Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930449I24Rik |
T |
A |
5: 146,441,690 (GRCm39) |
V279E |
possibly damaging |
Het |
Ache |
T |
C |
5: 137,289,152 (GRCm39) |
V286A |
possibly damaging |
Het |
Amotl1 |
T |
C |
9: 14,504,974 (GRCm39) |
N115S |
probably benign |
Het |
Aoah |
A |
T |
13: 21,163,696 (GRCm39) |
Y333F |
possibly damaging |
Het |
Ap4m1 |
A |
T |
5: 138,171,079 (GRCm39) |
R74* |
probably null |
Het |
Arhgef5 |
C |
T |
6: 43,256,432 (GRCm39) |
A1180V |
probably damaging |
Het |
Birc6 |
T |
C |
17: 74,926,835 (GRCm39) |
|
probably null |
Het |
Capn11 |
A |
G |
17: 45,953,392 (GRCm39) |
|
probably null |
Het |
Ccdc146 |
T |
A |
5: 21,527,756 (GRCm39) |
I187L |
probably benign |
Het |
Cfh |
A |
T |
1: 140,036,664 (GRCm39) |
C360S |
probably damaging |
Het |
Csmd1 |
T |
C |
8: 16,050,490 (GRCm39) |
N2249D |
probably damaging |
Het |
Cyb5r4 |
T |
G |
9: 86,939,282 (GRCm39) |
I355S |
probably damaging |
Het |
Dnm1l |
A |
T |
16: 16,132,251 (GRCm39) |
H653Q |
possibly damaging |
Het |
Frmd4a |
C |
T |
2: 4,337,889 (GRCm39) |
R32C |
probably benign |
Het |
Gm16503 |
C |
T |
4: 147,625,725 (GRCm39) |
S73L |
unknown |
Het |
Hnrnpll |
A |
T |
17: 80,357,234 (GRCm39) |
|
probably null |
Het |
Igf1r |
T |
A |
7: 67,844,826 (GRCm39) |
Y866* |
probably null |
Het |
Lct |
T |
C |
1: 128,231,963 (GRCm39) |
M629V |
probably damaging |
Het |
Mc1r |
A |
G |
8: 124,134,595 (GRCm39) |
N116S |
possibly damaging |
Het |
Micu2 |
T |
C |
14: 58,169,742 (GRCm39) |
K203E |
possibly damaging |
Het |
Mybpc1 |
C |
T |
10: 88,409,387 (GRCm39) |
W36* |
probably null |
Het |
Nsd1 |
C |
T |
13: 55,408,214 (GRCm39) |
T1286I |
probably damaging |
Het |
Or2a56 |
A |
G |
6: 42,932,689 (GRCm39) |
T86A |
probably benign |
Het |
Or51l14 |
T |
C |
7: 103,100,784 (GRCm39) |
M80T |
probably benign |
Het |
Pnpla3 |
C |
A |
15: 84,063,391 (GRCm39) |
N256K |
probably benign |
Het |
Polh |
A |
G |
17: 46,483,520 (GRCm39) |
S582P |
probably benign |
Het |
Rnaseh2a |
G |
A |
8: 85,686,702 (GRCm39) |
T149I |
possibly damaging |
Het |
Ryr1 |
A |
C |
7: 28,761,576 (GRCm39) |
Y3190* |
probably null |
Het |
Sec31b |
T |
A |
19: 44,520,149 (GRCm39) |
M212L |
probably benign |
Het |
Smc4 |
A |
G |
3: 68,938,800 (GRCm39) |
E950G |
probably benign |
Het |
Tlr1 |
A |
T |
5: 65,083,060 (GRCm39) |
S506T |
probably damaging |
Het |
Tmem181a |
T |
A |
17: 6,346,061 (GRCm39) |
L185H |
probably damaging |
Het |
Tmprss6 |
C |
T |
15: 78,330,899 (GRCm39) |
V43M |
probably damaging |
Het |
Vegfc |
A |
G |
8: 54,612,445 (GRCm39) |
Y156C |
probably damaging |
Het |
Vmn1r39 |
T |
C |
6: 66,781,703 (GRCm39) |
H205R |
possibly damaging |
Het |
Wnk2 |
C |
T |
13: 49,244,313 (GRCm39) |
D508N |
probably damaging |
Het |
Zan |
T |
C |
5: 137,422,240 (GRCm39) |
N2793D |
unknown |
Het |
|
Other mutations in Tmem236 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00490:Tmem236
|
APN |
2 |
14,224,189 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01363:Tmem236
|
APN |
2 |
14,179,441 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01980:Tmem236
|
APN |
2 |
14,223,716 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02749:Tmem236
|
APN |
2 |
14,224,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R0172:Tmem236
|
UTSW |
2 |
14,223,694 (GRCm39) |
missense |
probably benign |
0.06 |
R1470:Tmem236
|
UTSW |
2 |
14,223,732 (GRCm39) |
missense |
probably benign |
0.22 |
R1470:Tmem236
|
UTSW |
2 |
14,223,732 (GRCm39) |
missense |
probably benign |
0.22 |
R1519:Tmem236
|
UTSW |
2 |
14,197,091 (GRCm39) |
missense |
probably benign |
0.00 |
R1923:Tmem236
|
UTSW |
2 |
14,224,117 (GRCm39) |
missense |
probably damaging |
1.00 |
R2147:Tmem236
|
UTSW |
2 |
14,223,861 (GRCm39) |
missense |
probably benign |
0.03 |
R4551:Tmem236
|
UTSW |
2 |
14,223,964 (GRCm39) |
missense |
probably benign |
0.02 |
R4904:Tmem236
|
UTSW |
2 |
14,200,803 (GRCm39) |
missense |
probably benign |
|
R5168:Tmem236
|
UTSW |
2 |
14,197,139 (GRCm39) |
critical splice donor site |
probably null |
|
R5283:Tmem236
|
UTSW |
2 |
14,179,644 (GRCm39) |
missense |
probably benign |
0.01 |
R5306:Tmem236
|
UTSW |
2 |
14,223,975 (GRCm39) |
nonsense |
probably null |
|
R5334:Tmem236
|
UTSW |
2 |
14,223,871 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6516:Tmem236
|
UTSW |
2 |
14,200,791 (GRCm39) |
missense |
probably benign |
0.00 |
R6604:Tmem236
|
UTSW |
2 |
14,179,512 (GRCm39) |
missense |
probably benign |
0.03 |
R7689:Tmem236
|
UTSW |
2 |
14,197,076 (GRCm39) |
missense |
probably damaging |
0.99 |
R8390:Tmem236
|
UTSW |
2 |
14,224,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R9157:Tmem236
|
UTSW |
2 |
14,223,889 (GRCm39) |
missense |
probably benign |
0.00 |
R9630:Tmem236
|
UTSW |
2 |
14,223,815 (GRCm39) |
missense |
probably benign |
|
X0062:Tmem236
|
UTSW |
2 |
14,224,089 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Tmem236
|
UTSW |
2 |
14,179,538 (GRCm39) |
nonsense |
probably null |
|
|