Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A730071L15Rik |
G |
A |
11: 6,150,439 (GRCm39) |
W137* |
probably null |
Het |
Acads |
G |
A |
5: 115,250,417 (GRCm39) |
T169I |
probably benign |
Het |
Adgrg7 |
T |
A |
16: 56,570,787 (GRCm39) |
N414Y |
probably damaging |
Het |
Ankrd35 |
T |
A |
3: 96,577,742 (GRCm39) |
S6T |
probably damaging |
Het |
Armc3 |
A |
G |
2: 19,206,630 (GRCm39) |
|
probably null |
Het |
Atp9a |
C |
A |
2: 168,496,140 (GRCm39) |
V555F |
possibly damaging |
Het |
Bltp1 |
A |
G |
3: 37,075,630 (GRCm39) |
Y3610C |
probably damaging |
Het |
Cars2 |
C |
T |
8: 11,566,198 (GRCm39) |
V443I |
probably benign |
Het |
Cblc |
A |
G |
7: 19,526,821 (GRCm39) |
L137P |
probably damaging |
Het |
Ccdc198 |
T |
C |
14: 49,481,270 (GRCm39) |
|
probably null |
Het |
Cdk5r1 |
T |
A |
11: 80,369,021 (GRCm39) |
C229* |
probably null |
Het |
Cep85 |
C |
G |
4: 133,883,167 (GRCm39) |
A241P |
probably benign |
Het |
Cfap54 |
T |
C |
10: 92,710,877 (GRCm39) |
Y2728C |
unknown |
Het |
Ckap5 |
T |
A |
2: 91,400,597 (GRCm39) |
W650R |
probably damaging |
Het |
Cnot11 |
C |
T |
1: 39,579,148 (GRCm39) |
Q12* |
probably null |
Het |
Commd6 |
A |
T |
14: 101,874,534 (GRCm39) |
D19E |
probably damaging |
Het |
Crygc |
C |
T |
1: 65,112,361 (GRCm39) |
G71D |
possibly damaging |
Het |
Cstf3 |
A |
G |
2: 104,486,076 (GRCm39) |
K439E |
probably benign |
Het |
Cyp11b2 |
G |
T |
15: 74,727,340 (GRCm39) |
H114N |
probably benign |
Het |
Cyp2d40 |
T |
C |
15: 82,645,687 (GRCm39) |
D106G |
probably benign |
Het |
Dhx8 |
T |
A |
11: 101,655,618 (GRCm39) |
V1117E |
probably damaging |
Het |
Duoxa1 |
G |
T |
2: 122,134,462 (GRCm39) |
L219I |
probably damaging |
Het |
Dynap |
A |
T |
18: 70,374,253 (GRCm39) |
I91N |
probably damaging |
Het |
Elfn1 |
G |
T |
5: 139,958,900 (GRCm39) |
G635W |
probably damaging |
Het |
Fan1 |
A |
T |
7: 64,014,377 (GRCm39) |
I618N |
probably damaging |
Het |
Fras1 |
A |
G |
5: 96,876,410 (GRCm39) |
D2381G |
probably damaging |
Het |
Fxyd6 |
T |
A |
9: 45,302,851 (GRCm39) |
|
probably null |
Het |
Gpr137b |
A |
T |
13: 13,538,094 (GRCm39) |
W286R |
probably damaging |
Het |
Gpsm3 |
A |
T |
17: 34,809,536 (GRCm39) |
|
probably null |
Het |
Has1 |
C |
T |
17: 18,064,122 (GRCm39) |
V506I |
probably benign |
Het |
Hoxd10 |
T |
A |
2: 74,522,616 (GRCm39) |
V98D |
probably benign |
Het |
Htr2b |
T |
A |
1: 86,027,615 (GRCm39) |
D297V |
probably benign |
Het |
Hydin |
G |
C |
8: 111,265,007 (GRCm39) |
R2730P |
probably benign |
Het |
I830077J02Rik |
T |
C |
3: 105,833,830 (GRCm39) |
N109D |
possibly damaging |
Het |
Igf2r |
A |
T |
17: 12,922,263 (GRCm39) |
F1284I |
probably damaging |
Het |
Ildr2 |
C |
G |
1: 166,098,144 (GRCm39) |
D167E |
probably damaging |
Het |
Ipo9 |
T |
C |
1: 135,314,046 (GRCm39) |
D949G |
probably benign |
Het |
Itga10 |
T |
C |
3: 96,564,030 (GRCm39) |
F895L |
probably damaging |
Het |
Itpr1 |
A |
G |
6: 108,365,153 (GRCm39) |
N27S |
probably damaging |
Het |
Klra4 |
C |
A |
6: 130,042,162 (GRCm39) |
R35L |
probably benign |
Het |
Map3k2 |
T |
A |
18: 32,359,682 (GRCm39) |
C512S |
probably benign |
Het |
Mertk |
A |
G |
2: 128,601,150 (GRCm39) |
|
probably null |
Het |
Mgat2 |
T |
A |
12: 69,232,407 (GRCm39) |
I327N |
probably damaging |
Het |
Mogat1 |
T |
C |
1: 78,499,496 (GRCm39) |
I59T |
probably damaging |
Het |
Mrpl2 |
A |
T |
17: 46,958,382 (GRCm39) |
M55L |
probably benign |
Het |
Nxpe3 |
T |
C |
16: 55,664,685 (GRCm39) |
M512V |
possibly damaging |
Het |
Pcdh15 |
T |
C |
10: 74,286,052 (GRCm39) |
L769P |
probably damaging |
Het |
Pcmtd2 |
T |
G |
2: 181,486,231 (GRCm39) |
V117G |
probably damaging |
Het |
Pdia2 |
A |
T |
17: 26,415,578 (GRCm39) |
|
probably null |
Het |
Repin1 |
A |
T |
6: 48,574,859 (GRCm39) |
Q593L |
possibly damaging |
Het |
Rnf213 |
C |
T |
11: 119,340,692 (GRCm39) |
T3517I |
probably benign |
Het |
Rxfp2 |
A |
T |
5: 149,942,210 (GRCm39) |
|
probably benign |
Het |
Slc35a3 |
T |
A |
3: 116,506,417 (GRCm39) |
Q5L |
probably null |
Het |
Stab2 |
T |
A |
10: 86,778,054 (GRCm39) |
N758I |
probably damaging |
Het |
Sulf1 |
T |
A |
1: 12,908,658 (GRCm39) |
I557N |
probably damaging |
Het |
Tbc1d8 |
T |
C |
1: 39,428,455 (GRCm39) |
I497V |
possibly damaging |
Het |
Ticam2 |
A |
C |
18: 46,693,998 (GRCm39) |
S30A |
probably benign |
Het |
Timp3 |
T |
C |
10: 86,181,638 (GRCm39) |
S170P |
possibly damaging |
Het |
Top1mt |
C |
T |
15: 75,547,973 (GRCm39) |
E38K |
probably benign |
Het |
Tpp1 |
G |
A |
7: 105,398,171 (GRCm39) |
L331F |
probably damaging |
Het |
Trpm7 |
A |
T |
2: 126,654,941 (GRCm39) |
D1332E |
probably benign |
Het |
Ttc23 |
A |
G |
7: 67,319,476 (GRCm39) |
E112G |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,715,296 (GRCm39) |
|
probably benign |
Het |
Ttn |
T |
A |
2: 76,726,934 (GRCm39) |
|
probably benign |
Het |
Ubr3 |
T |
A |
2: 69,850,969 (GRCm39) |
C1796S |
probably damaging |
Het |
Ugt2b34 |
C |
T |
5: 87,040,675 (GRCm39) |
V416I |
probably benign |
Het |
Uqcrb |
A |
G |
13: 67,048,827 (GRCm39) |
|
probably benign |
Het |
Vps26b |
A |
G |
9: 26,921,760 (GRCm39) |
L255P |
probably benign |
Het |
Wdr59 |
A |
G |
8: 112,223,512 (GRCm39) |
V154A |
probably damaging |
Het |
|
Other mutations in Skint8 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00772:Skint8
|
APN |
4 |
111,796,120 (GRCm39) |
missense |
probably benign |
0.05 |
IGL01411:Skint8
|
APN |
4 |
111,794,103 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02973:Skint8
|
APN |
4 |
111,796,790 (GRCm39) |
missense |
probably benign |
0.09 |
IGL03154:Skint8
|
APN |
4 |
111,796,707 (GRCm39) |
splice site |
probably null |
|
FR4976:Skint8
|
UTSW |
4 |
111,796,099 (GRCm39) |
missense |
probably benign |
0.02 |
R0309:Skint8
|
UTSW |
4 |
111,796,064 (GRCm39) |
missense |
probably benign |
0.02 |
R0448:Skint8
|
UTSW |
4 |
111,794,087 (GRCm39) |
missense |
probably damaging |
1.00 |
R0483:Skint8
|
UTSW |
4 |
111,796,020 (GRCm39) |
splice site |
probably benign |
|
R0586:Skint8
|
UTSW |
4 |
111,794,126 (GRCm39) |
missense |
probably damaging |
1.00 |
R1076:Skint8
|
UTSW |
4 |
111,784,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R1169:Skint8
|
UTSW |
4 |
111,785,710 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1588:Skint8
|
UTSW |
4 |
111,785,924 (GRCm39) |
nonsense |
probably null |
|
R1707:Skint8
|
UTSW |
4 |
111,796,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R1865:Skint8
|
UTSW |
4 |
111,794,192 (GRCm39) |
missense |
probably damaging |
1.00 |
R1954:Skint8
|
UTSW |
4 |
111,807,278 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2147:Skint8
|
UTSW |
4 |
111,794,274 (GRCm39) |
missense |
probably damaging |
1.00 |
R2896:Skint8
|
UTSW |
4 |
111,807,333 (GRCm39) |
missense |
probably null |
|
R4945:Skint8
|
UTSW |
4 |
111,796,805 (GRCm39) |
missense |
probably damaging |
0.96 |
R5019:Skint8
|
UTSW |
4 |
111,785,845 (GRCm39) |
missense |
probably damaging |
0.99 |
R5281:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5284:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5289:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5309:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5310:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5588:Skint8
|
UTSW |
4 |
111,794,089 (GRCm39) |
missense |
probably benign |
0.01 |
R5636:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5637:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5638:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5639:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5719:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5720:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5754:Skint8
|
UTSW |
4 |
111,807,387 (GRCm39) |
missense |
probably benign |
|
R5850:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R5855:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R6036:Skint8
|
UTSW |
4 |
111,807,390 (GRCm39) |
missense |
probably damaging |
0.98 |
R6525:Skint8
|
UTSW |
4 |
111,785,935 (GRCm39) |
missense |
probably damaging |
0.98 |
R6554:Skint8
|
UTSW |
4 |
111,784,413 (GRCm39) |
missense |
probably benign |
0.35 |
R6578:Skint8
|
UTSW |
4 |
111,794,159 (GRCm39) |
missense |
probably benign |
0.03 |
R7000:Skint8
|
UTSW |
4 |
111,794,222 (GRCm39) |
missense |
probably benign |
0.16 |
R7317:Skint8
|
UTSW |
4 |
111,796,717 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7336:Skint8
|
UTSW |
4 |
111,796,769 (GRCm39) |
missense |
probably benign |
0.32 |
R7412:Skint8
|
UTSW |
4 |
111,785,758 (GRCm39) |
missense |
probably benign |
0.07 |
R7480:Skint8
|
UTSW |
4 |
111,785,784 (GRCm39) |
nonsense |
probably null |
|
R8027:Skint8
|
UTSW |
4 |
111,785,936 (GRCm39) |
missense |
probably benign |
0.36 |
R8204:Skint8
|
UTSW |
4 |
111,796,090 (GRCm39) |
missense |
probably benign |
0.03 |
R8963:Skint8
|
UTSW |
4 |
111,794,241 (GRCm39) |
missense |
probably benign |
0.03 |
R9084:Skint8
|
UTSW |
4 |
111,794,210 (GRCm39) |
missense |
probably benign |
0.11 |
R9249:Skint8
|
UTSW |
4 |
111,794,159 (GRCm39) |
missense |
probably damaging |
0.98 |
R9283:Skint8
|
UTSW |
4 |
111,785,644 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1177:Skint8
|
UTSW |
4 |
111,794,251 (GRCm39) |
missense |
probably benign |
0.39 |
|