Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
G |
A |
11: 119,900,977 (GRCm39) |
P1083S |
probably benign |
Het |
Abcb5 |
T |
A |
12: 118,908,641 (GRCm39) |
N101I |
possibly damaging |
Het |
Adrb2 |
A |
G |
18: 62,312,624 (GRCm39) |
V67A |
possibly damaging |
Het |
Agk |
T |
A |
6: 40,345,504 (GRCm39) |
|
probably null |
Het |
Akap10 |
A |
T |
11: 61,777,603 (GRCm39) |
M586K |
probably damaging |
Het |
Akt3 |
A |
T |
1: 176,877,756 (GRCm39) |
Y337* |
probably null |
Het |
Armc1 |
A |
G |
3: 19,198,562 (GRCm39) |
F133L |
possibly damaging |
Het |
Bank1 |
T |
C |
3: 135,799,069 (GRCm39) |
E424G |
probably damaging |
Het |
Cacna1a |
A |
G |
8: 85,306,834 (GRCm39) |
E1363G |
probably damaging |
Het |
Cacna1d |
C |
A |
14: 29,764,743 (GRCm39) |
A2076S |
probably damaging |
Het |
Ccdc73 |
T |
A |
2: 104,821,869 (GRCm39) |
L606* |
probably null |
Het |
Ccdc8 |
C |
T |
7: 16,730,562 (GRCm39) |
Q684* |
probably null |
Het |
Ces1b |
T |
A |
8: 93,793,648 (GRCm39) |
K314* |
probably null |
Het |
Ces1e |
T |
A |
8: 93,941,756 (GRCm39) |
N238I |
probably damaging |
Het |
Chd4 |
A |
G |
6: 125,091,263 (GRCm39) |
N1238S |
probably benign |
Het |
Cmtr2 |
T |
A |
8: 110,949,611 (GRCm39) |
D640E |
probably damaging |
Het |
Col7a1 |
C |
T |
9: 108,787,196 (GRCm39) |
T559I |
unknown |
Het |
Comt |
T |
C |
16: 18,226,771 (GRCm39) |
K205R |
probably benign |
Het |
Dbp |
A |
T |
7: 45,357,828 (GRCm39) |
E232V |
probably damaging |
Het |
Dcbld2 |
A |
G |
16: 58,276,493 (GRCm39) |
T470A |
possibly damaging |
Het |
Eml6 |
T |
A |
11: 29,704,987 (GRCm39) |
D1519V |
probably damaging |
Het |
Evpl |
T |
A |
11: 116,128,732 (GRCm39) |
H31L |
possibly damaging |
Het |
Exoc1 |
T |
A |
5: 76,711,186 (GRCm39) |
I86N |
probably damaging |
Het |
Fat3 |
C |
T |
9: 15,826,357 (GRCm39) |
E4532K |
possibly damaging |
Het |
Fgfr3 |
T |
C |
5: 33,889,503 (GRCm39) |
S301P |
probably benign |
Het |
Gas2l1 |
C |
T |
11: 5,014,254 (GRCm39) |
V69I |
probably damaging |
Het |
Gm2042 |
T |
A |
12: 87,924,854 (GRCm39) |
I107K |
probably damaging |
Het |
Gucy1b1 |
T |
C |
3: 81,947,054 (GRCm39) |
D385G |
probably null |
Het |
Ints1 |
T |
A |
5: 139,750,930 (GRCm39) |
E824D |
probably damaging |
Het |
Itfg1 |
T |
C |
8: 86,561,707 (GRCm39) |
D142G |
probably benign |
Het |
Kcnh7 |
T |
A |
2: 62,680,721 (GRCm39) |
I289L |
probably benign |
Het |
Klf12 |
G |
A |
14: 100,347,212 (GRCm39) |
Q40* |
probably null |
Het |
Mcm4 |
A |
C |
16: 15,447,226 (GRCm39) |
N579K |
possibly damaging |
Het |
Mfsd2b |
A |
T |
12: 4,917,358 (GRCm39) |
F179I |
possibly damaging |
Het |
Mmp11 |
C |
T |
10: 75,764,208 (GRCm39) |
V86M |
probably damaging |
Het |
Mogs |
T |
C |
6: 83,092,863 (GRCm39) |
V101A |
probably damaging |
Het |
Narf |
T |
A |
11: 121,133,452 (GRCm39) |
H84Q |
probably benign |
Het |
Or5ak4 |
C |
A |
2: 85,162,142 (GRCm39) |
M33I |
probably benign |
Het |
Otog |
A |
C |
7: 45,898,495 (GRCm39) |
E204D |
probably benign |
Het |
Parp8 |
G |
A |
13: 117,031,651 (GRCm39) |
H354Y |
possibly damaging |
Het |
Pcnx1 |
C |
A |
12: 82,011,254 (GRCm39) |
D1238E |
probably damaging |
Het |
Pi4ka |
A |
G |
16: 17,194,846 (GRCm39) |
L184P |
possibly damaging |
Het |
Pkd1l3 |
C |
T |
8: 110,351,081 (GRCm39) |
T642I |
probably damaging |
Het |
Pkhd1l1 |
G |
A |
15: 44,453,059 (GRCm39) |
E3995K |
probably benign |
Het |
Prdm9 |
A |
T |
17: 15,765,218 (GRCm39) |
Y521N |
probably benign |
Het |
Prex2 |
A |
G |
1: 11,254,680 (GRCm39) |
S1105G |
probably damaging |
Het |
Prss35 |
T |
A |
9: 86,638,153 (GRCm39) |
F308I |
probably damaging |
Het |
Rab22a |
C |
T |
2: 173,542,848 (GRCm39) |
A167V |
probably benign |
Het |
Rims2 |
A |
G |
15: 39,430,369 (GRCm39) |
Q871R |
possibly damaging |
Het |
Rorb |
A |
T |
19: 18,934,611 (GRCm39) |
M253K |
probably benign |
Het |
Ryr3 |
T |
C |
2: 112,482,955 (GRCm39) |
D4269G |
probably damaging |
Het |
Snx11 |
T |
C |
11: 96,660,732 (GRCm39) |
|
probably benign |
Het |
Son |
A |
G |
16: 91,454,076 (GRCm39) |
Q941R |
probably damaging |
Het |
Sptbn2 |
G |
T |
19: 4,797,813 (GRCm39) |
R1880L |
probably benign |
Het |
Sun1 |
G |
A |
5: 139,201,014 (GRCm39) |
|
probably null |
Het |
Tprn |
A |
G |
2: 25,154,050 (GRCm39) |
R451G |
probably benign |
Het |
Trbv30 |
T |
A |
6: 41,258,311 (GRCm39) |
M1K |
probably null |
Het |
Ttn |
C |
A |
2: 76,568,565 (GRCm39) |
G25697W |
probably damaging |
Het |
Ubb |
T |
G |
11: 62,442,353 (GRCm39) |
|
probably null |
Het |
Unc13b |
C |
T |
4: 43,239,331 (GRCm39) |
R1038C |
probably damaging |
Het |
Usp7 |
T |
C |
16: 8,514,775 (GRCm39) |
M687V |
probably benign |
Het |
Zfp160 |
G |
A |
17: 21,240,996 (GRCm39) |
M21I |
probably benign |
Het |
Zfp868 |
T |
C |
8: 70,064,747 (GRCm39) |
N196S |
probably benign |
Het |
Zup1 |
A |
T |
10: 33,804,025 (GRCm39) |
I483N |
probably damaging |
Het |
|
Other mutations in Jaml |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00595:Jaml
|
APN |
9 |
45,012,287 (GRCm39) |
unclassified |
probably benign |
|
IGL00771:Jaml
|
APN |
9 |
45,005,105 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01139:Jaml
|
APN |
9 |
45,012,317 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02669:Jaml
|
APN |
9 |
45,015,489 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL03405:Jaml
|
APN |
9 |
45,005,107 (GRCm39) |
missense |
possibly damaging |
0.61 |
R0207:Jaml
|
UTSW |
9 |
45,005,065 (GRCm39) |
missense |
probably benign |
0.01 |
R1962:Jaml
|
UTSW |
9 |
45,015,495 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2119:Jaml
|
UTSW |
9 |
45,012,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R2120:Jaml
|
UTSW |
9 |
45,012,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Jaml
|
UTSW |
9 |
45,012,362 (GRCm39) |
missense |
probably damaging |
1.00 |
R2358:Jaml
|
UTSW |
9 |
45,012,361 (GRCm39) |
missense |
possibly damaging |
0.95 |
R3917:Jaml
|
UTSW |
9 |
45,012,449 (GRCm39) |
unclassified |
probably benign |
|
R4801:Jaml
|
UTSW |
9 |
45,012,362 (GRCm39) |
missense |
possibly damaging |
0.57 |
R4802:Jaml
|
UTSW |
9 |
45,012,362 (GRCm39) |
missense |
possibly damaging |
0.57 |
R5224:Jaml
|
UTSW |
9 |
45,015,564 (GRCm39) |
missense |
probably damaging |
1.00 |
R5739:Jaml
|
UTSW |
9 |
45,000,026 (GRCm39) |
missense |
probably damaging |
1.00 |
R5760:Jaml
|
UTSW |
9 |
45,009,052 (GRCm39) |
missense |
probably benign |
0.02 |
R6033:Jaml
|
UTSW |
9 |
45,000,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R6033:Jaml
|
UTSW |
9 |
45,000,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R6174:Jaml
|
UTSW |
9 |
45,000,071 (GRCm39) |
missense |
probably damaging |
1.00 |
R6245:Jaml
|
UTSW |
9 |
45,009,217 (GRCm39) |
missense |
probably damaging |
1.00 |
R6797:Jaml
|
UTSW |
9 |
45,000,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R8184:Jaml
|
UTSW |
9 |
45,000,110 (GRCm39) |
missense |
probably damaging |
1.00 |
R9642:Jaml
|
UTSW |
9 |
45,000,116 (GRCm39) |
missense |
probably damaging |
1.00 |
|