Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadacl2fm1 |
C |
T |
3: 59,840,110 (GRCm39) |
R61C |
probably damaging |
Het |
Ackr4 |
A |
G |
9: 103,976,860 (GRCm39) |
V29A |
probably benign |
Het |
Adgrb1 |
T |
C |
15: 74,458,656 (GRCm39) |
F313L |
probably benign |
Het |
Arfgef2 |
C |
T |
2: 166,709,342 (GRCm39) |
R1140W |
probably damaging |
Het |
Arhgef15 |
A |
T |
11: 68,837,199 (GRCm39) |
N797K |
probably benign |
Het |
Arhgef5 |
A |
G |
6: 43,250,275 (GRCm39) |
E342G |
probably damaging |
Het |
Asb2 |
T |
A |
12: 103,291,530 (GRCm39) |
N466Y |
possibly damaging |
Het |
Atp8a1 |
A |
T |
5: 67,932,064 (GRCm39) |
|
probably null |
Het |
Cacna1b |
A |
G |
2: 24,497,492 (GRCm39) |
S2140P |
probably damaging |
Het |
Camsap2 |
G |
C |
1: 136,208,738 (GRCm39) |
P918R |
probably damaging |
Het |
Cdk7 |
G |
T |
13: 100,843,022 (GRCm39) |
D202E |
probably benign |
Het |
Cenpj |
G |
T |
14: 56,801,427 (GRCm39) |
A182E |
probably benign |
Het |
Clstn3 |
A |
G |
6: 124,409,128 (GRCm39) |
|
probably benign |
Het |
Col9a2 |
C |
T |
4: 120,909,485 (GRCm39) |
|
probably benign |
Het |
D630045J12Rik |
A |
G |
6: 38,116,385 (GRCm39) |
M1745T |
probably damaging |
Het |
Dnah11 |
A |
C |
12: 118,007,509 (GRCm39) |
N2156K |
probably damaging |
Het |
Dock3 |
G |
T |
9: 106,874,195 (GRCm39) |
Y425* |
probably null |
Het |
Eng |
A |
T |
2: 32,569,005 (GRCm39) |
T511S |
probably benign |
Het |
Gcfc2 |
A |
T |
6: 81,920,444 (GRCm39) |
S410C |
probably null |
Het |
Grik3 |
T |
A |
4: 125,579,958 (GRCm39) |
Y568N |
probably damaging |
Het |
H2-M10.4 |
A |
G |
17: 36,771,375 (GRCm39) |
W268R |
probably damaging |
Het |
Hepacam2 |
A |
T |
6: 3,467,505 (GRCm39) |
|
probably benign |
Het |
Hrct1 |
C |
A |
4: 43,727,384 (GRCm39) |
T8K |
possibly damaging |
Het |
Idua |
T |
A |
5: 108,829,618 (GRCm39) |
F447I |
probably damaging |
Het |
Il2ra |
T |
C |
2: 11,686,828 (GRCm39) |
|
probably benign |
Het |
Ipcef1 |
A |
G |
10: 6,870,062 (GRCm39) |
S113P |
probably damaging |
Het |
Klk1b9 |
T |
A |
7: 43,628,854 (GRCm39) |
N119K |
possibly damaging |
Het |
Krtap9-3 |
C |
A |
11: 99,488,663 (GRCm39) |
C73F |
probably damaging |
Het |
Loxhd1 |
T |
A |
18: 77,492,562 (GRCm39) |
F1334L |
possibly damaging |
Het |
Med1 |
A |
G |
11: 98,046,515 (GRCm39) |
|
probably benign |
Het |
Med13 |
A |
G |
11: 86,191,682 (GRCm39) |
|
probably benign |
Het |
Mtor |
C |
A |
4: 148,549,432 (GRCm39) |
H605Q |
probably benign |
Het |
Muc19 |
A |
G |
15: 91,777,218 (GRCm39) |
|
noncoding transcript |
Het |
Mybphl |
T |
C |
3: 108,282,731 (GRCm39) |
V207A |
probably damaging |
Het |
Nptxr |
A |
T |
15: 79,673,916 (GRCm39) |
C366S |
probably null |
Het |
Or5b105 |
G |
A |
19: 13,080,642 (GRCm39) |
R3C |
possibly damaging |
Het |
Or5p73 |
A |
G |
7: 108,064,750 (GRCm39) |
D73G |
probably damaging |
Het |
Or8h9 |
G |
T |
2: 86,789,748 (GRCm39) |
T18K |
probably damaging |
Het |
Pcdhb18 |
T |
C |
18: 37,623,240 (GRCm39) |
I190T |
possibly damaging |
Het |
Pde3b |
A |
G |
7: 114,097,216 (GRCm39) |
T428A |
probably benign |
Het |
Pgbd1 |
A |
C |
13: 21,618,651 (GRCm39) |
L2R |
probably damaging |
Het |
Pkp4 |
A |
G |
2: 59,096,780 (GRCm39) |
I61V |
probably damaging |
Het |
Pold4 |
T |
G |
19: 4,282,593 (GRCm39) |
Y58* |
probably null |
Het |
Polr1d |
A |
C |
5: 147,015,490 (GRCm39) |
|
probably null |
Het |
Prex2 |
T |
A |
1: 11,355,368 (GRCm39) |
D1556E |
probably damaging |
Het |
Psmd1 |
T |
C |
1: 86,061,463 (GRCm39) |
V891A |
possibly damaging |
Het |
Rasip1 |
C |
A |
7: 45,281,999 (GRCm39) |
P501T |
probably damaging |
Het |
Scgb2b27 |
C |
A |
7: 33,711,562 (GRCm39) |
E96* |
probably null |
Het |
Sec16b |
G |
T |
1: 157,380,505 (GRCm39) |
G359* |
probably null |
Het |
Secisbp2 |
A |
G |
13: 51,833,881 (GRCm39) |
T674A |
probably benign |
Het |
Serpinb6c |
G |
A |
13: 34,081,379 (GRCm39) |
S90L |
probably benign |
Het |
Sgsm2 |
A |
G |
11: 74,759,067 (GRCm39) |
I170T |
probably damaging |
Het |
Slc28a1 |
A |
T |
7: 80,767,454 (GRCm39) |
|
probably benign |
Het |
Slc35d1 |
T |
C |
4: 103,065,351 (GRCm39) |
T177A |
probably damaging |
Het |
Spg11 |
C |
T |
2: 121,886,177 (GRCm39) |
|
probably null |
Het |
Spint1 |
T |
C |
2: 119,078,826 (GRCm39) |
|
probably benign |
Het |
Spta1 |
A |
G |
1: 174,020,526 (GRCm39) |
H545R |
probably damaging |
Het |
Tada3 |
A |
T |
6: 113,343,968 (GRCm39) |
L227Q |
probably damaging |
Het |
Tln1 |
C |
T |
4: 43,549,151 (GRCm39) |
V644M |
probably damaging |
Het |
Unc79 |
G |
A |
12: 103,058,286 (GRCm39) |
V1016I |
probably benign |
Het |
Usf3 |
C |
A |
16: 44,037,269 (GRCm39) |
A583E |
probably damaging |
Het |
Ush2a |
A |
C |
1: 188,263,958 (GRCm39) |
I1612L |
probably damaging |
Het |
Vmn2r6 |
T |
C |
3: 64,447,333 (GRCm39) |
T578A |
probably benign |
Het |
Zmat4 |
T |
A |
8: 24,392,083 (GRCm39) |
M13K |
probably damaging |
Het |
|
Other mutations in Gsr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02471:Gsr
|
APN |
8 |
34,172,612 (GRCm39) |
splice site |
probably benign |
|
IGL02481:Gsr
|
APN |
8 |
34,175,569 (GRCm39) |
splice site |
probably benign |
|
IGL02941:Gsr
|
APN |
8 |
34,179,453 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03242:Gsr
|
APN |
8 |
34,175,627 (GRCm39) |
missense |
probably benign |
|
IGL03293:Gsr
|
APN |
8 |
34,185,024 (GRCm39) |
splice site |
probably benign |
|
R0490:Gsr
|
UTSW |
8 |
34,161,540 (GRCm39) |
splice site |
probably benign |
|
R0492:Gsr
|
UTSW |
8 |
34,171,603 (GRCm39) |
splice site |
probably benign |
|
R0524:Gsr
|
UTSW |
8 |
34,159,208 (GRCm39) |
critical splice donor site |
probably null |
|
R1104:Gsr
|
UTSW |
8 |
34,159,949 (GRCm39) |
missense |
probably damaging |
1.00 |
R1976:Gsr
|
UTSW |
8 |
34,170,288 (GRCm39) |
splice site |
probably null |
|
R2507:Gsr
|
UTSW |
8 |
34,170,316 (GRCm39) |
missense |
probably benign |
0.45 |
R2508:Gsr
|
UTSW |
8 |
34,170,316 (GRCm39) |
missense |
probably benign |
0.45 |
R3726:Gsr
|
UTSW |
8 |
34,161,565 (GRCm39) |
missense |
probably benign |
0.11 |
R4573:Gsr
|
UTSW |
8 |
34,183,881 (GRCm39) |
missense |
probably benign |
0.00 |
R4623:Gsr
|
UTSW |
8 |
34,170,333 (GRCm39) |
missense |
probably damaging |
0.99 |
R4639:Gsr
|
UTSW |
8 |
34,187,284 (GRCm39) |
missense |
probably damaging |
1.00 |
R4713:Gsr
|
UTSW |
8 |
34,170,347 (GRCm39) |
critical splice donor site |
probably null |
|
R4717:Gsr
|
UTSW |
8 |
34,183,886 (GRCm39) |
nonsense |
probably null |
|
R4992:Gsr
|
UTSW |
8 |
34,183,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R5099:Gsr
|
UTSW |
8 |
34,161,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R6019:Gsr
|
UTSW |
8 |
34,183,835 (GRCm39) |
missense |
probably damaging |
0.97 |
R7046:Gsr
|
UTSW |
8 |
34,185,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R7570:Gsr
|
UTSW |
8 |
34,159,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R8955:Gsr
|
UTSW |
8 |
34,183,936 (GRCm39) |
missense |
possibly damaging |
0.78 |
R9362:Gsr
|
UTSW |
8 |
34,179,406 (GRCm39) |
missense |
probably damaging |
1.00 |
|