Other mutations in this stock |
Total: 111 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca16 |
T |
A |
7: 120,113,825 (GRCm39) |
W899R |
probably damaging |
Het |
Abca5 |
A |
T |
11: 110,163,323 (GRCm39) |
W1631R |
possibly damaging |
Het |
Actg2 |
T |
A |
6: 83,504,350 (GRCm39) |
D25V |
probably damaging |
Het |
Akap10 |
G |
C |
11: 61,806,331 (GRCm39) |
D132E |
probably damaging |
Het |
Angptl2 |
G |
T |
2: 33,132,394 (GRCm39) |
E334* |
probably null |
Het |
Aprt |
T |
C |
8: 123,301,674 (GRCm39) |
R165G |
probably benign |
Het |
Bmp1 |
A |
G |
14: 70,729,524 (GRCm39) |
F549S |
probably damaging |
Het |
Capzb |
C |
T |
4: 139,007,864 (GRCm39) |
T215I |
probably benign |
Het |
Car14 |
C |
T |
3: 95,811,684 (GRCm39) |
M1I |
probably null |
Het |
Ccdc148 |
T |
A |
2: 58,713,648 (GRCm39) |
Q501L |
probably benign |
Het |
Ccdc32 |
G |
A |
2: 118,857,828 (GRCm39) |
T12I |
probably damaging |
Het |
Ccnf |
G |
A |
17: 24,443,986 (GRCm39) |
S594L |
probably damaging |
Het |
Cdadc1 |
C |
T |
14: 59,811,283 (GRCm39) |
C409Y |
probably damaging |
Het |
Cdh23 |
G |
T |
10: 60,148,356 (GRCm39) |
S2670R |
probably damaging |
Het |
Cdh8 |
T |
A |
8: 100,006,306 (GRCm39) |
K94* |
probably null |
Het |
Cdhr2 |
A |
T |
13: 54,865,505 (GRCm39) |
Y193F |
probably damaging |
Het |
Cdon |
T |
A |
9: 35,365,711 (GRCm39) |
Y153* |
probably null |
Het |
Chd1 |
G |
A |
17: 15,953,303 (GRCm39) |
G413R |
probably damaging |
Het |
Cit |
A |
T |
5: 116,125,060 (GRCm39) |
T1582S |
probably benign |
Het |
Clec4a3 |
T |
C |
6: 122,941,299 (GRCm39) |
L98P |
probably benign |
Het |
Cpa4 |
T |
A |
6: 30,583,644 (GRCm39) |
D253E |
probably damaging |
Het |
Cyp2c40 |
T |
A |
19: 39,795,612 (GRCm39) |
N189I |
possibly damaging |
Het |
Daam2 |
G |
T |
17: 49,797,050 (GRCm39) |
A245E |
probably benign |
Het |
Dennd5b |
A |
G |
6: 148,970,156 (GRCm39) |
F121S |
probably damaging |
Het |
Dgkd |
A |
G |
1: 87,854,671 (GRCm39) |
T658A |
probably benign |
Het |
Dmwd |
T |
A |
7: 18,814,265 (GRCm39) |
L305Q |
probably damaging |
Het |
Dnah5 |
A |
T |
15: 28,314,001 (GRCm39) |
Y1939F |
probably damaging |
Het |
Dock5 |
T |
C |
14: 68,058,776 (GRCm39) |
T512A |
probably damaging |
Het |
Dop1b |
T |
A |
16: 93,552,402 (GRCm39) |
D398E |
probably benign |
Het |
Eef1akmt4 |
A |
G |
16: 20,437,279 (GRCm39) |
H207R |
probably damaging |
Het |
Egfr |
T |
C |
11: 16,841,266 (GRCm39) |
V719A |
probably damaging |
Het |
Ep300 |
A |
T |
15: 81,470,784 (GRCm39) |
|
probably benign |
Het |
Epha4 |
A |
G |
1: 77,366,668 (GRCm39) |
|
probably null |
Het |
Erc2 |
T |
G |
14: 27,598,161 (GRCm39) |
|
probably null |
Het |
Ergic1 |
A |
T |
17: 26,857,801 (GRCm39) |
Y209F |
possibly damaging |
Het |
Fbxw28 |
A |
G |
9: 109,155,701 (GRCm39) |
I357T |
probably damaging |
Het |
Flnb |
A |
T |
14: 7,926,478 (GRCm38) |
T1841S |
probably benign |
Het |
Foxc1 |
G |
A |
13: 31,992,011 (GRCm39) |
S274N |
probably benign |
Het |
Fto |
C |
T |
8: 92,136,071 (GRCm39) |
T115M |
probably damaging |
Het |
Gm10228 |
C |
G |
16: 88,838,187 (GRCm39) |
C39S |
unknown |
Het |
Gm7334 |
T |
C |
17: 51,005,743 (GRCm39) |
F10L |
possibly damaging |
Het |
Hfm1 |
A |
G |
5: 107,029,727 (GRCm39) |
Y785H |
probably damaging |
Het |
Hivep1 |
T |
A |
13: 42,312,937 (GRCm39) |
S1726T |
probably benign |
Het |
Htt |
G |
T |
5: 35,009,534 (GRCm39) |
C1505F |
probably damaging |
Het |
Hydin |
T |
C |
8: 111,232,475 (GRCm39) |
S1665P |
possibly damaging |
Het |
Ifi209 |
T |
A |
1: 173,470,445 (GRCm39) |
N344K |
probably damaging |
Het |
Ifnar2 |
T |
C |
16: 91,196,181 (GRCm39) |
M262T |
probably benign |
Het |
Ighv7-3 |
T |
A |
12: 114,116,827 (GRCm39) |
S112C |
probably damaging |
Het |
Igkv4-86 |
A |
G |
6: 68,887,563 (GRCm39) |
S59P |
probably benign |
Het |
Iglv1 |
A |
G |
16: 18,904,239 (GRCm39) |
|
probably benign |
Het |
Ipo7 |
T |
A |
7: 109,652,006 (GRCm39) |
D928E |
possibly damaging |
Het |
Itgae |
G |
T |
11: 73,014,095 (GRCm39) |
|
probably null |
Het |
Kbtbd12 |
T |
A |
6: 88,595,179 (GRCm39) |
Q217L |
probably benign |
Het |
Kcnma1 |
T |
A |
14: 23,350,074 (GRCm39) |
Y1155F |
possibly damaging |
Het |
Kif14 |
A |
G |
1: 136,444,121 (GRCm39) |
E1371G |
probably benign |
Het |
Lilrb4a |
A |
T |
10: 51,367,142 (GRCm39) |
Y10F |
probably benign |
Het |
Lrp2 |
A |
T |
2: 69,333,732 (GRCm39) |
V1503E |
probably damaging |
Het |
Mfsd6 |
A |
T |
1: 52,747,799 (GRCm39) |
D355E |
probably benign |
Het |
Mri1 |
T |
C |
8: 84,977,657 (GRCm39) |
H226R |
|
Het |
Mroh4 |
C |
T |
15: 74,496,554 (GRCm39) |
E278K |
probably damaging |
Het |
Muc4 |
T |
A |
16: 32,574,739 (GRCm39) |
L1063H |
probably benign |
Het |
Mzf1 |
A |
T |
7: 12,778,018 (GRCm39) |
I541N |
probably damaging |
Het |
Nlrp10 |
T |
A |
7: 108,525,033 (GRCm39) |
E149V |
probably damaging |
Het |
Notch4 |
G |
A |
17: 34,801,392 (GRCm39) |
C1080Y |
probably damaging |
Het |
Nova1 |
T |
G |
12: 46,767,481 (GRCm39) |
I147L |
unknown |
Het |
Ogdh |
A |
G |
11: 6,288,558 (GRCm39) |
M223V |
probably benign |
Het |
Or2a56 |
T |
C |
6: 42,932,723 (GRCm39) |
I97T |
probably benign |
Het |
Or2y1e |
G |
T |
11: 49,218,498 (GRCm39) |
A87S |
probably benign |
Het |
Or4n4 |
A |
T |
14: 50,518,945 (GRCm39) |
I255N |
probably damaging |
Het |
Or6c66b |
G |
T |
10: 129,377,324 (GRCm39) |
R306L |
probably benign |
Het |
P3h3 |
T |
C |
6: 124,831,395 (GRCm39) |
Q330R |
probably benign |
Het |
Pcdhb10 |
A |
G |
18: 37,544,935 (GRCm39) |
T4A |
not run |
Het |
Pkd2l2 |
A |
T |
18: 34,566,340 (GRCm39) |
|
probably null |
Het |
Plekhb1 |
C |
T |
7: 100,294,870 (GRCm39) |
V168I |
probably benign |
Het |
Plxna4 |
C |
T |
6: 32,200,915 (GRCm39) |
R753H |
probably damaging |
Het |
Pramel17 |
T |
C |
4: 101,694,338 (GRCm39) |
I182V |
possibly damaging |
Het |
Prex1 |
G |
C |
2: 166,555,629 (GRCm39) |
P4A |
unknown |
Het |
Ptgdr |
A |
G |
14: 45,096,535 (GRCm39) |
V59A |
probably damaging |
Het |
Ralgapa1 |
T |
A |
12: 55,804,740 (GRCm39) |
I519F |
probably benign |
Het |
Rbpms |
A |
G |
8: 34,279,481 (GRCm39) |
I170T |
probably benign |
Het |
Sec31b |
T |
A |
19: 44,512,274 (GRCm39) |
|
probably null |
Het |
Skint11 |
A |
T |
4: 114,084,905 (GRCm39) |
Y138F |
probably benign |
Het |
Slain2 |
A |
G |
5: 73,105,953 (GRCm39) |
Y196C |
probably damaging |
Het |
Slco1b2 |
T |
A |
6: 141,621,950 (GRCm39) |
C503* |
probably null |
Het |
Slfn3 |
A |
T |
11: 83,105,614 (GRCm39) |
Y537F |
possibly damaging |
Het |
Slu7 |
T |
C |
11: 43,335,592 (GRCm39) |
Y443H |
probably damaging |
Het |
Sorl1 |
T |
A |
9: 41,955,205 (GRCm39) |
E683D |
probably damaging |
Het |
Sos1 |
T |
A |
17: 80,721,142 (GRCm39) |
I893L |
probably benign |
Het |
St8sia2 |
T |
A |
7: 73,593,069 (GRCm39) |
Y329F |
probably damaging |
Het |
Stra6l |
C |
A |
4: 45,869,570 (GRCm39) |
S212* |
probably null |
Het |
Syne3 |
C |
T |
12: 104,963,754 (GRCm39) |
|
probably benign |
Het |
Tenm4 |
T |
A |
7: 96,544,899 (GRCm39) |
I2342N |
probably benign |
Het |
Tescl |
T |
A |
7: 24,032,688 (GRCm39) |
E212D |
probably benign |
Het |
Trip11 |
A |
G |
12: 101,811,114 (GRCm39) |
S1879P |
probably benign |
Het |
Ube2c |
A |
T |
2: 164,613,211 (GRCm39) |
|
probably null |
Het |
Umodl1 |
T |
A |
17: 31,205,430 (GRCm39) |
I675N |
probably benign |
Het |
Vipr2 |
T |
C |
12: 116,086,338 (GRCm39) |
F121S |
probably damaging |
Het |
Vmn1r206 |
A |
T |
13: 22,804,839 (GRCm39) |
S123T |
possibly damaging |
Het |
Vmn1r58 |
A |
G |
7: 5,413,912 (GRCm39) |
V106A |
probably damaging |
Het |
Vmn2r112 |
A |
G |
17: 22,822,099 (GRCm39) |
Y259C |
probably damaging |
Het |
Vmn2r66 |
T |
C |
7: 84,654,909 (GRCm39) |
K467E |
probably benign |
Het |
Vmn2r98 |
T |
C |
17: 19,300,797 (GRCm39) |
F600L |
probably benign |
Het |
Vps13a |
T |
A |
19: 16,723,364 (GRCm39) |
N278I |
possibly damaging |
Het |
Vwa5a |
A |
C |
9: 38,652,458 (GRCm39) |
D747A |
possibly damaging |
Het |
Xdh |
G |
A |
17: 74,241,829 (GRCm39) |
P157S |
possibly damaging |
Het |
Xrn1 |
G |
A |
9: 95,880,401 (GRCm39) |
|
probably null |
Het |
Zfp362 |
T |
A |
4: 128,680,824 (GRCm39) |
H180L |
probably benign |
Het |
Zfp560 |
A |
T |
9: 20,258,619 (GRCm39) |
W748R |
possibly damaging |
Het |
Zfp808 |
A |
T |
13: 62,320,478 (GRCm39) |
Q569L |
probably benign |
Het |
Zfp93 |
T |
A |
7: 23,974,643 (GRCm39) |
D209E |
possibly damaging |
Het |
Zftraf1 |
A |
T |
15: 76,542,747 (GRCm39) |
Y138N |
probably damaging |
Het |
|
Other mutations in Nasp |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00657:Nasp
|
APN |
4 |
116,461,416 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00780:Nasp
|
APN |
4 |
116,461,196 (GRCm39) |
nonsense |
probably null |
|
IGL00833:Nasp
|
APN |
4 |
116,459,933 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02232:Nasp
|
APN |
4 |
116,461,997 (GRCm39) |
missense |
probably damaging |
0.99 |
R0023:Nasp
|
UTSW |
4 |
116,462,968 (GRCm39) |
splice site |
probably benign |
|
R0023:Nasp
|
UTSW |
4 |
116,462,968 (GRCm39) |
splice site |
probably benign |
|
R0179:Nasp
|
UTSW |
4 |
116,459,354 (GRCm39) |
missense |
probably damaging |
1.00 |
R0385:Nasp
|
UTSW |
4 |
116,467,892 (GRCm39) |
missense |
probably benign |
0.02 |
R1707:Nasp
|
UTSW |
4 |
116,476,133 (GRCm39) |
missense |
probably damaging |
0.99 |
R1945:Nasp
|
UTSW |
4 |
116,479,965 (GRCm39) |
missense |
possibly damaging |
0.62 |
R2061:Nasp
|
UTSW |
4 |
116,468,323 (GRCm39) |
missense |
probably benign |
0.12 |
R4983:Nasp
|
UTSW |
4 |
116,459,382 (GRCm39) |
missense |
probably damaging |
0.99 |
R5064:Nasp
|
UTSW |
4 |
116,469,167 (GRCm39) |
critical splice donor site |
probably null |
|
R5687:Nasp
|
UTSW |
4 |
116,463,002 (GRCm39) |
intron |
probably benign |
|
R5713:Nasp
|
UTSW |
4 |
116,471,558 (GRCm39) |
missense |
probably benign |
0.34 |
R5839:Nasp
|
UTSW |
4 |
116,459,288 (GRCm39) |
critical splice donor site |
probably null |
|
R6145:Nasp
|
UTSW |
4 |
116,468,274 (GRCm39) |
missense |
probably benign |
0.19 |
R6159:Nasp
|
UTSW |
4 |
116,461,086 (GRCm39) |
splice site |
probably null |
|
R6234:Nasp
|
UTSW |
4 |
116,479,979 (GRCm39) |
missense |
possibly damaging |
0.51 |
R6286:Nasp
|
UTSW |
4 |
116,461,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R6483:Nasp
|
UTSW |
4 |
116,476,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R6899:Nasp
|
UTSW |
4 |
116,461,530 (GRCm39) |
missense |
probably damaging |
1.00 |
R7276:Nasp
|
UTSW |
4 |
116,471,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R7412:Nasp
|
UTSW |
4 |
116,467,785 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8166:Nasp
|
UTSW |
4 |
116,468,112 (GRCm39) |
missense |
probably benign |
0.38 |
R8692:Nasp
|
UTSW |
4 |
116,469,280 (GRCm39) |
critical splice acceptor site |
probably null |
|
R9093:Nasp
|
UTSW |
4 |
116,468,017 (GRCm39) |
missense |
probably benign |
0.06 |
R9175:Nasp
|
UTSW |
4 |
116,471,576 (GRCm39) |
missense |
probably damaging |
0.98 |
|