Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aox3 |
T |
C |
1: 58,191,719 (GRCm39) |
F424L |
probably benign |
Het |
Arhgap11a |
T |
C |
2: 113,671,077 (GRCm39) |
T301A |
probably damaging |
Het |
Atp9a |
C |
A |
2: 168,495,481 (GRCm39) |
R575L |
probably damaging |
Het |
Brca2 |
G |
A |
5: 150,491,078 (GRCm39) |
D3088N |
probably damaging |
Het |
Brd3 |
G |
A |
2: 27,349,812 (GRCm39) |
T247I |
probably damaging |
Het |
Btbd8 |
A |
G |
5: 107,656,446 (GRCm39) |
H903R |
probably damaging |
Het |
Cacna1i |
A |
G |
15: 80,275,933 (GRCm39) |
N1908S |
probably benign |
Het |
Ccdc40 |
A |
T |
11: 119,122,797 (GRCm39) |
|
probably null |
Het |
Cdyl |
T |
C |
13: 36,047,226 (GRCm39) |
V389A |
probably damaging |
Het |
Col28a1 |
A |
G |
6: 8,014,963 (GRCm39) |
F814S |
probably damaging |
Het |
Cstf3 |
T |
C |
2: 104,476,976 (GRCm39) |
F149S |
probably damaging |
Het |
Dglucy |
T |
C |
12: 100,804,784 (GRCm39) |
Y122H |
probably damaging |
Het |
Dram1 |
T |
C |
10: 88,161,203 (GRCm39) |
D222G |
probably damaging |
Het |
Ets2 |
G |
A |
16: 95,512,802 (GRCm39) |
R96H |
probably damaging |
Het |
Gm11563 |
T |
A |
11: 99,549,527 (GRCm39) |
R76* |
probably null |
Het |
Gm17093 |
A |
C |
14: 44,758,277 (GRCm39) |
|
probably benign |
Het |
Gpi1 |
A |
T |
7: 33,920,347 (GRCm39) |
V136D |
probably damaging |
Het |
Hfm1 |
G |
A |
5: 107,059,410 (GRCm39) |
T204M |
possibly damaging |
Het |
Itgae |
T |
C |
11: 73,006,963 (GRCm39) |
I403T |
probably damaging |
Het |
Krt75 |
A |
T |
15: 101,476,537 (GRCm39) |
D409E |
probably damaging |
Het |
Limk2 |
T |
G |
11: 3,305,340 (GRCm39) |
T76P |
probably benign |
Het |
Mtus2 |
A |
T |
5: 148,015,030 (GRCm39) |
M608L |
probably benign |
Het |
Obscn |
C |
A |
11: 58,899,421 (GRCm39) |
E979* |
probably null |
Het |
Or52ab7 |
T |
G |
7: 102,978,480 (GRCm39) |
F262L |
probably benign |
Het |
P2rx7 |
C |
T |
5: 122,796,831 (GRCm39) |
A166V |
probably damaging |
Het |
Pomgnt2 |
T |
C |
9: 121,811,854 (GRCm39) |
E309G |
probably benign |
Het |
Sbno2 |
A |
T |
10: 79,905,458 (GRCm39) |
Y199* |
probably null |
Het |
Setd2 |
C |
A |
9: 110,446,499 (GRCm39) |
|
probably null |
Het |
Slc66a1 |
A |
G |
4: 139,028,384 (GRCm39) |
V186A |
probably benign |
Het |
Vmn2r84 |
T |
A |
10: 130,222,277 (GRCm39) |
I648F |
probably damaging |
Het |
Vrtn |
C |
T |
12: 84,696,980 (GRCm39) |
R577W |
probably benign |
Het |
Znhit6 |
A |
G |
3: 145,283,853 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Gm21738 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00990:Gm21738
|
APN |
14 |
19,418,885 (GRCm38) |
missense |
probably benign |
|
IGL01010:Gm21738
|
APN |
14 |
19,417,361 (GRCm38) |
missense |
probably benign |
0.03 |
IGL01018:Gm21738
|
APN |
14 |
19,418,856 (GRCm38) |
missense |
probably benign |
0.39 |
IGL01865:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01869:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01873:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01877:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01878:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01879:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01880:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01882:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01883:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01884:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01885:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01886:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01888:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01891:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01892:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01893:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01894:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01895:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01896:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01898:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01899:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01900:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01901:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01902:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01903:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01904:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01905:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01906:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01908:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01909:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01910:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01912:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01913:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01914:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01915:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01916:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01917:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01918:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01919:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01922:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01923:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01924:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01925:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01926:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01932:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01940:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
IGL01949:Gm21738
|
APN |
14 |
19,416,979 (GRCm38) |
missense |
probably benign |
0.01 |
PIT4131001:Gm21738
|
UTSW |
14 |
19,417,330 (GRCm38) |
missense |
probably benign |
0.00 |
PIT4142001:Gm21738
|
UTSW |
14 |
19,417,330 (GRCm38) |
missense |
probably benign |
0.00 |
R0831:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R0831:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R0976:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1029:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R1146:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1231:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1231:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R1402:Gm21738
|
UTSW |
14 |
19,415,963 (GRCm38) |
missense |
probably benign |
|
R1402:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R1638:Gm21738
|
UTSW |
14 |
19,418,908 (GRCm38) |
missense |
probably benign |
|
R1874:Gm21738
|
UTSW |
14 |
19,418,824 (GRCm38) |
missense |
possibly damaging |
0.64 |
R4392:Gm21738
|
UTSW |
14 |
19,417,178 (GRCm38) |
missense |
probably benign |
|
R4393:Gm21738
|
UTSW |
14 |
19,417,178 (GRCm38) |
missense |
probably benign |
|
R5049:Gm21738
|
UTSW |
14 |
19,415,957 (GRCm38) |
missense |
probably benign |
0.01 |
R5257:Gm21738
|
UTSW |
14 |
19,415,942 (GRCm38) |
missense |
probably benign |
|
R6756:Gm21738
|
UTSW |
14 |
19,418,824 (GRCm38) |
missense |
possibly damaging |
0.64 |
R6915:Gm21738
|
UTSW |
14 |
19,415,933 (GRCm38) |
missense |
probably benign |
|
V5622:Gm21738
|
UTSW |
14 |
19,417,180 (GRCm38) |
missense |
probably damaging |
1.00 |
|