Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acap2 |
T |
C |
16: 30,926,946 (GRCm39) |
Y516C |
probably benign |
Het |
Adam22 |
C |
T |
5: 8,186,805 (GRCm39) |
|
probably null |
Het |
Akap8l |
T |
C |
17: 32,557,799 (GRCm39) |
|
probably null |
Het |
Casr |
T |
C |
16: 36,336,120 (GRCm39) |
Y63C |
probably damaging |
Het |
Ccdc178 |
T |
C |
18: 22,048,047 (GRCm39) |
D781G |
possibly damaging |
Het |
Col9a1 |
C |
A |
1: 24,247,283 (GRCm39) |
P168Q |
probably damaging |
Het |
Dnm2 |
T |
C |
9: 21,397,019 (GRCm39) |
|
probably null |
Het |
Dst |
C |
T |
1: 34,310,482 (GRCm39) |
T6325M |
probably damaging |
Het |
Ercc4 |
C |
A |
16: 12,927,888 (GRCm39) |
D19E |
probably damaging |
Het |
Gm1110 |
C |
A |
9: 26,813,786 (GRCm39) |
V198L |
probably benign |
Het |
Grm7 |
A |
T |
6: 111,335,958 (GRCm39) |
I790F |
probably damaging |
Het |
Habp2 |
A |
G |
19: 56,306,249 (GRCm39) |
D445G |
possibly damaging |
Het |
Kat7 |
G |
A |
11: 95,166,631 (GRCm39) |
T517I |
probably damaging |
Het |
Kbtbd11 |
T |
A |
8: 15,079,178 (GRCm39) |
D592E |
possibly damaging |
Het |
Lgals8 |
T |
A |
13: 12,469,713 (GRCm39) |
Q82L |
probably benign |
Het |
Lmtk3 |
A |
G |
7: 45,444,277 (GRCm39) |
|
probably benign |
Het |
Map2 |
A |
T |
1: 66,459,345 (GRCm39) |
D1530V |
probably damaging |
Het |
Map2k6 |
G |
A |
11: 110,387,167 (GRCm39) |
V180I |
probably damaging |
Het |
Map3k5 |
T |
A |
10: 19,902,035 (GRCm39) |
|
probably null |
Het |
Mtor |
A |
G |
4: 148,623,327 (GRCm39) |
E2059G |
probably benign |
Het |
Myh10 |
A |
G |
11: 68,673,953 (GRCm39) |
D660G |
probably damaging |
Het |
Myo16 |
T |
A |
8: 10,488,803 (GRCm39) |
V658E |
probably damaging |
Het |
Nckap5 |
A |
T |
1: 125,953,487 (GRCm39) |
S1090T |
possibly damaging |
Het |
Nhlrc3 |
T |
C |
3: 53,363,875 (GRCm39) |
H217R |
probably damaging |
Het |
Ntrk3 |
T |
A |
7: 78,166,520 (GRCm39) |
I118F |
probably damaging |
Het |
Or14a259 |
T |
A |
7: 86,013,414 (GRCm39) |
I44F |
probably benign |
Het |
Or1e29 |
A |
T |
11: 73,667,655 (GRCm39) |
L166* |
probably null |
Het |
Or4p20 |
C |
T |
2: 88,253,461 (GRCm39) |
V303M |
probably benign |
Het |
Paxip1 |
T |
C |
5: 27,947,499 (GRCm39) |
Y1053C |
probably damaging |
Het |
Pfkfb4 |
T |
A |
9: 108,834,677 (GRCm39) |
F117I |
probably benign |
Het |
Pp2d1 |
T |
C |
17: 53,822,424 (GRCm39) |
Y214C |
probably benign |
Het |
Prr7 |
C |
A |
13: 55,620,613 (GRCm39) |
S207* |
probably null |
Het |
Ptprh |
T |
A |
7: 4,555,921 (GRCm39) |
Q715L |
possibly damaging |
Het |
Rasgrp1 |
A |
T |
2: 117,115,646 (GRCm39) |
D647E |
probably damaging |
Het |
Rnf20 |
T |
A |
4: 49,648,344 (GRCm39) |
M384K |
possibly damaging |
Het |
Rps6kb1 |
A |
T |
11: 86,424,896 (GRCm39) |
C37S |
possibly damaging |
Het |
Serpinb9f |
C |
A |
13: 33,518,592 (GRCm39) |
T364K |
probably benign |
Het |
Sorbs1 |
C |
T |
19: 40,285,075 (GRCm39) |
A641T |
probably damaging |
Het |
Srrm2 |
T |
C |
17: 24,035,719 (GRCm39) |
|
probably benign |
Het |
Stag3 |
C |
T |
5: 138,299,528 (GRCm39) |
S849L |
possibly damaging |
Het |
Syt15 |
A |
T |
14: 33,944,989 (GRCm39) |
S179C |
probably damaging |
Het |
Tapbp |
T |
C |
17: 34,139,300 (GRCm39) |
F90L |
possibly damaging |
Het |
Timm23 |
A |
T |
14: 31,920,944 (GRCm39) |
D49E |
probably damaging |
Het |
Tmcc1 |
C |
CAT |
6: 116,019,831 (GRCm39) |
|
probably null |
Het |
Tmem174 |
A |
C |
13: 98,773,757 (GRCm39) |
S24R |
possibly damaging |
Het |
Tmem63a |
A |
G |
1: 180,788,679 (GRCm39) |
S339G |
probably benign |
Het |
Tsc22d2 |
A |
G |
3: 58,323,627 (GRCm39) |
Y173C |
probably damaging |
Het |
Ubap2 |
A |
G |
4: 41,199,714 (GRCm39) |
|
probably null |
Het |
Upp1 |
T |
A |
11: 9,086,033 (GRCm39) |
V290E |
probably benign |
Het |
Uqcc4 |
T |
C |
17: 25,403,699 (GRCm39) |
V13A |
probably benign |
Het |
Usp17lb |
A |
T |
7: 104,490,639 (GRCm39) |
M96K |
probably benign |
Het |
Wdr20rt |
A |
G |
12: 65,274,187 (GRCm39) |
E449G |
probably damaging |
Het |
Zkscan8 |
A |
T |
13: 21,705,082 (GRCm39) |
S286T |
probably benign |
Het |
|
Other mutations in Gm8674 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
R0355:Gm8674
|
UTSW |
13 |
50,055,975 (GRCm39) |
exon |
noncoding transcript |
|
R0357:Gm8674
|
UTSW |
13 |
50,056,149 (GRCm39) |
exon |
noncoding transcript |
|
R0627:Gm8674
|
UTSW |
13 |
50,053,751 (GRCm39) |
exon |
noncoding transcript |
|
R0833:Gm8674
|
UTSW |
13 |
50,058,611 (GRCm39) |
exon |
noncoding transcript |
|
R1300:Gm8674
|
UTSW |
13 |
50,055,758 (GRCm39) |
exon |
noncoding transcript |
|
R1452:Gm8674
|
UTSW |
13 |
50,054,553 (GRCm39) |
exon |
noncoding transcript |
|
R1542:Gm8674
|
UTSW |
13 |
50,054,039 (GRCm39) |
exon |
noncoding transcript |
|
R1613:Gm8674
|
UTSW |
13 |
50,056,474 (GRCm39) |
intron |
noncoding transcript |
|
R1643:Gm8674
|
UTSW |
13 |
50,055,394 (GRCm39) |
exon |
noncoding transcript |
|
R1732:Gm8674
|
UTSW |
13 |
50,055,962 (GRCm39) |
exon |
noncoding transcript |
|
R1824:Gm8674
|
UTSW |
13 |
50,054,844 (GRCm39) |
exon |
noncoding transcript |
|
R1840:Gm8674
|
UTSW |
13 |
50,055,801 (GRCm39) |
exon |
noncoding transcript |
|
R1915:Gm8674
|
UTSW |
13 |
50,054,889 (GRCm39) |
exon |
noncoding transcript |
|
R1934:Gm8674
|
UTSW |
13 |
50,055,471 (GRCm39) |
exon |
noncoding transcript |
|
R2040:Gm8674
|
UTSW |
13 |
50,055,705 (GRCm39) |
exon |
noncoding transcript |
|
R2421:Gm8674
|
UTSW |
13 |
50,054,699 (GRCm39) |
exon |
noncoding transcript |
|
R3423:Gm8674
|
UTSW |
13 |
50,055,792 (GRCm39) |
exon |
noncoding transcript |
|
R3425:Gm8674
|
UTSW |
13 |
50,055,792 (GRCm39) |
exon |
noncoding transcript |
|
R3886:Gm8674
|
UTSW |
13 |
50,056,199 (GRCm39) |
splice site |
noncoding transcript |
|
R4083:Gm8674
|
UTSW |
13 |
50,055,047 (GRCm39) |
exon |
noncoding transcript |
|
R4343:Gm8674
|
UTSW |
13 |
50,053,742 (GRCm39) |
exon |
noncoding transcript |
|
R4570:Gm8674
|
UTSW |
13 |
50,056,570 (GRCm39) |
intron |
noncoding transcript |
|
R4936:Gm8674
|
UTSW |
13 |
50,054,791 (GRCm39) |
exon |
noncoding transcript |
|
R4967:Gm8674
|
UTSW |
13 |
50,056,034 (GRCm39) |
exon |
noncoding transcript |
|
R5065:Gm8674
|
UTSW |
13 |
50,056,613 (GRCm39) |
intron |
noncoding transcript |
|
R5067:Gm8674
|
UTSW |
13 |
50,053,870 (GRCm39) |
exon |
noncoding transcript |
|
R5120:Gm8674
|
UTSW |
13 |
50,055,984 (GRCm39) |
exon |
noncoding transcript |
|
R5208:Gm8674
|
UTSW |
13 |
50,055,957 (GRCm39) |
exon |
noncoding transcript |
|
R5268:Gm8674
|
UTSW |
13 |
50,055,390 (GRCm39) |
exon |
noncoding transcript |
|
R5471:Gm8674
|
UTSW |
13 |
50,054,849 (GRCm39) |
exon |
noncoding transcript |
|
R5773:Gm8674
|
UTSW |
13 |
50,055,912 (GRCm39) |
exon |
noncoding transcript |
|
R5809:Gm8674
|
UTSW |
13 |
50,055,924 (GRCm39) |
exon |
noncoding transcript |
|
R8162:Gm8674
|
UTSW |
13 |
50,054,407 (GRCm39) |
missense |
noncoding transcript |
|
R8239:Gm8674
|
UTSW |
13 |
50,054,262 (GRCm39) |
missense |
noncoding transcript |
|
Z1088:Gm8674
|
UTSW |
13 |
50,055,284 (GRCm39) |
exon |
noncoding transcript |
|
Z1088:Gm8674
|
UTSW |
13 |
50,054,830 (GRCm39) |
exon |
noncoding transcript |
|
|