Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts20 |
T |
A |
15: 94,241,923 (GRCm39) |
D695V |
probably damaging |
Het |
Ahnak |
T |
C |
19: 8,990,251 (GRCm39) |
|
probably benign |
Het |
Akap4 |
T |
A |
X: 6,942,423 (GRCm39) |
M242K |
probably benign |
Het |
Cd207 |
T |
C |
6: 83,652,839 (GRCm39) |
D97G |
probably benign |
Het |
Cdc20 |
A |
G |
4: 118,292,749 (GRCm39) |
V333A |
possibly damaging |
Het |
Cdhr2 |
A |
G |
13: 54,865,948 (GRCm39) |
|
probably benign |
Het |
Cfhr1 |
T |
A |
1: 139,481,322 (GRCm39) |
Y186F |
probably benign |
Het |
Cnbd1 |
T |
A |
4: 18,907,098 (GRCm39) |
I159F |
probably benign |
Het |
Cyp2j11 |
A |
C |
4: 96,227,332 (GRCm39) |
M228R |
probably benign |
Het |
Dach1 |
C |
A |
14: 98,077,640 (GRCm39) |
S581I |
possibly damaging |
Het |
Dbnl |
A |
G |
11: 5,743,722 (GRCm39) |
D71G |
possibly damaging |
Het |
F8 |
T |
A |
X: 74,330,993 (GRCm39) |
T966S |
possibly damaging |
Het |
Filip1 |
T |
A |
9: 79,805,528 (GRCm39) |
L75F |
probably benign |
Het |
Foxi2 |
A |
G |
7: 135,013,736 (GRCm39) |
Y322C |
probably benign |
Het |
Ftsj3 |
A |
G |
11: 106,146,458 (GRCm39) |
V7A |
probably benign |
Het |
Gm8362 |
A |
T |
14: 18,145,196 (GRCm39) |
S204T |
probably benign |
Het |
Ibtk |
C |
A |
9: 85,614,675 (GRCm39) |
|
probably benign |
Het |
Marf1 |
C |
T |
16: 13,964,600 (GRCm39) |
V267I |
possibly damaging |
Het |
Mmp27 |
T |
A |
9: 7,573,416 (GRCm39) |
D169E |
probably damaging |
Het |
Or10ag53 |
C |
A |
2: 87,082,806 (GRCm39) |
T175K |
probably damaging |
Het |
Or4a74 |
C |
T |
2: 89,440,191 (GRCm39) |
C85Y |
probably benign |
Het |
Or4k1 |
A |
T |
14: 50,377,511 (GRCm39) |
M195K |
probably benign |
Het |
P4ha2 |
G |
T |
11: 54,010,131 (GRCm39) |
C296F |
probably damaging |
Het |
Scart2 |
A |
T |
7: 139,876,017 (GRCm39) |
Q543L |
probably benign |
Het |
Slc38a5 |
T |
C |
X: 8,137,750 (GRCm39) |
|
probably benign |
Het |
Sorbs2 |
G |
T |
8: 46,198,460 (GRCm39) |
R36L |
possibly damaging |
Het |
Vmn2r115 |
G |
A |
17: 23,564,971 (GRCm39) |
R286K |
probably benign |
Het |
|
Other mutations in Tmem207 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02140:Tmem207
|
APN |
16 |
26,335,490 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02249:Tmem207
|
APN |
16 |
26,336,617 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02394:Tmem207
|
APN |
16 |
26,335,586 (GRCm39) |
splice site |
probably benign |
|
IGL03380:Tmem207
|
APN |
16 |
26,345,407 (GRCm39) |
missense |
probably damaging |
1.00 |
R0058:Tmem207
|
UTSW |
16 |
26,343,579 (GRCm39) |
splice site |
probably benign |
|
R0058:Tmem207
|
UTSW |
16 |
26,343,579 (GRCm39) |
splice site |
probably benign |
|
R1839:Tmem207
|
UTSW |
16 |
26,343,571 (GRCm39) |
missense |
possibly damaging |
0.80 |
R4943:Tmem207
|
UTSW |
16 |
26,336,603 (GRCm39) |
nonsense |
probably null |
|
R7348:Tmem207
|
UTSW |
16 |
26,335,577 (GRCm39) |
missense |
possibly damaging |
0.68 |
R7947:Tmem207
|
UTSW |
16 |
26,335,495 (GRCm39) |
missense |
possibly damaging |
0.82 |
R9358:Tmem207
|
UTSW |
16 |
26,345,434 (GRCm39) |
missense |
probably benign |
0.07 |
R9464:Tmem207
|
UTSW |
16 |
26,345,413 (GRCm39) |
missense |
|
|
R9564:Tmem207
|
UTSW |
16 |
26,335,499 (GRCm39) |
nonsense |
probably null |
|
|