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 |
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 |
Shc4 |
T |
A |
2: 125,565,285 (GRCm39) |
S5C |
probably damaging |
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 Mcidas |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01013:Mcidas
|
APN |
13 |
113,134,119 (GRCm39) |
splice site |
probably benign |
|
IGL01355:Mcidas
|
APN |
13 |
113,135,603 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02000:Mcidas
|
APN |
13 |
113,133,974 (GRCm39) |
missense |
probably benign |
|
IGL02019:Mcidas
|
APN |
13 |
113,133,377 (GRCm39) |
missense |
probably benign |
0.00 |
R0145:Mcidas
|
UTSW |
13 |
113,130,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R0412:Mcidas
|
UTSW |
13 |
113,135,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R1293:Mcidas
|
UTSW |
13 |
113,133,926 (GRCm39) |
missense |
probably benign |
|
R2011:Mcidas
|
UTSW |
13 |
113,130,515 (GRCm39) |
missense |
possibly damaging |
0.84 |
R4183:Mcidas
|
UTSW |
13 |
113,130,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R4905:Mcidas
|
UTSW |
13 |
113,134,038 (GRCm39) |
missense |
possibly damaging |
0.82 |
R4905:Mcidas
|
UTSW |
13 |
113,130,951 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5615:Mcidas
|
UTSW |
13 |
113,133,959 (GRCm39) |
missense |
probably benign |
0.01 |
R5997:Mcidas
|
UTSW |
13 |
113,135,120 (GRCm39) |
missense |
probably damaging |
0.99 |
R6848:Mcidas
|
UTSW |
13 |
113,130,419 (GRCm39) |
missense |
probably benign |
|
R7387:Mcidas
|
UTSW |
13 |
113,130,622 (GRCm39) |
missense |
probably benign |
0.03 |
R7398:Mcidas
|
UTSW |
13 |
113,133,416 (GRCm39) |
missense |
probably benign |
|
R7742:Mcidas
|
UTSW |
13 |
113,135,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R7797:Mcidas
|
UTSW |
13 |
113,135,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R7872:Mcidas
|
UTSW |
13 |
113,135,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R7873:Mcidas
|
UTSW |
13 |
113,135,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R7920:Mcidas
|
UTSW |
13 |
113,135,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R8859:Mcidas
|
UTSW |
13 |
113,130,664 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9342:Mcidas
|
UTSW |
13 |
113,130,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R9761:Mcidas
|
UTSW |
13 |
113,135,453 (GRCm39) |
missense |
probably benign |
0.04 |
X0066:Mcidas
|
UTSW |
13 |
113,133,981 (GRCm39) |
missense |
probably damaging |
0.97 |
|