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 |
Skint8 |
T |
C |
4: 111,785,968 (GRCm39) |
L138P |
probably damaging |
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 Slc35a3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01285:Slc35a3
|
APN |
3 |
116,488,262 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02092:Slc35a3
|
APN |
3 |
116,474,781 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02424:Slc35a3
|
APN |
3 |
116,488,267 (GRCm39) |
missense |
possibly damaging |
0.92 |
IGL03304:Slc35a3
|
APN |
3 |
116,480,960 (GRCm39) |
missense |
probably damaging |
1.00 |
R1465:Slc35a3
|
UTSW |
3 |
116,480,983 (GRCm39) |
missense |
probably benign |
0.44 |
R1465:Slc35a3
|
UTSW |
3 |
116,480,983 (GRCm39) |
missense |
probably benign |
0.44 |
R1753:Slc35a3
|
UTSW |
3 |
116,471,597 (GRCm39) |
missense |
possibly damaging |
0.79 |
R2035:Slc35a3
|
UTSW |
3 |
116,480,972 (GRCm39) |
missense |
probably damaging |
1.00 |
R2265:Slc35a3
|
UTSW |
3 |
116,467,285 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2266:Slc35a3
|
UTSW |
3 |
116,467,285 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2267:Slc35a3
|
UTSW |
3 |
116,467,285 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2268:Slc35a3
|
UTSW |
3 |
116,467,285 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4073:Slc35a3
|
UTSW |
3 |
116,468,887 (GRCm39) |
missense |
probably benign |
0.05 |
R5187:Slc35a3
|
UTSW |
3 |
116,474,794 (GRCm39) |
missense |
probably damaging |
1.00 |
R5490:Slc35a3
|
UTSW |
3 |
116,474,839 (GRCm39) |
nonsense |
probably null |
|
R7270:Slc35a3
|
UTSW |
3 |
116,505,455 (GRCm39) |
intron |
probably benign |
|
R7964:Slc35a3
|
UTSW |
3 |
116,480,984 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8747:Slc35a3
|
UTSW |
3 |
116,488,219 (GRCm39) |
missense |
probably damaging |
1.00 |
R9556:Slc35a3
|
UTSW |
3 |
116,474,763 (GRCm39) |
missense |
possibly damaging |
0.63 |
|