Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
G |
T |
11: 109,837,997 (GRCm39) |
S1085* |
probably null |
Het |
Akap9 |
T |
G |
5: 4,001,705 (GRCm39) |
S94A |
probably damaging |
Het |
Akap9 |
T |
A |
5: 4,115,856 (GRCm39) |
N3425K |
probably damaging |
Het |
Anapc7 |
T |
A |
5: 122,578,182 (GRCm39) |
I389N |
probably benign |
Het |
Aqp7 |
G |
A |
4: 41,045,321 (GRCm39) |
R20* |
probably null |
Het |
Cacna1h |
C |
T |
17: 25,602,457 (GRCm39) |
G1524R |
probably damaging |
Het |
Cacng4 |
T |
C |
11: 107,685,196 (GRCm39) |
Y32C |
probably damaging |
Het |
Cep120 |
A |
C |
18: 53,847,839 (GRCm39) |
S673R |
probably benign |
Het |
Cep162 |
T |
C |
9: 87,135,986 (GRCm39) |
E19G |
possibly damaging |
Het |
Cpxm2 |
C |
T |
7: 131,661,540 (GRCm39) |
V416I |
probably benign |
Het |
Dapk1 |
A |
G |
13: 60,874,424 (GRCm39) |
T427A |
probably benign |
Het |
Ecm1 |
A |
T |
3: 95,641,586 (GRCm39) |
D549E |
probably benign |
Het |
Efemp1 |
T |
A |
11: 28,871,428 (GRCm39) |
N342K |
probably damaging |
Het |
Erc2 |
T |
C |
14: 27,993,526 (GRCm39) |
|
probably benign |
Het |
Fhip2b |
C |
T |
14: 70,825,130 (GRCm39) |
R402H |
probably benign |
Het |
Galnt13 |
T |
C |
2: 54,747,926 (GRCm39) |
V269A |
probably damaging |
Het |
Gm6465 |
T |
G |
5: 11,899,020 (GRCm39) |
L171R |
probably damaging |
Het |
Gpatch1 |
A |
G |
7: 34,994,703 (GRCm39) |
V521A |
probably benign |
Het |
Heatr5b |
A |
T |
17: 79,103,914 (GRCm39) |
V1087E |
possibly damaging |
Het |
Ikzf2 |
A |
T |
1: 69,578,057 (GRCm39) |
V484D |
probably damaging |
Het |
Ints4 |
T |
A |
7: 97,190,360 (GRCm39) |
V953E |
probably damaging |
Het |
Iqce |
T |
C |
5: 140,685,480 (GRCm39) |
D15G |
possibly damaging |
Het |
Kif3a |
T |
A |
11: 53,461,368 (GRCm39) |
N4K |
possibly damaging |
Het |
Lrch4 |
A |
T |
5: 137,635,271 (GRCm39) |
I254F |
probably damaging |
Het |
Ly75 |
A |
T |
2: 60,129,516 (GRCm39) |
V1623D |
probably damaging |
Het |
Mapt |
T |
A |
11: 104,180,828 (GRCm39) |
|
probably benign |
Het |
Mast1 |
A |
T |
8: 85,639,875 (GRCm39) |
|
probably null |
Het |
Mcc |
G |
T |
18: 44,892,363 (GRCm39) |
Q84K |
probably benign |
Het |
Mtfr2 |
G |
A |
10: 20,224,149 (GRCm39) |
V28M |
probably benign |
Het |
Myh8 |
T |
A |
11: 67,180,520 (GRCm39) |
Y585* |
probably null |
Het |
Napsa |
T |
C |
7: 44,231,917 (GRCm39) |
V202A |
probably damaging |
Het |
Nsd2 |
A |
G |
5: 34,001,080 (GRCm39) |
K199R |
probably null |
Het |
Ntpcr |
C |
T |
8: 126,462,837 (GRCm39) |
A18V |
probably benign |
Het |
Or2aj4 |
A |
T |
16: 19,385,426 (GRCm39) |
M69K |
probably damaging |
Het |
Or2g25 |
G |
T |
17: 37,970,368 (GRCm39) |
N285K |
probably damaging |
Het |
Or56b35 |
T |
A |
7: 104,963,439 (GRCm39) |
I76N |
probably damaging |
Het |
Or5g9 |
G |
T |
2: 85,552,472 (GRCm39) |
C241F |
probably damaging |
Het |
Or8b9 |
A |
G |
9: 37,766,477 (GRCm39) |
D121G |
probably damaging |
Het |
Os9 |
A |
G |
10: 126,935,573 (GRCm39) |
V299A |
probably benign |
Het |
Pcdhb7 |
T |
C |
18: 37,476,915 (GRCm39) |
S684P |
possibly damaging |
Het |
Phf19 |
A |
C |
2: 34,787,067 (GRCm39) |
|
probably null |
Het |
Pkd1l3 |
G |
A |
8: 110,357,908 (GRCm39) |
|
probably null |
Het |
Pkhd1 |
A |
G |
1: 20,429,134 (GRCm39) |
I2422T |
probably damaging |
Het |
Plxna2 |
T |
A |
1: 194,326,258 (GRCm39) |
V64E |
possibly damaging |
Het |
Psme4 |
T |
A |
11: 30,762,038 (GRCm39) |
C459* |
probably null |
Het |
Ptk6 |
T |
C |
2: 180,841,433 (GRCm39) |
S159G |
probably benign |
Het |
Rhd |
T |
C |
4: 134,617,650 (GRCm39) |
I329T |
possibly damaging |
Het |
Scfd1 |
A |
G |
12: 51,492,494 (GRCm39) |
Y601C |
probably damaging |
Het |
Shroom3 |
T |
C |
5: 93,110,148 (GRCm39) |
S1753P |
probably damaging |
Het |
Slc8a1 |
A |
C |
17: 81,749,630 (GRCm39) |
|
probably null |
Het |
Spg7 |
T |
A |
8: 123,803,669 (GRCm39) |
L233Q |
probably damaging |
Het |
Strip1 |
C |
A |
3: 107,529,198 (GRCm39) |
R353L |
probably damaging |
Het |
Ubr1 |
T |
C |
2: 120,764,823 (GRCm39) |
N544D |
possibly damaging |
Het |
Ubr4 |
A |
G |
4: 139,204,469 (GRCm39) |
T4794A |
possibly damaging |
Het |
Usp24 |
A |
G |
4: 106,266,095 (GRCm39) |
|
probably benign |
Het |
Vmn1r193 |
A |
T |
13: 22,403,984 (GRCm39) |
C3S |
probably benign |
Het |
Yju2b |
G |
T |
8: 84,987,163 (GRCm39) |
|
probably benign |
Het |
Zdhhc5 |
C |
T |
2: 84,520,836 (GRCm39) |
R447H |
probably benign |
Het |
Zfp202 |
A |
G |
9: 40,123,124 (GRCm39) |
I629V |
probably benign |
Het |
Zfp462 |
T |
A |
4: 55,023,441 (GRCm39) |
C990S |
probably damaging |
Het |
|
Other mutations in Mgat4f |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01554:Mgat4f
|
APN |
1 |
134,317,696 (GRCm39) |
missense |
probably damaging |
1.00 |
P0005:Mgat4f
|
UTSW |
1 |
134,315,646 (GRCm39) |
missense |
probably benign |
0.00 |
R0498:Mgat4f
|
UTSW |
1 |
134,318,610 (GRCm39) |
missense |
possibly damaging |
0.69 |
R0563:Mgat4f
|
UTSW |
1 |
134,317,777 (GRCm39) |
missense |
probably benign |
0.00 |
R0731:Mgat4f
|
UTSW |
1 |
134,317,713 (GRCm39) |
missense |
probably benign |
|
R1558:Mgat4f
|
UTSW |
1 |
134,318,512 (GRCm39) |
missense |
probably damaging |
1.00 |
R2146:Mgat4f
|
UTSW |
1 |
134,318,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2148:Mgat4f
|
UTSW |
1 |
134,318,251 (GRCm39) |
missense |
probably damaging |
1.00 |
R2901:Mgat4f
|
UTSW |
1 |
134,318,662 (GRCm39) |
missense |
probably damaging |
0.99 |
R3897:Mgat4f
|
UTSW |
1 |
134,318,176 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4543:Mgat4f
|
UTSW |
1 |
134,317,531 (GRCm39) |
missense |
probably benign |
0.31 |
R4937:Mgat4f
|
UTSW |
1 |
134,317,714 (GRCm39) |
missense |
probably benign |
0.00 |
R5490:Mgat4f
|
UTSW |
1 |
134,317,666 (GRCm39) |
missense |
probably damaging |
1.00 |
R5684:Mgat4f
|
UTSW |
1 |
134,317,660 (GRCm39) |
missense |
probably benign |
0.04 |
R5823:Mgat4f
|
UTSW |
1 |
134,318,655 (GRCm39) |
missense |
probably damaging |
0.98 |
R6488:Mgat4f
|
UTSW |
1 |
134,318,626 (GRCm39) |
missense |
probably damaging |
1.00 |
R7177:Mgat4f
|
UTSW |
1 |
134,318,163 (GRCm39) |
missense |
probably benign |
0.08 |
R7201:Mgat4f
|
UTSW |
1 |
134,318,206 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7671:Mgat4f
|
UTSW |
1 |
134,317,800 (GRCm39) |
missense |
probably benign |
0.27 |
R7749:Mgat4f
|
UTSW |
1 |
134,318,250 (GRCm39) |
missense |
probably benign |
0.45 |
R8385:Mgat4f
|
UTSW |
1 |
134,318,376 (GRCm39) |
missense |
probably benign |
0.00 |
R9393:Mgat4f
|
UTSW |
1 |
134,318,596 (GRCm39) |
missense |
probably benign |
0.02 |
Z1177:Mgat4f
|
UTSW |
1 |
134,317,896 (GRCm39) |
missense |
probably damaging |
1.00 |
|