Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
A |
G |
8: 87,258,197 (GRCm39) |
I773T |
probably benign |
Het |
Adamtsl1 |
T |
A |
4: 86,260,960 (GRCm39) |
I1057N |
possibly damaging |
Het |
Anxa5 |
G |
A |
3: 36,504,821 (GRCm39) |
A247V |
probably damaging |
Het |
Ascc3 |
T |
G |
10: 50,611,425 (GRCm39) |
W1589G |
probably damaging |
Het |
Atp2b2 |
G |
A |
6: 113,770,743 (GRCm39) |
P389S |
probably damaging |
Het |
Bpifa6 |
T |
A |
2: 153,824,851 (GRCm39) |
S9T |
probably benign |
Het |
Cfhr4 |
T |
A |
1: 139,682,009 (GRCm39) |
T196S |
probably damaging |
Het |
Chd8 |
A |
G |
14: 52,442,783 (GRCm39) |
V589A |
probably benign |
Het |
Chrnb2 |
T |
C |
3: 89,671,713 (GRCm39) |
M1V |
probably null |
Het |
Col16a1 |
T |
A |
4: 129,960,889 (GRCm39) |
V449E |
unknown |
Het |
Cttnbp2nl |
T |
G |
3: 104,913,173 (GRCm39) |
K237T |
probably damaging |
Het |
Dazap1 |
T |
G |
10: 80,114,060 (GRCm39) |
|
probably null |
Het |
Fam187b |
T |
A |
7: 30,688,545 (GRCm39) |
V22E |
probably damaging |
Het |
Fcgbpl1 |
A |
G |
7: 27,837,040 (GRCm39) |
R320G |
probably damaging |
Het |
H2-T24 |
T |
A |
17: 36,325,878 (GRCm39) |
I238F |
probably damaging |
Het |
Hectd4 |
A |
G |
5: 121,471,087 (GRCm39) |
E2658G |
probably benign |
Het |
Herc1 |
A |
C |
9: 66,388,192 (GRCm39) |
I3826L |
probably benign |
Het |
Hinfp |
A |
G |
9: 44,211,060 (GRCm39) |
C67R |
probably damaging |
Het |
Hp1bp3 |
C |
T |
4: 137,964,520 (GRCm39) |
S348F |
probably damaging |
Het |
Hspg2 |
T |
C |
4: 137,279,198 (GRCm39) |
Y3094H |
probably damaging |
Het |
Htr1f |
A |
G |
16: 64,747,091 (GRCm39) |
V67A |
probably damaging |
Het |
Iqcc |
T |
G |
4: 129,510,392 (GRCm39) |
E374D |
probably damaging |
Het |
Kcnj9 |
T |
C |
1: 172,153,765 (GRCm39) |
T120A |
probably damaging |
Het |
Kitl |
C |
T |
10: 99,923,226 (GRCm39) |
P208S |
probably benign |
Het |
Lpcat4 |
A |
G |
2: 112,077,093 (GRCm39) |
Y479C |
probably damaging |
Het |
Lrrc74b |
T |
C |
16: 17,371,016 (GRCm39) |
N227S |
probably damaging |
Het |
Mdc1 |
T |
A |
17: 36,163,473 (GRCm39) |
V1007D |
probably damaging |
Het |
Mocos |
T |
G |
18: 24,812,819 (GRCm39) |
I571S |
probably benign |
Het |
Myh8 |
A |
G |
11: 67,183,014 (GRCm39) |
N659D |
probably damaging |
Het |
Naip2 |
A |
G |
13: 100,320,296 (GRCm39) |
V240A |
probably benign |
Het |
Nap1l1 |
T |
C |
10: 111,321,370 (GRCm39) |
S37P |
probably benign |
Het |
Nin |
T |
G |
12: 70,097,915 (GRCm39) |
K515T |
probably damaging |
Het |
Npl |
T |
A |
1: 153,384,864 (GRCm39) |
K258* |
probably null |
Het |
Ntn4 |
T |
A |
10: 93,480,569 (GRCm39) |
S98T |
possibly damaging |
Het |
Or10x1 |
T |
C |
1: 174,197,152 (GRCm39) |
V223A |
probably damaging |
Het |
Or2z8 |
C |
T |
8: 72,812,244 (GRCm39) |
T240M |
probably damaging |
Het |
Or5k14 |
C |
A |
16: 58,693,269 (GRCm39) |
M81I |
probably benign |
Het |
Ppox |
C |
A |
1: 171,106,849 (GRCm39) |
A192S |
possibly damaging |
Het |
Prkdc |
T |
C |
16: 15,531,517 (GRCm39) |
L1380S |
probably benign |
Het |
Psd4 |
C |
A |
2: 24,295,363 (GRCm39) |
A839E |
probably damaging |
Het |
Ptprn2 |
T |
G |
12: 116,685,711 (GRCm39) |
F57V |
probably damaging |
Het |
R3hdm2 |
T |
A |
10: 127,334,322 (GRCm39) |
M915K |
probably damaging |
Het |
Rab26 |
C |
T |
17: 24,749,759 (GRCm39) |
|
probably null |
Het |
Rnf213 |
A |
G |
11: 119,321,187 (GRCm39) |
E1215G |
probably benign |
Het |
Rprd2 |
T |
C |
3: 95,681,673 (GRCm39) |
K407E |
probably damaging |
Het |
Siah3 |
G |
A |
14: 75,693,574 (GRCm39) |
V27I |
possibly damaging |
Het |
Slc14a2 |
T |
A |
18: 78,235,338 (GRCm39) |
N280Y |
probably damaging |
Het |
Slc25a35 |
A |
G |
11: 68,862,786 (GRCm39) |
Y247C |
probably damaging |
Het |
Slc29a4 |
A |
G |
5: 142,691,285 (GRCm39) |
D55G |
probably benign |
Het |
Slc35d1 |
C |
T |
4: 103,065,378 (GRCm39) |
V189I |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,067,884 (GRCm39) |
R322* |
probably null |
Het |
Stac3 |
A |
T |
10: 127,339,519 (GRCm39) |
R138S |
probably damaging |
Het |
Tmem260 |
T |
A |
14: 48,720,779 (GRCm39) |
C306* |
probably null |
Het |
Tspyl1 |
A |
G |
10: 34,159,085 (GRCm39) |
N270S |
probably damaging |
Het |
Ugt2a2 |
T |
A |
5: 87,622,720 (GRCm39) |
K293* |
probably null |
Het |
Vmn2r102 |
A |
C |
17: 19,899,025 (GRCm39) |
T456P |
probably benign |
Het |
Vmn2r90 |
T |
A |
17: 17,932,511 (GRCm39) |
S139R |
probably benign |
Het |
Zmym2 |
A |
G |
14: 57,180,715 (GRCm39) |
N876D |
probably benign |
Het |
|
Other mutations in Ptprt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:Ptprt
|
APN |
2 |
161,652,544 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00565:Ptprt
|
APN |
2 |
161,402,111 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00925:Ptprt
|
APN |
2 |
161,498,083 (GRCm39) |
missense |
possibly damaging |
0.52 |
IGL01344:Ptprt
|
APN |
2 |
161,393,737 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01432:Ptprt
|
APN |
2 |
162,109,999 (GRCm39) |
splice site |
probably benign |
|
IGL02008:Ptprt
|
APN |
2 |
161,769,593 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02040:Ptprt
|
APN |
2 |
162,079,992 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02172:Ptprt
|
APN |
2 |
161,397,422 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02231:Ptprt
|
APN |
2 |
162,119,966 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02231:Ptprt
|
APN |
2 |
162,079,980 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02232:Ptprt
|
APN |
2 |
161,372,437 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02277:Ptprt
|
APN |
2 |
161,389,301 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02447:Ptprt
|
APN |
2 |
162,120,027 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02601:Ptprt
|
APN |
2 |
161,608,227 (GRCm39) |
missense |
probably benign |
0.10 |
IGL02623:Ptprt
|
APN |
2 |
161,449,372 (GRCm39) |
splice site |
probably benign |
|
IGL03379:Ptprt
|
APN |
2 |
161,397,379 (GRCm39) |
nonsense |
probably null |
|
Poverina
|
UTSW |
2 |
161,743,417 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL03055:Ptprt
|
UTSW |
2 |
161,375,533 (GRCm39) |
missense |
probably damaging |
0.96 |
R0064:Ptprt
|
UTSW |
2 |
161,769,711 (GRCm39) |
splice site |
probably benign |
|
R0129:Ptprt
|
UTSW |
2 |
162,119,990 (GRCm39) |
missense |
probably benign |
0.35 |
R0131:Ptprt
|
UTSW |
2 |
162,120,030 (GRCm39) |
missense |
probably benign |
0.00 |
R0131:Ptprt
|
UTSW |
2 |
162,120,030 (GRCm39) |
missense |
probably benign |
0.00 |
R0316:Ptprt
|
UTSW |
2 |
161,449,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R0454:Ptprt
|
UTSW |
2 |
161,395,742 (GRCm39) |
missense |
probably damaging |
0.96 |
R0488:Ptprt
|
UTSW |
2 |
161,395,745 (GRCm39) |
missense |
probably damaging |
0.99 |
R0573:Ptprt
|
UTSW |
2 |
161,393,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R0614:Ptprt
|
UTSW |
2 |
161,654,040 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0834:Ptprt
|
UTSW |
2 |
161,654,059 (GRCm39) |
splice site |
probably null |
|
R1023:Ptprt
|
UTSW |
2 |
161,400,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R1184:Ptprt
|
UTSW |
2 |
161,769,692 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1253:Ptprt
|
UTSW |
2 |
162,120,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R1476:Ptprt
|
UTSW |
2 |
161,769,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R1515:Ptprt
|
UTSW |
2 |
162,079,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R1595:Ptprt
|
UTSW |
2 |
161,652,469 (GRCm39) |
critical splice donor site |
probably null |
|
R1939:Ptprt
|
UTSW |
2 |
161,769,560 (GRCm39) |
missense |
probably benign |
0.45 |
R1987:Ptprt
|
UTSW |
2 |
161,608,241 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1987:Ptprt
|
UTSW |
2 |
161,400,818 (GRCm39) |
missense |
probably damaging |
1.00 |
R2049:Ptprt
|
UTSW |
2 |
161,376,465 (GRCm39) |
missense |
probably damaging |
1.00 |
R2140:Ptprt
|
UTSW |
2 |
161,653,908 (GRCm39) |
missense |
probably damaging |
1.00 |
R2421:Ptprt
|
UTSW |
2 |
162,119,960 (GRCm39) |
splice site |
probably benign |
|
R3432:Ptprt
|
UTSW |
2 |
161,769,449 (GRCm39) |
missense |
probably damaging |
1.00 |
R3619:Ptprt
|
UTSW |
2 |
161,408,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R3757:Ptprt
|
UTSW |
2 |
161,653,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R3758:Ptprt
|
UTSW |
2 |
161,653,950 (GRCm39) |
missense |
probably damaging |
1.00 |
R3834:Ptprt
|
UTSW |
2 |
161,389,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R3835:Ptprt
|
UTSW |
2 |
161,389,307 (GRCm39) |
missense |
probably damaging |
1.00 |
R3915:Ptprt
|
UTSW |
2 |
161,397,475 (GRCm39) |
splice site |
probably benign |
|
R4003:Ptprt
|
UTSW |
2 |
161,408,037 (GRCm39) |
splice site |
probably benign |
|
R4387:Ptprt
|
UTSW |
2 |
161,769,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R4519:Ptprt
|
UTSW |
2 |
161,406,609 (GRCm39) |
missense |
probably damaging |
1.00 |
R4618:Ptprt
|
UTSW |
2 |
161,395,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R4677:Ptprt
|
UTSW |
2 |
161,743,366 (GRCm39) |
critical splice donor site |
probably null |
|
R4866:Ptprt
|
UTSW |
2 |
161,402,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R5088:Ptprt
|
UTSW |
2 |
162,080,095 (GRCm39) |
missense |
probably benign |
0.01 |
R5173:Ptprt
|
UTSW |
2 |
161,769,676 (GRCm39) |
missense |
probably benign |
0.01 |
R5215:Ptprt
|
UTSW |
2 |
162,120,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R5383:Ptprt
|
UTSW |
2 |
161,539,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R5398:Ptprt
|
UTSW |
2 |
161,769,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R5518:Ptprt
|
UTSW |
2 |
162,120,143 (GRCm39) |
missense |
probably damaging |
0.99 |
R5711:Ptprt
|
UTSW |
2 |
161,652,524 (GRCm39) |
missense |
probably damaging |
0.98 |
R5735:Ptprt
|
UTSW |
2 |
161,376,484 (GRCm39) |
missense |
probably damaging |
0.98 |
R5834:Ptprt
|
UTSW |
2 |
161,402,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R5872:Ptprt
|
UTSW |
2 |
161,977,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R5926:Ptprt
|
UTSW |
2 |
161,406,606 (GRCm39) |
missense |
probably benign |
0.00 |
R6210:Ptprt
|
UTSW |
2 |
162,109,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R6285:Ptprt
|
UTSW |
2 |
161,743,417 (GRCm39) |
missense |
possibly damaging |
0.70 |
R6298:Ptprt
|
UTSW |
2 |
161,395,779 (GRCm39) |
missense |
probably damaging |
1.00 |
R6406:Ptprt
|
UTSW |
2 |
161,395,703 (GRCm39) |
missense |
probably damaging |
0.98 |
R6499:Ptprt
|
UTSW |
2 |
161,376,507 (GRCm39) |
missense |
probably benign |
0.32 |
R6613:Ptprt
|
UTSW |
2 |
161,372,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R6622:Ptprt
|
UTSW |
2 |
161,395,760 (GRCm39) |
missense |
probably damaging |
1.00 |
R7218:Ptprt
|
UTSW |
2 |
161,389,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R7247:Ptprt
|
UTSW |
2 |
161,375,443 (GRCm39) |
missense |
probably benign |
0.15 |
R7576:Ptprt
|
UTSW |
2 |
161,449,225 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7733:Ptprt
|
UTSW |
2 |
161,417,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R7735:Ptprt
|
UTSW |
2 |
161,417,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R7813:Ptprt
|
UTSW |
2 |
161,372,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R8031:Ptprt
|
UTSW |
2 |
161,977,377 (GRCm39) |
missense |
probably damaging |
1.00 |
R8074:Ptprt
|
UTSW |
2 |
161,769,581 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8151:Ptprt
|
UTSW |
2 |
162,120,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R8236:Ptprt
|
UTSW |
2 |
161,528,988 (GRCm39) |
critical splice donor site |
probably null |
|
R8308:Ptprt
|
UTSW |
2 |
161,769,566 (GRCm39) |
missense |
probably benign |
0.00 |
R8348:Ptprt
|
UTSW |
2 |
161,400,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R8362:Ptprt
|
UTSW |
2 |
161,393,667 (GRCm39) |
missense |
probably damaging |
1.00 |
R8365:Ptprt
|
UTSW |
2 |
161,743,451 (GRCm39) |
missense |
probably benign |
0.05 |
R8448:Ptprt
|
UTSW |
2 |
161,400,806 (GRCm39) |
missense |
probably damaging |
1.00 |
R8512:Ptprt
|
UTSW |
2 |
161,400,783 (GRCm39) |
missense |
probably benign |
0.00 |
R8715:Ptprt
|
UTSW |
2 |
161,372,463 (GRCm39) |
missense |
probably damaging |
1.00 |
R9004:Ptprt
|
UTSW |
2 |
161,608,314 (GRCm39) |
missense |
probably benign |
0.04 |
R9046:Ptprt
|
UTSW |
2 |
161,372,361 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9222:Ptprt
|
UTSW |
2 |
161,402,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R9297:Ptprt
|
UTSW |
2 |
161,417,698 (GRCm39) |
missense |
probably benign |
|
R9318:Ptprt
|
UTSW |
2 |
161,417,698 (GRCm39) |
missense |
probably benign |
|
R9476:Ptprt
|
UTSW |
2 |
161,397,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R9510:Ptprt
|
UTSW |
2 |
161,397,381 (GRCm39) |
missense |
probably damaging |
1.00 |
R9571:Ptprt
|
UTSW |
2 |
161,395,732 (GRCm39) |
missense |
probably benign |
0.10 |
X0064:Ptprt
|
UTSW |
2 |
161,769,403 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Ptprt
|
UTSW |
2 |
162,080,041 (GRCm39) |
missense |
possibly damaging |
0.86 |
Z1177:Ptprt
|
UTSW |
2 |
162,204,868 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1177:Ptprt
|
UTSW |
2 |
161,574,807 (GRCm39) |
missense |
probably damaging |
1.00 |
|