Other mutations in this stock |
Total: 49 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700123K08Rik |
T |
G |
5: 138,561,809 (GRCm39) |
T126P |
probably damaging |
Het |
Asic2 |
T |
C |
11: 80,782,563 (GRCm39) |
|
probably benign |
Het |
B430305J03Rik |
A |
G |
3: 61,271,562 (GRCm39) |
|
probably benign |
Het |
Bbs7 |
A |
G |
3: 36,664,741 (GRCm39) |
F47L |
possibly damaging |
Het |
Bcl2l14 |
G |
T |
6: 134,400,804 (GRCm39) |
G75V |
probably benign |
Het |
Btnl4 |
T |
C |
17: 34,694,901 (GRCm39) |
H4R |
probably benign |
Het |
Champ1 |
C |
A |
8: 13,928,739 (GRCm39) |
P299Q |
probably damaging |
Het |
Cimap3 |
T |
A |
3: 105,921,820 (GRCm39) |
E34D |
probably benign |
Het |
Cldnd2 |
A |
G |
7: 43,091,082 (GRCm39) |
K5E |
probably benign |
Het |
Ctr9 |
T |
A |
7: 110,642,631 (GRCm39) |
L401* |
probably null |
Het |
Cyp2c29 |
G |
A |
19: 39,279,291 (GRCm39) |
G96D |
possibly damaging |
Het |
Enpp4 |
A |
T |
17: 44,412,315 (GRCm39) |
L298H |
probably damaging |
Het |
Git1 |
T |
C |
11: 77,391,513 (GRCm39) |
C222R |
possibly damaging |
Het |
Gpam |
T |
C |
19: 55,076,635 (GRCm39) |
T189A |
probably damaging |
Het |
Hgfac |
T |
G |
5: 35,201,158 (GRCm39) |
|
probably null |
Het |
Hivep3 |
T |
A |
4: 119,991,162 (GRCm39) |
S2221T |
probably damaging |
Het |
Ifi47 |
T |
C |
11: 48,986,604 (GRCm39) |
Y124H |
probably damaging |
Het |
Il1a |
T |
C |
2: 129,148,575 (GRCm39) |
E45G |
probably damaging |
Het |
Itga11 |
T |
A |
9: 62,642,635 (GRCm39) |
I186N |
probably damaging |
Het |
Krt16 |
A |
T |
11: 100,137,162 (GRCm39) |
|
probably benign |
Het |
Mapk13 |
A |
G |
17: 28,995,387 (GRCm39) |
T203A |
probably damaging |
Het |
Mrpl37 |
T |
A |
4: 106,923,839 (GRCm39) |
I52F |
probably damaging |
Het |
Mtrex |
C |
T |
13: 113,027,881 (GRCm39) |
V660M |
probably damaging |
Het |
Nr1i2 |
A |
G |
16: 38,069,654 (GRCm39) |
F417L |
probably benign |
Het |
Or10ag59 |
T |
A |
2: 87,405,576 (GRCm39) |
S49R |
probably benign |
Het |
Or6c215 |
G |
A |
10: 129,637,702 (GRCm39) |
Q231* |
probably null |
Het |
Osbpl1a |
T |
C |
18: 13,047,550 (GRCm39) |
|
probably benign |
Het |
Parg |
C |
T |
14: 31,964,186 (GRCm39) |
T112M |
probably damaging |
Het |
Pou6f1 |
T |
C |
15: 100,477,821 (GRCm39) |
T166A |
possibly damaging |
Het |
Ptpru |
T |
G |
4: 131,504,086 (GRCm39) |
|
probably benign |
Het |
Rab6a |
T |
C |
7: 100,285,970 (GRCm39) |
|
probably null |
Het |
Rnf207 |
C |
T |
4: 152,396,869 (GRCm39) |
R425H |
probably benign |
Het |
Rusf1 |
A |
G |
7: 127,875,582 (GRCm39) |
L257P |
probably damaging |
Het |
Slc27a2 |
A |
G |
2: 126,420,912 (GRCm39) |
M468V |
probably benign |
Het |
Slc30a1 |
A |
G |
1: 191,639,441 (GRCm39) |
H108R |
possibly damaging |
Het |
Sned1 |
A |
G |
1: 93,163,930 (GRCm39) |
|
probably benign |
Het |
Sptbn4 |
A |
T |
7: 27,065,014 (GRCm39) |
F2095Y |
probably null |
Het |
Sspo |
A |
T |
6: 48,437,237 (GRCm39) |
|
probably benign |
Het |
Tbx19 |
A |
G |
1: 164,967,740 (GRCm39) |
S336P |
probably benign |
Het |
Tmem101 |
T |
A |
11: 102,044,119 (GRCm39) |
D256V |
probably damaging |
Het |
Trbv20 |
T |
G |
6: 41,165,210 (GRCm39) |
L2V |
unknown |
Het |
Trpc7 |
A |
G |
13: 56,970,274 (GRCm39) |
S382P |
probably damaging |
Het |
Tut4 |
C |
A |
4: 108,386,473 (GRCm39) |
Y1114* |
probably null |
Het |
Uhmk1 |
T |
C |
1: 170,040,095 (GRCm39) |
T91A |
possibly damaging |
Het |
Vmn2r10 |
T |
A |
5: 109,143,788 (GRCm39) |
R721* |
probably null |
Het |
Vmn2r94 |
T |
A |
17: 18,478,453 (GRCm39) |
Y98F |
possibly damaging |
Het |
Zfp532 |
A |
G |
18: 65,756,672 (GRCm39) |
R202G |
probably damaging |
Het |
Zfp827 |
T |
C |
8: 79,787,601 (GRCm39) |
S256P |
probably damaging |
Het |
Zzef1 |
T |
C |
11: 72,792,214 (GRCm39) |
I2266T |
probably damaging |
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 |
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 |
IGL03136:Prtg
|
APN |
9 |
72,764,267 (GRCm39) |
missense |
possibly damaging |
0.91 |
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 |
|