Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
A |
T |
14: 118,849,162 (GRCm39) |
S536R |
probably damaging |
Het |
Acacb |
G |
A |
5: 114,386,815 (GRCm39) |
|
silent |
Het |
Acsm1 |
T |
C |
7: 119,258,325 (GRCm39) |
Y473H |
probably benign |
Het |
Adam30 |
T |
A |
3: 98,070,034 (GRCm39) |
C622* |
probably null |
Het |
Adprs |
C |
T |
4: 126,210,632 (GRCm39) |
V283M |
probably damaging |
Het |
AI606181 |
G |
T |
19: 41,582,032 (GRCm39) |
R67S |
unknown |
Het |
Btbd3 |
A |
G |
2: 138,125,453 (GRCm39) |
I212M |
probably benign |
Het |
C1s1 |
C |
T |
6: 124,509,499 (GRCm39) |
|
probably null |
Het |
C7 |
T |
A |
15: 5,040,409 (GRCm39) |
T539S |
|
Het |
Cd5l |
A |
C |
3: 87,275,972 (GRCm39) |
D314A |
probably damaging |
Het |
Celsr3 |
T |
A |
9: 108,706,151 (GRCm39) |
V878E |
possibly damaging |
Het |
Cfap74 |
T |
C |
4: 155,503,121 (GRCm39) |
S38P |
|
Het |
Chst2 |
C |
T |
9: 95,288,347 (GRCm39) |
|
probably benign |
Het |
Deaf1 |
T |
C |
7: 140,904,078 (GRCm39) |
T103A |
probably damaging |
Het |
Deup1 |
T |
A |
9: 15,511,140 (GRCm39) |
D213V |
probably damaging |
Het |
Dhrs1 |
A |
G |
14: 55,978,638 (GRCm39) |
|
probably null |
Het |
Dnah7a |
A |
G |
1: 53,701,501 (GRCm39) |
V218A |
possibly damaging |
Het |
Dock7 |
G |
A |
4: 98,833,448 (GRCm39) |
Q1950* |
probably null |
Het |
Ehf |
G |
A |
2: 103,097,173 (GRCm39) |
R283W |
|
Het |
Elovl3 |
A |
T |
19: 46,123,087 (GRCm39) |
N221I |
possibly damaging |
Het |
Gm11938 |
A |
T |
11: 99,493,966 (GRCm39) |
V43E |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,630,795 (GRCm39) |
|
probably benign |
Het |
Hnf4g |
A |
G |
3: 3,708,096 (GRCm39) |
N115S |
probably benign |
Het |
Hnrnpr |
A |
T |
4: 136,056,737 (GRCm39) |
N246Y |
probably damaging |
Het |
Itpka |
A |
G |
2: 119,579,894 (GRCm39) |
E211G |
probably damaging |
Het |
Krt78 |
TAGGCACGGTCACCTGGCCTCCATATTCTCTCCCAGGCACGGTCACCTGGCCTCCACATTCTCCTCTAGGCACGGTCACCTGGCCTCCATATTCTCTCCCAGGCACGGTCACCTGGCCTCCAGATTCTCTTCCAGGCATGGTCACCTGGCCTCCATATTCTCTTCCAGGCACGGTCACCTGGCCTCCA |
TAGGCACGGTCACCTGGCCTCCACATTCTCCTCTAGGCACGGTCACCTGGCCTCCATATTCTCTCCCAGGCACGGTCACCTGGCCTCCAGATTCTCTTCCAGGCATGGTCACCTGGCCTCCATATTCTCTTCCAGGCACGGTCACCTGGCCTCCA |
15: 101,855,211 (GRCm39) |
|
probably benign |
Het |
Lcorl |
A |
T |
5: 45,931,516 (GRCm39) |
|
probably benign |
Het |
Lypd9 |
T |
A |
11: 58,338,209 (GRCm39) |
E61V |
probably benign |
Het |
Mier2 |
G |
A |
10: 79,384,274 (GRCm39) |
R166W |
probably damaging |
Het |
Mov10 |
A |
G |
3: 104,707,332 (GRCm39) |
Y606H |
probably benign |
Het |
Naa38 |
T |
G |
11: 69,287,148 (GRCm39) |
V76G |
probably damaging |
Het |
Nelfe |
C |
A |
17: 35,073,334 (GRCm39) |
P290T |
possibly damaging |
Het |
Nfil3 |
A |
T |
13: 53,121,609 (GRCm39) |
Y432N |
probably damaging |
Het |
Nipbl |
T |
C |
15: 8,356,608 (GRCm39) |
K1593E |
probably damaging |
Het |
Nlrc3 |
G |
C |
16: 3,776,807 (GRCm39) |
L56V |
possibly damaging |
Het |
Nlrp1a |
A |
T |
11: 71,014,735 (GRCm39) |
F172I |
possibly damaging |
Het |
Ntn4 |
T |
A |
10: 93,569,466 (GRCm39) |
|
probably benign |
Het |
Nudt2 |
G |
A |
4: 41,480,288 (GRCm39) |
R57Q |
probably damaging |
Het |
Obsl1 |
A |
C |
1: 75,482,027 (GRCm39) |
L281W |
probably benign |
Het |
Olfm4 |
A |
T |
14: 80,255,607 (GRCm39) |
N250I |
unknown |
Het |
Or10aa3 |
T |
A |
1: 173,878,413 (GRCm39) |
V158E |
probably damaging |
Het |
Or1x6 |
G |
A |
11: 50,938,938 (GRCm39) |
M1I |
probably null |
Het |
Or2m13 |
T |
A |
16: 19,226,173 (GRCm39) |
I198F |
probably benign |
Het |
Or2r2 |
T |
C |
6: 42,463,903 (GRCm39) |
S75G |
probably damaging |
Het |
Or5p50 |
A |
G |
7: 107,422,628 (GRCm39) |
I16T |
possibly damaging |
Het |
Pappa |
A |
T |
4: 65,074,426 (GRCm39) |
T327S |
probably damaging |
Het |
Pcdhb4 |
T |
G |
18: 37,440,714 (GRCm39) |
M8R |
probably benign |
Het |
Phf21b |
T |
A |
15: 84,671,563 (GRCm39) |
I444F |
probably damaging |
Het |
Pkd1l2 |
A |
C |
8: 117,769,037 (GRCm39) |
V1205G |
probably benign |
Het |
Plec |
T |
C |
15: 76,060,232 (GRCm39) |
Y3235C |
probably damaging |
Het |
Pnmt |
C |
T |
11: 98,278,832 (GRCm39) |
T266I |
possibly damaging |
Het |
Ppfia2 |
T |
A |
10: 106,655,220 (GRCm39) |
D262E |
probably benign |
Het |
Rabggta |
A |
T |
14: 55,955,913 (GRCm39) |
L448Q |
probably damaging |
Het |
Rap1gds1 |
C |
T |
3: 138,661,177 (GRCm39) |
R449H |
probably benign |
Het |
Rictor |
T |
A |
15: 6,801,610 (GRCm39) |
|
probably benign |
Het |
Rttn |
T |
C |
18: 89,027,556 (GRCm39) |
F557S |
probably damaging |
Het |
Ryr3 |
A |
G |
2: 112,465,748 (GRCm39) |
C4809R |
probably damaging |
Het |
Sacs |
A |
C |
14: 61,441,992 (GRCm39) |
D1346A |
probably benign |
Het |
Slain1 |
T |
A |
14: 103,923,191 (GRCm39) |
S261T |
probably damaging |
Het |
Slc22a4 |
C |
T |
11: 53,881,664 (GRCm39) |
W351* |
probably null |
Het |
Smpd3 |
C |
T |
8: 106,984,058 (GRCm39) |
G554S |
probably benign |
Het |
Spag17 |
C |
T |
3: 99,934,942 (GRCm39) |
S716F |
possibly damaging |
Het |
Spata31f1e |
C |
T |
4: 42,792,546 (GRCm39) |
G529S |
probably benign |
Het |
Spg11 |
C |
T |
2: 121,900,413 (GRCm39) |
M1546I |
probably benign |
Het |
Spmip11 |
T |
G |
15: 98,486,493 (GRCm39) |
S88A |
possibly damaging |
Het |
Stac3 |
C |
T |
10: 127,339,454 (GRCm39) |
L117F |
probably damaging |
Het |
Surf6 |
A |
G |
2: 26,782,536 (GRCm39) |
W264R |
probably damaging |
Het |
Taar7e |
T |
C |
10: 23,913,810 (GRCm39) |
V100A |
probably damaging |
Het |
Tenm3 |
T |
C |
8: 48,795,688 (GRCm39) |
H534R |
probably damaging |
Het |
Tinagl1 |
C |
A |
4: 130,067,823 (GRCm39) |
R57L |
probably damaging |
Het |
Tnfrsf11a |
G |
A |
1: 105,754,854 (GRCm39) |
A309T |
possibly damaging |
Het |
Traf6 |
A |
G |
2: 101,527,333 (GRCm39) |
Y361C |
possibly damaging |
Het |
Ttn |
A |
T |
2: 76,777,334 (GRCm39) |
|
probably benign |
Het |
Ufl1 |
A |
T |
4: 25,254,778 (GRCm39) |
Y559* |
probably null |
Het |
Upk1b |
A |
T |
16: 38,607,570 (GRCm39) |
N52K |
probably damaging |
Het |
Uqcrb |
A |
G |
13: 67,053,363 (GRCm39) |
S5P |
probably benign |
Het |
Use1 |
A |
G |
8: 71,819,688 (GRCm39) |
Y3C |
unknown |
Het |
Usp9y |
T |
A |
Y: 1,434,993 (GRCm39) |
I279L |
possibly damaging |
Het |
Vmn1r142 |
A |
G |
7: 21,862,796 (GRCm39) |
L222P |
probably damaging |
Het |
Vmn1r184 |
A |
C |
7: 25,967,177 (GRCm39) |
N308H |
probably benign |
Het |
Vmn2r14 |
C |
A |
5: 109,367,893 (GRCm39) |
M366I |
probably benign |
Het |
Vmn2r73 |
G |
T |
7: 85,521,904 (GRCm39) |
S145Y |
probably damaging |
Het |
Wdfy1 |
A |
T |
1: 79,692,697 (GRCm39) |
W207R |
probably damaging |
Het |
Zbtb38 |
A |
T |
9: 96,569,100 (GRCm39) |
N661K |
probably benign |
Het |
Zkscan3 |
G |
T |
13: 21,572,383 (GRCm39) |
H416Q |
possibly damaging |
Het |
|
Other mutations in Mgat5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00479:Mgat5
|
APN |
1 |
127,315,204 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00813:Mgat5
|
APN |
1 |
127,312,543 (GRCm39) |
missense |
probably benign |
|
IGL01795:Mgat5
|
APN |
1 |
127,396,968 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01830:Mgat5
|
APN |
1 |
127,339,869 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01879:Mgat5
|
APN |
1 |
127,325,287 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02322:Mgat5
|
APN |
1 |
127,310,722 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02621:Mgat5
|
APN |
1 |
127,325,326 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02695:Mgat5
|
APN |
1 |
127,339,868 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03142:Mgat5
|
APN |
1 |
127,339,960 (GRCm39) |
missense |
probably damaging |
1.00 |
Cowlick
|
UTSW |
1 |
127,399,301 (GRCm39) |
missense |
probably benign |
0.36 |
Curls
|
UTSW |
1 |
127,248,371 (GRCm39) |
missense |
possibly damaging |
0.77 |
R0518:Mgat5
|
UTSW |
1 |
127,312,584 (GRCm39) |
missense |
probably damaging |
1.00 |
R0594:Mgat5
|
UTSW |
1 |
127,339,985 (GRCm39) |
missense |
probably damaging |
0.96 |
R1480:Mgat5
|
UTSW |
1 |
127,387,716 (GRCm39) |
missense |
probably damaging |
1.00 |
R1501:Mgat5
|
UTSW |
1 |
127,325,378 (GRCm39) |
critical splice donor site |
probably null |
|
R1712:Mgat5
|
UTSW |
1 |
127,248,375 (GRCm39) |
missense |
probably benign |
0.34 |
R1744:Mgat5
|
UTSW |
1 |
127,407,206 (GRCm39) |
missense |
probably damaging |
1.00 |
R1862:Mgat5
|
UTSW |
1 |
127,387,706 (GRCm39) |
missense |
probably damaging |
1.00 |
R1994:Mgat5
|
UTSW |
1 |
127,387,696 (GRCm39) |
missense |
possibly damaging |
0.82 |
R2054:Mgat5
|
UTSW |
1 |
127,325,344 (GRCm39) |
missense |
probably damaging |
1.00 |
R2150:Mgat5
|
UTSW |
1 |
127,396,987 (GRCm39) |
missense |
probably damaging |
1.00 |
R2303:Mgat5
|
UTSW |
1 |
127,374,036 (GRCm39) |
missense |
probably benign |
0.00 |
R2566:Mgat5
|
UTSW |
1 |
127,234,741 (GRCm39) |
missense |
probably benign |
0.01 |
R3498:Mgat5
|
UTSW |
1 |
127,312,571 (GRCm39) |
missense |
possibly damaging |
0.55 |
R3788:Mgat5
|
UTSW |
1 |
127,294,180 (GRCm39) |
missense |
probably benign |
|
R4674:Mgat5
|
UTSW |
1 |
127,318,495 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Mgat5
|
UTSW |
1 |
127,396,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R4875:Mgat5
|
UTSW |
1 |
127,396,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R5175:Mgat5
|
UTSW |
1 |
127,387,649 (GRCm39) |
missense |
probably damaging |
0.97 |
R5310:Mgat5
|
UTSW |
1 |
127,315,251 (GRCm39) |
critical splice donor site |
probably null |
|
R5337:Mgat5
|
UTSW |
1 |
127,387,658 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5597:Mgat5
|
UTSW |
1 |
127,325,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R5599:Mgat5
|
UTSW |
1 |
127,325,303 (GRCm39) |
missense |
probably damaging |
1.00 |
R5861:Mgat5
|
UTSW |
1 |
127,315,129 (GRCm39) |
missense |
probably damaging |
1.00 |
R5956:Mgat5
|
UTSW |
1 |
127,310,676 (GRCm39) |
missense |
probably benign |
0.10 |
R6042:Mgat5
|
UTSW |
1 |
127,387,636 (GRCm39) |
missense |
probably damaging |
1.00 |
R6223:Mgat5
|
UTSW |
1 |
127,310,716 (GRCm39) |
missense |
possibly damaging |
0.86 |
R6492:Mgat5
|
UTSW |
1 |
127,399,301 (GRCm39) |
missense |
probably benign |
0.36 |
R6662:Mgat5
|
UTSW |
1 |
127,396,974 (GRCm39) |
missense |
probably damaging |
1.00 |
R6960:Mgat5
|
UTSW |
1 |
127,248,371 (GRCm39) |
missense |
possibly damaging |
0.77 |
R6981:Mgat5
|
UTSW |
1 |
127,318,588 (GRCm39) |
missense |
probably damaging |
0.98 |
R7110:Mgat5
|
UTSW |
1 |
127,310,716 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7133:Mgat5
|
UTSW |
1 |
127,292,926 (GRCm39) |
missense |
probably benign |
|
R7142:Mgat5
|
UTSW |
1 |
127,339,924 (GRCm39) |
missense |
probably damaging |
1.00 |
R7151:Mgat5
|
UTSW |
1 |
127,373,999 (GRCm39) |
missense |
probably damaging |
0.97 |
R7506:Mgat5
|
UTSW |
1 |
127,294,192 (GRCm39) |
missense |
probably benign |
0.24 |
R7790:Mgat5
|
UTSW |
1 |
127,339,941 (GRCm39) |
missense |
probably benign |
0.23 |
R7980:Mgat5
|
UTSW |
1 |
127,407,248 (GRCm39) |
missense |
probably benign |
0.13 |
R8548:Mgat5
|
UTSW |
1 |
127,248,409 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9127:Mgat5
|
UTSW |
1 |
127,294,197 (GRCm39) |
missense |
probably benign |
0.14 |
R9279:Mgat5
|
UTSW |
1 |
127,325,348 (GRCm39) |
missense |
probably damaging |
1.00 |
R9599:Mgat5
|
UTSW |
1 |
127,248,445 (GRCm39) |
missense |
probably benign |
0.02 |
X0028:Mgat5
|
UTSW |
1 |
127,294,222 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Mgat5
|
UTSW |
1 |
127,410,429 (GRCm39) |
missense |
probably damaging |
1.00 |
|