Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgap17 |
G |
A |
7: 122,893,750 (GRCm39) |
P557S |
probably benign |
Het |
Atad5 |
G |
T |
11: 80,000,910 (GRCm39) |
D1014Y |
possibly damaging |
Het |
Bmp6 |
T |
A |
13: 38,530,359 (GRCm39) |
S151T |
probably benign |
Het |
Bmp6 |
C |
T |
13: 38,682,795 (GRCm39) |
Q459* |
probably null |
Het |
Ccdc39 |
A |
G |
3: 33,880,612 (GRCm39) |
Y452H |
probably damaging |
Het |
Cenpj |
A |
G |
14: 56,780,329 (GRCm39) |
Y961H |
probably damaging |
Het |
Col6a6 |
A |
T |
9: 105,655,166 (GRCm39) |
Y852N |
probably damaging |
Het |
Cpne8 |
A |
G |
15: 90,456,218 (GRCm39) |
I156T |
probably benign |
Het |
Cul1 |
T |
A |
6: 47,492,010 (GRCm39) |
L430Q |
probably damaging |
Het |
Dhx30 |
A |
G |
9: 109,914,296 (GRCm39) |
S1031P |
probably benign |
Het |
Dhx9 |
A |
T |
1: 153,338,335 (GRCm39) |
F774I |
possibly damaging |
Het |
Gbp2b |
A |
T |
3: 142,312,576 (GRCm39) |
I320L |
probably benign |
Het |
Gemin6 |
T |
A |
17: 80,533,115 (GRCm39) |
V16D |
possibly damaging |
Het |
Gpr158 |
T |
A |
2: 21,581,751 (GRCm39) |
V410D |
possibly damaging |
Het |
H2-DMb2 |
C |
T |
17: 34,366,904 (GRCm39) |
T112M |
probably damaging |
Het |
Hecw2 |
T |
C |
1: 53,990,033 (GRCm39) |
T114A |
|
Het |
Herc2 |
G |
T |
7: 55,738,059 (GRCm39) |
R234L |
probably damaging |
Het |
Igsf11 |
A |
G |
16: 38,829,243 (GRCm39) |
I46V |
probably benign |
Het |
Izumo1r |
C |
T |
9: 14,813,705 (GRCm39) |
G38S |
possibly damaging |
Het |
Katna1 |
A |
G |
10: 7,614,600 (GRCm39) |
D36G |
probably benign |
Het |
Kdm1b |
G |
T |
13: 47,231,832 (GRCm39) |
R697L |
probably damaging |
Het |
Kif1b |
T |
A |
4: 149,338,196 (GRCm39) |
I483F |
probably damaging |
Het |
Krt1 |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
AAGCTGCCACCCCCAAAGCCACCACCGCCGTAGCTGCCACCCCCAAAGCCACCAC |
15: 101,758,813 (GRCm39) |
|
probably benign |
Het |
Lrp1b |
G |
A |
2: 41,158,417 (GRCm39) |
T1714I |
|
Het |
Man2a2 |
A |
G |
7: 80,003,067 (GRCm39) |
L1014P |
probably damaging |
Het |
Marf1 |
T |
C |
16: 13,935,169 (GRCm39) |
E1533G |
probably damaging |
Het |
Mfsd2a |
A |
T |
4: 122,845,623 (GRCm39) |
I176N |
probably damaging |
Het |
Mterf1b |
T |
A |
5: 4,246,961 (GRCm39) |
F201I |
possibly damaging |
Het |
Neurod2 |
T |
C |
11: 98,218,507 (GRCm39) |
E219G |
probably damaging |
Het |
Nln |
T |
C |
13: 104,209,486 (GRCm39) |
E29G |
probably benign |
Het |
Obscn |
G |
A |
11: 58,892,861 (GRCm39) |
T6795M |
possibly damaging |
Het |
Or1e1c |
G |
T |
11: 73,266,186 (GRCm39) |
V207F |
probably benign |
Het |
Or1i2 |
A |
G |
10: 78,447,635 (GRCm39) |
V280A |
possibly damaging |
Het |
Or1n1 |
C |
A |
2: 36,749,539 (GRCm39) |
A274S |
probably benign |
Het |
Or4c118 |
C |
T |
2: 88,975,074 (GRCm39) |
V98I |
probably benign |
Het |
Otog |
A |
T |
7: 45,895,948 (GRCm39) |
I138F |
probably damaging |
Het |
Pdcd2l |
G |
A |
7: 33,884,192 (GRCm39) |
Q337* |
probably null |
Het |
Ptprk |
A |
T |
10: 28,442,497 (GRCm39) |
N859I |
probably damaging |
Het |
Pygl |
G |
T |
12: 70,274,368 (GRCm39) |
|
probably benign |
Het |
Sema4d |
C |
T |
13: 51,863,018 (GRCm39) |
A447T |
probably benign |
Het |
Slc27a6 |
A |
T |
18: 58,712,888 (GRCm39) |
S237C |
probably benign |
Het |
Smarcc1 |
G |
A |
9: 110,051,199 (GRCm39) |
M1006I |
possibly damaging |
Het |
Sult2a2 |
G |
T |
7: 13,472,192 (GRCm39) |
G130C |
probably damaging |
Het |
Trpm7 |
T |
A |
2: 126,663,131 (GRCm39) |
H1039L |
probably benign |
Het |
Wdr64 |
T |
G |
1: 175,599,893 (GRCm39) |
N573K |
probably benign |
Het |
Zbtb48 |
T |
C |
4: 152,104,496 (GRCm39) |
I611V |
probably benign |
Het |
Zer1 |
T |
C |
2: 30,001,062 (GRCm39) |
S120G |
possibly damaging |
Het |
Zswim4 |
C |
T |
8: 84,940,699 (GRCm39) |
R800Q |
probably damaging |
Het |
|
Other mutations in Fezf2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01895:Fezf2
|
APN |
14 |
12,342,498 (GRCm38) |
makesense |
probably null |
|
IGL02008:Fezf2
|
APN |
14 |
12,343,705 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02238:Fezf2
|
APN |
14 |
12,344,494 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02428:Fezf2
|
APN |
14 |
12,344,494 (GRCm38) |
missense |
probably damaging |
0.98 |
IGL02588:Fezf2
|
APN |
14 |
12,343,687 (GRCm38) |
missense |
probably damaging |
1.00 |
K3955:Fezf2
|
UTSW |
14 |
12,345,097 (GRCm38) |
missense |
probably damaging |
1.00 |
R0266:Fezf2
|
UTSW |
14 |
12,342,607 (GRCm38) |
missense |
probably damaging |
1.00 |
R0281:Fezf2
|
UTSW |
14 |
12,343,977 (GRCm38) |
missense |
probably damaging |
1.00 |
R0849:Fezf2
|
UTSW |
14 |
12,342,607 (GRCm38) |
missense |
probably damaging |
1.00 |
R1061:Fezf2
|
UTSW |
14 |
12,342,713 (GRCm38) |
missense |
probably damaging |
1.00 |
R1107:Fezf2
|
UTSW |
14 |
12,342,624 (GRCm38) |
missense |
probably damaging |
1.00 |
R1326:Fezf2
|
UTSW |
14 |
12,342,644 (GRCm38) |
missense |
probably benign |
0.12 |
R1914:Fezf2
|
UTSW |
14 |
12,343,988 (GRCm38) |
missense |
probably damaging |
1.00 |
R1955:Fezf2
|
UTSW |
14 |
12,342,644 (GRCm38) |
missense |
probably benign |
0.12 |
R1980:Fezf2
|
UTSW |
14 |
12,344,405 (GRCm38) |
missense |
probably benign |
0.04 |
R1981:Fezf2
|
UTSW |
14 |
12,344,405 (GRCm38) |
missense |
probably benign |
0.04 |
R1982:Fezf2
|
UTSW |
14 |
12,344,405 (GRCm38) |
missense |
probably benign |
0.04 |
R1988:Fezf2
|
UTSW |
14 |
12,344,350 (GRCm38) |
missense |
probably damaging |
0.98 |
R4023:Fezf2
|
UTSW |
14 |
12,343,986 (GRCm38) |
missense |
probably damaging |
1.00 |
R4025:Fezf2
|
UTSW |
14 |
12,343,986 (GRCm38) |
missense |
probably damaging |
1.00 |
R4026:Fezf2
|
UTSW |
14 |
12,343,986 (GRCm38) |
missense |
probably damaging |
1.00 |
R5373:Fezf2
|
UTSW |
14 |
12,344,803 (GRCm38) |
missense |
possibly damaging |
0.67 |
R6982:Fezf2
|
UTSW |
14 |
12,343,645 (GRCm38) |
missense |
probably damaging |
1.00 |
R7650:Fezf2
|
UTSW |
14 |
12,342,653 (GRCm38) |
missense |
probably damaging |
0.97 |
R7677:Fezf2
|
UTSW |
14 |
12,344,941 (GRCm38) |
missense |
probably benign |
0.38 |
R7898:Fezf2
|
UTSW |
14 |
12,342,701 (GRCm38) |
missense |
possibly damaging |
0.82 |
Z1177:Fezf2
|
UTSW |
14 |
12,344,765 (GRCm38) |
missense |
probably benign |
0.19 |
|