Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adad1 |
A |
T |
3: 37,137,489 (GRCm39) |
I307F |
probably damaging |
Het |
Adam15 |
G |
A |
3: 89,247,769 (GRCm39) |
A789V |
possibly damaging |
Het |
Btnl6 |
T |
A |
17: 34,734,648 (GRCm39) |
D38V |
possibly damaging |
Het |
Cd59b |
G |
A |
2: 103,909,273 (GRCm39) |
C18Y |
probably damaging |
Het |
Clstn1 |
T |
G |
4: 149,716,299 (GRCm39) |
I255R |
probably damaging |
Het |
Dpp10 |
A |
G |
1: 123,613,999 (GRCm39) |
L99P |
possibly damaging |
Het |
Efr3b |
C |
T |
12: 4,033,391 (GRCm39) |
V139I |
probably benign |
Het |
Emc1 |
A |
T |
4: 139,098,295 (GRCm39) |
T759S |
probably benign |
Het |
Fndc1 |
C |
T |
17: 7,984,230 (GRCm39) |
G1232E |
unknown |
Het |
Gjb3 |
C |
T |
4: 127,220,157 (GRCm39) |
G125D |
probably damaging |
Het |
Helb |
A |
G |
10: 119,938,693 (GRCm39) |
S594P |
possibly damaging |
Het |
Hycc2 |
C |
A |
1: 58,579,350 (GRCm39) |
R229L |
probably damaging |
Het |
Ildr1 |
T |
C |
16: 36,542,712 (GRCm39) |
S371P |
probably damaging |
Het |
Kif1b |
T |
A |
4: 149,299,433 (GRCm39) |
R946W |
probably damaging |
Het |
Lrp12 |
T |
C |
15: 39,741,300 (GRCm39) |
T472A |
probably damaging |
Het |
Lyst |
A |
G |
13: 13,886,230 (GRCm39) |
D3031G |
probably benign |
Het |
Med12l |
A |
T |
3: 59,169,397 (GRCm39) |
T1596S |
possibly damaging |
Het |
Myom1 |
A |
C |
17: 71,379,076 (GRCm39) |
|
probably null |
Het |
Nhlrc2 |
T |
A |
19: 56,559,086 (GRCm39) |
Y190* |
probably null |
Het |
Nol4 |
A |
T |
18: 22,956,398 (GRCm39) |
N115K |
probably damaging |
Het |
Nrg1 |
T |
A |
8: 32,308,291 (GRCm39) |
|
probably null |
Het |
Or7g26 |
T |
A |
9: 19,229,999 (GRCm39) |
H56Q |
probably damaging |
Het |
Oxld1 |
A |
C |
11: 120,347,714 (GRCm39) |
L161R |
probably damaging |
Het |
Phex |
A |
G |
X: 155,969,271 (GRCm39) |
S568P |
probably damaging |
Het |
Pkd1 |
T |
G |
17: 24,788,673 (GRCm39) |
S810R |
probably benign |
Het |
Plin2 |
G |
T |
4: 86,582,723 (GRCm39) |
C84* |
probably null |
Het |
Ppfia3 |
A |
T |
7: 45,004,362 (GRCm39) |
|
probably benign |
Het |
Ptpn14 |
A |
G |
1: 189,582,587 (GRCm39) |
N478S |
probably benign |
Het |
Pygl |
A |
G |
12: 70,237,908 (GRCm39) |
M801T |
probably benign |
Het |
Recql5 |
A |
G |
11: 115,785,917 (GRCm39) |
Y619H |
probably benign |
Het |
Scn3a |
C |
A |
2: 65,356,899 (GRCm39) |
D182Y |
possibly damaging |
Het |
Serpinb6e |
T |
C |
13: 34,016,785 (GRCm39) |
E316G |
possibly damaging |
Het |
Shroom4 |
A |
G |
X: 6,495,998 (GRCm39) |
E386G |
possibly damaging |
Het |
Slc4a2 |
A |
G |
5: 24,634,432 (GRCm39) |
S24G |
probably benign |
Het |
Slc4a4 |
A |
G |
5: 89,277,508 (GRCm39) |
I282V |
probably benign |
Het |
Slc8b1 |
C |
T |
5: 120,658,918 (GRCm39) |
R148C |
probably damaging |
Het |
Stag2 |
A |
G |
X: 41,360,202 (GRCm39) |
|
probably benign |
Het |
Styx |
T |
A |
14: 45,609,922 (GRCm39) |
H195Q |
probably benign |
Het |
Sufu |
A |
G |
19: 46,439,349 (GRCm39) |
I190V |
probably benign |
Het |
Svep1 |
A |
G |
4: 58,145,341 (GRCm39) |
|
probably benign |
Het |
Tbc1d31 |
T |
C |
15: 57,801,344 (GRCm39) |
I293T |
probably benign |
Het |
Timp4 |
T |
A |
6: 115,223,444 (GRCm39) |
I160F |
probably damaging |
Het |
Tmem87a |
A |
T |
2: 120,234,534 (GRCm39) |
V3E |
probably damaging |
Het |
Utp4 |
T |
A |
8: 107,632,873 (GRCm39) |
H285Q |
probably benign |
Het |
Vrk1 |
T |
G |
12: 106,028,912 (GRCm39) |
S305A |
probably benign |
Het |
Zfp329 |
G |
T |
7: 12,545,106 (GRCm39) |
H139Q |
possibly damaging |
Het |
|
Other mutations in Bspry |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00418:Bspry
|
APN |
4 |
62,414,342 (GRCm39) |
missense |
probably benign |
0.44 |
IGL02186:Bspry
|
APN |
4 |
62,414,226 (GRCm39) |
splice site |
probably benign |
|
IGL02644:Bspry
|
APN |
4 |
62,414,565 (GRCm39) |
missense |
probably damaging |
1.00 |
R0041:Bspry
|
UTSW |
4 |
62,404,791 (GRCm39) |
missense |
probably damaging |
1.00 |
R0306:Bspry
|
UTSW |
4 |
62,414,394 (GRCm39) |
missense |
probably damaging |
1.00 |
R0560:Bspry
|
UTSW |
4 |
62,404,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R1919:Bspry
|
UTSW |
4 |
62,413,034 (GRCm39) |
missense |
probably damaging |
1.00 |
R3038:Bspry
|
UTSW |
4 |
62,415,220 (GRCm39) |
missense |
probably benign |
0.36 |
R4431:Bspry
|
UTSW |
4 |
62,400,904 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4690:Bspry
|
UTSW |
4 |
62,404,762 (GRCm39) |
missense |
probably damaging |
0.98 |
R4735:Bspry
|
UTSW |
4 |
62,404,762 (GRCm39) |
missense |
probably damaging |
0.98 |
R5432:Bspry
|
UTSW |
4 |
62,400,952 (GRCm39) |
missense |
probably benign |
0.01 |
R5684:Bspry
|
UTSW |
4 |
62,414,519 (GRCm39) |
missense |
possibly damaging |
0.81 |
R7209:Bspry
|
UTSW |
4 |
62,404,852 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7680:Bspry
|
UTSW |
4 |
62,414,828 (GRCm39) |
makesense |
probably null |
|
R7708:Bspry
|
UTSW |
4 |
62,414,337 (GRCm39) |
missense |
probably benign |
0.36 |
R9631:Bspry
|
UTSW |
4 |
62,400,955 (GRCm39) |
critical splice donor site |
probably null |
|
X0025:Bspry
|
UTSW |
4 |
62,398,435 (GRCm39) |
missense |
unknown |
|
|