Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abraxas1 |
A |
G |
5: 100,954,698 (GRCm39) |
V247A |
probably damaging |
Het |
Acot13 |
G |
T |
13: 25,002,133 (GRCm39) |
T103K |
probably damaging |
Het |
Acsl6 |
A |
T |
11: 54,251,901 (GRCm39) |
I683F |
probably damaging |
Het |
Acss2 |
A |
T |
2: 155,402,953 (GRCm39) |
H577L |
probably damaging |
Het |
Ahctf1 |
A |
T |
1: 179,614,638 (GRCm39) |
V382D |
probably damaging |
Het |
Aldob |
T |
C |
4: 49,538,858 (GRCm39) |
H220R |
probably damaging |
Het |
Ankrd1 |
C |
T |
19: 36,094,218 (GRCm39) |
V169M |
probably damaging |
Het |
Atp5f1a |
G |
A |
18: 77,869,015 (GRCm39) |
R413H |
possibly damaging |
Het |
Cep76 |
A |
G |
18: 67,762,975 (GRCm39) |
F283L |
probably damaging |
Het |
Chrna5 |
A |
T |
9: 54,912,391 (GRCm39) |
D397V |
probably benign |
Het |
Coro7 |
T |
C |
16: 4,488,400 (GRCm39) |
D90G |
probably damaging |
Het |
Csnk1g3 |
A |
G |
18: 54,081,177 (GRCm39) |
N383D |
probably benign |
Het |
Cwf19l2 |
C |
A |
9: 3,477,889 (GRCm39) |
Q865K |
probably damaging |
Het |
Cyth2 |
C |
A |
7: 45,460,378 (GRCm39) |
W149C |
probably damaging |
Het |
Dgkh |
C |
A |
14: 78,856,026 (GRCm39) |
R349L |
probably damaging |
Het |
Dnajc1 |
G |
T |
2: 18,224,704 (GRCm39) |
T383N |
possibly damaging |
Het |
Efcab3 |
T |
A |
11: 104,605,571 (GRCm39) |
|
probably null |
Het |
Extl3 |
A |
T |
14: 65,313,181 (GRCm39) |
M667K |
probably damaging |
Het |
Fam149a |
G |
T |
8: 45,811,678 (GRCm39) |
A75E |
|
Het |
Fgd4 |
T |
G |
16: 16,240,590 (GRCm39) |
Q713P |
probably damaging |
Het |
Frat2 |
T |
A |
19: 41,836,215 (GRCm39) |
I46F |
probably damaging |
Het |
Gzmc |
A |
G |
14: 56,469,017 (GRCm39) |
V234A |
probably damaging |
Het |
H2-Q4 |
A |
G |
17: 35,599,134 (GRCm39) |
N135D |
probably damaging |
Het |
Ighv1-85 |
A |
T |
12: 115,963,937 (GRCm39) |
V21D |
possibly damaging |
Het |
Itprid1 |
A |
G |
6: 55,955,320 (GRCm39) |
Q976R |
possibly damaging |
Het |
Kcna6 |
A |
T |
6: 126,715,983 (GRCm39) |
V302E |
probably damaging |
Het |
Kdm3b |
G |
T |
18: 34,942,293 (GRCm39) |
V795L |
possibly damaging |
Het |
Kdm5b |
G |
A |
1: 134,545,578 (GRCm39) |
R913H |
probably damaging |
Het |
Lpp |
T |
A |
16: 24,426,876 (GRCm39) |
M1K |
probably null |
Het |
Med12l |
T |
C |
3: 59,172,355 (GRCm39) |
S1704P |
probably damaging |
Het |
Mfsd10 |
G |
T |
5: 34,793,456 (GRCm39) |
S95* |
probably null |
Het |
Napepld |
C |
T |
5: 21,880,721 (GRCm39) |
E225K |
probably benign |
Het |
Ndfip2 |
T |
C |
14: 105,535,448 (GRCm39) |
F245L |
probably damaging |
Het |
Oaf |
G |
A |
9: 43,134,077 (GRCm39) |
R215C |
probably damaging |
Het |
Or10k2 |
A |
G |
8: 84,268,526 (GRCm39) |
H251R |
probably damaging |
Het |
Or13a20 |
C |
T |
7: 140,232,374 (GRCm39) |
H161Y |
probably damaging |
Het |
Or51i1 |
A |
G |
7: 103,670,736 (GRCm39) |
I263T |
possibly damaging |
Het |
Or52z15 |
A |
G |
7: 103,332,407 (GRCm39) |
I161V |
probably benign |
Het |
Or5p6 |
A |
G |
7: 107,631,199 (GRCm39) |
I117T |
probably benign |
Het |
Or8b47 |
A |
G |
9: 38,435,675 (GRCm39) |
T216A |
probably benign |
Het |
Pcdhgb2 |
A |
T |
18: 37,825,273 (GRCm39) |
I755F |
possibly damaging |
Het |
Pde4dip |
A |
G |
3: 97,622,490 (GRCm39) |
L1573P |
probably damaging |
Het |
Peg3 |
A |
T |
7: 6,713,650 (GRCm39) |
V524E |
probably damaging |
Het |
Phc1 |
G |
T |
6: 122,310,329 (GRCm39) |
T126N |
probably damaging |
Het |
Phf1 |
C |
A |
17: 27,154,291 (GRCm39) |
Y169* |
probably null |
Het |
Pramel25 |
A |
T |
4: 143,520,563 (GRCm39) |
D269V |
probably benign |
Het |
Prl3a1 |
G |
A |
13: 27,456,442 (GRCm39) |
E99K |
probably damaging |
Het |
Prss57 |
G |
A |
10: 79,623,213 (GRCm39) |
A78V |
probably damaging |
Het |
Rgsl1 |
A |
T |
1: 153,701,783 (GRCm39) |
C224S |
possibly damaging |
Het |
Rtn4 |
T |
C |
11: 29,643,274 (GRCm39) |
V29A |
unknown |
Het |
Selplg |
G |
A |
5: 113,957,481 (GRCm39) |
T275M |
probably damaging |
Het |
Skint11 |
C |
T |
4: 114,102,076 (GRCm39) |
T363I |
possibly damaging |
Het |
Slc22a29 |
T |
A |
19: 8,170,851 (GRCm39) |
I289F |
probably benign |
Het |
Slc26a2 |
A |
G |
18: 61,331,776 (GRCm39) |
S552P |
probably benign |
Het |
Sptb |
T |
A |
12: 76,655,300 (GRCm39) |
K1480* |
probably null |
Het |
Sptbn1 |
C |
A |
11: 30,092,153 (GRCm39) |
M537I |
probably damaging |
Het |
Sqor |
A |
T |
2: 122,627,008 (GRCm39) |
H43L |
probably benign |
Het |
Srcin1 |
C |
A |
11: 97,416,926 (GRCm39) |
E913* |
probably null |
Het |
Srgap1 |
A |
G |
10: 121,621,397 (GRCm39) |
L1032P |
probably damaging |
Het |
Stc2 |
T |
C |
11: 31,315,413 (GRCm39) |
K142R |
probably benign |
Het |
Stox1 |
A |
C |
10: 62,495,305 (GRCm39) |
N989K |
probably damaging |
Het |
Tert |
T |
A |
13: 73,776,314 (GRCm39) |
L355H |
probably damaging |
Het |
Tfb2m |
A |
G |
1: 179,358,926 (GRCm39) |
F319S |
probably damaging |
Het |
Trps1 |
A |
G |
15: 50,695,273 (GRCm39) |
F341L |
probably damaging |
Het |
Ttk |
T |
C |
9: 83,725,732 (GRCm39) |
V218A |
probably benign |
Het |
Vmn1r159 |
A |
G |
7: 22,542,696 (GRCm39) |
I112T |
probably benign |
Het |
Vps8 |
C |
A |
16: 21,351,070 (GRCm39) |
Q916K |
probably benign |
Het |
Wdr12 |
A |
T |
1: 60,121,225 (GRCm39) |
D364E |
probably damaging |
Het |
Ylpm1 |
A |
G |
12: 85,104,042 (GRCm39) |
E2019G |
probably damaging |
Het |
Zfp267 |
C |
A |
3: 36,219,738 (GRCm39) |
T587N |
probably benign |
Het |
Zfp507 |
A |
G |
7: 35,493,963 (GRCm39) |
L360P |
probably damaging |
Het |
|
Other mutations in Ptprb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01295:Ptprb
|
APN |
10 |
116,198,553 (GRCm39) |
missense |
probably benign |
0.15 |
IGL01354:Ptprb
|
APN |
10 |
116,179,796 (GRCm39) |
missense |
probably benign |
0.24 |
IGL01404:Ptprb
|
APN |
10 |
116,175,341 (GRCm39) |
missense |
probably benign |
0.14 |
IGL01410:Ptprb
|
APN |
10 |
116,138,179 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL01412:Ptprb
|
APN |
10 |
116,179,820 (GRCm39) |
missense |
probably benign |
0.27 |
IGL01731:Ptprb
|
APN |
10 |
116,208,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02003:Ptprb
|
APN |
10 |
116,203,410 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02110:Ptprb
|
APN |
10 |
116,167,108 (GRCm39) |
splice site |
probably benign |
|
IGL02178:Ptprb
|
APN |
10 |
116,158,437 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02304:Ptprb
|
APN |
10 |
116,167,164 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02324:Ptprb
|
APN |
10 |
116,155,238 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02388:Ptprb
|
APN |
10 |
116,203,426 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02640:Ptprb
|
APN |
10 |
116,174,569 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02698:Ptprb
|
APN |
10 |
116,199,185 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02876:Ptprb
|
APN |
10 |
116,184,116 (GRCm39) |
splice site |
probably benign |
|
IGL02879:Ptprb
|
APN |
10 |
116,163,873 (GRCm39) |
missense |
probably benign |
|
IGL02982:Ptprb
|
APN |
10 |
116,158,533 (GRCm39) |
missense |
probably benign |
0.20 |
IGL03146:Ptprb
|
APN |
10 |
116,164,032 (GRCm39) |
missense |
probably benign |
0.14 |
IGL03351:Ptprb
|
APN |
10 |
116,175,487 (GRCm39) |
missense |
probably benign |
0.03 |
R0306:Ptprb
|
UTSW |
10 |
116,179,893 (GRCm39) |
missense |
probably benign |
0.04 |
R0385:Ptprb
|
UTSW |
10 |
116,186,083 (GRCm39) |
missense |
probably benign |
0.00 |
R0600:Ptprb
|
UTSW |
10 |
116,204,712 (GRCm39) |
missense |
possibly damaging |
0.63 |
R0613:Ptprb
|
UTSW |
10 |
116,138,283 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0613:Ptprb
|
UTSW |
10 |
116,138,230 (GRCm39) |
missense |
possibly damaging |
0.59 |
R0850:Ptprb
|
UTSW |
10 |
116,175,415 (GRCm39) |
missense |
probably damaging |
1.00 |
R0850:Ptprb
|
UTSW |
10 |
116,138,030 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1331:Ptprb
|
UTSW |
10 |
116,203,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R1413:Ptprb
|
UTSW |
10 |
116,175,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R1418:Ptprb
|
UTSW |
10 |
116,155,375 (GRCm39) |
missense |
probably benign |
0.00 |
R1545:Ptprb
|
UTSW |
10 |
116,216,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R1562:Ptprb
|
UTSW |
10 |
116,175,372 (GRCm39) |
missense |
probably benign |
0.00 |
R1752:Ptprb
|
UTSW |
10 |
116,176,895 (GRCm39) |
missense |
probably benign |
0.44 |
R1837:Ptprb
|
UTSW |
10 |
116,177,531 (GRCm39) |
missense |
probably benign |
0.00 |
R1940:Ptprb
|
UTSW |
10 |
116,155,515 (GRCm39) |
splice site |
probably benign |
|
R1958:Ptprb
|
UTSW |
10 |
116,177,441 (GRCm39) |
missense |
probably benign |
0.10 |
R2029:Ptprb
|
UTSW |
10 |
116,182,958 (GRCm39) |
missense |
probably benign |
0.37 |
R2031:Ptprb
|
UTSW |
10 |
116,153,448 (GRCm39) |
missense |
probably benign |
|
R2101:Ptprb
|
UTSW |
10 |
116,150,943 (GRCm39) |
splice site |
probably benign |
|
R2209:Ptprb
|
UTSW |
10 |
116,205,262 (GRCm39) |
missense |
probably damaging |
1.00 |
R3016:Ptprb
|
UTSW |
10 |
116,193,200 (GRCm39) |
missense |
possibly damaging |
0.64 |
R3076:Ptprb
|
UTSW |
10 |
116,179,931 (GRCm39) |
missense |
probably damaging |
0.99 |
R3821:Ptprb
|
UTSW |
10 |
116,185,979 (GRCm39) |
missense |
probably benign |
0.11 |
R3824:Ptprb
|
UTSW |
10 |
116,186,694 (GRCm39) |
missense |
probably benign |
0.05 |
R3825:Ptprb
|
UTSW |
10 |
116,186,694 (GRCm39) |
missense |
probably benign |
0.05 |
R3841:Ptprb
|
UTSW |
10 |
116,182,887 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3953:Ptprb
|
UTSW |
10 |
116,177,399 (GRCm39) |
missense |
probably benign |
0.00 |
R4125:Ptprb
|
UTSW |
10 |
116,189,754 (GRCm39) |
missense |
probably benign |
0.12 |
R4227:Ptprb
|
UTSW |
10 |
116,138,130 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4385:Ptprb
|
UTSW |
10 |
116,182,772 (GRCm39) |
missense |
probably benign |
|
R4731:Ptprb
|
UTSW |
10 |
116,155,238 (GRCm39) |
missense |
probably benign |
0.03 |
R5009:Ptprb
|
UTSW |
10 |
116,184,032 (GRCm39) |
missense |
possibly damaging |
0.61 |
R5104:Ptprb
|
UTSW |
10 |
116,158,364 (GRCm39) |
missense |
probably benign |
0.17 |
R5114:Ptprb
|
UTSW |
10 |
116,184,088 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5145:Ptprb
|
UTSW |
10 |
116,179,820 (GRCm39) |
missense |
probably benign |
0.27 |
R5214:Ptprb
|
UTSW |
10 |
116,205,229 (GRCm39) |
missense |
possibly damaging |
0.75 |
R5382:Ptprb
|
UTSW |
10 |
116,189,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R5553:Ptprb
|
UTSW |
10 |
116,186,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5585:Ptprb
|
UTSW |
10 |
116,216,759 (GRCm39) |
missense |
probably damaging |
0.98 |
R5586:Ptprb
|
UTSW |
10 |
116,189,732 (GRCm39) |
missense |
probably damaging |
1.00 |
R5808:Ptprb
|
UTSW |
10 |
116,175,392 (GRCm39) |
missense |
probably benign |
0.00 |
R5875:Ptprb
|
UTSW |
10 |
116,184,071 (GRCm39) |
missense |
probably benign |
0.00 |
R6051:Ptprb
|
UTSW |
10 |
116,176,995 (GRCm39) |
nonsense |
probably null |
|
R6383:Ptprb
|
UTSW |
10 |
116,182,912 (GRCm39) |
nonsense |
probably null |
|
R6511:Ptprb
|
UTSW |
10 |
116,182,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R6817:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R6826:Ptprb
|
UTSW |
10 |
116,153,277 (GRCm39) |
missense |
probably benign |
0.26 |
R6958:Ptprb
|
UTSW |
10 |
116,113,153 (GRCm39) |
missense |
probably benign |
0.32 |
R7103:Ptprb
|
UTSW |
10 |
116,174,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R7129:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R7181:Ptprb
|
UTSW |
10 |
116,204,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R7215:Ptprb
|
UTSW |
10 |
116,174,681 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7289:Ptprb
|
UTSW |
10 |
116,164,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R7315:Ptprb
|
UTSW |
10 |
116,198,284 (GRCm39) |
missense |
possibly damaging |
0.83 |
R7319:Ptprb
|
UTSW |
10 |
116,177,309 (GRCm39) |
missense |
probably benign |
0.01 |
R7381:Ptprb
|
UTSW |
10 |
116,177,038 (GRCm39) |
missense |
probably benign |
|
R7412:Ptprb
|
UTSW |
10 |
116,177,043 (GRCm39) |
missense |
probably benign |
|
R7483:Ptprb
|
UTSW |
10 |
116,119,334 (GRCm39) |
missense |
probably benign |
0.01 |
R7495:Ptprb
|
UTSW |
10 |
116,177,353 (GRCm39) |
missense |
probably benign |
0.12 |
R7508:Ptprb
|
UTSW |
10 |
116,189,896 (GRCm39) |
nonsense |
probably null |
|
R7571:Ptprb
|
UTSW |
10 |
116,175,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R7586:Ptprb
|
UTSW |
10 |
116,179,779 (GRCm39) |
missense |
probably damaging |
0.97 |
R7623:Ptprb
|
UTSW |
10 |
116,205,214 (GRCm39) |
missense |
possibly damaging |
0.63 |
R7694:Ptprb
|
UTSW |
10 |
116,208,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R7744:Ptprb
|
UTSW |
10 |
116,113,389 (GRCm39) |
missense |
probably benign |
0.10 |
R7752:Ptprb
|
UTSW |
10 |
116,205,333 (GRCm39) |
missense |
probably benign |
0.37 |
R7826:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R7833:Ptprb
|
UTSW |
10 |
116,151,156 (GRCm39) |
missense |
probably benign |
0.01 |
R7834:Ptprb
|
UTSW |
10 |
116,175,329 (GRCm39) |
missense |
probably benign |
0.00 |
R7896:Ptprb
|
UTSW |
10 |
116,205,362 (GRCm39) |
splice site |
probably null |
|
R7901:Ptprb
|
UTSW |
10 |
116,205,333 (GRCm39) |
missense |
probably benign |
0.37 |
R7912:Ptprb
|
UTSW |
10 |
116,158,392 (GRCm39) |
missense |
probably damaging |
1.00 |
R7941:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R8147:Ptprb
|
UTSW |
10 |
116,153,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R8202:Ptprb
|
UTSW |
10 |
116,189,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R8339:Ptprb
|
UTSW |
10 |
116,119,356 (GRCm39) |
missense |
probably benign |
0.14 |
R8400:Ptprb
|
UTSW |
10 |
116,119,477 (GRCm39) |
small deletion |
probably benign |
|
R8504:Ptprb
|
UTSW |
10 |
116,176,936 (GRCm39) |
missense |
probably benign |
0.27 |
R8679:Ptprb
|
UTSW |
10 |
116,203,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R8786:Ptprb
|
UTSW |
10 |
116,155,306 (GRCm39) |
missense |
probably benign |
0.40 |
R8914:Ptprb
|
UTSW |
10 |
116,158,567 (GRCm39) |
nonsense |
probably null |
|
R8980:Ptprb
|
UTSW |
10 |
116,119,526 (GRCm39) |
missense |
probably benign |
0.07 |
R8982:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
R9256:Ptprb
|
UTSW |
10 |
116,219,776 (GRCm39) |
missense |
probably damaging |
1.00 |
R9288:Ptprb
|
UTSW |
10 |
116,155,353 (GRCm39) |
missense |
probably benign |
0.03 |
R9369:Ptprb
|
UTSW |
10 |
116,151,057 (GRCm39) |
missense |
probably benign |
0.00 |
R9448:Ptprb
|
UTSW |
10 |
116,149,819 (GRCm39) |
nonsense |
probably null |
|
R9467:Ptprb
|
UTSW |
10 |
116,158,390 (GRCm39) |
missense |
probably benign |
0.00 |
R9468:Ptprb
|
UTSW |
10 |
116,113,274 (GRCm39) |
missense |
probably benign |
0.00 |
R9481:Ptprb
|
UTSW |
10 |
116,155,353 (GRCm39) |
missense |
probably benign |
0.03 |
R9486:Ptprb
|
UTSW |
10 |
116,155,494 (GRCm39) |
nonsense |
probably null |
|
R9513:Ptprb
|
UTSW |
10 |
116,138,142 (GRCm39) |
missense |
probably benign |
0.00 |
R9529:Ptprb
|
UTSW |
10 |
116,174,519 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9535:Ptprb
|
UTSW |
10 |
116,158,431 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9614:Ptprb
|
UTSW |
10 |
116,203,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R9686:Ptprb
|
UTSW |
10 |
116,204,694 (GRCm39) |
missense |
probably damaging |
1.00 |
RF041:Ptprb
|
UTSW |
10 |
116,119,582 (GRCm39) |
small deletion |
probably benign |
|
X0020:Ptprb
|
UTSW |
10 |
116,138,085 (GRCm39) |
missense |
possibly damaging |
0.62 |
Z1176:Ptprb
|
UTSW |
10 |
116,138,061 (GRCm39) |
frame shift |
probably null |
|
Z1177:Ptprb
|
UTSW |
10 |
116,198,547 (GRCm39) |
critical splice acceptor site |
probably null |
|
|