Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
Acot10 |
A |
T |
15: 20,666,612 (GRCm39) |
L43Q |
probably damaging |
Het |
Alms1 |
G |
A |
6: 85,597,870 (GRCm39) |
V1368I |
probably benign |
Het |
Als2cl |
T |
C |
9: 110,713,115 (GRCm39) |
S2P |
probably benign |
Het |
AW209491 |
T |
C |
13: 14,812,158 (GRCm39) |
V337A |
probably damaging |
Het |
Bace2 |
A |
G |
16: 97,237,856 (GRCm39) |
T436A |
probably benign |
Het |
BC023105 |
A |
G |
18: 60,575,356 (GRCm39) |
|
noncoding transcript |
Het |
Blvra |
T |
C |
2: 126,937,075 (GRCm39) |
V176A |
probably damaging |
Het |
Casp2 |
G |
A |
6: 42,244,828 (GRCm39) |
A76T |
probably damaging |
Het |
Ccdc88c |
A |
G |
12: 100,911,332 (GRCm39) |
L34P |
probably damaging |
Het |
Cep250 |
G |
A |
2: 155,834,552 (GRCm39) |
R2159K |
probably damaging |
Het |
Col6a2 |
T |
A |
10: 76,442,003 (GRCm39) |
|
probably null |
Het |
Cse1l |
T |
C |
2: 166,783,970 (GRCm39) |
Y488H |
probably benign |
Het |
Dip2c |
G |
T |
13: 9,687,137 (GRCm39) |
G1254C |
probably damaging |
Het |
Dnajb12 |
T |
A |
10: 59,730,136 (GRCm39) |
S270R |
possibly damaging |
Het |
Dnajc28 |
G |
A |
16: 91,413,755 (GRCm39) |
T187M |
probably damaging |
Het |
Dscaml1 |
G |
A |
9: 45,643,366 (GRCm39) |
A1262T |
probably benign |
Het |
Dtwd2 |
A |
C |
18: 49,831,373 (GRCm39) |
|
probably benign |
Het |
Fadd |
C |
A |
7: 144,134,488 (GRCm39) |
K132N |
possibly damaging |
Het |
Fndc3c1 |
T |
C |
X: 105,487,897 (GRCm39) |
N462S |
probably benign |
Het |
Fzd3 |
A |
G |
14: 65,472,616 (GRCm39) |
V384A |
probably benign |
Het |
Gm6370 |
T |
C |
5: 146,430,702 (GRCm39) |
S296P |
probably benign |
Het |
Gsdmc |
T |
A |
15: 63,651,876 (GRCm39) |
H245L |
probably benign |
Het |
H13 |
T |
C |
2: 152,523,029 (GRCm39) |
I114T |
probably damaging |
Het |
Hhipl2 |
A |
G |
1: 183,204,920 (GRCm39) |
R78G |
probably benign |
Het |
Hrh3 |
C |
A |
2: 179,744,643 (GRCm39) |
R99L |
possibly damaging |
Het |
Ldc1 |
A |
T |
4: 130,112,967 (GRCm39) |
L143Q |
probably damaging |
Het |
Man2c1 |
A |
G |
9: 57,044,055 (GRCm39) |
N330S |
probably damaging |
Het |
Muc19 |
T |
A |
15: 91,781,816 (GRCm39) |
|
noncoding transcript |
Het |
Myh14 |
T |
G |
7: 44,277,974 (GRCm39) |
M1092L |
probably benign |
Het |
Neb |
A |
G |
2: 52,038,778 (GRCm39) |
I2899T |
probably benign |
Het |
Neb |
T |
A |
2: 52,134,137 (GRCm39) |
Q3282L |
probably damaging |
Het |
Nqo2 |
A |
T |
13: 34,163,620 (GRCm39) |
Q93L |
probably benign |
Het |
Or4a2 |
C |
A |
2: 89,248,444 (GRCm39) |
L104F |
probably benign |
Het |
Or51i2 |
T |
C |
7: 103,689,609 (GRCm39) |
V202A |
probably damaging |
Het |
Pcsk1 |
A |
G |
13: 75,244,488 (GRCm39) |
N122S |
probably damaging |
Het |
Pdzrn4 |
A |
G |
15: 92,668,745 (GRCm39) |
I966V |
probably benign |
Het |
Phldb1 |
G |
A |
9: 44,627,128 (GRCm39) |
T439I |
possibly damaging |
Het |
Pign |
A |
G |
1: 105,481,540 (GRCm39) |
|
probably benign |
Het |
Pkn1 |
A |
T |
8: 84,417,828 (GRCm39) |
D120E |
probably benign |
Het |
Ptpru |
A |
G |
4: 131,546,348 (GRCm39) |
Y301H |
probably damaging |
Het |
Raly |
C |
T |
2: 154,699,378 (GRCm39) |
Q61* |
probably null |
Het |
Rpl24 |
T |
C |
16: 55,791,723 (GRCm39) |
V148A |
probably benign |
Het |
S100a16 |
A |
G |
3: 90,449,379 (GRCm39) |
N18S |
probably damaging |
Het |
Sec31b |
G |
T |
19: 44,512,968 (GRCm39) |
T507N |
possibly damaging |
Het |
Sgca |
T |
C |
11: 94,863,396 (GRCm39) |
T27A |
possibly damaging |
Het |
Slc22a12 |
C |
A |
19: 6,590,658 (GRCm39) |
R203L |
probably damaging |
Het |
Ssbp3 |
C |
A |
4: 106,904,393 (GRCm39) |
|
probably benign |
Het |
Sucnr1 |
C |
G |
3: 59,994,215 (GRCm39) |
R248G |
probably damaging |
Het |
Tbr1 |
C |
T |
2: 61,642,076 (GRCm39) |
P184L |
probably benign |
Het |
Thsd7b |
A |
T |
1: 130,044,356 (GRCm39) |
D1112V |
probably benign |
Het |
Tnc |
A |
G |
4: 63,933,188 (GRCm39) |
V692A |
probably damaging |
Het |
Top2a |
C |
A |
11: 98,913,786 (GRCm39) |
K18N |
probably damaging |
Het |
Topbp1 |
G |
T |
9: 103,187,158 (GRCm39) |
R121L |
probably damaging |
Het |
Unc79 |
T |
C |
12: 103,025,629 (GRCm39) |
C339R |
probably damaging |
Het |
Wdfy3 |
C |
T |
5: 102,047,924 (GRCm39) |
|
probably null |
Het |
Zbtb3 |
G |
C |
19: 8,780,384 (GRCm39) |
|
probably benign |
Het |
Zfp715 |
T |
A |
7: 42,947,304 (GRCm39) |
K885N |
possibly damaging |
Het |
|
Other mutations in Or13a18 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00340:Or13a18
|
APN |
7 |
140,190,666 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02408:Or13a18
|
APN |
7 |
140,190,844 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02496:Or13a18
|
APN |
7 |
140,190,081 (GRCm39) |
start codon destroyed |
probably benign |
|
IGL03003:Or13a18
|
APN |
7 |
140,190,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0538:Or13a18
|
UTSW |
7 |
140,190,297 (GRCm39) |
missense |
probably damaging |
1.00 |
R1350:Or13a18
|
UTSW |
7 |
140,190,622 (GRCm39) |
missense |
probably damaging |
0.96 |
R1466:Or13a18
|
UTSW |
7 |
140,190,882 (GRCm39) |
missense |
probably benign |
0.01 |
R1466:Or13a18
|
UTSW |
7 |
140,190,882 (GRCm39) |
missense |
probably benign |
0.01 |
R2008:Or13a18
|
UTSW |
7 |
140,190,498 (GRCm39) |
missense |
probably damaging |
1.00 |
R4110:Or13a18
|
UTSW |
7 |
140,190,178 (GRCm39) |
missense |
possibly damaging |
0.89 |
R4255:Or13a18
|
UTSW |
7 |
140,190,500 (GRCm39) |
nonsense |
probably null |
|
R4622:Or13a18
|
UTSW |
7 |
140,190,611 (GRCm39) |
nonsense |
probably null |
|
R4809:Or13a18
|
UTSW |
7 |
140,190,987 (GRCm39) |
missense |
probably damaging |
0.98 |
R4826:Or13a18
|
UTSW |
7 |
140,190,232 (GRCm39) |
missense |
probably benign |
0.02 |
R4989:Or13a18
|
UTSW |
7 |
140,190,304 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5177:Or13a18
|
UTSW |
7 |
140,190,102 (GRCm39) |
missense |
probably benign |
0.00 |
R5261:Or13a18
|
UTSW |
7 |
140,190,576 (GRCm39) |
missense |
probably benign |
0.00 |
R5770:Or13a18
|
UTSW |
7 |
140,190,856 (GRCm39) |
missense |
probably damaging |
1.00 |
R5863:Or13a18
|
UTSW |
7 |
140,190,544 (GRCm39) |
missense |
probably damaging |
0.97 |
R6082:Or13a18
|
UTSW |
7 |
140,190,594 (GRCm39) |
missense |
probably benign |
0.00 |
R6705:Or13a18
|
UTSW |
7 |
140,190,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R7216:Or13a18
|
UTSW |
7 |
140,190,373 (GRCm39) |
missense |
possibly damaging |
0.87 |
R7443:Or13a18
|
UTSW |
7 |
140,190,961 (GRCm39) |
missense |
probably damaging |
1.00 |
R7485:Or13a18
|
UTSW |
7 |
140,190,091 (GRCm39) |
missense |
probably benign |
0.02 |
R7806:Or13a18
|
UTSW |
7 |
140,190,685 (GRCm39) |
missense |
probably benign |
0.00 |
R8373:Or13a18
|
UTSW |
7 |
140,190,208 (GRCm39) |
missense |
possibly damaging |
0.88 |
R8884:Or13a18
|
UTSW |
7 |
140,190,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R9278:Or13a18
|
UTSW |
7 |
140,190,936 (GRCm39) |
missense |
probably damaging |
1.00 |
R9595:Or13a18
|
UTSW |
7 |
140,190,939 (GRCm39) |
missense |
probably damaging |
0.97 |
|