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 |
Mfsd9 |
C |
A |
1: 40,829,638 (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 |
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 Ppil6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01110:Ppil6
|
APN |
10 |
41,374,406 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02964:Ppil6
|
APN |
10 |
41,383,479 (GRCm39) |
missense |
probably benign |
0.13 |
R0827:Ppil6
|
UTSW |
10 |
41,370,500 (GRCm39) |
unclassified |
probably benign |
|
R1661:Ppil6
|
UTSW |
10 |
41,390,176 (GRCm39) |
missense |
probably benign |
0.03 |
R2302:Ppil6
|
UTSW |
10 |
41,377,795 (GRCm39) |
missense |
probably damaging |
1.00 |
R2844:Ppil6
|
UTSW |
10 |
41,377,689 (GRCm39) |
splice site |
probably benign |
|
R4258:Ppil6
|
UTSW |
10 |
41,383,531 (GRCm39) |
nonsense |
probably null |
|
R5098:Ppil6
|
UTSW |
10 |
41,366,616 (GRCm39) |
missense |
probably null |
1.00 |
R5455:Ppil6
|
UTSW |
10 |
41,374,541 (GRCm39) |
missense |
probably benign |
0.15 |
R5530:Ppil6
|
UTSW |
10 |
41,383,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R6683:Ppil6
|
UTSW |
10 |
41,374,427 (GRCm39) |
missense |
probably benign |
|
R7288:Ppil6
|
UTSW |
10 |
41,374,524 (GRCm39) |
missense |
probably benign |
0.03 |
R7843:Ppil6
|
UTSW |
10 |
41,377,862 (GRCm39) |
missense |
probably benign |
|
R9424:Ppil6
|
UTSW |
10 |
41,379,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R9590:Ppil6
|
UTSW |
10 |
41,366,478 (GRCm39) |
start codon destroyed |
probably null |
0.95 |
R9630:Ppil6
|
UTSW |
10 |
41,370,550 (GRCm39) |
missense |
probably benign |
0.26 |
|