Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts2 |
A |
G |
11: 50,683,505 (GRCm39) |
Q929R |
probably benign |
Het |
Aplf |
A |
T |
6: 87,635,946 (GRCm39) |
D122E |
probably damaging |
Het |
Atp2a3 |
T |
A |
11: 72,878,810 (GRCm39) |
L874Q |
probably damaging |
Het |
Atp2b2 |
A |
T |
6: 113,770,691 (GRCm39) |
L406Q |
probably damaging |
Het |
Atp6v1b1 |
A |
G |
6: 83,733,891 (GRCm39) |
D374G |
probably benign |
Het |
Bcas1 |
T |
A |
2: 170,220,708 (GRCm39) |
R239* |
probably null |
Het |
Bhmt2 |
A |
G |
13: 93,805,854 (GRCm39) |
V56A |
probably damaging |
Het |
Cage1 |
T |
C |
13: 38,207,233 (GRCm39) |
E204G |
probably damaging |
Het |
Ccdc157 |
G |
A |
11: 4,094,035 (GRCm39) |
A532V |
probably benign |
Het |
Cd300lb |
G |
A |
11: 114,819,303 (GRCm39) |
R109* |
probably null |
Het |
Clca4c-ps |
T |
C |
3: 144,585,516 (GRCm39) |
|
noncoding transcript |
Het |
Ctnna3 |
G |
T |
10: 64,781,777 (GRCm39) |
V747F |
probably benign |
Het |
Cyp2c29 |
A |
T |
19: 39,318,866 (GRCm39) |
I488F |
probably benign |
Het |
Cyp3a25 |
T |
C |
5: 145,935,362 (GRCm39) |
M85V |
possibly damaging |
Het |
Dnah7b |
T |
A |
1: 46,266,090 (GRCm39) |
Y2220N |
probably damaging |
Het |
Espl1 |
A |
G |
15: 102,224,099 (GRCm39) |
I1217V |
probably benign |
Het |
Exoc2 |
A |
G |
13: 30,999,304 (GRCm39) |
S918P |
probably benign |
Het |
Fer1l4 |
T |
A |
2: 155,873,172 (GRCm39) |
I1303F |
possibly damaging |
Het |
Gm28047 |
A |
T |
15: 102,455,662 (GRCm39) |
I234K |
probably damaging |
Het |
Gpcpd1 |
A |
G |
2: 132,410,630 (GRCm39) |
V19A |
probably damaging |
Het |
Gprin3 |
A |
G |
6: 59,331,458 (GRCm39) |
V283A |
probably benign |
Het |
Greb1 |
A |
G |
12: 16,767,209 (GRCm39) |
F331S |
probably benign |
Het |
Iigp1c |
T |
G |
18: 60,379,470 (GRCm39) |
V335G |
probably damaging |
Het |
Jkamp |
A |
G |
12: 72,141,591 (GRCm39) |
Y198C |
probably damaging |
Het |
Klk1b11 |
G |
T |
7: 43,649,165 (GRCm39) |
C234F |
probably damaging |
Het |
Nacad |
T |
C |
11: 6,552,649 (GRCm39) |
T181A |
probably benign |
Het |
Or1e23 |
A |
G |
11: 73,407,375 (GRCm39) |
S217P |
probably benign |
Het |
Or2m13 |
A |
T |
16: 19,225,914 (GRCm39) |
L285Q |
possibly damaging |
Het |
Or5ak4 |
T |
A |
2: 85,161,465 (GRCm39) |
Y259F |
probably damaging |
Het |
Pitpnm3 |
A |
T |
11: 71,962,274 (GRCm39) |
I227N |
probably benign |
Het |
Pnn |
A |
G |
12: 59,116,995 (GRCm39) |
E189G |
probably damaging |
Het |
Pnpla2 |
C |
A |
7: 141,038,122 (GRCm39) |
P197T |
probably damaging |
Het |
Pnpla6 |
A |
G |
8: 3,567,327 (GRCm39) |
T62A |
probably benign |
Het |
Ptprq |
G |
T |
10: 107,482,419 (GRCm39) |
D1051E |
probably damaging |
Het |
Rag2 |
C |
T |
2: 101,460,376 (GRCm39) |
R229C |
probably damaging |
Het |
Serinc1 |
A |
T |
10: 57,399,204 (GRCm39) |
I196N |
probably damaging |
Het |
Slc26a4 |
C |
T |
12: 31,578,853 (GRCm39) |
|
probably benign |
Het |
Slc26a9 |
T |
C |
1: 131,680,583 (GRCm39) |
C43R |
probably damaging |
Het |
Slc2a3 |
A |
T |
6: 122,716,931 (GRCm39) |
Y44N |
probably benign |
Het |
Smad5 |
T |
G |
13: 56,883,603 (GRCm39) |
|
probably benign |
Het |
Sugct |
C |
A |
13: 17,819,450 (GRCm39) |
V132F |
possibly damaging |
Het |
Supt6 |
T |
C |
11: 78,117,030 (GRCm39) |
E568G |
possibly damaging |
Het |
Tfpt |
T |
C |
7: 3,631,982 (GRCm39) |
T43A |
probably damaging |
Het |
Timp4 |
A |
T |
6: 115,224,240 (GRCm39) |
V143E |
possibly damaging |
Het |
Tns1 |
T |
C |
1: 74,031,290 (GRCm39) |
D275G |
possibly damaging |
Het |
Trib1 |
A |
G |
15: 59,523,449 (GRCm39) |
E161G |
probably damaging |
Het |
Trpc7 |
A |
T |
13: 57,008,743 (GRCm39) |
L308Q |
probably damaging |
Het |
Ush1c |
A |
T |
7: 45,858,722 (GRCm39) |
V522E |
possibly damaging |
Het |
Usp28 |
T |
C |
9: 48,935,265 (GRCm39) |
V449A |
probably damaging |
Het |
Vmn1r82 |
A |
G |
7: 12,039,273 (GRCm39) |
Y64C |
probably damaging |
Het |
Wwox |
G |
A |
8: 115,438,805 (GRCm39) |
M290I |
probably benign |
Het |
|
Other mutations in Grb14 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00780:Grb14
|
APN |
2 |
64,745,062 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02902:Grb14
|
APN |
2 |
64,768,762 (GRCm39) |
missense |
probably damaging |
1.00 |
R0066:Grb14
|
UTSW |
2 |
64,768,836 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0066:Grb14
|
UTSW |
2 |
64,768,836 (GRCm39) |
critical splice acceptor site |
probably null |
|
R0658:Grb14
|
UTSW |
2 |
64,745,071 (GRCm39) |
nonsense |
probably null |
|
R0681:Grb14
|
UTSW |
2 |
64,747,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R1215:Grb14
|
UTSW |
2 |
64,747,608 (GRCm39) |
missense |
probably benign |
0.01 |
R1781:Grb14
|
UTSW |
2 |
64,805,899 (GRCm39) |
critical splice donor site |
probably null |
|
R1932:Grb14
|
UTSW |
2 |
64,743,146 (GRCm39) |
missense |
probably damaging |
1.00 |
R2034:Grb14
|
UTSW |
2 |
64,753,873 (GRCm39) |
splice site |
probably benign |
|
R4405:Grb14
|
UTSW |
2 |
64,783,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R4505:Grb14
|
UTSW |
2 |
64,852,912 (GRCm39) |
missense |
probably damaging |
0.97 |
R4580:Grb14
|
UTSW |
2 |
64,783,947 (GRCm39) |
missense |
probably benign |
0.29 |
R5216:Grb14
|
UTSW |
2 |
64,747,653 (GRCm39) |
missense |
probably benign |
0.00 |
R5367:Grb14
|
UTSW |
2 |
64,747,653 (GRCm39) |
missense |
probably benign |
0.00 |
R5369:Grb14
|
UTSW |
2 |
64,747,653 (GRCm39) |
missense |
probably benign |
0.00 |
R5382:Grb14
|
UTSW |
2 |
64,745,078 (GRCm39) |
missense |
probably damaging |
1.00 |
R5457:Grb14
|
UTSW |
2 |
64,747,442 (GRCm39) |
missense |
probably damaging |
1.00 |
R5816:Grb14
|
UTSW |
2 |
64,747,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R6062:Grb14
|
UTSW |
2 |
64,852,964 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7114:Grb14
|
UTSW |
2 |
64,747,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R8290:Grb14
|
UTSW |
2 |
64,805,929 (GRCm39) |
missense |
probably benign |
0.02 |
R8540:Grb14
|
UTSW |
2 |
64,851,478 (GRCm39) |
missense |
probably benign |
0.14 |
R9318:Grb14
|
UTSW |
2 |
64,852,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R9474:Grb14
|
UTSW |
2 |
64,768,744 (GRCm39) |
missense |
probably damaging |
0.96 |
R9572:Grb14
|
UTSW |
2 |
64,763,680 (GRCm39) |
missense |
probably damaging |
0.99 |
X0021:Grb14
|
UTSW |
2 |
64,766,769 (GRCm39) |
missense |
probably null |
0.26 |
|