Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700028K03Rik |
A |
T |
5: 107,693,607 (GRCm39) |
I75L |
probably benign |
Het |
Abca2 |
T |
C |
2: 25,333,817 (GRCm39) |
L1755P |
probably damaging |
Het |
Adam6b |
A |
T |
12: 113,454,364 (GRCm39) |
I394L |
probably benign |
Het |
Ano2 |
T |
A |
6: 126,016,471 (GRCm39) |
N1001K |
probably benign |
Het |
Arap2 |
A |
T |
5: 62,906,259 (GRCm39) |
N253K |
probably damaging |
Het |
Ascc3 |
T |
C |
10: 50,604,227 (GRCm39) |
C1316R |
probably benign |
Het |
Atox1 |
T |
C |
11: 55,341,343 (GRCm39) |
Y64C |
probably benign |
Het |
Atp13a1 |
A |
G |
8: 70,259,702 (GRCm39) |
T1098A |
possibly damaging |
Het |
Casr |
T |
C |
16: 36,330,728 (GRCm39) |
E202G |
possibly damaging |
Het |
Cct2 |
T |
C |
10: 116,889,018 (GRCm39) |
T494A |
probably benign |
Het |
Cd209e |
T |
A |
8: 3,899,158 (GRCm39) |
N185Y |
probably damaging |
Het |
Celsr1 |
A |
G |
15: 85,917,088 (GRCm39) |
L295P |
probably damaging |
Het |
Cyp26a1 |
A |
G |
19: 37,686,499 (GRCm39) |
T48A |
possibly damaging |
Het |
Elovl3 |
A |
G |
19: 46,121,567 (GRCm39) |
S37G |
probably benign |
Het |
Fbh1 |
T |
G |
2: 11,774,706 (GRCm39) |
D13A |
possibly damaging |
Het |
Fpr-rs4 |
CAGGAA |
CA |
17: 18,242,596 (GRCm39) |
|
probably null |
Het |
Frem3 |
G |
T |
8: 81,342,455 (GRCm39) |
V1583L |
possibly damaging |
Het |
Gm21863 |
C |
A |
12: 20,004,515 (GRCm39) |
Q4K |
possibly damaging |
Het |
Gm266 |
T |
C |
12: 111,452,132 (GRCm39) |
T25A |
possibly damaging |
Het |
Greb1 |
T |
C |
12: 16,752,651 (GRCm39) |
H897R |
probably damaging |
Het |
Hells |
A |
G |
19: 38,943,474 (GRCm39) |
D565G |
probably damaging |
Het |
Hfm1 |
C |
T |
5: 107,049,684 (GRCm39) |
V426I |
probably damaging |
Het |
Ints6 |
G |
A |
14: 62,951,138 (GRCm39) |
T297I |
probably damaging |
Het |
Itga10 |
C |
T |
3: 96,559,054 (GRCm39) |
|
probably benign |
Het |
Kmt2b |
A |
T |
7: 30,268,845 (GRCm39) |
M2628K |
probably damaging |
Het |
Ktn1 |
T |
G |
14: 47,938,069 (GRCm39) |
|
probably benign |
Het |
Lyst |
T |
A |
13: 13,815,807 (GRCm39) |
D1230E |
probably benign |
Het |
Mboat1 |
T |
C |
13: 30,425,300 (GRCm39) |
|
probably null |
Het |
Moxd2 |
T |
C |
6: 40,861,887 (GRCm39) |
|
probably null |
Het |
Mtmr4 |
T |
C |
11: 87,495,916 (GRCm39) |
M527T |
probably damaging |
Het |
Myt1 |
T |
A |
2: 181,467,717 (GRCm39) |
N1050K |
probably damaging |
Het |
Ncoa6 |
A |
T |
2: 155,248,000 (GRCm39) |
V1768E |
probably damaging |
Het |
Nelfcd |
G |
A |
2: 174,261,875 (GRCm39) |
C48Y |
probably damaging |
Het |
Opn3 |
G |
A |
1: 175,491,145 (GRCm39) |
A296V |
possibly damaging |
Het |
Or13a22 |
T |
C |
7: 140,073,295 (GRCm39) |
I248T |
probably benign |
Het |
Or2z8 |
T |
A |
8: 72,811,607 (GRCm39) |
F28I |
possibly damaging |
Het |
Pam |
T |
C |
1: 97,792,167 (GRCm39) |
E418G |
possibly damaging |
Het |
Prrc2c |
A |
T |
1: 162,525,126 (GRCm39) |
N493K |
probably damaging |
Het |
Ptpn18 |
A |
G |
1: 34,509,300 (GRCm39) |
Q165R |
probably damaging |
Het |
Ptpro |
C |
A |
6: 137,363,162 (GRCm39) |
|
probably benign |
Het |
Ralgapa1 |
A |
G |
12: 55,833,107 (GRCm39) |
F132S |
probably damaging |
Het |
Robo1 |
T |
C |
16: 72,730,630 (GRCm39) |
C244R |
probably damaging |
Het |
Robo3 |
A |
C |
9: 37,338,760 (GRCm39) |
V316G |
probably damaging |
Het |
Rsl1 |
T |
C |
13: 67,330,145 (GRCm39) |
S198P |
probably damaging |
Het |
Rsph9 |
T |
C |
17: 46,445,910 (GRCm39) |
D220G |
probably damaging |
Het |
Rxfp2 |
A |
C |
5: 149,993,677 (GRCm39) |
I580L |
probably benign |
Het |
Septin7 |
G |
A |
9: 25,199,532 (GRCm39) |
A144T |
possibly damaging |
Het |
Sfn |
T |
C |
4: 133,328,603 (GRCm39) |
K160E |
probably benign |
Het |
Ski |
A |
G |
4: 155,306,029 (GRCm39) |
Y317H |
probably damaging |
Het |
Skic3 |
A |
C |
13: 76,328,222 (GRCm39) |
R1423S |
probably damaging |
Het |
Slc22a22 |
A |
T |
15: 57,110,936 (GRCm39) |
Y430* |
probably null |
Het |
Src |
A |
G |
2: 157,299,030 (GRCm39) |
K9R |
probably benign |
Het |
Srm |
C |
T |
4: 148,678,453 (GRCm39) |
P255L |
possibly damaging |
Het |
Stpg4 |
T |
A |
17: 87,730,075 (GRCm39) |
N90I |
probably damaging |
Het |
Sytl2 |
T |
A |
7: 90,031,069 (GRCm39) |
|
probably benign |
Het |
Tbpl2 |
T |
C |
2: 23,984,871 (GRCm39) |
K92R |
probably benign |
Het |
Tlcd4 |
G |
T |
3: 121,024,975 (GRCm39) |
|
probably benign |
Het |
Tmem38a |
T |
A |
8: 73,335,096 (GRCm39) |
N178K |
probably damaging |
Het |
Tnfaip3 |
T |
C |
10: 18,883,900 (GRCm39) |
D160G |
possibly damaging |
Het |
Vegfb |
T |
A |
19: 6,963,407 (GRCm39) |
H119L |
possibly damaging |
Het |
Vmn2r111 |
T |
A |
17: 22,767,395 (GRCm39) |
I701F |
probably damaging |
Het |
Vmn2r95 |
C |
T |
17: 18,661,561 (GRCm39) |
L436F |
probably damaging |
Het |
Wdr47 |
T |
C |
3: 108,530,688 (GRCm39) |
C394R |
probably benign |
Het |
Ythdc2 |
T |
A |
18: 44,988,241 (GRCm39) |
Y16* |
probably null |
Het |
Zer1 |
G |
A |
2: 29,998,286 (GRCm39) |
L342F |
probably damaging |
Het |
Zfp353-ps |
A |
G |
8: 42,535,333 (GRCm39) |
|
noncoding transcript |
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 |
|
R2214:Gm8674
|
UTSW |
13 |
50,055,396 (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 |
|
|