Other mutations in this stock |
Total: 59 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029F12Rik |
T |
C |
13: 97,166,738 (GRCm39) |
T93A |
unknown |
Het |
Adgrg6 |
T |
A |
10: 14,302,515 (GRCm39) |
H938L |
probably benign |
Het |
Aff1 |
A |
G |
5: 103,997,365 (GRCm39) |
Y1153C |
probably damaging |
Het |
Akr1c20 |
T |
A |
13: 4,564,388 (GRCm39) |
I42L |
probably benign |
Het |
Atad2b |
T |
A |
12: 5,082,064 (GRCm39) |
N1324K |
probably benign |
Het |
Aurka |
T |
A |
2: 172,201,760 (GRCm39) |
I270F |
probably damaging |
Het |
Camk2g |
A |
T |
14: 20,815,498 (GRCm39) |
D189E |
probably damaging |
Het |
Cc2d2b |
A |
G |
19: 40,804,299 (GRCm39) |
D942G |
unknown |
Het |
Ccnd1 |
A |
C |
7: 144,491,770 (GRCm39) |
S90A |
probably benign |
Het |
Cfap77 |
G |
T |
2: 28,852,741 (GRCm39) |
T177K |
probably damaging |
Het |
Chd9 |
A |
G |
8: 91,721,220 (GRCm39) |
N1003D |
unknown |
Het |
Chga |
C |
G |
12: 102,525,613 (GRCm39) |
Q85E |
possibly damaging |
Het |
Cnot1 |
T |
C |
8: 96,496,209 (GRCm39) |
S322G |
probably benign |
Het |
Cyp8b1 |
C |
A |
9: 121,744,294 (GRCm39) |
S346I |
probably benign |
Het |
Cysltr2 |
T |
A |
14: 73,266,906 (GRCm39) |
H268L |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 117,884,704 (GRCm39) |
T3783A |
probably benign |
Het |
Dock3 |
C |
T |
9: 106,959,713 (GRCm39) |
V109I |
probably benign |
Het |
Dscc1 |
A |
G |
15: 54,953,674 (GRCm39) |
C50R |
probably benign |
Het |
Dtx3l |
T |
A |
16: 35,753,277 (GRCm39) |
D443V |
probably damaging |
Het |
Ephb6 |
A |
G |
6: 41,592,911 (GRCm39) |
H383R |
probably benign |
Het |
Fdft1 |
A |
G |
14: 63,400,869 (GRCm39) |
I88T |
probably damaging |
Het |
Fmo3 |
C |
A |
1: 162,794,524 (GRCm39) |
W182L |
probably benign |
Het |
Folh1 |
T |
A |
7: 86,406,158 (GRCm39) |
Q305L |
probably benign |
Het |
Gale |
C |
T |
4: 135,692,975 (GRCm39) |
Q73* |
probably null |
Het |
Gm9195 |
T |
C |
14: 72,699,885 (GRCm39) |
M1154V |
unknown |
Het |
Grip1 |
G |
A |
10: 119,874,569 (GRCm39) |
E778K |
possibly damaging |
Het |
Gtsf1l |
T |
C |
2: 162,929,052 (GRCm39) |
T144A |
probably benign |
Het |
Itpkc |
T |
C |
7: 26,927,222 (GRCm39) |
T231A |
probably benign |
Het |
Kng2 |
C |
A |
16: 22,822,737 (GRCm39) |
C205F |
probably damaging |
Het |
Ldlrap1 |
T |
G |
4: 134,476,661 (GRCm39) |
N244T |
probably benign |
Het |
Lingo2 |
A |
G |
4: 35,709,750 (GRCm39) |
F77L |
possibly damaging |
Het |
Lpcat2b |
A |
T |
5: 107,581,438 (GRCm39) |
T256S |
possibly damaging |
Het |
Lrit2 |
A |
G |
14: 36,790,936 (GRCm39) |
D205G |
probably damaging |
Het |
Lrrc34 |
T |
C |
3: 30,697,467 (GRCm39) |
D88G |
probably damaging |
Het |
Macf1 |
T |
C |
4: 123,366,136 (GRCm39) |
E2875G |
probably benign |
Het |
Med13 |
G |
T |
11: 86,177,345 (GRCm39) |
Q1584K |
possibly damaging |
Het |
Ndufv2 |
A |
G |
17: 66,394,503 (GRCm39) |
Y121H |
probably damaging |
Het |
Or4f52 |
T |
A |
2: 111,061,521 (GRCm39) |
I206F |
probably damaging |
Het |
Peg12 |
T |
C |
7: 62,113,297 (GRCm39) |
T267A |
unknown |
Het |
Pkig |
A |
G |
2: 163,567,375 (GRCm39) |
|
probably null |
Het |
Prkch |
C |
G |
12: 73,747,078 (GRCm39) |
T319S |
probably benign |
Het |
Rhobtb1 |
T |
C |
10: 69,115,202 (GRCm39) |
S534P |
probably damaging |
Het |
Riok2 |
A |
G |
17: 17,607,814 (GRCm39) |
N454S |
probably benign |
Het |
Ryr2 |
T |
A |
13: 11,701,935 (GRCm39) |
K2907N |
possibly damaging |
Het |
Sdc3 |
C |
T |
4: 130,546,048 (GRCm39) |
P136S |
unknown |
Het |
Slc37a3 |
G |
A |
6: 39,322,844 (GRCm39) |
L371F |
probably damaging |
Het |
Slc3a1 |
A |
T |
17: 85,371,419 (GRCm39) |
H657L |
probably damaging |
Het |
Slc7a13 |
T |
A |
4: 19,819,033 (GRCm39) |
Y78N |
probably benign |
Het |
Slfn8 |
G |
T |
11: 82,907,838 (GRCm39) |
A235E |
probably damaging |
Het |
Snap91 |
T |
A |
9: 86,707,094 (GRCm39) |
D232V |
possibly damaging |
Het |
Stap2 |
C |
A |
17: 56,309,914 (GRCm39) |
S79I |
probably damaging |
Het |
Stra6l |
T |
C |
4: 45,884,602 (GRCm39) |
V544A |
probably damaging |
Het |
Syn2 |
T |
C |
6: 115,251,219 (GRCm39) |
|
probably null |
Het |
Tctn1 |
G |
A |
5: 122,388,527 (GRCm39) |
P284S |
possibly damaging |
Het |
Terb2 |
G |
A |
2: 122,018,475 (GRCm39) |
M77I |
probably benign |
Het |
Trim80 |
G |
T |
11: 115,338,757 (GRCm39) |
R529L |
possibly damaging |
Het |
Washc2 |
T |
C |
6: 116,186,048 (GRCm39) |
L86P |
possibly damaging |
Het |
Zfp74 |
A |
T |
7: 29,631,845 (GRCm39) |
F133Y |
probably benign |
Het |
Zfp987 |
T |
A |
4: 146,060,752 (GRCm39) |
N61K |
probably benign |
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 |
100,356,204 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
R9765:Naip5
|
UTSW |
13 |
100,367,269 (GRCm39) |
missense |
probably damaging |
0.99 |
|