Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Akap13 |
G |
A |
7: 75,380,213 (GRCm39) |
R462H |
probably damaging |
Het |
Ammecr1l |
T |
C |
18: 31,905,152 (GRCm39) |
F131S |
probably damaging |
Het |
Apbb1ip |
A |
C |
2: 22,709,648 (GRCm39) |
D35A |
unknown |
Het |
Arhgap12 |
A |
T |
18: 6,111,976 (GRCm39) |
D129E |
probably benign |
Het |
Arpc1b |
A |
G |
5: 145,061,492 (GRCm39) |
D163G |
probably damaging |
Het |
Atxn7l1 |
A |
T |
12: 33,396,023 (GRCm39) |
T251S |
probably benign |
Het |
Best1 |
T |
C |
19: 9,969,027 (GRCm39) |
I230V |
possibly damaging |
Het |
Brca2 |
A |
G |
5: 150,483,613 (GRCm39) |
T2888A |
possibly damaging |
Het |
Cad |
T |
C |
5: 31,215,450 (GRCm39) |
V87A |
probably damaging |
Het |
Ccdc168 |
A |
T |
1: 44,099,994 (GRCm39) |
I368K |
possibly damaging |
Het |
Ccdc39 |
C |
T |
3: 33,869,560 (GRCm39) |
|
probably null |
Het |
Clcn1 |
T |
A |
6: 42,284,523 (GRCm39) |
C548* |
probably null |
Het |
Col18a1 |
A |
G |
10: 76,890,068 (GRCm39) |
S1678P |
probably damaging |
Het |
Col6a6 |
T |
C |
9: 105,651,987 (GRCm39) |
N1008S |
possibly damaging |
Het |
Defb41 |
A |
T |
1: 18,321,519 (GRCm39) |
C32S |
possibly damaging |
Het |
Dnah6 |
T |
C |
6: 73,072,171 (GRCm39) |
N2437S |
probably damaging |
Het |
Drosha |
T |
C |
15: 12,834,408 (GRCm39) |
Y171H |
unknown |
Het |
Ehd1 |
T |
C |
19: 6,344,613 (GRCm39) |
L291P |
probably damaging |
Het |
Eif3c |
A |
T |
7: 126,147,069 (GRCm39) |
H734Q |
possibly damaging |
Het |
Erich5 |
A |
T |
15: 34,471,502 (GRCm39) |
T244S |
probably benign |
Het |
Fam186b |
T |
A |
15: 99,177,613 (GRCm39) |
H571L |
probably benign |
Het |
Fer1l5 |
A |
G |
1: 36,426,271 (GRCm39) |
K360E |
probably benign |
Het |
Fga |
A |
T |
3: 82,938,158 (GRCm39) |
I178F |
probably damaging |
Het |
Gale |
A |
T |
4: 135,694,987 (GRCm39) |
T320S |
probably benign |
Het |
Gm11232 |
A |
T |
4: 71,675,465 (GRCm39) |
S99T |
probably benign |
Het |
Gpr137 |
C |
T |
19: 6,917,803 (GRCm39) |
W94* |
probably null |
Het |
Grm7 |
T |
A |
6: 111,223,280 (GRCm39) |
M440K |
possibly damaging |
Het |
Hacd4 |
A |
G |
4: 88,353,286 (GRCm39) |
F69L |
probably damaging |
Het |
Hdac7 |
T |
A |
15: 97,706,251 (GRCm39) |
H304L |
probably damaging |
Het |
Herc1 |
T |
A |
9: 66,358,224 (GRCm39) |
I2435N |
probably benign |
Het |
Itgb7 |
G |
A |
15: 102,124,957 (GRCm39) |
R755W |
probably damaging |
Het |
Kdm3b |
G |
T |
18: 34,926,129 (GRCm39) |
A90S |
probably benign |
Het |
Mcmdc2 |
G |
A |
1: 9,981,946 (GRCm39) |
M1I |
probably null |
Het |
Mitd1 |
A |
G |
1: 37,918,639 (GRCm39) |
|
probably null |
Het |
Myh10 |
A |
T |
11: 68,688,235 (GRCm39) |
Q1232L |
probably benign |
Het |
Myo1a |
C |
A |
10: 127,547,027 (GRCm39) |
N362K |
probably damaging |
Het |
N4bp1 |
G |
A |
8: 87,579,789 (GRCm39) |
T671I |
probably damaging |
Het |
Nav3 |
A |
T |
10: 109,659,138 (GRCm39) |
D826E |
probably damaging |
Het |
Negr1 |
C |
T |
3: 156,866,297 (GRCm39) |
T282M |
probably damaging |
Het |
Notch1 |
G |
A |
2: 26,354,917 (GRCm39) |
H1837Y |
possibly damaging |
Het |
Or2m12 |
A |
T |
16: 19,104,851 (GRCm39) |
V214E |
probably benign |
Het |
Or52e19b |
A |
T |
7: 103,032,413 (GRCm39) |
F265L |
probably benign |
Het |
Or5m13 |
T |
A |
2: 85,748,407 (GRCm39) |
I46N |
probably damaging |
Het |
Or7e177 |
A |
G |
9: 20,212,093 (GRCm39) |
N200S |
probably benign |
Het |
Pard6a |
T |
C |
8: 106,428,881 (GRCm39) |
C47R |
probably benign |
Het |
Parp2 |
T |
C |
14: 51,057,247 (GRCm39) |
|
probably null |
Het |
Pck1 |
C |
A |
2: 172,999,064 (GRCm39) |
A410D |
probably damaging |
Het |
Pdzph1 |
G |
A |
17: 59,191,008 (GRCm39) |
L85F |
probably damaging |
Het |
Piezo2 |
A |
G |
18: 63,279,873 (GRCm39) |
S1P |
probably damaging |
Het |
Pld1 |
T |
A |
3: 28,140,025 (GRCm39) |
V615D |
probably damaging |
Het |
Plekha7 |
T |
G |
7: 115,907,164 (GRCm39) |
I23L |
probably benign |
Het |
Prkcz |
T |
G |
4: 155,346,968 (GRCm39) |
D388A |
probably damaging |
Het |
Rab36 |
A |
G |
10: 74,888,335 (GRCm39) |
R260G |
probably benign |
Het |
Reln |
C |
A |
5: 22,209,229 (GRCm39) |
R1116S |
probably damaging |
Het |
Rskr |
A |
T |
11: 78,184,210 (GRCm39) |
M225L |
probably benign |
Het |
Rundc3b |
T |
G |
5: 8,619,505 (GRCm39) |
K151Q |
probably damaging |
Het |
Scaf11 |
A |
G |
15: 96,316,988 (GRCm39) |
S859P |
probably damaging |
Het |
Slc25a32 |
C |
T |
15: 38,963,281 (GRCm39) |
R180H |
probably benign |
Het |
Slc4a9 |
G |
A |
18: 36,665,196 (GRCm39) |
G443E |
possibly damaging |
Het |
Slmap |
T |
A |
14: 26,150,965 (GRCm39) |
K534N |
probably damaging |
Het |
Sncaip |
G |
A |
18: 52,971,088 (GRCm39) |
A3T |
probably damaging |
Het |
Spata31d1c |
G |
T |
13: 65,180,991 (GRCm39) |
S30I |
probably damaging |
Het |
Srrm1 |
A |
T |
4: 135,051,313 (GRCm39) |
V789E |
unknown |
Het |
Srrm2 |
A |
T |
17: 24,027,489 (GRCm39) |
|
probably benign |
Het |
Taf15 |
C |
T |
11: 83,375,678 (GRCm39) |
Q48* |
probably null |
Het |
Tek |
A |
T |
4: 94,687,403 (GRCm39) |
D172V |
probably benign |
Het |
Tmem232 |
T |
C |
17: 65,785,366 (GRCm39) |
Y198C |
probably damaging |
Het |
Tns3 |
A |
T |
11: 8,398,779 (GRCm39) |
V1191E |
probably damaging |
Het |
Togaram1 |
A |
G |
12: 65,067,088 (GRCm39) |
D1710G |
probably damaging |
Het |
Trav16d-dv11 |
T |
C |
14: 53,285,122 (GRCm39) |
I66T |
probably benign |
Het |
Ttn |
T |
A |
2: 76,577,289 (GRCm39) |
T24535S |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,730,087 (GRCm39) |
L911* |
probably null |
Het |
Ube4a |
A |
G |
9: 44,861,130 (GRCm39) |
S227P |
probably damaging |
Het |
Ubqln1 |
T |
C |
13: 58,339,569 (GRCm39) |
T352A |
probably benign |
Het |
Vmn1r174 |
C |
T |
7: 23,454,182 (GRCm39) |
P283S |
probably damaging |
Het |
Vmn1r59 |
T |
C |
7: 5,457,053 (GRCm39) |
T236A |
probably damaging |
Het |
Vmn2r3 |
T |
C |
3: 64,182,311 (GRCm39) |
I463V |
probably benign |
Het |
Wdr95 |
A |
G |
5: 149,497,461 (GRCm39) |
D213G |
probably damaging |
Het |
Zbtb49 |
T |
A |
5: 38,370,669 (GRCm39) |
H404L |
probably damaging |
Het |
Zfp879 |
A |
G |
11: 50,728,757 (GRCm39) |
M79T |
probably benign |
Het |
Zmiz2 |
G |
A |
11: 6,352,441 (GRCm39) |
C600Y |
probably damaging |
Het |
|
Other mutations in St7l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00785:St7l
|
APN |
3 |
104,780,895 (GRCm39) |
splice site |
probably benign |
|
IGL00919:St7l
|
APN |
3 |
104,833,782 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00945:St7l
|
APN |
3 |
104,833,798 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01644:St7l
|
APN |
3 |
104,826,772 (GRCm39) |
nonsense |
probably null |
|
IGL02158:St7l
|
APN |
3 |
104,782,148 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02164:St7l
|
APN |
3 |
104,829,597 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02331:St7l
|
APN |
3 |
104,833,904 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03220:St7l
|
APN |
3 |
104,782,139 (GRCm39) |
splice site |
probably benign |
|
R0118:St7l
|
UTSW |
3 |
104,796,619 (GRCm39) |
missense |
probably damaging |
0.97 |
R0320:St7l
|
UTSW |
3 |
104,778,229 (GRCm39) |
nonsense |
probably null |
|
R0345:St7l
|
UTSW |
3 |
104,803,125 (GRCm39) |
splice site |
probably benign |
|
R0714:St7l
|
UTSW |
3 |
104,782,244 (GRCm39) |
missense |
probably benign |
0.06 |
R0784:St7l
|
UTSW |
3 |
104,778,240 (GRCm39) |
missense |
probably benign |
0.13 |
R1664:St7l
|
UTSW |
3 |
104,778,214 (GRCm39) |
missense |
probably damaging |
1.00 |
R1719:St7l
|
UTSW |
3 |
104,778,303 (GRCm39) |
missense |
probably benign |
0.00 |
R1800:St7l
|
UTSW |
3 |
104,826,812 (GRCm39) |
missense |
probably damaging |
1.00 |
R1882:St7l
|
UTSW |
3 |
104,775,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R3692:St7l
|
UTSW |
3 |
104,798,870 (GRCm39) |
missense |
probably benign |
0.27 |
R3879:St7l
|
UTSW |
3 |
104,833,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R5130:St7l
|
UTSW |
3 |
104,803,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R5271:St7l
|
UTSW |
3 |
104,775,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R5887:St7l
|
UTSW |
3 |
104,782,244 (GRCm39) |
missense |
probably benign |
0.06 |
R6191:St7l
|
UTSW |
3 |
104,775,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R6252:St7l
|
UTSW |
3 |
104,826,819 (GRCm39) |
critical splice donor site |
probably null |
|
R7307:St7l
|
UTSW |
3 |
104,796,669 (GRCm39) |
missense |
probably benign |
0.03 |
R7442:St7l
|
UTSW |
3 |
104,796,645 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7860:St7l
|
UTSW |
3 |
104,833,893 (GRCm39) |
missense |
probably benign |
0.05 |
R8934:St7l
|
UTSW |
3 |
104,796,634 (GRCm39) |
missense |
probably damaging |
1.00 |
R8935:St7l
|
UTSW |
3 |
104,778,204 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:St7l
|
UTSW |
3 |
104,772,625 (GRCm39) |
critical splice donor site |
probably null |
|
|