Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700028J19Rik |
T |
A |
7: 43,879,974 (GRCm39) |
|
probably benign |
Het |
Abcb5 |
A |
T |
12: 118,896,348 (GRCm39) |
|
probably null |
Het |
Abcg1 |
G |
T |
17: 31,317,260 (GRCm39) |
E191* |
probably null |
Het |
Als2 |
A |
G |
1: 59,218,250 (GRCm39) |
Y1263H |
possibly damaging |
Het |
Amer2 |
T |
A |
14: 60,617,026 (GRCm39) |
L281* |
probably null |
Het |
Anxa6 |
T |
C |
11: 54,887,196 (GRCm39) |
N361D |
probably benign |
Het |
Ap1g1 |
A |
T |
8: 110,564,415 (GRCm39) |
N320I |
probably damaging |
Het |
Aqr |
T |
C |
2: 113,986,746 (GRCm39) |
D208G |
possibly damaging |
Het |
Arnt2 |
T |
C |
7: 83,912,473 (GRCm39) |
T545A |
probably benign |
Het |
Aspm |
G |
A |
1: 139,415,026 (GRCm39) |
V2701I |
probably benign |
Het |
Atad2 |
A |
G |
15: 57,980,194 (GRCm39) |
V106A |
possibly damaging |
Het |
Bbs2 |
A |
C |
8: 94,814,061 (GRCm39) |
F186V |
probably damaging |
Het |
Catsperg2 |
G |
A |
7: 29,400,613 (GRCm39) |
P247L |
probably damaging |
Het |
Cfap57 |
G |
T |
4: 118,426,656 (GRCm39) |
Q1098K |
probably benign |
Het |
Cxcr6 |
A |
G |
9: 123,639,811 (GRCm39) |
T271A |
probably benign |
Het |
Dock1 |
A |
G |
7: 134,374,091 (GRCm39) |
E579G |
probably benign |
Het |
Frem3 |
A |
G |
8: 81,421,932 (GRCm39) |
T2111A |
probably damaging |
Het |
Galnt1 |
A |
T |
18: 24,397,586 (GRCm39) |
D229V |
possibly damaging |
Het |
Gbp2b |
A |
C |
3: 142,313,919 (GRCm39) |
M400L |
probably benign |
Het |
Gm1123 |
T |
A |
9: 98,891,486 (GRCm39) |
|
probably null |
Het |
Gtpbp6 |
T |
C |
5: 110,252,805 (GRCm39) |
H349R |
probably damaging |
Het |
Hyal5 |
A |
G |
6: 24,876,691 (GRCm39) |
K188R |
probably benign |
Het |
Insrr |
T |
C |
3: 87,707,803 (GRCm39) |
|
probably null |
Het |
Kcnn1 |
A |
T |
8: 71,305,374 (GRCm39) |
C322S |
probably damaging |
Het |
Kdelr1 |
GTCTA |
G |
7: 45,531,041 (GRCm39) |
|
probably null |
Het |
Kif23 |
T |
C |
9: 61,852,691 (GRCm39) |
T8A |
probably benign |
Het |
Lrrk2 |
A |
T |
15: 91,687,504 (GRCm39) |
R2198* |
probably null |
Het |
Mcl1 |
T |
G |
3: 95,567,109 (GRCm39) |
D177E |
possibly damaging |
Het |
Mrps11 |
A |
T |
7: 78,441,628 (GRCm39) |
T137S |
probably benign |
Het |
Mtbp |
A |
G |
15: 55,426,168 (GRCm39) |
Y90C |
probably damaging |
Het |
Nkpd1 |
C |
T |
7: 19,257,498 (GRCm39) |
Q276* |
probably null |
Het |
Nxt1 |
G |
T |
2: 148,517,673 (GRCm39) |
W138L |
possibly damaging |
Het |
Or5al1 |
T |
C |
2: 85,990,139 (GRCm39) |
T192A |
probably damaging |
Het |
Or5h17 |
T |
A |
16: 58,820,709 (GRCm39) |
F220L |
probably benign |
Het |
Or5t17 |
T |
A |
2: 86,832,621 (GRCm39) |
S103T |
probably benign |
Het |
Osbpl7 |
C |
A |
11: 96,951,103 (GRCm39) |
P478H |
probably damaging |
Het |
Phf8-ps |
T |
A |
17: 33,285,746 (GRCm39) |
H352L |
probably benign |
Het |
Pitpna |
T |
A |
11: 75,511,095 (GRCm39) |
F222I |
probably damaging |
Het |
Plekhh2 |
A |
T |
17: 84,877,310 (GRCm39) |
R552W |
probably damaging |
Het |
Plxnb2 |
C |
T |
15: 89,051,235 (GRCm39) |
R328H |
probably damaging |
Het |
Pmaip1 |
C |
T |
18: 66,594,055 (GRCm39) |
T65I |
probably benign |
Het |
Ppil4 |
T |
G |
10: 7,674,186 (GRCm39) |
I110S |
probably damaging |
Het |
Prpf38a |
A |
G |
4: 108,427,351 (GRCm39) |
|
probably null |
Het |
Psme4 |
G |
A |
11: 30,759,837 (GRCm39) |
G320D |
probably damaging |
Het |
Rab17 |
C |
A |
1: 90,886,679 (GRCm39) |
R191L |
probably benign |
Het |
Rhag |
A |
T |
17: 41,142,222 (GRCm39) |
M222L |
possibly damaging |
Het |
Rims2 |
A |
T |
15: 39,300,602 (GRCm39) |
H111L |
possibly damaging |
Het |
Slc2a8 |
T |
C |
2: 32,871,801 (GRCm39) |
I51V |
possibly damaging |
Het |
Slc34a1 |
T |
C |
13: 55,549,085 (GRCm39) |
|
probably null |
Het |
Slf1 |
T |
C |
13: 77,231,598 (GRCm39) |
T594A |
possibly damaging |
Het |
Sox6 |
A |
T |
7: 115,178,392 (GRCm39) |
|
probably null |
Het |
Spata13 |
C |
T |
14: 60,928,652 (GRCm39) |
S70L |
probably benign |
Het |
Stard13 |
A |
G |
5: 150,986,592 (GRCm39) |
I188T |
possibly damaging |
Het |
Stard9 |
A |
G |
2: 120,535,803 (GRCm39) |
D4020G |
probably damaging |
Het |
Tdp1 |
A |
G |
12: 99,868,611 (GRCm39) |
K255R |
possibly damaging |
Het |
Tns2 |
G |
T |
15: 102,015,538 (GRCm39) |
A124S |
probably benign |
Het |
Top2b |
T |
A |
14: 16,413,666 (GRCm38) |
W1045R |
probably damaging |
Het |
Trav12-2 |
T |
C |
14: 53,854,122 (GRCm39) |
V32A |
probably damaging |
Het |
Vps13c |
G |
T |
9: 67,870,455 (GRCm39) |
R3198L |
possibly damaging |
Het |
Wee1 |
TCCCC |
TCCC |
7: 109,723,776 (GRCm39) |
|
probably null |
Het |
Zfp52 |
T |
A |
17: 21,782,013 (GRCm39) |
S620R |
probably benign |
Het |
Zfp62 |
T |
A |
11: 49,107,044 (GRCm39) |
C378* |
probably null |
Het |
Zfp638 |
C |
A |
6: 83,906,969 (GRCm39) |
P378H |
probably 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 |
|
IGL02388:Setx
|
APN |
2 |
29,063,665 (GRCm39) |
missense |
probably damaging |
1.00 |
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 |
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 |
|
|