Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
AA467197 |
T |
C |
2: 122,480,237 (GRCm39) |
Y33H |
probably damaging |
Het |
Abcc10 |
T |
C |
17: 46,623,273 (GRCm39) |
R880G |
probably benign |
Het |
Abcg2 |
T |
A |
6: 58,646,221 (GRCm39) |
Y246N |
probably benign |
Het |
Abhd18 |
A |
G |
3: 40,888,061 (GRCm39) |
M302V |
probably benign |
Het |
Ablim2 |
A |
G |
5: 36,032,235 (GRCm39) |
D568G |
possibly damaging |
Het |
Alpk2 |
T |
C |
18: 65,440,542 (GRCm39) |
R284G |
possibly damaging |
Het |
AU021092 |
T |
C |
16: 5,034,649 (GRCm39) |
Y191C |
probably damaging |
Het |
Bdp1 |
T |
A |
13: 100,200,985 (GRCm39) |
T751S |
probably benign |
Het |
Brme1 |
A |
T |
8: 84,893,952 (GRCm39) |
E373V |
probably damaging |
Het |
Ccdc136 |
A |
G |
6: 29,412,929 (GRCm39) |
E438G |
probably damaging |
Het |
Cul2 |
C |
A |
18: 3,399,912 (GRCm39) |
N15K |
probably benign |
Het |
Eml2 |
C |
A |
7: 18,913,220 (GRCm39) |
Q73K |
probably damaging |
Het |
Epha6 |
C |
A |
16: 59,826,030 (GRCm39) |
R588S |
probably damaging |
Het |
Eppk1 |
C |
T |
15: 75,994,319 (GRCm39) |
R854Q |
probably benign |
Het |
Fbxw28 |
C |
T |
9: 109,155,604 (GRCm39) |
W389* |
probably null |
Het |
Fcgbpl1 |
T |
A |
7: 27,842,158 (GRCm39) |
C698S |
probably damaging |
Het |
Gbp4 |
A |
T |
5: 105,284,703 (GRCm39) |
V62E |
probably benign |
Het |
Gtf2h1 |
C |
A |
7: 46,464,768 (GRCm39) |
T401K |
possibly damaging |
Het |
Hif1a |
G |
T |
12: 73,984,428 (GRCm39) |
M294I |
probably benign |
Het |
Irak2 |
A |
G |
6: 113,663,903 (GRCm39) |
N484S |
probably benign |
Het |
Kcnj16 |
A |
G |
11: 110,916,441 (GRCm39) |
T368A |
probably benign |
Het |
Kcnq1 |
G |
A |
7: 142,917,403 (GRCm39) |
G588D |
probably damaging |
Het |
Kcnq5 |
G |
A |
1: 21,549,648 (GRCm39) |
R360C |
probably damaging |
Het |
Nckap5 |
T |
G |
1: 125,942,357 (GRCm39) |
E1582D |
probably damaging |
Het |
Nrip3 |
A |
G |
7: 109,362,735 (GRCm39) |
I183T |
possibly damaging |
Het |
Or10g9 |
T |
A |
9: 39,912,241 (GRCm39) |
H94L |
probably benign |
Het |
Or4c117 |
A |
G |
2: 88,956,058 (GRCm39) |
F6L |
probably benign |
Het |
Pcdha2 |
C |
T |
18: 37,074,619 (GRCm39) |
S750L |
probably damaging |
Het |
Pik3r2 |
T |
C |
8: 71,223,079 (GRCm39) |
Y447C |
probably damaging |
Het |
Poteg |
T |
C |
8: 27,938,068 (GRCm39) |
Y75H |
probably benign |
Het |
Proser1 |
G |
C |
3: 53,385,977 (GRCm39) |
G620R |
probably damaging |
Het |
Prpsap1 |
A |
T |
11: 116,369,439 (GRCm39) |
L164H |
probably damaging |
Het |
Rfc3 |
A |
T |
5: 151,568,381 (GRCm39) |
V195E |
possibly damaging |
Het |
She |
A |
G |
3: 89,739,174 (GRCm39) |
T122A |
probably benign |
Het |
Spata31e1 |
A |
G |
13: 49,941,273 (GRCm39) |
S56P |
probably damaging |
Het |
Srpra |
A |
G |
9: 35,126,133 (GRCm39) |
E442G |
probably benign |
Het |
Sult2a6 |
T |
A |
7: 13,984,357 (GRCm39) |
R124S |
probably damaging |
Het |
Synm |
T |
C |
7: 67,383,511 (GRCm39) |
T1384A |
probably benign |
Het |
Tenm3 |
A |
G |
8: 48,746,544 (GRCm39) |
V1087A |
probably damaging |
Het |
Ticam1 |
T |
A |
17: 56,578,340 (GRCm39) |
I252L |
probably benign |
Het |
Trbv31 |
C |
A |
6: 41,534,697 (GRCm39) |
D89Y |
possibly damaging |
Het |
Trpc7 |
G |
A |
13: 56,970,282 (GRCm39) |
T434I |
probably benign |
Het |
Tubgcp4 |
T |
A |
2: 121,024,634 (GRCm39) |
I603N |
probably benign |
Het |
Ugt3a1 |
A |
G |
15: 9,310,669 (GRCm39) |
N317S |
possibly damaging |
Het |
Vdac1 |
C |
T |
11: 52,267,330 (GRCm39) |
T77I |
possibly damaging |
Het |
Vmn2r113 |
A |
T |
17: 23,177,753 (GRCm39) |
R846* |
probably null |
Het |
Zc3h12d |
GCCC |
GCC |
10: 7,715,735 (GRCm39) |
|
probably null |
Het |
Zranb2 |
G |
T |
3: 157,252,312 (GRCm39) |
R310S |
unknown |
Het |
|
Other mutations in Sarm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01476:Sarm1
|
APN |
11 |
78,381,637 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01484:Sarm1
|
APN |
11 |
78,381,839 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02591:Sarm1
|
APN |
11 |
78,378,178 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Sarm1
|
UTSW |
11 |
78,378,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R0282:Sarm1
|
UTSW |
11 |
78,365,806 (GRCm39) |
nonsense |
probably null |
|
R1583:Sarm1
|
UTSW |
11 |
78,374,153 (GRCm39) |
nonsense |
probably null |
|
R1800:Sarm1
|
UTSW |
11 |
78,381,820 (GRCm39) |
missense |
possibly damaging |
0.87 |
R2101:Sarm1
|
UTSW |
11 |
78,366,115 (GRCm39) |
missense |
probably damaging |
1.00 |
R2131:Sarm1
|
UTSW |
11 |
78,366,133 (GRCm39) |
missense |
probably benign |
0.00 |
R4474:Sarm1
|
UTSW |
11 |
78,387,927 (GRCm39) |
missense |
probably benign |
0.01 |
R5191:Sarm1
|
UTSW |
11 |
78,387,945 (GRCm39) |
nonsense |
probably null |
|
R5280:Sarm1
|
UTSW |
11 |
78,374,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Sarm1
|
UTSW |
11 |
78,388,265 (GRCm39) |
missense |
probably benign |
|
R5954:Sarm1
|
UTSW |
11 |
78,381,428 (GRCm39) |
nonsense |
probably null |
|
R6027:Sarm1
|
UTSW |
11 |
78,374,384 (GRCm39) |
missense |
probably benign |
|
R7343:Sarm1
|
UTSW |
11 |
78,388,083 (GRCm39) |
missense |
possibly damaging |
0.71 |
R9075:Sarm1
|
UTSW |
11 |
78,374,023 (GRCm39) |
missense |
probably benign |
0.00 |
R9533:Sarm1
|
UTSW |
11 |
78,373,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R9786:Sarm1
|
UTSW |
11 |
78,365,743 (GRCm39) |
missense |
probably benign |
0.01 |
R9788:Sarm1
|
UTSW |
11 |
78,378,863 (GRCm39) |
missense |
probably damaging |
1.00 |
V7732:Sarm1
|
UTSW |
11 |
78,378,891 (GRCm39) |
missense |
probably benign |
0.03 |
|