Other mutations in this stock |
Total: 30 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca13 |
A |
G |
11: 9,353,834 (GRCm39) |
T3719A |
probably damaging |
Het |
Abcb5 |
A |
G |
12: 118,831,705 (GRCm39) |
S1216P |
probably damaging |
Het |
Abl1 |
A |
G |
2: 31,668,989 (GRCm39) |
T104A |
probably damaging |
Het |
Adgrg6 |
A |
T |
10: 14,296,202 (GRCm39) |
M1066K |
possibly damaging |
Het |
Armc1 |
T |
C |
3: 19,198,594 (GRCm39) |
N122S |
probably benign |
Het |
Fat1 |
C |
T |
8: 45,504,307 (GRCm39) |
T4600M |
probably damaging |
Het |
Hrh1 |
T |
A |
6: 114,458,123 (GRCm39) |
I468N |
probably damaging |
Het |
Krt34 |
A |
T |
11: 99,930,916 (GRCm39) |
L162Q |
probably damaging |
Het |
Macrod2 |
A |
T |
2: 140,294,492 (GRCm39) |
|
probably benign |
Het |
Nap1l1 |
C |
T |
10: 111,328,839 (GRCm39) |
T256I |
probably benign |
Het |
Or12e1 |
A |
G |
2: 87,022,192 (GRCm39) |
I54V |
probably benign |
Het |
Or5h22 |
T |
C |
16: 58,895,132 (GRCm39) |
I104V |
probably benign |
Het |
Or6k4 |
A |
G |
1: 173,964,679 (GRCm39) |
Y123C |
possibly damaging |
Het |
Pard6a |
T |
A |
8: 106,429,309 (GRCm39) |
|
probably null |
Het |
Pmm2 |
G |
A |
16: 8,466,532 (GRCm39) |
R119Q |
probably damaging |
Het |
Por |
C |
T |
5: 135,763,040 (GRCm39) |
Q517* |
probably null |
Het |
Ppil6 |
T |
C |
10: 41,374,473 (GRCm39) |
I118T |
probably benign |
Het |
Psg26 |
A |
G |
7: 18,213,999 (GRCm39) |
V221A |
possibly damaging |
Het |
Ptpru |
C |
A |
4: 131,496,803 (GRCm39) |
|
probably benign |
Het |
Rpl27a |
T |
A |
7: 109,118,832 (GRCm39) |
V15E |
probably benign |
Het |
Setd1b |
T |
C |
5: 123,296,527 (GRCm39) |
|
probably benign |
Het |
Slc17a1 |
A |
G |
13: 24,058,714 (GRCm39) |
N56S |
probably damaging |
Het |
Sybu |
A |
T |
15: 44,536,201 (GRCm39) |
D508E |
probably damaging |
Het |
Tada2b |
A |
C |
5: 36,633,686 (GRCm39) |
N222K |
probably damaging |
Het |
Tbcb |
T |
C |
7: 29,930,627 (GRCm39) |
|
probably null |
Het |
Tmprss11f |
C |
A |
5: 86,692,691 (GRCm39) |
G78* |
probably null |
Het |
Vmn2r65 |
T |
C |
7: 84,589,708 (GRCm39) |
Y736C |
probably damaging |
Het |
Zc3h7a |
G |
A |
16: 10,967,242 (GRCm39) |
P517S |
probably benign |
Het |
Zfp280d |
A |
G |
9: 72,229,868 (GRCm39) |
T392A |
possibly damaging |
Het |
Zfp318 |
T |
A |
17: 46,719,942 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Mfsd9 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00946:Mfsd9
|
APN |
1 |
40,812,940 (GRCm39) |
missense |
probably benign |
0.22 |
R0631:Mfsd9
|
UTSW |
1 |
40,829,634 (GRCm39) |
splice site |
probably benign |
|
R1644:Mfsd9
|
UTSW |
1 |
40,812,958 (GRCm39) |
missense |
probably benign |
0.39 |
R4204:Mfsd9
|
UTSW |
1 |
40,820,670 (GRCm39) |
missense |
probably damaging |
1.00 |
R4761:Mfsd9
|
UTSW |
1 |
40,813,635 (GRCm39) |
missense |
possibly damaging |
0.61 |
R4777:Mfsd9
|
UTSW |
1 |
40,820,700 (GRCm39) |
missense |
possibly damaging |
0.64 |
R5109:Mfsd9
|
UTSW |
1 |
40,813,365 (GRCm39) |
missense |
probably damaging |
0.98 |
R6712:Mfsd9
|
UTSW |
1 |
40,825,601 (GRCm39) |
splice site |
probably null |
|
R8776:Mfsd9
|
UTSW |
1 |
40,812,915 (GRCm39) |
makesense |
probably null |
|
R8776-TAIL:Mfsd9
|
UTSW |
1 |
40,812,915 (GRCm39) |
makesense |
probably null |
|
R8839:Mfsd9
|
UTSW |
1 |
40,813,554 (GRCm39) |
missense |
probably benign |
|
R9411:Mfsd9
|
UTSW |
1 |
40,829,692 (GRCm39) |
missense |
probably damaging |
0.98 |
R9478:Mfsd9
|
UTSW |
1 |
40,812,941 (GRCm39) |
missense |
probably benign |
0.00 |
R9499:Mfsd9
|
UTSW |
1 |
40,813,152 (GRCm39) |
missense |
probably damaging |
0.96 |
R9551:Mfsd9
|
UTSW |
1 |
40,813,152 (GRCm39) |
missense |
probably damaging |
0.96 |
|