Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adss2 |
A |
T |
1: 177,612,508 (GRCm39) |
H80Q |
probably damaging |
Het |
Ahi1 |
A |
G |
10: 20,847,959 (GRCm39) |
N456D |
probably damaging |
Het |
Alpk2 |
T |
G |
18: 65,439,673 (GRCm39) |
E573D |
probably damaging |
Het |
Axin2 |
G |
A |
11: 108,814,501 (GRCm39) |
V130M |
probably damaging |
Het |
Cadm4 |
T |
C |
7: 24,202,184 (GRCm39) |
L341P |
possibly damaging |
Het |
Col20a1 |
G |
A |
2: 180,641,559 (GRCm39) |
C625Y |
probably damaging |
Het |
Col6a3 |
T |
G |
1: 90,731,655 (GRCm39) |
I1533L |
possibly damaging |
Het |
Dusp10 |
A |
T |
1: 183,769,697 (GRCm39) |
|
probably null |
Het |
Dysf |
T |
A |
6: 84,171,368 (GRCm39) |
I1837N |
probably damaging |
Het |
Fbxw19 |
A |
G |
9: 109,322,614 (GRCm39) |
S119P |
probably benign |
Het |
Il22ra1 |
C |
A |
4: 135,478,395 (GRCm39) |
P489T |
possibly damaging |
Het |
Il7r |
A |
T |
15: 9,508,085 (GRCm39) |
N412K |
possibly damaging |
Het |
Kdr |
A |
T |
5: 76,122,420 (GRCm39) |
Y502N |
probably benign |
Het |
Med12l |
T |
A |
3: 59,001,076 (GRCm39) |
L713H |
probably damaging |
Het |
Nfxl1 |
A |
G |
5: 72,707,771 (GRCm39) |
|
probably benign |
Het |
Or4a70 |
A |
G |
2: 89,324,182 (GRCm39) |
V158A |
probably benign |
Het |
Piezo1 |
T |
A |
8: 123,208,877 (GRCm39) |
E2495D |
probably damaging |
Het |
Pkhd1l1 |
T |
C |
15: 44,410,325 (GRCm39) |
F2611L |
probably benign |
Het |
Pld2 |
T |
C |
11: 70,432,132 (GRCm39) |
C84R |
probably damaging |
Het |
Prss3l |
A |
G |
6: 41,420,357 (GRCm39) |
V123A |
possibly damaging |
Het |
Scfd2 |
G |
T |
5: 74,691,707 (GRCm39) |
P192T |
possibly damaging |
Het |
Tmc2 |
T |
C |
2: 130,102,086 (GRCm39) |
|
probably benign |
Het |
Tmem217 |
T |
C |
17: 29,745,566 (GRCm39) |
R55G |
probably benign |
Het |
Unc80 |
A |
G |
1: 66,734,592 (GRCm39) |
D3205G |
possibly damaging |
Het |
Vps13c |
A |
G |
9: 67,793,566 (GRCm39) |
N440D |
probably damaging |
Het |
Wdr35 |
T |
C |
12: 9,055,838 (GRCm39) |
|
probably benign |
Het |
Zfp110 |
T |
A |
7: 12,583,723 (GRCm39) |
H790Q |
probably damaging |
Het |
|
Other mutations in Tm4sf19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02468:Tm4sf19
|
APN |
16 |
32,226,533 (GRCm39) |
splice site |
probably benign |
|
IGL02573:Tm4sf19
|
APN |
16 |
32,226,678 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02938:Tm4sf19
|
APN |
16 |
32,224,733 (GRCm39) |
missense |
probably damaging |
0.98 |
R1306:Tm4sf19
|
UTSW |
16 |
32,226,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R1450:Tm4sf19
|
UTSW |
16 |
32,226,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R1522:Tm4sf19
|
UTSW |
16 |
32,224,820 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1895:Tm4sf19
|
UTSW |
16 |
32,226,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R4407:Tm4sf19
|
UTSW |
16 |
32,226,712 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5527:Tm4sf19
|
UTSW |
16 |
32,226,739 (GRCm39) |
missense |
probably damaging |
1.00 |
R6166:Tm4sf19
|
UTSW |
16 |
32,226,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R6949:Tm4sf19
|
UTSW |
16 |
32,224,676 (GRCm39) |
missense |
probably benign |
0.01 |
R7269:Tm4sf19
|
UTSW |
16 |
32,224,814 (GRCm39) |
missense |
probably damaging |
0.98 |
R7316:Tm4sf19
|
UTSW |
16 |
32,226,466 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7993:Tm4sf19
|
UTSW |
16 |
32,226,458 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1177:Tm4sf19
|
UTSW |
16 |
32,224,741 (GRCm39) |
missense |
probably damaging |
1.00 |
|