Other mutations in this stock |
Total: 79 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930562C15Rik |
T |
C |
16: 4,667,508 (GRCm39) |
S300P |
unknown |
Het |
Abhd17a |
T |
A |
10: 80,420,008 (GRCm39) |
K226* |
probably null |
Het |
Alkbh7 |
T |
A |
17: 57,305,508 (GRCm39) |
H108Q |
probably damaging |
Het |
Ankrd44 |
A |
C |
1: 54,806,069 (GRCm39) |
H112Q |
probably damaging |
Het |
Capn3 |
A |
G |
2: 120,333,935 (GRCm39) |
E790G |
probably damaging |
Het |
Cd47 |
C |
A |
16: 49,728,440 (GRCm39) |
N330K |
possibly damaging |
Het |
Cd55 |
A |
G |
1: 130,390,343 (GRCm39) |
S22P |
possibly damaging |
Het |
Cdc25a |
A |
G |
9: 109,718,154 (GRCm39) |
I373V |
probably damaging |
Het |
Cfap43 |
T |
C |
19: 47,779,912 (GRCm39) |
I514V |
probably benign |
Het |
Cfap73 |
A |
T |
5: 120,768,200 (GRCm39) |
M186K |
probably benign |
Het |
Chd9 |
A |
G |
8: 91,728,394 (GRCm39) |
D1270G |
unknown |
Het |
Ciita |
A |
G |
16: 10,330,121 (GRCm39) |
T802A |
probably benign |
Het |
Dlgap2 |
A |
G |
8: 14,793,296 (GRCm39) |
E430G |
probably benign |
Het |
Dlx1 |
C |
A |
2: 71,360,513 (GRCm39) |
S59* |
probably null |
Het |
Dnaaf3 |
T |
C |
7: 4,531,076 (GRCm39) |
N119S |
probably damaging |
Het |
Dnah11 |
T |
G |
12: 118,004,830 (GRCm39) |
I2164L |
possibly damaging |
Het |
Dnah11 |
T |
C |
12: 118,090,624 (GRCm39) |
K1079R |
probably benign |
Het |
Dnah12 |
C |
T |
14: 26,576,837 (GRCm39) |
T3029I |
probably damaging |
Het |
Dppa3 |
A |
T |
6: 122,606,918 (GRCm39) |
Y136F |
probably damaging |
Het |
Enox1 |
T |
A |
14: 77,958,284 (GRCm39) |
M611K |
probably benign |
Het |
Farp2 |
T |
C |
1: 93,488,040 (GRCm39) |
F89S |
probably damaging |
Het |
Fbn2 |
C |
T |
18: 58,186,099 (GRCm39) |
V1750M |
probably benign |
Het |
Frs3 |
A |
G |
17: 48,013,620 (GRCm39) |
T181A |
probably damaging |
Het |
Heatr4 |
T |
A |
12: 84,004,644 (GRCm39) |
I726F |
possibly damaging |
Het |
Ighg1 |
T |
G |
12: 113,290,216 (GRCm39) |
E375A |
|
Het |
Ikzf4 |
G |
T |
10: 128,470,252 (GRCm39) |
Q476K |
possibly damaging |
Het |
Kcnh1 |
G |
T |
1: 192,187,945 (GRCm39) |
C829F |
probably benign |
Het |
Krtap19-4 |
T |
C |
16: 88,681,797 (GRCm39) |
Y53C |
unknown |
Het |
Loricrin |
C |
A |
3: 91,988,705 (GRCm39) |
G194C |
unknown |
Het |
Lrp1 |
A |
C |
10: 127,393,097 (GRCm39) |
D2720E |
probably benign |
Het |
Lrp4 |
A |
G |
2: 91,322,368 (GRCm39) |
Y1068C |
probably damaging |
Het |
Mbnl1 |
A |
G |
3: 60,511,244 (GRCm39) |
N67D |
probably benign |
Het |
Mrpl21 |
A |
G |
19: 3,336,998 (GRCm39) |
E123G |
probably benign |
Het |
Mst1 |
A |
T |
9: 107,958,485 (GRCm39) |
D65V |
probably damaging |
Het |
Myo15b |
T |
A |
11: 115,767,921 (GRCm39) |
|
probably null |
Het |
Myo5a |
A |
G |
9: 75,028,052 (GRCm39) |
Y79C |
probably damaging |
Het |
Oas1c |
A |
T |
5: 120,940,957 (GRCm39) |
W279R |
probably damaging |
Het |
Or4f4-ps1 |
A |
T |
2: 111,330,532 (GRCm39) |
M312L |
probably benign |
Het |
Or4k77 |
A |
T |
2: 111,199,882 (GRCm39) |
I302L |
probably benign |
Het |
Or51f5 |
A |
G |
7: 102,430,913 (GRCm39) |
I77V |
probably benign |
Het |
Pcdh9 |
C |
T |
14: 93,253,216 (GRCm39) |
G1149D |
possibly damaging |
Het |
Pcid2 |
G |
A |
8: 13,129,907 (GRCm39) |
T283I |
probably benign |
Het |
Pdhx |
A |
G |
2: 102,858,760 (GRCm39) |
V348A |
probably benign |
Het |
Pi16 |
C |
A |
17: 29,538,208 (GRCm39) |
P7Q |
possibly damaging |
Het |
Psmb3 |
T |
A |
11: 97,602,023 (GRCm39) |
M131K |
probably null |
Het |
Raph1 |
A |
G |
1: 60,542,032 (GRCm39) |
Y309H |
unknown |
Het |
Rasgrf1 |
A |
G |
9: 89,866,341 (GRCm39) |
N593S |
probably damaging |
Het |
Rbm38 |
A |
C |
2: 172,863,990 (GRCm39) |
E53A |
possibly damaging |
Het |
Rufy3 |
A |
G |
5: 88,797,715 (GRCm39) |
T631A |
probably benign |
Het |
Sbno1 |
A |
T |
5: 124,543,722 (GRCm39) |
D272E |
probably benign |
Het |
Scamp1 |
T |
A |
13: 94,361,415 (GRCm39) |
Y207F |
probably damaging |
Het |
Scn8a |
T |
A |
15: 100,866,984 (GRCm39) |
S263R |
probably damaging |
Het |
Setbp1 |
T |
G |
18: 78,798,960 (GRCm39) |
T1407P |
probably damaging |
Het |
Skor2 |
T |
C |
18: 76,948,096 (GRCm39) |
L606P |
possibly damaging |
Het |
Slc35f6 |
A |
G |
5: 30,814,796 (GRCm39) |
N241S |
probably benign |
Het |
Slc36a2 |
T |
G |
11: 55,059,744 (GRCm39) |
D247A |
probably benign |
Het |
Smim10l1 |
T |
A |
6: 133,084,895 (GRCm39) |
F87L |
unknown |
Het |
Son |
T |
C |
16: 91,461,889 (GRCm39) |
S2265P |
unknown |
Het |
Spta1 |
A |
G |
1: 174,050,203 (GRCm39) |
N1748D |
probably damaging |
Het |
Sptbn2 |
A |
G |
19: 4,774,201 (GRCm39) |
D84G |
probably damaging |
Het |
Tasor2 |
T |
A |
13: 3,640,521 (GRCm39) |
L205F |
probably damaging |
Het |
Tbc1d24 |
G |
A |
17: 24,404,266 (GRCm39) |
R293C |
probably damaging |
Het |
Tex15 |
A |
G |
8: 34,036,268 (GRCm39) |
T65A |
probably benign |
Het |
Thyn1 |
A |
G |
9: 26,916,506 (GRCm39) |
Y97C |
probably damaging |
Het |
Tmem64 |
T |
C |
4: 15,266,700 (GRCm39) |
L250P |
probably damaging |
Het |
Tnfrsf9 |
A |
T |
4: 151,019,991 (GRCm39) |
K217N |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,898,039 (GRCm39) |
T896A |
probably benign |
Het |
Trpm1 |
T |
A |
7: 63,854,333 (GRCm39) |
I285N |
possibly damaging |
Het |
Try5 |
T |
A |
6: 41,288,637 (GRCm39) |
D194V |
probably damaging |
Het |
U2surp |
G |
A |
9: 95,372,215 (GRCm39) |
R316* |
probably null |
Het |
Ubr2 |
G |
T |
17: 47,246,360 (GRCm39) |
S1618* |
probably null |
Het |
Ugp2 |
T |
C |
11: 21,273,271 (GRCm39) |
I449M |
probably damaging |
Het |
Umodl1 |
A |
G |
17: 31,201,236 (GRCm39) |
|
probably null |
Het |
Vmn2r31 |
C |
T |
7: 7,390,105 (GRCm39) |
V538I |
probably benign |
Het |
Vmn2r31 |
A |
T |
7: 7,397,397 (GRCm39) |
M287K |
probably damaging |
Het |
Wwc2 |
A |
G |
8: 48,311,919 (GRCm39) |
V748A |
unknown |
Het |
Zfp800 |
A |
C |
6: 28,243,662 (GRCm39) |
H434Q |
probably benign |
Het |
Zfp869 |
A |
G |
8: 70,159,356 (GRCm39) |
C406R |
probably damaging |
Het |
Zhx1 |
A |
G |
15: 57,917,733 (GRCm39) |
V171A |
probably benign |
Het |
|
Other mutations in Fam149a |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00226:Fam149a
|
APN |
8 |
45,792,380 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00229:Fam149a
|
APN |
8 |
45,804,823 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01089:Fam149a
|
APN |
8 |
45,801,564 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01578:Fam149a
|
APN |
8 |
45,803,479 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03095:Fam149a
|
APN |
8 |
45,794,265 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03112:Fam149a
|
APN |
8 |
45,801,580 (GRCm39) |
missense |
possibly damaging |
0.78 |
guangxi
|
UTSW |
8 |
45,834,778 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT1430001:Fam149a
|
UTSW |
8 |
45,804,743 (GRCm39) |
missense |
probably benign |
0.00 |
R0111:Fam149a
|
UTSW |
8 |
45,794,183 (GRCm39) |
splice site |
probably benign |
|
R0113:Fam149a
|
UTSW |
8 |
45,794,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R0452:Fam149a
|
UTSW |
8 |
45,808,686 (GRCm39) |
missense |
probably damaging |
1.00 |
R0604:Fam149a
|
UTSW |
8 |
45,798,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1441:Fam149a
|
UTSW |
8 |
45,808,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R1672:Fam149a
|
UTSW |
8 |
45,792,411 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1861:Fam149a
|
UTSW |
8 |
45,792,399 (GRCm39) |
nonsense |
probably null |
|
R1981:Fam149a
|
UTSW |
8 |
45,834,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R2173:Fam149a
|
UTSW |
8 |
45,806,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R2211:Fam149a
|
UTSW |
8 |
45,794,046 (GRCm39) |
missense |
probably damaging |
0.99 |
R3807:Fam149a
|
UTSW |
8 |
45,834,647 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4176:Fam149a
|
UTSW |
8 |
45,794,321 (GRCm39) |
missense |
probably benign |
0.41 |
R4913:Fam149a
|
UTSW |
8 |
45,806,920 (GRCm39) |
missense |
probably damaging |
1.00 |
R5158:Fam149a
|
UTSW |
8 |
45,803,472 (GRCm39) |
missense |
possibly damaging |
0.51 |
R5172:Fam149a
|
UTSW |
8 |
45,797,690 (GRCm39) |
missense |
probably damaging |
0.99 |
R5436:Fam149a
|
UTSW |
8 |
45,801,508 (GRCm39) |
missense |
probably benign |
0.21 |
R6060:Fam149a
|
UTSW |
8 |
45,811,799 (GRCm39) |
intron |
probably benign |
|
R6426:Fam149a
|
UTSW |
8 |
45,834,611 (GRCm39) |
missense |
probably benign |
|
R6590:Fam149a
|
UTSW |
8 |
45,802,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6596:Fam149a
|
UTSW |
8 |
45,834,667 (GRCm39) |
missense |
probably benign |
0.25 |
R6690:Fam149a
|
UTSW |
8 |
45,802,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6730:Fam149a
|
UTSW |
8 |
45,834,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R6734:Fam149a
|
UTSW |
8 |
45,834,478 (GRCm39) |
missense |
probably benign |
|
R6916:Fam149a
|
UTSW |
8 |
45,803,443 (GRCm39) |
missense |
probably damaging |
1.00 |
R7088:Fam149a
|
UTSW |
8 |
45,803,582 (GRCm39) |
missense |
probably benign |
0.08 |
R7352:Fam149a
|
UTSW |
8 |
45,794,034 (GRCm39) |
missense |
probably damaging |
0.98 |
R7454:Fam149a
|
UTSW |
8 |
45,801,583 (GRCm39) |
missense |
probably benign |
0.29 |
R7591:Fam149a
|
UTSW |
8 |
45,803,472 (GRCm39) |
missense |
possibly damaging |
0.89 |
R7788:Fam149a
|
UTSW |
8 |
45,834,554 (GRCm39) |
missense |
probably damaging |
1.00 |
R7846:Fam149a
|
UTSW |
8 |
45,811,678 (GRCm39) |
missense |
|
|
R7915:Fam149a
|
UTSW |
8 |
45,794,280 (GRCm39) |
missense |
probably benign |
|
R8036:Fam149a
|
UTSW |
8 |
45,802,048 (GRCm39) |
missense |
probably benign |
0.00 |
R8181:Fam149a
|
UTSW |
8 |
45,834,755 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8239:Fam149a
|
UTSW |
8 |
45,803,490 (GRCm39) |
missense |
possibly damaging |
0.48 |
R8246:Fam149a
|
UTSW |
8 |
45,834,655 (GRCm39) |
missense |
probably benign |
0.00 |
R8532:Fam149a
|
UTSW |
8 |
45,801,991 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8856:Fam149a
|
UTSW |
8 |
45,834,611 (GRCm39) |
missense |
|
|
R8986:Fam149a
|
UTSW |
8 |
45,811,837 (GRCm39) |
missense |
|
|
R9448:Fam149a
|
UTSW |
8 |
45,792,411 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9704:Fam149a
|
UTSW |
8 |
45,795,502 (GRCm39) |
missense |
probably benign |
0.24 |
R9794:Fam149a
|
UTSW |
8 |
45,834,449 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1176:Fam149a
|
UTSW |
8 |
45,795,495 (GRCm39) |
missense |
possibly damaging |
0.92 |
|