Other mutations in this stock |
Total: 60 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
A |
G |
5: 8,968,671 (GRCm39) |
I337V |
probably benign |
Het |
Abl2 |
A |
G |
1: 156,450,184 (GRCm39) |
D117G |
probably damaging |
Het |
Arhgap5 |
T |
A |
12: 52,563,365 (GRCm39) |
L112* |
probably null |
Het |
Brinp3 |
C |
G |
1: 146,777,748 (GRCm39) |
L732V |
possibly damaging |
Het |
Ccdc168 |
A |
T |
1: 44,099,694 (GRCm39) |
I468N |
possibly damaging |
Het |
Cfap91 |
T |
A |
16: 38,155,980 (GRCm39) |
H81L |
probably damaging |
Het |
Cmya5 |
T |
G |
13: 93,228,169 (GRCm39) |
K2306N |
probably damaging |
Het |
Col16a1 |
A |
C |
4: 129,959,294 (GRCm39) |
K680T |
unknown |
Het |
Col28a1 |
T |
A |
6: 7,998,499 (GRCm39) |
T1137S |
possibly damaging |
Het |
Crnn |
A |
T |
3: 93,056,452 (GRCm39) |
T413S |
possibly damaging |
Het |
Csf1 |
A |
G |
3: 107,655,495 (GRCm39) |
L512P |
possibly damaging |
Het |
Dlx3 |
C |
A |
11: 95,011,461 (GRCm39) |
A105D |
possibly damaging |
Het |
Dnah3 |
T |
G |
7: 119,550,900 (GRCm39) |
T161P |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,342,794 (GRCm39) |
D3435G |
probably damaging |
Het |
Dpp10 |
A |
G |
1: 123,295,524 (GRCm39) |
I541T |
probably benign |
Het |
Efcc1 |
T |
C |
6: 87,728,838 (GRCm39) |
V431A |
possibly damaging |
Het |
Enpp5 |
T |
C |
17: 44,391,868 (GRCm39) |
I99T |
probably benign |
Het |
Gm11232 |
C |
T |
4: 71,675,583 (GRCm39) |
W59* |
probably null |
Het |
Gxylt2 |
A |
T |
6: 100,727,383 (GRCm39) |
T166S |
probably benign |
Het |
Herc6 |
A |
T |
6: 57,628,791 (GRCm39) |
|
probably null |
Het |
Itga2 |
T |
C |
13: 115,005,753 (GRCm39) |
I476V |
probably benign |
Het |
Kcnq5 |
T |
C |
1: 21,539,710 (GRCm39) |
T403A |
possibly damaging |
Het |
Klhl42 |
A |
G |
6: 146,993,538 (GRCm39) |
K170R |
probably benign |
Het |
Klk13 |
T |
C |
7: 43,370,582 (GRCm39) |
|
probably null |
Het |
Krt32 |
G |
T |
11: 99,972,050 (GRCm39) |
R433S |
probably benign |
Het |
Lrp1 |
G |
T |
10: 127,375,217 (GRCm39) |
T4461N |
probably damaging |
Het |
Mapk10 |
A |
T |
5: 103,124,256 (GRCm39) |
M256K |
probably null |
Het |
Mogat2 |
T |
C |
7: 98,872,905 (GRCm39) |
K93R |
probably damaging |
Het |
Myh1 |
G |
T |
11: 67,101,254 (GRCm39) |
V677L |
probably damaging |
Het |
Oog4 |
G |
A |
4: 143,165,544 (GRCm39) |
T201M |
possibly damaging |
Het |
Or4a70 |
C |
T |
2: 89,324,036 (GRCm39) |
G207R |
possibly damaging |
Het |
Pik3c2a |
T |
C |
7: 115,975,621 (GRCm39) |
T649A |
probably damaging |
Het |
Plec |
T |
A |
15: 76,061,555 (GRCm39) |
H2794L |
possibly damaging |
Het |
Pros1 |
T |
A |
16: 62,744,913 (GRCm39) |
N509K |
probably damaging |
Het |
Psme3ip1 |
G |
A |
8: 95,309,636 (GRCm39) |
L119F |
probably benign |
Het |
Psme4 |
T |
A |
11: 30,722,700 (GRCm39) |
|
probably null |
Het |
Ptprf |
A |
G |
4: 118,070,011 (GRCm39) |
V1457A |
probably benign |
Het |
Rad50 |
A |
G |
11: 53,543,055 (GRCm39) |
|
probably null |
Het |
Rfx5 |
C |
T |
3: 94,866,053 (GRCm39) |
P451S |
unknown |
Het |
Scpppq1 |
G |
T |
5: 104,219,123 (GRCm39) |
|
probably null |
Het |
Sdk1 |
G |
T |
5: 141,984,598 (GRCm39) |
V728L |
probably benign |
Het |
Sfxn4 |
T |
C |
19: 60,847,112 (GRCm39) |
D57G |
probably benign |
Het |
Slc10a4 |
A |
G |
5: 73,169,650 (GRCm39) |
D425G |
probably benign |
Het |
Slc17a5 |
C |
T |
9: 78,495,174 (GRCm39) |
A26T |
probably benign |
Het |
Slc22a26 |
A |
T |
19: 7,760,509 (GRCm39) |
|
probably null |
Het |
Slc22a30 |
A |
G |
19: 8,382,055 (GRCm39) |
L72P |
probably damaging |
Het |
Slco6c1 |
T |
C |
1: 97,009,146 (GRCm39) |
T447A |
possibly damaging |
Het |
Slco6d1 |
A |
G |
1: 98,349,172 (GRCm39) |
N81S |
probably damaging |
Het |
Stard9 |
T |
C |
2: 120,495,483 (GRCm39) |
|
probably null |
Het |
Tecpr1 |
T |
C |
5: 144,145,417 (GRCm39) |
E610G |
possibly damaging |
Het |
Tmem81 |
G |
T |
1: 132,435,301 (GRCm39) |
V36L |
possibly damaging |
Het |
Trabd2b |
G |
T |
4: 114,467,194 (GRCm39) |
K474N |
probably benign |
Het |
Tspan33 |
T |
C |
6: 29,713,519 (GRCm39) |
F149L |
probably benign |
Het |
Ttn |
A |
G |
2: 76,606,683 (GRCm39) |
Y18076H |
probably damaging |
Het |
Utrn |
G |
A |
10: 12,516,764 (GRCm39) |
R2277C |
probably damaging |
Het |
Vmn2r101 |
T |
A |
17: 19,831,652 (GRCm39) |
D549E |
probably damaging |
Het |
Vmn2r107 |
T |
A |
17: 20,576,138 (GRCm39) |
I156K |
probably benign |
Het |
Wwc2 |
T |
G |
8: 48,316,955 (GRCm39) |
S713R |
unknown |
Het |
Xndc1 |
C |
A |
7: 101,730,687 (GRCm39) |
|
probably null |
Het |
Zfp810 |
A |
G |
9: 22,201,833 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Naip5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00096:Naip5
|
APN |
13 |
100,382,683 (GRCm39) |
nonsense |
probably null |
|
IGL00493:Naip5
|
APN |
13 |
100,367,279 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01294:Naip5
|
APN |
13 |
100,353,588 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01405:Naip5
|
APN |
13 |
100,358,453 (GRCm39) |
missense |
probably benign |
0.11 |
IGL01568:Naip5
|
APN |
13 |
100,353,609 (GRCm39) |
missense |
probably benign |
0.26 |
IGL01804:Naip5
|
APN |
13 |
100,358,092 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02012:Naip5
|
APN |
13 |
100,359,847 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02183:Naip5
|
APN |
13 |
100,358,150 (GRCm39) |
missense |
probably benign |
0.41 |
IGL02449:Naip5
|
APN |
13 |
100,358,683 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02815:Naip5
|
APN |
13 |
100,359,239 (GRCm39) |
missense |
probably benign |
|
IGL02992:Naip5
|
APN |
13 |
100,359,536 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03027:Naip5
|
APN |
13 |
100,359,524 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03234:Naip5
|
APN |
13 |
100,349,135 (GRCm39) |
missense |
probably damaging |
1.00 |
inwood2
|
UTSW |
13 |
100,359,522 (GRCm39) |
nonsense |
probably null |
|
inwood3
|
UTSW |
13 |
100,358,411 (GRCm39) |
nonsense |
probably null |
|
Nuchal
|
UTSW |
13 |
100,351,171 (GRCm39) |
missense |
possibly damaging |
0.82 |
PIT4131001:Naip5
|
UTSW |
13 |
100,356,268 (GRCm39) |
missense |
probably benign |
0.00 |
PIT4131001:Naip5
|
UTSW |
13 |
100,356,247 (GRCm39) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,359,622 (GRCm39) |
missense |
probably benign |
|
R0001:Naip5
|
UTSW |
13 |
100,351,158 (GRCm39) |
critical splice donor site |
probably null |
|
R0462:Naip5
|
UTSW |
13 |
100,358,240 (GRCm39) |
missense |
probably damaging |
1.00 |
R0636:Naip5
|
UTSW |
13 |
100,356,196 (GRCm39) |
missense |
probably benign |
|
R0674:Naip5
|
UTSW |
13 |
100,359,707 (GRCm39) |
missense |
probably benign |
0.04 |
R0764:Naip5
|
UTSW |
13 |
100,353,613 (GRCm39) |
missense |
probably benign |
0.03 |
R0837:Naip5
|
UTSW |
13 |
100,367,251 (GRCm39) |
missense |
probably benign |
|
R1179:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R1302:Naip5
|
UTSW |
13 |
100,358,099 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1441:Naip5
|
UTSW |
13 |
100,356,225 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1513:Naip5
|
UTSW |
13 |
100,358,714 (GRCm39) |
missense |
probably benign |
|
R1638:Naip5
|
UTSW |
13 |
100,349,177 (GRCm39) |
missense |
probably damaging |
1.00 |
R1651:Naip5
|
UTSW |
13 |
100,358,419 (GRCm39) |
missense |
probably benign |
0.41 |
R1707:Naip5
|
UTSW |
13 |
100,379,363 (GRCm39) |
missense |
probably damaging |
1.00 |
R1835:Naip5
|
UTSW |
13 |
100,359,726 (GRCm39) |
nonsense |
probably null |
|
R1836:Naip5
|
UTSW |
13 |
100,356,195 (GRCm39) |
missense |
probably benign |
0.18 |
R1972:Naip5
|
UTSW |
13 |
100,349,278 (GRCm39) |
missense |
probably damaging |
0.98 |
R2080:Naip5
|
UTSW |
13 |
100,358,041 (GRCm39) |
missense |
probably damaging |
1.00 |
R2333:Naip5
|
UTSW |
13 |
100,359,679 (GRCm39) |
missense |
probably damaging |
1.00 |
R2348:Naip5
|
UTSW |
13 |
100,356,246 (GRCm39) |
missense |
probably benign |
0.01 |
R3055:Naip5
|
UTSW |
13 |
100,358,386 (GRCm39) |
missense |
probably benign |
0.23 |
R3401:Naip5
|
UTSW |
13 |
100,358,411 (GRCm39) |
nonsense |
probably null |
|
R3723:Naip5
|
UTSW |
13 |
100,359,522 (GRCm39) |
nonsense |
probably null |
|
R3775:Naip5
|
UTSW |
13 |
100,359,902 (GRCm39) |
missense |
probably benign |
0.00 |
R3775:Naip5
|
UTSW |
13 |
100,359,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,359,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4019:Naip5
|
UTSW |
13 |
100,359,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,359,902 (GRCm39) |
missense |
probably benign |
0.00 |
R4020:Naip5
|
UTSW |
13 |
100,359,883 (GRCm39) |
missense |
probably benign |
0.00 |
R4074:Naip5
|
UTSW |
13 |
100,382,572 (GRCm39) |
missense |
probably damaging |
1.00 |
R4082:Naip5
|
UTSW |
13 |
100,382,338 (GRCm39) |
missense |
probably damaging |
1.00 |
R4105:Naip5
|
UTSW |
13 |
100,356,247 (GRCm39) |
missense |
probably benign |
|
R4227:Naip5
|
UTSW |
13 |
100,349,276 (GRCm39) |
missense |
probably damaging |
0.99 |
R4639:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4640:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4641:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4644:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4645:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R4700:Naip5
|
UTSW |
13 |
100,359,922 (GRCm39) |
missense |
possibly damaging |
0.62 |
R4727:Naip5
|
UTSW |
13 |
100,358,378 (GRCm39) |
missense |
possibly damaging |
0.81 |
R4729:Naip5
|
UTSW |
13 |
100,358,639 (GRCm39) |
missense |
possibly damaging |
0.75 |
R4816:Naip5
|
UTSW |
13 |
100,356,189 (GRCm39) |
missense |
probably benign |
0.32 |
R4816:Naip5
|
UTSW |
13 |
100,356,195 (GRCm39) |
missense |
probably benign |
0.01 |
R4816:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R4869:Naip5
|
UTSW |
13 |
100,381,639 (GRCm39) |
missense |
probably damaging |
1.00 |
R5162:Naip5
|
UTSW |
13 |
100,359,914 (GRCm39) |
missense |
possibly damaging |
0.78 |
R5244:Naip5
|
UTSW |
13 |
100,382,170 (GRCm39) |
missense |
probably benign |
0.08 |
R5411:Naip5
|
UTSW |
13 |
100,382,254 (GRCm39) |
missense |
possibly damaging |
0.54 |
R5632:Naip5
|
UTSW |
13 |
100,367,170 (GRCm39) |
splice site |
probably null |
|
R5760:Naip5
|
UTSW |
13 |
100,379,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R5916:Naip5
|
UTSW |
13 |
100,359,209 (GRCm39) |
missense |
probably benign |
0.02 |
R6302:Naip5
|
UTSW |
13 |
100,359,674 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6304:Naip5
|
UTSW |
13 |
100,359,674 (GRCm39) |
missense |
possibly damaging |
0.76 |
R6411:Naip5
|
UTSW |
13 |
100,359,913 (GRCm39) |
missense |
probably benign |
0.01 |
R6474:Naip5
|
UTSW |
13 |
100,351,171 (GRCm39) |
missense |
possibly damaging |
0.82 |
R6499:Naip5
|
UTSW |
13 |
100,358,102 (GRCm39) |
missense |
probably benign |
|
R6544:Naip5
|
UTSW |
13 |
100,359,652 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6827:Naip5
|
UTSW |
13 |
100,382,437 (GRCm39) |
missense |
possibly damaging |
0.48 |
R6954:Naip5
|
UTSW |
13 |
100,359,922 (GRCm39) |
missense |
probably damaging |
0.99 |
R7052:Naip5
|
UTSW |
13 |
100,358,855 (GRCm39) |
missense |
probably benign |
0.01 |
R7138:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R7141:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R7375:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7401:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7401:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7447:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7447:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7466:Naip5
|
UTSW |
13 |
100,358,494 (GRCm39) |
nonsense |
probably null |
|
R7491:Naip5
|
UTSW |
13 |
100,353,579 (GRCm39) |
missense |
probably benign |
0.18 |
R7559:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7559:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7562:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7562:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7588:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7588:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7589:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7589:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7590:Naip5
|
UTSW |
13 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
R7590:Naip5
|
UTSW |
13 |
100,356,205 (GRCm39) |
missense |
not run |
|
R7742:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R7886:Naip5
|
UTSW |
13 |
100,382,689 (GRCm39) |
missense |
probably benign |
0.28 |
R7996:Naip5
|
UTSW |
13 |
100,358,164 (GRCm39) |
missense |
probably damaging |
1.00 |
R8026:Naip5
|
UTSW |
13 |
100,382,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R8046:Naip5
|
UTSW |
13 |
100,358,741 (GRCm39) |
missense |
probably benign |
|
R8319:Naip5
|
UTSW |
13 |
100,358,167 (GRCm39) |
missense |
probably benign |
0.12 |
R8471:Naip5
|
UTSW |
13 |
100,358,153 (GRCm39) |
missense |
probably damaging |
0.99 |
R8480:Naip5
|
UTSW |
13 |
100,358,743 (GRCm39) |
missense |
probably damaging |
1.00 |
R8496:Naip5
|
UTSW |
13 |
100,349,247 (GRCm39) |
missense |
probably benign |
0.00 |
R8500:Naip5
|
UTSW |
13 |
100,359,220 (GRCm39) |
missense |
probably damaging |
0.98 |
R8712:Naip5
|
UTSW |
13 |
100,359,604 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8780:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8781:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8788:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8817:Naip5
|
UTSW |
13 |
100,349,207 (GRCm39) |
missense |
probably benign |
0.01 |
R8833:Naip5
|
UTSW |
13 |
100,359,442 (GRCm39) |
missense |
probably damaging |
0.97 |
R8835:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R8958:Naip5
|
UTSW |
13 |
100,354,117 (GRCm39) |
nonsense |
probably null |
|
R9031:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9032:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9074:Naip5
|
UTSW |
13 |
100,358,264 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9098:Naip5
|
UTSW |
13 |
100,366,127 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9204:Naip5
|
UTSW |
13 |
100,359,008 (GRCm39) |
missense |
probably damaging |
1.00 |
R9223:Naip5
|
UTSW |
13 |
100,364,184 (GRCm39) |
missense |
probably benign |
0.05 |
R9358:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9389:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9403:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9518:Naip5
|
UTSW |
13 |
100,358,367 (GRCm39) |
missense |
probably benign |
|
R9568:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9568:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9569:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9569:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9570:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9572:Naip5
|
UTSW |
13 |
100,359,821 (GRCm39) |
missense |
probably benign |
0.00 |
R9581:Naip5
|
UTSW |
13 |
100,351,194 (GRCm39) |
missense |
probably benign |
0.11 |
R9627:Naip5
|
UTSW |
13 |
100,356,338 (GRCm39) |
missense |
probably benign |
|
R9725:Naip5
|
UTSW |
13 |
100,358,784 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9763:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R9764:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
R9765:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
|