Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700019A02Rik |
A |
C |
1: 53,221,025 (GRCm39) |
D68E |
possibly damaging |
Het |
Abca3 |
T |
C |
17: 24,618,954 (GRCm39) |
V870A |
possibly damaging |
Het |
Aldh3a2 |
A |
T |
11: 61,139,885 (GRCm39) |
F416I |
probably damaging |
Het |
Armc6 |
A |
T |
8: 70,678,098 (GRCm39) |
L77Q |
possibly damaging |
Het |
Asb17 |
A |
G |
3: 153,556,570 (GRCm39) |
I226V |
probably benign |
Het |
Aspm |
A |
G |
1: 139,396,406 (GRCm39) |
I862V |
probably benign |
Het |
Atr |
T |
A |
9: 95,753,502 (GRCm39) |
D701E |
probably damaging |
Het |
Baz1b |
C |
T |
5: 135,247,097 (GRCm39) |
L849F |
possibly damaging |
Het |
Cbr1 |
T |
C |
16: 93,405,677 (GRCm39) |
V97A |
probably benign |
Het |
Cep295 |
G |
A |
9: 15,243,306 (GRCm39) |
Q1669* |
probably null |
Het |
Cfap54 |
T |
C |
10: 92,820,089 (GRCm39) |
T1242A |
possibly damaging |
Het |
Chrm3 |
T |
A |
13: 9,928,350 (GRCm39) |
T229S |
possibly damaging |
Het |
Cimip4 |
C |
A |
15: 78,270,474 (GRCm39) |
R98M |
probably damaging |
Het |
Col14a1 |
A |
C |
15: 55,251,975 (GRCm39) |
I544L |
unknown |
Het |
Crocc |
T |
C |
4: 140,752,776 (GRCm39) |
E1208G |
probably damaging |
Het |
Cyp2j8 |
A |
T |
4: 96,358,713 (GRCm39) |
|
probably benign |
Het |
Dcbld2 |
T |
C |
16: 58,285,713 (GRCm39) |
I624T |
possibly damaging |
Het |
Ddah1 |
A |
C |
3: 145,597,227 (GRCm39) |
I258L |
probably benign |
Het |
Dnah6 |
G |
A |
6: 73,026,114 (GRCm39) |
Q3460* |
probably null |
Het |
Dync2h1 |
T |
A |
9: 7,140,911 (GRCm39) |
D1372V |
probably damaging |
Het |
Egln1 |
G |
A |
8: 125,674,980 (GRCm39) |
R272* |
probably null |
Het |
Elf1 |
A |
G |
14: 79,804,620 (GRCm39) |
D95G |
possibly damaging |
Het |
Fkbp5 |
A |
G |
17: 28,621,729 (GRCm39) |
F374L |
probably damaging |
Het |
Fli1 |
T |
C |
9: 32,372,540 (GRCm39) |
|
probably benign |
Het |
Gabbr2 |
T |
C |
4: 46,846,436 (GRCm39) |
T158A |
probably damaging |
Het |
Gp2 |
A |
C |
7: 119,049,302 (GRCm39) |
Y412D |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,610,283 (GRCm39) |
V1462A |
possibly damaging |
Het |
Ide |
T |
C |
19: 37,258,160 (GRCm39) |
|
probably null |
Het |
Kalrn |
T |
C |
16: 34,134,648 (GRCm39) |
K372R |
possibly damaging |
Het |
Kcnj16 |
A |
G |
11: 110,916,067 (GRCm39) |
D243G |
possibly damaging |
Het |
Kif7 |
A |
G |
7: 79,363,905 (GRCm39) |
M1T |
probably null |
Het |
Klri2 |
A |
T |
6: 129,709,174 (GRCm39) |
L226Q |
probably damaging |
Het |
Kremen1 |
T |
C |
11: 5,165,373 (GRCm39) |
|
probably null |
Het |
Lama3 |
T |
C |
18: 12,646,788 (GRCm39) |
|
probably benign |
Het |
Lmln |
C |
A |
16: 32,908,581 (GRCm39) |
R336S |
probably benign |
Het |
Lrch4 |
T |
A |
5: 137,635,818 (GRCm39) |
D266E |
probably benign |
Het |
Lrrc28 |
C |
T |
7: 67,209,677 (GRCm39) |
R174H |
probably damaging |
Het |
Mib1 |
T |
A |
18: 10,798,474 (GRCm39) |
D778E |
probably damaging |
Het |
Msra |
T |
C |
14: 64,360,775 (GRCm39) |
I125V |
possibly damaging |
Het |
Or10c1 |
A |
G |
17: 37,522,244 (GRCm39) |
F167L |
probably damaging |
Het |
Or4k37 |
T |
A |
2: 111,158,964 (GRCm39) |
S67T |
probably damaging |
Het |
Or4p19 |
A |
T |
2: 88,242,555 (GRCm39) |
V149E |
possibly damaging |
Het |
Or52e18 |
A |
G |
7: 104,609,747 (GRCm39) |
F64S |
probably damaging |
Het |
Or6c75 |
C |
A |
10: 129,337,491 (GRCm39) |
T246N |
probably damaging |
Het |
Or8d23 |
A |
G |
9: 38,841,955 (GRCm39) |
M163V |
possibly damaging |
Het |
Pes1 |
T |
A |
11: 3,926,824 (GRCm39) |
Y369N |
probably damaging |
Het |
Pgam2 |
T |
C |
11: 5,751,773 (GRCm39) |
D221G |
possibly damaging |
Het |
Prl2c5 |
T |
C |
13: 13,365,265 (GRCm39) |
V137A |
possibly damaging |
Het |
Rasal1 |
T |
A |
5: 120,814,914 (GRCm39) |
D721E |
possibly damaging |
Het |
Sass6 |
G |
T |
3: 116,412,381 (GRCm39) |
E385D |
possibly damaging |
Het |
Sema5a |
A |
G |
15: 32,460,418 (GRCm39) |
R60G |
probably benign |
Het |
Sesn1 |
T |
C |
10: 41,779,762 (GRCm39) |
S399P |
probably damaging |
Het |
Skic2 |
G |
A |
17: 35,067,398 (GRCm39) |
L47F |
probably damaging |
Het |
Slc10a2 |
C |
T |
8: 5,141,755 (GRCm39) |
V210M |
probably damaging |
Het |
Slc8a3 |
C |
T |
12: 81,362,331 (GRCm39) |
G163S |
probably damaging |
Het |
Sorbs2 |
T |
C |
8: 46,212,234 (GRCm39) |
|
probably benign |
Het |
Speer4f1 |
T |
C |
5: 17,684,490 (GRCm39) |
W173R |
probably damaging |
Het |
Spon2 |
C |
A |
5: 33,374,108 (GRCm39) |
G92W |
probably damaging |
Het |
Sycp2 |
A |
T |
2: 178,037,009 (GRCm39) |
|
probably benign |
Het |
Tfb1m |
A |
G |
17: 3,605,241 (GRCm39) |
V84A |
probably damaging |
Het |
Tmem18 |
G |
T |
12: 30,637,198 (GRCm39) |
|
probably null |
Het |
Tom1l1 |
A |
G |
11: 90,547,210 (GRCm39) |
L290S |
possibly damaging |
Het |
Tube1 |
T |
G |
10: 39,021,711 (GRCm39) |
|
probably null |
Het |
Ugt2b35 |
T |
A |
5: 87,155,156 (GRCm39) |
|
probably null |
Het |
Unc93b1 |
T |
A |
19: 3,992,403 (GRCm39) |
Y269N |
probably benign |
Het |
Usp16 |
T |
C |
16: 87,259,030 (GRCm39) |
|
probably null |
Het |
Vmn1r38 |
A |
T |
6: 66,753,370 (GRCm39) |
S249T |
probably benign |
Het |
Vmn1r42 |
T |
A |
6: 89,821,733 (GRCm39) |
M279L |
possibly damaging |
Het |
Zdhhc23 |
T |
A |
16: 43,791,829 (GRCm39) |
T315S |
possibly damaging |
Het |
Zfp472 |
T |
C |
17: 33,194,900 (GRCm39) |
F12L |
probably benign |
Het |
Zfr2 |
T |
C |
10: 81,083,225 (GRCm39) |
S634P |
probably benign |
Het |
|
Other mutations in Cnga3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01636:Cnga3
|
APN |
1 |
37,299,874 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL01677:Cnga3
|
APN |
1 |
37,283,999 (GRCm39) |
nonsense |
probably null |
|
IGL02475:Cnga3
|
APN |
1 |
37,297,072 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03145:Cnga3
|
APN |
1 |
37,300,755 (GRCm39) |
missense |
probably damaging |
1.00 |
R1622:Cnga3
|
UTSW |
1 |
37,283,909 (GRCm39) |
splice site |
probably benign |
|
R1678:Cnga3
|
UTSW |
1 |
37,300,579 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1938:Cnga3
|
UTSW |
1 |
37,300,954 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2968:Cnga3
|
UTSW |
1 |
37,300,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R2969:Cnga3
|
UTSW |
1 |
37,300,159 (GRCm39) |
missense |
probably damaging |
1.00 |
R3406:Cnga3
|
UTSW |
1 |
37,301,146 (GRCm39) |
missense |
probably benign |
0.00 |
R3694:Cnga3
|
UTSW |
1 |
37,300,821 (GRCm39) |
missense |
probably damaging |
1.00 |
R4079:Cnga3
|
UTSW |
1 |
37,280,946 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4850:Cnga3
|
UTSW |
1 |
37,297,087 (GRCm39) |
nonsense |
probably null |
|
R4907:Cnga3
|
UTSW |
1 |
37,281,023 (GRCm39) |
critical splice donor site |
probably null |
|
R5802:Cnga3
|
UTSW |
1 |
37,300,006 (GRCm39) |
missense |
probably damaging |
0.98 |
R6135:Cnga3
|
UTSW |
1 |
37,271,318 (GRCm39) |
start gained |
probably benign |
|
R6586:Cnga3
|
UTSW |
1 |
37,300,359 (GRCm39) |
missense |
probably damaging |
0.99 |
R6997:Cnga3
|
UTSW |
1 |
37,283,965 (GRCm39) |
missense |
probably benign |
0.34 |
R7630:Cnga3
|
UTSW |
1 |
37,297,127 (GRCm39) |
missense |
probably damaging |
1.00 |
R7799:Cnga3
|
UTSW |
1 |
37,300,852 (GRCm39) |
missense |
probably damaging |
1.00 |
R8552:Cnga3
|
UTSW |
1 |
37,284,060 (GRCm39) |
missense |
probably benign |
|
R8859:Cnga3
|
UTSW |
1 |
37,299,852 (GRCm39) |
missense |
possibly damaging |
0.91 |
R8968:Cnga3
|
UTSW |
1 |
37,300,460 (GRCm39) |
missense |
probably benign |
0.23 |
|