Other mutations in this stock |
Total: 68 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb6 |
T |
C |
1: 75,151,479 (GRCm39) |
|
probably null |
Het |
Abcc9 |
G |
A |
6: 142,571,371 (GRCm39) |
|
probably benign |
Het |
Acss2 |
T |
C |
2: 155,416,575 (GRCm39) |
|
probably benign |
Het |
Atp8b4 |
G |
A |
2: 126,217,725 (GRCm39) |
T597I |
probably damaging |
Het |
Btaf1 |
A |
T |
19: 36,961,015 (GRCm39) |
N796I |
probably benign |
Het |
Caskin2 |
T |
C |
11: 115,690,905 (GRCm39) |
|
probably null |
Het |
Cdhr2 |
A |
G |
13: 54,884,349 (GRCm39) |
N1295D |
probably benign |
Het |
Cog3 |
G |
A |
14: 75,962,239 (GRCm39) |
T534M |
probably benign |
Het |
Cpne1 |
A |
G |
2: 155,919,561 (GRCm39) |
S303P |
probably damaging |
Het |
Cs |
G |
A |
10: 128,187,086 (GRCm39) |
G74S |
possibly damaging |
Het |
Cyb5r4 |
G |
T |
9: 86,929,533 (GRCm39) |
S229I |
probably damaging |
Het |
Ddr1 |
C |
T |
17: 35,997,400 (GRCm39) |
A531T |
probably benign |
Het |
Ect2l |
C |
T |
10: 18,018,810 (GRCm39) |
V529M |
probably damaging |
Het |
Edaradd |
C |
A |
13: 12,493,161 (GRCm39) |
R177L |
possibly damaging |
Het |
Esf1 |
T |
C |
2: 140,006,148 (GRCm39) |
D333G |
possibly damaging |
Het |
Fam8a1 |
T |
A |
13: 46,827,814 (GRCm39) |
L334H |
probably damaging |
Het |
Fbxl18 |
A |
G |
5: 142,871,558 (GRCm39) |
I559T |
probably damaging |
Het |
Fcrl2 |
A |
C |
3: 87,164,851 (GRCm39) |
V225G |
probably benign |
Het |
Ido1 |
C |
T |
8: 25,077,819 (GRCm39) |
V83M |
probably damaging |
Het |
Iffo1 |
T |
G |
6: 125,130,030 (GRCm39) |
C419G |
probably damaging |
Het |
Igfals |
A |
T |
17: 25,100,439 (GRCm39) |
Y510F |
probably benign |
Het |
Ipo9 |
A |
T |
1: 135,313,210 (GRCm39) |
Y1006* |
probably null |
Het |
Itgb4 |
C |
T |
11: 115,874,983 (GRCm39) |
R447W |
probably benign |
Het |
Jmjd1c |
T |
A |
10: 67,065,785 (GRCm39) |
S1737T |
probably benign |
Het |
Klhl32 |
C |
T |
4: 24,800,805 (GRCm39) |
|
probably null |
Het |
Klk1b11 |
T |
A |
7: 43,427,810 (GRCm39) |
C173S |
probably damaging |
Het |
Klk1b24 |
A |
T |
7: 43,840,889 (GRCm39) |
M106L |
probably benign |
Het |
Lamp1 |
G |
A |
8: 13,221,388 (GRCm39) |
|
probably null |
Het |
Mapk4 |
A |
T |
18: 74,103,365 (GRCm39) |
V48E |
probably damaging |
Het |
Marchf6 |
A |
T |
15: 31,486,082 (GRCm39) |
D395E |
probably damaging |
Het |
Mdp1 |
A |
G |
14: 55,896,465 (GRCm39) |
F157S |
probably damaging |
Het |
Mettl21e |
A |
T |
1: 44,250,255 (GRCm39) |
F50L |
probably damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,077,153 (GRCm39) |
I35T |
probably benign |
Het |
Natd1 |
T |
C |
11: 60,796,892 (GRCm39) |
Y91C |
probably damaging |
Het |
Nbas |
T |
A |
12: 13,633,476 (GRCm39) |
Y2294N |
probably damaging |
Het |
Nrcam |
A |
G |
12: 44,610,841 (GRCm39) |
T520A |
probably benign |
Het |
Nrf1 |
A |
G |
6: 30,117,061 (GRCm39) |
T324A |
probably benign |
Het |
Or10a2 |
G |
A |
7: 106,673,394 (GRCm39) |
A120T |
probably damaging |
Het |
Or4k51 |
T |
A |
2: 111,585,326 (GRCm39) |
I244N |
probably damaging |
Het |
Or52a5 |
A |
C |
7: 103,427,182 (GRCm39) |
D123E |
probably damaging |
Het |
Or5m11b |
A |
G |
2: 85,806,500 (GRCm39) |
I304M |
probably benign |
Het |
Pam |
C |
T |
1: 97,792,123 (GRCm39) |
V433I |
probably benign |
Het |
Pck1 |
T |
A |
2: 173,000,353 (GRCm39) |
Y595N |
probably damaging |
Het |
Per2 |
C |
T |
1: 91,373,223 (GRCm39) |
|
probably null |
Het |
Piezo2 |
G |
C |
18: 63,278,162 (GRCm39) |
F247L |
possibly damaging |
Het |
Pkdcc |
A |
G |
17: 83,523,337 (GRCm39) |
Y148C |
probably damaging |
Het |
Plod2 |
A |
G |
9: 92,475,876 (GRCm39) |
T320A |
probably benign |
Het |
Ppip5k1 |
G |
A |
2: 121,147,157 (GRCm39) |
R1155C |
probably benign |
Het |
Ppp1r15b |
C |
T |
1: 133,059,382 (GRCm39) |
|
probably benign |
Het |
Prkn |
C |
T |
17: 11,456,536 (GRCm39) |
A119V |
probably damaging |
Het |
Ptprz1 |
G |
T |
6: 22,986,133 (GRCm39) |
C311F |
probably damaging |
Het |
Rab11fip3 |
A |
T |
17: 26,235,038 (GRCm39) |
V44E |
probably damaging |
Het |
Rpl5 |
T |
A |
5: 108,051,514 (GRCm39) |
|
probably benign |
Het |
Sdk1 |
A |
G |
5: 141,921,853 (GRCm39) |
N283S |
probably damaging |
Het |
Shank3 |
T |
A |
15: 89,405,529 (GRCm39) |
N418K |
probably benign |
Het |
Shmt2 |
T |
C |
10: 127,353,668 (GRCm39) |
D499G |
probably benign |
Het |
Slc25a46 |
A |
G |
18: 31,716,293 (GRCm39) |
L403S |
probably damaging |
Het |
Slc5a1 |
A |
G |
5: 33,303,955 (GRCm39) |
T257A |
probably benign |
Het |
Snrnp35 |
T |
C |
5: 124,628,535 (GRCm39) |
V116A |
probably benign |
Het |
Spag9 |
T |
A |
11: 93,981,538 (GRCm39) |
F593I |
probably damaging |
Het |
Tmem171 |
C |
A |
13: 98,828,574 (GRCm39) |
R192L |
probably benign |
Het |
Trappc3l |
T |
A |
10: 33,978,703 (GRCm39) |
L169Q |
unknown |
Het |
Ube2s |
T |
C |
7: 4,811,431 (GRCm39) |
E148G |
probably damaging |
Het |
Uspl1 |
T |
C |
5: 149,146,521 (GRCm39) |
F424S |
probably damaging |
Het |
Vmn1r2 |
T |
C |
4: 3,172,261 (GRCm39) |
V60A |
probably benign |
Het |
Wdfy4 |
T |
C |
14: 32,829,575 (GRCm39) |
|
probably null |
Het |
Zfp735 |
C |
T |
11: 73,602,964 (GRCm39) |
S636L |
possibly damaging |
Het |
Zswim9 |
G |
A |
7: 12,995,094 (GRCm39) |
S354F |
probably 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 |
R4674:Rttn
|
UTSW |
18 |
89,029,135 (GRCm39) |
splice site |
probably null |
|
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 |
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 |
|
|