Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adcy7 |
T |
C |
8: 89,048,431 (GRCm39) |
S625P |
probably damaging |
Het |
Agpat1 |
T |
C |
17: 34,830,586 (GRCm39) |
V170A |
probably damaging |
Het |
Alg9 |
C |
T |
9: 50,720,080 (GRCm39) |
Q519* |
probably null |
Het |
Apol8 |
C |
T |
15: 77,634,336 (GRCm39) |
R80H |
probably benign |
Het |
Arhgap25 |
G |
T |
6: 87,465,287 (GRCm39) |
S118* |
probably null |
Het |
Arhgap30 |
T |
A |
1: 171,225,086 (GRCm39) |
Y47* |
probably null |
Het |
Arhgap42 |
C |
T |
9: 9,011,434 (GRCm39) |
D451N |
probably damaging |
Het |
Cabp2 |
T |
A |
19: 4,135,582 (GRCm39) |
F91I |
probably damaging |
Het |
Ccdc30 |
T |
C |
4: 119,230,943 (GRCm39) |
E108G |
probably benign |
Het |
Cfap99 |
T |
C |
5: 34,458,763 (GRCm39) |
S53P |
probably damaging |
Het |
Clec5a |
C |
T |
6: 40,556,361 (GRCm39) |
R135H |
possibly damaging |
Het |
Cops8 |
T |
G |
1: 90,531,325 (GRCm39) |
D18E |
probably benign |
Het |
Cped1 |
A |
T |
6: 22,233,480 (GRCm39) |
M779L |
possibly damaging |
Het |
Cyp4x1 |
G |
A |
4: 114,967,263 (GRCm39) |
H438Y |
probably damaging |
Het |
Disc1 |
A |
T |
8: 125,815,014 (GRCm39) |
T293S |
probably benign |
Het |
Ercc1 |
T |
C |
7: 19,084,102 (GRCm39) |
L113S |
probably damaging |
Het |
Ermp1 |
G |
T |
19: 29,593,196 (GRCm39) |
N765K |
probably benign |
Het |
Fam83c |
A |
G |
2: 155,676,740 (GRCm39) |
I10T |
probably benign |
Het |
Farp1 |
T |
C |
14: 121,513,008 (GRCm39) |
V788A |
probably benign |
Het |
Fbn1 |
C |
G |
2: 125,319,489 (GRCm39) |
G92R |
probably damaging |
Het |
Fsd1 |
T |
A |
17: 56,302,881 (GRCm39) |
M328K |
probably benign |
Het |
Fzd3 |
C |
A |
14: 65,440,262 (GRCm39) |
S636I |
probably benign |
Het |
Gapvd1 |
A |
G |
2: 34,594,330 (GRCm39) |
S886P |
probably damaging |
Het |
Gatad2b |
T |
A |
3: 90,249,029 (GRCm39) |
D22E |
probably benign |
Het |
Gm7168 |
A |
T |
17: 14,169,238 (GRCm39) |
K202* |
probably null |
Het |
Gmps |
T |
C |
3: 63,887,690 (GRCm39) |
I54T |
probably damaging |
Het |
Gp6 |
A |
G |
7: 4,397,114 (GRCm39) |
I107T |
probably benign |
Het |
Gpat2 |
T |
C |
2: 127,273,267 (GRCm39) |
V217A |
possibly damaging |
Het |
Hdlbp |
T |
A |
1: 93,344,917 (GRCm39) |
I863F |
probably damaging |
Het |
Hmcn1 |
A |
C |
1: 150,624,841 (GRCm39) |
I1021M |
possibly damaging |
Het |
Igkv6-14 |
C |
T |
6: 70,412,087 (GRCm39) |
A66T |
probably benign |
Het |
Ippk |
C |
T |
13: 49,599,818 (GRCm39) |
P226S |
|
Het |
Iqch |
A |
G |
9: 63,361,855 (GRCm39) |
I925T |
probably benign |
Het |
Kcnt1 |
A |
G |
2: 25,791,223 (GRCm39) |
E522G |
possibly damaging |
Het |
Kremen2 |
C |
G |
17: 23,962,776 (GRCm39) |
E103D |
probably damaging |
Het |
Lig4 |
G |
T |
8: 10,023,485 (GRCm39) |
N98K |
probably benign |
Het |
Lrrc3b |
T |
G |
14: 15,358,232 (GRCm38) |
I125L |
probably benign |
Het |
Lrrc4 |
T |
C |
6: 28,829,902 (GRCm39) |
D148G |
probably damaging |
Het |
Lrsam1 |
A |
G |
2: 32,837,901 (GRCm39) |
Y218H |
possibly damaging |
Het |
Mmrn2 |
G |
A |
14: 34,119,593 (GRCm39) |
V191I |
probably benign |
Het |
Nadk |
T |
A |
4: 155,655,127 (GRCm39) |
|
probably null |
Het |
Napb |
C |
A |
2: 148,551,351 (GRCm39) |
A61S |
possibly damaging |
Het |
Ncan |
T |
A |
8: 70,561,221 (GRCm39) |
D582V |
possibly damaging |
Het |
Ncl |
T |
C |
1: 86,284,364 (GRCm39) |
D244G |
possibly damaging |
Het |
Nlrp14 |
A |
G |
7: 106,791,715 (GRCm39) |
N800S |
possibly damaging |
Het |
Nlrp9b |
C |
T |
7: 19,753,260 (GRCm39) |
T55M |
probably benign |
Het |
Nobox |
G |
A |
6: 43,282,951 (GRCm39) |
T228I |
probably benign |
Het |
Npffr1 |
C |
A |
10: 61,449,750 (GRCm39) |
P8H |
possibly damaging |
Het |
Nrg2 |
T |
C |
18: 36,154,156 (GRCm39) |
Y587C |
probably damaging |
Het |
Nsd1 |
T |
G |
13: 55,393,434 (GRCm39) |
V448G |
probably benign |
Het |
Or2w1 |
T |
A |
13: 21,317,371 (GRCm39) |
V142D |
probably benign |
Het |
Or5e1 |
G |
T |
7: 108,354,438 (GRCm39) |
C125F |
probably damaging |
Het |
Or8k41 |
T |
G |
2: 86,313,412 (GRCm39) |
I225L |
probably damaging |
Het |
Or9g20 |
A |
G |
2: 85,630,011 (GRCm39) |
L201P |
probably damaging |
Het |
Peg10 |
T |
TCCC |
6: 4,756,451 (GRCm39) |
|
probably benign |
Het |
Ppp5c |
T |
C |
7: 16,742,932 (GRCm39) |
T229A |
probably benign |
Het |
Pramel51 |
T |
C |
12: 88,143,850 (GRCm39) |
Y329C |
probably benign |
Het |
Prr5 |
C |
T |
15: 84,577,993 (GRCm39) |
R101C |
probably damaging |
Het |
Psg22 |
T |
C |
7: 18,456,987 (GRCm39) |
M290T |
probably benign |
Het |
Pzp |
C |
T |
6: 128,490,694 (GRCm39) |
|
probably null |
Het |
Rapgef6 |
T |
C |
11: 54,516,784 (GRCm39) |
V347A |
probably benign |
Het |
Sema3f |
A |
T |
9: 107,565,275 (GRCm39) |
I259K |
possibly damaging |
Het |
Sgpp1 |
A |
T |
12: 75,763,374 (GRCm39) |
L269Q |
probably damaging |
Het |
Slc22a8 |
A |
C |
19: 8,582,903 (GRCm39) |
I195L |
probably benign |
Het |
Slc35a5 |
T |
C |
16: 44,962,551 (GRCm39) |
T425A |
unknown |
Het |
Spata31e1 |
G |
A |
13: 49,939,548 (GRCm39) |
R721C |
probably benign |
Het |
Stard13 |
G |
A |
5: 150,986,970 (GRCm39) |
T180I |
probably damaging |
Het |
Stard9 |
G |
A |
2: 120,534,911 (GRCm39) |
G3723S |
probably benign |
Het |
Svil |
A |
T |
18: 5,062,385 (GRCm39) |
T902S |
probably damaging |
Het |
Tnfaip8l3 |
T |
A |
9: 53,934,421 (GRCm39) |
R185W |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,590,393 (GRCm39) |
D21105E |
probably benign |
Het |
Vmn2r109 |
T |
A |
17: 20,774,729 (GRCm39) |
M209L |
probably benign |
Het |
Vmn2r125 |
A |
G |
4: 156,703,642 (GRCm39) |
H340R |
probably damaging |
Het |
Zfp946 |
T |
C |
17: 22,674,481 (GRCm39) |
C412R |
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 |
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 |
|
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 |
|
|