Other mutations in this stock |
Total: 73 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts7 |
A |
G |
9: 90,075,397 (GRCm39) |
E1043G |
probably benign |
Het |
Agps |
T |
G |
2: 75,684,850 (GRCm39) |
|
probably benign |
Het |
Ahnak |
A |
G |
19: 8,993,503 (GRCm39) |
E4929G |
possibly damaging |
Het |
Arl6ip4 |
T |
A |
5: 124,256,146 (GRCm39) |
|
probably benign |
Het |
Cdhr17 |
T |
C |
5: 17,006,547 (GRCm39) |
L88P |
possibly damaging |
Het |
Clca3a2 |
G |
T |
3: 144,525,158 (GRCm39) |
H25N |
probably benign |
Het |
Cubn |
C |
T |
2: 13,283,262 (GRCm39) |
D3559N |
probably damaging |
Het |
Dmac2 |
T |
A |
7: 25,320,345 (GRCm39) |
W15R |
probably benign |
Het |
Dzank1 |
T |
C |
2: 144,355,344 (GRCm39) |
E117G |
probably benign |
Het |
Eml2 |
A |
G |
7: 18,913,743 (GRCm39) |
T187A |
probably benign |
Het |
Eml5 |
A |
G |
12: 98,822,287 (GRCm39) |
V747A |
probably damaging |
Het |
Esr1 |
T |
A |
10: 4,919,271 (GRCm39) |
S454T |
probably damaging |
Het |
Evc2 |
A |
G |
5: 37,537,895 (GRCm39) |
T528A |
probably benign |
Het |
Fbxo5 |
T |
C |
10: 5,752,325 (GRCm39) |
N96S |
probably damaging |
Het |
Fcnb |
T |
C |
2: 27,969,636 (GRCm39) |
T144A |
probably damaging |
Het |
Fgf20 |
T |
A |
8: 40,739,951 (GRCm39) |
|
probably benign |
Het |
Gcg |
T |
C |
2: 62,306,408 (GRCm39) |
|
probably benign |
Het |
Gfm2 |
T |
A |
13: 97,299,369 (GRCm39) |
Y363* |
probably null |
Het |
Grwd1 |
C |
T |
7: 45,475,381 (GRCm39) |
R387Q |
probably benign |
Het |
Herc1 |
A |
G |
9: 66,412,129 (GRCm39) |
N4783S |
probably damaging |
Het |
Hydin |
C |
A |
8: 110,994,047 (GRCm39) |
A27E |
unknown |
Het |
Iigp1c |
T |
A |
18: 60,353,820 (GRCm39) |
|
probably benign |
Het |
Ikbip |
A |
G |
10: 90,932,249 (GRCm39) |
T298A |
possibly damaging |
Het |
Il1rap |
A |
G |
16: 26,541,724 (GRCm39) |
N655S |
possibly damaging |
Het |
Kif21b |
C |
T |
1: 136,077,162 (GRCm39) |
R395C |
probably damaging |
Het |
Kif3a |
ATTGACG |
A |
11: 53,484,248 (GRCm39) |
|
probably benign |
Het |
Klhl40 |
A |
G |
9: 121,609,002 (GRCm39) |
D389G |
probably benign |
Het |
Ly6g |
A |
G |
15: 75,030,529 (GRCm39) |
T116A |
probably damaging |
Het |
Mast2 |
A |
G |
4: 116,165,900 (GRCm39) |
L1276P |
probably damaging |
Het |
Mitf |
A |
G |
6: 97,990,704 (GRCm39) |
Q369R |
possibly damaging |
Het |
Mtus2 |
T |
A |
5: 148,243,453 (GRCm39) |
Y192* |
probably null |
Het |
Nav1 |
T |
A |
1: 135,388,095 (GRCm39) |
E1109D |
unknown |
Het |
Nav2 |
A |
G |
7: 49,246,904 (GRCm39) |
E2143G |
probably damaging |
Het |
Nedd4 |
A |
G |
9: 72,584,656 (GRCm39) |
Q119R |
possibly damaging |
Het |
Nek9 |
A |
G |
12: 85,359,841 (GRCm39) |
V537A |
probably damaging |
Het |
Notum |
G |
T |
11: 120,550,974 (GRCm39) |
T64K |
|
Het |
Nudcd2 |
A |
G |
11: 40,630,026 (GRCm39) |
N144S |
probably damaging |
Het |
Nup205 |
A |
G |
6: 35,176,792 (GRCm39) |
E596G |
probably benign |
Het |
Olfml1 |
T |
A |
7: 107,167,007 (GRCm39) |
L12Q |
possibly damaging |
Het |
Or4f60 |
T |
A |
2: 111,902,718 (GRCm39) |
D70V |
probably damaging |
Het |
Or51k1 |
C |
T |
7: 103,661,336 (GRCm39) |
C191Y |
probably damaging |
Het |
Or52n2c |
A |
T |
7: 104,574,305 (GRCm39) |
M222K |
probably benign |
Het |
Or56b2 |
T |
A |
7: 104,337,260 (GRCm39) |
F13I |
probably benign |
Het |
Or6b13 |
A |
G |
7: 139,782,563 (GRCm39) |
V40A |
probably benign |
Het |
Ovgp1 |
T |
C |
3: 105,893,883 (GRCm39) |
|
probably benign |
Het |
Padi4 |
T |
C |
4: 140,479,926 (GRCm39) |
N409S |
probably damaging |
Het |
Pam |
T |
A |
1: 97,903,620 (GRCm39) |
T38S |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,208,868 (GRCm39) |
I1382V |
possibly damaging |
Het |
Pla2g12a |
A |
T |
3: 129,684,080 (GRCm39) |
Q153L |
possibly damaging |
Het |
Pla2g4e |
T |
A |
2: 120,019,910 (GRCm39) |
H180L |
probably benign |
Het |
Pou2af2 |
T |
A |
9: 51,202,998 (GRCm39) |
H52L |
probably benign |
Het |
Pprc1 |
A |
G |
19: 46,050,868 (GRCm39) |
T169A |
unknown |
Het |
Prrc2c |
A |
G |
1: 162,505,622 (GRCm39) |
I2592T |
possibly damaging |
Het |
Ptchd3 |
T |
A |
11: 121,722,956 (GRCm39) |
I348N |
probably damaging |
Het |
Ralgps1 |
T |
C |
2: 33,226,571 (GRCm39) |
D40G |
probably damaging |
Het |
Rbm19 |
T |
C |
5: 120,256,810 (GRCm39) |
F41S |
probably damaging |
Het |
Rbsn |
T |
C |
6: 92,166,797 (GRCm39) |
M616V |
probably benign |
Het |
Ryr1 |
A |
T |
7: 28,751,813 (GRCm39) |
M3660K |
possibly damaging |
Het |
Sidt2 |
A |
T |
9: 45,861,396 (GRCm39) |
V246E |
probably damaging |
Het |
Slc4a4 |
T |
C |
5: 89,347,568 (GRCm39) |
W770R |
probably damaging |
Het |
Spata31d1c |
T |
A |
13: 65,184,680 (GRCm39) |
S741T |
probably damaging |
Het |
Stk19 |
T |
G |
17: 35,051,432 (GRCm39) |
Y108S |
possibly damaging |
Het |
Stox2 |
T |
C |
8: 47,645,441 (GRCm39) |
E673G |
possibly damaging |
Het |
Tax1bp1 |
T |
A |
6: 52,714,116 (GRCm39) |
C271S |
probably benign |
Het |
Tmem161a |
C |
A |
8: 70,631,572 (GRCm39) |
R167S |
probably damaging |
Het |
Tnrc6c |
T |
A |
11: 117,605,105 (GRCm39) |
V80E |
probably damaging |
Het |
Trpa1 |
G |
A |
1: 14,963,465 (GRCm39) |
H586Y |
probably damaging |
Het |
Tsr1 |
A |
G |
11: 74,799,056 (GRCm39) |
T746A |
probably damaging |
Het |
Uqcrfs1 |
T |
C |
13: 30,724,794 (GRCm39) |
I249V |
probably damaging |
Het |
Vmn2r84 |
C |
A |
10: 130,229,976 (GRCm39) |
E45D |
probably benign |
Het |
Vnn3 |
A |
G |
10: 23,741,607 (GRCm39) |
E304G |
probably damaging |
Het |
Zfp541 |
G |
A |
7: 15,816,029 (GRCm39) |
V839M |
possibly damaging |
Het |
Zfp62 |
A |
G |
11: 49,108,350 (GRCm39) |
K814E |
probably benign |
Het |
|
Other mutations in Gstt2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01571:Gstt2
|
APN |
10 |
75,670,005 (GRCm39) |
splice site |
probably benign |
|
IGL01710:Gstt2
|
APN |
10 |
75,669,579 (GRCm39) |
splice site |
probably benign |
|
IGL02642:Gstt2
|
APN |
10 |
75,668,652 (GRCm39) |
missense |
probably benign |
0.17 |
IGL03375:Gstt2
|
APN |
10 |
75,668,655 (GRCm39) |
splice site |
probably null |
|
R0389:Gstt2
|
UTSW |
10 |
75,668,266 (GRCm39) |
missense |
probably damaging |
1.00 |
R1751:Gstt2
|
UTSW |
10 |
75,670,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1767:Gstt2
|
UTSW |
10 |
75,670,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R1971:Gstt2
|
UTSW |
10 |
75,668,499 (GRCm39) |
missense |
probably benign |
0.10 |
R2367:Gstt2
|
UTSW |
10 |
75,668,524 (GRCm39) |
missense |
probably benign |
0.44 |
R5027:Gstt2
|
UTSW |
10 |
75,667,726 (GRCm39) |
missense |
probably damaging |
0.99 |
R7457:Gstt2
|
UTSW |
10 |
75,668,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R7579:Gstt2
|
UTSW |
10 |
75,670,019 (GRCm39) |
missense |
probably benign |
0.00 |
R7910:Gstt2
|
UTSW |
10 |
75,667,736 (GRCm39) |
missense |
probably benign |
0.25 |
R7912:Gstt2
|
UTSW |
10 |
75,668,418 (GRCm39) |
missense |
probably benign |
0.27 |
R8282:Gstt2
|
UTSW |
10 |
75,668,291 (GRCm39) |
missense |
probably benign |
0.00 |
R8348:Gstt2
|
UTSW |
10 |
75,668,526 (GRCm39) |
missense |
probably damaging |
0.98 |
R8448:Gstt2
|
UTSW |
10 |
75,668,526 (GRCm39) |
missense |
probably damaging |
0.98 |
R8488:Gstt2
|
UTSW |
10 |
75,667,823 (GRCm39) |
missense |
possibly damaging |
0.69 |
R9259:Gstt2
|
UTSW |
10 |
75,669,511 (GRCm39) |
missense |
possibly damaging |
0.77 |
|