Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A830018L16Rik |
T |
G |
1: 12,021,252 (GRCm39) |
S420R |
probably damaging |
Het |
Acat2 |
C |
T |
17: 13,166,346 (GRCm39) |
D219N |
probably damaging |
Het |
Anapc10 |
G |
A |
8: 80,446,308 (GRCm39) |
R46Q |
possibly damaging |
Het |
Ankub1 |
G |
A |
3: 57,573,039 (GRCm39) |
R228* |
probably null |
Het |
Arhgap21 |
T |
C |
2: 20,917,102 (GRCm39) |
N91S |
probably benign |
Het |
Arhgap32 |
T |
A |
9: 32,162,018 (GRCm39) |
V323D |
probably benign |
Het |
Bcas1 |
C |
T |
2: 170,212,369 (GRCm39) |
|
probably null |
Het |
Cd109 |
C |
T |
9: 78,588,119 (GRCm39) |
P716S |
probably damaging |
Het |
Chd4 |
C |
T |
6: 125,078,866 (GRCm39) |
P267L |
possibly damaging |
Het |
Cpne7 |
G |
T |
8: 123,860,552 (GRCm39) |
V502F |
probably damaging |
Het |
Cracd |
G |
A |
5: 77,014,122 (GRCm39) |
|
probably null |
Het |
Dlgap4 |
C |
T |
2: 156,604,657 (GRCm39) |
A921V |
probably benign |
Het |
Faap24 |
G |
T |
7: 35,092,465 (GRCm39) |
R151S |
probably benign |
Het |
Fam98a |
A |
G |
17: 75,854,657 (GRCm39) |
S51P |
probably damaging |
Het |
Fbxl8 |
A |
G |
8: 105,994,938 (GRCm39) |
D150G |
possibly damaging |
Het |
Fut10 |
A |
G |
8: 31,749,950 (GRCm39) |
K412R |
probably benign |
Het |
G0s2 |
T |
C |
1: 192,955,076 (GRCm39) |
S3G |
probably benign |
Het |
Gm1527 |
T |
C |
3: 28,974,767 (GRCm39) |
Y527H |
probably benign |
Het |
Gsdmc3 |
T |
C |
15: 63,733,510 (GRCm39) |
K227R |
possibly damaging |
Het |
Gtf2ird2 |
A |
G |
5: 134,242,848 (GRCm39) |
Y354C |
probably damaging |
Het |
Hmcn2 |
T |
A |
2: 31,344,869 (GRCm39) |
N4685K |
probably damaging |
Het |
Itgad |
A |
T |
7: 127,791,279 (GRCm39) |
Y717F |
probably benign |
Het |
Kcnh5 |
C |
T |
12: 75,161,166 (GRCm39) |
W247* |
probably null |
Het |
Kcnt1 |
C |
A |
2: 25,806,048 (GRCm39) |
S1212R |
probably benign |
Het |
Kirrel1 |
A |
G |
3: 86,995,791 (GRCm39) |
V381A |
probably damaging |
Het |
Loxl1 |
T |
A |
9: 58,219,481 (GRCm39) |
Q230L |
probably damaging |
Het |
Magi1 |
T |
C |
6: 93,655,308 (GRCm39) |
E1446G |
probably benign |
Het |
Man1a |
A |
G |
10: 53,795,330 (GRCm39) |
V550A |
possibly damaging |
Het |
Muc16 |
T |
A |
9: 18,549,925 (GRCm39) |
H5456L |
probably benign |
Het |
Nhsl1 |
A |
G |
10: 18,391,867 (GRCm39) |
K207R |
probably damaging |
Het |
Nlrp4a |
A |
C |
7: 26,148,670 (GRCm39) |
|
probably null |
Het |
Nr6a1 |
T |
C |
2: 38,621,085 (GRCm39) |
M407V |
possibly damaging |
Het |
Or13c7b |
A |
G |
4: 43,820,711 (GRCm39) |
S217P |
probably damaging |
Het |
Or2b2b |
T |
G |
13: 21,858,737 (GRCm39) |
I126L |
possibly damaging |
Het |
Or2z2 |
G |
T |
11: 58,346,489 (GRCm39) |
F95L |
probably benign |
Het |
Or6c206 |
T |
C |
10: 129,097,469 (GRCm39) |
I213T |
probably damaging |
Het |
Ovgp1 |
A |
G |
3: 105,881,626 (GRCm39) |
|
probably benign |
Het |
Ovol3 |
G |
T |
7: 29,933,791 (GRCm39) |
F110L |
probably damaging |
Het |
Pcsk5 |
T |
C |
19: 17,549,821 (GRCm39) |
T724A |
probably benign |
Het |
Phtf2 |
G |
T |
5: 20,970,799 (GRCm39) |
T653N |
probably damaging |
Het |
Plch1 |
A |
T |
3: 63,688,663 (GRCm39) |
|
probably null |
Het |
Prkce |
A |
T |
17: 86,800,757 (GRCm39) |
E391V |
probably benign |
Het |
Prob1 |
A |
G |
18: 35,788,038 (GRCm39) |
V72A |
probably benign |
Het |
Prrc2b |
C |
A |
2: 32,084,402 (GRCm39) |
P289Q |
probably benign |
Het |
Ptbp3 |
A |
T |
4: 59,514,280 (GRCm39) |
N114K |
probably benign |
Het |
Rho |
T |
A |
6: 115,909,135 (GRCm39) |
L57H |
probably damaging |
Het |
Slc44a5 |
A |
C |
3: 153,975,626 (GRCm39) |
D679A |
probably damaging |
Het |
Slit2 |
A |
T |
5: 48,407,239 (GRCm39) |
D898V |
probably damaging |
Het |
Spag16 |
C |
T |
1: 69,909,487 (GRCm39) |
R195C |
probably damaging |
Het |
Tmprss11a |
T |
G |
5: 86,591,993 (GRCm39) |
D60A |
possibly damaging |
Het |
Ttn |
T |
A |
2: 76,565,293 (GRCm39) |
R28311S |
probably damaging |
Het |
Wfikkn1 |
T |
C |
17: 26,097,352 (GRCm39) |
D324G |
probably damaging |
Het |
Zan |
A |
C |
5: 137,410,845 (GRCm39) |
|
probably null |
Het |
Zfp945 |
A |
T |
17: 23,070,727 (GRCm39) |
C412S |
possibly damaging |
Het |
|
Other mutations in Mgat4d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00542:Mgat4d
|
APN |
8 |
84,081,425 (GRCm39) |
missense |
probably benign |
0.21 |
IGL01634:Mgat4d
|
APN |
8 |
84,094,745 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01987:Mgat4d
|
APN |
8 |
84,094,731 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02084:Mgat4d
|
APN |
8 |
84,095,610 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0546:Mgat4d
|
UTSW |
8 |
84,082,350 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1322:Mgat4d
|
UTSW |
8 |
84,092,354 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1526:Mgat4d
|
UTSW |
8 |
84,095,666 (GRCm39) |
missense |
probably benign |
0.25 |
R1617:Mgat4d
|
UTSW |
8 |
84,092,340 (GRCm39) |
missense |
probably damaging |
1.00 |
R2223:Mgat4d
|
UTSW |
8 |
84,082,301 (GRCm39) |
splice site |
probably benign |
|
R3157:Mgat4d
|
UTSW |
8 |
84,081,450 (GRCm39) |
missense |
probably benign |
|
R3421:Mgat4d
|
UTSW |
8 |
84,084,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R3422:Mgat4d
|
UTSW |
8 |
84,084,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R4387:Mgat4d
|
UTSW |
8 |
84,098,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R4796:Mgat4d
|
UTSW |
8 |
84,084,749 (GRCm39) |
missense |
probably damaging |
1.00 |
R4805:Mgat4d
|
UTSW |
8 |
84,084,787 (GRCm39) |
splice site |
probably null |
|
R5054:Mgat4d
|
UTSW |
8 |
84,094,837 (GRCm39) |
splice site |
probably null |
|
R6366:Mgat4d
|
UTSW |
8 |
84,095,580 (GRCm39) |
splice site |
probably null |
|
R6927:Mgat4d
|
UTSW |
8 |
84,081,496 (GRCm39) |
missense |
probably benign |
0.03 |
R7053:Mgat4d
|
UTSW |
8 |
84,098,261 (GRCm39) |
missense |
probably damaging |
0.98 |
R7554:Mgat4d
|
UTSW |
8 |
84,082,402 (GRCm39) |
missense |
probably benign |
0.00 |
R7965:Mgat4d
|
UTSW |
8 |
84,084,722 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8111:Mgat4d
|
UTSW |
8 |
84,094,776 (GRCm39) |
missense |
probably damaging |
0.96 |
R8344:Mgat4d
|
UTSW |
8 |
84,094,762 (GRCm39) |
missense |
probably benign |
0.01 |
Z1176:Mgat4d
|
UTSW |
8 |
84,094,741 (GRCm39) |
missense |
probably benign |
0.39 |
Z1176:Mgat4d
|
UTSW |
8 |
84,075,150 (GRCm39) |
missense |
probably benign |
0.04 |
|