Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrv1 |
A |
T |
13: 81,679,795 (GRCm39) |
V1848E |
probably damaging |
Het |
Alpk3 |
A |
G |
7: 80,727,343 (GRCm39) |
K158E |
probably damaging |
Het |
Arrdc4 |
T |
A |
7: 68,389,756 (GRCm39) |
E356D |
probably damaging |
Het |
Asb4 |
A |
G |
6: 5,423,591 (GRCm39) |
N246S |
probably damaging |
Het |
Ccdc150 |
A |
T |
1: 54,404,130 (GRCm39) |
|
probably benign |
Het |
Ctsj |
G |
A |
13: 61,150,312 (GRCm39) |
P230L |
probably benign |
Het |
Dync1i2 |
C |
T |
2: 71,058,164 (GRCm39) |
|
probably benign |
Het |
Eme1 |
A |
G |
11: 94,536,277 (GRCm39) |
L564P |
probably damaging |
Het |
Fabp3 |
C |
T |
4: 130,206,180 (GRCm39) |
T57I |
probably benign |
Het |
Frg1 |
A |
G |
8: 41,864,254 (GRCm39) |
|
probably benign |
Het |
Fzd2 |
A |
T |
11: 102,496,206 (GRCm39) |
S217C |
possibly damaging |
Het |
Gaa |
G |
T |
11: 119,165,730 (GRCm39) |
R81L |
probably damaging |
Het |
Gfral |
A |
G |
9: 76,074,341 (GRCm39) |
V368A |
probably benign |
Het |
Gm10774 |
T |
C |
2: 126,551,392 (GRCm39) |
Y29C |
probably benign |
Het |
Gucy1a2 |
T |
A |
9: 3,759,830 (GRCm39) |
N545K |
probably damaging |
Het |
Herc2 |
T |
C |
7: 55,796,444 (GRCm39) |
S1939P |
probably benign |
Het |
Ifnk |
T |
C |
4: 35,152,231 (GRCm39) |
I53T |
probably benign |
Het |
Iqub |
G |
A |
6: 24,505,627 (GRCm39) |
L94F |
possibly damaging |
Het |
Kpna1 |
C |
T |
16: 35,853,749 (GRCm39) |
R460* |
probably null |
Het |
Masp1 |
T |
C |
16: 23,310,865 (GRCm39) |
E189G |
probably damaging |
Het |
Mogat1 |
A |
G |
1: 78,500,250 (GRCm39) |
I105V |
probably benign |
Het |
Mpi |
A |
G |
9: 57,452,472 (GRCm39) |
|
probably benign |
Het |
Msh2 |
C |
A |
17: 87,987,488 (GRCm39) |
D209E |
probably benign |
Het |
Nsf |
G |
A |
11: 103,719,364 (GRCm39) |
T646I |
probably damaging |
Het |
Or10g9b |
A |
T |
9: 39,917,390 (GRCm39) |
V285D |
possibly damaging |
Het |
Or4c10b |
C |
T |
2: 89,711,550 (GRCm39) |
P127S |
probably damaging |
Het |
Or5b24 |
T |
A |
19: 12,912,329 (GRCm39) |
S76T |
possibly damaging |
Het |
Or6b2 |
G |
A |
1: 92,407,612 (GRCm39) |
H244Y |
probably damaging |
Het |
Otogl |
T |
A |
10: 107,722,374 (GRCm39) |
I327F |
probably damaging |
Het |
Pappa2 |
T |
C |
1: 158,682,552 (GRCm39) |
D832G |
probably damaging |
Het |
Pax5 |
G |
T |
4: 44,697,512 (GRCm39) |
|
probably benign |
Het |
Pfkfb4 |
A |
G |
9: 108,836,794 (GRCm39) |
E163G |
probably benign |
Het |
Phc1 |
T |
C |
6: 122,300,416 (GRCm39) |
|
probably benign |
Het |
Piwil1 |
T |
C |
5: 128,824,957 (GRCm39) |
S552P |
probably benign |
Het |
Ppfia3 |
A |
C |
7: 45,001,639 (GRCm39) |
D424E |
probably benign |
Het |
Prss16 |
A |
G |
13: 22,191,138 (GRCm39) |
|
probably benign |
Het |
Rbsn |
A |
G |
6: 92,178,711 (GRCm39) |
|
probably null |
Het |
Rexo1 |
C |
T |
10: 80,380,239 (GRCm39) |
S919N |
probably benign |
Het |
Sec31a |
T |
C |
5: 100,510,032 (GRCm39) |
N1152D |
probably damaging |
Het |
Sel1l3 |
A |
T |
5: 53,274,445 (GRCm39) |
F1012I |
possibly damaging |
Het |
Sema4c |
A |
G |
1: 36,589,646 (GRCm39) |
V539A |
probably benign |
Het |
Sf3b5 |
A |
G |
10: 12,884,575 (GRCm39) |
E70G |
possibly damaging |
Het |
Tmcc2 |
TTGCTGCTGCTGCTGCTGC |
TTGCTGCTGCTGCTGC |
1: 132,285,493 (GRCm39) |
|
probably benign |
Het |
Tor1aip2 |
T |
C |
1: 155,940,483 (GRCm39) |
V263A |
possibly damaging |
Het |
Unc45b |
A |
G |
11: 82,813,733 (GRCm39) |
E380G |
probably damaging |
Het |
Usp16 |
C |
T |
16: 87,271,536 (GRCm39) |
T364M |
possibly damaging |
Het |
Wwox |
T |
C |
8: 115,438,776 (GRCm39) |
S281P |
probably damaging |
Het |
Zfp110 |
A |
G |
7: 12,580,721 (GRCm39) |
|
probably null |
Het |
Zfp335 |
G |
A |
2: 164,738,043 (GRCm39) |
A856V |
probably benign |
Het |
Zfp652 |
G |
A |
11: 95,640,608 (GRCm39) |
E178K |
possibly damaging |
Het |
|
Other mutations in Ptpro |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00334:Ptpro
|
APN |
6 |
137,371,907 (GRCm39) |
critical splice donor site |
probably null |
|
IGL00844:Ptpro
|
APN |
6 |
137,391,237 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00983:Ptpro
|
APN |
6 |
137,395,246 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01073:Ptpro
|
APN |
6 |
137,354,086 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01832:Ptpro
|
APN |
6 |
137,370,666 (GRCm39) |
missense |
possibly damaging |
0.93 |
IGL02308:Ptpro
|
APN |
6 |
137,431,698 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02387:Ptpro
|
APN |
6 |
137,387,978 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02605:Ptpro
|
APN |
6 |
137,357,316 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02666:Ptpro
|
APN |
6 |
137,355,057 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03275:Ptpro
|
APN |
6 |
137,427,004 (GRCm39) |
missense |
probably damaging |
1.00 |
Brau
|
UTSW |
6 |
137,431,596 (GRCm39) |
missense |
probably damaging |
1.00 |
court
|
UTSW |
6 |
137,370,673 (GRCm39) |
nonsense |
probably null |
|
Hoff
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
Jester
|
UTSW |
6 |
137,426,915 (GRCm39) |
missense |
probably damaging |
1.00 |
mann
|
UTSW |
6 |
137,388,114 (GRCm39) |
splice site |
probably null |
|
R0017:Ptpro
|
UTSW |
6 |
137,393,825 (GRCm39) |
missense |
probably benign |
0.03 |
R0017:Ptpro
|
UTSW |
6 |
137,393,825 (GRCm39) |
missense |
probably benign |
0.03 |
R0020:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0022:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0023:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0024:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0094:Ptpro
|
UTSW |
6 |
137,363,350 (GRCm39) |
missense |
probably benign |
0.08 |
R0094:Ptpro
|
UTSW |
6 |
137,363,350 (GRCm39) |
missense |
probably benign |
0.08 |
R0103:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0106:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0316:Ptpro
|
UTSW |
6 |
137,353,987 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0427:Ptpro
|
UTSW |
6 |
137,345,294 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0456:Ptpro
|
UTSW |
6 |
137,391,228 (GRCm39) |
missense |
probably benign |
0.04 |
R0536:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0537:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0552:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0555:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0664:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0708:Ptpro
|
UTSW |
6 |
137,363,251 (GRCm39) |
missense |
probably benign |
0.26 |
R0730:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0735:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0738:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0786:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0811:Ptpro
|
UTSW |
6 |
137,345,077 (GRCm39) |
missense |
probably benign |
0.00 |
R0812:Ptpro
|
UTSW |
6 |
137,345,077 (GRCm39) |
missense |
probably benign |
0.00 |
R0881:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R0973:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1145:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1145:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1146:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1259:Ptpro
|
UTSW |
6 |
137,369,739 (GRCm39) |
missense |
probably damaging |
0.98 |
R1340:Ptpro
|
UTSW |
6 |
137,418,079 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1381:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1382:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1385:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1396:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1401:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1416:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1422:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1448:Ptpro
|
UTSW |
6 |
137,418,114 (GRCm39) |
missense |
probably damaging |
1.00 |
R1513:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1518:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1526:Ptpro
|
UTSW |
6 |
137,438,724 (GRCm39) |
missense |
probably damaging |
1.00 |
R1540:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1571:Ptpro
|
UTSW |
6 |
137,355,128 (GRCm39) |
missense |
probably benign |
|
R1573:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1587:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1588:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1649:Ptpro
|
UTSW |
6 |
137,421,015 (GRCm39) |
nonsense |
probably null |
|
R1700:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1701:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1745:Ptpro
|
UTSW |
6 |
137,377,643 (GRCm39) |
missense |
probably benign |
0.03 |
R1772:Ptpro
|
UTSW |
6 |
137,407,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Ptpro
|
UTSW |
6 |
137,377,617 (GRCm39) |
splice site |
probably benign |
|
R1958:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R1967:Ptpro
|
UTSW |
6 |
137,393,863 (GRCm39) |
missense |
probably benign |
0.38 |
R2025:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R2026:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R2040:Ptpro
|
UTSW |
6 |
137,363,162 (GRCm39) |
splice site |
probably benign |
|
R2115:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R2117:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R2130:Ptpro
|
UTSW |
6 |
137,388,114 (GRCm39) |
splice site |
probably null |
|
R2161:Ptpro
|
UTSW |
6 |
137,426,885 (GRCm39) |
missense |
probably benign |
0.01 |
R2431:Ptpro
|
UTSW |
6 |
137,420,583 (GRCm39) |
nonsense |
probably null |
|
R2915:Ptpro
|
UTSW |
6 |
137,391,239 (GRCm39) |
start gained |
probably benign |
|
R2988:Ptpro
|
UTSW |
6 |
137,420,597 (GRCm39) |
nonsense |
probably null |
|
R3772:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3773:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3795:Ptpro
|
UTSW |
6 |
137,357,307 (GRCm39) |
missense |
probably benign |
|
R3885:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3886:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3887:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3888:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R3893:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4032:Ptpro
|
UTSW |
6 |
137,438,740 (GRCm39) |
missense |
probably damaging |
1.00 |
R4133:Ptpro
|
UTSW |
6 |
137,397,370 (GRCm39) |
missense |
probably damaging |
1.00 |
R4377:Ptpro
|
UTSW |
6 |
137,357,264 (GRCm39) |
missense |
probably benign |
0.26 |
R4455:Ptpro
|
UTSW |
6 |
137,370,657 (GRCm39) |
missense |
probably damaging |
1.00 |
R4613:Ptpro
|
UTSW |
6 |
137,393,834 (GRCm39) |
nonsense |
probably null |
|
R4827:Ptpro
|
UTSW |
6 |
137,419,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R4863:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R4870:Ptpro
|
UTSW |
6 |
137,354,130 (GRCm39) |
missense |
probably damaging |
0.96 |
R4910:Ptpro
|
UTSW |
6 |
137,345,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R4932:Ptpro
|
UTSW |
6 |
137,388,103 (GRCm39) |
nonsense |
probably null |
|
R4941:Ptpro
|
UTSW |
6 |
137,369,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R4989:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5009:Ptpro
|
UTSW |
6 |
137,354,130 (GRCm39) |
missense |
probably damaging |
0.96 |
R5032:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5033:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5162:Ptpro
|
UTSW |
6 |
137,420,592 (GRCm39) |
missense |
probably damaging |
1.00 |
R5393:Ptpro
|
UTSW |
6 |
137,357,222 (GRCm39) |
missense |
probably benign |
0.04 |
R5423:Ptpro
|
UTSW |
6 |
137,419,705 (GRCm39) |
missense |
probably damaging |
1.00 |
R5782:Ptpro
|
UTSW |
6 |
137,376,496 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6103:Ptpro
|
UTSW |
6 |
137,377,704 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6239:Ptpro
|
UTSW |
6 |
137,357,606 (GRCm39) |
missense |
probably benign |
0.28 |
R6488:Ptpro
|
UTSW |
6 |
137,370,673 (GRCm39) |
nonsense |
probably null |
|
R6494:Ptpro
|
UTSW |
6 |
137,359,640 (GRCm39) |
missense |
probably benign |
0.20 |
R6746:Ptpro
|
UTSW |
6 |
137,371,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R6763:Ptpro
|
UTSW |
6 |
137,395,279 (GRCm39) |
splice site |
probably null |
|
R6888:Ptpro
|
UTSW |
6 |
137,357,198 (GRCm39) |
missense |
probably benign |
0.30 |
R6983:Ptpro
|
UTSW |
6 |
137,426,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R7019:Ptpro
|
UTSW |
6 |
137,357,476 (GRCm39) |
missense |
probably benign |
|
R7218:Ptpro
|
UTSW |
6 |
137,431,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R7236:Ptpro
|
UTSW |
6 |
137,345,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R7299:Ptpro
|
UTSW |
6 |
137,418,142 (GRCm39) |
critical splice donor site |
probably null |
|
R7381:Ptpro
|
UTSW |
6 |
137,376,559 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7493:Ptpro
|
UTSW |
6 |
137,359,647 (GRCm39) |
missense |
probably benign |
0.01 |
R7733:Ptpro
|
UTSW |
6 |
137,391,284 (GRCm39) |
nonsense |
probably null |
|
R7793:Ptpro
|
UTSW |
6 |
137,393,818 (GRCm39) |
missense |
probably damaging |
0.99 |
R7804:Ptpro
|
UTSW |
6 |
137,376,599 (GRCm39) |
splice site |
probably null |
|
R7833:Ptpro
|
UTSW |
6 |
137,393,861 (GRCm39) |
nonsense |
probably null |
|
R7859:Ptpro
|
UTSW |
6 |
137,369,805 (GRCm39) |
critical splice donor site |
probably null |
|
R7873:Ptpro
|
UTSW |
6 |
137,407,737 (GRCm39) |
missense |
probably benign |
0.44 |
R8042:Ptpro
|
UTSW |
6 |
137,393,881 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8859:Ptpro
|
UTSW |
6 |
137,403,782 (GRCm39) |
nonsense |
probably null |
|
R8979:Ptpro
|
UTSW |
6 |
137,345,140 (GRCm39) |
missense |
probably benign |
|
R9138:Ptpro
|
UTSW |
6 |
137,388,113 (GRCm39) |
critical splice donor site |
probably null |
|
R9309:Ptpro
|
UTSW |
6 |
137,431,656 (GRCm39) |
missense |
probably damaging |
1.00 |
R9420:Ptpro
|
UTSW |
6 |
137,420,933 (GRCm39) |
missense |
probably benign |
0.08 |
R9612:Ptpro
|
UTSW |
6 |
137,391,318 (GRCm39) |
missense |
probably benign |
0.31 |
R9625:Ptpro
|
UTSW |
6 |
137,371,873 (GRCm39) |
missense |
probably damaging |
1.00 |
R9697:Ptpro
|
UTSW |
6 |
137,363,288 (GRCm39) |
missense |
probably damaging |
1.00 |
R9715:Ptpro
|
UTSW |
6 |
137,345,108 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Ptpro
|
UTSW |
6 |
137,355,138 (GRCm39) |
missense |
probably damaging |
1.00 |
|