Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930567H17Rik |
C |
T |
X: 69,438,135 (GRCm39) |
A53T |
probably benign |
Het |
Abca13 |
A |
T |
11: 9,206,205 (GRCm39) |
K168N |
probably damaging |
Het |
Ajuba |
T |
C |
14: 54,806,983 (GRCm39) |
R490G |
probably damaging |
Het |
Akap6 |
T |
A |
12: 53,186,454 (GRCm39) |
N1289K |
probably damaging |
Het |
Ankfy1 |
G |
A |
11: 72,605,310 (GRCm39) |
|
probably null |
Het |
Arhgap21 |
A |
G |
2: 20,891,948 (GRCm39) |
V161A |
probably damaging |
Het |
Arhgef18 |
T |
C |
8: 3,500,317 (GRCm39) |
I541T |
possibly damaging |
Het |
Atg14 |
T |
C |
14: 47,788,802 (GRCm39) |
K184E |
probably benign |
Het |
Casp8 |
T |
C |
1: 58,883,929 (GRCm39) |
V432A |
probably damaging |
Het |
Cela1 |
T |
C |
15: 100,580,794 (GRCm39) |
Y91C |
probably damaging |
Het |
Chrnb3 |
C |
A |
8: 27,884,021 (GRCm39) |
L253M |
probably damaging |
Het |
Col24a1 |
G |
T |
3: 145,230,037 (GRCm39) |
G1493* |
probably null |
Het |
Dnah7a |
C |
T |
1: 53,486,524 (GRCm39) |
E3346K |
probably benign |
Het |
Dock5 |
A |
T |
14: 67,993,941 (GRCm39) |
S1845T |
probably benign |
Het |
Dtx3 |
A |
G |
10: 127,029,058 (GRCm39) |
I60T |
possibly damaging |
Het |
Eif1ad8 |
A |
T |
12: 87,563,935 (GRCm39) |
D90V |
probably damaging |
Het |
F2rl1 |
A |
G |
13: 95,649,796 (GRCm39) |
L362P |
probably damaging |
Het |
Gm26678 |
T |
C |
3: 54,540,504 (GRCm39) |
|
noncoding transcript |
Het |
Impg1 |
A |
G |
9: 80,252,611 (GRCm39) |
L523P |
probably damaging |
Het |
Ip6k2 |
G |
A |
9: 108,682,847 (GRCm39) |
R319Q |
probably benign |
Het |
Klhl23 |
T |
C |
2: 69,654,516 (GRCm39) |
F129L |
probably damaging |
Het |
Krt71 |
T |
C |
15: 101,643,129 (GRCm39) |
T460A |
probably benign |
Het |
Madd |
C |
T |
2: 90,997,373 (GRCm39) |
R746Q |
probably benign |
Het |
Med12l |
T |
G |
3: 59,164,644 (GRCm39) |
|
probably null |
Het |
Mrps30 |
T |
C |
13: 118,523,376 (GRCm39) |
D132G |
probably damaging |
Het |
Myh6 |
T |
G |
14: 55,197,819 (GRCm39) |
M440L |
probably benign |
Het |
Myh7 |
T |
A |
14: 55,228,575 (GRCm39) |
S205C |
probably benign |
Het |
Nxpe4 |
A |
T |
9: 48,310,137 (GRCm39) |
T467S |
probably damaging |
Het |
Or13a20 |
T |
C |
7: 140,232,653 (GRCm39) |
Y254H |
probably damaging |
Het |
Or1e17 |
A |
G |
11: 73,831,182 (GRCm39) |
T37A |
possibly damaging |
Het |
Or7g30 |
T |
A |
9: 19,352,886 (GRCm39) |
L226I |
probably damaging |
Het |
Pcdh7 |
G |
A |
5: 57,876,631 (GRCm39) |
G62D |
possibly damaging |
Het |
Pde3b |
A |
G |
7: 114,120,923 (GRCm39) |
T683A |
possibly damaging |
Het |
Plcb2 |
A |
T |
2: 118,540,047 (GRCm39) |
L1082Q |
probably damaging |
Het |
Rin2 |
C |
T |
2: 145,702,366 (GRCm39) |
T354I |
probably benign |
Het |
Rufy4 |
T |
C |
1: 74,186,822 (GRCm39) |
C537R |
probably damaging |
Het |
Skint11 |
C |
A |
4: 114,101,856 (GRCm39) |
Q99K |
probably benign |
Het |
Slc6a6 |
T |
C |
6: 91,718,257 (GRCm39) |
V357A |
probably damaging |
Het |
Slitrk6 |
T |
C |
14: 110,987,580 (GRCm39) |
E709G |
probably benign |
Het |
Spc24 |
T |
C |
9: 21,667,498 (GRCm39) |
|
probably null |
Het |
Tas2r140 |
A |
T |
6: 133,031,915 (GRCm39) |
V281D |
probably damaging |
Het |
Tfcp2l1 |
G |
A |
1: 118,589,795 (GRCm39) |
R285H |
probably benign |
Het |
Tmem132d |
A |
G |
5: 128,509,389 (GRCm39) |
S14P |
possibly damaging |
Het |
Tulp2 |
A |
G |
7: 45,171,298 (GRCm39) |
K360E |
probably damaging |
Het |
Vmn1r60 |
A |
G |
7: 5,547,803 (GRCm39) |
V99A |
probably benign |
Het |
Zfp599 |
T |
A |
9: 22,161,041 (GRCm39) |
K375* |
probably null |
Het |
|
Other mutations in Gal3st2c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Gal3st2c
|
APN |
1 |
93,936,771 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01469:Gal3st2c
|
APN |
1 |
93,937,039 (GRCm39) |
missense |
probably benign |
0.18 |
PIT4431001:Gal3st2c
|
UTSW |
1 |
93,935,834 (GRCm39) |
missense |
probably damaging |
1.00 |
R0110:Gal3st2c
|
UTSW |
1 |
93,937,219 (GRCm39) |
missense |
probably benign |
0.03 |
R0602:Gal3st2c
|
UTSW |
1 |
93,936,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R0846:Gal3st2c
|
UTSW |
1 |
93,934,669 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1577:Gal3st2c
|
UTSW |
1 |
93,934,650 (GRCm39) |
missense |
probably damaging |
0.98 |
R1900:Gal3st2c
|
UTSW |
1 |
93,936,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R1902:Gal3st2c
|
UTSW |
1 |
93,936,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R2143:Gal3st2c
|
UTSW |
1 |
93,937,173 (GRCm39) |
nonsense |
probably null |
|
R2846:Gal3st2c
|
UTSW |
1 |
93,924,122 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3737:Gal3st2c
|
UTSW |
1 |
93,937,050 (GRCm39) |
missense |
possibly damaging |
0.79 |
R4623:Gal3st2c
|
UTSW |
1 |
93,937,178 (GRCm39) |
missense |
possibly damaging |
0.59 |
R5177:Gal3st2c
|
UTSW |
1 |
93,936,930 (GRCm39) |
nonsense |
probably null |
|
R5590:Gal3st2c
|
UTSW |
1 |
93,936,023 (GRCm39) |
critical splice donor site |
probably null |
|
R7529:Gal3st2c
|
UTSW |
1 |
93,937,039 (GRCm39) |
missense |
probably benign |
0.18 |
R7559:Gal3st2c
|
UTSW |
1 |
93,937,075 (GRCm39) |
missense |
probably damaging |
1.00 |
R9525:Gal3st2c
|
UTSW |
1 |
93,935,928 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Gal3st2c
|
UTSW |
1 |
93,935,867 (GRCm39) |
missense |
probably benign |
0.02 |
|