Other mutations in this stock |
Total: 31 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abi3bp |
T |
C |
16: 56,412,999 (GRCm39) |
S314P |
probably damaging |
Het |
Abra |
T |
C |
15: 41,732,802 (GRCm39) |
H88R |
probably benign |
Het |
Bsn |
A |
G |
9: 107,987,617 (GRCm39) |
|
probably benign |
Het |
Chd3 |
A |
C |
11: 69,251,886 (GRCm39) |
C123G |
probably damaging |
Het |
Clca3b |
A |
C |
3: 144,547,171 (GRCm39) |
|
probably null |
Het |
Cnot7 |
G |
T |
8: 40,952,386 (GRCm39) |
P190T |
probably damaging |
Het |
Cps1 |
A |
T |
1: 67,212,031 (GRCm39) |
|
probably benign |
Het |
Dennd2d |
A |
G |
3: 106,407,220 (GRCm39) |
T424A |
probably benign |
Het |
Dnhd1 |
C |
T |
7: 105,327,516 (GRCm39) |
R54C |
probably damaging |
Het |
Efhd1 |
G |
A |
1: 87,192,334 (GRCm39) |
E55K |
probably damaging |
Het |
Ep300 |
T |
C |
15: 81,495,638 (GRCm39) |
|
probably benign |
Het |
Ezh1 |
G |
T |
11: 101,090,166 (GRCm39) |
H529Q |
probably damaging |
Het |
Klhl3 |
A |
T |
13: 58,198,878 (GRCm39) |
S201T |
possibly damaging |
Het |
Krt1c |
A |
G |
15: 101,724,953 (GRCm39) |
F219S |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 41,172,172 (GRCm39) |
D751N |
probably damaging |
Het |
Lyst |
T |
A |
13: 13,838,629 (GRCm39) |
C1848* |
probably null |
Het |
Macf1 |
A |
G |
4: 123,284,842 (GRCm39) |
|
probably null |
Het |
Med10 |
T |
C |
13: 69,961,819 (GRCm39) |
|
probably benign |
Het |
Msh4 |
T |
A |
3: 153,592,593 (GRCm39) |
T170S |
probably damaging |
Het |
Or52n3 |
T |
C |
7: 104,530,141 (GRCm39) |
C76R |
probably damaging |
Het |
Pelp1 |
T |
A |
11: 70,297,153 (GRCm39) |
|
probably benign |
Het |
Prex2 |
G |
A |
1: 11,367,963 (GRCm39) |
V1595I |
probably benign |
Het |
Prpf8 |
C |
T |
11: 75,392,660 (GRCm39) |
R1617* |
probably null |
Het |
Rabep1 |
T |
A |
11: 70,825,385 (GRCm39) |
L684Q |
probably damaging |
Het |
Slc22a4 |
G |
A |
11: 53,874,435 (GRCm39) |
|
probably benign |
Het |
Smox |
T |
C |
2: 131,362,037 (GRCm39) |
F153S |
probably damaging |
Het |
Tma16 |
A |
G |
8: 66,939,062 (GRCm39) |
|
probably null |
Het |
Unc80 |
G |
T |
1: 66,665,675 (GRCm39) |
R1814L |
possibly damaging |
Het |
Vmn2r108 |
C |
T |
17: 20,691,987 (GRCm39) |
D179N |
possibly damaging |
Het |
Washc2 |
A |
G |
6: 116,236,126 (GRCm39) |
E1199G |
probably benign |
Het |
Zic1 |
C |
A |
9: 91,244,525 (GRCm39) |
|
probably null |
Het |
|
Other mutations in 1700001J03Rik |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02141:1700001J03Rik
|
APN |
5 |
146,120,275 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02475:1700001J03Rik
|
APN |
5 |
146,119,343 (GRCm39) |
utr 3 prime |
probably benign |
|
R0682:1700001J03Rik
|
UTSW |
5 |
146,121,650 (GRCm39) |
missense |
probably benign |
0.05 |
R1808:1700001J03Rik
|
UTSW |
5 |
146,121,691 (GRCm39) |
nonsense |
probably null |
|
R2083:1700001J03Rik
|
UTSW |
5 |
146,121,681 (GRCm39) |
missense |
possibly damaging |
0.75 |
R2919:1700001J03Rik
|
UTSW |
5 |
146,122,001 (GRCm39) |
missense |
probably benign |
0.00 |
R3753:1700001J03Rik
|
UTSW |
5 |
146,121,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R4764:1700001J03Rik
|
UTSW |
5 |
146,122,029 (GRCm39) |
missense |
probably benign |
0.00 |
R7242:1700001J03Rik
|
UTSW |
5 |
146,121,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R7578:1700001J03Rik
|
UTSW |
5 |
146,120,343 (GRCm39) |
missense |
probably damaging |
1.00 |
R7784:1700001J03Rik
|
UTSW |
5 |
146,119,638 (GRCm39) |
splice site |
probably null |
|
R9176:1700001J03Rik
|
UTSW |
5 |
146,121,004 (GRCm39) |
missense |
probably damaging |
1.00 |
|