Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
T |
C |
7: 119,877,472 (GRCm39) |
L1040P |
possibly damaging |
Het |
Acot11 |
C |
A |
4: 106,612,502 (GRCm39) |
|
probably null |
Het |
Aldoart2 |
C |
A |
12: 55,612,899 (GRCm39) |
Q275K |
probably damaging |
Het |
Auts2 |
T |
C |
5: 131,501,288 (GRCm39) |
T42A |
probably damaging |
Het |
Bora |
C |
T |
14: 99,299,003 (GRCm39) |
L187F |
probably damaging |
Het |
Cbln4 |
A |
G |
2: 171,884,059 (GRCm39) |
S54P |
possibly damaging |
Het |
Celsr3 |
T |
A |
9: 108,721,140 (GRCm39) |
L2661Q |
probably damaging |
Het |
Cfap65 |
T |
C |
1: 74,946,772 (GRCm39) |
T1313A |
probably damaging |
Het |
Dbndd2 |
C |
A |
2: 164,332,225 (GRCm39) |
|
probably benign |
Het |
Dennd4a |
A |
G |
9: 64,746,126 (GRCm39) |
D4G |
possibly damaging |
Het |
Dmxl1 |
T |
A |
18: 50,090,348 (GRCm39) |
|
probably benign |
Het |
Dnah7b |
T |
C |
1: 46,240,478 (GRCm39) |
C1532R |
probably damaging |
Het |
Erbb3 |
A |
T |
10: 128,412,816 (GRCm39) |
H591Q |
probably benign |
Het |
Exosc4 |
T |
C |
15: 76,213,770 (GRCm39) |
L198P |
probably damaging |
Het |
F2r |
A |
T |
13: 95,754,837 (GRCm39) |
C16S |
possibly damaging |
Het |
Gtf2h4 |
A |
T |
17: 35,981,125 (GRCm39) |
I234N |
possibly damaging |
Het |
Ift27 |
A |
T |
15: 78,049,448 (GRCm39) |
V84D |
probably damaging |
Het |
Ints10 |
C |
T |
8: 69,263,256 (GRCm39) |
A389V |
probably benign |
Het |
Irs1 |
TGGGGTGGACATCGAACTGAAGGAG |
TG |
1: 82,265,453 (GRCm39) |
913 |
probably null |
Het |
Klrc2 |
T |
A |
6: 129,637,471 (GRCm39) |
T17S |
possibly damaging |
Het |
Matr3 |
T |
A |
18: 35,705,428 (GRCm39) |
S118T |
probably damaging |
Het |
Msh3 |
A |
G |
13: 92,402,549 (GRCm39) |
|
probably benign |
Het |
Myo5c |
A |
G |
9: 75,191,434 (GRCm39) |
M1103V |
probably benign |
Het |
Niban2 |
C |
A |
2: 32,812,590 (GRCm39) |
Y446* |
probably null |
Het |
Or2y1e |
T |
A |
11: 49,219,124 (GRCm39) |
D295E |
probably benign |
Het |
Or5e1 |
T |
C |
7: 108,354,612 (GRCm39) |
L183P |
probably damaging |
Het |
Or6z3 |
A |
T |
7: 6,463,753 (GRCm39) |
M82L |
probably benign |
Het |
Osbpl3 |
A |
T |
6: 50,329,764 (GRCm39) |
D88E |
possibly damaging |
Het |
Pou1f1 |
C |
T |
16: 65,328,728 (GRCm39) |
T149I |
probably damaging |
Het |
Ppp1r12b |
G |
T |
1: 134,883,471 (GRCm39) |
A17E |
probably benign |
Het |
Pstpip2 |
T |
A |
18: 77,962,032 (GRCm39) |
Y267* |
probably null |
Het |
Rcor1 |
A |
G |
12: 111,063,986 (GRCm39) |
D95G |
probably damaging |
Het |
Rttn |
T |
C |
18: 89,119,809 (GRCm39) |
L1748P |
probably damaging |
Het |
Slco2a1 |
A |
G |
9: 102,963,031 (GRCm39) |
K629E |
possibly damaging |
Het |
Smarcc1 |
A |
G |
9: 109,964,696 (GRCm39) |
|
probably benign |
Het |
Son |
A |
G |
16: 91,472,397 (GRCm39) |
K360E |
probably benign |
Het |
Stab1 |
A |
T |
14: 30,865,629 (GRCm39) |
M1753K |
probably benign |
Het |
Syne2 |
A |
G |
12: 76,026,593 (GRCm39) |
I3474V |
probably damaging |
Het |
Tmem63c |
A |
T |
12: 87,133,192 (GRCm39) |
T736S |
possibly damaging |
Het |
Tmpo |
G |
A |
10: 90,998,503 (GRCm39) |
P428L |
possibly damaging |
Het |
Tmprss11a |
G |
T |
5: 86,570,432 (GRCm39) |
Q176K |
probably damaging |
Het |
Trappc4 |
A |
G |
9: 44,315,322 (GRCm39) |
S219P |
probably damaging |
Het |
Vmn2r117 |
G |
T |
17: 23,696,859 (GRCm39) |
P183T |
probably damaging |
Het |
Vmn2r54 |
C |
T |
7: 12,363,598 (GRCm39) |
V432I |
probably benign |
Het |
Vtcn1 |
G |
A |
3: 100,799,909 (GRCm39) |
G257R |
probably benign |
Het |
Yipf1 |
T |
A |
4: 107,202,288 (GRCm39) |
M217K |
possibly damaging |
Het |
Zfc3h1 |
T |
C |
10: 115,236,647 (GRCm39) |
S374P |
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,577,828 (GRCm39) |
H1095R |
probably benign |
Het |
Zfp661 |
A |
T |
2: 127,420,564 (GRCm39) |
H78Q |
probably benign |
Het |
Zfp957 |
T |
C |
14: 79,450,849 (GRCm39) |
T317A |
unknown |
Het |
Zfyve9 |
T |
A |
4: 108,584,688 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Mfsd6l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00503:Mfsd6l
|
APN |
11 |
68,447,299 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02292:Mfsd6l
|
APN |
11 |
68,448,576 (GRCm39) |
missense |
probably benign |
0.00 |
R0086:Mfsd6l
|
UTSW |
11 |
68,447,391 (GRCm39) |
missense |
probably benign |
0.26 |
R0180:Mfsd6l
|
UTSW |
11 |
68,447,371 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1547:Mfsd6l
|
UTSW |
11 |
68,447,434 (GRCm39) |
missense |
probably damaging |
0.98 |
R4831:Mfsd6l
|
UTSW |
11 |
68,447,331 (GRCm39) |
missense |
probably benign |
0.00 |
R5237:Mfsd6l
|
UTSW |
11 |
68,448,096 (GRCm39) |
missense |
probably benign |
0.26 |
R5244:Mfsd6l
|
UTSW |
11 |
68,448,001 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5867:Mfsd6l
|
UTSW |
11 |
68,448,036 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5961:Mfsd6l
|
UTSW |
11 |
68,447,368 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7337:Mfsd6l
|
UTSW |
11 |
68,448,109 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7343:Mfsd6l
|
UTSW |
11 |
68,447,874 (GRCm39) |
missense |
possibly damaging |
0.74 |
R7526:Mfsd6l
|
UTSW |
11 |
68,448,864 (GRCm39) |
missense |
probably damaging |
1.00 |
R7686:Mfsd6l
|
UTSW |
11 |
68,448,052 (GRCm39) |
missense |
probably benign |
0.01 |
R7715:Mfsd6l
|
UTSW |
11 |
68,448,376 (GRCm39) |
missense |
probably damaging |
1.00 |
R8555:Mfsd6l
|
UTSW |
11 |
68,447,898 (GRCm39) |
missense |
probably benign |
0.05 |
R9015:Mfsd6l
|
UTSW |
11 |
68,447,536 (GRCm39) |
missense |
probably benign |
0.00 |
Z1177:Mfsd6l
|
UTSW |
11 |
68,448,540 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Mfsd6l
|
UTSW |
11 |
68,447,808 (GRCm39) |
missense |
possibly damaging |
0.80 |
|