Other mutations in this stock |
Total: 78 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca1 |
C |
T |
4: 53,081,954 (GRCm39) |
D769N |
possibly damaging |
Het |
Abcb6 |
A |
G |
1: 75,156,653 (GRCm39) |
L37P |
possibly damaging |
Het |
Abcg1 |
G |
T |
17: 31,324,504 (GRCm39) |
A250S |
probably benign |
Het |
Acsf3 |
C |
T |
8: 123,540,373 (GRCm39) |
H524Y |
possibly damaging |
Het |
Agbl4 |
A |
G |
4: 110,518,039 (GRCm39) |
K110R |
unknown |
Het |
Arfgap2 |
G |
A |
2: 91,096,644 (GRCm39) |
|
probably null |
Het |
B4galt4 |
T |
C |
16: 38,586,383 (GRCm39) |
|
probably null |
Het |
Bex6 |
G |
T |
16: 32,005,224 (GRCm39) |
D11Y |
probably damaging |
Het |
Bhlhe40 |
TG |
TGG |
6: 108,641,818 (GRCm39) |
254 |
probably null |
Het |
C8b |
A |
T |
4: 104,647,811 (GRCm39) |
D334V |
probably damaging |
Het |
Capn11 |
T |
C |
17: 45,954,681 (GRCm39) |
Q152R |
probably null |
Het |
Ccdc171 |
C |
A |
4: 83,499,003 (GRCm39) |
Q234K |
probably damaging |
Het |
Cemip2 |
C |
A |
19: 21,829,695 (GRCm39) |
A1268E |
probably benign |
Het |
Clec2h |
A |
G |
6: 128,650,966 (GRCm39) |
D82G |
probably benign |
Het |
Creld2 |
A |
G |
15: 88,710,632 (GRCm39) |
D349G |
probably damaging |
Het |
D430041D05Rik |
A |
G |
2: 103,979,128 (GRCm39) |
*1415Q |
probably null |
Het |
Dnmt3a |
T |
C |
12: 3,952,768 (GRCm39) |
V755A |
possibly damaging |
Het |
Doc2a |
G |
T |
7: 126,450,164 (GRCm39) |
V201L |
probably benign |
Het |
Fan1 |
T |
A |
7: 64,022,234 (GRCm39) |
N340Y |
probably damaging |
Het |
Fbn1 |
G |
T |
2: 125,193,889 (GRCm39) |
D1359E |
possibly damaging |
Het |
Fcnb |
T |
C |
2: 27,969,707 (GRCm39) |
Y120C |
probably damaging |
Het |
Fras1 |
T |
A |
5: 96,842,778 (GRCm39) |
D1665E |
probably benign |
Het |
Fry |
A |
T |
5: 150,419,232 (GRCm39) |
D524V |
|
Het |
Garem1 |
A |
G |
18: 21,281,621 (GRCm39) |
L245P |
probably damaging |
Het |
Gdf6 |
A |
G |
4: 9,859,712 (GRCm39) |
S265G |
probably benign |
Het |
Gm5591 |
T |
C |
7: 38,218,363 (GRCm39) |
I837V |
probably benign |
Het |
Gpr61 |
T |
C |
3: 108,058,211 (GRCm39) |
Y150C |
probably damaging |
Het |
Grin2b |
A |
T |
6: 135,710,225 (GRCm39) |
L1107Q |
probably damaging |
Het |
Helb |
A |
G |
10: 119,941,483 (GRCm39) |
S402P |
probably benign |
Het |
Htt |
A |
G |
5: 34,977,444 (GRCm39) |
T777A |
probably benign |
Het |
Iffo2 |
A |
G |
4: 139,341,164 (GRCm39) |
D383G |
probably benign |
Het |
Ikzf3 |
G |
T |
11: 98,407,753 (GRCm39) |
Y29* |
probably null |
Het |
Ints2 |
A |
T |
11: 86,146,179 (GRCm39) |
M143K |
probably benign |
Het |
Jmjd1c |
T |
C |
10: 67,090,274 (GRCm39) |
V2292A |
not run |
Het |
Katnip |
A |
G |
7: 125,442,188 (GRCm39) |
E725G |
probably benign |
Het |
Lamb1 |
C |
A |
12: 31,353,046 (GRCm39) |
Q916K |
probably benign |
Het |
Lrrtm4 |
G |
A |
6: 79,999,528 (GRCm39) |
M313I |
probably benign |
Het |
Lum |
A |
G |
10: 97,404,425 (GRCm39) |
I107V |
probably benign |
Het |
Ly6h |
T |
C |
15: 75,437,061 (GRCm39) |
E126G |
probably benign |
Het |
Map3k5 |
G |
A |
10: 20,007,860 (GRCm39) |
V1230M |
probably damaging |
Het |
Mcoln1 |
T |
C |
8: 3,558,378 (GRCm39) |
F211L |
probably benign |
Het |
Mink1 |
G |
A |
11: 70,494,594 (GRCm39) |
W258* |
probably null |
Het |
Muc16 |
G |
T |
9: 18,571,298 (GRCm39) |
S407* |
probably null |
Het |
Ngef |
G |
A |
1: 87,473,744 (GRCm39) |
Q13* |
probably null |
Het |
Nxpe5 |
T |
A |
5: 138,237,573 (GRCm39) |
Y44* |
probably null |
Het |
Or13d1 |
T |
A |
4: 52,971,106 (GRCm39) |
L162M |
probably benign |
Het |
Or4a77 |
A |
G |
2: 89,487,671 (GRCm39) |
V38A |
probably benign |
Het |
Or5t9 |
A |
G |
2: 86,660,052 (GRCm39) |
R319G |
probably benign |
Het |
Or7e178 |
T |
A |
9: 20,225,476 (GRCm39) |
I247F |
probably damaging |
Het |
Or8g24 |
A |
T |
9: 38,989,862 (GRCm39) |
Y60N |
probably damaging |
Het |
Or8h8 |
C |
A |
2: 86,753,151 (GRCm39) |
A242S |
probably benign |
Het |
Orc3 |
C |
A |
4: 34,595,223 (GRCm39) |
E249* |
probably null |
Het |
Otogl |
A |
T |
10: 107,598,287 (GRCm39) |
C2288S |
probably damaging |
Het |
Pde1b |
A |
G |
15: 103,433,238 (GRCm39) |
E249G |
probably damaging |
Het |
Phf2 |
T |
C |
13: 48,976,558 (GRCm39) |
E219G |
unknown |
Het |
Rbm19 |
T |
A |
5: 120,278,440 (GRCm39) |
|
probably null |
Het |
Rcc2 |
G |
A |
4: 140,429,586 (GRCm39) |
C40Y |
probably benign |
Het |
Sbk2 |
A |
G |
7: 4,960,289 (GRCm39) |
Y294H |
possibly damaging |
Het |
Selenoo |
T |
C |
15: 88,976,942 (GRCm39) |
I198T |
possibly damaging |
Het |
Sema3f |
T |
C |
9: 107,559,800 (GRCm39) |
E729G |
probably benign |
Het |
Serpinb1b |
A |
T |
13: 33,269,293 (GRCm39) |
T9S |
probably benign |
Het |
Sfxn4 |
T |
C |
19: 60,832,690 (GRCm39) |
T235A |
probably damaging |
Het |
Shc4 |
A |
T |
2: 125,491,154 (GRCm39) |
Y461* |
probably null |
Het |
Slc22a15 |
T |
C |
3: 101,771,926 (GRCm39) |
D391G |
probably benign |
Het |
Slc22a23 |
G |
T |
13: 34,489,167 (GRCm39) |
Y239* |
probably null |
Het |
Slc24a2 |
G |
A |
4: 86,909,750 (GRCm39) |
A656V |
probably damaging |
Het |
Slc2a5 |
A |
T |
4: 150,227,590 (GRCm39) |
I470F |
probably damaging |
Het |
Sptbn4 |
T |
C |
7: 27,063,694 (GRCm39) |
E2249G |
possibly damaging |
Het |
Tdrd7 |
C |
A |
4: 46,034,309 (GRCm39) |
S1051R |
probably benign |
Het |
Tnfrsf18 |
G |
A |
4: 156,112,802 (GRCm39) |
A163T |
probably benign |
Het |
Ube3b |
T |
C |
5: 114,544,846 (GRCm39) |
V596A |
possibly damaging |
Het |
Vmn2r10 |
T |
A |
5: 109,149,955 (GRCm39) |
N363I |
probably benign |
Het |
Vmn2r15 |
T |
A |
5: 109,440,956 (GRCm39) |
I301F |
probably damaging |
Het |
Yod1 |
C |
T |
1: 130,646,806 (GRCm39) |
Q228* |
probably null |
Het |
Zfp433 |
A |
T |
10: 81,556,124 (GRCm39) |
K209* |
probably null |
Het |
Zfp865 |
G |
A |
7: 5,033,445 (GRCm39) |
V477I |
probably benign |
Het |
Zfp937 |
T |
A |
2: 150,081,421 (GRCm39) |
Y484N |
probably benign |
Het |
Zfp951 |
T |
G |
5: 104,962,312 (GRCm39) |
H418P |
probably damaging |
Het |
|
Other mutations in Tas2r139 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00863:Tas2r139
|
APN |
6 |
42,118,055 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01593:Tas2r139
|
APN |
6 |
42,117,891 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01835:Tas2r139
|
APN |
6 |
42,118,366 (GRCm39) |
missense |
probably benign |
0.21 |
IGL02990:Tas2r139
|
APN |
6 |
42,118,038 (GRCm39) |
missense |
probably damaging |
1.00 |
R0517:Tas2r139
|
UTSW |
6 |
42,118,425 (GRCm39) |
missense |
probably damaging |
0.98 |
R1106:Tas2r139
|
UTSW |
6 |
42,118,479 (GRCm39) |
missense |
probably benign |
0.36 |
R1352:Tas2r139
|
UTSW |
6 |
42,117,874 (GRCm39) |
missense |
probably benign |
0.28 |
R4352:Tas2r139
|
UTSW |
6 |
42,118,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R4632:Tas2r139
|
UTSW |
6 |
42,118,432 (GRCm39) |
missense |
probably damaging |
1.00 |
R4785:Tas2r139
|
UTSW |
6 |
42,118,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R4947:Tas2r139
|
UTSW |
6 |
42,118,500 (GRCm39) |
missense |
possibly damaging |
0.82 |
R5888:Tas2r139
|
UTSW |
6 |
42,118,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R6796:Tas2r139
|
UTSW |
6 |
42,118,526 (GRCm39) |
missense |
probably damaging |
1.00 |
R8075:Tas2r139
|
UTSW |
6 |
42,118,154 (GRCm39) |
missense |
probably benign |
0.00 |
R8319:Tas2r139
|
UTSW |
6 |
42,118,720 (GRCm39) |
missense |
probably benign |
0.01 |
R9087:Tas2r139
|
UTSW |
6 |
42,118,168 (GRCm39) |
missense |
probably damaging |
1.00 |
R9185:Tas2r139
|
UTSW |
6 |
42,118,099 (GRCm39) |
missense |
probably benign |
0.25 |
R9803:Tas2r139
|
UTSW |
6 |
42,118,066 (GRCm39) |
missense |
probably damaging |
1.00 |
|