Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
A |
T |
9: 53,334,317 (GRCm39) |
M187L |
possibly damaging |
Het |
9930012K11Rik |
T |
C |
14: 70,394,686 (GRCm39) |
E156G |
possibly damaging |
Het |
Acad9 |
C |
T |
3: 36,130,139 (GRCm39) |
A194V |
probably damaging |
Het |
Agps |
T |
A |
2: 75,683,128 (GRCm39) |
V151E |
probably benign |
Het |
Akr1c19 |
T |
A |
13: 4,296,818 (GRCm39) |
L288Q |
probably damaging |
Het |
Carmil1 |
T |
G |
13: 24,197,377 (GRCm39) |
D1353A |
probably damaging |
Het |
Ccz1 |
T |
A |
5: 143,949,897 (GRCm39) |
I43F |
probably damaging |
Het |
Cep70 |
G |
A |
9: 99,157,638 (GRCm39) |
C179Y |
probably damaging |
Het |
Comt |
A |
T |
16: 18,229,440 (GRCm39) |
L196H |
probably damaging |
Het |
Cspg5 |
A |
T |
9: 110,076,023 (GRCm39) |
D253V |
probably damaging |
Het |
Dars2 |
A |
G |
1: 160,874,378 (GRCm39) |
V437A |
possibly damaging |
Het |
Dcaf5 |
A |
G |
12: 80,395,164 (GRCm39) |
I335T |
probably damaging |
Het |
Ddn |
T |
C |
15: 98,703,906 (GRCm39) |
K462R |
possibly damaging |
Het |
Dscaml1 |
T |
C |
9: 45,654,044 (GRCm39) |
|
probably null |
Het |
Eef1ece2 |
T |
C |
16: 20,451,341 (GRCm39) |
S325P |
probably benign |
Het |
Ethe1 |
A |
G |
7: 24,307,377 (GRCm39) |
Y197C |
probably damaging |
Het |
Evc |
A |
T |
5: 37,479,527 (GRCm39) |
L269* |
probably null |
Het |
Fam161a |
T |
C |
11: 22,970,001 (GRCm39) |
S60P |
possibly damaging |
Het |
Fam20b |
A |
G |
1: 156,509,012 (GRCm39) |
V400A |
probably benign |
Het |
Fam53b |
T |
A |
7: 132,361,390 (GRCm39) |
S213C |
possibly damaging |
Het |
Flot2 |
A |
G |
11: 77,945,612 (GRCm39) |
I45V |
probably benign |
Het |
Gemin4 |
A |
C |
11: 76,103,579 (GRCm39) |
L394R |
probably damaging |
Het |
Glis2 |
T |
G |
16: 4,429,182 (GRCm39) |
S128R |
possibly damaging |
Het |
Gm3696 |
A |
G |
14: 18,435,009 (GRCm39) |
Y92H |
probably damaging |
Het |
Gpbp1l1 |
T |
C |
4: 116,447,442 (GRCm39) |
V374A |
probably benign |
Het |
Grm1 |
T |
C |
10: 10,565,440 (GRCm39) |
N956S |
probably benign |
Het |
Hbb-bh1 |
T |
C |
7: 103,492,238 (GRCm39) |
E27G |
probably damaging |
Het |
Hmcn1 |
A |
T |
1: 150,458,088 (GRCm39) |
C5233S |
probably damaging |
Het |
Hmgcr |
C |
T |
13: 96,803,105 (GRCm39) |
C30Y |
probably damaging |
Het |
Hoxb6 |
A |
G |
11: 96,183,651 (GRCm39) |
|
probably benign |
Het |
Igf2 |
T |
C |
7: 142,209,555 (GRCm39) |
Q35R |
possibly damaging |
Het |
Ighv1-4 |
C |
T |
12: 114,450,941 (GRCm39) |
V56I |
probably benign |
Het |
Kif13a |
C |
T |
13: 46,905,931 (GRCm39) |
V671M |
possibly damaging |
Het |
Lmtk2 |
C |
T |
5: 144,111,178 (GRCm39) |
Q633* |
probably null |
Het |
Mesd |
T |
C |
7: 83,544,957 (GRCm39) |
Y136H |
probably damaging |
Het |
Mga |
T |
A |
2: 119,795,269 (GRCm39) |
S2984R |
possibly damaging |
Het |
Mkrn3 |
T |
C |
7: 62,068,675 (GRCm39) |
N372S |
probably benign |
Het |
Mtpap |
A |
G |
18: 4,387,068 (GRCm39) |
I373V |
probably benign |
Het |
Mycbp2 |
G |
A |
14: 103,358,027 (GRCm39) |
T4589M |
probably damaging |
Het |
Myh2 |
A |
G |
11: 67,079,195 (GRCm39) |
Q921R |
probably benign |
Het |
Myom1 |
A |
G |
17: 71,352,544 (GRCm39) |
D324G |
possibly damaging |
Het |
Nat10 |
T |
C |
2: 103,584,514 (GRCm39) |
K88E |
probably benign |
Het |
Ncapd3 |
A |
G |
9: 26,981,254 (GRCm39) |
R915G |
probably damaging |
Het |
Nek4 |
T |
C |
14: 30,679,249 (GRCm39) |
Y190H |
probably damaging |
Het |
Nfasc |
A |
C |
1: 132,529,790 (GRCm39) |
Y797D |
probably damaging |
Het |
Ngp |
A |
G |
9: 110,249,978 (GRCm39) |
D92G |
probably benign |
Het |
Nos2 |
A |
C |
11: 78,820,680 (GRCm39) |
H95P |
probably damaging |
Het |
Nr3c1 |
ACGTC |
ACGTCGTC |
18: 39,619,513 (GRCm39) |
|
probably benign |
Het |
Or10ag59 |
C |
T |
2: 87,405,863 (GRCm39) |
T145I |
probably benign |
Het |
Or5bw2 |
C |
A |
7: 6,573,715 (GRCm39) |
H242N |
probably damaging |
Het |
Or5p73 |
T |
C |
7: 108,064,642 (GRCm39) |
I37T |
possibly damaging |
Het |
Or5t18 |
A |
T |
2: 86,636,967 (GRCm39) |
H125Q |
possibly damaging |
Het |
Otogl |
T |
A |
10: 107,606,471 (GRCm39) |
D2154V |
probably benign |
Het |
Pdss1 |
T |
A |
2: 22,825,653 (GRCm39) |
|
probably null |
Het |
Pex5 |
A |
T |
6: 124,375,022 (GRCm39) |
L609* |
probably null |
Het |
Pglyrp4 |
C |
A |
3: 90,640,281 (GRCm39) |
A177D |
probably damaging |
Het |
Phactr4 |
A |
G |
4: 132,104,489 (GRCm39) |
|
probably null |
Het |
Phf8-ps |
T |
C |
17: 33,284,501 (GRCm39) |
D767G |
probably benign |
Het |
Pik3cd |
G |
C |
4: 149,744,171 (GRCm39) |
N193K |
probably benign |
Het |
Prr36 |
TACCTCTTC |
T |
8: 4,265,163 (GRCm39) |
|
probably benign |
Het |
Prss38 |
A |
T |
11: 59,266,384 (GRCm39) |
W25R |
probably benign |
Het |
Prss8 |
T |
A |
7: 127,526,056 (GRCm39) |
Q189L |
probably damaging |
Het |
Psd |
T |
A |
19: 46,303,240 (GRCm39) |
D713V |
probably damaging |
Het |
Rad51ap2 |
C |
T |
12: 11,507,692 (GRCm39) |
T538I |
probably benign |
Het |
Rarres1 |
T |
C |
3: 67,422,517 (GRCm39) |
T78A |
probably benign |
Het |
Rbl2 |
G |
T |
8: 91,828,922 (GRCm39) |
G651* |
probably null |
Het |
Rev3l |
A |
T |
10: 39,699,601 (GRCm39) |
Q1366L |
probably damaging |
Het |
Rundc1 |
T |
C |
11: 101,320,413 (GRCm39) |
S215P |
probably benign |
Het |
Sanbr |
A |
T |
11: 23,572,479 (GRCm39) |
C130S |
probably benign |
Het |
Scarf2 |
G |
A |
16: 17,620,837 (GRCm39) |
W168* |
probably null |
Het |
Sh2d7 |
A |
G |
9: 54,448,186 (GRCm39) |
D69G |
possibly damaging |
Het |
Slc26a4 |
A |
T |
12: 31,579,527 (GRCm39) |
Y578* |
probably null |
Het |
Slc2a9 |
A |
T |
5: 38,610,538 (GRCm39) |
L87Q |
probably damaging |
Het |
Slc39a10 |
A |
T |
1: 46,849,230 (GRCm39) |
H795Q |
probably damaging |
Het |
Spata13 |
C |
T |
14: 60,993,871 (GRCm39) |
R1108W |
probably damaging |
Het |
Sqle |
T |
C |
15: 59,187,901 (GRCm39) |
S70P |
probably benign |
Het |
Syncrip |
A |
T |
9: 88,346,716 (GRCm39) |
F263I |
probably damaging |
Het |
Synj2 |
T |
C |
17: 6,088,220 (GRCm39) |
S1424P |
possibly damaging |
Het |
Tax1bp3 |
A |
T |
11: 73,071,941 (GRCm39) |
T89S |
possibly damaging |
Het |
Tcaim |
G |
A |
9: 122,648,092 (GRCm39) |
|
probably null |
Het |
Tcp10c |
T |
C |
17: 13,582,438 (GRCm39) |
I240T |
possibly damaging |
Het |
Ttll8 |
G |
T |
15: 88,801,442 (GRCm39) |
N415K |
probably benign |
Het |
Tut7 |
T |
C |
13: 59,969,463 (GRCm39) |
E144G |
probably benign |
Het |
Ugcg |
T |
C |
4: 59,217,111 (GRCm39) |
S212P |
possibly damaging |
Het |
Vmn2r32 |
T |
C |
7: 7,482,807 (GRCm39) |
K56E |
probably benign |
Het |
Vmn2r55 |
T |
C |
7: 12,386,000 (GRCm39) |
E660G |
probably damaging |
Het |
Vmn2r7 |
T |
C |
3: 64,598,301 (GRCm39) |
N752S |
probably benign |
Het |
Vps54 |
T |
A |
11: 21,225,005 (GRCm39) |
M167K |
probably benign |
Het |
Vwa2 |
A |
C |
19: 56,897,791 (GRCm39) |
M699L |
probably benign |
Het |
Wdr59 |
A |
G |
8: 112,192,494 (GRCm39) |
V689A |
|
Het |
Whamm |
T |
G |
7: 81,235,995 (GRCm39) |
N399K |
probably damaging |
Het |
Zfp760 |
A |
G |
17: 21,941,760 (GRCm39) |
K312E |
probably benign |
Het |
Zkscan3 |
C |
A |
13: 21,578,983 (GRCm39) |
V171L |
probably benign |
Het |
|
Other mutations in Ak9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
Mean
|
UTSW |
10 |
41,233,559 (GRCm39) |
missense |
possibly damaging |
0.59 |
BB006:Ak9
|
UTSW |
10 |
41,259,944 (GRCm39) |
missense |
|
|
BB016:Ak9
|
UTSW |
10 |
41,259,944 (GRCm39) |
missense |
|
|
R0057:Ak9
|
UTSW |
10 |
41,268,724 (GRCm39) |
missense |
probably benign |
0.04 |
R0605:Ak9
|
UTSW |
10 |
41,221,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R0658:Ak9
|
UTSW |
10 |
41,223,218 (GRCm39) |
missense |
probably damaging |
0.98 |
R1696:Ak9
|
UTSW |
10 |
41,203,585 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1738:Ak9
|
UTSW |
10 |
41,211,917 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1815:Ak9
|
UTSW |
10 |
41,213,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R2900:Ak9
|
UTSW |
10 |
41,300,751 (GRCm39) |
missense |
unknown |
|
R3123:Ak9
|
UTSW |
10 |
41,234,576 (GRCm39) |
missense |
possibly damaging |
0.46 |
R3715:Ak9
|
UTSW |
10 |
41,233,508 (GRCm39) |
missense |
probably damaging |
0.96 |
R4092:Ak9
|
UTSW |
10 |
41,265,140 (GRCm39) |
missense |
probably benign |
0.29 |
R4193:Ak9
|
UTSW |
10 |
41,211,941 (GRCm39) |
missense |
probably benign |
0.14 |
R4598:Ak9
|
UTSW |
10 |
41,259,907 (GRCm39) |
missense |
probably damaging |
1.00 |
R4621:Ak9
|
UTSW |
10 |
41,282,887 (GRCm39) |
missense |
possibly damaging |
0.55 |
R4681:Ak9
|
UTSW |
10 |
41,303,234 (GRCm39) |
missense |
unknown |
|
R4707:Ak9
|
UTSW |
10 |
41,221,456 (GRCm39) |
missense |
probably benign |
0.36 |
R4908:Ak9
|
UTSW |
10 |
41,296,678 (GRCm39) |
missense |
unknown |
|
R4952:Ak9
|
UTSW |
10 |
41,296,585 (GRCm39) |
missense |
probably benign |
0.07 |
R5162:Ak9
|
UTSW |
10 |
41,233,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5446:Ak9
|
UTSW |
10 |
41,296,505 (GRCm39) |
missense |
possibly damaging |
0.70 |
R5494:Ak9
|
UTSW |
10 |
41,223,165 (GRCm39) |
missense |
probably damaging |
1.00 |
R5517:Ak9
|
UTSW |
10 |
41,216,887 (GRCm39) |
missense |
probably benign |
0.23 |
R5849:Ak9
|
UTSW |
10 |
41,224,045 (GRCm39) |
missense |
probably benign |
0.31 |
R5858:Ak9
|
UTSW |
10 |
41,299,023 (GRCm39) |
missense |
unknown |
|
R5920:Ak9
|
UTSW |
10 |
41,296,672 (GRCm39) |
missense |
probably benign |
0.30 |
R5952:Ak9
|
UTSW |
10 |
41,233,559 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5955:Ak9
|
UTSW |
10 |
41,234,560 (GRCm39) |
missense |
probably damaging |
1.00 |
R6050:Ak9
|
UTSW |
10 |
41,265,108 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6087:Ak9
|
UTSW |
10 |
41,258,828 (GRCm39) |
missense |
probably benign |
0.01 |
R6190:Ak9
|
UTSW |
10 |
41,298,404 (GRCm39) |
missense |
unknown |
|
R6190:Ak9
|
UTSW |
10 |
41,298,403 (GRCm39) |
missense |
unknown |
|
R6197:Ak9
|
UTSW |
10 |
41,193,826 (GRCm39) |
missense |
probably damaging |
0.98 |
R6220:Ak9
|
UTSW |
10 |
41,246,095 (GRCm39) |
missense |
unknown |
|
R6250:Ak9
|
UTSW |
10 |
41,265,030 (GRCm39) |
missense |
possibly damaging |
0.54 |
R6315:Ak9
|
UTSW |
10 |
41,282,837 (GRCm39) |
missense |
possibly damaging |
0.55 |
R6331:Ak9
|
UTSW |
10 |
41,258,825 (GRCm39) |
missense |
probably damaging |
0.99 |
R6812:Ak9
|
UTSW |
10 |
41,243,163 (GRCm39) |
missense |
unknown |
|
R6847:Ak9
|
UTSW |
10 |
41,233,797 (GRCm39) |
splice site |
probably null |
|
R7128:Ak9
|
UTSW |
10 |
41,300,713 (GRCm39) |
missense |
unknown |
|
R7253:Ak9
|
UTSW |
10 |
41,308,480 (GRCm39) |
missense |
unknown |
|
R7401:Ak9
|
UTSW |
10 |
41,299,000 (GRCm39) |
missense |
unknown |
|
R7478:Ak9
|
UTSW |
10 |
41,265,087 (GRCm39) |
missense |
|
|
R7698:Ak9
|
UTSW |
10 |
41,224,072 (GRCm39) |
missense |
|
|
R7758:Ak9
|
UTSW |
10 |
41,223,128 (GRCm39) |
missense |
|
|
R7806:Ak9
|
UTSW |
10 |
41,309,080 (GRCm39) |
critical splice acceptor site |
probably null |
|
R7894:Ak9
|
UTSW |
10 |
41,296,535 (GRCm39) |
missense |
unknown |
|
R7929:Ak9
|
UTSW |
10 |
41,259,944 (GRCm39) |
missense |
|
|
R7941:Ak9
|
UTSW |
10 |
41,285,133 (GRCm39) |
missense |
unknown |
|
R8032:Ak9
|
UTSW |
10 |
41,300,616 (GRCm39) |
missense |
unknown |
|
R8143:Ak9
|
UTSW |
10 |
41,213,588 (GRCm39) |
nonsense |
probably null |
|
R8298:Ak9
|
UTSW |
10 |
41,265,054 (GRCm39) |
missense |
|
|
R8301:Ak9
|
UTSW |
10 |
41,300,712 (GRCm39) |
missense |
|
|
R8355:Ak9
|
UTSW |
10 |
41,275,700 (GRCm39) |
missense |
|
|
R8703:Ak9
|
UTSW |
10 |
41,201,120 (GRCm39) |
missense |
|
|
R8728:Ak9
|
UTSW |
10 |
41,282,959 (GRCm39) |
missense |
|
|
R8757:Ak9
|
UTSW |
10 |
41,299,036 (GRCm39) |
missense |
unknown |
|
R8798:Ak9
|
UTSW |
10 |
41,258,847 (GRCm39) |
missense |
|
|
R8868:Ak9
|
UTSW |
10 |
41,258,869 (GRCm39) |
nonsense |
probably null |
|
R8868:Ak9
|
UTSW |
10 |
41,193,842 (GRCm39) |
critical splice donor site |
probably null |
|
R9088:Ak9
|
UTSW |
10 |
41,282,870 (GRCm39) |
missense |
|
|
R9090:Ak9
|
UTSW |
10 |
41,300,623 (GRCm39) |
missense |
unknown |
|
R9165:Ak9
|
UTSW |
10 |
41,309,235 (GRCm39) |
missense |
unknown |
|
R9195:Ak9
|
UTSW |
10 |
41,283,479 (GRCm39) |
missense |
|
|
R9271:Ak9
|
UTSW |
10 |
41,300,623 (GRCm39) |
missense |
unknown |
|
R9297:Ak9
|
UTSW |
10 |
41,299,081 (GRCm39) |
missense |
unknown |
|
R9302:Ak9
|
UTSW |
10 |
41,196,486 (GRCm39) |
missense |
|
|
R9309:Ak9
|
UTSW |
10 |
41,192,364 (GRCm39) |
critical splice donor site |
probably null |
|
R9318:Ak9
|
UTSW |
10 |
41,299,081 (GRCm39) |
missense |
unknown |
|
R9393:Ak9
|
UTSW |
10 |
41,285,068 (GRCm39) |
missense |
unknown |
|
R9541:Ak9
|
UTSW |
10 |
41,243,173 (GRCm39) |
missense |
|
|
R9579:Ak9
|
UTSW |
10 |
41,213,576 (GRCm39) |
missense |
|
|
R9618:Ak9
|
UTSW |
10 |
41,203,627 (GRCm39) |
missense |
|
|
R9697:Ak9
|
UTSW |
10 |
41,298,968 (GRCm39) |
nonsense |
probably null |
|
R9753:Ak9
|
UTSW |
10 |
41,259,496 (GRCm39) |
missense |
|
|
Z1176:Ak9
|
UTSW |
10 |
41,299,019 (GRCm39) |
missense |
unknown |
|
Z1176:Ak9
|
UTSW |
10 |
41,224,247 (GRCm39) |
missense |
|
|
|