Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5730522E02Rik |
A |
G |
11: 25,719,122 (GRCm39) |
L7S |
unknown |
Het |
Abr |
C |
T |
11: 76,316,121 (GRCm39) |
W571* |
probably null |
Het |
Adam18 |
A |
T |
8: 25,131,852 (GRCm39) |
C420S |
probably damaging |
Het |
Akap5 |
G |
T |
12: 76,376,649 (GRCm39) |
E694* |
probably null |
Het |
Bbs1 |
T |
C |
19: 4,941,019 (GRCm39) |
K565R |
probably benign |
Het |
Brix1 |
A |
G |
15: 10,478,852 (GRCm39) |
F189S |
probably damaging |
Het |
Cnot4 |
C |
A |
6: 35,028,176 (GRCm39) |
R480L |
probably damaging |
Het |
Ctu2 |
A |
G |
8: 123,205,940 (GRCm39) |
|
probably benign |
Het |
Dhcr7 |
A |
G |
7: 143,401,103 (GRCm39) |
H422R |
probably damaging |
Het |
Dock1 |
A |
G |
7: 134,770,118 (GRCm39) |
M1793V |
probably benign |
Het |
Dock7 |
A |
G |
4: 98,892,028 (GRCm39) |
F853L |
probably damaging |
Het |
Fkbp15 |
G |
A |
4: 62,258,466 (GRCm39) |
|
probably benign |
Het |
Ftsj3 |
C |
T |
11: 106,144,639 (GRCm39) |
D117N |
probably damaging |
Het |
Gphn |
A |
G |
12: 78,528,107 (GRCm39) |
I142V |
possibly damaging |
Het |
Hsd3b1 |
G |
A |
3: 98,760,301 (GRCm39) |
A230V |
probably damaging |
Het |
Hydin |
G |
A |
8: 111,145,156 (GRCm39) |
A836T |
probably benign |
Het |
Ift52 |
G |
T |
2: 162,867,254 (GRCm39) |
E71* |
probably null |
Het |
Ms4a14 |
T |
C |
19: 11,281,775 (GRCm39) |
D261G |
possibly damaging |
Het |
Nid1 |
G |
A |
13: 13,675,084 (GRCm39) |
V935I |
probably benign |
Het |
Nrap |
T |
C |
19: 56,330,687 (GRCm39) |
K1008E |
possibly damaging |
Het |
Nup210 |
A |
C |
6: 91,005,843 (GRCm39) |
V1340G |
probably benign |
Het |
Or2aj4 |
A |
T |
16: 19,385,103 (GRCm39) |
F177I |
probably damaging |
Het |
Or5b94 |
T |
A |
19: 12,652,331 (GRCm39) |
I254N |
probably damaging |
Het |
Or8d6 |
T |
C |
9: 39,854,332 (GRCm39) |
Y259H |
probably damaging |
Het |
Pcdhb15 |
C |
A |
18: 37,608,067 (GRCm39) |
T433N |
probably damaging |
Het |
Pdcd6ip |
T |
A |
9: 113,520,567 (GRCm39) |
N139I |
probably damaging |
Het |
Pgbd1 |
A |
G |
13: 21,617,609 (GRCm39) |
V80A |
possibly damaging |
Het |
Pigw |
A |
G |
11: 84,768,603 (GRCm39) |
I242T |
probably benign |
Het |
Ptpn13 |
T |
A |
5: 103,691,329 (GRCm39) |
N1065K |
possibly damaging |
Het |
Qrich1 |
G |
A |
9: 108,422,117 (GRCm39) |
R577H |
probably damaging |
Het |
Ryr3 |
G |
A |
2: 112,506,319 (GRCm39) |
|
probably benign |
Het |
Selenoi |
T |
C |
5: 30,462,725 (GRCm39) |
Y197H |
probably damaging |
Het |
Slc47a2 |
A |
G |
11: 61,201,591 (GRCm39) |
C343R |
probably benign |
Het |
Smurf2 |
A |
T |
11: 106,721,874 (GRCm39) |
D527E |
probably benign |
Het |
Spam1 |
C |
T |
6: 24,797,010 (GRCm39) |
|
probably benign |
Het |
Stkld1 |
T |
C |
2: 26,841,435 (GRCm39) |
V460A |
probably benign |
Het |
Tgoln1 |
G |
A |
6: 72,591,096 (GRCm39) |
R339W |
probably damaging |
Het |
Tprg1 |
T |
C |
16: 25,231,512 (GRCm39) |
|
probably benign |
Het |
Treml1 |
T |
G |
17: 48,671,879 (GRCm39) |
|
probably benign |
Het |
Ttc39b |
A |
T |
4: 83,155,517 (GRCm39) |
V497E |
probably damaging |
Het |
Vmn1r223 |
A |
G |
13: 23,433,933 (GRCm39) |
T176A |
possibly damaging |
Het |
Vmn2r75 |
A |
T |
7: 85,797,911 (GRCm39) |
I634N |
possibly damaging |
Het |
Vps13c |
A |
G |
9: 67,857,592 (GRCm39) |
E2608G |
probably damaging |
Het |
Zfp575 |
A |
G |
7: 24,285,381 (GRCm39) |
C87R |
probably damaging |
Het |
Zfp790 |
T |
A |
7: 29,529,320 (GRCm39) |
Y668* |
probably null |
Het |
|
Other mutations in Prtg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00597:Prtg
|
APN |
9 |
72,716,926 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00942:Prtg
|
APN |
9 |
72,799,622 (GRCm39) |
missense |
possibly damaging |
0.82 |
IGL01821:Prtg
|
APN |
9 |
72,819,219 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01901:Prtg
|
APN |
9 |
72,762,348 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02143:Prtg
|
APN |
9 |
72,799,606 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02232:Prtg
|
APN |
9 |
72,758,771 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02451:Prtg
|
APN |
9 |
72,764,281 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02510:Prtg
|
APN |
9 |
72,798,151 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02739:Prtg
|
APN |
9 |
72,758,867 (GRCm39) |
missense |
possibly damaging |
0.92 |
FR4548:Prtg
|
UTSW |
9 |
72,764,363 (GRCm39) |
critical splice donor site |
probably benign |
|
FR4589:Prtg
|
UTSW |
9 |
72,764,147 (GRCm39) |
missense |
probably damaging |
1.00 |
FR4737:Prtg
|
UTSW |
9 |
72,764,363 (GRCm39) |
critical splice donor site |
probably benign |
|
R0130:Prtg
|
UTSW |
9 |
72,716,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R0321:Prtg
|
UTSW |
9 |
72,755,307 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0390:Prtg
|
UTSW |
9 |
72,752,240 (GRCm39) |
missense |
probably benign |
0.24 |
R0900:Prtg
|
UTSW |
9 |
72,752,225 (GRCm39) |
missense |
probably benign |
|
R1121:Prtg
|
UTSW |
9 |
72,813,449 (GRCm39) |
missense |
probably benign |
0.15 |
R1438:Prtg
|
UTSW |
9 |
72,818,032 (GRCm39) |
splice site |
probably benign |
|
R1537:Prtg
|
UTSW |
9 |
72,717,039 (GRCm39) |
missense |
probably benign |
0.00 |
R1590:Prtg
|
UTSW |
9 |
72,750,089 (GRCm39) |
missense |
probably benign |
|
R1626:Prtg
|
UTSW |
9 |
72,752,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R1965:Prtg
|
UTSW |
9 |
72,755,604 (GRCm39) |
missense |
probably benign |
0.27 |
R1993:Prtg
|
UTSW |
9 |
72,752,178 (GRCm39) |
missense |
probably benign |
|
R2351:Prtg
|
UTSW |
9 |
72,764,106 (GRCm39) |
missense |
probably damaging |
1.00 |
R3737:Prtg
|
UTSW |
9 |
72,749,991 (GRCm39) |
nonsense |
probably null |
|
R3921:Prtg
|
UTSW |
9 |
72,755,629 (GRCm39) |
missense |
probably damaging |
0.98 |
R4035:Prtg
|
UTSW |
9 |
72,749,991 (GRCm39) |
nonsense |
probably null |
|
R4378:Prtg
|
UTSW |
9 |
72,750,042 (GRCm39) |
missense |
possibly damaging |
0.91 |
R4687:Prtg
|
UTSW |
9 |
72,798,080 (GRCm39) |
missense |
probably damaging |
1.00 |
R5469:Prtg
|
UTSW |
9 |
72,799,247 (GRCm39) |
missense |
probably damaging |
0.98 |
R5556:Prtg
|
UTSW |
9 |
72,758,986 (GRCm39) |
missense |
probably damaging |
1.00 |
R5563:Prtg
|
UTSW |
9 |
72,764,180 (GRCm39) |
missense |
probably damaging |
1.00 |
R5710:Prtg
|
UTSW |
9 |
72,716,922 (GRCm39) |
missense |
probably damaging |
1.00 |
R5738:Prtg
|
UTSW |
9 |
72,819,288 (GRCm39) |
missense |
probably benign |
0.16 |
R5868:Prtg
|
UTSW |
9 |
72,716,999 (GRCm39) |
nonsense |
probably null |
|
R5961:Prtg
|
UTSW |
9 |
72,764,228 (GRCm39) |
missense |
probably benign |
|
R5964:Prtg
|
UTSW |
9 |
72,799,536 (GRCm39) |
missense |
probably benign |
0.41 |
R6217:Prtg
|
UTSW |
9 |
72,812,076 (GRCm39) |
missense |
probably damaging |
1.00 |
R6306:Prtg
|
UTSW |
9 |
72,813,468 (GRCm39) |
missense |
probably benign |
0.42 |
R6395:Prtg
|
UTSW |
9 |
72,819,414 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6455:Prtg
|
UTSW |
9 |
72,815,138 (GRCm39) |
missense |
probably damaging |
1.00 |
R6673:Prtg
|
UTSW |
9 |
72,758,964 (GRCm39) |
missense |
probably damaging |
0.99 |
R6985:Prtg
|
UTSW |
9 |
72,758,783 (GRCm39) |
missense |
probably damaging |
1.00 |
R7014:Prtg
|
UTSW |
9 |
72,799,267 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7233:Prtg
|
UTSW |
9 |
72,819,273 (GRCm39) |
missense |
probably benign |
0.00 |
R7261:Prtg
|
UTSW |
9 |
72,815,117 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7324:Prtg
|
UTSW |
9 |
72,798,122 (GRCm39) |
missense |
probably damaging |
0.96 |
R7372:Prtg
|
UTSW |
9 |
72,758,848 (GRCm39) |
nonsense |
probably null |
|
R7808:Prtg
|
UTSW |
9 |
72,749,979 (GRCm39) |
missense |
possibly damaging |
0.81 |
R8069:Prtg
|
UTSW |
9 |
72,752,265 (GRCm39) |
missense |
probably benign |
0.10 |
R8262:Prtg
|
UTSW |
9 |
72,813,520 (GRCm39) |
missense |
probably benign |
0.00 |
R8280:Prtg
|
UTSW |
9 |
72,813,433 (GRCm39) |
missense |
probably damaging |
0.99 |
R8290:Prtg
|
UTSW |
9 |
72,798,077 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Prtg
|
UTSW |
9 |
72,798,156 (GRCm39) |
critical splice donor site |
probably null |
|
R8773:Prtg
|
UTSW |
9 |
72,819,583 (GRCm39) |
makesense |
probably null |
|
R9020:Prtg
|
UTSW |
9 |
72,799,277 (GRCm39) |
missense |
probably damaging |
0.98 |
R9104:Prtg
|
UTSW |
9 |
72,755,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R9166:Prtg
|
UTSW |
9 |
72,764,107 (GRCm39) |
missense |
probably damaging |
1.00 |
R9186:Prtg
|
UTSW |
9 |
72,764,159 (GRCm39) |
missense |
probably benign |
0.34 |
R9256:Prtg
|
UTSW |
9 |
72,758,977 (GRCm39) |
missense |
probably damaging |
0.99 |
R9277:Prtg
|
UTSW |
9 |
72,716,929 (GRCm39) |
missense |
probably benign |
0.02 |
R9383:Prtg
|
UTSW |
9 |
72,757,143 (GRCm39) |
missense |
probably benign |
0.39 |
R9402:Prtg
|
UTSW |
9 |
72,819,253 (GRCm39) |
missense |
probably benign |
0.37 |
R9564:Prtg
|
UTSW |
9 |
72,766,153 (GRCm39) |
missense |
probably damaging |
0.99 |
R9644:Prtg
|
UTSW |
9 |
72,813,493 (GRCm39) |
missense |
probably damaging |
0.99 |
R9700:Prtg
|
UTSW |
9 |
72,762,313 (GRCm39) |
missense |
probably benign |
|
X0028:Prtg
|
UTSW |
9 |
72,758,998 (GRCm39) |
missense |
possibly damaging |
0.55 |
X0064:Prtg
|
UTSW |
9 |
72,812,174 (GRCm39) |
splice site |
probably null |
|
Z1176:Prtg
|
UTSW |
9 |
72,801,250 (GRCm39) |
missense |
probably damaging |
1.00 |
|