Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamtsl5 |
A |
G |
10: 80,177,747 (GRCm39) |
V305A |
possibly damaging |
Het |
Adgrl4 |
A |
G |
3: 151,198,012 (GRCm39) |
T91A |
probably benign |
Het |
Ano6 |
A |
G |
15: 95,865,595 (GRCm39) |
I860V |
probably benign |
Het |
B3galnt1 |
A |
G |
3: 69,482,866 (GRCm39) |
S132P |
probably damaging |
Het |
Bltp1 |
T |
C |
3: 37,062,592 (GRCm39) |
I3368T |
probably damaging |
Het |
Btbd10 |
A |
T |
7: 112,946,266 (GRCm39) |
V33E |
probably benign |
Het |
Cacna1g |
A |
T |
11: 94,330,548 (GRCm39) |
V989D |
probably damaging |
Het |
Celsr3 |
A |
G |
9: 108,712,989 (GRCm39) |
D1807G |
probably benign |
Het |
Chd6 |
A |
G |
2: 160,854,987 (GRCm39) |
M807T |
probably damaging |
Het |
Cpxm2 |
T |
C |
7: 131,672,589 (GRCm39) |
D320G |
probably damaging |
Het |
Cryzl1 |
A |
C |
16: 91,489,413 (GRCm39) |
|
probably null |
Het |
Dcbld2 |
A |
T |
16: 58,253,736 (GRCm39) |
K158* |
probably null |
Het |
Depdc5 |
A |
G |
5: 33,069,575 (GRCm39) |
N437S |
probably benign |
Het |
Dock7 |
G |
A |
4: 98,855,464 (GRCm39) |
S1496L |
probably benign |
Het |
Eea1 |
T |
G |
10: 95,864,274 (GRCm39) |
I931R |
probably benign |
Het |
Eif2ak4 |
C |
A |
2: 118,266,722 (GRCm39) |
L714I |
probably damaging |
Het |
Enpep |
A |
G |
3: 129,125,509 (GRCm39) |
|
probably null |
Het |
Fam83b |
T |
A |
9: 76,409,413 (GRCm39) |
K238* |
probably null |
Het |
Fam83f |
A |
G |
15: 80,576,312 (GRCm39) |
Y321C |
possibly damaging |
Het |
Fanci |
A |
G |
7: 79,067,687 (GRCm39) |
I42V |
probably benign |
Het |
Flg2 |
A |
T |
3: 93,121,728 (GRCm39) |
R1299S |
unknown |
Het |
Gak |
G |
T |
5: 108,771,202 (GRCm39) |
C102* |
probably null |
Het |
Gcnt7 |
A |
G |
2: 172,295,993 (GRCm39) |
L277P |
probably damaging |
Het |
Gucy2d |
A |
G |
7: 98,099,168 (GRCm39) |
E329G |
probably benign |
Het |
Hacd1 |
T |
C |
2: 14,040,755 (GRCm39) |
I167V |
probably damaging |
Het |
Hdlbp |
T |
A |
1: 93,345,389 (GRCm39) |
D662V |
possibly damaging |
Het |
Hspa4 |
A |
T |
11: 53,155,883 (GRCm39) |
V674E |
probably benign |
Het |
Hunk |
A |
G |
16: 90,290,320 (GRCm39) |
Q442R |
possibly damaging |
Het |
Lce1j |
A |
T |
3: 92,696,729 (GRCm39) |
C16* |
probably null |
Het |
Lrat |
A |
T |
3: 82,810,799 (GRCm39) |
M74K |
probably damaging |
Het |
Lrig2 |
G |
A |
3: 104,374,509 (GRCm39) |
R191C |
probably damaging |
Het |
Lrrc37a |
A |
C |
11: 103,351,666 (GRCm39) |
F2558L |
unknown |
Het |
Mctp1 |
T |
A |
13: 76,879,930 (GRCm39) |
|
probably null |
Het |
Mecom |
T |
A |
3: 30,194,535 (GRCm39) |
|
probably benign |
Het |
Ms4a15 |
T |
G |
19: 10,970,534 (GRCm39) |
E3A |
probably benign |
Het |
Myo1d |
T |
C |
11: 80,448,300 (GRCm39) |
I942V |
probably benign |
Het |
Neu2 |
A |
G |
1: 87,524,600 (GRCm39) |
Y195C |
probably damaging |
Het |
Nipa1 |
A |
T |
7: 55,669,252 (GRCm39) |
V22E |
probably benign |
Het |
Or4n4b |
A |
T |
14: 50,535,924 (GRCm39) |
L281I |
probably benign |
Het |
Or6c35 |
T |
C |
10: 129,169,580 (GRCm39) |
S277P |
possibly damaging |
Het |
Or8k25 |
T |
A |
2: 86,244,381 (GRCm39) |
N5I |
probably damaging |
Het |
Pik3r4 |
A |
G |
9: 105,562,389 (GRCm39) |
T1223A |
possibly damaging |
Het |
Ppl |
T |
C |
16: 4,910,305 (GRCm39) |
D811G |
probably damaging |
Het |
Prep |
T |
A |
10: 44,991,203 (GRCm39) |
Y290N |
probably damaging |
Het |
Ptk6 |
A |
T |
2: 180,840,895 (GRCm39) |
H215Q |
probably benign |
Het |
Rad50 |
A |
G |
11: 53,582,971 (GRCm39) |
I474T |
possibly damaging |
Het |
Rnf213 |
T |
A |
11: 119,343,513 (GRCm39) |
V3626E |
possibly damaging |
Het |
Scn4a |
C |
T |
11: 106,236,502 (GRCm39) |
V253M |
probably damaging |
Het |
Snta1 |
T |
A |
2: 154,219,069 (GRCm39) |
D422V |
probably damaging |
Het |
Spata31h1 |
G |
T |
10: 82,131,150 (GRCm39) |
T620K |
probably benign |
Het |
Stk38 |
A |
G |
17: 29,203,086 (GRCm39) |
L160P |
probably benign |
Het |
Tapbp |
T |
C |
17: 34,145,072 (GRCm39) |
F323S |
probably damaging |
Het |
Uggt1 |
C |
T |
1: 36,212,531 (GRCm39) |
R937Q |
probably benign |
Het |
Vash2 |
G |
A |
1: 190,710,484 (GRCm39) |
P57L |
probably damaging |
Het |
Vmn1r4 |
G |
A |
6: 56,933,852 (GRCm39) |
V119I |
probably benign |
Het |
Vmn2r74 |
T |
C |
7: 85,610,599 (GRCm39) |
D31G |
probably benign |
Het |
Zfp114 |
T |
C |
7: 23,877,206 (GRCm39) |
V16A |
possibly damaging |
Het |
|
Other mutations in Mgst1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02135:Mgst1
|
APN |
6 |
138,124,766 (GRCm39) |
missense |
probably damaging |
0.99 |
R0319:Mgst1
|
UTSW |
6 |
138,133,155 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0613:Mgst1
|
UTSW |
6 |
138,133,243 (GRCm39) |
missense |
probably damaging |
1.00 |
R0634:Mgst1
|
UTSW |
6 |
138,133,329 (GRCm39) |
missense |
probably damaging |
1.00 |
R0730:Mgst1
|
UTSW |
6 |
138,124,667 (GRCm39) |
missense |
probably benign |
0.03 |
R0862:Mgst1
|
UTSW |
6 |
138,124,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4447:Mgst1
|
UTSW |
6 |
138,118,662 (GRCm39) |
intron |
probably benign |
|
R4569:Mgst1
|
UTSW |
6 |
138,133,213 (GRCm39) |
missense |
probably damaging |
0.99 |
R4644:Mgst1
|
UTSW |
6 |
138,133,368 (GRCm39) |
missense |
probably damaging |
1.00 |
R4701:Mgst1
|
UTSW |
6 |
138,127,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R4930:Mgst1
|
UTSW |
6 |
138,130,507 (GRCm39) |
missense |
probably benign |
0.00 |
R5688:Mgst1
|
UTSW |
6 |
138,118,798 (GRCm39) |
intron |
probably benign |
|
R6307:Mgst1
|
UTSW |
6 |
138,127,827 (GRCm39) |
missense |
probably benign |
0.44 |
R6697:Mgst1
|
UTSW |
6 |
138,124,751 (GRCm39) |
missense |
probably damaging |
1.00 |
R6741:Mgst1
|
UTSW |
6 |
138,127,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R6755:Mgst1
|
UTSW |
6 |
138,124,770 (GRCm39) |
missense |
probably damaging |
0.99 |
R6791:Mgst1
|
UTSW |
6 |
138,118,805 (GRCm39) |
intron |
probably benign |
|
R7295:Mgst1
|
UTSW |
6 |
138,124,754 (GRCm39) |
missense |
probably benign |
0.11 |
R7440:Mgst1
|
UTSW |
6 |
138,127,842 (GRCm39) |
missense |
probably benign |
|
R7532:Mgst1
|
UTSW |
6 |
138,130,504 (GRCm39) |
missense |
probably benign |
0.29 |
R8486:Mgst1
|
UTSW |
6 |
138,120,026 (GRCm39) |
missense |
probably benign |
0.00 |
R8954:Mgst1
|
UTSW |
6 |
138,119,967 (GRCm39) |
intron |
probably benign |
|
R9326:Mgst1
|
UTSW |
6 |
138,120,023 (GRCm39) |
missense |
probably benign |
0.29 |
R9784:Mgst1
|
UTSW |
6 |
138,124,799 (GRCm39) |
missense |
probably damaging |
1.00 |
|