Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy4 |
A |
G |
14: 56,019,092 (GRCm39) |
V155A |
probably benign |
Het |
Arfgef2 |
A |
G |
2: 166,695,208 (GRCm39) |
Y527C |
probably damaging |
Het |
Brca1 |
C |
T |
11: 101,415,303 (GRCm39) |
G944R |
probably benign |
Het |
C2cd2 |
A |
G |
16: 97,687,286 (GRCm39) |
|
probably null |
Het |
Cass4 |
T |
C |
2: 172,269,879 (GRCm39) |
F654L |
unknown |
Het |
Ccdc178 |
A |
T |
18: 21,977,944 (GRCm39) |
|
probably null |
Het |
Cct4 |
T |
C |
11: 22,946,040 (GRCm39) |
|
probably null |
Het |
Cish |
T |
C |
9: 107,174,227 (GRCm39) |
V5A |
possibly damaging |
Het |
Col5a1 |
G |
A |
2: 27,848,340 (GRCm39) |
|
probably benign |
Het |
Col6a3 |
G |
T |
1: 90,703,455 (GRCm39) |
N3037K |
unknown |
Het |
Csmd2 |
T |
A |
4: 128,432,980 (GRCm39) |
C3012* |
probably null |
Het |
Dclk2 |
T |
C |
3: 86,700,608 (GRCm39) |
|
probably null |
Het |
Dhx38 |
A |
T |
8: 110,282,772 (GRCm39) |
D631E |
probably damaging |
Het |
Eif2ak2 |
C |
A |
17: 79,183,652 (GRCm39) |
A66S |
probably damaging |
Het |
Ephx2 |
A |
G |
14: 66,361,782 (GRCm39) |
|
probably null |
Het |
Fbxw10 |
T |
G |
11: 62,748,587 (GRCm39) |
C405G |
possibly damaging |
Het |
Galnt13 |
G |
T |
2: 54,950,497 (GRCm39) |
G393* |
probably null |
Het |
Gm5591 |
G |
T |
7: 38,219,183 (GRCm39) |
H563Q |
probably damaging |
Het |
Gtf3c5 |
A |
G |
2: 28,459,373 (GRCm39) |
I394T |
probably benign |
Het |
Hectd4 |
G |
A |
5: 121,477,581 (GRCm39) |
A2835T |
possibly damaging |
Het |
Herc2 |
A |
G |
7: 55,818,652 (GRCm39) |
D2781G |
possibly damaging |
Het |
Kmt2b |
G |
T |
7: 30,268,802 (GRCm39) |
H2642Q |
probably damaging |
Het |
Lars1 |
A |
T |
18: 42,354,684 (GRCm39) |
D754E |
probably damaging |
Het |
Lrpprc |
A |
C |
17: 85,059,745 (GRCm39) |
S690A |
probably benign |
Het |
Map3k6 |
A |
G |
4: 132,976,193 (GRCm39) |
T805A |
probably benign |
Het |
Mthfd1l |
T |
G |
10: 3,934,147 (GRCm39) |
S160A |
probably benign |
Het |
Mtmr6 |
G |
A |
14: 60,519,544 (GRCm39) |
|
probably null |
Het |
Mybpc2 |
A |
T |
7: 44,158,488 (GRCm39) |
M698K |
probably damaging |
Het |
Myh8 |
T |
A |
11: 67,190,586 (GRCm39) |
L1304M |
probably damaging |
Het |
Mylip |
T |
A |
13: 45,557,947 (GRCm39) |
V117E |
probably benign |
Het |
Npc1l1 |
T |
C |
11: 6,165,129 (GRCm39) |
Q1061R |
probably benign |
Het |
Or12e13 |
A |
G |
2: 87,664,081 (GRCm39) |
R233G |
probably benign |
Het |
Or5d37 |
A |
T |
2: 87,923,589 (GRCm39) |
Y230* |
probably null |
Het |
Pkd2l2 |
G |
A |
18: 34,561,232 (GRCm39) |
M413I |
probably damaging |
Het |
Plch2 |
C |
T |
4: 155,138,980 (GRCm39) |
G19D |
unknown |
Het |
Pramel17 |
T |
C |
4: 101,693,130 (GRCm39) |
K290R |
probably benign |
Het |
Psg22 |
A |
C |
7: 18,458,350 (GRCm39) |
Y347S |
probably damaging |
Het |
Ptpre |
C |
A |
7: 135,270,765 (GRCm39) |
Q314K |
probably damaging |
Het |
Rgs6 |
T |
C |
12: 83,032,144 (GRCm39) |
S54P |
probably damaging |
Het |
Sbds |
C |
A |
5: 130,279,726 (GRCm39) |
V130F |
possibly damaging |
Het |
Slc1a7 |
G |
A |
4: 107,869,473 (GRCm39) |
V513M |
probably benign |
Het |
Slc24a2 |
A |
T |
4: 87,094,552 (GRCm39) |
D322E |
probably benign |
Het |
Slc7a4 |
A |
C |
16: 17,392,315 (GRCm39) |
V373G |
possibly damaging |
Het |
Sulf1 |
G |
A |
1: 12,908,825 (GRCm39) |
V613M |
probably damaging |
Het |
Syt1 |
T |
C |
10: 108,472,434 (GRCm39) |
D150G |
probably damaging |
Het |
Tnpo3 |
C |
A |
6: 29,551,900 (GRCm39) |
V888F |
probably benign |
Het |
Trim9 |
T |
C |
12: 70,393,608 (GRCm39) |
H112R |
probably benign |
Het |
Vmn2r80 |
T |
C |
10: 78,984,711 (GRCm39) |
I21T |
probably benign |
Het |
Wdr41 |
C |
A |
13: 95,149,654 (GRCm39) |
A286E |
possibly damaging |
Het |
Wnt8b |
T |
A |
19: 44,500,396 (GRCm39) |
C328S |
probably damaging |
Het |
Ybx3 |
A |
T |
6: 131,345,400 (GRCm39) |
Y324* |
probably null |
Het |
Zmynd15 |
T |
A |
11: 70,351,767 (GRCm39) |
H124Q |
probably benign |
Het |
|
Other mutations in Slc45a4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00325:Slc45a4
|
APN |
15 |
73,459,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02506:Slc45a4
|
APN |
15 |
73,453,687 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02642:Slc45a4
|
APN |
15 |
73,458,664 (GRCm39) |
missense |
probably benign |
|
IGL03195:Slc45a4
|
APN |
15 |
73,456,272 (GRCm39) |
missense |
possibly damaging |
0.89 |
nosey
|
UTSW |
15 |
73,457,953 (GRCm39) |
missense |
probably damaging |
1.00 |
Undefined
|
UTSW |
15 |
73,456,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R0048:Slc45a4
|
UTSW |
15 |
73,477,285 (GRCm39) |
splice site |
probably benign |
|
R0189:Slc45a4
|
UTSW |
15 |
73,453,763 (GRCm39) |
missense |
probably benign |
0.00 |
R0240:Slc45a4
|
UTSW |
15 |
73,453,755 (GRCm39) |
missense |
probably benign |
0.02 |
R0240:Slc45a4
|
UTSW |
15 |
73,453,755 (GRCm39) |
missense |
probably benign |
0.02 |
R0828:Slc45a4
|
UTSW |
15 |
73,458,665 (GRCm39) |
missense |
probably benign |
0.01 |
R1172:Slc45a4
|
UTSW |
15 |
73,477,278 (GRCm39) |
splice site |
probably benign |
|
R1331:Slc45a4
|
UTSW |
15 |
73,458,596 (GRCm39) |
missense |
probably benign |
0.00 |
R1739:Slc45a4
|
UTSW |
15 |
73,457,887 (GRCm39) |
missense |
probably damaging |
1.00 |
R2310:Slc45a4
|
UTSW |
15 |
73,461,409 (GRCm39) |
missense |
probably damaging |
1.00 |
R4695:Slc45a4
|
UTSW |
15 |
73,453,924 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4904:Slc45a4
|
UTSW |
15 |
73,458,691 (GRCm39) |
missense |
probably benign |
0.18 |
R4974:Slc45a4
|
UTSW |
15 |
73,456,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Slc45a4
|
UTSW |
15 |
73,453,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Slc45a4
|
UTSW |
15 |
73,453,825 (GRCm39) |
missense |
probably damaging |
1.00 |
R6114:Slc45a4
|
UTSW |
15 |
73,477,453 (GRCm39) |
missense |
probably damaging |
0.96 |
R7057:Slc45a4
|
UTSW |
15 |
73,459,487 (GRCm39) |
missense |
probably damaging |
1.00 |
R7221:Slc45a4
|
UTSW |
15 |
73,458,259 (GRCm39) |
missense |
probably benign |
0.06 |
R7288:Slc45a4
|
UTSW |
15 |
73,458,785 (GRCm39) |
nonsense |
probably null |
|
R7331:Slc45a4
|
UTSW |
15 |
73,477,489 (GRCm39) |
missense |
probably benign |
0.02 |
R7874:Slc45a4
|
UTSW |
15 |
73,456,184 (GRCm39) |
splice site |
probably null |
|
R7901:Slc45a4
|
UTSW |
15 |
73,477,621 (GRCm39) |
start gained |
probably benign |
|
R8188:Slc45a4
|
UTSW |
15 |
73,456,383 (GRCm39) |
missense |
probably benign |
0.42 |
R8315:Slc45a4
|
UTSW |
15 |
73,461,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R8827:Slc45a4
|
UTSW |
15 |
73,458,316 (GRCm39) |
missense |
probably benign |
|
R8856:Slc45a4
|
UTSW |
15 |
73,457,966 (GRCm39) |
missense |
probably damaging |
1.00 |
R9089:Slc45a4
|
UTSW |
15 |
73,457,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R9278:Slc45a4
|
UTSW |
15 |
73,458,206 (GRCm39) |
missense |
probably benign |
0.14 |
|