Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts4 |
T |
C |
1: 171,080,170 (GRCm39) |
F44S |
probably damaging |
Het |
Ap3b1 |
A |
T |
13: 94,613,501 (GRCm39) |
T667S |
probably benign |
Het |
Camsap1 |
T |
C |
2: 25,819,937 (GRCm39) |
Y1516C |
probably benign |
Het |
Ccl17 |
A |
G |
8: 95,537,100 (GRCm39) |
M1V |
probably null |
Het |
Cfhr1 |
T |
A |
1: 139,478,606 (GRCm39) |
T255S |
probably benign |
Het |
Clcn6 |
T |
C |
4: 148,093,245 (GRCm39) |
N812D |
probably damaging |
Het |
Cyp2b10 |
T |
C |
7: 25,616,764 (GRCm39) |
F402L |
probably damaging |
Het |
Dgkz |
A |
C |
2: 91,766,234 (GRCm39) |
S776A |
probably benign |
Het |
Dnaaf2 |
A |
T |
12: 69,244,122 (GRCm39) |
L313Q |
probably damaging |
Het |
Dnah10 |
G |
A |
5: 124,878,924 (GRCm39) |
G2728S |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,178,949 (GRCm39) |
M874K |
probably benign |
Het |
Eef1akmt3 |
A |
T |
10: 126,869,147 (GRCm39) |
L109Q |
probably damaging |
Het |
Egf |
A |
G |
3: 129,530,434 (GRCm39) |
S243P |
probably benign |
Het |
Fbxw21 |
T |
C |
9: 108,974,607 (GRCm39) |
I304M |
possibly damaging |
Het |
Fcgr4 |
T |
C |
1: 170,847,699 (GRCm39) |
V99A |
probably damaging |
Het |
Fhdc1 |
T |
C |
3: 84,356,193 (GRCm39) |
E417G |
probably damaging |
Het |
Flnc |
G |
T |
6: 29,446,607 (GRCm39) |
G939V |
probably damaging |
Het |
Herc1 |
A |
G |
9: 66,315,436 (GRCm39) |
M1173V |
probably benign |
Het |
Itgb4 |
C |
T |
11: 115,870,212 (GRCm39) |
T64I |
probably benign |
Het |
Kif16b |
A |
G |
2: 142,553,820 (GRCm39) |
S993P |
probably damaging |
Het |
Kitl |
T |
A |
10: 99,899,947 (GRCm39) |
V84E |
probably damaging |
Het |
Klra17 |
A |
G |
6: 129,849,150 (GRCm39) |
|
probably null |
Het |
Map2k3 |
A |
G |
11: 60,837,572 (GRCm39) |
D224G |
probably benign |
Het |
Medag |
T |
G |
5: 149,345,672 (GRCm39) |
F4V |
probably benign |
Het |
Mob3b |
C |
T |
4: 34,985,993 (GRCm39) |
V182I |
probably benign |
Het |
Mvb12b |
G |
T |
2: 33,764,402 (GRCm39) |
T49K |
probably damaging |
Het |
Naaladl2 |
A |
G |
3: 24,112,378 (GRCm39) |
V568A |
possibly damaging |
Het |
Nbea |
T |
C |
3: 55,693,896 (GRCm39) |
E2174G |
probably benign |
Het |
Nmd3 |
T |
C |
3: 69,652,580 (GRCm39) |
Y389H |
probably benign |
Het |
Or13g1 |
A |
G |
7: 85,955,547 (GRCm39) |
I258T |
probably damaging |
Het |
Or4p19 |
C |
T |
2: 88,242,589 (GRCm39) |
E138K |
probably benign |
Het |
Pcare |
T |
C |
17: 72,057,037 (GRCm39) |
D880G |
probably damaging |
Het |
Pcdh1 |
T |
A |
18: 38,336,327 (GRCm39) |
N103Y |
probably damaging |
Het |
Pcm1 |
A |
G |
8: 41,781,815 (GRCm39) |
D1905G |
possibly damaging |
Het |
Plcd1 |
A |
G |
9: 118,901,667 (GRCm39) |
F619S |
probably damaging |
Het |
Ptdss1 |
T |
A |
13: 67,111,433 (GRCm39) |
D166E |
probably damaging |
Het |
Rnf213 |
T |
C |
11: 119,332,927 (GRCm39) |
V2713A |
probably damaging |
Het |
Sema4f |
T |
C |
6: 82,896,634 (GRCm39) |
N200D |
probably damaging |
Het |
Tjp1 |
A |
T |
7: 64,973,837 (GRCm39) |
N472K |
probably damaging |
Het |
Trav6n-5 |
T |
C |
14: 53,342,608 (GRCm39) |
Y49H |
probably benign |
Het |
Trbv2 |
A |
G |
6: 41,024,904 (GRCm39) |
T107A |
probably benign |
Het |
Unc13c |
T |
C |
9: 73,643,933 (GRCm39) |
N1177S |
possibly damaging |
Het |
Vmn1r212 |
A |
G |
13: 23,068,258 (GRCm39) |
V25A |
probably damaging |
Het |
Zfhx4 |
T |
G |
3: 5,468,487 (GRCm39) |
S2882A |
probably benign |
Het |
Zswim5 |
A |
C |
4: 116,819,818 (GRCm39) |
S408R |
probably benign |
Het |
|
Other mutations in Hspa2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00433:Hspa2
|
APN |
12 |
76,453,123 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02946:Hspa2
|
APN |
12 |
76,451,947 (GRCm39) |
missense |
probably damaging |
0.99 |
R0504:Hspa2
|
UTSW |
12 |
76,451,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R1191:Hspa2
|
UTSW |
12 |
76,452,655 (GRCm39) |
missense |
probably damaging |
1.00 |
R1204:Hspa2
|
UTSW |
12 |
76,451,641 (GRCm39) |
missense |
probably benign |
|
R1880:Hspa2
|
UTSW |
12 |
76,452,694 (GRCm39) |
missense |
possibly damaging |
0.72 |
R2234:Hspa2
|
UTSW |
12 |
76,451,419 (GRCm39) |
missense |
possibly damaging |
0.56 |
R2265:Hspa2
|
UTSW |
12 |
76,452,962 (GRCm39) |
missense |
probably benign |
0.05 |
R4036:Hspa2
|
UTSW |
12 |
76,452,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R4037:Hspa2
|
UTSW |
12 |
76,452,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R4038:Hspa2
|
UTSW |
12 |
76,452,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R4039:Hspa2
|
UTSW |
12 |
76,452,542 (GRCm39) |
missense |
probably damaging |
1.00 |
R4120:Hspa2
|
UTSW |
12 |
76,452,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R4673:Hspa2
|
UTSW |
12 |
76,452,514 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4720:Hspa2
|
UTSW |
12 |
76,451,639 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4948:Hspa2
|
UTSW |
12 |
76,452,761 (GRCm39) |
missense |
probably damaging |
1.00 |
R5492:Hspa2
|
UTSW |
12 |
76,451,308 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
R7422:Hspa2
|
UTSW |
12 |
76,452,884 (GRCm39) |
missense |
probably damaging |
0.98 |
R7698:Hspa2
|
UTSW |
12 |
76,452,083 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9292:Hspa2
|
UTSW |
12 |
76,452,047 (GRCm39) |
missense |
probably damaging |
1.00 |
|