Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ap3b1 |
T |
C |
13: 94,613,540 (GRCm39) |
S680P |
probably benign |
Het |
Carmil1 |
T |
C |
13: 24,251,189 (GRCm39) |
T844A |
probably benign |
Het |
Cfap57 |
C |
T |
4: 118,472,128 (GRCm39) |
V84I |
probably benign |
Het |
Clca4a |
A |
T |
3: 144,659,512 (GRCm39) |
D781E |
probably benign |
Het |
Col10a1 |
A |
G |
10: 34,271,638 (GRCm39) |
M537V |
probably benign |
Het |
Col5a2 |
A |
G |
1: 45,415,248 (GRCm39) |
M1497T |
probably benign |
Het |
Csmd1 |
T |
A |
8: 16,135,192 (GRCm39) |
I1655F |
probably damaging |
Het |
Cts3 |
A |
G |
13: 61,716,589 (GRCm39) |
S16P |
probably benign |
Het |
Cyp2c67 |
T |
C |
19: 39,604,084 (GRCm39) |
Y424C |
probably damaging |
Het |
Dip2c |
T |
C |
13: 9,672,741 (GRCm39) |
|
probably null |
Het |
Dnah5 |
T |
C |
15: 28,248,125 (GRCm39) |
|
probably null |
Het |
Dpp4 |
A |
G |
2: 62,190,627 (GRCm39) |
|
probably null |
Het |
Fam135b |
T |
G |
15: 71,350,991 (GRCm39) |
N295T |
possibly damaging |
Het |
Fign |
A |
G |
2: 63,810,916 (GRCm39) |
V118A |
probably benign |
Het |
Gpr108 |
A |
T |
17: 57,543,228 (GRCm39) |
Y480* |
probably null |
Het |
Lmf1 |
G |
A |
17: 25,873,445 (GRCm39) |
V317M |
probably damaging |
Het |
Lrrc30 |
C |
T |
17: 67,939,472 (GRCm39) |
G36E |
probably damaging |
Het |
Map2 |
T |
C |
1: 66,452,466 (GRCm39) |
V452A |
probably benign |
Het |
Mks1 |
C |
T |
11: 87,747,666 (GRCm39) |
T183M |
possibly damaging |
Het |
Mpg |
G |
A |
11: 32,179,517 (GRCm39) |
|
probably null |
Het |
Nat10 |
A |
G |
2: 103,557,131 (GRCm39) |
L841P |
possibly damaging |
Het |
Nbeal1 |
A |
G |
1: 60,316,386 (GRCm39) |
E1863G |
probably benign |
Het |
Neurl1b |
C |
G |
17: 26,657,720 (GRCm39) |
H219Q |
probably benign |
Het |
Nr2e3 |
T |
A |
9: 59,854,671 (GRCm39) |
I292F |
possibly damaging |
Het |
Nxn |
T |
C |
11: 76,163,285 (GRCm39) |
Y246C |
probably damaging |
Het |
Or1o3 |
A |
T |
17: 37,573,964 (GRCm39) |
M197K |
probably benign |
Het |
Or4f4b |
T |
C |
2: 111,313,823 (GRCm39) |
F44S |
probably damaging |
Het |
Or5ac15 |
T |
G |
16: 58,940,011 (GRCm39) |
T141P |
possibly damaging |
Het |
Or5h26 |
A |
G |
16: 58,988,080 (GRCm39) |
V142A |
probably benign |
Het |
Or8k17 |
A |
T |
2: 86,066,660 (GRCm39) |
L166* |
probably null |
Het |
Pcdha5 |
T |
A |
18: 37,093,544 (GRCm39) |
F18I |
probably benign |
Het |
Pcdhb17 |
A |
G |
18: 37,618,779 (GRCm39) |
K190E |
probably damaging |
Het |
Peg3 |
GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC |
GTGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTCCTGGCCATGGGGCTTATCATCATGGGGCTC |
7: 6,712,167 (GRCm39) |
|
probably benign |
Het |
Ppm1g |
G |
T |
5: 31,362,447 (GRCm39) |
Y284* |
probably null |
Het |
Rp1 |
A |
G |
1: 4,218,054 (GRCm39) |
V1026A |
unknown |
Het |
Scap |
C |
T |
9: 110,203,081 (GRCm39) |
R252C |
probably damaging |
Het |
Scn9a |
C |
A |
2: 66,366,580 (GRCm39) |
K734N |
probably benign |
Het |
Sema5a |
C |
T |
15: 32,682,471 (GRCm39) |
S955F |
probably damaging |
Het |
Serpinb10 |
A |
G |
1: 107,456,831 (GRCm39) |
|
probably null |
Het |
Sfi1 |
ACA |
ACATCTTCCCAAAGCCAGTCA |
11: 3,103,382 (GRCm39) |
|
probably benign |
Het |
Sh2d5 |
A |
G |
4: 137,986,467 (GRCm39) |
T397A |
probably benign |
Het |
Slc22a8 |
T |
C |
19: 8,587,409 (GRCm39) |
F490L |
probably benign |
Het |
Tbc1d19 |
A |
T |
5: 54,014,260 (GRCm39) |
Y296F |
probably damaging |
Het |
Tmppe |
T |
C |
9: 114,233,862 (GRCm39) |
S54P |
possibly damaging |
Het |
Vmn1r123 |
A |
T |
7: 20,896,795 (GRCm39) |
N229I |
probably benign |
Het |
Wdr36 |
T |
A |
18: 32,987,624 (GRCm39) |
|
probably null |
Het |
Wdr47 |
T |
A |
3: 108,550,480 (GRCm39) |
M835K |
possibly damaging |
Het |
Wscd2 |
A |
T |
5: 113,715,475 (GRCm39) |
K438N |
possibly damaging |
Het |
Xrcc6 |
T |
A |
15: 81,900,678 (GRCm39) |
|
probably null |
Het |
Xrn1 |
T |
A |
9: 95,903,906 (GRCm39) |
F1148I |
possibly damaging |
Het |
Zmynd8 |
T |
C |
2: 165,654,346 (GRCm39) |
D722G |
probably damaging |
Het |
|
Other mutations in Ky |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01515:Ky
|
APN |
9 |
102,419,304 (GRCm39) |
missense |
probably benign |
|
IGL02197:Ky
|
APN |
9 |
102,414,985 (GRCm39) |
missense |
possibly damaging |
0.63 |
PIT4802001:Ky
|
UTSW |
9 |
102,414,972 (GRCm39) |
missense |
probably benign |
0.00 |
R0384:Ky
|
UTSW |
9 |
102,419,289 (GRCm39) |
missense |
probably benign |
0.05 |
R0620:Ky
|
UTSW |
9 |
102,414,820 (GRCm39) |
missense |
probably benign |
0.04 |
R1099:Ky
|
UTSW |
9 |
102,414,923 (GRCm39) |
missense |
probably damaging |
1.00 |
R1754:Ky
|
UTSW |
9 |
102,419,126 (GRCm39) |
missense |
possibly damaging |
0.54 |
R2075:Ky
|
UTSW |
9 |
102,419,945 (GRCm39) |
missense |
probably damaging |
0.98 |
R2322:Ky
|
UTSW |
9 |
102,414,990 (GRCm39) |
critical splice donor site |
probably null |
|
R2415:Ky
|
UTSW |
9 |
102,419,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R3950:Ky
|
UTSW |
9 |
102,419,627 (GRCm39) |
nonsense |
probably null |
|
R4419:Ky
|
UTSW |
9 |
102,419,909 (GRCm39) |
missense |
probably damaging |
1.00 |
R4786:Ky
|
UTSW |
9 |
102,419,186 (GRCm39) |
missense |
probably benign |
0.02 |
R5261:Ky
|
UTSW |
9 |
102,414,798 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5529:Ky
|
UTSW |
9 |
102,419,274 (GRCm39) |
missense |
probably benign |
0.10 |
R6857:Ky
|
UTSW |
9 |
102,419,631 (GRCm39) |
missense |
probably damaging |
1.00 |
R6931:Ky
|
UTSW |
9 |
102,414,826 (GRCm39) |
missense |
probably damaging |
1.00 |
R7205:Ky
|
UTSW |
9 |
102,419,491 (GRCm39) |
missense |
probably damaging |
1.00 |
R7211:Ky
|
UTSW |
9 |
102,386,349 (GRCm39) |
missense |
probably benign |
0.08 |
R7570:Ky
|
UTSW |
9 |
102,419,528 (GRCm39) |
missense |
probably benign |
0.00 |
R7644:Ky
|
UTSW |
9 |
102,414,972 (GRCm39) |
missense |
probably benign |
0.00 |
R7910:Ky
|
UTSW |
9 |
102,419,141 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7988:Ky
|
UTSW |
9 |
102,402,614 (GRCm39) |
missense |
probably damaging |
1.00 |
R8708:Ky
|
UTSW |
9 |
102,402,590 (GRCm39) |
splice site |
probably benign |
|
R8726:Ky
|
UTSW |
9 |
102,405,102 (GRCm39) |
missense |
probably damaging |
1.00 |
R9146:Ky
|
UTSW |
9 |
102,419,405 (GRCm39) |
missense |
|
|
R9709:Ky
|
UTSW |
9 |
102,419,411 (GRCm39) |
missense |
probably damaging |
1.00 |
|