Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca2 |
A |
G |
2: 25,336,331 (GRCm39) |
I2201V |
probably benign |
Het |
Adam22 |
T |
C |
5: 8,145,007 (GRCm39) |
N817S |
probably damaging |
Het |
Alox12 |
C |
A |
11: 70,140,991 (GRCm39) |
R348L |
probably damaging |
Het |
Asb17 |
A |
T |
3: 153,559,143 (GRCm39) |
T285S |
probably benign |
Het |
Casp4 |
T |
C |
9: 5,324,733 (GRCm39) |
S182P |
possibly damaging |
Het |
Cenpe |
T |
C |
3: 134,944,155 (GRCm39) |
M985T |
possibly damaging |
Het |
Clcn1 |
C |
T |
6: 42,277,169 (GRCm39) |
P420L |
probably benign |
Het |
Coro2a |
T |
C |
4: 46,548,917 (GRCm39) |
I126V |
probably benign |
Het |
Cubn |
T |
C |
2: 13,432,778 (GRCm39) |
Y1181C |
probably damaging |
Het |
Cyp2d22 |
A |
T |
15: 82,258,179 (GRCm39) |
L147Q |
probably damaging |
Het |
Dna2 |
C |
T |
10: 62,784,966 (GRCm39) |
R28W |
probably benign |
Het |
Ecm1 |
G |
A |
3: 95,643,275 (GRCm39) |
R342C |
probably damaging |
Het |
Fat2 |
T |
C |
11: 55,200,800 (GRCm39) |
N758S |
probably damaging |
Het |
Fbxo43 |
T |
C |
15: 36,163,162 (GRCm39) |
D15G |
probably damaging |
Het |
Flt3 |
T |
C |
5: 147,281,323 (GRCm39) |
E803G |
probably damaging |
Het |
Folr1 |
T |
G |
7: 101,507,801 (GRCm39) |
D213A |
probably damaging |
Het |
Fus |
T |
C |
7: 127,579,094 (GRCm39) |
V359A |
probably damaging |
Het |
Gabrb3 |
C |
T |
7: 57,415,262 (GRCm39) |
R111* |
probably null |
Het |
Gm17324 |
T |
C |
9: 78,355,964 (GRCm39) |
|
probably benign |
Het |
Hormad2 |
A |
T |
11: 4,358,848 (GRCm39) |
|
probably null |
Het |
Ifi27l2b |
T |
A |
12: 103,422,780 (GRCm39) |
|
probably null |
Het |
Isg20 |
G |
T |
7: 78,569,891 (GRCm39) |
C176F |
probably benign |
Het |
Katnip |
C |
A |
7: 125,442,020 (GRCm39) |
S643Y |
probably damaging |
Het |
Krt15 |
C |
A |
11: 100,024,007 (GRCm39) |
V346L |
probably benign |
Het |
Liat1 |
A |
T |
11: 75,894,024 (GRCm39) |
I134F |
probably damaging |
Het |
Med13l |
A |
G |
5: 118,876,584 (GRCm39) |
K920R |
probably damaging |
Het |
Mlh3 |
A |
T |
12: 85,313,694 (GRCm39) |
F831I |
probably benign |
Het |
Mtmr9 |
A |
G |
14: 63,771,786 (GRCm39) |
S267P |
probably benign |
Het |
Mybpc1 |
C |
T |
10: 88,389,193 (GRCm39) |
A406T |
probably damaging |
Het |
Myh1 |
T |
C |
11: 67,102,196 (GRCm39) |
M829T |
probably benign |
Het |
Myo10 |
A |
G |
15: 25,780,497 (GRCm39) |
Q209R |
possibly damaging |
Het |
Nceh1 |
T |
A |
3: 27,293,701 (GRCm39) |
V153D |
probably damaging |
Het |
Oog3 |
A |
T |
4: 143,889,169 (GRCm39) |
I3N |
probably damaging |
Het |
Or1j19 |
A |
G |
2: 36,676,696 (GRCm39) |
D53G |
probably damaging |
Het |
Or2ag1b |
C |
T |
7: 106,288,187 (GRCm39) |
M250I |
probably benign |
Het |
Or4c103 |
T |
A |
2: 88,513,423 (GRCm39) |
I218F |
probably benign |
Het |
Or8c20 |
C |
A |
9: 38,260,658 (GRCm39) |
S87* |
probably null |
Het |
Pcnt |
G |
A |
10: 76,203,164 (GRCm39) |
T2646M |
probably benign |
Het |
Phf10 |
A |
T |
17: 15,166,512 (GRCm39) |
C453S |
probably damaging |
Het |
Plcb4 |
T |
A |
2: 135,812,367 (GRCm39) |
|
probably null |
Het |
Plekhh1 |
A |
G |
12: 79,123,482 (GRCm39) |
H1185R |
probably benign |
Het |
Prmt3 |
G |
T |
7: 49,476,602 (GRCm39) |
V404L |
probably benign |
Het |
Rars1 |
A |
G |
11: 35,711,921 (GRCm39) |
|
probably null |
Het |
Rasa2 |
G |
T |
9: 96,427,803 (GRCm39) |
N687K |
possibly damaging |
Het |
Rbm11 |
A |
G |
16: 75,393,423 (GRCm39) |
T40A |
probably damaging |
Het |
Rem2 |
T |
C |
14: 54,713,775 (GRCm39) |
V16A |
probably benign |
Het |
Rlf |
A |
T |
4: 121,007,588 (GRCm39) |
M574K |
possibly damaging |
Het |
Rpap3 |
A |
T |
15: 97,592,098 (GRCm39) |
V186D |
possibly damaging |
Het |
Sertad3 |
G |
A |
7: 27,176,048 (GRCm39) |
E161K |
probably damaging |
Het |
Sh3gl2 |
T |
C |
4: 85,304,130 (GRCm39) |
S278P |
probably benign |
Het |
Strn3 |
T |
C |
12: 51,680,401 (GRCm39) |
T400A |
probably benign |
Het |
Sycp2 |
A |
T |
2: 178,024,178 (GRCm39) |
I402N |
probably damaging |
Het |
Synj1 |
C |
T |
16: 90,784,290 (GRCm39) |
V283I |
probably benign |
Het |
Tas2r108 |
A |
G |
6: 40,471,000 (GRCm39) |
|
probably null |
Het |
Ttpal |
A |
G |
2: 163,457,323 (GRCm39) |
N265S |
probably benign |
Het |
Unc80 |
G |
A |
1: 66,677,116 (GRCm39) |
G2015D |
probably damaging |
Het |
Upf1 |
C |
T |
8: 70,796,017 (GRCm39) |
W138* |
probably null |
Het |
Vmn1r25 |
T |
G |
6: 57,955,786 (GRCm39) |
M168L |
probably benign |
Het |
Vmn2r18 |
A |
T |
5: 151,510,301 (GRCm39) |
F24Y |
probably benign |
Het |
Vmn2r4 |
G |
T |
3: 64,296,865 (GRCm39) |
T640N |
probably damaging |
Het |
Wdr75 |
T |
A |
1: 45,843,030 (GRCm39) |
|
probably null |
Het |
Zdbf2 |
T |
G |
1: 63,342,747 (GRCm39) |
S375R |
possibly damaging |
Het |
Zfp648 |
A |
G |
1: 154,080,138 (GRCm39) |
Q99R |
probably benign |
Het |
Zfp964 |
C |
T |
8: 70,115,654 (GRCm39) |
P85S |
probably benign |
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 |
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 |
R7846:Ptprb
|
UTSW |
10 |
116,119,453 (GRCm39) |
missense |
probably benign |
0.17 |
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 |
|
|