Other mutations in this stock |
Total: 88 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abhd15 |
C |
A |
11: 77,406,312 (GRCm39) |
H96Q |
possibly damaging |
Het |
Ankhd1 |
A |
G |
18: 36,788,653 (GRCm39) |
Q411R |
|
Het |
Ankrd34c |
A |
T |
9: 89,610,940 (GRCm39) |
V467E |
probably damaging |
Het |
Apobr |
A |
T |
7: 126,186,507 (GRCm39) |
R673* |
probably null |
Het |
Arhgap18 |
T |
C |
10: 26,722,107 (GRCm39) |
V98A |
possibly damaging |
Het |
Arhgap30 |
G |
T |
1: 171,235,957 (GRCm39) |
W777L |
possibly damaging |
Het |
Atp8a1 |
A |
G |
5: 67,779,977 (GRCm39) |
Y1154H |
unknown |
Het |
B3gntl1 |
A |
G |
11: 121,514,770 (GRCm39) |
F299S |
possibly damaging |
Het |
Baz2a |
C |
T |
10: 127,957,812 (GRCm39) |
T1055I |
probably benign |
Het |
Baz2b |
T |
C |
2: 59,743,331 (GRCm39) |
M1547V |
probably benign |
Het |
Bsn |
T |
C |
9: 107,993,292 (GRCm39) |
D820G |
probably damaging |
Het |
Castor1 |
T |
A |
11: 4,170,485 (GRCm39) |
N160K |
probably damaging |
Het |
Ccdc57 |
A |
G |
11: 120,812,578 (GRCm39) |
Y59H |
probably damaging |
Het |
Crim1 |
T |
A |
17: 78,651,871 (GRCm39) |
C532S |
probably damaging |
Het |
Csmd2 |
A |
C |
4: 128,200,168 (GRCm39) |
D451A |
|
Het |
Cyp2d22 |
A |
T |
15: 82,256,748 (GRCm39) |
I342K |
probably damaging |
Het |
Des |
A |
T |
1: 75,343,406 (GRCm39) |
T430S |
probably benign |
Het |
Dnah17 |
C |
T |
11: 118,016,503 (GRCm39) |
V283I |
probably benign |
Het |
Dnah9 |
C |
T |
11: 65,786,731 (GRCm39) |
G3634E |
probably benign |
Het |
Dst |
A |
G |
1: 34,228,943 (GRCm39) |
S2179G |
probably benign |
Het |
Elp1 |
C |
A |
4: 56,771,003 (GRCm39) |
R980L |
probably benign |
Het |
Esrp2 |
T |
A |
8: 106,858,775 (GRCm39) |
T621S |
possibly damaging |
Het |
Ext2 |
C |
T |
2: 93,534,836 (GRCm39) |
V643I |
probably benign |
Het |
Fastk |
G |
A |
5: 24,649,172 (GRCm39) |
P72S |
probably benign |
Het |
Fbxo28 |
A |
G |
1: 182,145,566 (GRCm39) |
I174T |
possibly damaging |
Het |
Fstl3 |
C |
T |
10: 79,614,411 (GRCm39) |
L38F |
probably damaging |
Het |
Golgb1 |
C |
T |
16: 36,739,181 (GRCm39) |
Q2548* |
probably null |
Het |
Gstm3 |
T |
C |
3: 107,874,956 (GRCm39) |
T99A |
probably benign |
Het |
H2bc15 |
A |
G |
13: 21,938,369 (GRCm39) |
D26G |
unknown |
Het |
Hadh |
T |
C |
3: 131,034,636 (GRCm39) |
N220S |
probably damaging |
Het |
Hnrnpab |
T |
C |
11: 51,497,240 (GRCm39) |
T51A |
probably benign |
Het |
Ints8 |
T |
A |
4: 11,213,811 (GRCm39) |
|
probably null |
Het |
Ipo7 |
T |
C |
7: 109,643,826 (GRCm39) |
V407A |
probably damaging |
Het |
Kics2 |
A |
T |
10: 121,586,273 (GRCm39) |
H196L |
probably damaging |
Het |
Kif20b |
T |
C |
19: 34,915,725 (GRCm39) |
S501P |
probably benign |
Het |
Krt39 |
T |
G |
11: 99,407,450 (GRCm39) |
Q348P |
probably damaging |
Het |
Lrp1b |
T |
A |
2: 40,488,456 (GRCm39) |
N4543I |
|
Het |
Macrod2 |
T |
C |
2: 141,652,534 (GRCm39) |
V199A |
probably benign |
Het |
Mast2 |
A |
G |
4: 116,167,701 (GRCm39) |
V1052A |
probably damaging |
Het |
Mfap4 |
T |
C |
11: 61,378,007 (GRCm39) |
F149S |
probably damaging |
Het |
Moap1 |
A |
G |
12: 102,708,526 (GRCm39) |
V341A |
unknown |
Het |
Mprip |
G |
T |
11: 59,628,403 (GRCm39) |
E283D |
possibly damaging |
Het |
Mrgpra2a |
A |
G |
7: 47,077,004 (GRCm39) |
F85L |
possibly damaging |
Het |
Mx1 |
T |
A |
16: 97,252,753 (GRCm39) |
|
probably null |
Het |
Ndc80 |
A |
T |
17: 71,807,294 (GRCm39) |
M554K |
probably benign |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Or52j3 |
A |
T |
7: 102,836,194 (GRCm39) |
I129F |
probably damaging |
Het |
Or5k1b |
T |
A |
16: 58,581,126 (GRCm39) |
K138* |
probably null |
Het |
Or6c38 |
T |
A |
10: 128,929,472 (GRCm39) |
I124F |
probably damaging |
Het |
Pck1 |
C |
T |
2: 172,996,569 (GRCm39) |
T161I |
probably damaging |
Het |
Pclo |
T |
A |
5: 14,726,959 (GRCm39) |
M1939K |
unknown |
Het |
Pcm1 |
T |
A |
8: 41,732,877 (GRCm39) |
N711K |
probably damaging |
Het |
Pkd2l1 |
A |
G |
19: 44,143,894 (GRCm39) |
V393A |
probably benign |
Het |
Pla2g15 |
G |
T |
8: 106,889,539 (GRCm39) |
A229S |
possibly damaging |
Het |
Plekhg1 |
G |
A |
10: 3,907,141 (GRCm39) |
R741Q |
|
Het |
Plod1 |
A |
G |
4: 148,010,626 (GRCm39) |
L275P |
possibly damaging |
Het |
Plvap |
G |
T |
8: 71,964,323 (GRCm39) |
T13K |
possibly damaging |
Het |
Plxna1 |
A |
T |
6: 89,314,320 (GRCm39) |
I707N |
probably damaging |
Het |
Pnma8b |
A |
G |
7: 16,680,843 (GRCm39) |
E609G |
probably benign |
Het |
Ptger4 |
C |
T |
15: 5,273,193 (GRCm39) |
|
probably benign |
Het |
Qars1 |
G |
T |
9: 108,386,132 (GRCm39) |
E108* |
probably null |
Het |
Rfpl4 |
C |
A |
7: 5,113,840 (GRCm39) |
D114Y |
probably damaging |
Het |
Rint1 |
A |
G |
5: 24,010,411 (GRCm39) |
T207A |
probably benign |
Het |
Rxfp1 |
A |
G |
3: 79,552,261 (GRCm39) |
I680T |
probably benign |
Het |
Skint2 |
A |
T |
4: 112,502,616 (GRCm39) |
K275N |
probably benign |
Het |
Slc29a3 |
A |
G |
10: 60,559,755 (GRCm39) |
V133A |
possibly damaging |
Het |
Slc9a2 |
A |
G |
1: 40,805,460 (GRCm39) |
K680E |
probably benign |
Het |
Smc1b |
A |
T |
15: 85,004,846 (GRCm39) |
F409L |
probably benign |
Het |
Sos2 |
A |
T |
12: 69,695,239 (GRCm39) |
M166K |
probably damaging |
Het |
Spata31h1 |
T |
C |
10: 82,123,554 (GRCm39) |
D3152G |
probably benign |
Het |
Tead1 |
A |
G |
7: 112,358,723 (GRCm39) |
I12V |
probably benign |
Het |
Tead3 |
C |
A |
17: 28,551,709 (GRCm39) |
K461N |
probably benign |
Het |
Tex12 |
C |
A |
9: 50,468,772 (GRCm39) |
A83S |
probably damaging |
Het |
Top6bl |
T |
G |
19: 4,746,068 (GRCm39) |
K199Q |
possibly damaging |
Het |
Ttc28 |
A |
G |
5: 111,325,525 (GRCm39) |
T319A |
unknown |
Het |
Ttn |
T |
C |
2: 76,728,593 (GRCm39) |
I5496V |
unknown |
Het |
Tubb4a |
T |
A |
17: 57,387,959 (GRCm39) |
I356F |
possibly damaging |
Het |
Txk |
A |
T |
5: 72,891,610 (GRCm39) |
W119R |
probably damaging |
Het |
Txnl4a |
A |
T |
18: 80,261,937 (GRCm39) |
I58F |
probably benign |
Het |
Uba6 |
A |
T |
5: 86,318,418 (GRCm39) |
Y44N |
probably damaging |
Het |
Usp40 |
T |
C |
1: 87,878,009 (GRCm39) |
T1093A |
probably benign |
Het |
Vmn1r194 |
T |
C |
13: 22,428,731 (GRCm39) |
I116T |
probably benign |
Het |
Vmn2r14 |
A |
G |
5: 109,368,176 (GRCm39) |
M272T |
possibly damaging |
Het |
Vmn2r85 |
C |
A |
10: 130,255,033 (GRCm39) |
M550I |
possibly damaging |
Het |
Vmn2r85 |
C |
A |
10: 130,261,534 (GRCm39) |
V268F |
probably damaging |
Het |
Vwa5b2 |
T |
A |
16: 20,416,890 (GRCm39) |
V529E |
probably damaging |
Het |
Zfp141 |
A |
T |
7: 42,124,821 (GRCm39) |
Y550* |
probably null |
Het |
Zik1 |
G |
A |
7: 10,224,156 (GRCm39) |
L314F |
probably damaging |
Het |
|
Other mutations in Immt |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01974:Immt
|
APN |
6 |
71,849,842 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02085:Immt
|
APN |
6 |
71,828,820 (GRCm39) |
missense |
probably benign |
0.30 |
IGL02493:Immt
|
APN |
6 |
71,821,700 (GRCm39) |
splice site |
probably benign |
|
Glut
|
UTSW |
6 |
71,838,024 (GRCm39) |
missense |
probably damaging |
1.00 |
P0045:Immt
|
UTSW |
6 |
71,845,601 (GRCm39) |
missense |
possibly damaging |
0.88 |
R0106:Immt
|
UTSW |
6 |
71,828,828 (GRCm39) |
missense |
probably benign |
0.22 |
R0106:Immt
|
UTSW |
6 |
71,828,828 (GRCm39) |
missense |
probably benign |
0.22 |
R0565:Immt
|
UTSW |
6 |
71,823,467 (GRCm39) |
splice site |
probably benign |
|
R0671:Immt
|
UTSW |
6 |
71,848,541 (GRCm39) |
missense |
possibly damaging |
0.95 |
R0676:Immt
|
UTSW |
6 |
71,828,828 (GRCm39) |
missense |
probably benign |
0.22 |
R0718:Immt
|
UTSW |
6 |
71,840,156 (GRCm39) |
missense |
probably damaging |
1.00 |
R0789:Immt
|
UTSW |
6 |
71,838,051 (GRCm39) |
missense |
probably damaging |
1.00 |
R0980:Immt
|
UTSW |
6 |
71,851,310 (GRCm39) |
missense |
probably benign |
0.19 |
R1332:Immt
|
UTSW |
6 |
71,823,256 (GRCm39) |
splice site |
probably benign |
|
R1688:Immt
|
UTSW |
6 |
71,833,995 (GRCm39) |
missense |
probably damaging |
1.00 |
R2106:Immt
|
UTSW |
6 |
71,848,499 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2149:Immt
|
UTSW |
6 |
71,821,659 (GRCm39) |
nonsense |
probably null |
|
R3706:Immt
|
UTSW |
6 |
71,839,346 (GRCm39) |
missense |
probably benign |
0.01 |
R4393:Immt
|
UTSW |
6 |
71,849,784 (GRCm39) |
missense |
probably benign |
0.04 |
R4543:Immt
|
UTSW |
6 |
71,828,762 (GRCm39) |
missense |
probably damaging |
0.97 |
R4645:Immt
|
UTSW |
6 |
71,833,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R4774:Immt
|
UTSW |
6 |
71,829,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R5535:Immt
|
UTSW |
6 |
71,829,768 (GRCm39) |
missense |
probably null |
1.00 |
R5920:Immt
|
UTSW |
6 |
71,840,180 (GRCm39) |
missense |
probably benign |
0.18 |
R7002:Immt
|
UTSW |
6 |
71,838,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R7266:Immt
|
UTSW |
6 |
71,851,689 (GRCm39) |
missense |
probably benign |
0.26 |
R7326:Immt
|
UTSW |
6 |
71,823,353 (GRCm39) |
missense |
probably damaging |
1.00 |
R7949:Immt
|
UTSW |
6 |
71,851,327 (GRCm39) |
nonsense |
probably null |
|
R8185:Immt
|
UTSW |
6 |
71,849,835 (GRCm39) |
nonsense |
probably null |
|
R8200:Immt
|
UTSW |
6 |
71,848,421 (GRCm39) |
missense |
probably damaging |
0.96 |
R8444:Immt
|
UTSW |
6 |
71,848,492 (GRCm39) |
nonsense |
probably null |
|
R8828:Immt
|
UTSW |
6 |
71,829,762 (GRCm39) |
nonsense |
probably null |
|
R9135:Immt
|
UTSW |
6 |
71,851,403 (GRCm39) |
missense |
probably damaging |
1.00 |
R9136:Immt
|
UTSW |
6 |
71,851,403 (GRCm39) |
missense |
probably damaging |
1.00 |
|