Other mutations in this stock |
Total: 84 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
T |
C |
5: 8,860,615 (GRCm39) |
I112T |
probably benign |
Het |
Acvr1b |
T |
C |
15: 101,100,939 (GRCm39) |
I367T |
possibly damaging |
Het |
Akr1b8 |
G |
A |
6: 34,333,359 (GRCm39) |
|
probably null |
Het |
Ash1l |
T |
C |
3: 88,979,783 (GRCm39) |
V2769A |
possibly damaging |
Het |
Asxl3 |
A |
T |
18: 22,650,795 (GRCm39) |
D928V |
probably damaging |
Het |
Atp1a4 |
A |
T |
1: 172,085,223 (GRCm39) |
V66E |
possibly damaging |
Het |
Cald1 |
AAGAGAGAGAGAGAG |
AAGAGAGAGAGAG |
6: 34,723,108 (GRCm39) |
|
probably null |
Het |
Cbx2 |
T |
A |
11: 118,919,935 (GRCm39) |
I500N |
probably damaging |
Het |
Ccdc82 |
A |
T |
9: 13,252,260 (GRCm39) |
H184L |
probably benign |
Het |
Cd84 |
A |
T |
1: 171,700,887 (GRCm39) |
H216L |
possibly damaging |
Het |
Ceacam15 |
T |
C |
7: 16,407,410 (GRCm39) |
T36A |
probably benign |
Het |
Cebpd |
A |
G |
16: 15,705,385 (GRCm39) |
D66G |
probably damaging |
Het |
Clec1b |
C |
A |
6: 129,377,097 (GRCm39) |
L47I |
probably damaging |
Het |
Cracr2b |
A |
G |
7: 141,043,451 (GRCm39) |
D43G |
probably damaging |
Het |
Crbn |
T |
A |
6: 106,767,932 (GRCm39) |
Q173L |
possibly damaging |
Het |
Cspg4 |
T |
C |
9: 56,805,489 (GRCm39) |
V2100A |
probably damaging |
Het |
Cyp46a1 |
T |
C |
12: 108,324,345 (GRCm39) |
L374P |
probably damaging |
Het |
Dhx16 |
T |
A |
17: 36,196,831 (GRCm39) |
V607E |
probably damaging |
Het |
Dido1 |
A |
G |
2: 180,329,352 (GRCm39) |
S357P |
probably damaging |
Het |
Dnah6 |
T |
A |
6: 73,169,405 (GRCm39) |
I399F |
probably benign |
Het |
Dock10 |
T |
C |
1: 80,584,337 (GRCm39) |
E123G |
possibly damaging |
Het |
Dstyk |
A |
G |
1: 132,391,128 (GRCm39) |
D843G |
probably benign |
Het |
Efcab12 |
C |
A |
6: 115,800,610 (GRCm39) |
V138F |
probably damaging |
Het |
Egf |
A |
G |
3: 129,511,689 (GRCm39) |
F493L |
probably damaging |
Het |
Ephx1 |
A |
G |
1: 180,822,256 (GRCm39) |
F220S |
probably damaging |
Het |
Exoc6 |
T |
C |
19: 37,597,530 (GRCm39) |
F644L |
probably damaging |
Het |
F13b |
A |
G |
1: 139,429,542 (GRCm39) |
Y20C |
unknown |
Het |
Fam184b |
T |
A |
5: 45,740,230 (GRCm39) |
K319* |
probably null |
Het |
Flrt2 |
T |
A |
12: 95,747,462 (GRCm39) |
L600* |
probably null |
Het |
Gbgt1 |
T |
C |
2: 28,388,453 (GRCm39) |
F46S |
possibly damaging |
Het |
Gli2 |
T |
C |
1: 118,763,759 (GRCm39) |
E1464G |
probably damaging |
Het |
Hdac9 |
A |
G |
12: 34,423,959 (GRCm39) |
V501A |
possibly damaging |
Het |
Heca |
T |
C |
10: 17,791,057 (GRCm39) |
H333R |
probably benign |
Het |
Hirip3 |
G |
A |
7: 126,463,834 (GRCm39) |
|
probably null |
Het |
Igsf8 |
G |
A |
1: 172,146,479 (GRCm39) |
W51* |
probably null |
Het |
Kif21a |
C |
A |
15: 90,824,748 (GRCm39) |
R1342L |
possibly damaging |
Het |
Krt73 |
T |
C |
15: 101,710,510 (GRCm39) |
N75D |
probably benign |
Het |
Macf1 |
T |
A |
4: 123,366,190 (GRCm39) |
Y1292F |
probably benign |
Het |
Macroh2a1 |
A |
C |
13: 56,230,997 (GRCm39) |
C297G |
possibly damaging |
Het |
Mapk14 |
A |
G |
17: 28,963,996 (GRCm39) |
|
probably null |
Het |
Mgat5 |
T |
A |
1: 127,318,495 (GRCm39) |
V330D |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,239,257 (GRCm39) |
|
probably null |
Het |
Naip1 |
A |
T |
13: 100,580,682 (GRCm39) |
F188L |
probably damaging |
Het |
Ncoa3 |
T |
C |
2: 165,901,731 (GRCm39) |
S1035P |
probably benign |
Het |
Ndn |
T |
A |
7: 61,998,570 (GRCm39) |
W139R |
probably damaging |
Het |
Nes |
T |
C |
3: 87,879,102 (GRCm39) |
V198A |
possibly damaging |
Het |
Or4c107 |
G |
T |
2: 88,789,216 (GRCm39) |
M135I |
probably damaging |
Het |
Or4c35 |
A |
G |
2: 89,808,250 (GRCm39) |
I43V |
possibly damaging |
Het |
Or51ab3 |
T |
G |
7: 103,201,183 (GRCm39) |
L64V |
probably damaging |
Het |
Or52p1 |
T |
A |
7: 104,267,631 (GRCm39) |
C248* |
probably null |
Het |
Or5b111 |
T |
A |
19: 13,291,178 (GRCm39) |
H157L |
probably benign |
Het |
Or5p72 |
T |
C |
7: 108,022,309 (GRCm39) |
V177A |
possibly damaging |
Het |
Pcf11 |
G |
A |
7: 92,308,985 (GRCm39) |
|
probably benign |
Het |
Pde1a |
TCC |
TC |
2: 79,728,525 (GRCm39) |
|
probably benign |
Het |
Pipox |
T |
G |
11: 77,784,596 (GRCm39) |
Q4P |
probably benign |
Het |
Pla2g4c |
C |
T |
7: 13,077,439 (GRCm39) |
T327I |
probably null |
Het |
Plppr1 |
C |
T |
4: 49,323,384 (GRCm39) |
R225W |
probably damaging |
Het |
Pnpla6 |
T |
A |
8: 3,571,412 (GRCm39) |
V145D |
probably damaging |
Het |
Pnpla7 |
T |
C |
2: 24,942,329 (GRCm39) |
Y83H |
probably damaging |
Het |
Rif1 |
T |
A |
2: 51,996,954 (GRCm39) |
L970Q |
probably null |
Het |
Rimklb |
C |
A |
6: 122,433,242 (GRCm39) |
E303* |
probably null |
Het |
Rpl13a |
A |
T |
7: 44,776,242 (GRCm39) |
|
probably benign |
Het |
Sf3b3 |
G |
A |
8: 111,571,137 (GRCm39) |
R10W |
probably damaging |
Het |
Skint4 |
G |
A |
4: 111,975,430 (GRCm39) |
C130Y |
probably damaging |
Het |
Snap91 |
A |
G |
9: 86,674,070 (GRCm39) |
S593P |
possibly damaging |
Het |
Ssb |
A |
G |
2: 69,699,194 (GRCm39) |
Q209R |
probably benign |
Het |
Stap1 |
A |
T |
5: 86,229,044 (GRCm39) |
I71L |
probably benign |
Het |
Syna |
C |
A |
5: 134,587,209 (GRCm39) |
R580L |
probably damaging |
Het |
Tacc2 |
T |
A |
7: 130,226,591 (GRCm39) |
M1111K |
possibly damaging |
Het |
Tanc2 |
T |
C |
11: 105,758,306 (GRCm39) |
L689P |
probably damaging |
Het |
Tasor2 |
T |
C |
13: 3,623,686 (GRCm39) |
E1406G |
possibly damaging |
Het |
Tcstv7b |
T |
C |
13: 120,702,362 (GRCm39) |
W53R |
probably damaging |
Het |
Tdrd5 |
A |
C |
1: 156,105,005 (GRCm39) |
C463W |
probably damaging |
Het |
Tet1 |
A |
G |
10: 62,674,627 (GRCm39) |
F1150L |
probably damaging |
Het |
Tia1 |
T |
A |
6: 86,397,382 (GRCm39) |
F118L |
probably damaging |
Het |
Trav3-1 |
A |
T |
14: 52,818,460 (GRCm39) |
T45S |
possibly damaging |
Het |
Uaca |
A |
T |
9: 60,761,711 (GRCm39) |
Y235F |
possibly damaging |
Het |
Ube4b |
T |
C |
4: 149,415,827 (GRCm39) |
N44S |
possibly damaging |
Het |
Vmn2r93 |
T |
A |
17: 18,525,255 (GRCm39) |
H304Q |
probably benign |
Het |
Wdr18 |
A |
G |
10: 79,801,069 (GRCm39) |
I161V |
probably benign |
Het |
Zfp112 |
A |
G |
7: 23,826,399 (GRCm39) |
H789R |
probably damaging |
Het |
Zfp873 |
A |
G |
10: 81,895,814 (GRCm39) |
T182A |
possibly damaging |
Het |
Zscan2 |
T |
A |
7: 80,525,150 (GRCm39) |
S290R |
probably damaging |
Het |
Zup1 |
A |
T |
10: 33,824,980 (GRCm39) |
D167E |
possibly damaging |
Het |
|
Other mutations in Rttn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00595:Rttn
|
APN |
18 |
88,992,464 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00788:Rttn
|
APN |
18 |
88,990,633 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00929:Rttn
|
APN |
18 |
89,047,059 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01392:Rttn
|
APN |
18 |
89,013,737 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01395:Rttn
|
APN |
18 |
89,147,894 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01701:Rttn
|
APN |
18 |
89,082,339 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02136:Rttn
|
APN |
18 |
89,064,252 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL02151:Rttn
|
APN |
18 |
89,038,329 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02165:Rttn
|
APN |
18 |
89,061,165 (GRCm39) |
missense |
probably benign |
|
IGL02228:Rttn
|
APN |
18 |
89,060,355 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02276:Rttn
|
APN |
18 |
89,066,578 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02612:Rttn
|
APN |
18 |
88,991,750 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02645:Rttn
|
APN |
18 |
89,128,810 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02716:Rttn
|
APN |
18 |
89,066,541 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02820:Rttn
|
APN |
18 |
89,047,122 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02961:Rttn
|
APN |
18 |
89,071,697 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02973:Rttn
|
APN |
18 |
88,990,618 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Rttn
|
APN |
18 |
88,997,814 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03082:Rttn
|
APN |
18 |
89,002,072 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03121:Rttn
|
APN |
18 |
88,993,875 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03135:Rttn
|
APN |
18 |
89,033,274 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03328:Rttn
|
APN |
18 |
89,061,152 (GRCm39) |
missense |
probably benign |
0.19 |
Fascisti
|
UTSW |
18 |
89,027,584 (GRCm39) |
splice site |
probably benign |
|
marcher
|
UTSW |
18 |
89,056,070 (GRCm39) |
missense |
probably damaging |
0.99 |
militaristi
|
UTSW |
18 |
89,029,040 (GRCm39) |
missense |
probably damaging |
1.00 |
Thoughtless
|
UTSW |
18 |
89,032,735 (GRCm39) |
missense |
probably damaging |
1.00 |
twister
|
UTSW |
18 |
89,064,286 (GRCm39) |
critical splice donor site |
probably null |
|
Vermiculus
|
UTSW |
18 |
89,108,557 (GRCm39) |
missense |
probably benign |
|
R0062:Rttn
|
UTSW |
18 |
89,029,090 (GRCm39) |
critical splice donor site |
probably null |
|
R0062:Rttn
|
UTSW |
18 |
89,029,090 (GRCm39) |
critical splice donor site |
probably null |
|
R0310:Rttn
|
UTSW |
18 |
89,027,584 (GRCm39) |
splice site |
probably benign |
|
R0330:Rttn
|
UTSW |
18 |
89,004,204 (GRCm39) |
splice site |
probably null |
|
R0363:Rttn
|
UTSW |
18 |
89,029,079 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Rttn
|
UTSW |
18 |
89,108,543 (GRCm39) |
splice site |
probably benign |
|
R0590:Rttn
|
UTSW |
18 |
88,997,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R0601:Rttn
|
UTSW |
18 |
89,061,090 (GRCm39) |
missense |
probably benign |
0.00 |
R0604:Rttn
|
UTSW |
18 |
88,995,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R0631:Rttn
|
UTSW |
18 |
89,007,670 (GRCm39) |
missense |
probably benign |
0.00 |
R0882:Rttn
|
UTSW |
18 |
88,991,813 (GRCm39) |
nonsense |
probably null |
|
R0885:Rttn
|
UTSW |
18 |
89,001,934 (GRCm39) |
missense |
probably benign |
0.03 |
R0900:Rttn
|
UTSW |
18 |
89,119,815 (GRCm39) |
missense |
probably benign |
0.13 |
R1077:Rttn
|
UTSW |
18 |
89,082,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R1444:Rttn
|
UTSW |
18 |
89,060,991 (GRCm39) |
missense |
probably benign |
0.04 |
R1460:Rttn
|
UTSW |
18 |
89,127,481 (GRCm39) |
splice site |
probably benign |
|
R1517:Rttn
|
UTSW |
18 |
89,131,474 (GRCm39) |
missense |
probably benign |
0.01 |
R1630:Rttn
|
UTSW |
18 |
89,061,078 (GRCm39) |
missense |
probably benign |
0.02 |
R1632:Rttn
|
UTSW |
18 |
89,027,460 (GRCm39) |
missense |
probably benign |
0.18 |
R1722:Rttn
|
UTSW |
18 |
88,991,655 (GRCm39) |
missense |
probably benign |
0.34 |
R1755:Rttn
|
UTSW |
18 |
89,027,441 (GRCm39) |
missense |
probably damaging |
1.00 |
R1881:Rttn
|
UTSW |
18 |
89,033,336 (GRCm39) |
missense |
probably damaging |
0.96 |
R1971:Rttn
|
UTSW |
18 |
89,108,557 (GRCm39) |
missense |
probably benign |
|
R2035:Rttn
|
UTSW |
18 |
89,038,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R2109:Rttn
|
UTSW |
18 |
89,004,197 (GRCm39) |
missense |
possibly damaging |
0.93 |
R2191:Rttn
|
UTSW |
18 |
89,113,772 (GRCm39) |
critical splice donor site |
probably null |
|
R2201:Rttn
|
UTSW |
18 |
89,029,067 (GRCm39) |
missense |
possibly damaging |
0.88 |
R2266:Rttn
|
UTSW |
18 |
89,082,295 (GRCm39) |
missense |
probably benign |
0.05 |
R3014:Rttn
|
UTSW |
18 |
89,032,744 (GRCm39) |
missense |
probably damaging |
1.00 |
R3052:Rttn
|
UTSW |
18 |
89,033,370 (GRCm39) |
splice site |
probably benign |
|
R3427:Rttn
|
UTSW |
18 |
89,113,775 (GRCm39) |
splice site |
probably null |
|
R3431:Rttn
|
UTSW |
18 |
89,113,695 (GRCm39) |
missense |
probably benign |
0.04 |
R3786:Rttn
|
UTSW |
18 |
89,056,018 (GRCm39) |
missense |
probably benign |
0.00 |
R3803:Rttn
|
UTSW |
18 |
88,995,831 (GRCm39) |
missense |
probably damaging |
0.96 |
R3980:Rttn
|
UTSW |
18 |
89,035,399 (GRCm39) |
missense |
probably benign |
0.12 |
R4035:Rttn
|
UTSW |
18 |
89,013,777 (GRCm39) |
missense |
probably benign |
0.03 |
R4170:Rttn
|
UTSW |
18 |
88,993,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R4223:Rttn
|
UTSW |
18 |
89,113,708 (GRCm39) |
missense |
probably damaging |
1.00 |
R4273:Rttn
|
UTSW |
18 |
89,110,020 (GRCm39) |
missense |
probably benign |
|
R4517:Rttn
|
UTSW |
18 |
89,047,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R4837:Rttn
|
UTSW |
18 |
89,108,539 (GRCm39) |
splice site |
probably null |
|
R4869:Rttn
|
UTSW |
18 |
89,061,138 (GRCm39) |
nonsense |
probably null |
|
R4881:Rttn
|
UTSW |
18 |
89,119,809 (GRCm39) |
missense |
probably damaging |
1.00 |
R4959:Rttn
|
UTSW |
18 |
89,060,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R4973:Rttn
|
UTSW |
18 |
89,060,292 (GRCm39) |
missense |
probably damaging |
1.00 |
R4975:Rttn
|
UTSW |
18 |
89,082,209 (GRCm39) |
splice site |
probably null |
|
R5166:Rttn
|
UTSW |
18 |
89,031,218 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5243:Rttn
|
UTSW |
18 |
89,126,187 (GRCm39) |
missense |
possibly damaging |
0.74 |
R5594:Rttn
|
UTSW |
18 |
89,108,560 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5654:Rttn
|
UTSW |
18 |
89,066,556 (GRCm39) |
missense |
probably benign |
|
R5794:Rttn
|
UTSW |
18 |
89,013,693 (GRCm39) |
missense |
probably benign |
0.18 |
R5799:Rttn
|
UTSW |
18 |
89,056,070 (GRCm39) |
missense |
probably damaging |
0.99 |
R5955:Rttn
|
UTSW |
18 |
89,139,133 (GRCm39) |
missense |
probably damaging |
0.99 |
R5963:Rttn
|
UTSW |
18 |
89,091,819 (GRCm39) |
missense |
probably benign |
0.01 |
R5989:Rttn
|
UTSW |
18 |
88,991,750 (GRCm39) |
missense |
probably damaging |
1.00 |
R6004:Rttn
|
UTSW |
18 |
89,039,816 (GRCm39) |
missense |
probably damaging |
0.96 |
R6132:Rttn
|
UTSW |
18 |
89,133,770 (GRCm39) |
critical splice donor site |
probably null |
|
R6430:Rttn
|
UTSW |
18 |
89,039,809 (GRCm39) |
missense |
probably null |
0.18 |
R6436:Rttn
|
UTSW |
18 |
89,128,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R6681:Rttn
|
UTSW |
18 |
89,032,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R6994:Rttn
|
UTSW |
18 |
89,047,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R7049:Rttn
|
UTSW |
18 |
89,082,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R7078:Rttn
|
UTSW |
18 |
89,027,546 (GRCm39) |
missense |
probably benign |
0.03 |
R7083:Rttn
|
UTSW |
18 |
89,108,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R7250:Rttn
|
UTSW |
18 |
89,007,647 (GRCm39) |
missense |
probably benign |
0.03 |
R7402:Rttn
|
UTSW |
18 |
89,004,035 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7565:Rttn
|
UTSW |
18 |
89,078,603 (GRCm39) |
missense |
probably damaging |
1.00 |
R7588:Rttn
|
UTSW |
18 |
89,082,353 (GRCm39) |
missense |
probably damaging |
0.97 |
R8029:Rttn
|
UTSW |
18 |
89,108,598 (GRCm39) |
missense |
not run |
|
R8085:Rttn
|
UTSW |
18 |
89,071,672 (GRCm39) |
nonsense |
probably null |
|
R8113:Rttn
|
UTSW |
18 |
89,029,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R8355:Rttn
|
UTSW |
18 |
89,047,016 (GRCm39) |
missense |
probably benign |
0.05 |
R8531:Rttn
|
UTSW |
18 |
89,131,467 (GRCm39) |
missense |
probably benign |
0.00 |
R8992:Rttn
|
UTSW |
18 |
88,995,832 (GRCm39) |
missense |
probably benign |
0.24 |
R9008:Rttn
|
UTSW |
18 |
89,027,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R9139:Rttn
|
UTSW |
18 |
89,038,261 (GRCm39) |
missense |
probably benign |
0.30 |
R9210:Rttn
|
UTSW |
18 |
89,064,286 (GRCm39) |
critical splice donor site |
probably null |
|
R9212:Rttn
|
UTSW |
18 |
89,064,286 (GRCm39) |
critical splice donor site |
probably null |
|
R9286:Rttn
|
UTSW |
18 |
88,995,849 (GRCm39) |
missense |
probably benign |
0.06 |
R9368:Rttn
|
UTSW |
18 |
89,078,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R9632:Rttn
|
UTSW |
18 |
89,035,334 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9710:Rttn
|
UTSW |
18 |
89,035,334 (GRCm39) |
missense |
possibly damaging |
0.82 |
X0017:Rttn
|
UTSW |
18 |
89,131,526 (GRCm39) |
missense |
probably benign |
0.01 |
X0022:Rttn
|
UTSW |
18 |
88,991,791 (GRCm39) |
nonsense |
probably null |
|
|