Other mutations in this stock |
Total: 113 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
6030469F06Rik |
A |
G |
12: 31,234,914 (GRCm39) |
|
noncoding transcript |
Het |
Abca2 |
T |
G |
2: 25,337,846 (GRCm39) |
|
probably benign |
Het |
Adamts8 |
T |
A |
9: 30,862,673 (GRCm39) |
W86R |
probably benign |
Het |
Adipor2 |
A |
T |
6: 119,338,804 (GRCm39) |
W150R |
probably damaging |
Het |
Aff4 |
T |
A |
11: 53,263,351 (GRCm39) |
S124T |
probably damaging |
Het |
Ahnak |
G |
T |
19: 8,982,260 (GRCm39) |
K1181N |
probably damaging |
Het |
Ak2 |
C |
A |
4: 128,896,152 (GRCm39) |
|
probably benign |
Het |
Alkbh5 |
A |
G |
11: 60,429,873 (GRCm39) |
I209V |
probably benign |
Het |
Ankrd11 |
T |
C |
8: 123,619,463 (GRCm39) |
E1442G |
probably damaging |
Het |
Apba2 |
T |
A |
7: 64,345,297 (GRCm39) |
D162E |
probably benign |
Het |
Asic3 |
G |
A |
5: 24,618,819 (GRCm39) |
G37E |
probably damaging |
Het |
AU040320 |
A |
T |
4: 126,685,824 (GRCm39) |
K133N |
possibly damaging |
Het |
C1qtnf7 |
A |
G |
5: 43,766,481 (GRCm39) |
S34G |
probably benign |
Het |
Carf |
A |
G |
1: 60,165,065 (GRCm39) |
|
probably benign |
Het |
Ccdc148 |
T |
A |
2: 58,796,374 (GRCm39) |
R463* |
probably null |
Het |
Ccdc148 |
T |
C |
2: 58,824,455 (GRCm39) |
R329G |
probably damaging |
Het |
Ccdc185 |
A |
G |
1: 182,576,263 (GRCm39) |
I142T |
probably benign |
Het |
Cd274 |
T |
C |
19: 29,359,992 (GRCm39) |
|
probably benign |
Het |
Chrna10 |
G |
A |
7: 101,763,454 (GRCm39) |
P114S |
probably damaging |
Het |
Chst10 |
A |
G |
1: 38,904,772 (GRCm39) |
I311T |
probably damaging |
Het |
Cpne9 |
T |
C |
6: 113,271,698 (GRCm39) |
Y353H |
probably damaging |
Het |
Cubn |
G |
T |
2: 13,330,099 (GRCm39) |
A2594E |
possibly damaging |
Het |
Cyp3a13 |
T |
C |
5: 137,903,827 (GRCm39) |
N277S |
possibly damaging |
Het |
Dctn4 |
A |
G |
18: 60,671,478 (GRCm39) |
T117A |
probably damaging |
Het |
Ddah1 |
A |
T |
3: 145,559,029 (GRCm39) |
K96* |
probably null |
Het |
Ddx5 |
A |
C |
11: 106,675,711 (GRCm39) |
D326E |
probably benign |
Het |
Dlg2 |
T |
C |
7: 91,617,406 (GRCm39) |
S323P |
probably damaging |
Het |
Dnaaf1 |
C |
T |
8: 120,306,049 (GRCm39) |
H109Y |
probably damaging |
Het |
Dnah8 |
C |
A |
17: 30,914,147 (GRCm39) |
R1098S |
possibly damaging |
Het |
Dnajc13 |
T |
C |
9: 104,091,366 (GRCm39) |
T642A |
probably benign |
Het |
Dnajc18 |
A |
G |
18: 35,813,900 (GRCm39) |
S290P |
possibly damaging |
Het |
Dscam |
T |
A |
16: 96,602,453 (GRCm39) |
H663L |
possibly damaging |
Het |
Eefsec |
C |
T |
6: 88,353,182 (GRCm39) |
|
probably benign |
Het |
Emc1 |
A |
G |
4: 139,098,248 (GRCm39) |
N740S |
probably damaging |
Het |
Enpp2 |
C |
T |
15: 54,727,208 (GRCm39) |
G541D |
probably damaging |
Het |
Fam234b |
C |
T |
6: 135,205,490 (GRCm39) |
T485I |
probably benign |
Het |
Fbxl13 |
A |
T |
5: 21,688,989 (GRCm39) |
I773K |
probably benign |
Het |
Fmo4 |
A |
G |
1: 162,621,924 (GRCm39) |
F429S |
possibly damaging |
Het |
Fndc3b |
A |
G |
3: 27,494,334 (GRCm39) |
|
probably benign |
Het |
Frem1 |
T |
C |
4: 82,930,116 (GRCm39) |
S277G |
probably damaging |
Het |
Gaa |
A |
G |
11: 119,163,810 (GRCm39) |
I221V |
probably benign |
Het |
Gnptab |
A |
G |
10: 88,281,616 (GRCm39) |
|
probably benign |
Het |
Gphn |
T |
A |
12: 78,659,738 (GRCm39) |
|
probably benign |
Het |
Helz2 |
T |
C |
2: 180,881,447 (GRCm39) |
E345G |
probably damaging |
Het |
Ifna4 |
G |
T |
4: 88,760,237 (GRCm39) |
R47I |
probably damaging |
Het |
Igsf21 |
C |
A |
4: 139,761,836 (GRCm39) |
A281S |
probably benign |
Het |
Ikzf3 |
T |
A |
11: 98,407,731 (GRCm39) |
I37L |
probably benign |
Het |
Inpp5d |
A |
T |
1: 87,625,827 (GRCm39) |
|
probably benign |
Het |
Jag1 |
T |
C |
2: 136,957,568 (GRCm39) |
E48G |
probably damaging |
Het |
Jarid2 |
G |
T |
13: 45,001,857 (GRCm39) |
V57F |
probably damaging |
Het |
Kcnj4 |
A |
G |
15: 79,369,605 (GRCm39) |
L125P |
probably damaging |
Het |
Kif21b |
A |
G |
1: 136,083,891 (GRCm39) |
K713E |
possibly damaging |
Het |
Layn |
T |
A |
9: 50,968,886 (GRCm39) |
S286C |
probably damaging |
Het |
Lepr |
T |
A |
4: 101,592,878 (GRCm39) |
D164E |
probably benign |
Het |
Macroh2a1 |
A |
T |
13: 56,230,949 (GRCm39) |
S310T |
probably damaging |
Het |
Map3k1 |
T |
C |
13: 111,892,405 (GRCm39) |
H950R |
possibly damaging |
Het |
Map4k5 |
C |
A |
12: 69,852,124 (GRCm39) |
V801L |
possibly damaging |
Het |
Mapkbp1 |
T |
A |
2: 119,851,742 (GRCm39) |
S895T |
probably benign |
Het |
Mthfr |
T |
A |
4: 148,138,029 (GRCm39) |
|
probably benign |
Het |
Naca |
T |
A |
10: 127,884,157 (GRCm39) |
M2157K |
probably damaging |
Het |
Nav2 |
T |
C |
7: 49,011,952 (GRCm39) |
I61T |
probably damaging |
Het |
Nkx2-5 |
C |
A |
17: 27,058,253 (GRCm39) |
A234S |
probably benign |
Het |
Nol8 |
G |
A |
13: 49,830,264 (GRCm39) |
S1116N |
probably benign |
Het |
Nphp3 |
T |
C |
9: 103,909,078 (GRCm39) |
|
probably benign |
Het |
Nppa |
T |
C |
4: 148,085,304 (GRCm39) |
S5P |
probably benign |
Het |
Nup210 |
A |
G |
6: 91,030,551 (GRCm39) |
V123A |
possibly damaging |
Het |
Or13a21 |
G |
T |
7: 139,999,286 (GRCm39) |
N133K |
probably benign |
Het |
Osbpl11 |
A |
G |
16: 33,049,455 (GRCm39) |
K604R |
probably damaging |
Het |
Osbpl1a |
C |
T |
18: 13,047,615 (GRCm39) |
S113N |
probably benign |
Het |
P2rx4 |
C |
A |
5: 122,852,602 (GRCm39) |
P92Q |
probably damaging |
Het |
Pde9a |
A |
T |
17: 31,692,136 (GRCm39) |
Q148L |
probably benign |
Het |
Phf21b |
T |
A |
15: 84,689,160 (GRCm39) |
H122L |
probably damaging |
Het |
Pik3ca |
T |
A |
3: 32,515,990 (GRCm39) |
F977I |
probably damaging |
Het |
Pkd1l3 |
A |
G |
8: 110,363,059 (GRCm39) |
|
probably benign |
Het |
Potefam1 |
A |
G |
2: 111,055,748 (GRCm39) |
|
probably null |
Het |
Pp2d1 |
T |
G |
17: 53,823,015 (GRCm39) |
K17T |
possibly damaging |
Het |
Ppp4r2 |
A |
G |
6: 100,843,527 (GRCm39) |
E415G |
probably damaging |
Het |
Pramel19 |
T |
A |
4: 101,798,503 (GRCm39) |
L158Q |
probably damaging |
Het |
Prkg1 |
A |
G |
19: 30,556,270 (GRCm39) |
S559P |
probably damaging |
Het |
Prss45 |
A |
T |
9: 110,670,019 (GRCm39) |
Y276F |
possibly damaging |
Het |
Ptk7 |
G |
T |
17: 46,883,517 (GRCm39) |
N849K |
probably damaging |
Het |
Rnf121 |
A |
G |
7: 101,680,782 (GRCm39) |
I125T |
possibly damaging |
Het |
Rnf17 |
A |
G |
14: 56,699,368 (GRCm39) |
N502S |
probably damaging |
Het |
Sap25 |
T |
A |
5: 137,640,622 (GRCm39) |
Y167* |
probably null |
Het |
Sdk2 |
G |
A |
11: 113,720,906 (GRCm39) |
T1341I |
possibly damaging |
Het |
Sgcb |
A |
G |
5: 73,792,896 (GRCm39) |
V302A |
probably benign |
Het |
Skor1 |
T |
A |
9: 63,047,393 (GRCm39) |
M865L |
possibly damaging |
Het |
Slc25a45 |
T |
C |
19: 5,929,928 (GRCm39) |
|
probably benign |
Het |
Slc2a3 |
A |
G |
6: 122,714,269 (GRCm39) |
|
probably benign |
Het |
Slc35g1 |
C |
A |
19: 38,391,665 (GRCm39) |
L316I |
probably benign |
Het |
Slco1a8 |
C |
T |
6: 141,938,243 (GRCm39) |
W225* |
probably null |
Het |
Spint4 |
T |
A |
2: 164,540,568 (GRCm39) |
L33H |
probably damaging |
Het |
Sptlc3 |
A |
T |
2: 139,389,154 (GRCm39) |
D178V |
probably benign |
Het |
Stoml1 |
A |
G |
9: 58,167,709 (GRCm39) |
|
probably benign |
Het |
Tbc1d2 |
T |
A |
4: 46,606,491 (GRCm39) |
Y818F |
possibly damaging |
Het |
Tbc1d24 |
A |
T |
17: 24,400,197 (GRCm39) |
|
probably null |
Het |
Teddm2 |
C |
T |
1: 153,726,277 (GRCm39) |
W146* |
probably null |
Het |
Ttn |
T |
A |
2: 76,589,338 (GRCm39) |
D12948V |
probably damaging |
Het |
Txndc8 |
T |
C |
4: 58,000,274 (GRCm39) |
T102A |
probably damaging |
Het |
Uxs1 |
G |
A |
1: 43,804,076 (GRCm39) |
Q280* |
probably null |
Het |
Vmn1r167 |
T |
C |
7: 23,204,681 (GRCm39) |
T112A |
possibly damaging |
Het |
Vmn1r195 |
A |
T |
13: 22,463,348 (GRCm39) |
I273L |
probably benign |
Het |
Vmn1r28 |
T |
A |
6: 58,242,217 (GRCm39) |
M20K |
probably benign |
Het |
Vmn1r53 |
G |
A |
6: 90,200,914 (GRCm39) |
L137F |
probably benign |
Het |
Vmn2r105 |
G |
A |
17: 20,449,004 (GRCm39) |
|
probably benign |
Het |
Vps13b |
C |
T |
15: 35,709,630 (GRCm39) |
A1859V |
probably benign |
Het |
Vwa5b2 |
A |
G |
16: 20,415,019 (GRCm39) |
H347R |
probably benign |
Het |
Wnk2 |
G |
A |
13: 49,235,451 (GRCm39) |
P655S |
probably damaging |
Het |
Zan |
T |
G |
5: 137,418,191 (GRCm39) |
D2969A |
unknown |
Het |
Zbtb24 |
A |
G |
10: 41,331,075 (GRCm39) |
H334R |
probably damaging |
Het |
Zfp108 |
A |
G |
7: 23,959,973 (GRCm39) |
D188G |
probably benign |
Het |
Zfp784 |
A |
T |
7: 5,038,800 (GRCm39) |
C253S |
possibly damaging |
Het |
Zfr |
T |
G |
15: 12,146,458 (GRCm39) |
C336W |
probably damaging |
Het |
|
Other mutations in Adh1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00424:Adh1
|
APN |
3 |
137,988,260 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00510:Adh1
|
APN |
3 |
137,995,668 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01326:Adh1
|
APN |
3 |
137,992,672 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01662:Adh1
|
APN |
3 |
137,988,512 (GRCm39) |
missense |
possibly damaging |
0.96 |
IGL02090:Adh1
|
APN |
3 |
137,988,546 (GRCm39) |
missense |
possibly damaging |
0.95 |
PIT4687001:Adh1
|
UTSW |
3 |
137,995,596 (GRCm39) |
missense |
probably damaging |
1.00 |
R0413:Adh1
|
UTSW |
3 |
137,986,193 (GRCm39) |
missense |
probably benign |
0.00 |
R0882:Adh1
|
UTSW |
3 |
137,992,558 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1426:Adh1
|
UTSW |
3 |
137,992,556 (GRCm39) |
missense |
probably damaging |
1.00 |
R1464:Adh1
|
UTSW |
3 |
137,994,508 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1901:Adh1
|
UTSW |
3 |
137,994,558 (GRCm39) |
missense |
probably benign |
0.00 |
R2056:Adh1
|
UTSW |
3 |
137,992,676 (GRCm39) |
missense |
probably damaging |
1.00 |
R2095:Adh1
|
UTSW |
3 |
137,988,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R3155:Adh1
|
UTSW |
3 |
137,986,250 (GRCm39) |
missense |
probably damaging |
0.99 |
R3752:Adh1
|
UTSW |
3 |
137,994,555 (GRCm39) |
missense |
probably benign |
|
R3795:Adh1
|
UTSW |
3 |
137,985,526 (GRCm39) |
missense |
possibly damaging |
0.85 |
R4351:Adh1
|
UTSW |
3 |
137,986,258 (GRCm39) |
missense |
probably benign |
0.21 |
R4698:Adh1
|
UTSW |
3 |
137,988,274 (GRCm39) |
missense |
probably benign |
0.05 |
R4747:Adh1
|
UTSW |
3 |
137,994,642 (GRCm39) |
missense |
probably damaging |
1.00 |
R5626:Adh1
|
UTSW |
3 |
137,986,171 (GRCm39) |
missense |
probably benign |
0.04 |
R6014:Adh1
|
UTSW |
3 |
137,992,559 (GRCm39) |
missense |
probably benign |
0.00 |
R6060:Adh1
|
UTSW |
3 |
137,992,544 (GRCm39) |
missense |
probably damaging |
1.00 |
R6225:Adh1
|
UTSW |
3 |
137,995,565 (GRCm39) |
missense |
probably benign |
0.04 |
R6637:Adh1
|
UTSW |
3 |
137,988,231 (GRCm39) |
nonsense |
probably null |
|
R7129:Adh1
|
UTSW |
3 |
137,986,235 (GRCm39) |
missense |
probably damaging |
0.98 |
R7288:Adh1
|
UTSW |
3 |
137,988,493 (GRCm39) |
missense |
probably benign |
|
R7291:Adh1
|
UTSW |
3 |
137,988,569 (GRCm39) |
missense |
probably damaging |
1.00 |
R7367:Adh1
|
UTSW |
3 |
137,996,312 (GRCm39) |
missense |
probably benign |
0.04 |
R7378:Adh1
|
UTSW |
3 |
137,994,648 (GRCm39) |
splice site |
probably null |
|
R7453:Adh1
|
UTSW |
3 |
137,995,702 (GRCm39) |
critical splice donor site |
probably null |
|
R7613:Adh1
|
UTSW |
3 |
137,992,592 (GRCm39) |
nonsense |
probably null |
|
R8848:Adh1
|
UTSW |
3 |
137,986,262 (GRCm39) |
missense |
probably benign |
0.12 |
R9513:Adh1
|
UTSW |
3 |
137,988,571 (GRCm39) |
nonsense |
probably null |
|
Z1187:Adh1
|
UTSW |
3 |
137,992,544 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1190:Adh1
|
UTSW |
3 |
137,992,544 (GRCm39) |
missense |
probably damaging |
1.00 |
|