Other mutations in this stock |
Total: 96 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2310030G06Rik |
A |
G |
9: 50,651,866 (GRCm39) |
Y121H |
probably damaging |
Het |
Abca13 |
G |
T |
11: 9,349,303 (GRCm39) |
G3626W |
probably damaging |
Het |
Acvr1c |
A |
G |
2: 58,174,973 (GRCm39) |
Y192H |
probably damaging |
Het |
Afm |
A |
T |
5: 90,698,200 (GRCm39) |
D534V |
probably damaging |
Het |
Agl |
T |
C |
3: 116,565,021 (GRCm39) |
E1076G |
probably benign |
Het |
Ahcyl |
T |
C |
16: 45,974,211 (GRCm39) |
K389E |
probably benign |
Het |
Angptl3 |
A |
T |
4: 98,925,757 (GRCm39) |
H361L |
probably benign |
Het |
Apob |
T |
C |
12: 8,061,421 (GRCm39) |
F3301S |
possibly damaging |
Het |
Arhgef33 |
T |
A |
17: 80,674,730 (GRCm39) |
C376S |
possibly damaging |
Het |
Atp6v1h |
T |
A |
1: 5,165,911 (GRCm39) |
L127Q |
probably damaging |
Het |
Bcl2l1 |
G |
A |
2: 152,671,870 (GRCm39) |
S14F |
probably damaging |
Het |
Bhmt1b |
T |
G |
18: 87,775,382 (GRCm39) |
F302V |
probably damaging |
Het |
Birc6 |
G |
A |
17: 74,930,853 (GRCm39) |
A2477T |
probably benign |
Het |
Bpifb9a |
G |
A |
2: 154,112,941 (GRCm39) |
A589T |
possibly damaging |
Het |
Casp9 |
C |
A |
4: 141,533,151 (GRCm39) |
T252K |
probably benign |
Het |
Cct4 |
G |
A |
11: 22,952,922 (GRCm39) |
D533N |
probably damaging |
Het |
Clcn6 |
A |
C |
4: 148,098,358 (GRCm39) |
I555S |
probably damaging |
Het |
Col4a4 |
A |
T |
1: 82,475,543 (GRCm39) |
|
probably null |
Het |
Cyp2d10 |
A |
T |
15: 82,288,129 (GRCm39) |
|
probably null |
Het |
D930048N14Rik |
A |
G |
11: 51,545,740 (GRCm39) |
|
probably benign |
Het |
Dlg5 |
T |
C |
14: 24,204,764 (GRCm39) |
|
probably null |
Het |
Dnah11 |
T |
C |
12: 118,002,430 (GRCm39) |
E2240G |
probably damaging |
Het |
Dnmt3a |
A |
G |
12: 3,916,088 (GRCm39) |
E17G |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,384,138 (GRCm39) |
T670A |
probably benign |
Het |
Dpy19l2 |
A |
G |
9: 24,580,618 (GRCm39) |
M241T |
probably benign |
Het |
Dpy19l4 |
A |
G |
4: 11,296,034 (GRCm39) |
S212P |
probably damaging |
Het |
Ephb6 |
T |
C |
6: 41,593,040 (GRCm39) |
F426S |
probably damaging |
Het |
F5 |
A |
T |
1: 164,026,402 (GRCm39) |
D1658V |
probably benign |
Het |
Faah |
A |
T |
4: 115,856,755 (GRCm39) |
V469E |
probably damaging |
Het |
Fas |
T |
C |
19: 34,294,013 (GRCm39) |
C123R |
probably damaging |
Het |
Fhod1 |
T |
C |
8: 106,065,546 (GRCm39) |
|
probably benign |
Het |
Filip1 |
A |
G |
9: 79,805,589 (GRCm39) |
V55A |
probably benign |
Het |
Frmpd1 |
G |
A |
4: 45,273,197 (GRCm39) |
R372Q |
probably damaging |
Het |
Glyctk |
C |
T |
9: 106,034,806 (GRCm39) |
G87S |
probably damaging |
Het |
Golga3 |
T |
C |
5: 110,357,744 (GRCm39) |
L1080P |
probably damaging |
Het |
Gpr137 |
T |
C |
19: 6,915,812 (GRCm39) |
T281A |
probably benign |
Het |
Grap2 |
T |
A |
15: 80,532,612 (GRCm39) |
|
probably null |
Het |
Hlcs |
T |
C |
16: 94,069,151 (GRCm39) |
D170G |
probably damaging |
Het |
Hook1 |
A |
G |
4: 95,901,493 (GRCm39) |
T484A |
probably benign |
Het |
Hoxa5 |
T |
A |
6: 52,180,771 (GRCm39) |
H187L |
probably benign |
Het |
Inpp1 |
G |
T |
1: 52,829,253 (GRCm39) |
S255R |
probably benign |
Het |
Inpp4b |
T |
A |
8: 82,494,786 (GRCm39) |
V67E |
probably damaging |
Het |
Iqgap3 |
A |
G |
3: 87,994,616 (GRCm39) |
N105S |
probably damaging |
Het |
Kcnq5 |
A |
G |
1: 21,539,692 (GRCm39) |
|
probably null |
Het |
Klhl1 |
T |
C |
14: 96,477,649 (GRCm39) |
N473S |
probably benign |
Het |
Klk1b24 |
C |
A |
7: 43,840,785 (GRCm39) |
T71N |
probably benign |
Het |
Loxhd1 |
A |
G |
18: 77,468,269 (GRCm39) |
|
probably null |
Het |
Lrp1b |
C |
T |
2: 41,001,071 (GRCm39) |
R2165Q |
probably benign |
Het |
Lrp2bp |
A |
T |
8: 46,478,272 (GRCm39) |
Q328L |
possibly damaging |
Het |
Lrrc63 |
T |
A |
14: 75,344,829 (GRCm39) |
K419N |
possibly damaging |
Het |
Lrrc9 |
A |
G |
12: 72,547,533 (GRCm39) |
N150S |
probably benign |
Het |
Lrrn4 |
C |
A |
2: 132,713,995 (GRCm39) |
C317F |
probably damaging |
Het |
Ltbp2 |
T |
C |
12: 84,860,074 (GRCm39) |
S627G |
probably damaging |
Het |
Macf1 |
A |
T |
4: 123,386,947 (GRCm39) |
S1224T |
probably damaging |
Het |
Meis2 |
A |
C |
2: 115,889,151 (GRCm39) |
H200Q |
probably benign |
Het |
Mesd |
C |
A |
7: 83,544,790 (GRCm39) |
A80E |
probably benign |
Het |
Mroh2a |
G |
C |
1: 88,185,524 (GRCm39) |
E1510D |
probably damaging |
Het |
Myo3a |
T |
C |
2: 22,467,939 (GRCm39) |
F398L |
probably benign |
Het |
Nanp |
A |
G |
2: 150,872,749 (GRCm39) |
C60R |
probably benign |
Het |
Nectin2 |
T |
G |
7: 19,464,041 (GRCm39) |
M313L |
probably benign |
Het |
Nek4 |
C |
T |
14: 30,678,844 (GRCm39) |
H123Y |
probably damaging |
Het |
Nploc4 |
A |
G |
11: 120,299,607 (GRCm39) |
V371A |
probably damaging |
Het |
Or11g7 |
A |
G |
14: 50,690,634 (GRCm39) |
T42A |
possibly damaging |
Het |
Or13c7b |
A |
G |
4: 43,820,723 (GRCm39) |
F213L |
probably benign |
Het |
Or52n4 |
T |
C |
7: 104,294,153 (GRCm39) |
N140S |
probably benign |
Het |
Or5b109 |
T |
A |
19: 13,212,265 (GRCm39) |
V217E |
possibly damaging |
Het |
Pcdh20 |
T |
A |
14: 88,706,673 (GRCm39) |
Q209L |
probably benign |
Het |
Pcdhb20 |
G |
A |
18: 37,637,750 (GRCm39) |
R92H |
probably damaging |
Het |
Pgap1 |
T |
C |
1: 54,567,714 (GRCm39) |
H377R |
probably benign |
Het |
Phyhipl |
G |
T |
10: 70,406,798 (GRCm39) |
P52Q |
probably damaging |
Het |
Pwwp2a |
T |
A |
11: 43,596,383 (GRCm39) |
V516E |
possibly damaging |
Het |
Rack1 |
T |
C |
11: 48,692,586 (GRCm39) |
V69A |
probably damaging |
Het |
Rexo5 |
T |
A |
7: 119,400,581 (GRCm39) |
|
probably null |
Het |
Rock1 |
G |
T |
18: 10,072,863 (GRCm39) |
Q1161K |
possibly damaging |
Het |
Rps6ka2 |
T |
C |
17: 7,560,266 (GRCm39) |
L568P |
probably damaging |
Het |
Seh1l |
T |
C |
18: 67,917,054 (GRCm39) |
S78P |
probably damaging |
Het |
Serpinb3b |
A |
T |
1: 107,083,573 (GRCm39) |
|
probably null |
Het |
Setd1a |
T |
C |
7: 127,387,512 (GRCm39) |
|
probably benign |
Het |
Setx |
G |
T |
2: 29,030,401 (GRCm39) |
|
probably null |
Het |
Sfi1 |
TCGC |
TC |
11: 3,096,254 (GRCm39) |
|
probably null |
Het |
Shc2 |
G |
T |
10: 79,467,136 (GRCm39) |
R146S |
probably damaging |
Het |
Skap2 |
T |
C |
6: 51,886,348 (GRCm39) |
T5A |
probably benign |
Het |
Slc35a3 |
T |
C |
3: 116,480,983 (GRCm39) |
I93M |
probably benign |
Het |
Sohlh1 |
C |
T |
2: 25,733,359 (GRCm39) |
G295D |
probably damaging |
Het |
Sult2a8 |
A |
C |
7: 14,150,208 (GRCm39) |
C168G |
probably benign |
Het |
Tbc1d4 |
T |
C |
14: 101,685,124 (GRCm39) |
I1176V |
possibly damaging |
Het |
Thada |
A |
T |
17: 84,744,104 (GRCm39) |
F735I |
possibly damaging |
Het |
Tle1 |
A |
C |
4: 72,058,068 (GRCm39) |
H52Q |
probably damaging |
Het |
Tmem101 |
A |
T |
11: 102,044,155 (GRCm39) |
V244E |
probably damaging |
Het |
Tnfrsf26 |
C |
A |
7: 143,171,668 (GRCm39) |
C95F |
probably damaging |
Het |
Uspl1 |
T |
C |
5: 149,150,842 (GRCm39) |
S482P |
probably benign |
Het |
Vmn2r118 |
G |
T |
17: 55,917,935 (GRCm39) |
N192K |
probably benign |
Het |
Vmn2r14 |
C |
T |
5: 109,368,195 (GRCm39) |
V266I |
possibly damaging |
Het |
Vmn2r51 |
A |
G |
7: 9,834,249 (GRCm39) |
I263T |
probably damaging |
Het |
Zfp937 |
T |
A |
2: 150,080,967 (GRCm39) |
C332* |
probably null |
Het |
Zscan21 |
T |
A |
5: 138,123,470 (GRCm39) |
S50T |
probably benign |
Het |
|
Other mutations in Ass1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01413:Ass1
|
APN |
2 |
31,366,934 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02152:Ass1
|
APN |
2 |
31,382,336 (GRCm39) |
missense |
probably damaging |
1.00 |
R0008:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0083:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0084:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0085:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0087:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0183:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0220:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0254:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0302:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0346:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0440:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0472:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0605:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R0644:Ass1
|
UTSW |
2 |
31,404,831 (GRCm39) |
missense |
probably damaging |
1.00 |
R1460:Ass1
|
UTSW |
2 |
31,404,753 (GRCm39) |
missense |
probably benign |
0.37 |
R1465:Ass1
|
UTSW |
2 |
31,410,428 (GRCm39) |
makesense |
probably null |
|
R1770:Ass1
|
UTSW |
2 |
31,376,528 (GRCm39) |
missense |
probably benign |
0.29 |
R1908:Ass1
|
UTSW |
2 |
31,383,160 (GRCm39) |
nonsense |
probably null |
|
R2361:Ass1
|
UTSW |
2 |
31,410,394 (GRCm39) |
missense |
probably benign |
0.02 |
R2430:Ass1
|
UTSW |
2 |
31,391,508 (GRCm39) |
missense |
probably damaging |
1.00 |
R3816:Ass1
|
UTSW |
2 |
31,400,117 (GRCm39) |
splice site |
probably benign |
|
R4614:Ass1
|
UTSW |
2 |
31,404,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R4628:Ass1
|
UTSW |
2 |
31,371,000 (GRCm39) |
missense |
probably damaging |
1.00 |
R5007:Ass1
|
UTSW |
2 |
31,391,544 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5069:Ass1
|
UTSW |
2 |
31,400,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R5081:Ass1
|
UTSW |
2 |
31,378,665 (GRCm39) |
critical splice donor site |
probably null |
|
R5315:Ass1
|
UTSW |
2 |
31,382,341 (GRCm39) |
missense |
probably benign |
0.21 |
R5370:Ass1
|
UTSW |
2 |
31,408,745 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6259:Ass1
|
UTSW |
2 |
31,378,654 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6541:Ass1
|
UTSW |
2 |
31,400,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R6731:Ass1
|
UTSW |
2 |
31,404,796 (GRCm39) |
missense |
probably damaging |
1.00 |
R6927:Ass1
|
UTSW |
2 |
31,404,813 (GRCm39) |
missense |
probably damaging |
1.00 |
R7811:Ass1
|
UTSW |
2 |
31,404,753 (GRCm39) |
missense |
probably benign |
0.37 |
R7995:Ass1
|
UTSW |
2 |
31,376,552 (GRCm39) |
missense |
probably benign |
0.00 |
R8504:Ass1
|
UTSW |
2 |
31,391,544 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8816:Ass1
|
UTSW |
2 |
31,383,189 (GRCm39) |
critical splice donor site |
probably benign |
|
R8865:Ass1
|
UTSW |
2 |
31,410,407 (GRCm39) |
missense |
probably benign |
0.00 |
R8930:Ass1
|
UTSW |
2 |
31,382,387 (GRCm39) |
missense |
probably damaging |
1.00 |
R8932:Ass1
|
UTSW |
2 |
31,382,387 (GRCm39) |
missense |
probably damaging |
1.00 |
|