Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
T |
A |
11: 9,265,339 (GRCm39) |
|
probably null |
Het |
Adamts19 |
A |
G |
18: 58,970,848 (GRCm39) |
Q144R |
possibly damaging |
Het |
Adgrb3 |
C |
A |
1: 25,570,956 (GRCm39) |
C507F |
probably damaging |
Het |
Atg9b |
T |
C |
5: 24,590,237 (GRCm39) |
*923W |
probably null |
Het |
Atp13a4 |
T |
C |
16: 29,239,653 (GRCm39) |
|
probably benign |
Het |
Baz2b |
G |
T |
2: 59,788,795 (GRCm39) |
R697S |
probably damaging |
Het |
Bicdl1 |
A |
G |
5: 115,799,537 (GRCm39) |
I184T |
probably benign |
Het |
Bpifb4 |
C |
T |
2: 153,784,903 (GRCm39) |
L204F |
possibly damaging |
Het |
Cep120 |
C |
T |
18: 53,851,561 (GRCm39) |
R577Q |
probably damaging |
Het |
Cplx4 |
T |
C |
18: 66,103,048 (GRCm39) |
E24G |
possibly damaging |
Het |
Dcxr |
T |
C |
11: 120,616,923 (GRCm39) |
T147A |
probably benign |
Het |
Dnajc10 |
C |
A |
2: 80,170,870 (GRCm39) |
H454N |
probably damaging |
Het |
Dsp |
G |
T |
13: 38,351,504 (GRCm39) |
G108* |
probably null |
Het |
Entpd6 |
T |
A |
2: 150,609,014 (GRCm39) |
I366K |
probably damaging |
Het |
Fam111a |
A |
G |
19: 12,565,057 (GRCm39) |
K269E |
probably benign |
Het |
Grid2ip |
T |
G |
5: 143,361,455 (GRCm39) |
V222G |
possibly damaging |
Het |
Hmcn2 |
T |
G |
2: 31,335,326 (GRCm39) |
V4421G |
probably benign |
Het |
Ifi207 |
T |
C |
1: 173,555,253 (GRCm39) |
T817A |
probably damaging |
Het |
Irak2 |
A |
T |
6: 113,670,683 (GRCm39) |
E533V |
probably damaging |
Het |
Katnip |
A |
G |
7: 125,464,523 (GRCm39) |
S1297G |
probably damaging |
Het |
Kbtbd6 |
T |
C |
14: 79,689,596 (GRCm39) |
F97S |
probably damaging |
Het |
Kctd14 |
A |
T |
7: 97,106,883 (GRCm39) |
E99V |
probably damaging |
Het |
Klhl10 |
A |
T |
11: 100,338,557 (GRCm39) |
Y432F |
probably benign |
Het |
Lrrc49 |
T |
C |
9: 60,592,335 (GRCm39) |
N53S |
possibly damaging |
Het |
Mief2 |
T |
A |
11: 60,621,288 (GRCm39) |
|
probably benign |
Het |
Mog |
A |
T |
17: 37,334,049 (GRCm39) |
S15T |
unknown |
Het |
Mpi |
T |
C |
9: 57,452,181 (GRCm39) |
D365G |
probably damaging |
Het |
Mpp7 |
A |
G |
18: 7,379,983 (GRCm39) |
|
probably null |
Het |
Nes |
A |
G |
3: 87,883,486 (GRCm39) |
T582A |
probably benign |
Het |
Nlrp14 |
A |
G |
7: 106,780,393 (GRCm39) |
D5G |
probably benign |
Het |
Nr1i3 |
C |
T |
1: 171,044,719 (GRCm39) |
T218I |
probably damaging |
Het |
Nup43 |
C |
T |
10: 7,554,433 (GRCm39) |
R339* |
probably null |
Het |
Nup58 |
T |
A |
14: 60,457,471 (GRCm39) |
R577S |
probably benign |
Het |
Olfr908 |
C |
T |
9: 38,427,897 (GRCm39) |
|
probably benign |
Het |
Or52n4b |
T |
A |
7: 108,144,092 (GRCm39) |
M120K |
probably damaging |
Het |
Or5d35 |
T |
A |
2: 87,855,207 (GRCm39) |
I47K |
probably damaging |
Het |
Or6c38 |
A |
T |
10: 128,929,537 (GRCm39) |
V102D |
possibly damaging |
Het |
Or9g20 |
G |
A |
2: 85,630,338 (GRCm39) |
S92F |
probably damaging |
Het |
Orc1 |
T |
C |
4: 108,436,765 (GRCm39) |
|
probably benign |
Het |
Pax6 |
C |
A |
2: 105,526,847 (GRCm39) |
P251Q |
probably benign |
Het |
Phactr3 |
C |
T |
2: 177,925,729 (GRCm39) |
R330W |
probably damaging |
Het |
Phldb1 |
G |
A |
9: 44,622,324 (GRCm39) |
R81W |
probably damaging |
Het |
Pip5k1c |
C |
T |
10: 81,151,774 (GRCm39) |
P656L |
probably benign |
Het |
Pkn3 |
T |
G |
2: 29,974,692 (GRCm39) |
|
probably null |
Het |
Plcb2 |
T |
A |
2: 118,543,615 (GRCm39) |
H752L |
probably benign |
Het |
Plch1 |
G |
A |
3: 63,660,746 (GRCm39) |
T291M |
probably damaging |
Het |
Plekhg1 |
A |
T |
10: 3,823,127 (GRCm39) |
M32L |
probably benign |
Het |
Plekhg1 |
A |
T |
10: 3,823,130 (GRCm39) |
T33S |
probably damaging |
Het |
Plk4 |
A |
G |
3: 40,759,625 (GRCm39) |
T174A |
probably damaging |
Het |
Ppip5k2 |
C |
A |
1: 97,648,792 (GRCm39) |
|
probably benign |
Het |
Prl2a1 |
G |
A |
13: 27,988,961 (GRCm39) |
V29M |
probably benign |
Het |
R3hcc1l |
T |
C |
19: 42,571,996 (GRCm39) |
|
probably benign |
Het |
Rasa3 |
C |
T |
8: 13,648,289 (GRCm39) |
G125D |
probably damaging |
Het |
Sema3f |
A |
T |
9: 107,566,919 (GRCm39) |
Y136* |
probably null |
Het |
Slc13a5 |
T |
A |
11: 72,141,672 (GRCm39) |
|
probably null |
Het |
Slc16a1 |
T |
C |
3: 104,560,880 (GRCm39) |
V395A |
possibly damaging |
Het |
Sparcl1 |
C |
T |
5: 104,236,356 (GRCm39) |
A466T |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,069,690 (GRCm39) |
|
probably benign |
Het |
Styxl1 |
G |
A |
5: 135,797,755 (GRCm39) |
R50* |
probably null |
Het |
Tex264 |
T |
A |
9: 106,550,901 (GRCm39) |
I99F |
possibly damaging |
Het |
Tgtp2 |
T |
C |
11: 48,949,811 (GRCm39) |
T254A |
probably damaging |
Het |
Tmem245 |
A |
C |
4: 56,937,989 (GRCm39) |
|
probably null |
Het |
Tnik |
A |
T |
3: 28,661,359 (GRCm39) |
T587S |
probably benign |
Het |
Tpr |
T |
G |
1: 150,288,864 (GRCm39) |
S648A |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,596,313 (GRCm39) |
E18454G |
probably damaging |
Het |
Utp20 |
A |
C |
10: 88,645,797 (GRCm39) |
H527Q |
probably benign |
Het |
Vmn1r1 |
A |
T |
1: 181,985,111 (GRCm39) |
S185T |
probably benign |
Het |
Vps54 |
C |
T |
11: 21,262,952 (GRCm39) |
H680Y |
probably damaging |
Het |
Vwa5b2 |
A |
G |
16: 20,419,553 (GRCm39) |
|
probably null |
Het |
Wscd1 |
T |
C |
11: 71,662,802 (GRCm39) |
|
probably null |
Het |
Zbtb41 |
C |
T |
1: 139,375,152 (GRCm39) |
P871S |
probably damaging |
Het |
Zcchc4 |
T |
C |
5: 52,953,549 (GRCm39) |
L186P |
possibly damaging |
Het |
Zdhhc13 |
A |
G |
7: 48,449,621 (GRCm39) |
Y73C |
probably benign |
Het |
Zfp12 |
A |
G |
5: 143,225,755 (GRCm39) |
E21G |
probably damaging |
Het |
|
Other mutations in Or4l15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02811:Or4l15
|
APN |
14 |
50,197,590 (GRCm39) |
utr 3 prime |
probably benign |
|
R0829:Or4l15
|
UTSW |
14 |
50,198,503 (GRCm39) |
missense |
probably benign |
0.03 |
R1513:Or4l15
|
UTSW |
14 |
50,198,558 (GRCm39) |
critical splice acceptor site |
probably null |
|
R2016:Or4l15
|
UTSW |
14 |
50,197,959 (GRCm39) |
missense |
probably benign |
0.00 |
R2936:Or4l15
|
UTSW |
14 |
50,197,611 (GRCm39) |
missense |
probably benign |
0.03 |
R3082:Or4l15
|
UTSW |
14 |
50,198,161 (GRCm39) |
missense |
probably damaging |
1.00 |
R3738:Or4l15
|
UTSW |
14 |
50,198,013 (GRCm39) |
missense |
possibly damaging |
0.60 |
R4830:Or4l15
|
UTSW |
14 |
50,197,681 (GRCm39) |
missense |
probably damaging |
1.00 |
R4839:Or4l15
|
UTSW |
14 |
50,197,646 (GRCm39) |
missense |
probably benign |
0.41 |
R5362:Or4l15
|
UTSW |
14 |
50,197,986 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5695:Or4l15
|
UTSW |
14 |
50,198,080 (GRCm39) |
missense |
probably benign |
0.00 |
R6187:Or4l15
|
UTSW |
14 |
50,198,526 (GRCm39) |
start codon destroyed |
probably null |
0.99 |
R7371:Or4l15
|
UTSW |
14 |
50,198,563 (GRCm39) |
splice site |
probably null |
|
R7611:Or4l15
|
UTSW |
14 |
50,198,368 (GRCm39) |
missense |
probably benign |
0.03 |
R9243:Or4l15
|
UTSW |
14 |
50,197,881 (GRCm39) |
missense |
probably benign |
0.06 |
|