Other mutations in this stock |
Total: 75 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930455H04Rik |
C |
A |
3: 116,762,120 (GRCm39) |
|
probably benign |
Het |
Actn3 |
C |
T |
19: 4,921,798 (GRCm39) |
|
probably null |
Het |
Akap13 |
T |
A |
7: 75,184,601 (GRCm39) |
|
probably null |
Het |
Akap9 |
A |
T |
5: 4,094,048 (GRCm39) |
Q2190L |
possibly damaging |
Het |
Ankrd6 |
A |
T |
4: 32,823,452 (GRCm39) |
V190D |
possibly damaging |
Het |
Atrn |
T |
A |
2: 130,841,157 (GRCm39) |
D1186E |
probably benign |
Het |
Bank1 |
A |
T |
3: 135,989,934 (GRCm39) |
V52E |
probably damaging |
Het |
Blmh |
A |
G |
11: 76,857,883 (GRCm39) |
N342D |
probably benign |
Het |
Card6 |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
TTGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGTGGATGAGAGGGCTTAGCATGGGAGGACTGCGGATGAGAGGGCTTAGCATGGGAGGACTG |
15: 5,128,173 (GRCm39) |
|
probably benign |
Het |
Ces2f |
A |
G |
8: 105,677,669 (GRCm39) |
T225A |
probably damaging |
Het |
Clic6 |
G |
T |
16: 92,296,245 (GRCm39) |
D302Y |
probably damaging |
Het |
Clmn |
T |
A |
12: 104,763,341 (GRCm39) |
N95I |
probably damaging |
Het |
Cmya5 |
A |
T |
13: 93,232,840 (GRCm39) |
F749L |
probably benign |
Het |
Cramp1 |
A |
G |
17: 25,202,956 (GRCm39) |
F358L |
probably damaging |
Het |
Dhx38 |
T |
C |
8: 110,283,098 (GRCm39) |
D573G |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,584,471 (GRCm39) |
Y625H |
probably damaging |
Het |
Enpep |
A |
G |
3: 129,115,007 (GRCm39) |
|
probably null |
Het |
Fat1 |
T |
C |
8: 45,483,350 (GRCm39) |
L3146P |
probably damaging |
Het |
Gal3st2b |
G |
A |
1: 93,868,570 (GRCm39) |
S265N |
probably benign |
Het |
Glis3 |
G |
A |
19: 28,643,266 (GRCm39) |
A92V |
possibly damaging |
Het |
Gm266 |
T |
C |
12: 111,452,173 (GRCm39) |
D11G |
probably benign |
Het |
Hmcn2 |
A |
T |
2: 31,204,427 (GRCm39) |
M1L |
probably benign |
Het |
Kcnj15 |
G |
A |
16: 95,097,548 (GRCm39) |
|
probably benign |
Het |
Krt27 |
A |
G |
11: 99,239,551 (GRCm39) |
S310P |
probably damaging |
Het |
Lama2 |
A |
T |
10: 26,862,816 (GRCm39) |
D2982E |
probably damaging |
Het |
Lrfn3 |
A |
G |
7: 30,059,451 (GRCm39) |
V258A |
probably benign |
Het |
Lrit3 |
A |
T |
3: 129,594,193 (GRCm39) |
M128K |
probably damaging |
Het |
Ltbp3 |
A |
G |
19: 5,797,512 (GRCm39) |
T417A |
probably benign |
Het |
Micall1 |
A |
G |
15: 79,011,198 (GRCm39) |
S523G |
probably damaging |
Het |
Mmp21 |
G |
A |
7: 133,280,700 (GRCm39) |
A90V |
probably benign |
Het |
Mon2 |
T |
C |
10: 122,895,110 (GRCm39) |
N53S |
probably benign |
Het |
Muc15 |
T |
C |
2: 110,562,252 (GRCm39) |
|
probably null |
Het |
Myo15b |
A |
T |
11: 115,773,127 (GRCm39) |
M431L |
probably benign |
Het |
Nicn1 |
C |
T |
9: 108,171,708 (GRCm39) |
R163C |
possibly damaging |
Het |
Nt5c3 |
T |
C |
6: 56,861,701 (GRCm39) |
D195G |
probably damaging |
Het |
Or3a1b |
T |
A |
11: 74,012,874 (GRCm39) |
M253K |
probably benign |
Het |
Or52h1 |
A |
G |
7: 103,828,949 (GRCm39) |
L222P |
possibly damaging |
Het |
Pals1 |
T |
A |
12: 78,866,115 (GRCm39) |
D313E |
probably benign |
Het |
Pgrmc2 |
A |
G |
3: 41,037,125 (GRCm39) |
L102P |
probably damaging |
Het |
Plekha1 |
T |
G |
7: 130,502,241 (GRCm39) |
|
probably benign |
Het |
Pramel23 |
T |
C |
4: 143,423,562 (GRCm39) |
Y409C |
probably damaging |
Het |
Prss59 |
A |
T |
6: 40,902,999 (GRCm39) |
Y124* |
probably null |
Het |
Ralgapa1 |
T |
G |
12: 55,749,345 (GRCm39) |
I1233L |
probably damaging |
Het |
Rb1cc1 |
T |
A |
1: 6,333,441 (GRCm39) |
D68E |
probably benign |
Het |
Rere |
C |
A |
4: 150,699,331 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
A |
T |
11: 119,321,100 (GRCm39) |
H1185L |
possibly damaging |
Het |
Robo2 |
G |
T |
16: 73,770,150 (GRCm39) |
P529T |
probably damaging |
Het |
Robo2 |
G |
A |
16: 73,770,149 (GRCm39) |
P529L |
probably damaging |
Het |
Shprh |
A |
G |
10: 11,061,181 (GRCm39) |
T1165A |
possibly damaging |
Het |
Slc22a26 |
C |
T |
19: 7,768,390 (GRCm39) |
|
probably benign |
Het |
Slc43a1 |
T |
C |
2: 84,690,450 (GRCm39) |
L456P |
probably damaging |
Het |
Slc5a8 |
T |
C |
10: 88,740,885 (GRCm39) |
Y267H |
probably damaging |
Het |
Snrnp200 |
T |
C |
2: 127,068,902 (GRCm39) |
I927T |
probably benign |
Het |
Sorbs1 |
T |
C |
19: 40,362,006 (GRCm39) |
D156G |
probably benign |
Het |
Sox5 |
A |
T |
6: 143,853,169 (GRCm39) |
S370T |
probably benign |
Het |
Spen |
T |
C |
4: 141,201,374 (GRCm39) |
T2418A |
probably damaging |
Het |
St8sia6 |
A |
T |
2: 13,701,705 (GRCm39) |
L104H |
probably damaging |
Het |
Stox1 |
T |
A |
10: 62,500,430 (GRCm39) |
N710I |
probably damaging |
Het |
Syncrip |
T |
C |
9: 88,344,900 (GRCm39) |
|
probably benign |
Het |
Syt11 |
G |
A |
3: 88,655,051 (GRCm39) |
P417S |
probably damaging |
Het |
Taf2 |
A |
T |
15: 54,910,849 (GRCm39) |
N608K |
probably benign |
Het |
Tfcp2l1 |
G |
A |
1: 118,596,447 (GRCm39) |
G394E |
possibly damaging |
Het |
Tial1 |
A |
G |
7: 128,056,715 (GRCm39) |
I13T |
probably damaging |
Het |
Tmem108 |
T |
C |
9: 103,361,981 (GRCm39) |
D535G |
probably benign |
Het |
Tpp1 |
T |
C |
7: 105,396,626 (GRCm39) |
M464V |
probably benign |
Het |
Trrap |
C |
A |
5: 144,757,063 (GRCm39) |
N2108K |
probably damaging |
Het |
Tspan3 |
T |
C |
9: 56,053,883 (GRCm39) |
D156G |
probably benign |
Het |
Ttn |
C |
T |
2: 76,592,607 (GRCm39) |
V20842I |
probably benign |
Het |
Ubr4 |
T |
A |
4: 139,190,886 (GRCm39) |
W4078R |
probably damaging |
Het |
Uts2r |
G |
A |
11: 121,051,795 (GRCm39) |
V220M |
possibly damaging |
Het |
Vmn2r19 |
G |
A |
6: 123,293,283 (GRCm39) |
|
probably null |
Het |
Vmn2r3 |
A |
T |
3: 64,166,673 (GRCm39) |
F819L |
probably damaging |
Het |
Wdtc1 |
T |
C |
4: 133,031,470 (GRCm39) |
Y250C |
probably damaging |
Het |
Zan |
T |
C |
5: 137,393,888 (GRCm39) |
H4521R |
unknown |
Het |
Zfp219 |
A |
T |
14: 52,244,224 (GRCm39) |
C652S |
probably damaging |
Het |
|
Other mutations in Mettl25 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00310:Mettl25
|
APN |
10 |
105,662,295 (GRCm39) |
missense |
probably benign |
|
IGL00698:Mettl25
|
APN |
10 |
105,629,201 (GRCm39) |
missense |
probably null |
0.31 |
IGL00766:Mettl25
|
APN |
10 |
105,615,443 (GRCm39) |
splice site |
probably benign |
|
IGL01360:Mettl25
|
APN |
10 |
105,659,058 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01954:Mettl25
|
APN |
10 |
105,659,068 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02088:Mettl25
|
APN |
10 |
105,659,111 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02623:Mettl25
|
APN |
10 |
105,662,185 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03245:Mettl25
|
APN |
10 |
105,662,358 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL03134:Mettl25
|
UTSW |
10 |
105,661,888 (GRCm39) |
nonsense |
probably null |
|
R0238:Mettl25
|
UTSW |
10 |
105,662,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0238:Mettl25
|
UTSW |
10 |
105,662,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Mettl25
|
UTSW |
10 |
105,662,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R0239:Mettl25
|
UTSW |
10 |
105,662,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R1297:Mettl25
|
UTSW |
10 |
105,659,126 (GRCm39) |
missense |
probably benign |
0.11 |
R1482:Mettl25
|
UTSW |
10 |
105,662,451 (GRCm39) |
missense |
possibly damaging |
0.61 |
R1526:Mettl25
|
UTSW |
10 |
105,668,844 (GRCm39) |
missense |
possibly damaging |
0.56 |
R1542:Mettl25
|
UTSW |
10 |
105,661,981 (GRCm39) |
missense |
probably benign |
0.04 |
R1589:Mettl25
|
UTSW |
10 |
105,615,493 (GRCm39) |
missense |
probably damaging |
1.00 |
R1901:Mettl25
|
UTSW |
10 |
105,661,948 (GRCm39) |
missense |
probably damaging |
0.96 |
R1902:Mettl25
|
UTSW |
10 |
105,661,948 (GRCm39) |
missense |
probably damaging |
0.96 |
R2016:Mettl25
|
UTSW |
10 |
105,633,167 (GRCm39) |
missense |
probably benign |
0.00 |
R2355:Mettl25
|
UTSW |
10 |
105,599,316 (GRCm39) |
missense |
probably benign |
0.00 |
R2920:Mettl25
|
UTSW |
10 |
105,601,038 (GRCm39) |
splice site |
probably null |
|
R3149:Mettl25
|
UTSW |
10 |
105,662,214 (GRCm39) |
missense |
probably benign |
0.00 |
R4547:Mettl25
|
UTSW |
10 |
105,661,878 (GRCm39) |
missense |
probably damaging |
1.00 |
R4646:Mettl25
|
UTSW |
10 |
105,662,416 (GRCm39) |
missense |
probably damaging |
1.00 |
R4652:Mettl25
|
UTSW |
10 |
105,615,509 (GRCm39) |
nonsense |
probably null |
|
R5020:Mettl25
|
UTSW |
10 |
105,662,068 (GRCm39) |
missense |
possibly damaging |
0.87 |
R5435:Mettl25
|
UTSW |
10 |
105,615,447 (GRCm39) |
critical splice donor site |
probably null |
|
R6947:Mettl25
|
UTSW |
10 |
105,662,053 (GRCm39) |
missense |
probably benign |
0.00 |
R7075:Mettl25
|
UTSW |
10 |
105,665,785 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7729:Mettl25
|
UTSW |
10 |
105,601,871 (GRCm39) |
missense |
probably benign |
0.03 |
R8074:Mettl25
|
UTSW |
10 |
105,661,941 (GRCm39) |
missense |
probably benign |
0.02 |
R8108:Mettl25
|
UTSW |
10 |
105,659,040 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8415:Mettl25
|
UTSW |
10 |
105,662,002 (GRCm39) |
missense |
probably benign |
0.05 |
R8949:Mettl25
|
UTSW |
10 |
105,668,714 (GRCm39) |
missense |
probably benign |
0.00 |
R9497:Mettl25
|
UTSW |
10 |
105,677,090 (GRCm39) |
missense |
probably damaging |
0.98 |
R9772:Mettl25
|
UTSW |
10 |
105,633,127 (GRCm39) |
missense |
probably benign |
|
RF009:Mettl25
|
UTSW |
10 |
105,669,100 (GRCm39) |
intron |
probably benign |
|
Z1176:Mettl25
|
UTSW |
10 |
105,661,959 (GRCm39) |
missense |
possibly damaging |
0.95 |
|