Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921509C19Rik |
A |
C |
2: 151,314,845 (GRCm39) |
S278A |
possibly damaging |
Het |
Adamts20 |
T |
C |
15: 94,251,554 (GRCm39) |
D411G |
probably damaging |
Het |
Adgrl3 |
A |
G |
5: 81,871,987 (GRCm39) |
I894V |
possibly damaging |
Het |
Adprhl1 |
C |
T |
8: 13,273,069 (GRCm39) |
V1230I |
probably benign |
Het |
Agpat1 |
T |
A |
17: 34,829,883 (GRCm39) |
Y77N |
probably damaging |
Het |
Anpep |
A |
G |
7: 79,477,392 (GRCm39) |
V725A |
possibly damaging |
Het |
Apc |
T |
A |
18: 34,445,126 (GRCm39) |
I674K |
probably damaging |
Het |
Arhgef2 |
A |
G |
3: 88,551,262 (GRCm39) |
R808G |
probably damaging |
Het |
Asap1 |
A |
G |
15: 64,002,105 (GRCm39) |
V402A |
probably damaging |
Het |
Aspg |
T |
C |
12: 112,091,255 (GRCm39) |
V479A |
possibly damaging |
Het |
B3galnt2 |
G |
A |
13: 14,169,070 (GRCm39) |
V368M |
probably benign |
Het |
Bahcc1 |
T |
C |
11: 120,177,132 (GRCm39) |
S2007P |
probably damaging |
Het |
Cyfip2 |
A |
T |
11: 46,087,254 (GRCm39) |
I1212N |
possibly damaging |
Het |
Dnajc16 |
A |
T |
4: 141,491,124 (GRCm39) |
D675E |
probably damaging |
Het |
Dram2 |
T |
C |
3: 106,462,503 (GRCm39) |
F4L |
probably damaging |
Het |
Dsp |
A |
G |
13: 38,379,425 (GRCm39) |
T2057A |
probably benign |
Het |
Dync1h1 |
T |
G |
12: 110,602,887 (GRCm39) |
L2176R |
probably damaging |
Het |
Efhb |
A |
T |
17: 53,708,549 (GRCm39) |
I707N |
possibly damaging |
Het |
Eif2ak4 |
A |
G |
2: 118,302,377 (GRCm39) |
T1555A |
probably benign |
Het |
Erc1 |
G |
A |
6: 119,801,912 (GRCm39) |
T35I |
possibly damaging |
Het |
Esr2 |
C |
A |
12: 76,188,168 (GRCm39) |
M363I |
probably benign |
Het |
Etl4 |
A |
T |
2: 20,749,000 (GRCm39) |
N446I |
possibly damaging |
Het |
Evpl |
T |
A |
11: 116,113,782 (GRCm39) |
K1303* |
probably null |
Het |
Fam135b |
A |
T |
15: 71,335,529 (GRCm39) |
V555E |
probably damaging |
Het |
Fam186b |
A |
G |
15: 99,177,970 (GRCm39) |
L452P |
probably benign |
Het |
Fmn1 |
A |
T |
2: 113,271,956 (GRCm39) |
Q108L |
unknown |
Het |
Gcc2 |
A |
G |
10: 58,092,723 (GRCm39) |
T48A |
probably benign |
Het |
Gm6619 |
T |
G |
6: 131,467,354 (GRCm39) |
I73S |
possibly damaging |
Het |
Gm8267 |
T |
A |
14: 44,960,397 (GRCm39) |
D116V |
probably damaging |
Het |
Gtf3c3 |
G |
A |
1: 54,459,607 (GRCm39) |
T385M |
probably benign |
Het |
Iqgap2 |
C |
A |
13: 95,764,584 (GRCm39) |
M1553I |
probably benign |
Het |
Kcnk1 |
G |
T |
8: 126,722,307 (GRCm39) |
G37C |
probably damaging |
Het |
Kifc3 |
T |
C |
8: 95,864,615 (GRCm39) |
M32V |
probably benign |
Het |
Krt81 |
C |
A |
15: 101,359,251 (GRCm39) |
K222N |
possibly damaging |
Het |
Lrrc63 |
A |
G |
14: 75,363,697 (GRCm39) |
S145P |
possibly damaging |
Het |
Mybbp1a |
T |
A |
11: 72,342,101 (GRCm39) |
V1279E |
probably benign |
Het |
Niban3 |
A |
G |
8: 72,052,808 (GRCm39) |
D94G |
probably benign |
Het |
Or8u9 |
T |
A |
2: 86,001,354 (GRCm39) |
D269V |
probably damaging |
Het |
Pierce1 |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
TCTCTGGGGCAGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTCTGGGGCGGGCTTAGCCTTGGGCTCCCCCGGCTCCGGCTCCTC |
2: 28,356,122 (GRCm39) |
|
probably benign |
Het |
Pramel12 |
A |
G |
4: 143,145,410 (GRCm39) |
Y293C |
probably benign |
Het |
Ptpn18 |
T |
C |
1: 34,512,416 (GRCm39) |
V407A |
probably benign |
Het |
Ptpn9 |
T |
A |
9: 56,934,717 (GRCm39) |
Y160* |
probably null |
Het |
Ptprj |
T |
C |
2: 90,280,163 (GRCm39) |
K1045R |
possibly damaging |
Het |
Rundc3a |
G |
T |
11: 102,290,872 (GRCm39) |
|
probably null |
Het |
Scn11a |
C |
T |
9: 119,587,692 (GRCm39) |
V1351I |
probably benign |
Het |
Slc26a9 |
A |
G |
1: 131,690,556 (GRCm39) |
Y520C |
probably damaging |
Het |
Spata20 |
G |
A |
11: 94,374,867 (GRCm39) |
A245V |
probably benign |
Het |
Steap3 |
A |
C |
1: 120,169,248 (GRCm39) |
F350V |
probably benign |
Het |
Swt1 |
A |
T |
1: 151,286,815 (GRCm39) |
F226I |
probably benign |
Het |
Taar7f |
A |
G |
10: 23,925,885 (GRCm39) |
T160A |
possibly damaging |
Het |
Timd5 |
G |
A |
11: 46,419,382 (GRCm39) |
W66* |
probably null |
Het |
Upf2 |
A |
T |
2: 6,023,743 (GRCm39) |
I698F |
unknown |
Het |
Vmn2r84 |
T |
C |
10: 130,227,982 (GRCm39) |
T85A |
possibly damaging |
Het |
Zfp426 |
T |
C |
9: 20,382,147 (GRCm39) |
E280G |
possibly damaging |
Het |
Zfp810 |
C |
A |
9: 22,190,568 (GRCm39) |
E78* |
probably null |
Het |
Zfp937 |
GTGATAAGGCATTTGCACAAAACAGTCATCTCCTAACACATAAAAGAACACAT |
G |
2: 150,080,630 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Or11g26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02385:Or11g26
|
APN |
14 |
50,752,900 (GRCm39) |
missense |
probably damaging |
0.97 |
R0046:Or11g26
|
UTSW |
14 |
50,753,596 (GRCm39) |
makesense |
probably null |
|
R0369:Or11g26
|
UTSW |
14 |
50,753,282 (GRCm39) |
missense |
probably benign |
0.00 |
R0612:Or11g26
|
UTSW |
14 |
50,752,939 (GRCm39) |
missense |
probably benign |
|
R1588:Or11g26
|
UTSW |
14 |
50,753,584 (GRCm39) |
missense |
probably benign |
|
R1726:Or11g26
|
UTSW |
14 |
50,753,636 (GRCm39) |
splice site |
probably null |
|
R1998:Or11g26
|
UTSW |
14 |
50,752,813 (GRCm39) |
missense |
probably benign |
0.00 |
R2875:Or11g26
|
UTSW |
14 |
50,753,269 (GRCm39) |
missense |
probably benign |
0.06 |
R4009:Or11g26
|
UTSW |
14 |
50,753,419 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5119:Or11g26
|
UTSW |
14 |
50,752,966 (GRCm39) |
missense |
probably benign |
0.00 |
R5232:Or11g26
|
UTSW |
14 |
50,753,495 (GRCm39) |
missense |
probably damaging |
0.99 |
R5627:Or11g26
|
UTSW |
14 |
50,753,257 (GRCm39) |
missense |
probably benign |
|
R5930:Or11g26
|
UTSW |
14 |
50,753,249 (GRCm39) |
missense |
probably benign |
|
R6597:Or11g26
|
UTSW |
14 |
50,753,008 (GRCm39) |
missense |
probably benign |
0.11 |
R7596:Or11g26
|
UTSW |
14 |
50,753,002 (GRCm39) |
missense |
probably benign |
0.14 |
R8051:Or11g26
|
UTSW |
14 |
50,753,100 (GRCm39) |
missense |
probably benign |
0.00 |
R8294:Or11g26
|
UTSW |
14 |
50,753,083 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8329:Or11g26
|
UTSW |
14 |
50,753,015 (GRCm39) |
missense |
probably damaging |
0.99 |
R8380:Or11g26
|
UTSW |
14 |
50,753,297 (GRCm39) |
missense |
probably benign |
0.00 |
R9517:Or11g26
|
UTSW |
14 |
50,752,770 (GRCm39) |
missense |
probably benign |
|
R9647:Or11g26
|
UTSW |
14 |
50,753,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R9694:Or11g26
|
UTSW |
14 |
50,752,669 (GRCm39) |
missense |
probably benign |
|
R9796:Or11g26
|
UTSW |
14 |
50,753,229 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1088:Or11g26
|
UTSW |
14 |
50,752,984 (GRCm39) |
missense |
possibly damaging |
0.90 |
Z1176:Or11g26
|
UTSW |
14 |
50,753,522 (GRCm39) |
missense |
probably damaging |
1.00 |
|