Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Afdn |
C |
T |
17: 14,043,615 (GRCm39) |
H358Y |
probably benign |
Het |
Aoc1l2 |
T |
C |
6: 48,907,464 (GRCm39) |
S155P |
probably damaging |
Het |
Ccdc125 |
T |
A |
13: 100,830,995 (GRCm39) |
M394K |
probably benign |
Het |
Cfd |
C |
A |
10: 79,727,636 (GRCm39) |
H103Q |
probably damaging |
Het |
Cnot2 |
G |
A |
10: 116,334,058 (GRCm39) |
P371S |
possibly damaging |
Het |
Dedd2 |
T |
C |
7: 24,903,332 (GRCm39) |
E209G |
probably benign |
Het |
Dnah3 |
A |
G |
7: 119,522,197 (GRCm39) |
S3999P |
probably benign |
Het |
Fer1l5 |
T |
C |
1: 36,447,753 (GRCm39) |
|
probably null |
Het |
H6pd |
A |
T |
4: 150,069,578 (GRCm39) |
|
probably null |
Het |
Il25 |
T |
C |
14: 55,170,490 (GRCm39) |
I21T |
probably benign |
Het |
Kmt2c |
C |
T |
5: 25,614,291 (GRCm39) |
S143N |
probably damaging |
Het |
Marveld3 |
T |
C |
8: 110,688,681 (GRCm39) |
D20G |
possibly damaging |
Het |
Msl1 |
A |
G |
11: 98,690,882 (GRCm39) |
E122G |
probably damaging |
Het |
Obscn |
A |
T |
11: 58,919,421 (GRCm39) |
V6861E |
probably damaging |
Het |
Or5b97 |
A |
T |
19: 12,878,605 (GRCm39) |
C180S |
probably damaging |
Het |
Phc1 |
A |
T |
6: 122,313,845 (GRCm39) |
M29K |
possibly damaging |
Het |
Pkd1l3 |
T |
A |
8: 110,375,126 (GRCm39) |
|
probably null |
Het |
Prl5a1 |
G |
T |
13: 28,333,919 (GRCm39) |
V141F |
possibly damaging |
Het |
Psg20 |
A |
T |
7: 18,408,547 (GRCm39) |
V391D |
probably damaging |
Het |
Rasa3 |
T |
C |
8: 13,630,037 (GRCm39) |
E580G |
possibly damaging |
Het |
Ror1 |
T |
C |
4: 100,283,252 (GRCm39) |
V439A |
probably benign |
Het |
Rsl1 |
A |
G |
13: 67,325,206 (GRCm39) |
T81A |
probably benign |
Het |
Sgpp1 |
G |
C |
12: 75,782,243 (GRCm39) |
P32R |
probably benign |
Het |
Slc22a8 |
T |
C |
19: 8,586,656 (GRCm39) |
L389P |
probably benign |
Het |
Slc6a11 |
A |
G |
6: 114,111,859 (GRCm39) |
Y142C |
probably damaging |
Het |
Syt9 |
C |
T |
7: 107,024,503 (GRCm39) |
T132I |
probably damaging |
Het |
Thop1 |
T |
A |
10: 80,917,246 (GRCm39) |
I583N |
probably damaging |
Het |
Tom1l1 |
A |
G |
11: 90,575,886 (GRCm39) |
|
probably null |
Het |
Unk |
A |
G |
11: 115,941,581 (GRCm39) |
D276G |
probably damaging |
Het |
Zfp942 |
C |
A |
17: 22,147,733 (GRCm39) |
E299* |
probably null |
Het |
Zkscan6 |
A |
G |
11: 65,719,461 (GRCm39) |
T494A |
probably damaging |
Het |
Zscan25 |
T |
A |
5: 145,227,723 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Ptprh |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01766:Ptprh
|
APN |
7 |
4,583,915 (GRCm39) |
missense |
probably benign |
0.23 |
IGL02420:Ptprh
|
APN |
7 |
4,583,929 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02619:Ptprh
|
APN |
7 |
4,552,498 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02729:Ptprh
|
APN |
7 |
4,583,873 (GRCm39) |
missense |
probably damaging |
0.99 |
BB008:Ptprh
|
UTSW |
7 |
4,574,987 (GRCm39) |
missense |
probably benign |
0.03 |
BB018:Ptprh
|
UTSW |
7 |
4,574,987 (GRCm39) |
missense |
probably benign |
0.03 |
R0018:Ptprh
|
UTSW |
7 |
4,604,845 (GRCm39) |
critical splice donor site |
probably null |
|
R0049:Ptprh
|
UTSW |
7 |
4,576,361 (GRCm39) |
missense |
possibly damaging |
0.80 |
R0449:Ptprh
|
UTSW |
7 |
4,601,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R0477:Ptprh
|
UTSW |
7 |
4,600,997 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0626:Ptprh
|
UTSW |
7 |
4,567,271 (GRCm39) |
missense |
probably benign |
0.00 |
R0741:Ptprh
|
UTSW |
7 |
4,557,172 (GRCm39) |
critical splice donor site |
probably null |
|
R1068:Ptprh
|
UTSW |
7 |
4,552,462 (GRCm39) |
missense |
possibly damaging |
0.89 |
R1226:Ptprh
|
UTSW |
7 |
4,606,091 (GRCm39) |
nonsense |
probably null |
|
R1487:Ptprh
|
UTSW |
7 |
4,555,737 (GRCm39) |
missense |
probably damaging |
1.00 |
R1495:Ptprh
|
UTSW |
7 |
4,583,888 (GRCm39) |
missense |
probably benign |
0.02 |
R1537:Ptprh
|
UTSW |
7 |
4,552,698 (GRCm39) |
missense |
probably damaging |
1.00 |
R1601:Ptprh
|
UTSW |
7 |
4,555,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R1731:Ptprh
|
UTSW |
7 |
4,604,912 (GRCm39) |
missense |
probably benign |
0.00 |
R1920:Ptprh
|
UTSW |
7 |
4,552,394 (GRCm39) |
missense |
probably benign |
0.25 |
R2082:Ptprh
|
UTSW |
7 |
4,553,774 (GRCm39) |
missense |
probably damaging |
1.00 |
R2180:Ptprh
|
UTSW |
7 |
4,604,867 (GRCm39) |
missense |
probably benign |
0.26 |
R2214:Ptprh
|
UTSW |
7 |
4,555,921 (GRCm39) |
missense |
possibly damaging |
0.78 |
R2245:Ptprh
|
UTSW |
7 |
4,576,345 (GRCm39) |
missense |
probably benign |
0.09 |
R2271:Ptprh
|
UTSW |
7 |
4,606,132 (GRCm39) |
start gained |
probably benign |
|
R3693:Ptprh
|
UTSW |
7 |
4,557,234 (GRCm39) |
missense |
probably damaging |
0.99 |
R3713:Ptprh
|
UTSW |
7 |
4,574,969 (GRCm39) |
missense |
probably damaging |
1.00 |
R4081:Ptprh
|
UTSW |
7 |
4,583,987 (GRCm39) |
missense |
probably damaging |
0.99 |
R4205:Ptprh
|
UTSW |
7 |
4,600,991 (GRCm39) |
missense |
probably damaging |
1.00 |
R4689:Ptprh
|
UTSW |
7 |
4,600,996 (GRCm39) |
missense |
possibly damaging |
0.74 |
R4782:Ptprh
|
UTSW |
7 |
4,572,576 (GRCm39) |
missense |
probably benign |
0.08 |
R4838:Ptprh
|
UTSW |
7 |
4,576,429 (GRCm39) |
missense |
possibly damaging |
0.78 |
R4974:Ptprh
|
UTSW |
7 |
4,554,006 (GRCm39) |
splice site |
probably null |
|
R5218:Ptprh
|
UTSW |
7 |
4,600,919 (GRCm39) |
missense |
probably benign |
0.05 |
R5430:Ptprh
|
UTSW |
7 |
4,554,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R5533:Ptprh
|
UTSW |
7 |
4,552,504 (GRCm39) |
missense |
probably damaging |
1.00 |
R5544:Ptprh
|
UTSW |
7 |
4,583,909 (GRCm39) |
nonsense |
probably null |
|
R5547:Ptprh
|
UTSW |
7 |
4,557,221 (GRCm39) |
nonsense |
probably null |
|
R5869:Ptprh
|
UTSW |
7 |
4,604,939 (GRCm39) |
missense |
probably benign |
0.00 |
R5928:Ptprh
|
UTSW |
7 |
4,576,507 (GRCm39) |
missense |
probably damaging |
1.00 |
R6063:Ptprh
|
UTSW |
7 |
4,576,361 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6112:Ptprh
|
UTSW |
7 |
4,600,922 (GRCm39) |
missense |
probably benign |
0.01 |
R6493:Ptprh
|
UTSW |
7 |
4,583,989 (GRCm39) |
missense |
possibly damaging |
0.65 |
R6836:Ptprh
|
UTSW |
7 |
4,554,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R6859:Ptprh
|
UTSW |
7 |
4,552,370 (GRCm39) |
nonsense |
probably null |
|
R6868:Ptprh
|
UTSW |
7 |
4,604,864 (GRCm39) |
missense |
probably benign |
|
R7015:Ptprh
|
UTSW |
7 |
4,555,626 (GRCm39) |
critical splice donor site |
probably null |
|
R7092:Ptprh
|
UTSW |
7 |
4,583,860 (GRCm39) |
critical splice donor site |
probably null |
|
R7147:Ptprh
|
UTSW |
7 |
4,553,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R7177:Ptprh
|
UTSW |
7 |
4,572,480 (GRCm39) |
missense |
possibly damaging |
0.77 |
R7358:Ptprh
|
UTSW |
7 |
4,554,006 (GRCm39) |
splice site |
probably null |
|
R7436:Ptprh
|
UTSW |
7 |
4,555,742 (GRCm39) |
missense |
probably damaging |
1.00 |
R7512:Ptprh
|
UTSW |
7 |
4,574,780 (GRCm39) |
missense |
possibly damaging |
0.60 |
R7863:Ptprh
|
UTSW |
7 |
4,606,097 (GRCm39) |
start codon destroyed |
probably benign |
0.31 |
R7931:Ptprh
|
UTSW |
7 |
4,574,987 (GRCm39) |
missense |
probably benign |
0.03 |
R7973:Ptprh
|
UTSW |
7 |
4,583,887 (GRCm39) |
missense |
possibly damaging |
0.55 |
R8239:Ptprh
|
UTSW |
7 |
4,584,090 (GRCm39) |
missense |
probably damaging |
1.00 |
R8331:Ptprh
|
UTSW |
7 |
4,552,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R8688:Ptprh
|
UTSW |
7 |
4,554,022 (GRCm39) |
missense |
probably benign |
0.03 |
R8700:Ptprh
|
UTSW |
7 |
4,567,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R8716:Ptprh
|
UTSW |
7 |
4,567,273 (GRCm39) |
missense |
probably damaging |
1.00 |
R8970:Ptprh
|
UTSW |
7 |
4,583,944 (GRCm39) |
missense |
possibly damaging |
0.84 |
R9119:Ptprh
|
UTSW |
7 |
4,555,712 (GRCm39) |
missense |
probably benign |
0.25 |
R9203:Ptprh
|
UTSW |
7 |
4,574,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9213:Ptprh
|
UTSW |
7 |
4,583,911 (GRCm39) |
missense |
probably damaging |
0.99 |
R9250:Ptprh
|
UTSW |
7 |
4,576,289 (GRCm39) |
missense |
probably benign |
0.03 |
RF022:Ptprh
|
UTSW |
7 |
4,552,367 (GRCm39) |
missense |
probably benign |
|
Z1177:Ptprh
|
UTSW |
7 |
4,601,117 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Ptprh
|
UTSW |
7 |
4,600,970 (GRCm39) |
missense |
probably damaging |
0.99 |
|