Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4933415A04Rik |
A |
T |
11: 43,478,200 (GRCm39) |
|
probably benign |
Het |
A730018C14Rik |
A |
T |
12: 112,381,628 (GRCm39) |
|
noncoding transcript |
Het |
Abca5 |
A |
T |
11: 110,210,651 (GRCm39) |
L176Q |
probably damaging |
Het |
Aspm |
C |
A |
1: 139,404,614 (GRCm39) |
Q1315K |
probably benign |
Het |
Bpifb4 |
A |
G |
2: 153,782,888 (GRCm39) |
D31G |
probably benign |
Het |
Brf1 |
A |
G |
12: 112,937,083 (GRCm39) |
|
probably benign |
Het |
Card19 |
A |
C |
13: 49,361,621 (GRCm39) |
D3E |
probably benign |
Het |
Chd6 |
A |
G |
2: 160,809,822 (GRCm39) |
F1480L |
probably damaging |
Het |
Cldn25 |
A |
G |
9: 48,958,933 (GRCm39) |
|
noncoding transcript |
Het |
Col11a2 |
A |
G |
17: 34,276,249 (GRCm39) |
N799D |
probably damaging |
Het |
Cpb1 |
T |
C |
3: 20,320,697 (GRCm39) |
|
probably null |
Het |
Cyp2g1 |
T |
A |
7: 26,513,607 (GRCm39) |
I182N |
probably damaging |
Het |
Dntt |
A |
T |
19: 41,044,185 (GRCm39) |
|
probably benign |
Het |
Dscc1 |
C |
A |
15: 54,946,966 (GRCm39) |
C253F |
probably benign |
Het |
Dysf |
C |
A |
6: 84,090,318 (GRCm39) |
F956L |
probably benign |
Het |
Ephb6 |
T |
C |
6: 41,596,528 (GRCm39) |
|
probably benign |
Het |
Firrm |
T |
C |
1: 163,810,380 (GRCm39) |
|
probably benign |
Het |
Fkbp6 |
C |
T |
5: 135,368,858 (GRCm39) |
R234Q |
probably benign |
Het |
Gda |
T |
C |
19: 21,374,920 (GRCm39) |
D332G |
probably benign |
Het |
Ggt7 |
C |
T |
2: 155,336,813 (GRCm39) |
A560T |
possibly damaging |
Het |
Glis3 |
A |
T |
19: 28,509,268 (GRCm39) |
S239T |
possibly damaging |
Het |
Glyctk |
G |
A |
9: 106,033,168 (GRCm39) |
P124L |
probably benign |
Het |
Gm10845 |
T |
A |
14: 80,100,644 (GRCm39) |
|
noncoding transcript |
Het |
H13 |
A |
G |
2: 152,528,176 (GRCm39) |
K175R |
probably benign |
Het |
Igsf6 |
T |
A |
7: 120,673,677 (GRCm39) |
I18F |
probably benign |
Het |
Immt |
A |
G |
6: 71,828,828 (GRCm39) |
S128G |
probably benign |
Het |
Isy1 |
G |
A |
6: 87,796,167 (GRCm39) |
R257W |
probably damaging |
Het |
Kif13a |
G |
T |
13: 46,978,823 (GRCm39) |
|
probably benign |
Het |
L2hgdh |
A |
T |
12: 69,752,563 (GRCm39) |
Y239* |
probably null |
Het |
Lamp1 |
A |
G |
8: 13,224,550 (GRCm39) |
T405A |
probably damaging |
Het |
Lpin1 |
A |
T |
12: 16,590,980 (GRCm39) |
N817K |
possibly damaging |
Het |
Macf1 |
G |
A |
4: 123,302,357 (GRCm39) |
T715I |
probably benign |
Het |
Mapk12 |
T |
C |
15: 89,017,187 (GRCm39) |
|
probably benign |
Het |
Mdga2 |
A |
T |
12: 66,763,480 (GRCm39) |
N205K |
probably damaging |
Het |
Nat10 |
A |
G |
2: 103,587,550 (GRCm39) |
V55A |
probably damaging |
Het |
Nlrp10 |
T |
C |
7: 108,524,529 (GRCm39) |
E317G |
possibly damaging |
Het |
Nolc1 |
T |
A |
19: 46,068,528 (GRCm39) |
|
probably benign |
Het |
Nomo1 |
T |
C |
7: 45,687,056 (GRCm39) |
I72T |
probably damaging |
Het |
Or5b98 |
A |
G |
19: 12,931,720 (GRCm39) |
I256V |
probably benign |
Het |
Pappa2 |
C |
T |
1: 158,542,547 (GRCm39) |
C1780Y |
probably damaging |
Het |
Pgm2l1 |
A |
G |
7: 99,899,580 (GRCm39) |
M65V |
probably benign |
Het |
Pnisr |
T |
C |
4: 21,874,617 (GRCm39) |
|
probably benign |
Het |
Prss34 |
A |
T |
17: 25,517,700 (GRCm39) |
D25V |
probably damaging |
Het |
Ptpn1 |
T |
C |
2: 167,818,338 (GRCm39) |
|
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Racgap1 |
T |
C |
15: 99,540,839 (GRCm39) |
T4A |
possibly damaging |
Het |
Rap1gap2 |
A |
G |
11: 74,326,570 (GRCm39) |
C166R |
probably benign |
Het |
Rbm28 |
C |
A |
6: 29,127,802 (GRCm39) |
V705L |
probably benign |
Het |
Rgs1 |
C |
T |
1: 144,124,287 (GRCm39) |
V50M |
probably benign |
Het |
Rgs12 |
C |
T |
5: 35,124,008 (GRCm39) |
T597I |
probably benign |
Het |
Ros1 |
T |
C |
10: 52,018,363 (GRCm39) |
N765S |
possibly damaging |
Het |
Ruvbl1 |
A |
G |
6: 88,450,182 (GRCm39) |
R58G |
probably damaging |
Het |
Slc6a7 |
A |
G |
18: 61,135,295 (GRCm39) |
V411A |
probably benign |
Het |
Slco1a6 |
A |
T |
6: 142,103,116 (GRCm39) |
|
probably benign |
Het |
Smc1b |
A |
T |
15: 84,955,020 (GRCm39) |
D1077E |
probably damaging |
Het |
Srek1 |
G |
A |
13: 103,880,131 (GRCm39) |
H476Y |
unknown |
Het |
Strn3 |
A |
G |
12: 51,668,571 (GRCm39) |
V673A |
probably benign |
Het |
Tepsin |
T |
C |
11: 119,982,637 (GRCm39) |
|
probably null |
Het |
Tmem131l |
C |
T |
3: 83,842,122 (GRCm39) |
|
probably benign |
Het |
Tmem132c |
T |
C |
5: 127,631,733 (GRCm39) |
V664A |
possibly damaging |
Het |
Tmprss15 |
T |
C |
16: 78,800,277 (GRCm39) |
D602G |
probably damaging |
Het |
Trbv15 |
T |
C |
6: 41,118,199 (GRCm39) |
|
probably benign |
Het |
Trpm4 |
A |
G |
7: 44,968,664 (GRCm39) |
|
probably null |
Het |
Wdr70 |
A |
T |
15: 8,049,068 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Pygb |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00979:Pygb
|
APN |
2 |
150,661,833 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01395:Pygb
|
APN |
2 |
150,643,503 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01571:Pygb
|
APN |
2 |
150,672,393 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01960:Pygb
|
APN |
2 |
150,655,403 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03118:Pygb
|
APN |
2 |
150,662,731 (GRCm39) |
missense |
probably benign |
0.01 |
R0106:Pygb
|
UTSW |
2 |
150,648,123 (GRCm39) |
missense |
probably benign |
0.02 |
R0423:Pygb
|
UTSW |
2 |
150,665,904 (GRCm39) |
missense |
probably benign |
|
R0545:Pygb
|
UTSW |
2 |
150,657,626 (GRCm39) |
missense |
probably benign |
0.00 |
R0674:Pygb
|
UTSW |
2 |
150,657,054 (GRCm39) |
splice site |
probably null |
|
R1052:Pygb
|
UTSW |
2 |
150,628,858 (GRCm39) |
missense |
probably benign |
0.00 |
R1590:Pygb
|
UTSW |
2 |
150,659,583 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1706:Pygb
|
UTSW |
2 |
150,669,067 (GRCm39) |
missense |
probably damaging |
1.00 |
R1786:Pygb
|
UTSW |
2 |
150,658,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R2405:Pygb
|
UTSW |
2 |
150,662,695 (GRCm39) |
missense |
probably benign |
0.04 |
R3522:Pygb
|
UTSW |
2 |
150,670,473 (GRCm39) |
missense |
probably benign |
0.07 |
R4082:Pygb
|
UTSW |
2 |
150,668,391 (GRCm39) |
critical splice donor site |
probably null |
|
R4319:Pygb
|
UTSW |
2 |
150,657,534 (GRCm39) |
splice site |
probably benign |
|
R4662:Pygb
|
UTSW |
2 |
150,657,036 (GRCm39) |
missense |
probably benign |
|
R5072:Pygb
|
UTSW |
2 |
150,643,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R5665:Pygb
|
UTSW |
2 |
150,662,808 (GRCm39) |
splice site |
probably null |
|
R5874:Pygb
|
UTSW |
2 |
150,628,798 (GRCm39) |
missense |
probably benign |
0.11 |
R5910:Pygb
|
UTSW |
2 |
150,657,620 (GRCm39) |
missense |
probably benign |
0.00 |
R6610:Pygb
|
UTSW |
2 |
150,665,886 (GRCm39) |
splice site |
probably null |
|
R6820:Pygb
|
UTSW |
2 |
150,658,674 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7348:Pygb
|
UTSW |
2 |
150,628,903 (GRCm39) |
missense |
probably benign |
0.10 |
R7920:Pygb
|
UTSW |
2 |
150,628,922 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7936:Pygb
|
UTSW |
2 |
150,657,589 (GRCm39) |
missense |
probably benign |
0.28 |
R9226:Pygb
|
UTSW |
2 |
150,662,781 (GRCm39) |
missense |
possibly damaging |
0.58 |
R9308:Pygb
|
UTSW |
2 |
150,668,297 (GRCm39) |
missense |
probably benign |
0.15 |
R9618:Pygb
|
UTSW |
2 |
150,657,008 (GRCm39) |
missense |
|
|
|