Other mutations in this stock |
Total: 28 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Arl5b |
T |
C |
2: 15,074,746 (GRCm39) |
S76P |
probably benign |
Het |
Asap3 |
A |
C |
4: 135,933,879 (GRCm39) |
D17A |
probably damaging |
Het |
Ccdc24 |
C |
T |
4: 117,729,243 (GRCm39) |
R78H |
probably damaging |
Het |
Crp |
T |
C |
1: 172,526,568 (GRCm39) |
F218L |
probably benign |
Het |
Dab2 |
T |
C |
15: 6,459,306 (GRCm39) |
L385P |
probably benign |
Het |
Dip2c |
C |
A |
13: 9,660,791 (GRCm39) |
T855N |
probably damaging |
Het |
Dnai7 |
A |
T |
6: 145,137,302 (GRCm39) |
F269I |
possibly damaging |
Het |
Dync2i1 |
A |
T |
12: 116,205,400 (GRCm39) |
D396E |
probably benign |
Het |
Ep400 |
A |
G |
5: 110,887,460 (GRCm39) |
V541A |
probably damaging |
Het |
Gbgt1 |
A |
T |
2: 28,392,207 (GRCm39) |
|
probably null |
Het |
Gm6871 |
A |
T |
7: 41,195,845 (GRCm39) |
D297E |
possibly damaging |
Het |
Gpr107 |
T |
A |
2: 31,062,006 (GRCm39) |
F145I |
probably benign |
Het |
Itgb6 |
T |
G |
2: 60,450,696 (GRCm39) |
D581A |
probably benign |
Het |
Lce1a1 |
C |
T |
3: 92,554,470 (GRCm39) |
M1I |
probably null |
Het |
Lmbrd2 |
G |
A |
15: 9,157,382 (GRCm39) |
V207M |
probably damaging |
Het |
Muc5b |
T |
A |
7: 141,395,129 (GRCm39) |
V45E |
unknown |
Het |
Mybpc2 |
A |
G |
7: 44,154,806 (GRCm39) |
V977A |
probably damaging |
Het |
Oas1c |
T |
C |
5: 120,946,744 (GRCm39) |
T29A |
probably benign |
Het |
Pdzd2 |
G |
T |
15: 12,365,853 (GRCm39) |
|
probably null |
Het |
Plk2 |
T |
C |
13: 110,532,912 (GRCm39) |
Y158H |
possibly damaging |
Het |
Ptprq |
A |
G |
10: 107,443,983 (GRCm39) |
|
probably benign |
Het |
Rnf17 |
C |
T |
14: 56,658,539 (GRCm39) |
T76I |
probably damaging |
Het |
Serpinb1c |
T |
C |
13: 33,067,958 (GRCm39) |
K213E |
probably damaging |
Het |
Sidt2 |
A |
G |
9: 45,854,350 (GRCm39) |
V624A |
possibly damaging |
Het |
Sin3b |
T |
C |
8: 73,483,628 (GRCm39) |
V1005A |
probably benign |
Het |
Ubr4 |
T |
C |
4: 139,182,495 (GRCm39) |
V358A |
possibly damaging |
Het |
Zfp120 |
T |
C |
2: 149,961,748 (GRCm39) |
I67V |
possibly damaging |
Het |
Zfp942 |
A |
T |
17: 22,147,605 (GRCm39) |
H341Q |
probably damaging |
Het |
|
Other mutations in Prss1l |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00330:Prss1l
|
APN |
6 |
41,371,707 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01103:Prss1l
|
APN |
6 |
41,374,091 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01368:Prss1l
|
APN |
6 |
41,373,620 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL01458:Prss1l
|
APN |
6 |
41,373,621 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03114:Prss1l
|
APN |
6 |
41,374,012 (GRCm39) |
missense |
probably damaging |
1.00 |
R0167:Prss1l
|
UTSW |
6 |
41,373,195 (GRCm39) |
splice site |
probably benign |
|
R1548:Prss1l
|
UTSW |
6 |
41,372,945 (GRCm39) |
missense |
probably damaging |
1.00 |
R4584:Prss1l
|
UTSW |
6 |
41,373,701 (GRCm39) |
missense |
probably benign |
0.35 |
R5622:Prss1l
|
UTSW |
6 |
41,373,084 (GRCm39) |
missense |
probably damaging |
1.00 |
R5664:Prss1l
|
UTSW |
6 |
41,371,605 (GRCm39) |
missense |
probably benign |
0.04 |
R6222:Prss1l
|
UTSW |
6 |
41,374,100 (GRCm39) |
missense |
probably damaging |
0.98 |
R6325:Prss1l
|
UTSW |
6 |
41,373,590 (GRCm39) |
missense |
probably benign |
0.00 |
R7816:Prss1l
|
UTSW |
6 |
41,371,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R7986:Prss1l
|
UTSW |
6 |
41,373,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R8016:Prss1l
|
UTSW |
6 |
41,374,100 (GRCm39) |
missense |
probably damaging |
0.98 |
|