Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2210010C04Rik |
C |
T |
6: 41,033,145 (GRCm38) |
G85D |
probably benign |
Het |
4931440F15Rik |
A |
G |
11: 29,825,107 (GRCm38) |
S117P |
probably damaging |
Het |
Abcb1b |
G |
A |
5: 8,825,614 (GRCm38) |
V596I |
probably benign |
Het |
Agtpbp1 |
A |
T |
13: 59,466,070 (GRCm38) |
M1019K |
probably damaging |
Het |
Arfgef3 |
A |
G |
10: 18,603,523 (GRCm38) |
V1448A |
probably damaging |
Het |
Baz1a |
T |
A |
12: 54,916,823 (GRCm38) |
E828D |
probably damaging |
Het |
Ces1f |
A |
T |
8: 93,269,972 (GRCm38) |
|
probably null |
Het |
Cfap53 |
T |
A |
18: 74,299,343 (GRCm38) |
|
probably null |
Het |
Col6a4 |
T |
C |
9: 106,000,784 (GRCm38) |
Y1998C |
probably damaging |
Het |
Col9a2 |
A |
G |
4: 121,054,751 (GRCm38) |
T675A |
probably benign |
Het |
Dusp6 |
G |
A |
10: 99,263,977 (GRCm38) |
V96M |
possibly damaging |
Het |
Elmo1 |
T |
G |
13: 20,185,491 (GRCm38) |
M22R |
probably benign |
Het |
Gm19965 |
A |
G |
1: 116,821,836 (GRCm38) |
N416D |
|
Het |
Gpr162 |
A |
G |
6: 124,861,394 (GRCm38) |
Y98H |
probably damaging |
Het |
Igfals |
G |
A |
17: 24,881,626 (GRCm38) |
V564I |
probably benign |
Het |
Il4 |
C |
T |
11: 53,614,010 (GRCm38) |
R76H |
probably damaging |
Het |
Itgb1 |
T |
A |
8: 128,707,156 (GRCm38) |
N50K |
probably benign |
Het |
Itpr3 |
A |
T |
17: 27,095,925 (GRCm38) |
Y682F |
possibly damaging |
Het |
Jak3 |
C |
T |
8: 71,684,052 (GRCm38) |
P668S |
probably damaging |
Het |
Malrd1 |
A |
T |
2: 15,703,156 (GRCm38) |
N932I |
unknown |
Het |
Mast4 |
C |
A |
13: 103,333,930 (GRCm38) |
R88L |
probably benign |
Het |
Mfsd11 |
T |
G |
11: 116,873,335 (GRCm38) |
S381A |
probably benign |
Het |
Mrm3 |
A |
G |
11: 76,250,030 (GRCm38) |
D288G |
probably damaging |
Het |
Myg1 |
G |
T |
15: 102,336,937 (GRCm38) |
V198F |
probably damaging |
Het |
Npy6r |
T |
C |
18: 44,275,692 (GRCm38) |
I60T |
probably damaging |
Het |
Olfr1109 |
A |
T |
2: 87,093,046 (GRCm38) |
M117K |
possibly damaging |
Het |
Olfr1308 |
G |
T |
2: 111,960,527 (GRCm38) |
P182H |
probably damaging |
Het |
Olfr1341 |
A |
T |
4: 118,710,156 (GRCm38) |
M250L |
probably benign |
Het |
Olfr177 |
C |
T |
16: 58,872,613 (GRCm38) |
C179Y |
probably damaging |
Het |
Olfr530 |
T |
C |
7: 140,373,017 (GRCm38) |
T198A |
probably benign |
Het |
Olfr811 |
G |
A |
10: 129,801,671 (GRCm38) |
P285S |
probably damaging |
Het |
Ovgp1 |
CCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCATCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCACCACTGGCATTTCTAAGACCACCACTGGGGTTTCTAAGATCACCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCA |
CCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCACCACTGGCATTTCTAAGACCACCACTGGGGTTTCTAAGATCACCACTGGTGTTTCTAAGACCACCACTGGCATTTCTAAGACCA |
3: 105,986,525 (GRCm38) |
|
probably benign |
Het |
Oxtr |
C |
A |
6: 112,489,349 (GRCm38) |
R150L |
probably damaging |
Het |
Pappa |
A |
T |
4: 65,180,888 (GRCm38) |
Y548F |
probably damaging |
Het |
Pip4k2a |
T |
C |
2: 18,908,079 (GRCm38) |
K73R |
probably damaging |
Het |
Pla2g4f |
T |
A |
2: 120,302,300 (GRCm38) |
D685V |
probably damaging |
Het |
Ppp1r35 |
T |
A |
5: 137,779,315 (GRCm38) |
L81Q |
probably damaging |
Het |
Ptprf |
C |
A |
4: 118,236,039 (GRCm38) |
A469S |
probably benign |
Het |
Ranbp3l |
T |
A |
15: 9,057,223 (GRCm38) |
N322K |
probably damaging |
Het |
Rev3l |
T |
A |
10: 39,822,971 (GRCm38) |
Y1155N |
possibly damaging |
Het |
Rfesd |
T |
C |
13: 76,003,012 (GRCm38) |
Y96C |
probably damaging |
Het |
Runx1 |
C |
T |
16: 92,613,680 (GRCm38) |
V283I |
possibly damaging |
Het |
Sema5b |
A |
C |
16: 35,645,722 (GRCm38) |
Q125P |
probably damaging |
Het |
Spef2 |
A |
T |
15: 9,725,221 (GRCm38) |
M150K |
probably damaging |
Het |
Srcap |
T |
G |
7: 127,542,283 (GRCm38) |
L1745W |
probably damaging |
Het |
Srgap2 |
A |
G |
1: 131,355,627 (GRCm38) |
Y239H |
probably damaging |
Het |
Svil |
T |
A |
18: 5,090,811 (GRCm38) |
H1304Q |
possibly damaging |
Het |
Syne1 |
T |
C |
10: 5,229,193 (GRCm38) |
D4427G |
possibly damaging |
Het |
Tg |
T |
A |
15: 66,689,324 (GRCm38) |
M1065K |
probably benign |
Het |
Tgm2 |
T |
C |
2: 158,117,896 (GRCm38) |
T656A |
probably benign |
Het |
Ttc37 |
A |
G |
13: 76,127,039 (GRCm38) |
D403G |
probably benign |
Het |
Ubr4 |
A |
G |
4: 139,425,924 (GRCm38) |
K809E |
|
Het |
Vmn1r88 |
T |
C |
7: 13,178,619 (GRCm38) |
S301P |
probably damaging |
Het |
Wdr27 |
A |
G |
17: 14,891,718 (GRCm38) |
V671A |
possibly damaging |
Het |
Zbtb17 |
G |
A |
4: 141,465,820 (GRCm38) |
V550I |
possibly damaging |
Het |
Zeb2 |
A |
T |
2: 44,997,908 (GRCm38) |
I379N |
probably damaging |
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 |
R9223:Naip5
|
UTSW |
13 |
100,227,676 (GRCm38) |
missense |
probably benign |
0.05 |
R9358: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 |
|