Other mutations in this stock |
Total: 64 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ascc3 |
T |
A |
10: 50,718,289 (GRCm39) |
I1994N |
probably damaging |
Het |
BC061237 |
A |
G |
14: 44,738,730 (GRCm39) |
D43G |
probably benign |
Het |
Bckdhb |
A |
C |
9: 83,870,863 (GRCm39) |
E124D |
probably damaging |
Het |
Card6 |
T |
C |
15: 5,128,778 (GRCm39) |
T873A |
probably benign |
Het |
Cbs |
C |
A |
17: 31,835,048 (GRCm39) |
C476F |
probably benign |
Het |
Cckbr |
A |
C |
7: 105,075,376 (GRCm39) |
T49P |
probably benign |
Het |
Cd248 |
C |
T |
19: 5,119,534 (GRCm39) |
P461S |
probably damaging |
Het |
Cdh16 |
T |
C |
8: 105,342,959 (GRCm39) |
Y19C |
probably damaging |
Het |
Clip2 |
T |
C |
5: 134,551,847 (GRCm39) |
K92E |
probably damaging |
Het |
Cnnm2 |
T |
A |
19: 46,750,232 (GRCm39) |
C7* |
probably null |
Het |
Ctnnb1 |
T |
G |
9: 120,779,580 (GRCm39) |
|
probably benign |
Het |
Def8 |
T |
C |
8: 124,185,083 (GRCm39) |
|
probably benign |
Het |
Deup1 |
A |
G |
9: 15,511,009 (GRCm39) |
Y257H |
probably damaging |
Het |
Diaph1 |
C |
A |
18: 38,033,691 (GRCm39) |
|
probably benign |
Het |
Dnah12 |
A |
G |
14: 26,578,573 (GRCm39) |
M491V |
probably benign |
Het |
Eftud2 |
A |
C |
11: 102,737,013 (GRCm39) |
I590S |
probably damaging |
Het |
Ep300 |
T |
C |
15: 81,504,198 (GRCm39) |
|
probably benign |
Het |
Fam209 |
A |
G |
2: 172,314,618 (GRCm39) |
K36E |
probably damaging |
Het |
Fat3 |
G |
A |
9: 15,909,567 (GRCm39) |
S2145F |
probably damaging |
Het |
Flg |
A |
T |
3: 93,186,833 (GRCm39) |
Q95L |
probably benign |
Het |
Gabrr2 |
A |
G |
4: 33,081,348 (GRCm39) |
Y4C |
probably damaging |
Het |
Ggcx |
G |
A |
6: 72,395,355 (GRCm39) |
V149M |
probably damaging |
Het |
Gm10801 |
T |
G |
2: 98,494,246 (GRCm39) |
|
probably null |
Het |
H2-M10.1 |
T |
A |
17: 36,635,281 (GRCm39) |
Q250L |
possibly damaging |
Het |
Hecw2 |
A |
T |
1: 53,965,280 (GRCm39) |
N515K |
probably benign |
Het |
Hmcn1 |
A |
T |
1: 150,510,946 (GRCm39) |
D3592E |
probably damaging |
Het |
Klf5 |
T |
A |
14: 99,536,509 (GRCm39) |
F27I |
probably benign |
Het |
Krt1 |
T |
A |
15: 101,758,847 (GRCm39) |
S106C |
unknown |
Het |
Lrrc14b |
T |
C |
13: 74,511,787 (GRCm39) |
S98G |
probably benign |
Het |
Lrrc7 |
A |
G |
3: 157,866,333 (GRCm39) |
V1136A |
probably benign |
Het |
Map3k11 |
G |
T |
19: 5,752,311 (GRCm39) |
C831F |
probably benign |
Het |
Mccc2 |
T |
C |
13: 100,104,241 (GRCm39) |
T303A |
probably benign |
Het |
Mipep |
T |
C |
14: 61,046,444 (GRCm39) |
L322P |
probably damaging |
Het |
Mob1b |
T |
A |
5: 88,901,061 (GRCm39) |
I156K |
probably damaging |
Het |
Myd88 |
T |
C |
9: 119,166,882 (GRCm39) |
D225G |
possibly damaging |
Het |
Nos1ap |
T |
C |
1: 170,177,025 (GRCm39) |
Y126C |
probably damaging |
Het |
Nuak2 |
G |
T |
1: 132,259,223 (GRCm39) |
A342S |
possibly damaging |
Het |
Or10ah1-ps1 |
G |
T |
5: 143,123,152 (GRCm39) |
S290R |
probably benign |
Het |
Or4f15 |
A |
C |
2: 111,813,486 (GRCm39) |
M311R |
probably benign |
Het |
Or7e165 |
T |
G |
9: 19,695,011 (GRCm39) |
I194S |
probably benign |
Het |
Pcdhb16 |
A |
T |
18: 37,612,422 (GRCm39) |
I461F |
probably benign |
Het |
Pcdhga10 |
A |
C |
18: 37,882,534 (GRCm39) |
H765P |
probably benign |
Het |
Plxna4 |
C |
A |
6: 32,192,589 (GRCm39) |
D791Y |
probably damaging |
Het |
Pole |
T |
G |
5: 110,484,305 (GRCm39) |
I320M |
probably damaging |
Het |
Psg23 |
G |
T |
7: 18,345,966 (GRCm39) |
T243N |
probably damaging |
Het |
Ptma-ps1 |
A |
G |
7: 23,763,543 (GRCm39) |
|
noncoding transcript |
Het |
Ptprk |
A |
T |
10: 28,139,617 (GRCm39) |
Q114L |
probably benign |
Het |
Pum1 |
T |
C |
4: 130,491,393 (GRCm39) |
L774P |
probably damaging |
Het |
Rabgef1 |
A |
G |
5: 130,237,520 (GRCm39) |
|
probably benign |
Het |
Rasef |
A |
G |
4: 73,698,634 (GRCm39) |
V9A |
probably benign |
Het |
Rcbtb1 |
T |
A |
14: 59,465,804 (GRCm39) |
H382Q |
possibly damaging |
Het |
Robo4 |
CGG |
CG |
9: 37,322,786 (GRCm39) |
|
probably null |
Het |
Sacs |
T |
G |
14: 61,441,836 (GRCm39) |
I1294R |
probably damaging |
Het |
Slc19a3 |
A |
T |
1: 83,000,678 (GRCm39) |
F113Y |
probably damaging |
Het |
Snrnp48 |
G |
A |
13: 38,401,365 (GRCm39) |
S204N |
possibly damaging |
Het |
Sp3 |
A |
G |
2: 72,809,376 (GRCm39) |
|
probably benign |
Het |
St8sia6 |
G |
A |
2: 13,677,335 (GRCm39) |
H161Y |
probably benign |
Het |
Strip2 |
A |
T |
6: 29,917,074 (GRCm39) |
|
probably benign |
Het |
Trank1 |
T |
C |
9: 111,193,827 (GRCm39) |
V617A |
probably benign |
Het |
Uvssa |
T |
A |
5: 33,547,096 (GRCm39) |
S221T |
probably benign |
Het |
Vmn2r75 |
A |
T |
7: 85,813,494 (GRCm39) |
L436Q |
probably null |
Het |
Wdfy4 |
T |
C |
14: 32,769,237 (GRCm39) |
E2076G |
probably damaging |
Het |
Zfp407 |
C |
T |
18: 84,578,477 (GRCm39) |
V879I |
probably damaging |
Het |
Zmym4 |
A |
G |
4: 126,798,269 (GRCm39) |
I786T |
probably benign |
Het |
|
Other mutations in Dmrta1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02154:Dmrta1
|
APN |
4 |
89,580,150 (GRCm39) |
missense |
probably benign |
0.04 |
IGL02572:Dmrta1
|
APN |
4 |
89,579,795 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02875:Dmrta1
|
APN |
4 |
89,579,985 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02883:Dmrta1
|
APN |
4 |
89,577,011 (GRCm39) |
missense |
probably benign |
|
R0097:Dmrta1
|
UTSW |
4 |
89,577,109 (GRCm39) |
missense |
probably benign |
0.08 |
R0097:Dmrta1
|
UTSW |
4 |
89,577,109 (GRCm39) |
missense |
probably benign |
0.08 |
R0394:Dmrta1
|
UTSW |
4 |
89,580,276 (GRCm39) |
missense |
probably damaging |
1.00 |
R2093:Dmrta1
|
UTSW |
4 |
89,579,742 (GRCm39) |
missense |
probably benign |
|
R2132:Dmrta1
|
UTSW |
4 |
89,576,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R2133:Dmrta1
|
UTSW |
4 |
89,576,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R2401:Dmrta1
|
UTSW |
4 |
89,579,853 (GRCm39) |
missense |
probably benign |
0.00 |
R3694:Dmrta1
|
UTSW |
4 |
89,580,415 (GRCm39) |
nonsense |
probably null |
|
R3695:Dmrta1
|
UTSW |
4 |
89,580,415 (GRCm39) |
nonsense |
probably null |
|
R3891:Dmrta1
|
UTSW |
4 |
89,579,831 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3929:Dmrta1
|
UTSW |
4 |
89,579,681 (GRCm39) |
nonsense |
probably null |
|
R4620:Dmrta1
|
UTSW |
4 |
89,577,021 (GRCm39) |
missense |
probably benign |
0.05 |
R4927:Dmrta1
|
UTSW |
4 |
89,579,985 (GRCm39) |
missense |
probably damaging |
1.00 |
R4982:Dmrta1
|
UTSW |
4 |
89,576,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R5312:Dmrta1
|
UTSW |
4 |
89,580,284 (GRCm39) |
missense |
probably damaging |
0.99 |
R5437:Dmrta1
|
UTSW |
4 |
89,579,993 (GRCm39) |
missense |
possibly damaging |
0.71 |
R5637:Dmrta1
|
UTSW |
4 |
89,577,068 (GRCm39) |
missense |
probably benign |
|
R6185:Dmrta1
|
UTSW |
4 |
89,580,005 (GRCm39) |
missense |
probably damaging |
0.97 |
R6906:Dmrta1
|
UTSW |
4 |
89,580,203 (GRCm39) |
missense |
probably benign |
0.06 |
R7156:Dmrta1
|
UTSW |
4 |
89,576,700 (GRCm39) |
missense |
probably damaging |
0.99 |
R7201:Dmrta1
|
UTSW |
4 |
89,580,408 (GRCm39) |
nonsense |
probably null |
|
R7755:Dmrta1
|
UTSW |
4 |
89,580,170 (GRCm39) |
missense |
probably benign |
0.01 |
R7862:Dmrta1
|
UTSW |
4 |
89,576,561 (GRCm39) |
missense |
probably benign |
0.00 |
R7880:Dmrta1
|
UTSW |
4 |
89,577,081 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8714:Dmrta1
|
UTSW |
4 |
89,579,682 (GRCm39) |
missense |
probably benign |
|
R8841:Dmrta1
|
UTSW |
4 |
89,579,950 (GRCm39) |
missense |
probably benign |
0.00 |
R9028:Dmrta1
|
UTSW |
4 |
89,579,914 (GRCm39) |
missense |
probably damaging |
0.96 |
Z1177:Dmrta1
|
UTSW |
4 |
89,576,691 (GRCm39) |
missense |
probably benign |
0.37 |
Z1177:Dmrta1
|
UTSW |
4 |
89,576,645 (GRCm39) |
missense |
probably damaging |
0.97 |
Z1177:Dmrta1
|
UTSW |
4 |
89,576,735 (GRCm39) |
missense |
probably benign |
0.16 |
|