Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2ml1 |
G |
A |
6: 128,523,292 (GRCm39) |
Q1215* |
probably null |
Het |
Aldh2 |
C |
T |
5: 121,718,712 (GRCm39) |
G64R |
probably damaging |
Het |
Atp11a |
G |
A |
8: 12,911,939 (GRCm39) |
|
probably benign |
Het |
Bcl11b |
T |
C |
12: 107,955,993 (GRCm39) |
D52G |
probably damaging |
Het |
Bltp1 |
A |
G |
3: 37,065,715 (GRCm39) |
|
probably null |
Het |
Capg |
T |
A |
6: 72,532,537 (GRCm39) |
I34K |
possibly damaging |
Het |
Card11 |
T |
A |
5: 140,899,064 (GRCm39) |
I37F |
probably damaging |
Het |
Col27a1 |
G |
T |
4: 63,235,740 (GRCm39) |
R724L |
unknown |
Het |
Cryl1 |
T |
C |
14: 57,620,224 (GRCm39) |
E47G |
probably damaging |
Het |
Dgkb |
A |
T |
12: 38,150,424 (GRCm39) |
D70V |
possibly damaging |
Het |
Dscam |
T |
C |
16: 96,394,455 (GRCm39) |
E1949G |
probably damaging |
Het |
Dscam |
A |
G |
16: 96,449,437 (GRCm39) |
V1387A |
probably damaging |
Het |
Exph5 |
G |
A |
9: 53,286,617 (GRCm39) |
V1233M |
possibly damaging |
Het |
Fat3 |
A |
T |
9: 16,286,940 (GRCm39) |
V861E |
probably damaging |
Het |
Fgfr4 |
T |
G |
13: 55,304,711 (GRCm39) |
D184E |
possibly damaging |
Het |
Fkbp14 |
G |
T |
6: 54,562,837 (GRCm39) |
S49* |
probably null |
Het |
Gk2 |
T |
C |
5: 97,603,588 (GRCm39) |
I417V |
probably benign |
Het |
Kmt2e |
TGCCGCCGCCGCCGCCACCGCCGCCGCCGC |
TGCCGCCGCCGCCGCCGCCACCGCCGCCGCCGC |
5: 23,704,474 (GRCm39) |
|
probably benign |
Het |
Malrd1 |
C |
T |
2: 16,155,567 (GRCm39) |
P1992L |
unknown |
Het |
Mapk6 |
A |
T |
9: 75,302,830 (GRCm39) |
I221N |
probably damaging |
Het |
Mup9 |
A |
G |
4: 60,377,354 (GRCm39) |
V65A |
possibly damaging |
Het |
Myo15b |
A |
G |
11: 115,775,923 (GRCm39) |
D805G |
probably damaging |
Het |
Nup50l |
T |
C |
6: 96,142,096 (GRCm39) |
E316G |
possibly damaging |
Het |
Or52a5b |
A |
G |
7: 103,417,346 (GRCm39) |
I86T |
possibly damaging |
Het |
Or8k35 |
A |
T |
2: 86,424,283 (GRCm39) |
D296E |
probably benign |
Het |
Otof |
T |
A |
5: 30,532,978 (GRCm39) |
H1588L |
probably damaging |
Het |
Pakap |
A |
G |
4: 57,855,880 (GRCm39) |
D403G |
possibly damaging |
Het |
Pde4a |
A |
G |
9: 21,103,886 (GRCm39) |
K145R |
probably benign |
Het |
Pik3ap1 |
A |
T |
19: 41,310,065 (GRCm39) |
D418E |
probably benign |
Het |
Pilrb2 |
C |
A |
5: 137,866,852 (GRCm39) |
R217M |
possibly damaging |
Het |
Plcb2 |
T |
C |
2: 118,549,922 (GRCm39) |
N232S |
probably damaging |
Het |
Ppargc1b |
C |
A |
18: 61,440,747 (GRCm39) |
G724W |
probably damaging |
Het |
Ppp2r5d |
A |
G |
17: 47,015,782 (GRCm39) |
S2P |
probably benign |
Het |
Prr5l |
T |
G |
2: 101,547,769 (GRCm39) |
N252T |
probably benign |
Het |
Rbmyf5 |
A |
G |
Y: 3,298,867 (GRCm39) |
Y206H |
possibly damaging |
Homo |
Rilp |
A |
T |
11: 75,403,601 (GRCm39) |
K348* |
probably null |
Het |
Slc17a7 |
A |
G |
7: 44,824,299 (GRCm39) |
E505G |
possibly damaging |
Het |
Slc6a21 |
T |
A |
7: 44,929,309 (GRCm39) |
M1K |
probably null |
Het |
Sorcs1 |
T |
C |
19: 50,666,606 (GRCm39) |
T101A |
probably benign |
Het |
Sorl1 |
A |
T |
9: 42,010,559 (GRCm39) |
V137E |
probably damaging |
Het |
Stam2 |
T |
C |
2: 52,597,993 (GRCm39) |
I270V |
probably benign |
Het |
Synj2 |
G |
A |
17: 6,040,565 (GRCm39) |
A214T |
probably benign |
Het |
Tars3 |
G |
T |
7: 65,312,051 (GRCm39) |
C321F |
probably damaging |
Het |
Tcea1 |
T |
A |
1: 4,962,268 (GRCm39) |
D229E |
probably benign |
Het |
Tdrd9 |
C |
T |
12: 111,993,547 (GRCm39) |
R692W |
probably benign |
Het |
Tkfc |
T |
C |
19: 10,571,888 (GRCm39) |
T383A |
probably benign |
Het |
Traf1 |
T |
C |
2: 34,846,287 (GRCm39) |
D43G |
probably benign |
Het |
Tubgcp6 |
C |
T |
15: 89,007,080 (GRCm39) |
|
probably benign |
Het |
Vit |
A |
T |
17: 78,886,828 (GRCm39) |
Y152F |
probably damaging |
Het |
Vmn1r66 |
A |
T |
7: 10,008,412 (GRCm39) |
M207K |
possibly damaging |
Het |
|
Other mutations in Ginm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00272:Ginm1
|
APN |
10 |
7,668,460 (GRCm39) |
unclassified |
probably benign |
|
IGL02474:Ginm1
|
APN |
10 |
7,653,532 (GRCm39) |
splice site |
probably benign |
|
IGL02606:Ginm1
|
APN |
10 |
7,646,163 (GRCm39) |
missense |
probably damaging |
0.98 |
Juniper
|
UTSW |
10 |
7,655,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R0010:Ginm1
|
UTSW |
10 |
7,651,138 (GRCm39) |
splice site |
probably benign |
|
R0010:Ginm1
|
UTSW |
10 |
7,651,138 (GRCm39) |
splice site |
probably benign |
|
R0052:Ginm1
|
UTSW |
10 |
7,655,070 (GRCm39) |
missense |
possibly damaging |
0.92 |
R0052:Ginm1
|
UTSW |
10 |
7,655,070 (GRCm39) |
missense |
possibly damaging |
0.92 |
R1901:Ginm1
|
UTSW |
10 |
7,650,980 (GRCm39) |
critical splice donor site |
probably null |
|
R2106:Ginm1
|
UTSW |
10 |
7,651,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R5374:Ginm1
|
UTSW |
10 |
7,655,078 (GRCm39) |
missense |
probably damaging |
0.99 |
R5929:Ginm1
|
UTSW |
10 |
7,649,814 (GRCm39) |
missense |
probably benign |
0.16 |
R6062:Ginm1
|
UTSW |
10 |
7,651,097 (GRCm39) |
missense |
probably benign |
0.00 |
R6102:Ginm1
|
UTSW |
10 |
7,644,260 (GRCm39) |
missense |
probably benign |
0.00 |
R7326:Ginm1
|
UTSW |
10 |
7,653,614 (GRCm39) |
nonsense |
probably null |
|
R7417:Ginm1
|
UTSW |
10 |
7,649,844 (GRCm39) |
missense |
probably damaging |
0.99 |
R7663:Ginm1
|
UTSW |
10 |
7,651,126 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7757:Ginm1
|
UTSW |
10 |
7,655,119 (GRCm39) |
missense |
probably damaging |
1.00 |
R8237:Ginm1
|
UTSW |
10 |
7,668,419 (GRCm39) |
missense |
unknown |
|
R8437:Ginm1
|
UTSW |
10 |
7,646,130 (GRCm39) |
missense |
probably benign |
|
R9004:Ginm1
|
UTSW |
10 |
7,651,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R9239:Ginm1
|
UTSW |
10 |
7,649,825 (GRCm39) |
missense |
possibly damaging |
0.93 |
|