Other mutations in this stock |
Total: 34 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acnat1 |
T |
A |
4: 49,447,793 (GRCm39) |
T245S |
probably benign |
Het |
Agl |
T |
C |
3: 116,574,646 (GRCm39) |
I718V |
probably benign |
Het |
Cbs |
T |
A |
17: 31,844,005 (GRCm39) |
N209Y |
probably benign |
Het |
Cd163 |
T |
C |
6: 124,302,300 (GRCm39) |
C955R |
probably damaging |
Het |
Dnajb3 |
A |
G |
1: 88,132,662 (GRCm39) |
|
probably benign |
Het |
Dop1b |
G |
A |
16: 93,536,079 (GRCm39) |
R59Q |
possibly damaging |
Het |
Dtx1 |
A |
G |
5: 120,819,500 (GRCm39) |
L566P |
probably damaging |
Het |
Fgf14 |
G |
T |
14: 124,221,213 (GRCm39) |
P197Q |
probably damaging |
Het |
Gask1a |
A |
G |
9: 121,794,094 (GRCm39) |
R83G |
probably benign |
Het |
Gcc1 |
G |
A |
6: 28,420,661 (GRCm39) |
Q66* |
probably null |
Het |
Gypc |
T |
C |
18: 32,692,879 (GRCm39) |
|
probably benign |
Het |
Helz2 |
G |
A |
2: 180,876,819 (GRCm39) |
A1225V |
probably benign |
Het |
Herc1 |
A |
G |
9: 66,358,274 (GRCm39) |
T2452A |
probably benign |
Het |
Hoxc4 |
A |
G |
15: 102,943,152 (GRCm39) |
I2V |
probably benign |
Het |
Impa1 |
A |
G |
3: 10,394,025 (GRCm39) |
I14T |
probably benign |
Het |
Itih1 |
T |
A |
14: 30,658,677 (GRCm39) |
D400V |
probably damaging |
Het |
Lama3 |
T |
C |
18: 12,711,184 (GRCm39) |
Y3206H |
probably damaging |
Het |
Lce1k |
T |
A |
3: 92,714,192 (GRCm39) |
|
probably benign |
Het |
Myo15b |
A |
G |
11: 115,775,076 (GRCm39) |
E2168G |
probably benign |
Het |
Myom3 |
G |
T |
4: 135,541,614 (GRCm39) |
E1402* |
probably null |
Het |
Nfyb |
G |
T |
10: 82,590,867 (GRCm39) |
Q55K |
probably damaging |
Het |
Nobox |
T |
C |
6: 43,284,136 (GRCm39) |
K137E |
possibly damaging |
Het |
Pnlip |
T |
A |
19: 58,669,220 (GRCm39) |
D406E |
probably benign |
Het |
Pole |
A |
T |
5: 110,460,594 (GRCm39) |
|
probably benign |
Het |
Ppp2r2b |
T |
C |
18: 42,781,793 (GRCm39) |
Y336C |
possibly damaging |
Het |
Prkg1 |
T |
C |
19: 31,279,701 (GRCm39) |
T178A |
probably damaging |
Het |
Prr11 |
C |
T |
11: 86,994,371 (GRCm39) |
A92T |
possibly damaging |
Het |
Racgap1 |
G |
T |
15: 99,537,585 (GRCm39) |
S67R |
probably damaging |
Het |
Scn10a |
G |
A |
9: 119,445,771 (GRCm39) |
P1462S |
probably damaging |
Het |
Sptbn1 |
T |
C |
11: 30,147,747 (GRCm39) |
E29G |
probably benign |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Vmn2r72 |
T |
A |
7: 85,401,021 (GRCm39) |
T133S |
probably benign |
Het |
Zbtb20 |
A |
G |
16: 43,430,296 (GRCm39) |
H269R |
possibly damaging |
Het |
Zwilch |
A |
T |
9: 64,054,118 (GRCm39) |
N526K |
probably benign |
Het |
|
Other mutations in Mcpt4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00537:Mcpt4
|
APN |
14 |
56,298,487 (GRCm39) |
missense |
probably benign |
|
R0622:Mcpt4
|
UTSW |
14 |
56,298,119 (GRCm39) |
missense |
probably benign |
0.06 |
R1699:Mcpt4
|
UTSW |
14 |
56,297,416 (GRCm39) |
makesense |
probably null |
|
R4298:Mcpt4
|
UTSW |
14 |
56,298,444 (GRCm39) |
missense |
possibly damaging |
0.70 |
R4413:Mcpt4
|
UTSW |
14 |
56,297,993 (GRCm39) |
missense |
probably damaging |
0.98 |
R5191:Mcpt4
|
UTSW |
14 |
56,298,466 (GRCm39) |
missense |
probably benign |
0.00 |
R5378:Mcpt4
|
UTSW |
14 |
56,299,750 (GRCm39) |
splice site |
probably null |
|
R6650:Mcpt4
|
UTSW |
14 |
56,298,090 (GRCm39) |
missense |
possibly damaging |
0.82 |
R7062:Mcpt4
|
UTSW |
14 |
56,298,125 (GRCm39) |
missense |
probably benign |
0.09 |
R7730:Mcpt4
|
UTSW |
14 |
56,297,428 (GRCm39) |
missense |
probably benign |
|
R7809:Mcpt4
|
UTSW |
14 |
56,298,141 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8363:Mcpt4
|
UTSW |
14 |
56,299,692 (GRCm39) |
missense |
probably damaging |
1.00 |
R9368:Mcpt4
|
UTSW |
14 |
56,299,134 (GRCm39) |
missense |
probably damaging |
0.97 |
R9751:Mcpt4
|
UTSW |
14 |
56,297,511 (GRCm39) |
missense |
probably damaging |
1.00 |
X0019:Mcpt4
|
UTSW |
14 |
56,299,729 (GRCm39) |
start codon destroyed |
probably null |
0.94 |
Z1088:Mcpt4
|
UTSW |
14 |
56,297,967 (GRCm39) |
nonsense |
probably null |
|
|