Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930590J08Rik |
G |
A |
6: 91,900,118 (GRCm39) |
G424D |
probably damaging |
Het |
Aco1 |
T |
C |
4: 40,185,028 (GRCm39) |
V566A |
probably benign |
Het |
Adat1 |
G |
T |
8: 112,704,704 (GRCm39) |
T414K |
probably benign |
Het |
Alox12e |
A |
G |
11: 70,211,927 (GRCm39) |
V194A |
probably benign |
Het |
Anpep |
A |
G |
7: 79,491,644 (GRCm39) |
V119A |
probably benign |
Het |
Atat1 |
C |
A |
17: 36,219,849 (GRCm39) |
|
probably null |
Het |
Atp10a |
G |
A |
7: 58,469,432 (GRCm39) |
W1094* |
probably null |
Het |
Bcl11b |
T |
C |
12: 107,969,360 (GRCm39) |
R15G |
probably benign |
Het |
Bltp1 |
A |
G |
3: 37,087,456 (GRCm39) |
D4019G |
probably benign |
Het |
Btnl1 |
A |
G |
17: 34,598,468 (GRCm39) |
E28G |
probably benign |
Het |
Ccnd1 |
A |
G |
7: 144,493,306 (GRCm39) |
V42A |
probably benign |
Het |
Cdyl2 |
T |
A |
8: 117,309,923 (GRCm39) |
K344N |
probably damaging |
Het |
Cep68 |
A |
G |
11: 20,180,498 (GRCm39) |
M711T |
probably benign |
Het |
Cyp2j7 |
A |
G |
4: 96,118,211 (GRCm39) |
|
probably null |
Het |
Cyp3a25 |
A |
T |
5: 145,935,357 (GRCm39) |
D86E |
probably damaging |
Het |
Dclk1 |
G |
T |
3: 55,154,615 (GRCm39) |
R15L |
probably damaging |
Het |
Dpy19l1 |
T |
A |
9: 24,393,341 (GRCm39) |
K143* |
probably null |
Het |
Duox2 |
A |
G |
2: 122,111,483 (GRCm39) |
V1405A |
probably benign |
Het |
Filip1 |
T |
C |
9: 79,726,906 (GRCm39) |
E571G |
probably damaging |
Het |
Gpat2 |
G |
C |
2: 127,273,838 (GRCm39) |
G294R |
possibly damaging |
Het |
Jph1 |
T |
C |
1: 17,162,071 (GRCm39) |
N197S |
probably damaging |
Het |
Kcnt2 |
T |
C |
1: 140,437,322 (GRCm39) |
L535S |
probably damaging |
Het |
Lepr |
C |
A |
4: 101,622,151 (GRCm39) |
S361* |
probably null |
Het |
Lfng |
T |
A |
5: 140,600,151 (GRCm39) |
|
probably null |
Het |
Lpcat2 |
G |
A |
8: 93,613,209 (GRCm39) |
A250T |
probably benign |
Het |
Map3k4 |
A |
T |
17: 12,490,954 (GRCm39) |
M159K |
possibly damaging |
Het |
Notch3 |
A |
T |
17: 32,363,533 (GRCm39) |
C1177S |
probably damaging |
Het |
Olfml2b |
C |
T |
1: 170,496,800 (GRCm39) |
P477L |
probably benign |
Het |
Or51a5 |
A |
T |
7: 102,771,136 (GRCm39) |
F281Y |
probably benign |
Het |
Or5k16 |
T |
A |
16: 58,736,627 (GRCm39) |
I126L |
probably damaging |
Het |
Or6c33 |
A |
T |
10: 129,853,782 (GRCm39) |
H184L |
probably benign |
Het |
Pald1 |
G |
T |
10: 61,186,714 (GRCm39) |
F146L |
possibly damaging |
Het |
Pcdhga1 |
A |
G |
18: 37,796,022 (GRCm39) |
D342G |
probably damaging |
Het |
Plcb2 |
T |
C |
2: 118,545,949 (GRCm39) |
S579G |
probably damaging |
Het |
Prdm16 |
A |
T |
4: 154,425,824 (GRCm39) |
S654T |
probably benign |
Het |
Rab3gap2 |
C |
A |
1: 184,968,181 (GRCm39) |
L178I |
probably damaging |
Het |
Rbfox1 |
C |
T |
16: 7,042,214 (GRCm39) |
Q23* |
probably null |
Het |
Slc14a2 |
T |
G |
18: 78,190,190 (GRCm39) |
T920P |
probably benign |
Het |
Slc17a6 |
G |
A |
7: 51,317,211 (GRCm39) |
V411M |
probably benign |
Het |
Stard6 |
G |
A |
18: 70,609,459 (GRCm39) |
V33I |
probably benign |
Het |
Syce1 |
A |
T |
7: 140,358,978 (GRCm39) |
H178Q |
probably damaging |
Het |
Syne2 |
T |
A |
12: 76,151,754 (GRCm39) |
F1872I |
probably damaging |
Het |
Tor1aip1 |
T |
C |
1: 155,894,234 (GRCm39) |
E274G |
possibly damaging |
Het |
Trpm1 |
A |
T |
7: 63,918,045 (GRCm39) |
T462S |
probably benign |
Het |
Ugt3a1 |
C |
T |
15: 9,306,541 (GRCm39) |
A230V |
probably benign |
Het |
Vmn1r178 |
A |
G |
7: 23,592,984 (GRCm39) |
T11A |
possibly damaging |
Het |
Vmn2r69 |
A |
T |
7: 85,061,067 (GRCm39) |
N172K |
probably benign |
Het |
Whrn |
G |
T |
4: 63,336,829 (GRCm39) |
P136T |
possibly damaging |
Het |
Zfhx4 |
A |
G |
3: 5,478,170 (GRCm39) |
N3570S |
probably damaging |
Het |
Zfp689 |
A |
G |
7: 127,043,968 (GRCm39) |
S221P |
probably damaging |
Het |
|
Other mutations in Mab21l4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01954:Mab21l4
|
APN |
1 |
93,079,794 (GRCm39) |
missense |
probably damaging |
0.98 |
R0018:Mab21l4
|
UTSW |
1 |
93,082,327 (GRCm39) |
missense |
probably benign |
0.00 |
R0115:Mab21l4
|
UTSW |
1 |
93,087,447 (GRCm39) |
missense |
possibly damaging |
0.70 |
R0467:Mab21l4
|
UTSW |
1 |
93,080,766 (GRCm39) |
missense |
probably damaging |
1.00 |
R1452:Mab21l4
|
UTSW |
1 |
93,080,661 (GRCm39) |
missense |
probably damaging |
1.00 |
R1938:Mab21l4
|
UTSW |
1 |
93,079,730 (GRCm39) |
makesense |
probably null |
|
R3156:Mab21l4
|
UTSW |
1 |
93,087,764 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4740:Mab21l4
|
UTSW |
1 |
93,083,890 (GRCm39) |
missense |
probably benign |
0.01 |
R5260:Mab21l4
|
UTSW |
1 |
93,087,700 (GRCm39) |
missense |
probably damaging |
0.99 |
R5283:Mab21l4
|
UTSW |
1 |
93,087,575 (GRCm39) |
missense |
probably benign |
0.02 |
R5645:Mab21l4
|
UTSW |
1 |
93,080,668 (GRCm39) |
missense |
probably damaging |
1.00 |
R6738:Mab21l4
|
UTSW |
1 |
93,087,707 (GRCm39) |
missense |
probably benign |
0.30 |
R7184:Mab21l4
|
UTSW |
1 |
93,082,237 (GRCm39) |
missense |
probably benign |
0.00 |
R7227:Mab21l4
|
UTSW |
1 |
93,079,736 (GRCm39) |
missense |
probably benign |
0.00 |
R7562:Mab21l4
|
UTSW |
1 |
93,087,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R8001:Mab21l4
|
UTSW |
1 |
93,082,321 (GRCm39) |
missense |
probably damaging |
1.00 |
R8735:Mab21l4
|
UTSW |
1 |
93,082,208 (GRCm39) |
critical splice donor site |
probably null |
|
R8970:Mab21l4
|
UTSW |
1 |
93,087,533 (GRCm39) |
missense |
probably benign |
0.00 |
R9418:Mab21l4
|
UTSW |
1 |
93,087,710 (GRCm39) |
missense |
probably benign |
0.45 |
R9537:Mab21l4
|
UTSW |
1 |
93,080,884 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9599:Mab21l4
|
UTSW |
1 |
93,087,568 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9736:Mab21l4
|
UTSW |
1 |
93,087,661 (GRCm39) |
missense |
probably damaging |
0.99 |
|