Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1b |
G |
A |
5: 8,875,614 (GRCm39) |
V596I |
probably benign |
Het |
Agtpbp1 |
A |
T |
13: 59,613,884 (GRCm39) |
M1019K |
probably damaging |
Het |
Arfgef3 |
A |
G |
10: 18,479,271 (GRCm39) |
V1448A |
probably damaging |
Het |
Baz1a |
T |
A |
12: 54,963,608 (GRCm39) |
E828D |
probably damaging |
Het |
Ces1f |
A |
T |
8: 93,996,600 (GRCm39) |
|
probably null |
Het |
Cfap53 |
T |
A |
18: 74,432,414 (GRCm39) |
|
probably null |
Het |
Col6a4 |
T |
C |
9: 105,877,983 (GRCm39) |
Y1998C |
probably damaging |
Het |
Col9a2 |
A |
G |
4: 120,911,948 (GRCm39) |
T675A |
probably benign |
Het |
Dusp6 |
G |
A |
10: 99,099,839 (GRCm39) |
V96M |
possibly damaging |
Het |
Elmo1 |
T |
G |
13: 20,369,661 (GRCm39) |
M22R |
probably benign |
Het |
Fem1al |
A |
G |
11: 29,775,107 (GRCm39) |
S117P |
probably damaging |
Het |
Gm19965 |
A |
G |
1: 116,749,566 (GRCm39) |
N416D |
|
Het |
Gpr162 |
A |
G |
6: 124,838,357 (GRCm39) |
Y98H |
probably damaging |
Het |
Igfals |
G |
A |
17: 25,100,600 (GRCm39) |
V564I |
probably benign |
Het |
Il4 |
C |
T |
11: 53,504,837 (GRCm39) |
R76H |
probably damaging |
Het |
Itgb1 |
T |
A |
8: 129,433,637 (GRCm39) |
N50K |
probably benign |
Het |
Itpr3 |
A |
T |
17: 27,314,899 (GRCm39) |
Y682F |
possibly damaging |
Het |
Jak3 |
C |
T |
8: 72,136,696 (GRCm39) |
P668S |
probably damaging |
Het |
Malrd1 |
A |
T |
2: 15,707,967 (GRCm39) |
N932I |
unknown |
Het |
Mast4 |
C |
A |
13: 103,470,438 (GRCm39) |
R88L |
probably benign |
Het |
Mfsd11 |
T |
G |
11: 116,764,161 (GRCm39) |
S381A |
probably benign |
Het |
Mrm3 |
A |
G |
11: 76,140,856 (GRCm39) |
D288G |
probably damaging |
Het |
Myg1 |
G |
T |
15: 102,245,372 (GRCm39) |
V198F |
probably damaging |
Het |
Npy6r |
T |
C |
18: 44,408,759 (GRCm39) |
I60T |
probably damaging |
Het |
Or12j3 |
T |
C |
7: 139,952,930 (GRCm39) |
T198A |
probably benign |
Het |
Or13p3 |
A |
T |
4: 118,567,353 (GRCm39) |
M250L |
probably benign |
Het |
Or4f57 |
G |
T |
2: 111,790,872 (GRCm39) |
P182H |
probably damaging |
Het |
Or5aq6 |
A |
T |
2: 86,923,390 (GRCm39) |
M117K |
possibly damaging |
Het |
Or5k14 |
C |
T |
16: 58,692,976 (GRCm39) |
C179Y |
probably damaging |
Het |
Or6c215 |
G |
A |
10: 129,637,540 (GRCm39) |
P285S |
probably damaging |
Het |
Ovgp1 |
CCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCATCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCACCACTGGCATTTCTAAGACCACCACTGGGGTTTCTAAGATCACCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCA |
CCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCACCACTGGCATTTCTAAGACCACCACTGGGGTTTCTAAGATCACCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCA |
3: 105,893,841 (GRCm39) |
|
probably benign |
Het |
Oxtr |
C |
A |
6: 112,466,310 (GRCm39) |
R150L |
probably damaging |
Het |
Pappa |
A |
T |
4: 65,099,125 (GRCm39) |
Y548F |
probably damaging |
Het |
Pip4k2a |
T |
C |
2: 18,912,890 (GRCm39) |
K73R |
probably damaging |
Het |
Pla2g4f |
T |
A |
2: 120,132,781 (GRCm39) |
D685V |
probably damaging |
Het |
Ppp1r35 |
T |
A |
5: 137,777,577 (GRCm39) |
L81Q |
probably damaging |
Het |
Prss3b |
C |
T |
6: 41,010,079 (GRCm39) |
G85D |
probably benign |
Het |
Ptprf |
C |
A |
4: 118,093,236 (GRCm39) |
A469S |
probably benign |
Het |
Ranbp3l |
T |
A |
15: 9,057,304 (GRCm39) |
N322K |
probably damaging |
Het |
Rev3l |
T |
A |
10: 39,698,967 (GRCm39) |
Y1155N |
possibly damaging |
Het |
Rfesd |
T |
C |
13: 76,151,131 (GRCm39) |
Y96C |
probably damaging |
Het |
Runx1 |
C |
T |
16: 92,410,568 (GRCm39) |
V283I |
possibly damaging |
Het |
Sema5b |
A |
C |
16: 35,466,092 (GRCm39) |
Q125P |
probably damaging |
Het |
Skic3 |
A |
G |
13: 76,275,158 (GRCm39) |
D403G |
probably benign |
Het |
Spef2 |
A |
T |
15: 9,725,307 (GRCm39) |
M150K |
probably damaging |
Het |
Srcap |
T |
G |
7: 127,141,455 (GRCm39) |
L1745W |
probably damaging |
Het |
Srgap2 |
A |
G |
1: 131,283,365 (GRCm39) |
Y239H |
probably damaging |
Het |
Svil |
T |
A |
18: 5,090,811 (GRCm39) |
H1304Q |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,179,193 (GRCm39) |
D4427G |
possibly damaging |
Het |
Tg |
T |
A |
15: 66,561,173 (GRCm39) |
M1065K |
probably benign |
Het |
Tgm2 |
T |
C |
2: 157,959,816 (GRCm39) |
T656A |
probably benign |
Het |
Ubr4 |
A |
G |
4: 139,153,235 (GRCm39) |
K809E |
|
Het |
Vmn1r88 |
T |
C |
7: 12,912,546 (GRCm39) |
S301P |
probably damaging |
Het |
Wdr27 |
A |
G |
17: 15,111,980 (GRCm39) |
V671A |
possibly damaging |
Het |
Zbtb17 |
G |
A |
4: 141,193,131 (GRCm39) |
V550I |
possibly damaging |
Het |
Zeb2 |
A |
T |
2: 44,887,920 (GRCm39) |
I379N |
probably damaging |
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 |
|
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 |
|