Other mutations in this stock |
Total: 52 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
G |
A |
12: 55,126,768 (GRCm39) |
T32I |
probably benign |
Het |
4930486L24Rik |
T |
A |
13: 61,000,922 (GRCm39) |
I205L |
probably benign |
Het |
Aatk |
C |
T |
11: 119,901,508 (GRCm39) |
V963M |
probably damaging |
Het |
Adra1b |
C |
A |
11: 43,726,242 (GRCm39) |
R225L |
probably damaging |
Het |
Adrb1 |
T |
C |
19: 56,711,021 (GRCm39) |
V73A |
probably damaging |
Het |
Akt3 |
A |
T |
1: 176,877,756 (GRCm39) |
Y337* |
probably null |
Het |
BC035947 |
G |
T |
1: 78,475,527 (GRCm39) |
P335Q |
possibly damaging |
Het |
C2cd3 |
T |
C |
7: 100,104,553 (GRCm39) |
F2189L |
probably benign |
Het |
Capn9 |
A |
G |
8: 125,342,924 (GRCm39) |
I635V |
probably benign |
Het |
Cep55 |
T |
A |
19: 38,046,374 (GRCm39) |
D42E |
probably benign |
Het |
Cftr |
T |
A |
6: 18,274,607 (GRCm39) |
Y878* |
probably null |
Het |
Clpb |
A |
T |
7: 101,312,866 (GRCm39) |
|
probably benign |
Het |
Cpeb3 |
T |
C |
19: 37,022,089 (GRCm39) |
I569V |
possibly damaging |
Het |
Cpne6 |
A |
T |
14: 55,752,701 (GRCm39) |
D297V |
probably damaging |
Het |
Ddhd1 |
T |
C |
14: 45,894,976 (GRCm39) |
T165A |
probably benign |
Het |
Fam98b |
T |
C |
2: 117,093,402 (GRCm39) |
|
probably null |
Het |
Frem2 |
T |
C |
3: 53,561,744 (GRCm39) |
N921S |
probably benign |
Het |
Gbf1 |
T |
A |
19: 46,260,211 (GRCm39) |
V1039E |
probably benign |
Het |
Gmip |
A |
G |
8: 70,266,436 (GRCm39) |
E212G |
probably damaging |
Het |
Gpcpd1 |
C |
T |
2: 132,379,758 (GRCm39) |
|
probably benign |
Het |
Gtf2ird1 |
A |
T |
5: 134,392,766 (GRCm39) |
N796K |
probably damaging |
Het |
Hadhb |
T |
C |
5: 30,360,247 (GRCm39) |
|
probably benign |
Het |
Itga4 |
T |
A |
2: 79,119,609 (GRCm39) |
S472T |
probably damaging |
Het |
Kcna4 |
G |
A |
2: 107,125,670 (GRCm39) |
E135K |
possibly damaging |
Het |
Kmt2c |
G |
T |
5: 25,480,737 (GRCm39) |
|
probably null |
Het |
Lama1 |
T |
C |
17: 68,091,020 (GRCm39) |
I1620T |
unknown |
Het |
Lins1 |
A |
G |
7: 66,363,902 (GRCm39) |
E594G |
probably benign |
Het |
Lrrc38 |
T |
A |
4: 143,096,364 (GRCm39) |
M225K |
probably benign |
Het |
Mphosph9 |
A |
G |
5: 124,399,090 (GRCm39) |
I975T |
probably damaging |
Het |
Mrgprh |
T |
C |
17: 13,095,874 (GRCm39) |
F38S |
probably benign |
Het |
Myo1h |
G |
A |
5: 114,458,714 (GRCm39) |
G150R |
probably damaging |
Het |
Oas2 |
T |
G |
5: 120,876,863 (GRCm39) |
I391L |
possibly damaging |
Het |
Or4a70 |
T |
A |
2: 89,324,378 (GRCm39) |
R93* |
probably null |
Het |
Or5p72 |
T |
C |
7: 108,021,889 (GRCm39) |
I37T |
possibly damaging |
Het |
Or6c3b |
T |
A |
10: 129,527,391 (GRCm39) |
D173V |
possibly damaging |
Het |
Pdcd5 |
T |
C |
7: 35,342,063 (GRCm39) |
T182A |
probably damaging |
Het |
Pdlim7 |
T |
C |
13: 55,656,810 (GRCm39) |
D48G |
probably damaging |
Het |
Polr3b |
A |
C |
10: 84,464,489 (GRCm39) |
|
probably null |
Het |
Psmd5 |
C |
T |
2: 34,747,649 (GRCm39) |
|
probably null |
Het |
Rsf1 |
GGCG |
GGCGACGGCCGCG |
7: 97,229,113 (GRCm39) |
|
probably benign |
Homo |
Sdhb |
T |
C |
4: 140,703,501 (GRCm39) |
Y208H |
probably damaging |
Het |
Serinc5 |
G |
A |
13: 92,842,740 (GRCm39) |
V397I |
possibly damaging |
Het |
Sik2 |
A |
T |
9: 50,909,834 (GRCm39) |
M73K |
possibly damaging |
Het |
Slc41a1 |
A |
G |
1: 131,770,487 (GRCm39) |
|
probably null |
Het |
Slco1a1 |
T |
C |
6: 141,882,213 (GRCm39) |
I119V |
probably benign |
Het |
Srd5a1 |
T |
C |
13: 69,759,418 (GRCm39) |
|
probably benign |
Het |
Stab2 |
T |
C |
10: 86,754,948 (GRCm39) |
I1111V |
probably benign |
Het |
Stxbp6 |
G |
T |
12: 44,949,779 (GRCm39) |
|
probably null |
Het |
Tbc1d19 |
A |
G |
5: 53,992,591 (GRCm39) |
|
probably null |
Het |
Tnxb |
A |
T |
17: 34,929,710 (GRCm39) |
T2815S |
probably benign |
Het |
Txnip |
T |
A |
3: 96,467,623 (GRCm39) |
I363N |
probably damaging |
Het |
Zfp442 |
A |
T |
2: 150,251,499 (GRCm39) |
N134K |
possibly damaging |
Het |
|
Other mutations in Or7e178 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01992:Or7e178
|
APN |
9 |
20,226,015 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02412:Or7e178
|
APN |
9 |
20,225,935 (GRCm39) |
missense |
probably benign |
|
IGL03288:Or7e178
|
APN |
9 |
20,247,207 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03395:Or7e178
|
APN |
9 |
20,225,847 (GRCm39) |
missense |
probably damaging |
1.00 |
R0332:Or7e178
|
UTSW |
9 |
20,225,352 (GRCm39) |
missense |
probably benign |
0.00 |
R0346:Or7e178
|
UTSW |
9 |
20,225,707 (GRCm39) |
missense |
probably benign |
0.20 |
R0569:Or7e178
|
UTSW |
9 |
20,225,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R0798:Or7e178
|
UTSW |
9 |
20,225,495 (GRCm39) |
nonsense |
probably null |
|
R0865:Or7e178
|
UTSW |
9 |
20,226,045 (GRCm39) |
missense |
probably damaging |
1.00 |
R1082:Or7e178
|
UTSW |
9 |
20,225,765 (GRCm39) |
missense |
possibly damaging |
0.52 |
R1905:Or7e178
|
UTSW |
9 |
20,226,142 (GRCm39) |
missense |
probably benign |
|
R4245:Or7e178
|
UTSW |
9 |
20,225,629 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5566:Or7e178
|
UTSW |
9 |
20,225,265 (GRCm39) |
missense |
probably benign |
|
R6306:Or7e178
|
UTSW |
9 |
20,225,742 (GRCm39) |
missense |
probably benign |
0.25 |
R6721:Or7e178
|
UTSW |
9 |
20,225,576 (GRCm39) |
missense |
probably benign |
0.24 |
R6930:Or7e178
|
UTSW |
9 |
20,225,395 (GRCm39) |
missense |
probably damaging |
1.00 |
R7196:Or7e178
|
UTSW |
9 |
20,225,494 (GRCm39) |
missense |
probably benign |
0.38 |
R7711:Or7e178
|
UTSW |
9 |
20,225,319 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8023:Or7e178
|
UTSW |
9 |
20,225,545 (GRCm39) |
missense |
probably benign |
0.00 |
R8029:Or7e178
|
UTSW |
9 |
20,225,643 (GRCm39) |
missense |
possibly damaging |
0.59 |
R8050:Or7e178
|
UTSW |
9 |
20,225,941 (GRCm39) |
missense |
probably damaging |
1.00 |
R8058:Or7e178
|
UTSW |
9 |
20,225,476 (GRCm39) |
missense |
probably damaging |
0.99 |
R8159:Or7e178
|
UTSW |
9 |
20,226,015 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8201:Or7e178
|
UTSW |
9 |
20,225,908 (GRCm39) |
missense |
probably benign |
0.10 |
R9022:Or7e178
|
UTSW |
9 |
20,225,268 (GRCm39) |
missense |
probably damaging |
1.00 |
|