Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankle1 |
T |
C |
8: 71,861,337 (GRCm39) |
S391P |
probably damaging |
Het |
Ankmy1 |
T |
C |
1: 92,811,570 (GRCm39) |
Q606R |
probably benign |
Het |
Bmf |
A |
G |
2: 118,377,358 (GRCm39) |
L130P |
probably damaging |
Het |
Ccdc88c |
G |
A |
12: 100,889,570 (GRCm39) |
T1491I |
probably benign |
Het |
Cyp2c69 |
G |
A |
19: 39,864,663 (GRCm39) |
R272C |
probably benign |
Het |
Defa27 |
A |
G |
8: 21,806,354 (GRCm39) |
N78S |
probably benign |
Het |
Depdc5 |
T |
A |
5: 33,101,447 (GRCm39) |
D912E |
probably damaging |
Het |
Dsc3 |
C |
T |
18: 20,099,288 (GRCm39) |
D743N |
probably damaging |
Het |
Epcam |
T |
C |
17: 87,950,983 (GRCm39) |
V190A |
probably benign |
Het |
Exoc2 |
G |
A |
13: 31,060,756 (GRCm39) |
R583* |
probably null |
Het |
Extl1 |
T |
A |
4: 134,091,990 (GRCm39) |
I288F |
probably damaging |
Het |
Fam50b |
G |
A |
13: 34,931,084 (GRCm39) |
E187K |
possibly damaging |
Het |
Fcer2a |
T |
A |
8: 3,732,910 (GRCm39) |
Y299F |
probably benign |
Het |
Frmd4a |
G |
A |
2: 4,595,506 (GRCm39) |
G439R |
probably damaging |
Het |
Gal3st4 |
T |
C |
5: 138,269,100 (GRCm39) |
H120R |
probably benign |
Het |
Grid1 |
C |
A |
14: 35,043,642 (GRCm39) |
N332K |
probably damaging |
Het |
Igkv4-68 |
A |
G |
6: 69,281,896 (GRCm39) |
Y92H |
probably damaging |
Het |
Itga1 |
T |
C |
13: 115,148,772 (GRCm39) |
E283G |
probably damaging |
Het |
Ldlrad1 |
G |
A |
4: 107,066,688 (GRCm39) |
A8T |
probably benign |
Het |
Lrrc24 |
A |
G |
15: 76,602,248 (GRCm39) |
L169P |
probably benign |
Het |
Mcidas |
G |
A |
13: 113,135,521 (GRCm39) |
G315S |
probably damaging |
Het |
Mettl8 |
T |
C |
2: 70,812,243 (GRCm39) |
T131A |
probably benign |
Het |
Miip |
C |
T |
4: 147,947,375 (GRCm39) |
G236S |
probably benign |
Het |
Nbr1 |
T |
A |
11: 101,460,154 (GRCm39) |
D383E |
probably damaging |
Het |
Neto1 |
A |
T |
18: 86,479,198 (GRCm39) |
K167N |
probably benign |
Het |
Nkx6-1 |
A |
T |
5: 101,811,628 (GRCm39) |
L158Q |
unknown |
Het |
Nlrp5 |
G |
A |
7: 23,118,219 (GRCm39) |
V648M |
possibly damaging |
Het |
Nvl |
G |
T |
1: 180,924,722 (GRCm39) |
Q811K |
probably benign |
Het |
Or13a21 |
A |
G |
7: 139,999,027 (GRCm39) |
F220L |
possibly damaging |
Het |
Or13p3 |
C |
A |
4: 118,566,855 (GRCm39) |
H84N |
possibly damaging |
Het |
Or1j10 |
A |
G |
2: 36,267,453 (GRCm39) |
T222A |
probably benign |
Het |
Or3a1c |
T |
A |
11: 74,046,844 (GRCm39) |
L288Q |
probably damaging |
Het |
Pccb |
T |
C |
9: 100,881,316 (GRCm39) |
Y224C |
probably damaging |
Het |
Pcdh10 |
T |
C |
3: 45,334,657 (GRCm39) |
Y324H |
probably benign |
Het |
Pecam1 |
C |
A |
11: 106,586,658 (GRCm39) |
E286* |
probably null |
Het |
Prl7d1 |
A |
T |
13: 27,893,263 (GRCm39) |
L215Q |
probably damaging |
Het |
Ranbp2 |
T |
A |
10: 58,319,729 (GRCm39) |
Y2514* |
probably null |
Het |
Rgs11 |
A |
G |
17: 26,426,552 (GRCm39) |
H261R |
possibly damaging |
Het |
Samd15 |
A |
G |
12: 87,247,506 (GRCm39) |
T64A |
probably benign |
Het |
Shroom3 |
G |
A |
5: 93,067,508 (GRCm39) |
V109M |
probably damaging |
Het |
Spata13 |
T |
C |
14: 60,929,291 (GRCm39) |
I283T |
possibly damaging |
Het |
Sptbn2 |
C |
G |
19: 4,799,040 (GRCm39) |
R2037G |
probably benign |
Het |
Synj2bp |
G |
A |
12: 81,548,922 (GRCm39) |
P106S |
probably benign |
Het |
Tasor |
T |
C |
14: 27,203,340 (GRCm39) |
S289P |
|
Het |
Thoc1 |
T |
C |
18: 9,986,300 (GRCm39) |
V344A |
probably damaging |
Het |
Vmn1r71 |
A |
G |
7: 10,482,136 (GRCm39) |
L184S |
probably damaging |
Het |
Vps45 |
A |
G |
3: 95,926,936 (GRCm39) |
I537T |
probably benign |
Het |
|
Other mutations in Shc4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02298:Shc4
|
APN |
2 |
125,491,074 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03003:Shc4
|
APN |
2 |
125,565,253 (GRCm39) |
nonsense |
probably null |
|
R0167:Shc4
|
UTSW |
2 |
125,564,933 (GRCm39) |
missense |
probably benign |
0.00 |
R0784:Shc4
|
UTSW |
2 |
125,499,416 (GRCm39) |
missense |
probably benign |
0.08 |
R0959:Shc4
|
UTSW |
2 |
125,520,607 (GRCm39) |
critical splice donor site |
probably null |
|
R1099:Shc4
|
UTSW |
2 |
125,564,764 (GRCm39) |
missense |
probably benign |
0.03 |
R1864:Shc4
|
UTSW |
2 |
125,481,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R2198:Shc4
|
UTSW |
2 |
125,481,266 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3791:Shc4
|
UTSW |
2 |
125,565,251 (GRCm39) |
missense |
probably damaging |
0.97 |
R4324:Shc4
|
UTSW |
2 |
125,520,670 (GRCm39) |
missense |
probably benign |
0.23 |
R4424:Shc4
|
UTSW |
2 |
125,494,442 (GRCm39) |
missense |
probably benign |
|
R4611:Shc4
|
UTSW |
2 |
125,497,602 (GRCm39) |
missense |
probably benign |
0.29 |
R4745:Shc4
|
UTSW |
2 |
125,491,197 (GRCm39) |
missense |
probably damaging |
0.96 |
R5037:Shc4
|
UTSW |
2 |
125,471,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R5433:Shc4
|
UTSW |
2 |
125,481,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R5754:Shc4
|
UTSW |
2 |
125,512,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R8058:Shc4
|
UTSW |
2 |
125,491,154 (GRCm39) |
nonsense |
probably null |
|
R8314:Shc4
|
UTSW |
2 |
125,497,536 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8396:Shc4
|
UTSW |
2 |
125,471,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R8785:Shc4
|
UTSW |
2 |
125,491,064 (GRCm39) |
critical splice donor site |
probably null |
|
R9006:Shc4
|
UTSW |
2 |
125,514,394 (GRCm39) |
unclassified |
probably benign |
|
R9244:Shc4
|
UTSW |
2 |
125,497,589 (GRCm39) |
nonsense |
probably null |
|
R9332:Shc4
|
UTSW |
2 |
125,520,618 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Shc4
|
UTSW |
2 |
125,564,843 (GRCm39) |
missense |
probably benign |
0.37 |
|