294M |
possibly damaging |
Het |
| Isoc2b |
C |
T |
7: 4,854,061 (GRCm39) |
V104M |
probably damaging |
Het |
| Kif2c |
A |
C |
4: 117,024,280 (GRCm39) |
S311R |
probably benign |
Het |
| Morn3 |
G |
A |
5: 123,179,270 (GRCm39) |
A60V |
probably damaging |
Het |
| Oit3 |
T |
C |
10: 59,274,534 (GRCm39) |
N89D |
probably damaging |
Het |
| Or14c40 |
A |
T |
7: 86,313,293 (GRCm39) |
N141I |
probably damaging |
Het |
| Or4c116 |
G |
T |
2: 88,942,640 (GRCm39) |
T72N |
possibly damaging |
Het |
| Or4c127 |
T |
C |
2: 89,832,876 (GRCm39) |
V42A |
probably benign |
Het |
| Or5d44 |
T |
A |
2: 88,142,095 (GRCm39) |
Q15L |
noncoding transcript |
Het |
| Or8b48 |
A |
C |
9: 38,493,069 (GRCm39) |
R165S |
probably damaging |
Het |
| Pan2 |
C |
A |
10: 128,150,381 (GRCm39) |
N708K |
possibly damaging |
Het |
| Pcdha8 |
C |
A |
18: 37,127,753 (GRCm39) |
A745E |
probably benign |
Het |
| Pcyox1 |
C |
T |
6: 86,371,390 (GRCm39) |
|
probably null |
Het |
| Prl2c2 |
A |
T |
13: 13,176,713 (GRCm39) |
|
probably null |
Het |
| Samd1 |
T |
C |
8: 84,726,361 (GRCm39) |
S473P |
possibly damaging |
Het |
| Slc26a1 |
A |
T |
5: 108,819,773 (GRCm39) |
D475E |
probably damaging |
Het |
| Slco1c1 |
T |
C |
6: 141,493,535 (GRCm39) |
V239A |
possibly damaging |
Het |
| Smo |
T |
A |
6: 29,736,044 (GRCm39) |
L12Q |
unknown |
Homo |
| Srpk1 |
C |
T |
17: 28,821,727 (GRCm39) |
R229Q |
possibly damaging |
Het |
| Syn2 |
T |
A |
6: 115,216,362 (GRCm39) |
F191L |
probably damaging |
Het |
| Syngr2 |
T |
C |
11: 117,704,261 (GRCm39) |
V182A |
probably benign |
Het |
| Tarbp1 |
G |
A |
8: 127,174,139 (GRCm39) |
A889V |
probably benign |
Het |
| Tbc1d2b |
T |
C |
9: 90,108,262 (GRCm39) |
T430A |
probably benign |
Het |
| Tmem217 |
T |
A |
17: 29,745,484 (GRCm39) |
Y82F |
probably damaging |
Het |
| Ttll9 |
T |
A |
2: 152,841,220 (GRCm39) |
Y272* |
probably null |
Het |
| Uts2r |
A |
G |
11: 121,052,033 (GRCm39) |
Y299C |
probably damaging |
Het |
| Vsig8 |
T |
A |
1: 172,388,143 (GRCm39) |
M37K |
probably benign |
Het |
| Vwf |
G |
T |
6: 125,616,339 (GRCm39) |
D1218Y |
unknown |
Het |
| Wdr11 |
T |
G |
7: 129,226,036 (GRCm39) |
M727R |
probably benign |
Het |
| Wwc2 |
A |
G |
8: 48,353,826 (GRCm39) |
Y103H |
possibly damaging |
Het |
| Yod1 |
T |
A |
1: 130,647,008 (GRCm39) |
L295* |
probably null |
Het |
| Zfp113 |
G |
T |
5: 138,143,608 (GRCm39) |
S214* |
probably null |
Het |
| Zfp438 |
T |
A |
18: 5,213,780 (GRCm39) |
M393L |
probably benign |
Het |
| Zfp946 |
G |
A |
17: 22,674,752 (GRCm39) |
C502Y |
probably benign |
Het |
|
| Other mutations in Parp1 |
| Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
|---|
|
IGL01147:Parp1
|
APN |
1 |
180,417,145 (GRCm39) |
missense |
probably damaging |
0.99 |
|
IGL01316:Parp1
|
APN |
1 |
180,420,500 (GRCm39) |
splice site |
probably benign |
|
|
IGL01915:Parp1
|
APN |
1 |
180,425,907 (GRCm39) |
missense |
probably damaging |
1.00 |
|
IGL02016:Parp1
|
APN |
1 |
180,426,516 (GRCm39) |
splice site |
probably null |
|
|
IGL03328:Parp1
|
APN |
1 |
180,427,155 (GRCm39) |
splice site |
probably benign |
|
|
IGL03348:Parp1
|
APN |
1 |
180,405,272 (GRCm39) |
splice site |
probably benign |
|
|
IGL03368:Parp1
|
APN |
1 |
180,408,187 (GRCm39) |
missense |
probably benign |
0.01 |
|
R0541:Parp1
|
UTSW |
1 |
180,426,616 (GRCm39) |
missense |
probably benign |
0.05 |
|
R0648:Parp1
|
UTSW |
1 |
180,428,005 (GRCm39) |
splice site |
probably benign |
|
|
R1326:Parp1
|
UTSW |
1 |
180,428,023 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R1421:Parp1
|
UTSW |
1 |
180,427,653 (GRCm39) |
splice site |
probably benign |
|
|
R1438:Parp1
|
UTSW |
1 |
180,418,807 (GRCm39) |
missense |
probably benign |
0.08 |
|
R1781:Parp1
|
UTSW |
1 |
180,415,578 (GRCm39) |
missense |
probably benign |
0.04 |
|
R1800:Parp1
|
UTSW |
1 |
180,428,091 (GRCm39) |
splice site |
probably null |
|
|
R1900:Parp1
|
UTSW |
1 |
180,424,904 (GRCm39) |
missense |
probably damaging |
0.98 |
|
R1903:Parp1
|
UTSW |
1 |
180,416,235 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2869:Parp1
|
UTSW |
1 |
180,401,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2869:Parp1
|
UTSW |
1 |
180,401,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2871:Parp1
|
UTSW |
1 |
180,401,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2871:Parp1
|
UTSW |
1 |
180,401,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2872:Parp1
|
UTSW |
1 |
180,401,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2872:Parp1
|
UTSW |
1 |
180,401,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2873:Parp1
|
UTSW |
1 |
180,401,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R2874:Parp1
|
UTSW |
1 |
180,401,230 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4342:Parp1
|
UTSW |
1 |
180,414,894 (GRCm39) |
missense |
probably benign |
0.00 |
|
R4510:Parp1
|
UTSW |
1 |
180,418,841 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R4511:Parp1
|
UTSW |
1 |
180,418,841 (GRCm39) |
missense |
possibly damaging |
0.59 |
|
R4529:Parp1
|
UTSW |
1 |
180,418,877 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R4740:Parp1
|
UTSW |
1 |
180,417,033 (GRCm39) |
missense |
probably damaging |
0.99 |
|
R4876:Parp1
|
UTSW |
1 |
180,396,600 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
|
R6666:Parp1
|
UTSW |
1 |
180,413,516 (GRCm39) |
missense |
probably benign |
|
|
R6918:Parp1
|
UTSW |
1 |
180,416,235 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R6974:Parp1
|
UTSW |
1 |
180,417,071 (GRCm39) |
nonsense |
probably null |
|
|
R6996:Parp1
|
UTSW |
1 |
180,414,936 (GRCm39) |
missense |
possibly damaging |
0.46 |
|
R7034:Parp1
|
UTSW |
1 |
180,425,817 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7036:Parp1
|
UTSW |
1 |
180,425,817 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7068:Parp1
|
UTSW |
1 |
180,416,233 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R7156:Parp1
|
UTSW |
1 |
180,426,629 (GRCm39) |
missense |
possibly damaging |
0.91 |
|
R7326:Parp1
|
UTSW |
1 |
180,396,665 (GRCm39) |
missense |
possibly damaging |
0.94 |
|
R7603:Parp1
|
UTSW |
1 |
180,427,777 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7733:Parp1
|
UTSW |
1 |
180,427,777 (GRCm39) |
critical splice donor site |
probably null |
|
|
R7772:Parp1
|
UTSW |
1 |
180,416,963 (GRCm39) |
missense |
possibly damaging |
0.54 |
|
R8735:Parp1
|
UTSW |
1 |
180,396,690 (GRCm39) |
missense |
probably benign |
0.04 |
|
R8747:Parp1
|
UTSW |
1 |
180,422,275 (GRCm39) |
missense |
probably damaging |
1.00 |
|
R8782:Parp1
|
UTSW |
1 |
180,417,127 (GRCm39) |
missense |
probably benign |
0.01 |
|
R9243:Parp1
|
UTSW |
1 |
180,415,680 (GRCm39) |
missense |
probably benign |
0.30 |
|
R9268:Parp1
|
UTSW |
1 |
180,415,509 (GRCm39) |
missense |
possibly damaging |
0.95 |
|
| Predicted Primers |
PCR Primer
(F):5'- AAGCTCCCGAGTCTGTTCATC -3'
(R):5'- GAAATTTGGGAGCTCACGGTTG -3'
Sequencing Primer
(F):5'- CATCTCTTGGGTGAACCTGAGTAAC -3'
(R):5'- TTGCTGCCAGCTGAGGAAAG -3'
|
| Posted On |
2018-08-29 |
Incidental Mutation