Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2700097O09Rik |
A |
G |
12: 55,106,295 (GRCm39) |
S143P |
possibly damaging |
Het |
4930522H14Rik |
T |
C |
4: 109,362,654 (GRCm39) |
K218E |
possibly damaging |
Het |
Abcb1a |
T |
A |
5: 8,736,300 (GRCm39) |
|
probably null |
Het |
Adam39 |
A |
G |
8: 41,278,031 (GRCm39) |
T141A |
possibly damaging |
Het |
Adam6b |
T |
A |
12: 113,455,071 (GRCm39) |
S629R |
probably benign |
Het |
Ap3b2 |
C |
A |
7: 81,113,438 (GRCm39) |
E924* |
probably null |
Het |
Armc3 |
A |
T |
2: 19,314,858 (GRCm39) |
Y856F |
probably benign |
Het |
Asap1 |
A |
G |
15: 64,044,579 (GRCm39) |
L142P |
probably damaging |
Het |
Atg9a |
T |
A |
1: 75,162,734 (GRCm39) |
D427V |
probably damaging |
Het |
Atl2 |
G |
A |
17: 80,160,135 (GRCm39) |
A17V |
probably benign |
Het |
Atxn2l |
A |
T |
7: 126,095,639 (GRCm39) |
S379T |
probably damaging |
Het |
C1ql3 |
G |
T |
2: 13,015,453 (GRCm39) |
P69Q |
possibly damaging |
Het |
Cap2 |
A |
T |
13: 46,763,111 (GRCm39) |
I114F |
probably damaging |
Het |
Ccdc168 |
A |
G |
1: 44,096,950 (GRCm39) |
F1383L |
probably benign |
Het |
Ccdc168 |
T |
C |
1: 44,100,667 (GRCm39) |
I144V |
probably benign |
Het |
Cox16 |
T |
C |
12: 81,521,389 (GRCm39) |
N135S |
probably null |
Het |
Dnajc13 |
A |
T |
9: 104,108,234 (GRCm39) |
H180Q |
possibly damaging |
Het |
Dpy19l3 |
A |
T |
7: 35,424,835 (GRCm39) |
Y73* |
probably null |
Het |
Duox2 |
T |
A |
2: 122,123,877 (GRCm39) |
M436L |
probably benign |
Het |
Exoc6 |
T |
A |
19: 37,585,568 (GRCm39) |
M481K |
possibly damaging |
Het |
Fbxw2 |
GCCCCC |
GCCCCCCCC |
2: 34,702,829 (GRCm39) |
|
probably benign |
Het |
Fmn1 |
T |
A |
2: 113,195,557 (GRCm39) |
V419E |
unknown |
Het |
Fndc4 |
T |
C |
5: 31,450,795 (GRCm39) |
*232W |
probably null |
Het |
Foxc1 |
C |
T |
13: 31,992,595 (GRCm39) |
R469* |
probably null |
Het |
Fsip2 |
A |
G |
2: 82,810,155 (GRCm39) |
H2158R |
probably benign |
Het |
Ghdc |
C |
T |
11: 100,659,083 (GRCm39) |
G373D |
probably benign |
Het |
Gm10330 |
A |
T |
12: 23,830,032 (GRCm39) |
S50T |
probably benign |
Het |
Hlx |
G |
T |
1: 184,464,184 (GRCm39) |
A52D |
probably damaging |
Het |
Lonrf1 |
A |
G |
8: 36,690,108 (GRCm39) |
V650A |
probably damaging |
Het |
Map1a |
T |
C |
2: 121,130,918 (GRCm39) |
V578A |
possibly damaging |
Het |
Mbd3 |
C |
G |
10: 80,229,740 (GRCm39) |
D190H |
probably damaging |
Het |
Mia3 |
A |
G |
1: 183,120,121 (GRCm39) |
S85P |
probably benign |
Het |
Myrip |
T |
C |
9: 120,261,595 (GRCm39) |
F403L |
probably damaging |
Het |
Nox4 |
A |
G |
7: 86,954,097 (GRCm39) |
Y134C |
probably damaging |
Het |
Numb |
A |
G |
12: 83,842,217 (GRCm39) |
L642P |
probably damaging |
Het |
Pappa |
A |
T |
4: 65,099,185 (GRCm39) |
Y568F |
possibly damaging |
Het |
Pdzrn4 |
T |
C |
15: 92,575,593 (GRCm39) |
L333P |
probably benign |
Het |
Prl |
A |
T |
13: 27,241,619 (GRCm39) |
S3C |
probably damaging |
Het |
Ptprc |
T |
C |
1: 138,047,824 (GRCm39) |
T60A |
possibly damaging |
Het |
Rbm10 |
C |
T |
X: 20,503,903 (GRCm39) |
|
probably benign |
Het |
Slc7a7 |
C |
T |
14: 54,646,103 (GRCm39) |
R120H |
probably damaging |
Het |
Smpd1 |
T |
C |
7: 105,205,761 (GRCm39) |
|
probably null |
Het |
Spta1 |
A |
G |
1: 174,058,891 (GRCm39) |
E1942G |
probably damaging |
Het |
Tmem38a |
A |
G |
8: 73,333,479 (GRCm39) |
Y66C |
probably damaging |
Het |
Tnnt1 |
A |
T |
7: 4,510,524 (GRCm39) |
Y232* |
probably null |
Het |
Tpte |
T |
C |
8: 22,839,405 (GRCm39) |
|
probably null |
Het |
Virma |
T |
C |
4: 11,521,164 (GRCm39) |
V907A |
probably damaging |
Het |
Vmn1r174 |
C |
T |
7: 23,453,981 (GRCm39) |
Q216* |
probably null |
Het |
Zswim3 |
T |
C |
2: 164,661,901 (GRCm39) |
V127A |
probably benign |
Het |
|
Other mutations in Mcpt9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02947:Mcpt9
|
APN |
14 |
56,264,373 (GRCm39) |
nonsense |
probably null |
|
IGL03200:Mcpt9
|
APN |
14 |
56,264,390 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03218:Mcpt9
|
APN |
14 |
56,264,908 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03412:Mcpt9
|
APN |
14 |
56,265,484 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4434001:Mcpt9
|
UTSW |
14 |
56,266,686 (GRCm39) |
missense |
probably benign |
0.03 |
R0196:Mcpt9
|
UTSW |
14 |
56,265,453 (GRCm39) |
missense |
probably benign |
0.43 |
R1218:Mcpt9
|
UTSW |
14 |
56,266,125 (GRCm39) |
nonsense |
probably null |
|
R1962:Mcpt9
|
UTSW |
14 |
56,265,024 (GRCm39) |
missense |
probably benign |
0.01 |
R2232:Mcpt9
|
UTSW |
14 |
56,265,445 (GRCm39) |
missense |
probably benign |
0.00 |
R3911:Mcpt9
|
UTSW |
14 |
56,265,136 (GRCm39) |
missense |
probably benign |
0.29 |
R4441:Mcpt9
|
UTSW |
14 |
56,265,009 (GRCm39) |
missense |
probably damaging |
1.00 |
R4600:Mcpt9
|
UTSW |
14 |
56,266,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4603:Mcpt9
|
UTSW |
14 |
56,266,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4610:Mcpt9
|
UTSW |
14 |
56,266,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4611:Mcpt9
|
UTSW |
14 |
56,266,049 (GRCm39) |
missense |
probably damaging |
1.00 |
R4738:Mcpt9
|
UTSW |
14 |
56,264,456 (GRCm39) |
missense |
probably damaging |
0.98 |
R7146:Mcpt9
|
UTSW |
14 |
56,264,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R7475:Mcpt9
|
UTSW |
14 |
56,264,400 (GRCm39) |
missense |
probably damaging |
1.00 |
R8885:Mcpt9
|
UTSW |
14 |
56,265,153 (GRCm39) |
missense |
probably benign |
0.01 |
|