Other mutations in this stock |
Total: 36 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb11 |
T |
A |
2: 69,076,288 (GRCm39) |
D1140V |
probably damaging |
Het |
Ak1 |
G |
T |
2: 32,523,507 (GRCm39) |
|
probably benign |
Het |
Ano1 |
A |
T |
7: 144,190,848 (GRCm39) |
L411H |
probably benign |
Het |
Atad2 |
A |
T |
15: 57,967,921 (GRCm39) |
N569K |
probably benign |
Het |
Bst2 |
C |
A |
8: 71,989,830 (GRCm39) |
R81L |
probably damaging |
Het |
Cd4 |
G |
A |
6: 124,856,341 (GRCm39) |
T50I |
probably benign |
Het |
Chrna5 |
C |
T |
9: 54,911,683 (GRCm39) |
T57M |
possibly damaging |
Het |
Cp |
A |
T |
3: 20,031,369 (GRCm39) |
D602V |
possibly damaging |
Het |
Drd2 |
T |
C |
9: 49,312,115 (GRCm39) |
I156T |
probably damaging |
Het |
Elp4 |
G |
A |
2: 105,622,653 (GRCm39) |
R349W |
probably damaging |
Het |
Eml6 |
G |
A |
11: 29,705,021 (GRCm39) |
R1508* |
probably null |
Het |
Etl4 |
T |
C |
2: 20,748,667 (GRCm39) |
L335S |
probably damaging |
Het |
Fat3 |
A |
T |
9: 16,289,319 (GRCm39) |
I68K |
probably benign |
Het |
Fyco1 |
G |
T |
9: 123,657,944 (GRCm39) |
A744D |
probably damaging |
Het |
Gm22165 |
G |
T |
3: 64,012,886 (GRCm39) |
|
probably benign |
Het |
Gse1 |
T |
C |
8: 121,280,326 (GRCm39) |
M1T |
probably null |
Het |
Hs3st5 |
A |
T |
10: 36,709,404 (GRCm39) |
H313L |
probably damaging |
Het |
Hsd17b3 |
T |
C |
13: 64,210,719 (GRCm39) |
Y212C |
probably damaging |
Het |
Hyal5 |
G |
T |
6: 24,876,406 (GRCm39) |
S93I |
probably benign |
Het |
Itgb1 |
T |
C |
8: 129,449,315 (GRCm39) |
V578A |
probably benign |
Het |
Klf12 |
A |
T |
14: 100,347,294 (GRCm39) |
N12K |
possibly damaging |
Het |
Krt40 |
C |
T |
11: 99,432,045 (GRCm39) |
C222Y |
probably damaging |
Het |
Lrrn2 |
T |
C |
1: 132,864,965 (GRCm39) |
L10P |
probably damaging |
Het |
Lrsam1 |
T |
C |
2: 32,837,915 (GRCm39) |
Y213C |
probably damaging |
Het |
Mitf |
C |
A |
6: 97,994,892 (GRCm39) |
T277K |
possibly damaging |
Het |
Ncan |
C |
T |
8: 70,554,607 (GRCm39) |
R1070H |
probably benign |
Het |
Nr4a3 |
A |
G |
4: 48,083,201 (GRCm39) |
E578G |
probably benign |
Het |
Patj |
A |
G |
4: 98,301,287 (GRCm39) |
T191A |
possibly damaging |
Het |
Smad5 |
G |
A |
13: 56,883,630 (GRCm39) |
V339I |
probably benign |
Het |
Spem2 |
T |
A |
11: 69,708,065 (GRCm39) |
Y300F |
possibly damaging |
Het |
Trank1 |
T |
G |
9: 111,193,790 (GRCm39) |
S605A |
probably damaging |
Het |
Treml4 |
T |
A |
17: 48,571,877 (GRCm39) |
D93E |
possibly damaging |
Het |
Tsc22d2 |
T |
A |
3: 58,323,924 (GRCm39) |
V272E |
probably damaging |
Het |
Vmn2r19 |
T |
A |
6: 123,306,826 (GRCm39) |
F445I |
possibly damaging |
Het |
Zfp712 |
T |
A |
13: 67,190,230 (GRCm39) |
Q99L |
possibly damaging |
Het |
Zfp719 |
A |
T |
7: 43,233,611 (GRCm39) |
K10I |
probably benign |
Het |
|
Other mutations in Pign |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00485:Pign
|
APN |
1 |
105,525,448 (GRCm39) |
nonsense |
probably null |
|
IGL00770:Pign
|
APN |
1 |
105,525,481 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00774:Pign
|
APN |
1 |
105,525,481 (GRCm39) |
missense |
probably benign |
0.00 |
IGL00828:Pign
|
APN |
1 |
105,481,845 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL01523:Pign
|
APN |
1 |
105,580,903 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01953:Pign
|
APN |
1 |
105,516,764 (GRCm39) |
splice site |
probably benign |
|
IGL02389:Pign
|
APN |
1 |
105,574,506 (GRCm39) |
nonsense |
probably null |
|
PIT4810001:Pign
|
UTSW |
1 |
105,525,487 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0080:Pign
|
UTSW |
1 |
105,480,130 (GRCm39) |
missense |
probably damaging |
1.00 |
R0097:Pign
|
UTSW |
1 |
105,515,701 (GRCm39) |
splice site |
probably benign |
|
R0302:Pign
|
UTSW |
1 |
105,516,818 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0573:Pign
|
UTSW |
1 |
105,580,902 (GRCm39) |
missense |
probably damaging |
1.00 |
R0580:Pign
|
UTSW |
1 |
105,519,419 (GRCm39) |
missense |
probably benign |
0.03 |
R0946:Pign
|
UTSW |
1 |
105,519,422 (GRCm39) |
missense |
probably benign |
0.00 |
R1397:Pign
|
UTSW |
1 |
105,585,496 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Pign
|
UTSW |
1 |
105,512,727 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1462:Pign
|
UTSW |
1 |
105,512,727 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1751:Pign
|
UTSW |
1 |
105,580,917 (GRCm39) |
missense |
probably benign |
0.19 |
R1753:Pign
|
UTSW |
1 |
105,517,042 (GRCm39) |
missense |
possibly damaging |
0.65 |
R1767:Pign
|
UTSW |
1 |
105,580,917 (GRCm39) |
missense |
probably benign |
0.19 |
R1854:Pign
|
UTSW |
1 |
105,482,223 (GRCm39) |
missense |
probably damaging |
0.99 |
R1907:Pign
|
UTSW |
1 |
105,565,940 (GRCm39) |
missense |
possibly damaging |
0.50 |
R2845:Pign
|
UTSW |
1 |
105,585,521 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2846:Pign
|
UTSW |
1 |
105,585,521 (GRCm39) |
missense |
possibly damaging |
0.80 |
R3718:Pign
|
UTSW |
1 |
105,577,006 (GRCm39) |
critical splice donor site |
probably null |
|
R3970:Pign
|
UTSW |
1 |
105,583,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R4067:Pign
|
UTSW |
1 |
105,515,703 (GRCm39) |
critical splice donor site |
probably null |
|
R4110:Pign
|
UTSW |
1 |
105,481,540 (GRCm39) |
unclassified |
probably benign |
|
R4387:Pign
|
UTSW |
1 |
105,449,785 (GRCm39) |
missense |
possibly damaging |
0.48 |
R4393:Pign
|
UTSW |
1 |
105,449,751 (GRCm39) |
missense |
probably benign |
0.00 |
R4472:Pign
|
UTSW |
1 |
105,575,945 (GRCm39) |
missense |
probably benign |
0.29 |
R4519:Pign
|
UTSW |
1 |
105,525,391 (GRCm39) |
critical splice donor site |
probably null |
|
R4619:Pign
|
UTSW |
1 |
105,449,715 (GRCm39) |
utr 3 prime |
probably benign |
|
R4746:Pign
|
UTSW |
1 |
105,512,749 (GRCm39) |
missense |
probably benign |
0.33 |
R4859:Pign
|
UTSW |
1 |
105,575,892 (GRCm39) |
nonsense |
probably null |
|
R4893:Pign
|
UTSW |
1 |
105,574,436 (GRCm39) |
missense |
probably damaging |
1.00 |
R4953:Pign
|
UTSW |
1 |
105,572,227 (GRCm39) |
missense |
probably benign |
0.32 |
R5046:Pign
|
UTSW |
1 |
105,449,798 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5377:Pign
|
UTSW |
1 |
105,585,537 (GRCm39) |
missense |
probably benign |
0.12 |
R5388:Pign
|
UTSW |
1 |
105,583,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R5482:Pign
|
UTSW |
1 |
105,474,435 (GRCm39) |
missense |
probably benign |
0.44 |
R5594:Pign
|
UTSW |
1 |
105,574,594 (GRCm39) |
intron |
probably benign |
|
R5639:Pign
|
UTSW |
1 |
105,517,040 (GRCm39) |
missense |
probably benign |
0.09 |
R5778:Pign
|
UTSW |
1 |
105,519,447 (GRCm39) |
missense |
probably damaging |
1.00 |
R5821:Pign
|
UTSW |
1 |
105,516,788 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5928:Pign
|
UTSW |
1 |
105,485,792 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5979:Pign
|
UTSW |
1 |
105,516,999 (GRCm39) |
missense |
probably benign |
0.01 |
R6213:Pign
|
UTSW |
1 |
105,516,991 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6292:Pign
|
UTSW |
1 |
105,512,802 (GRCm39) |
missense |
possibly damaging |
0.69 |
R6343:Pign
|
UTSW |
1 |
105,512,820 (GRCm39) |
missense |
probably benign |
0.33 |
R6566:Pign
|
UTSW |
1 |
105,565,906 (GRCm39) |
critical splice donor site |
probably null |
|
R6856:Pign
|
UTSW |
1 |
105,481,620 (GRCm39) |
nonsense |
probably null |
|
R6954:Pign
|
UTSW |
1 |
105,481,622 (GRCm39) |
missense |
probably benign |
0.39 |
R7361:Pign
|
UTSW |
1 |
105,512,778 (GRCm39) |
missense |
probably benign |
0.01 |
R7582:Pign
|
UTSW |
1 |
105,577,092 (GRCm39) |
missense |
probably benign |
0.00 |
R7622:Pign
|
UTSW |
1 |
105,575,842 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7742:Pign
|
UTSW |
1 |
105,480,122 (GRCm39) |
missense |
probably benign |
|
R7892:Pign
|
UTSW |
1 |
105,585,401 (GRCm39) |
missense |
probably benign |
0.01 |
R8273:Pign
|
UTSW |
1 |
105,516,803 (GRCm39) |
missense |
probably benign |
0.00 |
R8352:Pign
|
UTSW |
1 |
105,575,917 (GRCm39) |
missense |
probably benign |
0.35 |
R8452:Pign
|
UTSW |
1 |
105,575,917 (GRCm39) |
missense |
probably benign |
0.35 |
R8826:Pign
|
UTSW |
1 |
105,481,827 (GRCm39) |
missense |
probably damaging |
1.00 |
R8841:Pign
|
UTSW |
1 |
105,485,634 (GRCm39) |
intron |
probably benign |
|
R8886:Pign
|
UTSW |
1 |
105,512,779 (GRCm39) |
missense |
probably benign |
|
R8904:Pign
|
UTSW |
1 |
105,519,359 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9074:Pign
|
UTSW |
1 |
105,556,246 (GRCm39) |
missense |
unknown |
|
R9197:Pign
|
UTSW |
1 |
105,516,818 (GRCm39) |
missense |
probably benign |
0.03 |
R9630:Pign
|
UTSW |
1 |
105,481,591 (GRCm39) |
missense |
probably benign |
0.23 |
R9702:Pign
|
UTSW |
1 |
105,485,212 (GRCm39) |
missense |
probably damaging |
1.00 |
X0025:Pign
|
UTSW |
1 |
105,585,359 (GRCm39) |
missense |
probably benign |
0.03 |
Z1177:Pign
|
UTSW |
1 |
105,585,545 (GRCm39) |
start codon destroyed |
probably null |
0.98 |
|