Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arhgef4 |
C |
T |
1: 34,771,304 (GRCm39) |
L1204F |
probably damaging |
Het |
Atp9b |
T |
C |
18: 80,822,115 (GRCm39) |
D495G |
probably benign |
Het |
B020011L13Rik |
G |
A |
1: 117,729,614 (GRCm39) |
V374I |
probably benign |
Het |
Babam1 |
T |
A |
8: 71,855,449 (GRCm39) |
V214D |
probably damaging |
Het |
Chpf2 |
T |
C |
5: 24,796,773 (GRCm39) |
V573A |
probably damaging |
Het |
Elmo3 |
T |
A |
8: 106,033,379 (GRCm39) |
I115N |
probably damaging |
Het |
Emc1 |
T |
A |
4: 139,092,874 (GRCm39) |
Y564N |
probably damaging |
Het |
Fam180a |
A |
C |
6: 35,292,322 (GRCm39) |
L28R |
probably damaging |
Het |
Fiz1 |
C |
T |
7: 5,011,400 (GRCm39) |
A373T |
possibly damaging |
Het |
Fnip2 |
A |
G |
3: 79,415,152 (GRCm39) |
F243L |
probably damaging |
Het |
Gabra5 |
A |
T |
7: 57,063,496 (GRCm39) |
N309K |
probably damaging |
Het |
Gm17654 |
A |
G |
14: 43,815,534 (GRCm39) |
L91P |
unknown |
Het |
Gm19684 |
G |
A |
17: 36,438,402 (GRCm39) |
|
probably null |
Het |
Gm9376 |
A |
T |
14: 118,504,669 (GRCm39) |
M34L |
unknown |
Het |
Hmgcr |
A |
G |
13: 96,802,366 (GRCm39) |
F106S |
probably damaging |
Het |
Hydin |
T |
G |
8: 111,081,574 (GRCm39) |
|
probably null |
Het |
Igf2bp3 |
A |
G |
6: 49,191,393 (GRCm39) |
Y5H |
probably damaging |
Het |
Igsf11 |
A |
G |
16: 38,829,336 (GRCm39) |
T77A |
probably benign |
Het |
Il20 |
A |
G |
1: 130,836,118 (GRCm39) |
Y142H |
probably benign |
Het |
Macf1 |
A |
T |
4: 123,342,042 (GRCm39) |
D2160E |
probably benign |
Het |
Melk |
A |
G |
4: 44,340,633 (GRCm39) |
Y310C |
probably damaging |
Het |
Mep1a |
C |
T |
17: 43,789,949 (GRCm39) |
V454M |
probably benign |
Het |
Mep1a |
A |
T |
17: 43,790,124 (GRCm39) |
N395K |
probably benign |
Het |
Mnt |
A |
G |
11: 74,727,242 (GRCm39) |
K43E |
probably damaging |
Het |
Nrap |
A |
G |
19: 56,335,616 (GRCm39) |
I853T |
probably damaging |
Het |
Or1j13 |
T |
C |
2: 36,370,032 (GRCm39) |
T37A |
probably benign |
Het |
Or8d1b |
T |
G |
9: 38,887,062 (GRCm39) |
L30R |
probably damaging |
Het |
Pdia4 |
A |
G |
6: 47,777,952 (GRCm39) |
S347P |
probably benign |
Het |
Pkd1l1 |
T |
G |
11: 8,794,649 (GRCm39) |
Q1837H |
probably benign |
Het |
Pramel11 |
T |
C |
4: 143,623,877 (GRCm39) |
N99S |
possibly damaging |
Het |
Pygo1 |
T |
A |
9: 72,852,711 (GRCm39) |
N299K |
probably damaging |
Het |
Sirpb1b |
A |
T |
3: 15,613,725 (GRCm39) |
V52E |
probably damaging |
Het |
Tdrd7 |
T |
A |
4: 45,994,517 (GRCm39) |
I305N |
probably damaging |
Het |
Trav14-1 |
T |
C |
14: 53,791,955 (GRCm39) |
S102P |
probably damaging |
Het |
Tsga10 |
C |
A |
1: 37,874,266 (GRCm39) |
|
probably benign |
Het |
Uso1 |
T |
A |
5: 92,347,711 (GRCm39) |
H837Q |
probably benign |
Het |
Vmn2r82 |
A |
T |
10: 79,231,727 (GRCm39) |
R575S |
probably benign |
Het |
Yae1d1 |
C |
A |
13: 18,167,861 (GRCm39) |
A11S |
probably benign |
Het |
Zfp277 |
A |
G |
12: 40,368,548 (GRCm39) |
I459T |
possibly damaging |
Het |
|
Other mutations in Ogfrl1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00913:Ogfrl1
|
APN |
1 |
23,409,171 (GRCm39) |
missense |
probably benign |
|
IGL02200:Ogfrl1
|
APN |
1 |
23,409,150 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4508001:Ogfrl1
|
UTSW |
1 |
23,409,351 (GRCm39) |
nonsense |
probably null |
|
R0012:Ogfrl1
|
UTSW |
1 |
23,409,206 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0735:Ogfrl1
|
UTSW |
1 |
23,414,835 (GRCm39) |
missense |
possibly damaging |
0.76 |
R1474:Ogfrl1
|
UTSW |
1 |
23,414,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R3837:Ogfrl1
|
UTSW |
1 |
23,409,041 (GRCm39) |
missense |
probably benign |
0.03 |
R4037:Ogfrl1
|
UTSW |
1 |
23,418,045 (GRCm39) |
splice site |
probably benign |
|
R4039:Ogfrl1
|
UTSW |
1 |
23,418,045 (GRCm39) |
splice site |
probably benign |
|
R4332:Ogfrl1
|
UTSW |
1 |
23,414,910 (GRCm39) |
missense |
probably damaging |
1.00 |
R4780:Ogfrl1
|
UTSW |
1 |
23,409,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R5056:Ogfrl1
|
UTSW |
1 |
23,418,130 (GRCm39) |
missense |
probably damaging |
0.97 |
R5994:Ogfrl1
|
UTSW |
1 |
23,418,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R6167:Ogfrl1
|
UTSW |
1 |
23,415,309 (GRCm39) |
missense |
probably damaging |
1.00 |
R6341:Ogfrl1
|
UTSW |
1 |
23,408,944 (GRCm39) |
missense |
probably benign |
0.04 |
R6342:Ogfrl1
|
UTSW |
1 |
23,408,944 (GRCm39) |
missense |
probably benign |
0.04 |
R6343:Ogfrl1
|
UTSW |
1 |
23,408,944 (GRCm39) |
missense |
probably benign |
0.04 |
R6363:Ogfrl1
|
UTSW |
1 |
23,409,194 (GRCm39) |
missense |
probably benign |
0.01 |
R6584:Ogfrl1
|
UTSW |
1 |
23,408,944 (GRCm39) |
missense |
probably benign |
0.04 |
R6586:Ogfrl1
|
UTSW |
1 |
23,408,944 (GRCm39) |
missense |
probably benign |
0.04 |
R7419:Ogfrl1
|
UTSW |
1 |
23,422,063 (GRCm39) |
nonsense |
probably null |
|
R8364:Ogfrl1
|
UTSW |
1 |
23,414,824 (GRCm39) |
nonsense |
probably null |
|
R8749:Ogfrl1
|
UTSW |
1 |
23,409,399 (GRCm39) |
missense |
probably damaging |
1.00 |
R9539:Ogfrl1
|
UTSW |
1 |
23,415,322 (GRCm39) |
missense |
probably damaging |
1.00 |
|