Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700056E22Rik |
T |
A |
1: 183,765,356 (GRCm39) |
R234S |
probably damaging |
Het |
Ace |
T |
A |
11: 105,870,092 (GRCm39) |
F806Y |
probably benign |
Het |
Ak8 |
A |
G |
2: 28,629,643 (GRCm39) |
T286A |
probably benign |
Het |
Apba2 |
T |
A |
7: 64,395,546 (GRCm39) |
F674Y |
probably damaging |
Het |
Apob |
A |
G |
12: 8,058,069 (GRCm39) |
I2184V |
probably benign |
Het |
Arhgap23 |
C |
T |
11: 97,356,854 (GRCm39) |
P884L |
probably benign |
Het |
Atg2a |
T |
C |
19: 6,294,554 (GRCm39) |
L90P |
probably damaging |
Het |
Bmi1 |
C |
T |
2: 18,689,114 (GRCm39) |
T266I |
probably damaging |
Het |
Cdh26 |
A |
G |
2: 178,104,517 (GRCm39) |
I301V |
probably damaging |
Het |
Cenpx |
A |
T |
11: 120,602,558 (GRCm39) |
H68Q |
unknown |
Het |
Cnot10 |
T |
C |
9: 114,439,738 (GRCm39) |
R524G |
probably benign |
Het |
Cnpy1 |
A |
T |
5: 28,414,206 (GRCm39) |
Y22* |
probably null |
Het |
Csmd3 |
C |
T |
15: 47,499,794 (GRCm39) |
R2114H |
|
Het |
Defa29 |
T |
A |
8: 21,816,062 (GRCm39) |
T102S |
probably benign |
Het |
Fras1 |
T |
C |
5: 96,744,711 (GRCm39) |
I582T |
probably benign |
Het |
Gm14295 |
G |
A |
2: 176,501,422 (GRCm39) |
C304Y |
probably damaging |
Het |
Gucy2d |
T |
C |
7: 98,093,046 (GRCm39) |
V141A |
possibly damaging |
Het |
Ifi47 |
A |
C |
11: 48,986,425 (GRCm39) |
Q64P |
probably damaging |
Het |
Irx3 |
G |
T |
8: 92,527,028 (GRCm39) |
S225R |
possibly damaging |
Het |
Itpr1 |
A |
G |
6: 108,340,581 (GRCm39) |
H289R |
probably benign |
Het |
Lamc3 |
A |
G |
2: 31,802,128 (GRCm39) |
D512G |
probably damaging |
Het |
Mcm3 |
C |
T |
1: 20,886,980 (GRCm39) |
V142I |
probably benign |
Het |
Med23 |
C |
A |
10: 24,784,632 (GRCm39) |
F1200L |
probably benign |
Het |
Ndst4 |
A |
T |
3: 125,364,439 (GRCm39) |
D372V |
possibly damaging |
Het |
Nob1 |
T |
A |
8: 108,148,230 (GRCm39) |
K71* |
probably null |
Het |
Ntrk3 |
A |
G |
7: 78,005,897 (GRCm39) |
I488T |
probably benign |
Het |
Pds5b |
G |
T |
5: 150,643,424 (GRCm39) |
C82F |
probably damaging |
Het |
Pkd1l3 |
T |
A |
8: 110,360,022 (GRCm39) |
V969E |
possibly damaging |
Het |
Ppme1 |
A |
T |
7: 99,984,298 (GRCm39) |
N307K |
probably benign |
Het |
Pus7l |
C |
T |
15: 94,425,856 (GRCm39) |
C515Y |
probably benign |
Het |
Rpp21 |
T |
A |
17: 36,568,591 (GRCm39) |
H22L |
possibly damaging |
Het |
Scamp3 |
T |
C |
3: 89,088,525 (GRCm39) |
F244L |
probably damaging |
Het |
Scgb1b7 |
A |
T |
7: 31,412,379 (GRCm39) |
K52* |
probably null |
Het |
Slc12a3 |
T |
C |
8: 95,060,695 (GRCm39) |
I261T |
probably damaging |
Het |
Slc19a3 |
C |
T |
1: 82,992,533 (GRCm39) |
R396H |
probably damaging |
Het |
Slc22a14 |
T |
C |
9: 119,009,922 (GRCm39) |
I58V |
probably benign |
Het |
Slc9a9 |
A |
C |
9: 95,111,092 (GRCm39) |
T637P |
probably damaging |
Het |
Snrnp40 |
T |
A |
4: 130,278,316 (GRCm39) |
C274S |
possibly damaging |
Het |
Sptbn1 |
A |
G |
11: 30,088,457 (GRCm39) |
V905A |
probably damaging |
Het |
Taok3 |
A |
G |
5: 117,404,102 (GRCm39) |
D759G |
possibly damaging |
Het |
Tas1r1 |
T |
C |
4: 152,117,033 (GRCm39) |
I200M |
probably benign |
Het |
Tnfrsf25 |
T |
C |
4: 152,204,139 (GRCm39) |
V360A |
possibly damaging |
Het |
Trim12a |
A |
T |
7: 103,953,544 (GRCm39) |
M189K |
possibly damaging |
Het |
Tspan32 |
T |
C |
7: 142,559,695 (GRCm39) |
F41L |
probably benign |
Het |
Tube1 |
T |
A |
10: 39,021,657 (GRCm39) |
S301T |
possibly damaging |
Het |
Usp8 |
T |
C |
2: 126,584,578 (GRCm39) |
S596P |
probably benign |
Het |
Virma |
T |
A |
4: 11,521,261 (GRCm39) |
|
probably null |
Het |
Vmn2r58 |
T |
C |
7: 41,513,722 (GRCm39) |
D307G |
probably benign |
Het |
Zeb2 |
T |
C |
2: 44,888,964 (GRCm39) |
K327R |
probably damaging |
Het |
Zfp54 |
C |
T |
17: 21,654,910 (GRCm39) |
T468M |
probably benign |
Het |
Zfp780b |
A |
T |
7: 27,662,551 (GRCm39) |
I668N |
possibly damaging |
Het |
|
Other mutations in Bhmt2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Bhmt2
|
APN |
13 |
93,803,279 (GRCm39) |
splice site |
probably benign |
|
IGL01665:Bhmt2
|
APN |
13 |
93,799,661 (GRCm39) |
nonsense |
probably null |
|
IGL02059:Bhmt2
|
APN |
13 |
93,803,171 (GRCm39) |
missense |
probably benign |
|
IGL02239:Bhmt2
|
APN |
13 |
93,799,687 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02267:Bhmt2
|
APN |
13 |
93,805,854 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03148:Bhmt2
|
APN |
13 |
93,803,161 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1171:Bhmt2
|
UTSW |
13 |
93,798,837 (GRCm39) |
missense |
probably benign |
0.00 |
R1517:Bhmt2
|
UTSW |
13 |
93,798,847 (GRCm39) |
missense |
probably damaging |
0.97 |
R1886:Bhmt2
|
UTSW |
13 |
93,798,998 (GRCm39) |
missense |
probably benign |
0.02 |
R2167:Bhmt2
|
UTSW |
13 |
93,799,012 (GRCm39) |
missense |
probably benign |
0.29 |
R4024:Bhmt2
|
UTSW |
13 |
93,799,839 (GRCm39) |
splice site |
probably benign |
|
R4823:Bhmt2
|
UTSW |
13 |
93,799,798 (GRCm39) |
missense |
probably benign |
|
R5273:Bhmt2
|
UTSW |
13 |
93,803,086 (GRCm39) |
missense |
possibly damaging |
0.84 |
R5333:Bhmt2
|
UTSW |
13 |
93,807,938 (GRCm39) |
missense |
probably benign |
0.00 |
R5738:Bhmt2
|
UTSW |
13 |
93,799,798 (GRCm39) |
missense |
probably benign |
|
R5955:Bhmt2
|
UTSW |
13 |
93,799,705 (GRCm39) |
missense |
probably benign |
0.00 |
R6281:Bhmt2
|
UTSW |
13 |
93,799,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R6858:Bhmt2
|
UTSW |
13 |
93,807,948 (GRCm39) |
missense |
probably damaging |
0.97 |
R6934:Bhmt2
|
UTSW |
13 |
93,798,819 (GRCm39) |
missense |
probably benign |
0.18 |
R6985:Bhmt2
|
UTSW |
13 |
93,799,830 (GRCm39) |
missense |
possibly damaging |
0.64 |
R7185:Bhmt2
|
UTSW |
13 |
93,799,779 (GRCm39) |
missense |
probably benign |
0.22 |
R7639:Bhmt2
|
UTSW |
13 |
93,799,822 (GRCm39) |
missense |
probably damaging |
1.00 |
R9224:Bhmt2
|
UTSW |
13 |
93,805,854 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Bhmt2
|
UTSW |
13 |
93,799,833 (GRCm39) |
missense |
probably damaging |
0.99 |
|