Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579C12Rik |
C |
A |
9: 89,034,884 (GRCm39) |
|
noncoding transcript |
Het |
Abra |
C |
A |
15: 41,732,430 (GRCm39) |
R212L |
probably damaging |
Het |
Actr1a |
T |
C |
19: 46,372,714 (GRCm39) |
E87G |
probably damaging |
Het |
Adam26a |
A |
G |
8: 44,022,578 (GRCm39) |
V304A |
possibly damaging |
Het |
Alg2 |
T |
A |
4: 47,471,670 (GRCm39) |
K379N |
probably benign |
Het |
Alk |
G |
T |
17: 72,181,933 (GRCm39) |
|
probably benign |
Het |
Aopep |
A |
G |
13: 63,163,597 (GRCm39) |
Y206C |
probably damaging |
Het |
Arhgef17 |
A |
G |
7: 100,531,475 (GRCm39) |
Y331H |
probably damaging |
Het |
Art3 |
A |
G |
5: 92,560,094 (GRCm39) |
|
probably benign |
Het |
Asap1 |
G |
A |
15: 64,007,647 (GRCm39) |
|
probably benign |
Het |
Atad2 |
A |
T |
15: 57,960,114 (GRCm39) |
|
probably null |
Het |
Atp8b5 |
G |
A |
4: 43,372,906 (GRCm39) |
R1150H |
probably damaging |
Het |
Bltp2 |
C |
T |
11: 78,178,755 (GRCm39) |
|
probably benign |
Het |
Brdt |
T |
C |
5: 107,507,324 (GRCm39) |
S575P |
probably benign |
Het |
Capn3 |
T |
A |
2: 120,316,963 (GRCm39) |
|
probably benign |
Het |
Casd1 |
T |
A |
6: 4,640,951 (GRCm39) |
Y691N |
probably damaging |
Het |
Ccdc127 |
T |
G |
13: 74,505,098 (GRCm39) |
H215Q |
possibly damaging |
Het |
Cenpe |
T |
C |
3: 134,974,740 (GRCm39) |
L2300P |
probably damaging |
Het |
Clasp1 |
T |
C |
1: 118,498,661 (GRCm39) |
F898L |
possibly damaging |
Het |
Clcn1 |
C |
A |
6: 42,290,925 (GRCm39) |
P933Q |
possibly damaging |
Het |
Cntn3 |
T |
A |
6: 102,222,032 (GRCm39) |
N489I |
probably benign |
Het |
Col16a1 |
T |
C |
4: 129,955,517 (GRCm39) |
|
probably benign |
Het |
Col24a1 |
G |
A |
3: 145,243,022 (GRCm39) |
|
probably null |
Het |
Col8a2 |
C |
T |
4: 126,205,417 (GRCm39) |
|
probably benign |
Het |
Cpd |
T |
C |
11: 76,675,208 (GRCm39) |
|
probably benign |
Het |
Csmd3 |
A |
T |
15: 47,522,588 (GRCm39) |
C2694S |
probably damaging |
Het |
Cyp2c40 |
T |
C |
19: 39,775,319 (GRCm39) |
Y311C |
probably benign |
Het |
Dennd5b |
T |
A |
6: 148,969,760 (GRCm39) |
N231I |
probably damaging |
Het |
Dgkh |
T |
A |
14: 78,816,232 (GRCm39) |
H936L |
probably benign |
Het |
Dmtf1 |
T |
C |
5: 9,170,347 (GRCm39) |
|
probably null |
Het |
Dnai2 |
T |
C |
11: 114,643,777 (GRCm39) |
V481A |
possibly damaging |
Het |
Dnai3 |
T |
C |
3: 145,788,801 (GRCm39) |
Y260C |
probably damaging |
Het |
Dpyd |
T |
G |
3: 118,710,780 (GRCm39) |
V396G |
probably damaging |
Het |
Elmo3 |
A |
G |
8: 106,035,213 (GRCm39) |
D448G |
probably damaging |
Het |
Emsy |
A |
T |
7: 98,290,822 (GRCm39) |
V100E |
probably damaging |
Het |
Erbb2 |
T |
C |
11: 98,303,563 (GRCm39) |
|
probably null |
Het |
Faah |
T |
C |
4: 115,865,432 (GRCm39) |
K85R |
probably benign |
Het |
Fam149a |
A |
T |
8: 45,792,399 (GRCm39) |
Y686* |
probably null |
Het |
Fat4 |
T |
C |
3: 39,064,633 (GRCm39) |
V4863A |
probably benign |
Het |
Fbxl8 |
A |
G |
8: 105,995,561 (GRCm39) |
T358A |
probably damaging |
Het |
Fcgbpl1 |
A |
G |
7: 27,854,157 (GRCm39) |
Y1707C |
probably damaging |
Het |
Fgfr3 |
A |
G |
5: 33,887,090 (GRCm39) |
T165A |
probably damaging |
Het |
Fnbp1l |
A |
T |
3: 122,354,581 (GRCm39) |
H180Q |
probably damaging |
Het |
Gm8180 |
T |
A |
14: 44,021,196 (GRCm39) |
H4L |
probably benign |
Het |
Gon4l |
T |
C |
3: 88,802,794 (GRCm39) |
V1135A |
probably damaging |
Het |
Gstcd |
G |
T |
3: 132,688,868 (GRCm39) |
N627K |
probably damaging |
Het |
Gtf2a1l |
G |
A |
17: 89,022,382 (GRCm39) |
V458I |
probably damaging |
Het |
Gtf3c3 |
T |
C |
1: 54,477,997 (GRCm39) |
E26G |
possibly damaging |
Het |
Hrct1 |
A |
T |
4: 43,727,404 (GRCm39) |
T15S |
probably benign |
Het |
Ift122 |
C |
A |
6: 115,868,889 (GRCm39) |
R459S |
probably damaging |
Het |
Irf1 |
T |
A |
11: 53,665,183 (GRCm39) |
C187S |
possibly damaging |
Het |
Kcnh7 |
A |
G |
2: 62,607,736 (GRCm39) |
V615A |
probably damaging |
Het |
Kif1c |
T |
C |
11: 70,594,168 (GRCm39) |
S61P |
probably damaging |
Het |
Mamdc2 |
T |
C |
19: 23,336,517 (GRCm39) |
T331A |
probably damaging |
Het |
Mark2 |
T |
C |
19: 7,268,128 (GRCm39) |
D25G |
possibly damaging |
Het |
Me2 |
T |
C |
18: 73,918,785 (GRCm39) |
D432G |
probably benign |
Het |
Mfap3 |
T |
C |
11: 57,419,032 (GRCm39) |
V64A |
probably benign |
Het |
Nadk2 |
T |
A |
15: 9,108,399 (GRCm39) |
M416K |
probably benign |
Het |
Ndufs1 |
C |
T |
1: 63,186,576 (GRCm39) |
G631D |
probably benign |
Het |
Nomo1 |
G |
A |
7: 45,727,525 (GRCm39) |
V1055I |
probably benign |
Het |
Nuggc |
T |
A |
14: 65,879,450 (GRCm39) |
|
probably benign |
Het |
Nwd2 |
T |
C |
5: 63,962,197 (GRCm39) |
S594P |
probably damaging |
Het |
Or13c3 |
T |
A |
4: 52,856,373 (GRCm39) |
I47L |
probably benign |
Het |
Or4a27 |
T |
G |
2: 88,559,674 (GRCm39) |
I90L |
probably damaging |
Het |
Or4b1b |
C |
A |
2: 90,112,502 (GRCm39) |
C139F |
probably damaging |
Het |
Or5b113 |
T |
A |
19: 13,342,705 (GRCm39) |
S238T |
possibly damaging |
Het |
Or6p1 |
T |
C |
1: 174,258,657 (GRCm39) |
I221T |
probably damaging |
Het |
Or8c10 |
C |
T |
9: 38,278,902 (GRCm39) |
S10L |
probably benign |
Het |
Pakap |
A |
G |
4: 57,709,468 (GRCm39) |
I138V |
probably damaging |
Het |
Pcyt2 |
G |
A |
11: 120,501,968 (GRCm39) |
P332S |
probably benign |
Het |
Phaf1 |
A |
G |
8: 105,966,703 (GRCm39) |
E150G |
probably null |
Het |
Phf14 |
A |
T |
6: 11,987,610 (GRCm39) |
M630L |
probably benign |
Het |
Piezo1 |
T |
C |
8: 123,222,489 (GRCm39) |
N919S |
possibly damaging |
Het |
Pif1 |
A |
T |
9: 65,496,735 (GRCm39) |
I283F |
probably damaging |
Het |
Pknox2 |
G |
A |
9: 36,834,957 (GRCm39) |
H171Y |
probably damaging |
Het |
Pramel17 |
A |
T |
4: 101,694,135 (GRCm39) |
D249E |
probably benign |
Het |
Prkg2 |
T |
A |
5: 99,095,275 (GRCm39) |
D632V |
probably damaging |
Het |
Prr29 |
G |
A |
11: 106,266,264 (GRCm39) |
A6T |
probably damaging |
Het |
Rims1 |
T |
A |
1: 22,635,639 (GRCm39) |
Y114F |
probably damaging |
Het |
Ryr1 |
A |
T |
7: 28,708,977 (GRCm39) |
D4796E |
unknown |
Het |
Scnn1b |
G |
A |
7: 121,513,484 (GRCm39) |
C399Y |
probably damaging |
Het |
Scp2 |
T |
C |
4: 107,948,518 (GRCm39) |
Y153C |
probably damaging |
Het |
Sema3d |
A |
G |
5: 12,547,570 (GRCm39) |
K164R |
probably benign |
Het |
Siglecf |
A |
G |
7: 43,004,967 (GRCm39) |
N399S |
probably benign |
Het |
Siglecf |
A |
G |
7: 43,001,648 (GRCm39) |
T153A |
probably benign |
Het |
Skint2 |
T |
C |
4: 112,504,315 (GRCm39) |
|
probably benign |
Het |
Slc22a8 |
G |
A |
19: 8,583,503 (GRCm39) |
R236H |
probably damaging |
Het |
Slc25a40 |
T |
A |
5: 8,492,431 (GRCm39) |
|
probably null |
Het |
Slc26a5 |
T |
C |
5: 22,021,956 (GRCm39) |
D490G |
possibly damaging |
Het |
Slc26a7 |
G |
T |
4: 14,522,873 (GRCm39) |
D482E |
probably benign |
Het |
Smarca2 |
A |
T |
19: 26,601,284 (GRCm39) |
M77L |
probably benign |
Het |
Sos2 |
A |
G |
12: 69,664,137 (GRCm39) |
L449P |
probably damaging |
Het |
Spaca1 |
A |
G |
4: 34,044,206 (GRCm39) |
V96A |
probably damaging |
Het |
Spata31d1b |
T |
A |
13: 59,865,150 (GRCm39) |
I766N |
possibly damaging |
Het |
Specc1l |
T |
C |
10: 75,145,693 (GRCm39) |
Y1113H |
probably damaging |
Het |
Speg |
A |
G |
1: 75,365,649 (GRCm39) |
R677G |
probably damaging |
Het |
Taf5l |
A |
T |
8: 124,724,729 (GRCm39) |
D363E |
probably damaging |
Het |
Tex56 |
A |
T |
13: 35,116,490 (GRCm39) |
I80F |
possibly damaging |
Het |
Tmem208 |
A |
G |
8: 106,061,438 (GRCm39) |
K155E |
possibly damaging |
Het |
Tppp2 |
A |
C |
14: 52,158,062 (GRCm39) |
N169T |
probably benign |
Het |
Trrap |
T |
A |
5: 144,752,727 (GRCm39) |
|
probably null |
Het |
Ttll6 |
T |
A |
11: 96,029,700 (GRCm39) |
Y204* |
probably null |
Het |
Ttn |
A |
T |
2: 76,602,992 (GRCm39) |
I18410K |
probably benign |
Het |
V1rd19 |
T |
A |
7: 23,703,149 (GRCm39) |
V205D |
probably damaging |
Het |
Vdac3 |
A |
T |
8: 23,070,515 (GRCm39) |
I132K |
possibly damaging |
Het |
Zc3h15 |
A |
G |
2: 83,494,334 (GRCm39) |
T421A |
unknown |
Het |
Zc3hc1 |
T |
C |
6: 30,374,837 (GRCm39) |
T235A |
probably benign |
Het |
Zcchc14 |
A |
G |
8: 122,335,990 (GRCm39) |
|
probably benign |
Het |
Zfp318 |
T |
A |
17: 46,722,366 (GRCm39) |
N1456K |
possibly damaging |
Het |
Zfp606 |
A |
G |
7: 12,214,858 (GRCm39) |
|
probably benign |
Het |
Zfp811 |
T |
A |
17: 33,016,399 (GRCm39) |
H546L |
probably damaging |
Het |
Zfp94 |
A |
T |
7: 24,008,541 (GRCm39) |
Y33N |
probably damaging |
Het |
Zfyve9 |
G |
T |
4: 108,539,492 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Vmn2r95 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01024:Vmn2r95
|
APN |
17 |
18,672,590 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL01479:Vmn2r95
|
APN |
17 |
18,664,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01890:Vmn2r95
|
APN |
17 |
18,671,737 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01986:Vmn2r95
|
APN |
17 |
18,660,473 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02113:Vmn2r95
|
APN |
17 |
18,660,169 (GRCm39) |
missense |
possibly damaging |
0.47 |
IGL02154:Vmn2r95
|
APN |
17 |
18,672,248 (GRCm39) |
missense |
probably benign |
0.16 |
IGL02190:Vmn2r95
|
APN |
17 |
18,672,038 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02412:Vmn2r95
|
APN |
17 |
18,660,218 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02550:Vmn2r95
|
APN |
17 |
18,671,994 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02679:Vmn2r95
|
APN |
17 |
18,664,116 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02691:Vmn2r95
|
APN |
17 |
18,672,120 (GRCm39) |
missense |
probably benign |
0.07 |
IGL02990:Vmn2r95
|
APN |
17 |
18,672,298 (GRCm39) |
nonsense |
probably null |
|
IGL03032:Vmn2r95
|
APN |
17 |
18,672,575 (GRCm39) |
missense |
probably benign |
0.00 |
R0416:Vmn2r95
|
UTSW |
17 |
18,661,664 (GRCm39) |
missense |
probably damaging |
1.00 |
R0448:Vmn2r95
|
UTSW |
17 |
18,672,005 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0514:Vmn2r95
|
UTSW |
17 |
18,671,844 (GRCm39) |
missense |
probably benign |
|
R0519:Vmn2r95
|
UTSW |
17 |
18,659,765 (GRCm39) |
missense |
probably damaging |
1.00 |
R0539:Vmn2r95
|
UTSW |
17 |
18,672,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R1501:Vmn2r95
|
UTSW |
17 |
18,660,118 (GRCm39) |
missense |
probably damaging |
0.99 |
R1598:Vmn2r95
|
UTSW |
17 |
18,672,575 (GRCm39) |
missense |
probably benign |
0.03 |
R1613:Vmn2r95
|
UTSW |
17 |
18,660,901 (GRCm39) |
splice site |
probably benign |
|
R1921:Vmn2r95
|
UTSW |
17 |
18,644,575 (GRCm39) |
missense |
probably benign |
0.11 |
R1986:Vmn2r95
|
UTSW |
17 |
18,671,805 (GRCm39) |
missense |
probably benign |
|
R2031:Vmn2r95
|
UTSW |
17 |
18,659,717 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2040:Vmn2r95
|
UTSW |
17 |
18,661,561 (GRCm39) |
missense |
probably damaging |
1.00 |
R3608:Vmn2r95
|
UTSW |
17 |
18,660,235 (GRCm39) |
missense |
possibly damaging |
0.47 |
R3727:Vmn2r95
|
UTSW |
17 |
18,661,744 (GRCm39) |
nonsense |
probably null |
|
R3953:Vmn2r95
|
UTSW |
17 |
18,660,358 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3955:Vmn2r95
|
UTSW |
17 |
18,660,358 (GRCm39) |
missense |
possibly damaging |
0.79 |
R3957:Vmn2r95
|
UTSW |
17 |
18,660,358 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4474:Vmn2r95
|
UTSW |
17 |
18,672,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R4672:Vmn2r95
|
UTSW |
17 |
18,672,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Vmn2r95
|
UTSW |
17 |
18,671,915 (GRCm39) |
missense |
probably damaging |
1.00 |
R5054:Vmn2r95
|
UTSW |
17 |
18,671,708 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5178:Vmn2r95
|
UTSW |
17 |
18,660,337 (GRCm39) |
missense |
probably benign |
0.01 |
R5980:Vmn2r95
|
UTSW |
17 |
18,661,624 (GRCm39) |
missense |
probably benign |
|
R6183:Vmn2r95
|
UTSW |
17 |
18,664,192 (GRCm39) |
missense |
probably damaging |
0.99 |
R6276:Vmn2r95
|
UTSW |
17 |
18,671,732 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6651:Vmn2r95
|
UTSW |
17 |
18,660,622 (GRCm39) |
missense |
probably damaging |
1.00 |
R6682:Vmn2r95
|
UTSW |
17 |
18,660,489 (GRCm39) |
missense |
probably damaging |
1.00 |
R6797:Vmn2r95
|
UTSW |
17 |
18,672,551 (GRCm39) |
utr 3 prime |
probably benign |
|
R6799:Vmn2r95
|
UTSW |
17 |
18,659,555 (GRCm39) |
missense |
probably damaging |
1.00 |
R6849:Vmn2r95
|
UTSW |
17 |
18,664,182 (GRCm39) |
missense |
probably damaging |
1.00 |
R6849:Vmn2r95
|
UTSW |
17 |
18,664,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R6982:Vmn2r95
|
UTSW |
17 |
18,672,323 (GRCm39) |
missense |
probably damaging |
1.00 |
R7203:Vmn2r95
|
UTSW |
17 |
18,661,577 (GRCm39) |
missense |
probably benign |
0.01 |
R7226:Vmn2r95
|
UTSW |
17 |
18,672,245 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7240:Vmn2r95
|
UTSW |
17 |
18,672,225 (GRCm39) |
missense |
probably benign |
0.15 |
R7383:Vmn2r95
|
UTSW |
17 |
18,660,734 (GRCm39) |
missense |
probably benign |
0.06 |
R7614:Vmn2r95
|
UTSW |
17 |
18,660,352 (GRCm39) |
missense |
probably benign |
|
R7755:Vmn2r95
|
UTSW |
17 |
18,644,367 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R7942:Vmn2r95
|
UTSW |
17 |
18,660,529 (GRCm39) |
missense |
possibly damaging |
0.74 |
R8355:Vmn2r95
|
UTSW |
17 |
18,660,352 (GRCm39) |
missense |
probably benign |
|
R8455:Vmn2r95
|
UTSW |
17 |
18,660,352 (GRCm39) |
missense |
probably benign |
|
R8478:Vmn2r95
|
UTSW |
17 |
18,672,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Vmn2r95
|
UTSW |
17 |
18,664,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R8752:Vmn2r95
|
UTSW |
17 |
18,661,738 (GRCm39) |
missense |
probably damaging |
0.98 |
R8788:Vmn2r95
|
UTSW |
17 |
18,671,790 (GRCm39) |
missense |
probably benign |
0.09 |
R8852:Vmn2r95
|
UTSW |
17 |
18,664,113 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9098:Vmn2r95
|
UTSW |
17 |
18,660,167 (GRCm39) |
missense |
possibly damaging |
0.88 |
R9202:Vmn2r95
|
UTSW |
17 |
18,644,394 (GRCm39) |
missense |
probably benign |
0.00 |
R9244:Vmn2r95
|
UTSW |
17 |
18,672,189 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9546:Vmn2r95
|
UTSW |
17 |
18,661,721 (GRCm39) |
missense |
probably benign |
0.01 |
R9665:Vmn2r95
|
UTSW |
17 |
18,660,607 (GRCm39) |
missense |
probably damaging |
0.99 |
Z1088:Vmn2r95
|
UTSW |
17 |
18,660,663 (GRCm39) |
missense |
probably benign |
0.01 |
|