Other mutations in this stock |
Total: 44 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aloxe3 |
A |
G |
11: 69,033,051 (GRCm39) |
K575R |
probably benign |
Het |
Atp10b |
T |
A |
11: 43,150,726 (GRCm39) |
*1475R |
probably null |
Het |
Baz2b |
T |
C |
2: 59,799,608 (GRCm39) |
D237G |
probably benign |
Het |
Cacna2d4 |
A |
C |
6: 119,219,876 (GRCm39) |
Q215H |
possibly damaging |
Het |
Capn15 |
G |
A |
17: 26,182,055 (GRCm39) |
R651C |
probably damaging |
Het |
Cby2 |
T |
C |
14: 75,820,654 (GRCm39) |
E357G |
probably damaging |
Het |
Ccdc28b |
A |
G |
4: 129,516,471 (GRCm39) |
V29A |
probably benign |
Het |
Cyb5rl |
A |
G |
4: 106,938,157 (GRCm39) |
T170A |
possibly damaging |
Het |
D330020A13Rik |
A |
G |
6: 120,271,890 (GRCm39) |
T189A |
unknown |
Het |
Emsy |
C |
A |
7: 98,268,512 (GRCm39) |
V524F |
possibly damaging |
Het |
Eppk1 |
T |
A |
15: 75,980,765 (GRCm39) |
N3315I |
probably damaging |
Het |
Erich2 |
T |
G |
2: 70,361,964 (GRCm39) |
|
probably benign |
Het |
Fkbp15 |
T |
C |
4: 62,242,365 (GRCm39) |
D529G |
probably damaging |
Het |
Gzmd |
T |
A |
14: 56,368,144 (GRCm39) |
Y105F |
possibly damaging |
Het |
Hpse |
G |
A |
5: 100,840,109 (GRCm39) |
T336M |
probably damaging |
Het |
Hrg |
A |
G |
16: 22,772,455 (GRCm39) |
D88G |
probably damaging |
Het |
Kif20b |
G |
A |
19: 34,914,253 (GRCm39) |
|
probably benign |
Het |
Kmt2a |
A |
G |
9: 44,733,174 (GRCm39) |
M2381T |
unknown |
Het |
Krtap5-3 |
T |
A |
7: 141,755,933 (GRCm39) |
C257S |
unknown |
Het |
Met |
C |
T |
6: 17,491,534 (GRCm39) |
R99W |
probably benign |
Het |
Nlrp4b |
A |
G |
7: 10,449,629 (GRCm39) |
R611G |
probably null |
Het |
Or10a3b |
A |
C |
7: 108,445,017 (GRCm39) |
S67A |
probably benign |
Het |
Or4b1d |
C |
T |
2: 89,969,472 (GRCm39) |
V4I |
probably benign |
Het |
Or8b1c |
T |
C |
9: 38,384,787 (GRCm39) |
V248A |
probably benign |
Het |
Or9m1 |
T |
A |
2: 87,733,189 (GRCm39) |
Y277F |
probably damaging |
Het |
Pclo |
A |
G |
5: 14,727,510 (GRCm39) |
I2123V |
unknown |
Het |
Phf10 |
G |
C |
17: 15,170,883 (GRCm39) |
A350G |
probably benign |
Het |
Pira2 |
T |
C |
7: 3,845,490 (GRCm39) |
Y298C |
probably damaging |
Het |
Pkhd1 |
A |
T |
1: 20,434,425 (GRCm39) |
Y2338N |
probably damaging |
Het |
Psme4 |
C |
T |
11: 30,788,957 (GRCm39) |
L1120F |
possibly damaging |
Het |
Safb2 |
A |
T |
17: 56,870,391 (GRCm39) |
H934Q |
possibly damaging |
Het |
Slc4a7 |
T |
A |
14: 14,775,346 (GRCm38) |
L884Q |
probably damaging |
Het |
Smc4 |
A |
C |
3: 68,934,894 (GRCm39) |
|
probably benign |
Het |
Spag16 |
T |
C |
1: 69,935,706 (GRCm39) |
V311A |
probably benign |
Het |
Sprr2j-ps |
T |
C |
3: 92,326,176 (GRCm39) |
V17A |
unknown |
Het |
Tenm3 |
T |
C |
8: 48,729,722 (GRCm39) |
Y1428C |
probably damaging |
Het |
Tent4b |
A |
G |
8: 88,977,350 (GRCm39) |
H384R |
probably benign |
Het |
Treml2 |
A |
G |
17: 48,609,775 (GRCm39) |
D69G |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,658,277 (GRCm39) |
K12368E |
unknown |
Het |
Usp17le |
T |
C |
7: 104,417,969 (GRCm39) |
D391G |
probably benign |
Het |
Usp28 |
G |
A |
9: 48,949,139 (GRCm39) |
R911Q |
probably benign |
Het |
Wdfy3 |
A |
C |
5: 101,993,058 (GRCm39) |
S3274R |
probably benign |
Het |
Ythdc2 |
T |
C |
18: 44,997,371 (GRCm39) |
V976A |
probably benign |
Het |
Zfp334 |
A |
G |
2: 165,223,408 (GRCm39) |
S212P |
possibly damaging |
Het |
|
Other mutations in Gbx2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01583:Gbx2
|
APN |
1 |
89,856,559 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01804:Gbx2
|
APN |
1 |
89,856,703 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02345:Gbx2
|
APN |
1 |
89,856,698 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02370:Gbx2
|
APN |
1 |
89,856,871 (GRCm39) |
splice site |
probably benign |
|
IGL02957:Gbx2
|
APN |
1 |
89,858,375 (GRCm39) |
missense |
probably benign |
0.02 |
IGL02959:Gbx2
|
APN |
1 |
89,856,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R2280:Gbx2
|
UTSW |
1 |
89,858,359 (GRCm39) |
missense |
probably damaging |
1.00 |
R2405:Gbx2
|
UTSW |
1 |
89,858,630 (GRCm39) |
start gained |
probably benign |
|
R2860:Gbx2
|
UTSW |
1 |
89,856,853 (GRCm39) |
missense |
probably damaging |
0.97 |
R2861:Gbx2
|
UTSW |
1 |
89,856,853 (GRCm39) |
missense |
probably damaging |
0.97 |
R5384:Gbx2
|
UTSW |
1 |
89,856,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R5587:Gbx2
|
UTSW |
1 |
89,860,844 (GRCm39) |
unclassified |
probably benign |
|
R5747:Gbx2
|
UTSW |
1 |
89,856,437 (GRCm39) |
missense |
probably damaging |
0.98 |
R5956:Gbx2
|
UTSW |
1 |
89,860,908 (GRCm39) |
unclassified |
probably benign |
|
R6053:Gbx2
|
UTSW |
1 |
89,858,159 (GRCm39) |
missense |
probably benign |
0.00 |
R6633:Gbx2
|
UTSW |
1 |
89,856,442 (GRCm39) |
frame shift |
probably null |
|
R7479:Gbx2
|
UTSW |
1 |
89,858,373 (GRCm39) |
missense |
probably benign |
0.02 |
R7505:Gbx2
|
UTSW |
1 |
89,856,455 (GRCm39) |
missense |
probably benign |
0.26 |
R7768:Gbx2
|
UTSW |
1 |
89,856,706 (GRCm39) |
missense |
probably benign |
0.09 |
R8184:Gbx2
|
UTSW |
1 |
89,856,550 (GRCm39) |
missense |
probably damaging |
1.00 |
R9599:Gbx2
|
UTSW |
1 |
89,856,635 (GRCm39) |
missense |
probably damaging |
1.00 |
|