Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930597O21Rik |
A |
T |
6: 66,873,097 (GRCm39) |
|
probably benign |
Het |
Abca8a |
A |
G |
11: 109,969,641 (GRCm39) |
|
probably benign |
Het |
Asphd1 |
A |
T |
7: 126,545,884 (GRCm39) |
|
probably benign |
Het |
Ccdc77 |
G |
A |
6: 120,308,858 (GRCm39) |
A301V |
probably benign |
Het |
Cep350 |
G |
T |
1: 155,829,499 (GRCm39) |
T135K |
probably benign |
Het |
Chrna7 |
A |
T |
7: 62,757,439 (GRCm39) |
D153E |
probably damaging |
Het |
Clec4b2 |
G |
T |
6: 123,179,187 (GRCm39) |
|
probably null |
Het |
Cyp2c67 |
T |
C |
19: 39,631,799 (GRCm39) |
N133D |
probably benign |
Het |
Dglucy |
T |
C |
12: 100,823,257 (GRCm39) |
I484T |
probably damaging |
Het |
Dtna |
G |
T |
18: 23,730,571 (GRCm39) |
M319I |
probably benign |
Het |
E2f5 |
T |
A |
3: 14,653,340 (GRCm39) |
M152K |
probably benign |
Het |
Emsy |
A |
T |
7: 98,290,873 (GRCm39) |
M58K |
probably damaging |
Het |
Epha1 |
A |
G |
6: 42,341,950 (GRCm39) |
Y367H |
probably damaging |
Het |
Etv1 |
A |
G |
12: 38,831,798 (GRCm39) |
S32G |
possibly damaging |
Het |
Fam114a1 |
A |
T |
5: 65,166,323 (GRCm39) |
|
probably benign |
Het |
Fbxo30 |
T |
A |
10: 11,166,122 (GRCm39) |
N281K |
probably benign |
Het |
Galnt12 |
G |
T |
4: 47,117,941 (GRCm39) |
R412L |
probably damaging |
Het |
Gm5786 |
T |
A |
12: 59,128,382 (GRCm39) |
|
noncoding transcript |
Het |
Gm9845 |
T |
C |
3: 39,412,616 (GRCm39) |
|
noncoding transcript |
Het |
Hecw2 |
A |
G |
1: 53,964,858 (GRCm39) |
V656A |
probably benign |
Het |
Hpse2 |
A |
T |
19: 43,282,692 (GRCm39) |
V187D |
probably damaging |
Het |
Itsn2 |
T |
A |
12: 4,679,557 (GRCm39) |
M122K |
possibly damaging |
Het |
Kcnj11 |
A |
G |
7: 45,749,213 (GRCm39) |
S37P |
probably benign |
Het |
Kif13b |
T |
C |
14: 65,037,807 (GRCm39) |
I1491T |
probably damaging |
Het |
Krt36 |
T |
A |
11: 99,995,990 (GRCm39) |
K145* |
probably null |
Het |
Loxhd1 |
A |
G |
18: 77,456,833 (GRCm39) |
I499V |
probably benign |
Het |
Map3k4 |
G |
T |
17: 12,490,497 (GRCm39) |
N311K |
probably damaging |
Het |
Mical2 |
C |
A |
7: 111,934,620 (GRCm39) |
H880N |
probably benign |
Het |
Myo1d |
A |
T |
11: 80,528,823 (GRCm39) |
C666* |
probably null |
Het |
Nlrx1 |
C |
T |
9: 44,175,302 (GRCm39) |
R158H |
probably benign |
Het |
Or10ag53 |
T |
A |
2: 87,082,295 (GRCm39) |
Y5N |
probably benign |
Het |
Or10q1 |
C |
A |
19: 13,726,994 (GRCm39) |
H175N |
possibly damaging |
Het |
Or13a17 |
A |
G |
7: 140,271,024 (GRCm39) |
T69A |
probably benign |
Het |
Or1e21 |
A |
T |
11: 73,344,106 (GRCm39) |
L311I |
probably benign |
Het |
Or4a78 |
T |
C |
2: 89,497,316 (GRCm39) |
S305G |
probably benign |
Het |
Pdgfrl |
A |
G |
8: 41,430,094 (GRCm39) |
R154G |
probably benign |
Het |
Pitpnb |
T |
C |
5: 111,478,699 (GRCm39) |
F7S |
possibly damaging |
Het |
Ppm1n |
G |
A |
7: 19,013,097 (GRCm39) |
R285C |
probably damaging |
Het |
Prdm11 |
A |
T |
2: 92,805,957 (GRCm39) |
I331N |
possibly damaging |
Het |
Ptprb |
C |
T |
10: 116,203,426 (GRCm39) |
P2066L |
probably damaging |
Het |
Ric8b |
T |
C |
10: 84,828,135 (GRCm39) |
|
probably benign |
Het |
Skil |
C |
A |
3: 31,165,787 (GRCm39) |
S368* |
probably null |
Het |
Slc1a5 |
G |
T |
7: 16,519,644 (GRCm39) |
|
probably null |
Het |
Trpm7 |
A |
C |
2: 126,661,811 (GRCm39) |
V1079G |
possibly damaging |
Het |
Tulp1 |
A |
G |
17: 28,577,633 (GRCm39) |
F2L |
probably damaging |
Het |
Ulbp3 |
A |
T |
10: 3,075,050 (GRCm39) |
|
noncoding transcript |
Het |
Zbtb17 |
A |
G |
4: 141,189,224 (GRCm39) |
Y48C |
probably damaging |
Het |
Zfp605 |
T |
A |
5: 110,275,506 (GRCm39) |
I208N |
possibly damaging |
Het |
|
Other mutations in Setx |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00688:Setx
|
APN |
2 |
29,038,457 (GRCm39) |
missense |
possibly damaging |
0.50 |
IGL00806:Setx
|
APN |
2 |
29,017,038 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01346:Setx
|
APN |
2 |
29,034,821 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01623:Setx
|
APN |
2 |
29,053,021 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02351:Setx
|
APN |
2 |
29,036,976 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02358:Setx
|
APN |
2 |
29,036,976 (GRCm39) |
missense |
probably benign |
0.45 |
IGL02378:Setx
|
APN |
2 |
29,063,738 (GRCm39) |
splice site |
probably benign |
|
IGL02408:Setx
|
APN |
2 |
29,023,942 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02425:Setx
|
APN |
2 |
29,038,420 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03023:Setx
|
APN |
2 |
29,035,914 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03351:Setx
|
APN |
2 |
29,051,811 (GRCm39) |
missense |
probably benign |
0.25 |
Addison
|
UTSW |
2 |
29,048,917 (GRCm39) |
missense |
probably damaging |
1.00 |
dallas
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
Denton
|
UTSW |
2 |
29,035,072 (GRCm39) |
missense |
possibly damaging |
0.81 |
doggie
|
UTSW |
2 |
29,054,562 (GRCm39) |
missense |
probably damaging |
1.00 |
Irving
|
UTSW |
2 |
29,029,233 (GRCm39) |
missense |
probably damaging |
0.99 |
G1Funyon:Setx
|
UTSW |
2 |
29,035,702 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03014:Setx
|
UTSW |
2 |
29,029,423 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4403001:Setx
|
UTSW |
2 |
29,023,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R0027:Setx
|
UTSW |
2 |
29,029,233 (GRCm39) |
missense |
probably damaging |
0.99 |
R0031:Setx
|
UTSW |
2 |
29,066,941 (GRCm39) |
missense |
probably benign |
0.02 |
R0070:Setx
|
UTSW |
2 |
29,051,537 (GRCm39) |
missense |
probably benign |
0.00 |
R0070:Setx
|
UTSW |
2 |
29,051,537 (GRCm39) |
missense |
probably benign |
0.00 |
R0092:Setx
|
UTSW |
2 |
29,036,305 (GRCm39) |
missense |
probably benign |
0.00 |
R0193:Setx
|
UTSW |
2 |
29,069,685 (GRCm39) |
missense |
probably benign |
0.21 |
R0281:Setx
|
UTSW |
2 |
29,069,655 (GRCm39) |
missense |
probably benign |
0.00 |
R0401:Setx
|
UTSW |
2 |
29,056,301 (GRCm39) |
nonsense |
probably null |
|
R0413:Setx
|
UTSW |
2 |
29,029,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R0517:Setx
|
UTSW |
2 |
29,047,145 (GRCm39) |
missense |
probably benign |
0.00 |
R0536:Setx
|
UTSW |
2 |
29,048,260 (GRCm39) |
missense |
possibly damaging |
0.46 |
R0617:Setx
|
UTSW |
2 |
29,036,819 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1183:Setx
|
UTSW |
2 |
29,070,104 (GRCm39) |
missense |
probably benign |
|
R1331:Setx
|
UTSW |
2 |
29,069,698 (GRCm39) |
missense |
probably benign |
|
R1465:Setx
|
UTSW |
2 |
29,030,401 (GRCm39) |
critical splice donor site |
probably null |
|
R1465:Setx
|
UTSW |
2 |
29,030,401 (GRCm39) |
critical splice donor site |
probably null |
|
R1467:Setx
|
UTSW |
2 |
29,048,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R1467:Setx
|
UTSW |
2 |
29,048,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R1482:Setx
|
UTSW |
2 |
29,053,004 (GRCm39) |
missense |
probably damaging |
0.99 |
R1599:Setx
|
UTSW |
2 |
29,030,385 (GRCm39) |
missense |
probably benign |
0.04 |
R1663:Setx
|
UTSW |
2 |
29,016,917 (GRCm39) |
missense |
probably damaging |
1.00 |
R1909:Setx
|
UTSW |
2 |
29,053,021 (GRCm39) |
missense |
possibly damaging |
0.70 |
R2117:Setx
|
UTSW |
2 |
29,020,313 (GRCm39) |
missense |
probably benign |
0.01 |
R2207:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2221:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2223:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2223:Setx
|
UTSW |
2 |
29,038,549 (GRCm39) |
missense |
possibly damaging |
0.89 |
R2273:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2274:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2275:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2309:Setx
|
UTSW |
2 |
29,048,916 (GRCm39) |
missense |
probably damaging |
1.00 |
R2328:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2328:Setx
|
UTSW |
2 |
29,044,072 (GRCm39) |
frame shift |
probably null |
|
R2329:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2331:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2332:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2429:Setx
|
UTSW |
2 |
29,069,910 (GRCm39) |
missense |
probably benign |
0.00 |
R2438:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2439:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2496:Setx
|
UTSW |
2 |
29,034,813 (GRCm39) |
missense |
probably benign |
0.11 |
R2858:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2859:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2884:Setx
|
UTSW |
2 |
29,038,637 (GRCm39) |
missense |
probably damaging |
0.98 |
R2885:Setx
|
UTSW |
2 |
29,038,637 (GRCm39) |
missense |
probably damaging |
0.98 |
R2886:Setx
|
UTSW |
2 |
29,038,637 (GRCm39) |
missense |
probably damaging |
0.98 |
R2915:Setx
|
UTSW |
2 |
29,062,336 (GRCm39) |
missense |
probably damaging |
0.99 |
R2921:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R2921:Setx
|
UTSW |
2 |
29,044,072 (GRCm39) |
small deletion |
probably benign |
|
R2923:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R3426:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R3609:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R3610:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R3731:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R3813:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R3835:Setx
|
UTSW |
2 |
29,035,072 (GRCm39) |
missense |
possibly damaging |
0.81 |
R3871:Setx
|
UTSW |
2 |
29,035,753 (GRCm39) |
missense |
probably damaging |
0.98 |
R4013:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R4014:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R4015:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R4017:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R4246:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R4248:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R4297:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R4298:Setx
|
UTSW |
2 |
29,044,073 (GRCm39) |
frame shift |
probably null |
|
R4539:Setx
|
UTSW |
2 |
29,069,760 (GRCm39) |
missense |
probably benign |
0.14 |
R4590:Setx
|
UTSW |
2 |
29,034,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R4632:Setx
|
UTSW |
2 |
29,038,627 (GRCm39) |
missense |
probably benign |
0.23 |
R4782:Setx
|
UTSW |
2 |
29,034,058 (GRCm39) |
missense |
probably damaging |
0.99 |
R4801:Setx
|
UTSW |
2 |
29,036,385 (GRCm39) |
missense |
probably benign |
0.14 |
R4802:Setx
|
UTSW |
2 |
29,036,385 (GRCm39) |
missense |
probably benign |
0.14 |
R4975:Setx
|
UTSW |
2 |
29,054,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R5040:Setx
|
UTSW |
2 |
29,029,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R5133:Setx
|
UTSW |
2 |
29,070,093 (GRCm39) |
missense |
probably benign |
0.02 |
R5208:Setx
|
UTSW |
2 |
29,056,379 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5237:Setx
|
UTSW |
2 |
29,036,995 (GRCm39) |
missense |
probably benign |
0.00 |
R5248:Setx
|
UTSW |
2 |
29,038,430 (GRCm39) |
missense |
probably benign |
0.26 |
R5288:Setx
|
UTSW |
2 |
29,024,045 (GRCm39) |
critical splice donor site |
probably null |
|
R5385:Setx
|
UTSW |
2 |
29,024,045 (GRCm39) |
critical splice donor site |
probably null |
|
R5387:Setx
|
UTSW |
2 |
29,037,606 (GRCm39) |
missense |
probably benign |
0.00 |
R5407:Setx
|
UTSW |
2 |
29,035,486 (GRCm39) |
missense |
probably benign |
0.00 |
R5685:Setx
|
UTSW |
2 |
29,061,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R6110:Setx
|
UTSW |
2 |
29,030,302 (GRCm39) |
missense |
probably damaging |
1.00 |
R6136:Setx
|
UTSW |
2 |
29,038,039 (GRCm39) |
missense |
probably benign |
0.01 |
R6310:Setx
|
UTSW |
2 |
29,066,947 (GRCm39) |
missense |
possibly damaging |
0.57 |
R6328:Setx
|
UTSW |
2 |
29,064,474 (GRCm39) |
intron |
probably benign |
|
R6358:Setx
|
UTSW |
2 |
29,061,360 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6384:Setx
|
UTSW |
2 |
29,063,570 (GRCm39) |
missense |
probably damaging |
1.00 |
R6400:Setx
|
UTSW |
2 |
29,020,286 (GRCm39) |
missense |
probably damaging |
0.97 |
R6572:Setx
|
UTSW |
2 |
29,063,706 (GRCm39) |
missense |
possibly damaging |
0.63 |
R6662:Setx
|
UTSW |
2 |
29,048,126 (GRCm39) |
missense |
probably damaging |
0.97 |
R6898:Setx
|
UTSW |
2 |
29,038,120 (GRCm39) |
missense |
probably benign |
0.00 |
R7188:Setx
|
UTSW |
2 |
29,038,184 (GRCm39) |
missense |
probably benign |
0.02 |
R7332:Setx
|
UTSW |
2 |
29,036,638 (GRCm39) |
missense |
probably benign |
0.00 |
R7357:Setx
|
UTSW |
2 |
29,020,313 (GRCm39) |
missense |
probably benign |
0.01 |
R7556:Setx
|
UTSW |
2 |
29,036,505 (GRCm39) |
missense |
possibly damaging |
0.88 |
R7646:Setx
|
UTSW |
2 |
29,067,561 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7802:Setx
|
UTSW |
2 |
29,037,033 (GRCm39) |
missense |
probably benign |
0.02 |
R7810:Setx
|
UTSW |
2 |
29,038,663 (GRCm39) |
missense |
probably benign |
0.43 |
R7831:Setx
|
UTSW |
2 |
29,069,866 (GRCm39) |
missense |
possibly damaging |
0.75 |
R7831:Setx
|
UTSW |
2 |
29,047,120 (GRCm39) |
missense |
probably damaging |
1.00 |
R7843:Setx
|
UTSW |
2 |
29,063,581 (GRCm39) |
missense |
probably damaging |
1.00 |
R7850:Setx
|
UTSW |
2 |
29,037,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R7858:Setx
|
UTSW |
2 |
29,051,562 (GRCm39) |
missense |
probably damaging |
1.00 |
R8121:Setx
|
UTSW |
2 |
29,035,046 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8284:Setx
|
UTSW |
2 |
29,035,348 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8301:Setx
|
UTSW |
2 |
29,035,702 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8752:Setx
|
UTSW |
2 |
29,048,992 (GRCm39) |
missense |
probably damaging |
0.97 |
R8785:Setx
|
UTSW |
2 |
29,035,275 (GRCm39) |
missense |
probably damaging |
1.00 |
R8871:Setx
|
UTSW |
2 |
29,038,114 (GRCm39) |
missense |
probably benign |
0.11 |
R8927:Setx
|
UTSW |
2 |
29,016,971 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8928:Setx
|
UTSW |
2 |
29,016,971 (GRCm39) |
missense |
possibly damaging |
0.59 |
R9182:Setx
|
UTSW |
2 |
29,061,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R9334:Setx
|
UTSW |
2 |
29,044,032 (GRCm39) |
nonsense |
probably null |
|
R9335:Setx
|
UTSW |
2 |
29,035,963 (GRCm39) |
missense |
probably benign |
0.00 |
R9491:Setx
|
UTSW |
2 |
29,037,835 (GRCm39) |
missense |
probably benign |
0.03 |
R9551:Setx
|
UTSW |
2 |
29,020,244 (GRCm39) |
missense |
possibly damaging |
0.80 |
R9627:Setx
|
UTSW |
2 |
29,034,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R9688:Setx
|
UTSW |
2 |
29,036,328 (GRCm39) |
missense |
probably damaging |
1.00 |
R9689:Setx
|
UTSW |
2 |
29,051,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R9747:Setx
|
UTSW |
2 |
29,064,377 (GRCm39) |
nonsense |
probably null |
|
R9780:Setx
|
UTSW |
2 |
29,016,999 (GRCm39) |
missense |
possibly damaging |
0.88 |
X0066:Setx
|
UTSW |
2 |
29,037,891 (GRCm39) |
nonsense |
probably null |
|
|