Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abtb2 |
A |
T |
2: 103,547,602 (GRCm39) |
Y992F |
probably benign |
Het |
Adgrg6 |
T |
A |
10: 14,342,976 (GRCm39) |
N324Y |
probably damaging |
Het |
Ampd3 |
T |
C |
7: 110,394,965 (GRCm39) |
F305L |
probably benign |
Het |
Ankrd35 |
A |
G |
3: 96,588,388 (GRCm39) |
|
probably null |
Het |
Api5 |
A |
G |
2: 94,260,064 (GRCm39) |
I64T |
possibly damaging |
Het |
Arhgap21 |
A |
G |
2: 20,860,399 (GRCm39) |
I1165T |
probably damaging |
Het |
Bdp1 |
T |
C |
13: 100,214,623 (GRCm39) |
|
probably null |
Het |
Capn3 |
T |
A |
2: 120,326,518 (GRCm39) |
I570N |
probably damaging |
Het |
Catsperg2 |
T |
C |
7: 29,418,990 (GRCm39) |
H232R |
possibly damaging |
Het |
Clcn7 |
T |
C |
17: 25,365,792 (GRCm39) |
L156P |
possibly damaging |
Het |
Cpa3 |
C |
A |
3: 20,276,376 (GRCm39) |
V286F |
probably benign |
Het |
Csrnp3 |
G |
A |
2: 65,853,153 (GRCm39) |
C527Y |
probably damaging |
Het |
Dock5 |
A |
T |
14: 68,065,887 (GRCm39) |
V372E |
probably benign |
Het |
Elmo1 |
T |
C |
13: 20,789,372 (GRCm39) |
L696P |
probably damaging |
Het |
Fam91a1 |
T |
C |
15: 58,303,045 (GRCm39) |
|
probably benign |
Het |
Gm12695 |
T |
A |
4: 96,650,988 (GRCm39) |
D155V |
probably null |
Het |
Hspa4l |
A |
G |
3: 40,736,055 (GRCm39) |
I559V |
probably benign |
Het |
Kdm1a |
G |
T |
4: 136,278,348 (GRCm39) |
|
probably benign |
Het |
Lrrc8d |
A |
T |
5: 105,974,683 (GRCm39) |
|
noncoding transcript |
Het |
Minpp1 |
A |
T |
19: 32,475,815 (GRCm39) |
Y316F |
possibly damaging |
Het |
Neto2 |
T |
C |
8: 86,390,064 (GRCm39) |
|
probably benign |
Het |
Nrxn2 |
T |
A |
19: 6,500,610 (GRCm39) |
D277E |
probably benign |
Het |
Ola1 |
A |
G |
2: 72,972,644 (GRCm39) |
|
probably benign |
Het |
Or4k48 |
A |
G |
2: 111,475,850 (GRCm39) |
V164A |
probably benign |
Het |
Or51r1 |
T |
C |
7: 102,228,602 (GRCm39) |
I300T |
probably damaging |
Het |
Or8c15 |
T |
A |
9: 38,120,532 (GRCm39) |
M61K |
probably damaging |
Het |
Pam |
A |
G |
1: 97,768,064 (GRCm39) |
V722A |
possibly damaging |
Het |
Pfdn6 |
T |
C |
17: 34,158,077 (GRCm39) |
Y90C |
probably benign |
Het |
Pkhd1 |
T |
A |
1: 20,621,126 (GRCm39) |
H844L |
possibly damaging |
Het |
Plk5 |
G |
A |
10: 80,198,896 (GRCm39) |
V422M |
probably damaging |
Het |
Psmc1 |
G |
T |
12: 100,085,386 (GRCm39) |
R249L |
probably damaging |
Het |
Ralgapa1 |
G |
T |
12: 55,759,450 (GRCm39) |
H1480Q |
possibly damaging |
Het |
Rars1 |
G |
A |
11: 35,715,353 (GRCm39) |
|
probably benign |
Het |
Rbm48 |
G |
A |
5: 3,640,600 (GRCm39) |
R260C |
possibly damaging |
Het |
Smarcc1 |
C |
T |
9: 110,051,068 (GRCm39) |
H963Y |
possibly damaging |
Het |
Spef2 |
T |
C |
15: 9,725,238 (GRCm39) |
E230G |
probably damaging |
Het |
Spg11 |
A |
G |
2: 121,922,741 (GRCm39) |
S903P |
probably benign |
Het |
Tas2r122 |
T |
C |
6: 132,688,572 (GRCm39) |
Y107C |
probably damaging |
Het |
Tpm3 |
C |
A |
3: 89,995,753 (GRCm39) |
N204K |
probably benign |
Het |
Wdr36 |
T |
C |
18: 32,985,044 (GRCm39) |
I450T |
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 |
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 |
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 |
|