Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl1 |
G |
A |
4: 86,168,084 (GRCm39) |
A476T |
probably benign |
Het |
Ajm1 |
T |
C |
2: 25,468,501 (GRCm39) |
E470G |
possibly damaging |
Het |
Aknad1 |
T |
C |
3: 108,659,339 (GRCm39) |
S118P |
probably damaging |
Het |
Arhgap20 |
A |
G |
9: 51,728,041 (GRCm39) |
T85A |
probably benign |
Het |
Astn2 |
A |
G |
4: 65,566,530 (GRCm39) |
L824P |
probably damaging |
Het |
Ccr1 |
C |
A |
9: 123,763,827 (GRCm39) |
K234N |
probably damaging |
Het |
Cfap46 |
T |
C |
7: 139,235,757 (GRCm39) |
R203G |
probably damaging |
Het |
Col8a1 |
A |
G |
16: 57,448,931 (GRCm39) |
I193T |
unknown |
Het |
Cpa2 |
T |
C |
6: 30,552,070 (GRCm39) |
|
probably benign |
Het |
Crabp1 |
T |
C |
9: 54,675,717 (GRCm39) |
L100P |
possibly damaging |
Het |
Cspp1 |
A |
T |
1: 10,174,511 (GRCm39) |
R655W |
probably damaging |
Het |
Ddx1 |
A |
T |
12: 13,287,818 (GRCm39) |
|
probably benign |
Het |
Dnah7b |
T |
G |
1: 46,138,772 (GRCm39) |
|
probably benign |
Het |
Dzip3 |
A |
G |
16: 48,771,921 (GRCm39) |
S583P |
probably damaging |
Het |
Exosc1 |
A |
G |
19: 41,921,676 (GRCm39) |
|
probably benign |
Het |
Fhip1a |
A |
G |
3: 85,580,550 (GRCm39) |
S552P |
probably benign |
Het |
Gas7 |
A |
T |
11: 67,543,751 (GRCm39) |
|
probably benign |
Het |
Gss |
A |
T |
2: 155,409,609 (GRCm39) |
|
probably benign |
Het |
Hdhd3 |
G |
A |
4: 62,417,757 (GRCm39) |
R140* |
probably null |
Het |
Irx2 |
T |
A |
13: 72,779,675 (GRCm39) |
S320T |
possibly damaging |
Het |
Kcnf1 |
T |
C |
12: 17,225,142 (GRCm39) |
S360G |
possibly damaging |
Het |
Klk1b4 |
T |
C |
7: 43,860,480 (GRCm39) |
L166P |
probably damaging |
Het |
Mettl27 |
T |
C |
5: 134,963,285 (GRCm39) |
|
probably benign |
Het |
Myrfl |
T |
A |
10: 116,675,354 (GRCm39) |
H193L |
probably benign |
Het |
Nbas |
C |
T |
12: 13,381,115 (GRCm39) |
|
probably benign |
Het |
Or10ac1 |
C |
A |
6: 42,515,020 (GRCm39) |
R312L |
probably benign |
Het |
Or52b2 |
A |
T |
7: 104,986,736 (GRCm39) |
Y62* |
probably null |
Het |
Papolg |
A |
G |
11: 23,832,257 (GRCm39) |
I177T |
probably damaging |
Het |
Pdcd1 |
A |
G |
1: 93,967,238 (GRCm39) |
V220A |
probably benign |
Het |
Psmc1 |
T |
C |
12: 100,085,341 (GRCm39) |
L234P |
probably damaging |
Het |
Rasa2 |
A |
T |
9: 96,434,457 (GRCm39) |
M610K |
possibly damaging |
Het |
Ryr3 |
A |
G |
2: 112,484,047 (GRCm39) |
F3930S |
probably damaging |
Het |
Sacs |
G |
A |
14: 61,440,944 (GRCm39) |
V997I |
probably benign |
Het |
Setdb2 |
A |
G |
14: 59,660,945 (GRCm39) |
|
probably benign |
Het |
Ssu2 |
C |
A |
6: 112,361,359 (GRCm39) |
L32F |
probably damaging |
Het |
Taar1 |
A |
T |
10: 23,797,181 (GRCm39) |
N293I |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,611,846 (GRCm39) |
|
probably benign |
Het |
Vmn2r49 |
T |
C |
7: 9,720,325 (GRCm39) |
M389V |
possibly damaging |
Het |
Wdr7 |
T |
C |
18: 63,998,371 (GRCm39) |
V1106A |
probably benign |
Het |
Zfp324 |
A |
G |
7: 12,700,185 (GRCm39) |
I15V |
probably benign |
Het |
|
Other mutations in Klri1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01328:Klri1
|
APN |
6 |
129,675,800 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01380:Klri1
|
APN |
6 |
129,675,761 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01608:Klri1
|
APN |
6 |
129,675,130 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL01778:Klri1
|
APN |
6 |
129,694,010 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1646:Klri1
|
UTSW |
6 |
129,680,299 (GRCm39) |
missense |
probably benign |
0.00 |
R1649:Klri1
|
UTSW |
6 |
129,675,204 (GRCm39) |
missense |
probably benign |
|
R1746:Klri1
|
UTSW |
6 |
129,675,118 (GRCm39) |
splice site |
probably null |
|
R1960:Klri1
|
UTSW |
6 |
129,674,347 (GRCm39) |
missense |
probably benign |
0.02 |
R6561:Klri1
|
UTSW |
6 |
129,693,964 (GRCm39) |
missense |
probably benign |
0.03 |
R6773:Klri1
|
UTSW |
6 |
129,680,510 (GRCm39) |
missense |
possibly damaging |
0.67 |
R8169:Klri1
|
UTSW |
6 |
129,694,070 (GRCm39) |
missense |
probably benign |
0.42 |
R8861:Klri1
|
UTSW |
6 |
129,675,164 (GRCm39) |
missense |
probably benign |
0.03 |
R8907:Klri1
|
UTSW |
6 |
129,680,283 (GRCm39) |
missense |
probably null |
0.01 |
R9122:Klri1
|
UTSW |
6 |
129,693,995 (GRCm39) |
nonsense |
probably null |
|
R9199:Klri1
|
UTSW |
6 |
129,674,264 (GRCm39) |
makesense |
probably null |
|
R9438:Klri1
|
UTSW |
6 |
129,675,879 (GRCm39) |
missense |
probably benign |
0.10 |
X0021:Klri1
|
UTSW |
6 |
129,693,874 (GRCm39) |
missense |
probably benign |
0.25 |
|