Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930507D05Rik |
C |
T |
10: 62,285,441 (GRCm39) |
A55V |
unknown |
Het |
Adra1b |
T |
G |
11: 43,667,028 (GRCm39) |
D403A |
probably benign |
Het |
Ankdd1b |
A |
T |
13: 96,597,405 (GRCm39) |
L9Q |
probably damaging |
Het |
Ankrd17 |
A |
T |
5: 90,426,204 (GRCm39) |
S789R |
possibly damaging |
Het |
B3galnt1 |
A |
G |
3: 69,482,326 (GRCm39) |
S312P |
probably damaging |
Het |
C4bp |
C |
T |
1: 130,583,750 (GRCm39) |
V73M |
probably damaging |
Het |
Ccdc121rt2 |
T |
C |
5: 112,598,019 (GRCm39) |
S189P |
probably benign |
Het |
Cenpe |
T |
A |
3: 134,957,305 (GRCm39) |
N1854K |
probably damaging |
Het |
Chrm2 |
A |
C |
6: 36,500,674 (GRCm39) |
Y177S |
probably damaging |
Het |
Clca4b |
C |
T |
3: 144,633,996 (GRCm39) |
V140I |
probably benign |
Het |
Csad |
A |
G |
15: 102,087,958 (GRCm39) |
S322P |
probably damaging |
Het |
Depdc1b |
T |
G |
13: 108,493,956 (GRCm39) |
Y115D |
probably damaging |
Het |
Dnah17 |
T |
C |
11: 118,020,023 (GRCm39) |
Y8C |
probably damaging |
Het |
Dsg3 |
T |
C |
18: 20,656,817 (GRCm39) |
|
probably null |
Het |
Elf5 |
A |
G |
2: 103,269,697 (GRCm39) |
T93A |
possibly damaging |
Het |
Eogt |
C |
T |
6: 97,122,353 (GRCm39) |
D27N |
possibly damaging |
Het |
Fam118b |
T |
C |
9: 35,146,633 (GRCm39) |
D78G |
probably damaging |
Het |
Fhip2a |
T |
A |
19: 57,370,166 (GRCm39) |
M470K |
probably benign |
Het |
Frem3 |
A |
G |
8: 81,337,781 (GRCm39) |
T25A |
probably benign |
Het |
Gab1 |
C |
A |
8: 81,515,226 (GRCm39) |
R364L |
possibly damaging |
Het |
Golm1 |
T |
C |
13: 59,813,375 (GRCm39) |
Y32C |
probably damaging |
Het |
Has1 |
A |
T |
17: 18,070,207 (GRCm39) |
V238E |
probably damaging |
Het |
Hkdc1 |
T |
C |
10: 62,219,583 (GRCm39) |
R907G |
possibly damaging |
Het |
Igkv4-61 |
C |
A |
6: 69,394,138 (GRCm39) |
A31S |
possibly damaging |
Het |
Krtap24-1 |
C |
T |
16: 88,408,761 (GRCm39) |
V122I |
probably damaging |
Het |
Lrrc10 |
T |
G |
10: 116,881,616 (GRCm39) |
L97V |
probably damaging |
Het |
Map3k20 |
T |
A |
2: 72,232,457 (GRCm39) |
M371K |
probably benign |
Het |
Mis18bp1 |
A |
T |
12: 65,205,317 (GRCm39) |
M2K |
possibly damaging |
Het |
Mob3b |
T |
A |
4: 34,954,049 (GRCm39) |
|
probably null |
Het |
Muc4 |
A |
G |
16: 32,570,607 (GRCm39) |
T556A |
possibly damaging |
Het |
Muc6 |
A |
C |
7: 141,224,032 (GRCm39) |
|
probably benign |
Het |
Ncapg |
A |
T |
5: 45,839,158 (GRCm39) |
L519F |
probably damaging |
Het |
Nfix |
A |
G |
8: 85,453,778 (GRCm39) |
S265P |
probably benign |
Het |
Or13p10 |
T |
A |
4: 118,522,808 (GRCm39) |
F31L |
possibly damaging |
Het |
Or4c121 |
T |
C |
2: 89,023,823 (GRCm39) |
K185R |
probably damaging |
Het |
Or4k49 |
T |
C |
2: 111,494,817 (GRCm39) |
V82A |
probably benign |
Het |
Or52e5 |
T |
C |
7: 104,719,514 (GRCm39) |
L280P |
probably damaging |
Het |
Or8g35 |
C |
A |
9: 39,381,112 (GRCm39) |
K303N |
probably benign |
Het |
Osgin2 |
T |
C |
4: 16,006,410 (GRCm39) |
T95A |
probably benign |
Het |
Pcdh7 |
G |
A |
5: 57,879,046 (GRCm39) |
G867D |
probably damaging |
Het |
Pcdhb22 |
T |
C |
18: 37,652,959 (GRCm39) |
S476P |
possibly damaging |
Het |
Phldb1 |
A |
G |
9: 44,623,197 (GRCm39) |
I619T |
probably damaging |
Het |
Ppp1r13l |
C |
T |
7: 19,105,256 (GRCm39) |
R343C |
probably damaging |
Het |
Rab2b |
T |
A |
14: 52,506,164 (GRCm39) |
|
probably benign |
Het |
Rims2 |
A |
T |
15: 39,373,092 (GRCm39) |
E972V |
probably damaging |
Het |
Slc26a9 |
G |
T |
1: 131,686,228 (GRCm39) |
C337F |
probably benign |
Het |
Spty2d1 |
A |
G |
7: 46,647,751 (GRCm39) |
S393P |
probably damaging |
Het |
Stkld1 |
A |
T |
2: 26,831,093 (GRCm39) |
N90I |
possibly damaging |
Het |
Svep1 |
T |
A |
4: 58,053,126 (GRCm39) |
R3406S |
probably benign |
Het |
Svil |
A |
T |
18: 5,040,171 (GRCm39) |
D48V |
probably benign |
Het |
Thsd7a |
T |
A |
6: 12,555,081 (GRCm39) |
K268* |
probably null |
Het |
Tmc6 |
A |
G |
11: 117,661,326 (GRCm39) |
L618P |
probably damaging |
Het |
Tmem231 |
G |
A |
8: 112,653,524 (GRCm39) |
|
probably benign |
Het |
Ube2q2l |
C |
A |
6: 136,378,099 (GRCm39) |
D244Y |
probably damaging |
Het |
Ubn1 |
A |
G |
16: 4,899,791 (GRCm39) |
H1101R |
probably benign |
Het |
Upf2 |
G |
A |
2: 6,032,150 (GRCm39) |
V899I |
unknown |
Het |
Ush2a |
A |
T |
1: 188,360,763 (GRCm39) |
N2161I |
probably damaging |
Het |
Usp25 |
A |
T |
16: 76,859,330 (GRCm39) |
D276V |
probably damaging |
Het |
Vmn2r68 |
T |
A |
7: 84,882,915 (GRCm39) |
H279L |
probably benign |
Het |
Vps13d |
G |
A |
4: 144,818,850 (GRCm39) |
R3019W |
probably damaging |
Het |
Vsig10 |
A |
T |
5: 117,486,361 (GRCm39) |
E423D |
probably benign |
Het |
Wdfy2 |
T |
A |
14: 63,162,582 (GRCm39) |
F95I |
probably benign |
Het |
Xrn1 |
A |
G |
9: 95,915,763 (GRCm39) |
|
probably null |
Het |
Zdhhc13 |
A |
G |
7: 48,461,149 (GRCm39) |
T362A |
possibly damaging |
Het |
Zfp984 |
C |
T |
4: 147,845,703 (GRCm39) |
S2N |
probably benign |
Het |
|
Other mutations in Parp4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00479:Parp4
|
APN |
14 |
56,853,917 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL00571:Parp4
|
APN |
14 |
56,884,810 (GRCm39) |
missense |
unknown |
|
IGL00737:Parp4
|
APN |
14 |
56,821,620 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00793:Parp4
|
APN |
14 |
56,840,334 (GRCm39) |
missense |
possibly damaging |
0.73 |
IGL01108:Parp4
|
APN |
14 |
56,844,897 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01131:Parp4
|
APN |
14 |
56,823,217 (GRCm39) |
splice site |
probably benign |
|
IGL01485:Parp4
|
APN |
14 |
56,859,661 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL01704:Parp4
|
APN |
14 |
56,839,783 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01993:Parp4
|
APN |
14 |
56,848,245 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL02125:Parp4
|
APN |
14 |
56,827,959 (GRCm39) |
missense |
probably benign |
0.33 |
IGL02851:Parp4
|
APN |
14 |
56,886,326 (GRCm39) |
missense |
unknown |
|
IGL02863:Parp4
|
APN |
14 |
56,886,243 (GRCm39) |
missense |
unknown |
|
IGL03065:Parp4
|
APN |
14 |
56,875,326 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03117:Parp4
|
APN |
14 |
56,840,313 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03271:Parp4
|
APN |
14 |
56,823,082 (GRCm39) |
missense |
probably benign |
0.10 |
IGL03309:Parp4
|
APN |
14 |
56,825,265 (GRCm39) |
missense |
probably benign |
0.11 |
IGL03408:Parp4
|
APN |
14 |
56,839,865 (GRCm39) |
missense |
probably damaging |
0.99 |
poisonous
|
UTSW |
14 |
56,873,205 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0515_Parp4_195
|
UTSW |
14 |
56,851,124 (GRCm39) |
missense |
probably damaging |
1.00 |
toxic
|
UTSW |
14 |
56,866,615 (GRCm39) |
missense |
probably benign |
0.28 |
venomous
|
UTSW |
14 |
56,827,355 (GRCm39) |
missense |
possibly damaging |
0.92 |
virulent
|
UTSW |
14 |
56,825,235 (GRCm39) |
missense |
probably damaging |
0.97 |
R0278:Parp4
|
UTSW |
14 |
56,844,980 (GRCm39) |
missense |
probably damaging |
0.99 |
R0320:Parp4
|
UTSW |
14 |
56,825,953 (GRCm39) |
critical splice donor site |
probably null |
|
R0445:Parp4
|
UTSW |
14 |
56,840,205 (GRCm39) |
splice site |
probably null |
|
R0452:Parp4
|
UTSW |
14 |
56,886,300 (GRCm39) |
missense |
unknown |
|
R0511:Parp4
|
UTSW |
14 |
56,873,172 (GRCm39) |
splice site |
probably benign |
|
R0515:Parp4
|
UTSW |
14 |
56,851,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R0608:Parp4
|
UTSW |
14 |
56,839,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R0800:Parp4
|
UTSW |
14 |
56,827,408 (GRCm39) |
missense |
probably benign |
0.00 |
R0959:Parp4
|
UTSW |
14 |
56,885,576 (GRCm39) |
missense |
unknown |
|
R1207:Parp4
|
UTSW |
14 |
56,885,339 (GRCm39) |
missense |
unknown |
|
R1207:Parp4
|
UTSW |
14 |
56,885,339 (GRCm39) |
missense |
unknown |
|
R1342:Parp4
|
UTSW |
14 |
56,827,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R1520:Parp4
|
UTSW |
14 |
56,835,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R1565:Parp4
|
UTSW |
14 |
56,827,329 (GRCm39) |
splice site |
probably benign |
|
R1574:Parp4
|
UTSW |
14 |
56,839,752 (GRCm39) |
missense |
probably damaging |
0.98 |
R1574:Parp4
|
UTSW |
14 |
56,839,752 (GRCm39) |
missense |
probably damaging |
0.98 |
R1649:Parp4
|
UTSW |
14 |
56,827,885 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1666:Parp4
|
UTSW |
14 |
56,861,620 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1781:Parp4
|
UTSW |
14 |
56,864,838 (GRCm39) |
splice site |
probably null |
|
R1799:Parp4
|
UTSW |
14 |
56,885,589 (GRCm39) |
missense |
unknown |
|
R1823:Parp4
|
UTSW |
14 |
56,827,329 (GRCm39) |
splice site |
probably benign |
|
R1859:Parp4
|
UTSW |
14 |
56,886,372 (GRCm39) |
missense |
unknown |
|
R1919:Parp4
|
UTSW |
14 |
56,861,474 (GRCm39) |
missense |
probably damaging |
1.00 |
R2000:Parp4
|
UTSW |
14 |
56,851,181 (GRCm39) |
missense |
probably damaging |
0.98 |
R2032:Parp4
|
UTSW |
14 |
56,866,553 (GRCm39) |
missense |
possibly damaging |
0.71 |
R2034:Parp4
|
UTSW |
14 |
56,871,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R2177:Parp4
|
UTSW |
14 |
56,896,746 (GRCm39) |
missense |
unknown |
|
R2291:Parp4
|
UTSW |
14 |
56,851,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R2865:Parp4
|
UTSW |
14 |
56,851,181 (GRCm39) |
missense |
probably damaging |
0.98 |
R3012:Parp4
|
UTSW |
14 |
56,832,873 (GRCm39) |
critical splice donor site |
probably null |
|
R3841:Parp4
|
UTSW |
14 |
56,825,235 (GRCm39) |
missense |
probably damaging |
0.97 |
R3913:Parp4
|
UTSW |
14 |
56,857,975 (GRCm39) |
missense |
probably damaging |
1.00 |
R4064:Parp4
|
UTSW |
14 |
56,861,597 (GRCm39) |
missense |
probably benign |
0.06 |
R4201:Parp4
|
UTSW |
14 |
56,829,848 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4288:Parp4
|
UTSW |
14 |
56,844,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R4360:Parp4
|
UTSW |
14 |
56,866,661 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4506:Parp4
|
UTSW |
14 |
56,889,761 (GRCm39) |
missense |
unknown |
|
R4577:Parp4
|
UTSW |
14 |
56,827,867 (GRCm39) |
missense |
probably benign |
0.33 |
R4633:Parp4
|
UTSW |
14 |
56,885,048 (GRCm39) |
missense |
unknown |
|
R4762:Parp4
|
UTSW |
14 |
56,848,267 (GRCm39) |
missense |
probably damaging |
1.00 |
R4836:Parp4
|
UTSW |
14 |
56,823,195 (GRCm39) |
missense |
probably benign |
0.00 |
R4974:Parp4
|
UTSW |
14 |
56,827,355 (GRCm39) |
missense |
possibly damaging |
0.92 |
R5049:Parp4
|
UTSW |
14 |
56,873,188 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5479:Parp4
|
UTSW |
14 |
56,861,552 (GRCm39) |
missense |
probably benign |
0.01 |
R5683:Parp4
|
UTSW |
14 |
56,884,886 (GRCm39) |
nonsense |
probably null |
|
R5884:Parp4
|
UTSW |
14 |
56,852,207 (GRCm39) |
missense |
probably damaging |
1.00 |
R5965:Parp4
|
UTSW |
14 |
56,861,489 (GRCm39) |
missense |
probably benign |
0.11 |
R6001:Parp4
|
UTSW |
14 |
56,878,740 (GRCm39) |
missense |
probably benign |
0.01 |
R6027:Parp4
|
UTSW |
14 |
56,866,615 (GRCm39) |
missense |
probably benign |
0.28 |
R6230:Parp4
|
UTSW |
14 |
56,844,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R6242:Parp4
|
UTSW |
14 |
56,832,856 (GRCm39) |
nonsense |
probably null |
|
R6355:Parp4
|
UTSW |
14 |
56,839,757 (GRCm39) |
missense |
possibly damaging |
0.61 |
R6414:Parp4
|
UTSW |
14 |
56,864,838 (GRCm39) |
splice site |
probably null |
|
R6477:Parp4
|
UTSW |
14 |
56,884,694 (GRCm39) |
missense |
probably benign |
0.00 |
R6542:Parp4
|
UTSW |
14 |
56,885,339 (GRCm39) |
missense |
unknown |
|
R6759:Parp4
|
UTSW |
14 |
56,857,947 (GRCm39) |
missense |
probably benign |
0.10 |
R6995:Parp4
|
UTSW |
14 |
56,851,196 (GRCm39) |
missense |
probably damaging |
0.97 |
R7002:Parp4
|
UTSW |
14 |
56,839,861 (GRCm39) |
missense |
probably damaging |
1.00 |
R7026:Parp4
|
UTSW |
14 |
56,858,049 (GRCm39) |
missense |
probably benign |
0.01 |
R7062:Parp4
|
UTSW |
14 |
56,852,216 (GRCm39) |
missense |
possibly damaging |
0.48 |
R7101:Parp4
|
UTSW |
14 |
56,827,430 (GRCm39) |
missense |
probably benign |
0.02 |
R7124:Parp4
|
UTSW |
14 |
56,840,256 (GRCm39) |
missense |
probably benign |
0.11 |
R7162:Parp4
|
UTSW |
14 |
56,886,333 (GRCm39) |
missense |
unknown |
|
R7293:Parp4
|
UTSW |
14 |
56,885,303 (GRCm39) |
small deletion |
probably benign |
|
R7297:Parp4
|
UTSW |
14 |
56,885,138 (GRCm39) |
missense |
not run |
|
R7337:Parp4
|
UTSW |
14 |
56,839,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R7539:Parp4
|
UTSW |
14 |
56,873,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R7575:Parp4
|
UTSW |
14 |
56,875,375 (GRCm39) |
missense |
probably benign |
0.28 |
R7808:Parp4
|
UTSW |
14 |
56,873,205 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7854:Parp4
|
UTSW |
14 |
56,896,805 (GRCm39) |
missense |
unknown |
|
R7960:Parp4
|
UTSW |
14 |
56,832,708 (GRCm39) |
splice site |
probably null |
|
R8152:Parp4
|
UTSW |
14 |
56,884,703 (GRCm39) |
missense |
probably benign |
0.00 |
R8344:Parp4
|
UTSW |
14 |
56,886,186 (GRCm39) |
missense |
unknown |
|
R8416:Parp4
|
UTSW |
14 |
56,825,271 (GRCm39) |
critical splice donor site |
probably null |
|
R8726:Parp4
|
UTSW |
14 |
56,866,556 (GRCm39) |
missense |
probably benign |
0.04 |
R8752:Parp4
|
UTSW |
14 |
56,886,073 (GRCm39) |
missense |
unknown |
|
R8804:Parp4
|
UTSW |
14 |
56,853,900 (GRCm39) |
nonsense |
probably null |
|
R9046:Parp4
|
UTSW |
14 |
56,864,927 (GRCm39) |
missense |
probably damaging |
0.98 |
R9176:Parp4
|
UTSW |
14 |
56,873,274 (GRCm39) |
missense |
possibly damaging |
0.54 |
R9303:Parp4
|
UTSW |
14 |
56,852,224 (GRCm39) |
critical splice donor site |
probably null |
|
R9303:Parp4
|
UTSW |
14 |
56,832,790 (GRCm39) |
frame shift |
probably null |
|
R9305:Parp4
|
UTSW |
14 |
56,852,224 (GRCm39) |
critical splice donor site |
probably null |
|
R9305:Parp4
|
UTSW |
14 |
56,832,790 (GRCm39) |
frame shift |
probably null |
|
R9360:Parp4
|
UTSW |
14 |
56,878,775 (GRCm39) |
critical splice donor site |
probably null |
|
R9430:Parp4
|
UTSW |
14 |
56,866,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R9491:Parp4
|
UTSW |
14 |
56,832,828 (GRCm39) |
missense |
probably damaging |
0.99 |
R9729:Parp4
|
UTSW |
14 |
56,885,888 (GRCm39) |
missense |
unknown |
|
RF020:Parp4
|
UTSW |
14 |
56,884,806 (GRCm39) |
missense |
unknown |
|
Z1177:Parp4
|
UTSW |
14 |
56,829,824 (GRCm39) |
missense |
probably damaging |
1.00 |
|