Other mutations in this stock |
Total: 91 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc12 |
C |
T |
8: 87,293,173 (GRCm39) |
G5D |
possibly damaging |
Het |
Adamts9 |
T |
C |
6: 92,867,101 (GRCm39) |
K95R |
probably damaging |
Het |
Adap1 |
G |
T |
5: 139,259,246 (GRCm39) |
L314M |
probably benign |
Het |
Alkbh1 |
T |
A |
12: 87,475,864 (GRCm39) |
E306V |
possibly damaging |
Het |
Alpk2 |
T |
A |
18: 65,438,972 (GRCm39) |
D1274V |
possibly damaging |
Het |
Ankrd31 |
A |
C |
13: 97,014,746 (GRCm39) |
K1188N |
possibly damaging |
Het |
Aox1 |
T |
A |
1: 58,369,965 (GRCm39) |
M759K |
probably damaging |
Het |
Atp13a3 |
T |
A |
16: 30,155,061 (GRCm39) |
D961V |
probably damaging |
Het |
Bcl11a |
G |
A |
11: 24,108,321 (GRCm39) |
G100R |
probably damaging |
Het |
Bpifc |
G |
A |
10: 85,812,122 (GRCm39) |
A362V |
probably damaging |
Het |
Btaf1 |
C |
T |
19: 36,950,408 (GRCm39) |
T546I |
probably benign |
Het |
Casd1 |
C |
A |
6: 4,619,834 (GRCm39) |
P193Q |
probably damaging |
Het |
Cdhr1 |
T |
C |
14: 36,811,422 (GRCm39) |
T230A |
probably benign |
Het |
Celsr3 |
T |
G |
9: 108,706,041 (GRCm39) |
D841E |
probably damaging |
Het |
Cenpj |
T |
C |
14: 56,789,433 (GRCm39) |
D872G |
probably benign |
Het |
Cep95 |
G |
T |
11: 106,706,422 (GRCm39) |
A559S |
probably damaging |
Het |
Chpt1 |
A |
T |
10: 88,311,306 (GRCm39) |
C62* |
probably null |
Het |
Cspg4b |
T |
A |
13: 113,456,981 (GRCm39) |
I1009N |
possibly damaging |
Het |
Cspp1 |
A |
G |
1: 10,134,559 (GRCm39) |
K103R |
probably damaging |
Het |
Ctla4 |
T |
C |
1: 60,951,837 (GRCm39) |
V122A |
probably benign |
Het |
Cyp3a11 |
A |
G |
5: 145,799,237 (GRCm39) |
F317L |
possibly damaging |
Het |
Daam1 |
T |
C |
12: 71,993,025 (GRCm39) |
L338P |
unknown |
Het |
Dcc |
T |
A |
18: 71,815,238 (GRCm39) |
I379L |
probably benign |
Het |
Dennd2c |
C |
A |
3: 103,038,925 (GRCm39) |
C24* |
probably null |
Het |
Dnai3 |
G |
A |
3: 145,772,648 (GRCm39) |
S466L |
probably benign |
Het |
Dnajc12 |
A |
G |
10: 63,233,053 (GRCm39) |
I65V |
probably benign |
Het |
Dock3 |
T |
A |
9: 106,785,631 (GRCm39) |
M208L |
probably benign |
Het |
Dsg1b |
T |
C |
18: 20,537,848 (GRCm39) |
I588T |
possibly damaging |
Het |
Eif1b |
T |
C |
9: 120,323,206 (GRCm39) |
L22S |
probably benign |
Het |
Ep300 |
T |
A |
15: 81,532,708 (GRCm39) |
S1649T |
unknown |
Het |
Eps15 |
CAAA |
CAA |
4: 109,162,900 (GRCm39) |
|
probably null |
Het |
Ercc6 |
A |
T |
14: 32,291,943 (GRCm39) |
E1102D |
probably benign |
Het |
Gsdmc3 |
T |
C |
15: 63,732,090 (GRCm39) |
N312S |
probably benign |
Het |
Guca2b |
A |
T |
4: 119,514,890 (GRCm39) |
L57Q |
probably damaging |
Het |
Heatr5b |
G |
T |
17: 79,069,526 (GRCm39) |
H1740Q |
probably benign |
Het |
Hecw1 |
G |
A |
13: 14,697,592 (GRCm39) |
|
probably benign |
Het |
Icam5 |
A |
G |
9: 20,948,217 (GRCm39) |
H675R |
probably benign |
Het |
Il18rap |
T |
C |
1: 40,564,049 (GRCm39) |
F56L |
probably benign |
Het |
Iqgap3 |
T |
A |
3: 87,997,037 (GRCm39) |
|
probably null |
Het |
Itsn1 |
T |
C |
16: 91,664,984 (GRCm39) |
|
probably benign |
Het |
Jakmip3 |
A |
T |
7: 138,622,585 (GRCm39) |
D315V |
probably damaging |
Het |
Kif24 |
A |
G |
4: 41,413,959 (GRCm39) |
Y328H |
probably damaging |
Het |
Kmt2a |
A |
T |
9: 44,744,171 (GRCm39) |
|
probably benign |
Het |
Kng1 |
A |
G |
16: 22,898,475 (GRCm39) |
E625G |
probably damaging |
Het |
Man2b1 |
C |
T |
8: 85,823,675 (GRCm39) |
T973I |
probably benign |
Het |
Masp2 |
G |
A |
4: 148,687,210 (GRCm39) |
V31M |
probably damaging |
Het |
Myo18b |
C |
T |
5: 113,013,601 (GRCm39) |
R785H |
possibly damaging |
Het |
Naa15 |
G |
A |
3: 51,350,212 (GRCm39) |
G103D |
probably damaging |
Het |
Or4f15 |
A |
G |
2: 111,813,969 (GRCm39) |
V150A |
probably benign |
Het |
Or5m11b |
A |
G |
2: 85,805,926 (GRCm39) |
Y113C |
probably damaging |
Het |
Or7e177 |
T |
A |
9: 20,211,899 (GRCm39) |
D134E |
probably damaging |
Het |
Papln |
A |
G |
12: 83,829,789 (GRCm39) |
N970S |
probably benign |
Het |
Pick1 |
T |
A |
15: 79,135,928 (GRCm39) |
|
probably null |
Het |
Pigr |
A |
C |
1: 130,769,498 (GRCm39) |
D103A |
probably benign |
Het |
Plekhf1 |
A |
C |
7: 37,921,029 (GRCm39) |
F180V |
possibly damaging |
Het |
Plxnc1 |
A |
G |
10: 94,669,504 (GRCm39) |
|
probably null |
Het |
Polr3f |
A |
G |
2: 144,376,308 (GRCm39) |
I136V |
probably damaging |
Het |
Ppp2r2c |
T |
C |
5: 37,097,468 (GRCm39) |
M218T |
possibly damaging |
Het |
Prox2 |
C |
T |
12: 85,136,420 (GRCm39) |
V466I |
probably damaging |
Het |
Prrc2a |
G |
A |
17: 35,373,909 (GRCm39) |
L1479F |
probably damaging |
Het |
Rbm24 |
T |
A |
13: 46,575,313 (GRCm39) |
|
probably null |
Het |
Rcc1l |
A |
T |
5: 134,195,560 (GRCm39) |
|
probably null |
Het |
Ripk4 |
A |
C |
16: 97,556,323 (GRCm39) |
L140R |
probably damaging |
Het |
Rmnd1 |
A |
T |
10: 4,372,135 (GRCm39) |
L188Q |
probably damaging |
Het |
Rnf170 |
C |
T |
8: 26,630,992 (GRCm39) |
P249S |
probably damaging |
Het |
Rras |
A |
G |
7: 44,667,595 (GRCm39) |
|
probably null |
Het |
Rsf1 |
G |
A |
7: 97,229,117 (GRCm39) |
|
probably benign |
Het |
Scn7a |
T |
A |
2: 66,530,458 (GRCm39) |
D629V |
probably damaging |
Het |
Sipa1l3 |
A |
G |
7: 29,087,558 (GRCm39) |
S556P |
probably damaging |
Het |
Smarca2 |
C |
T |
19: 26,608,292 (GRCm39) |
A117V |
probably damaging |
Het |
Snca |
C |
T |
6: 60,792,702 (GRCm39) |
A69T |
probably damaging |
Het |
Snx2 |
T |
C |
18: 53,342,737 (GRCm39) |
|
probably null |
Het |
Spp1 |
T |
A |
5: 104,587,242 (GRCm39) |
S109T |
possibly damaging |
Het |
Stoml3 |
T |
C |
3: 53,414,937 (GRCm39) |
L243P |
probably damaging |
Het |
Sycp1 |
A |
G |
3: 102,816,277 (GRCm39) |
M419T |
probably damaging |
Het |
Thoc1 |
T |
C |
18: 9,993,330 (GRCm39) |
V563A |
probably benign |
Het |
Tmprss11g |
T |
C |
5: 86,635,281 (GRCm39) |
I398V |
probably damaging |
Het |
Tox3 |
A |
G |
8: 90,975,566 (GRCm39) |
L355P |
probably damaging |
Het |
Tpp1 |
A |
G |
7: 105,396,223 (GRCm39) |
I492T |
probably benign |
Het |
Trim21 |
A |
T |
7: 102,213,289 (GRCm39) |
L3Q |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,738,080 (GRCm39) |
V4153G |
probably benign |
Het |
Ttn |
T |
C |
2: 76,744,638 (GRCm39) |
|
probably benign |
Het |
Unc80 |
A |
G |
1: 66,560,756 (GRCm39) |
E828G |
possibly damaging |
Het |
Vav3 |
A |
G |
3: 109,416,170 (GRCm39) |
N263S |
possibly damaging |
Het |
Vmn1r183 |
A |
C |
7: 23,754,982 (GRCm39) |
T262P |
possibly damaging |
Het |
Vmn2r67 |
G |
A |
7: 84,799,142 (GRCm39) |
P522S |
possibly damaging |
Het |
Vps35 |
T |
A |
8: 86,026,086 (GRCm39) |
M1L |
probably benign |
Het |
Xpo7 |
A |
T |
14: 70,942,130 (GRCm39) |
L79* |
probably null |
Het |
Zc3h14 |
G |
A |
12: 98,726,087 (GRCm39) |
R324H |
probably damaging |
Het |
Zfp330 |
T |
C |
8: 83,499,613 (GRCm39) |
T6A |
probably damaging |
Het |
Zfp948 |
T |
A |
17: 21,807,286 (GRCm39) |
H159Q |
unknown |
Het |
|
Other mutations in Susd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00740:Susd2
|
APN |
10 |
75,473,882 (GRCm39) |
missense |
probably benign |
0.02 |
IGL00907:Susd2
|
APN |
10 |
75,476,765 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01155:Susd2
|
APN |
10 |
75,476,726 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01677:Susd2
|
APN |
10 |
75,475,265 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02146:Susd2
|
APN |
10 |
75,474,267 (GRCm39) |
missense |
possibly damaging |
0.79 |
IGL02273:Susd2
|
APN |
10 |
75,476,772 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02386:Susd2
|
APN |
10 |
75,475,929 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02475:Susd2
|
APN |
10 |
75,473,333 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03218:Susd2
|
APN |
10 |
75,478,459 (GRCm39) |
missense |
probably benign |
|
PIT4418001:Susd2
|
UTSW |
10 |
75,474,183 (GRCm39) |
missense |
probably benign |
0.24 |
R0135:Susd2
|
UTSW |
10 |
75,474,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R0396:Susd2
|
UTSW |
10 |
75,475,745 (GRCm39) |
missense |
probably damaging |
1.00 |
R0401:Susd2
|
UTSW |
10 |
75,474,437 (GRCm39) |
splice site |
probably benign |
|
R0608:Susd2
|
UTSW |
10 |
75,474,069 (GRCm39) |
missense |
probably benign |
0.45 |
R0636:Susd2
|
UTSW |
10 |
75,475,184 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Susd2
|
UTSW |
10 |
75,473,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R1470:Susd2
|
UTSW |
10 |
75,473,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R1619:Susd2
|
UTSW |
10 |
75,473,878 (GRCm39) |
missense |
possibly damaging |
0.66 |
R1634:Susd2
|
UTSW |
10 |
75,473,389 (GRCm39) |
missense |
probably benign |
0.04 |
R1866:Susd2
|
UTSW |
10 |
75,475,566 (GRCm39) |
missense |
probably damaging |
0.98 |
R4354:Susd2
|
UTSW |
10 |
75,475,562 (GRCm39) |
missense |
probably damaging |
0.99 |
R4451:Susd2
|
UTSW |
10 |
75,475,232 (GRCm39) |
missense |
probably damaging |
1.00 |
R4721:Susd2
|
UTSW |
10 |
75,473,964 (GRCm39) |
missense |
probably benign |
0.00 |
R5546:Susd2
|
UTSW |
10 |
75,478,052 (GRCm39) |
missense |
probably benign |
0.01 |
R5768:Susd2
|
UTSW |
10 |
75,473,853 (GRCm39) |
missense |
probably damaging |
0.98 |
R5769:Susd2
|
UTSW |
10 |
75,473,853 (GRCm39) |
missense |
probably damaging |
0.98 |
R5770:Susd2
|
UTSW |
10 |
75,473,853 (GRCm39) |
missense |
probably damaging |
0.98 |
R5771:Susd2
|
UTSW |
10 |
75,473,853 (GRCm39) |
missense |
probably damaging |
0.98 |
R5960:Susd2
|
UTSW |
10 |
75,475,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R6152:Susd2
|
UTSW |
10 |
75,473,853 (GRCm39) |
missense |
probably damaging |
0.98 |
R6153:Susd2
|
UTSW |
10 |
75,473,853 (GRCm39) |
missense |
probably damaging |
0.98 |
R6259:Susd2
|
UTSW |
10 |
75,473,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R7106:Susd2
|
UTSW |
10 |
75,473,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R7232:Susd2
|
UTSW |
10 |
75,475,685 (GRCm39) |
missense |
probably damaging |
1.00 |
R7297:Susd2
|
UTSW |
10 |
75,478,402 (GRCm39) |
missense |
probably benign |
0.19 |
R7326:Susd2
|
UTSW |
10 |
75,478,399 (GRCm39) |
missense |
probably benign |
0.00 |
R7905:Susd2
|
UTSW |
10 |
75,475,491 (GRCm39) |
nonsense |
probably null |
|
R8512:Susd2
|
UTSW |
10 |
75,475,485 (GRCm39) |
missense |
probably benign |
0.13 |
R8888:Susd2
|
UTSW |
10 |
75,475,452 (GRCm39) |
missense |
possibly damaging |
0.58 |
R8895:Susd2
|
UTSW |
10 |
75,475,452 (GRCm39) |
missense |
possibly damaging |
0.58 |
X0025:Susd2
|
UTSW |
10 |
75,476,406 (GRCm39) |
nonsense |
probably null |
|
Z1177:Susd2
|
UTSW |
10 |
75,476,312 (GRCm39) |
missense |
probably damaging |
0.98 |
|