Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9630041A04Rik |
C |
A |
9: 101,942,994 (GRCm38) |
D204E |
possibly damaging |
Het |
Aldh3a2 |
A |
G |
11: 61,265,211 (GRCm38) |
S80P |
probably benign |
Het |
Bcl6b |
A |
T |
11: 70,226,574 (GRCm38) |
Y407* |
probably null |
Het |
Cel |
TTA |
TTATA |
2: 28,559,429 (GRCm38) |
|
probably null |
Het |
Cerkl |
A |
T |
2: 79,341,330 (GRCm38) |
C395S |
probably damaging |
Het |
Chst5 |
C |
A |
8: 111,890,860 (GRCm38) |
V43L |
probably benign |
Het |
Clip1 |
A |
T |
5: 123,646,274 (GRCm38) |
F271I |
probably damaging |
Het |
Clspn |
A |
G |
4: 126,590,618 (GRCm38) |
T1190A |
possibly damaging |
Het |
Col20a1 |
A |
T |
2: 181,006,735 (GRCm38) |
E938D |
probably damaging |
Het |
Ctgf |
T |
C |
10: 24,595,958 (GRCm38) |
V49A |
probably benign |
Het |
Dmrta2 |
G |
A |
4: 109,982,582 (GRCm38) |
V509M |
probably damaging |
Het |
Dnah7b |
T |
A |
1: 46,322,260 (GRCm38) |
M3440K |
probably benign |
Het |
Erlin1 |
A |
G |
19: 44,040,745 (GRCm38) |
|
probably null |
Het |
Fam24b |
A |
G |
7: 131,326,140 (GRCm38) |
S107P |
probably benign |
Het |
Fancm |
T |
A |
12: 65,102,584 (GRCm38) |
I708N |
probably benign |
Het |
Fbxo11 |
A |
T |
17: 88,015,696 (GRCm38) |
D12E |
|
Het |
Fbxw13 |
T |
C |
9: 109,195,048 (GRCm38) |
D39G |
probably damaging |
Het |
Gabrb3 |
T |
G |
7: 57,816,404 (GRCm38) |
L322R |
probably damaging |
Het |
Gm10696 |
A |
C |
3: 94,175,643 (GRCm38) |
L287R |
probably damaging |
Het |
Gm5239 |
A |
T |
18: 35,536,619 (GRCm38) |
I13F |
possibly damaging |
Het |
Heatr1 |
A |
G |
13: 12,404,921 (GRCm38) |
Y375C |
probably benign |
Het |
Helq |
A |
T |
5: 100,798,437 (GRCm38) |
S13T |
possibly damaging |
Het |
Helz |
A |
G |
11: 107,619,092 (GRCm38) |
T514A |
probably benign |
Het |
Hook3 |
A |
G |
8: 26,032,524 (GRCm38) |
V32A |
|
Het |
Htra4 |
A |
G |
8: 25,037,032 (GRCm38) |
I249T |
possibly damaging |
Het |
Htt |
G |
T |
5: 34,905,348 (GRCm38) |
V2809L |
probably benign |
Het |
Ifi203 |
T |
A |
1: 173,937,871 (GRCm38) |
I46F |
probably benign |
Het |
Kcna2 |
A |
T |
3: 107,104,990 (GRCm38) |
I296F |
possibly damaging |
Het |
Kndc1 |
A |
G |
7: 139,921,441 (GRCm38) |
E882G |
possibly damaging |
Het |
Krtap16-1 |
A |
T |
11: 99,985,245 (GRCm38) |
D444E |
probably benign |
Het |
Lrrtm3 |
ATTTT |
ATTTTT |
10: 64,089,256 (GRCm38) |
|
probably null |
Het |
Mdga2 |
C |
T |
12: 66,568,860 (GRCm38) |
D658N |
possibly damaging |
Het |
Mkrn1 |
T |
C |
6: 39,401,249 (GRCm38) |
K316R |
possibly damaging |
Het |
Mmd2 |
C |
T |
5: 142,567,911 (GRCm38) |
C165Y |
probably damaging |
Het |
Mpdz |
A |
G |
4: 81,284,630 (GRCm38) |
F1843L |
probably damaging |
Het |
Mrc2 |
G |
A |
11: 105,329,267 (GRCm38) |
R338Q |
probably damaging |
Het |
Nav2 |
C |
A |
7: 49,552,851 (GRCm38) |
S1461Y |
probably damaging |
Het |
Nol8 |
T |
A |
13: 49,661,262 (GRCm38) |
V282D |
possibly damaging |
Het |
Nup98 |
C |
A |
7: 102,184,960 (GRCm38) |
G265V |
possibly damaging |
Het |
Olfr1049 |
G |
T |
2: 86,255,200 (GRCm38) |
F164L |
possibly damaging |
Het |
Olfr1311 |
T |
A |
2: 112,021,172 (GRCm38) |
K227N |
possibly damaging |
Het |
Olfr1318 |
T |
A |
2: 112,156,128 (GRCm38) |
M59K |
possibly damaging |
Het |
Olfr132 |
C |
T |
17: 38,131,121 (GRCm38) |
E24K |
possibly damaging |
Het |
Olfr1532-ps1 |
A |
G |
7: 106,914,773 (GRCm38) |
T192A |
possibly damaging |
Het |
Olfr356 |
T |
C |
2: 36,937,899 (GRCm38) |
F260S |
probably damaging |
Het |
Otogl |
T |
A |
10: 107,854,344 (GRCm38) |
E888D |
probably damaging |
Het |
Pcdhgc4 |
A |
G |
18: 37,815,632 (GRCm38) |
I34V |
possibly damaging |
Het |
Ppp1r12b |
T |
C |
1: 134,879,638 (GRCm38) |
R417G |
probably benign |
Het |
Rtn4 |
A |
G |
11: 29,706,778 (GRCm38) |
S311G |
probably benign |
Het |
Serinc3 |
A |
G |
2: 163,636,892 (GRCm38) |
V105A |
probably benign |
Het |
Serpina3f |
A |
G |
12: 104,217,185 (GRCm38) |
D102G |
possibly damaging |
Het |
Sik3 |
A |
G |
9: 46,155,474 (GRCm38) |
I184V |
probably damaging |
Het |
Tex35 |
A |
T |
1: 157,107,866 (GRCm38) |
C21S |
probably benign |
Het |
Tfap2b |
T |
C |
1: 19,212,425 (GRCm38) |
|
probably null |
Het |
Thbs4 |
C |
T |
13: 92,761,490 (GRCm38) |
C607Y |
probably damaging |
Het |
Tmem144 |
A |
T |
3: 79,827,657 (GRCm38) |
N151K |
probably benign |
Het |
Tomm70a |
T |
A |
16: 57,142,803 (GRCm38) |
M395K |
probably benign |
Het |
Trim43b |
A |
C |
9: 89,085,610 (GRCm38) |
H324Q |
probably benign |
Het |
Vmn2r116 |
A |
T |
17: 23,401,167 (GRCm38) |
Y625F |
probably damaging |
Het |
Yipf3 |
A |
T |
17: 46,248,872 (GRCm38) |
N38I |
probably damaging |
Het |
Zfp804b |
T |
A |
5: 6,771,496 (GRCm38) |
E522D |
probably benign |
Het |
|
Other mutations in Naip5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00096:Naip5
|
APN |
13 |
100,246,175 (GRCm38) |
nonsense |
probably null |
|
IGL00493:Naip5
|
APN |
13 |
100,230,771 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL01294:Naip5
|
APN |
13 |
100,217,080 (GRCm38) |
missense |
probably damaging |
0.99 |
IGL01405:Naip5
|
APN |
13 |
100,221,945 (GRCm38) |
missense |
probably benign |
0.11 |
IGL01568:Naip5
|
APN |
13 |
100,217,101 (GRCm38) |
missense |
probably benign |
0.26 |
IGL01804:Naip5
|
APN |
13 |
100,221,584 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02012:Naip5
|
APN |
13 |
100,223,339 (GRCm38) |
missense |
probably benign |
0.01 |
IGL02183:Naip5
|
APN |
13 |
100,221,642 (GRCm38) |
missense |
probably benign |
0.41 |
IGL02449:Naip5
|
APN |
13 |
100,222,175 (GRCm38) |
missense |
probably benign |
0.34 |
IGL02815:Naip5
|
APN |
13 |
100,222,731 (GRCm38) |
missense |
probably benign |
|
IGL02992:Naip5
|
APN |
13 |
100,223,028 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL03027:Naip5
|
APN |
13 |
100,223,016 (GRCm38) |
missense |
probably benign |
0.00 |
IGL03234:Naip5
|
APN |
13 |
100,212,627 (GRCm38) |
missense |
probably damaging |
1.00 |
inwood2
|
UTSW |
13 |
100,223,014 (GRCm38) |
nonsense |
probably null |
|
inwood3
|
UTSW |
13 |
100,221,903 (GRCm38) |
nonsense |
probably null |
|
Nuchal
|
UTSW |
13 |
100,214,663 (GRCm38) |
missense |
possibly damaging |
0.82 |
PIT4131001:Naip5
|
UTSW |
13 |
100,219,760 (GRCm38) |
missense |
probably benign |
0.00 |
PIT4131001:Naip5
|
UTSW |
13 |
100,219,739 (GRCm38) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,223,114 (GRCm38) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,214,650 (GRCm38) |
critical splice donor site |
probably null |
|
R0462:Naip5
|
UTSW |
13 |
100,221,732 (GRCm38) |
missense |
probably damaging |
1.00 |
R0636:Naip5
|
UTSW |
13 |
100,219,688 (GRCm38) |
missense |
probably benign |
|
R0674:Naip5
|
UTSW |
13 |
100,223,199 (GRCm38) |
missense |
probably benign |
0.04 |
R0764:Naip5
|
UTSW |
13 |
100,217,105 (GRCm38) |
missense |
probably benign |
0.03 |
R0837:Naip5
|
UTSW |
13 |
100,230,743 (GRCm38) |
missense |
probably benign |
|
R1179:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R1302:Naip5
|
UTSW |
13 |
100,221,591 (GRCm38) |
missense |
possibly damaging |
0.91 |
R1441:Naip5
|
UTSW |
13 |
100,219,717 (GRCm38) |
missense |
possibly damaging |
0.95 |
R1513:Naip5
|
UTSW |
13 |
100,222,206 (GRCm38) |
missense |
probably benign |
|
R1638:Naip5
|
UTSW |
13 |
100,212,669 (GRCm38) |
missense |
probably damaging |
1.00 |
R1651:Naip5
|
UTSW |
13 |
100,221,911 (GRCm38) |
missense |
probably benign |
0.41 |
R1707:Naip5
|
UTSW |
13 |
100,242,855 (GRCm38) |
missense |
probably damaging |
1.00 |
R1835:Naip5
|
UTSW |
13 |
100,223,218 (GRCm38) |
nonsense |
probably null |
|
R1836:Naip5
|
UTSW |
13 |
100,219,687 (GRCm38) |
missense |
probably benign |
0.18 |
R1972:Naip5
|
UTSW |
13 |
100,212,770 (GRCm38) |
missense |
probably damaging |
0.98 |
R2080:Naip5
|
UTSW |
13 |
100,221,533 (GRCm38) |
missense |
probably damaging |
1.00 |
R2333:Naip5
|
UTSW |
13 |
100,223,171 (GRCm38) |
missense |
probably damaging |
1.00 |
R2348:Naip5
|
UTSW |
13 |
100,219,738 (GRCm38) |
missense |
probably benign |
0.01 |
R3055:Naip5
|
UTSW |
13 |
100,221,878 (GRCm38) |
missense |
probably benign |
0.23 |
R3401:Naip5
|
UTSW |
13 |
100,221,903 (GRCm38) |
nonsense |
probably null |
|
R3723:Naip5
|
UTSW |
13 |
100,223,014 (GRCm38) |
nonsense |
probably null |
|
R3775:Naip5
|
UTSW |
13 |
100,223,394 (GRCm38) |
missense |
probably benign |
0.00 |
R3775:Naip5
|
UTSW |
13 |
100,223,375 (GRCm38) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,223,375 (GRCm38) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,223,394 (GRCm38) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,223,394 (GRCm38) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,223,375 (GRCm38) |
missense |
probably benign |
0.00 |
R4074:Naip5
|
UTSW |
13 |
100,246,064 (GRCm38) |
missense |
probably damaging |
1.00 |
R4082:Naip5
|
UTSW |
13 |
100,245,830 (GRCm38) |
missense |
probably damaging |
1.00 |
R4105:Naip5
|
UTSW |
13 |
100,219,739 (GRCm38) |
missense |
probably benign |
|
R4227:Naip5
|
UTSW |
13 |
100,212,768 (GRCm38) |
missense |
probably damaging |
0.99 |
R4639:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4640:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4641:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4644:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4645:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R4700:Naip5
|
UTSW |
13 |
100,223,414 (GRCm38) |
missense |
possibly damaging |
0.62 |
R4727:Naip5
|
UTSW |
13 |
100,221,870 (GRCm38) |
missense |
possibly damaging |
0.81 |
R4729:Naip5
|
UTSW |
13 |
100,222,131 (GRCm38) |
missense |
possibly damaging |
0.75 |
R4816:Naip5
|
UTSW |
13 |
100,219,681 (GRCm38) |
missense |
probably benign |
0.32 |
R4816:Naip5
|
UTSW |
13 |
100,219,687 (GRCm38) |
missense |
probably benign |
0.01 |
R4816:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R4869:Naip5
|
UTSW |
13 |
100,245,131 (GRCm38) |
missense |
probably damaging |
1.00 |
R5162:Naip5
|
UTSW |
13 |
100,223,406 (GRCm38) |
missense |
possibly damaging |
0.78 |
R5244:Naip5
|
UTSW |
13 |
100,245,662 (GRCm38) |
missense |
probably benign |
0.08 |
R5411:Naip5
|
UTSW |
13 |
100,245,746 (GRCm38) |
missense |
possibly damaging |
0.54 |
R5632:Naip5
|
UTSW |
13 |
100,230,662 (GRCm38) |
splice site |
probably null |
|
R5760:Naip5
|
UTSW |
13 |
100,242,838 (GRCm38) |
missense |
probably damaging |
1.00 |
R5916:Naip5
|
UTSW |
13 |
100,222,701 (GRCm38) |
missense |
probably benign |
0.02 |
R6302:Naip5
|
UTSW |
13 |
100,223,166 (GRCm38) |
missense |
possibly damaging |
0.76 |
R6304:Naip5
|
UTSW |
13 |
100,223,166 (GRCm38) |
missense |
possibly damaging |
0.76 |
R6411:Naip5
|
UTSW |
13 |
100,223,405 (GRCm38) |
missense |
probably benign |
0.01 |
R6474:Naip5
|
UTSW |
13 |
100,214,663 (GRCm38) |
missense |
possibly damaging |
0.82 |
R6499:Naip5
|
UTSW |
13 |
100,221,594 (GRCm38) |
missense |
probably benign |
|
R6544:Naip5
|
UTSW |
13 |
100,223,144 (GRCm38) |
missense |
possibly damaging |
0.50 |
R6827:Naip5
|
UTSW |
13 |
100,245,929 (GRCm38) |
missense |
possibly damaging |
0.48 |
R6954:Naip5
|
UTSW |
13 |
100,223,414 (GRCm38) |
missense |
probably damaging |
0.99 |
R7052:Naip5
|
UTSW |
13 |
100,222,347 (GRCm38) |
missense |
probably benign |
0.01 |
R7138:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R7141:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R7375:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7375:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7401:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7401:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7447:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7447:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7466:Naip5
|
UTSW |
13 |
100,221,986 (GRCm38) |
nonsense |
probably null |
|
R7491:Naip5
|
UTSW |
13 |
100,217,071 (GRCm38) |
missense |
probably benign |
0.18 |
R7559:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7559:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7562:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7562:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7588:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7588:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7589:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7589:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7590:Naip5
|
UTSW |
13 |
100,219,696 (GRCm38) |
missense |
probably benign |
0.00 |
R7590:Naip5
|
UTSW |
13 |
100,219,697 (GRCm38) |
missense |
not run |
|
R7742:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R7886:Naip5
|
UTSW |
13 |
100,246,181 (GRCm38) |
missense |
probably benign |
0.28 |
R7996:Naip5
|
UTSW |
13 |
100,221,656 (GRCm38) |
missense |
probably damaging |
1.00 |
R8026:Naip5
|
UTSW |
13 |
100,245,898 (GRCm38) |
missense |
probably damaging |
1.00 |
R8046:Naip5
|
UTSW |
13 |
100,222,233 (GRCm38) |
missense |
probably benign |
|
R8319:Naip5
|
UTSW |
13 |
100,221,659 (GRCm38) |
missense |
probably benign |
0.12 |
R8471:Naip5
|
UTSW |
13 |
100,221,645 (GRCm38) |
missense |
probably damaging |
0.99 |
R8480:Naip5
|
UTSW |
13 |
100,222,235 (GRCm38) |
missense |
probably damaging |
1.00 |
R8496:Naip5
|
UTSW |
13 |
100,212,739 (GRCm38) |
missense |
probably benign |
0.00 |
R8500:Naip5
|
UTSW |
13 |
100,222,712 (GRCm38) |
missense |
probably damaging |
0.98 |
R8712:Naip5
|
UTSW |
13 |
100,223,096 (GRCm38) |
missense |
possibly damaging |
0.61 |
R8780:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R8781:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R8788:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R8817:Naip5
|
UTSW |
13 |
100,212,699 (GRCm38) |
missense |
probably benign |
0.01 |
R8833:Naip5
|
UTSW |
13 |
100,222,934 (GRCm38) |
missense |
probably damaging |
0.97 |
R8835:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R8958:Naip5
|
UTSW |
13 |
100,217,609 (GRCm38) |
nonsense |
probably null |
|
R9031:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9032:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9074:Naip5
|
UTSW |
13 |
100,221,756 (GRCm38) |
missense |
possibly damaging |
0.92 |
R9098:Naip5
|
UTSW |
13 |
100,229,619 (GRCm38) |
missense |
possibly damaging |
0.67 |
R9204:Naip5
|
UTSW |
13 |
100,222,500 (GRCm38) |
missense |
probably damaging |
1.00 |
R9358:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9389:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9403:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9518:Naip5
|
UTSW |
13 |
100,221,859 (GRCm38) |
missense |
probably benign |
|
R9568:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
R9568:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9569:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
R9569:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9570:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
R9572:Naip5
|
UTSW |
13 |
100,223,313 (GRCm38) |
missense |
probably benign |
0.00 |
R9581:Naip5
|
UTSW |
13 |
100,214,686 (GRCm38) |
missense |
probably benign |
0.11 |
R9627:Naip5
|
UTSW |
13 |
100,219,830 (GRCm38) |
missense |
probably benign |
|
R9725:Naip5
|
UTSW |
13 |
100,222,276 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9763:Naip5
|
UTSW |
13 |
100,230,761 (GRCm38) |
missense |
probably damaging |
0.99 |
R9764:Naip5
|
UTSW |
13 |
100,230,761 (GRCm38) |
missense |
probably damaging |
0.99 |
R9765:Naip5
|
UTSW |
13 |
100,230,761 (GRCm38) |
missense |
probably damaging |
0.99 |
|