Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb1a |
G |
A |
5: 8,752,216 (GRCm39) |
G426S |
probably damaging |
Het |
Casp4 |
A |
T |
9: 5,328,573 (GRCm39) |
|
probably benign |
Het |
Ccdc40 |
T |
A |
11: 119,144,229 (GRCm39) |
F988Y |
probably damaging |
Het |
Ccdc9b |
T |
C |
2: 118,590,098 (GRCm39) |
T249A |
probably benign |
Het |
Chd5 |
T |
A |
4: 152,464,389 (GRCm39) |
V1516E |
probably benign |
Het |
Chrnd |
T |
A |
1: 87,123,389 (GRCm39) |
|
probably null |
Het |
Col5a3 |
C |
A |
9: 20,683,738 (GRCm39) |
G1506V |
unknown |
Het |
Csgalnact2 |
A |
T |
6: 118,106,215 (GRCm39) |
C34* |
probably null |
Het |
Ddx23 |
T |
C |
15: 98,549,832 (GRCm39) |
K195E |
probably benign |
Het |
Dhps |
T |
G |
8: 85,800,880 (GRCm39) |
S240A |
probably benign |
Het |
Dnah5 |
T |
A |
15: 28,234,599 (GRCm39) |
|
probably null |
Het |
Dock10 |
T |
C |
1: 80,514,676 (GRCm39) |
T1414A |
probably benign |
Het |
Dock4 |
A |
G |
12: 40,805,812 (GRCm39) |
D928G |
probably damaging |
Het |
Dolpp1 |
T |
C |
2: 30,285,658 (GRCm39) |
|
probably benign |
Het |
Dse |
T |
A |
10: 34,028,601 (GRCm39) |
I830F |
probably damaging |
Het |
Elmod1 |
C |
T |
9: 53,843,091 (GRCm39) |
R29Q |
probably damaging |
Het |
Ephx4 |
T |
A |
5: 107,577,518 (GRCm39) |
|
probably null |
Het |
Evi5 |
A |
T |
5: 107,968,302 (GRCm39) |
M215K |
probably damaging |
Het |
Fbxl4 |
T |
C |
4: 22,390,678 (GRCm39) |
L287P |
probably damaging |
Het |
Gbp9 |
G |
A |
5: 105,230,724 (GRCm39) |
S400L |
probably damaging |
Het |
Gm6291 |
T |
C |
18: 6,371,365 (GRCm39) |
|
noncoding transcript |
Het |
Gmcl1 |
A |
T |
6: 86,688,596 (GRCm39) |
D301E |
probably benign |
Het |
Gna14 |
C |
T |
19: 16,580,692 (GRCm39) |
R177C |
possibly damaging |
Het |
Golph3 |
C |
T |
15: 12,339,756 (GRCm39) |
R90C |
probably damaging |
Het |
Gpr142 |
T |
A |
11: 114,689,785 (GRCm39) |
C12* |
probably null |
Het |
Hat1 |
T |
A |
2: 71,239,357 (GRCm39) |
N43K |
possibly damaging |
Het |
Hivep1 |
A |
T |
13: 42,310,694 (GRCm39) |
E978V |
possibly damaging |
Het |
Hormad1 |
G |
A |
3: 95,467,044 (GRCm39) |
|
probably null |
Het |
Kalrn |
C |
T |
16: 33,795,805 (GRCm39) |
|
probably benign |
Het |
Mars1 |
T |
C |
10: 127,132,418 (GRCm39) |
T860A |
probably benign |
Het |
Mdn1 |
A |
T |
4: 32,695,400 (GRCm39) |
L1146F |
probably damaging |
Het |
Met |
A |
G |
6: 17,531,581 (GRCm39) |
T620A |
probably benign |
Het |
Mppe1 |
T |
C |
18: 67,358,834 (GRCm39) |
E378G |
probably benign |
Het |
Mybpc3 |
T |
A |
2: 90,955,010 (GRCm39) |
V481D |
probably damaging |
Het |
Myh14 |
A |
T |
7: 44,256,133 (GRCm39) |
L1924Q |
probably damaging |
Het |
Mylip |
G |
T |
13: 45,562,178 (GRCm39) |
E327* |
probably null |
Het |
Naip1 |
C |
T |
13: 100,559,636 (GRCm39) |
G1123R |
probably benign |
Het |
Ncam1 |
T |
A |
9: 49,418,343 (GRCm39) |
T986S |
probably benign |
Het |
Or13p4 |
T |
C |
4: 118,547,314 (GRCm39) |
I112V |
probably damaging |
Het |
Or4x13 |
T |
C |
2: 90,231,800 (GRCm39) |
I265T |
probably benign |
Het |
Phactr2 |
C |
T |
10: 13,121,261 (GRCm39) |
G480S |
probably damaging |
Het |
Por |
A |
G |
5: 135,744,838 (GRCm39) |
I34V |
probably benign |
Het |
Ppp2r5b |
C |
T |
19: 6,284,764 (GRCm39) |
R33H |
probably damaging |
Het |
Prkdc |
C |
A |
16: 15,570,693 (GRCm39) |
Y2325* |
probably null |
Het |
Prx |
A |
G |
7: 27,214,709 (GRCm39) |
E73G |
probably damaging |
Het |
Rbms2 |
C |
A |
10: 127,981,556 (GRCm39) |
A126S |
possibly damaging |
Het |
Rhoq |
C |
T |
17: 87,302,117 (GRCm39) |
A111V |
probably damaging |
Het |
Rpl14 |
T |
A |
9: 120,403,240 (GRCm39) |
|
probably benign |
Het |
Serbp1 |
A |
G |
6: 67,249,870 (GRCm39) |
*75W |
probably null |
Het |
Sptbn1 |
C |
A |
11: 30,073,978 (GRCm39) |
V1351F |
probably damaging |
Het |
Supt16 |
A |
G |
14: 52,401,979 (GRCm39) |
V897A |
probably benign |
Het |
Tfdp1 |
T |
A |
8: 13,407,038 (GRCm39) |
|
probably null |
Het |
Ttn |
T |
A |
2: 76,780,487 (GRCm39) |
Y1088F |
probably damaging |
Het |
Vmn2r105 |
G |
T |
17: 20,448,929 (GRCm39) |
Q83K |
probably benign |
Het |
Wdr76 |
A |
T |
2: 121,359,323 (GRCm39) |
S221C |
probably damaging |
Het |
Zfhx2 |
G |
T |
14: 55,303,348 (GRCm39) |
F1545L |
probably benign |
Het |
Zfp318 |
A |
G |
17: 46,709,959 (GRCm39) |
I561V |
probably damaging |
Het |
|
Other mutations in Naip6 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00677:Naip6
|
APN |
13 |
100,452,525 (GRCm39) |
missense |
probably benign |
0.03 |
IGL01123:Naip6
|
APN |
13 |
100,440,946 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01151:Naip6
|
APN |
13 |
100,435,601 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01382:Naip6
|
APN |
13 |
100,436,364 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01415:Naip6
|
APN |
13 |
100,439,798 (GRCm39) |
missense |
probably benign |
0.17 |
IGL01654:Naip6
|
APN |
13 |
100,435,853 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01662:Naip6
|
APN |
13 |
100,436,862 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01726:Naip6
|
APN |
13 |
100,439,760 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01810:Naip6
|
APN |
13 |
100,424,603 (GRCm39) |
splice site |
probably benign |
|
IGL01867:Naip6
|
APN |
13 |
100,436,820 (GRCm39) |
missense |
probably benign |
0.40 |
IGL01926:Naip6
|
APN |
13 |
100,436,704 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01964:Naip6
|
APN |
13 |
100,435,238 (GRCm39) |
splice site |
probably benign |
|
IGL02145:Naip6
|
APN |
13 |
100,433,486 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02160:Naip6
|
APN |
13 |
100,435,933 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02214:Naip6
|
APN |
13 |
100,452,567 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02342:Naip6
|
APN |
13 |
100,439,748 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL02568:Naip6
|
APN |
13 |
100,452,780 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02573:Naip6
|
APN |
13 |
100,435,979 (GRCm39) |
nonsense |
probably null |
|
IGL02680:Naip6
|
APN |
13 |
100,420,256 (GRCm39) |
missense |
probably benign |
|
IGL02829:Naip6
|
APN |
13 |
100,437,273 (GRCm39) |
missense |
probably benign |
0.11 |
IGL02833:Naip6
|
APN |
13 |
100,436,121 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02851:Naip6
|
APN |
13 |
100,437,168 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02860:Naip6
|
APN |
13 |
100,436,984 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02886:Naip6
|
APN |
13 |
100,436,984 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL03155:Naip6
|
APN |
13 |
100,452,932 (GRCm39) |
missense |
possibly damaging |
0.62 |
R0032:Naip6
|
UTSW |
13 |
100,439,745 (GRCm39) |
missense |
probably benign |
0.00 |
R0310:Naip6
|
UTSW |
13 |
100,444,721 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0437:Naip6
|
UTSW |
13 |
100,433,432 (GRCm39) |
missense |
possibly damaging |
0.75 |
R0472:Naip6
|
UTSW |
13 |
100,438,768 (GRCm39) |
missense |
probably benign |
0.02 |
R0560:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R0638:Naip6
|
UTSW |
13 |
100,437,036 (GRCm39) |
missense |
probably benign |
0.00 |
R0792:Naip6
|
UTSW |
13 |
100,420,274 (GRCm39) |
missense |
possibly damaging |
0.78 |
R0963:Naip6
|
UTSW |
13 |
100,452,983 (GRCm39) |
missense |
probably benign |
0.11 |
R1102:Naip6
|
UTSW |
13 |
100,440,923 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1278:Naip6
|
UTSW |
13 |
100,436,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R1462:Naip6
|
UTSW |
13 |
100,436,748 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1462:Naip6
|
UTSW |
13 |
100,436,748 (GRCm39) |
missense |
possibly damaging |
0.64 |
R1544:Naip6
|
UTSW |
13 |
100,452,983 (GRCm39) |
missense |
probably benign |
|
R1595:Naip6
|
UTSW |
13 |
100,435,602 (GRCm39) |
missense |
probably damaging |
0.96 |
R1749:Naip6
|
UTSW |
13 |
100,444,763 (GRCm39) |
missense |
probably benign |
0.03 |
R1838:Naip6
|
UTSW |
13 |
100,452,644 (GRCm39) |
missense |
probably damaging |
0.99 |
R1863:Naip6
|
UTSW |
13 |
100,437,067 (GRCm39) |
missense |
probably benign |
0.03 |
R1914:Naip6
|
UTSW |
13 |
100,435,936 (GRCm39) |
missense |
probably benign |
0.13 |
R2001:Naip6
|
UTSW |
13 |
100,437,237 (GRCm39) |
missense |
probably benign |
0.44 |
R2082:Naip6
|
UTSW |
13 |
100,440,852 (GRCm39) |
splice site |
probably null |
|
R2143:Naip6
|
UTSW |
13 |
100,436,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R2174:Naip6
|
UTSW |
13 |
100,435,495 (GRCm39) |
missense |
probably benign |
|
R2266:Naip6
|
UTSW |
13 |
100,420,067 (GRCm39) |
missense |
possibly damaging |
0.46 |
R2284:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2285:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2286:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2351:Naip6
|
UTSW |
13 |
100,420,169 (GRCm39) |
missense |
probably damaging |
1.00 |
R2363:Naip6
|
UTSW |
13 |
100,452,928 (GRCm39) |
missense |
possibly damaging |
0.90 |
R2445:Naip6
|
UTSW |
13 |
100,437,176 (GRCm39) |
missense |
probably damaging |
0.99 |
R2971:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R2975:Naip6
|
UTSW |
13 |
100,424,695 (GRCm39) |
missense |
probably damaging |
1.00 |
R3081:Naip6
|
UTSW |
13 |
100,436,961 (GRCm39) |
missense |
probably benign |
|
R3082:Naip6
|
UTSW |
13 |
100,452,925 (GRCm39) |
missense |
probably benign |
0.00 |
R3122:Naip6
|
UTSW |
13 |
100,453,031 (GRCm39) |
missense |
probably benign |
0.00 |
R3417:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R3943:Naip6
|
UTSW |
13 |
100,431,247 (GRCm39) |
missense |
probably benign |
0.01 |
R3944:Naip6
|
UTSW |
13 |
100,431,247 (GRCm39) |
missense |
probably benign |
0.01 |
R4080:Naip6
|
UTSW |
13 |
100,435,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R4166:Naip6
|
UTSW |
13 |
100,452,657 (GRCm39) |
missense |
probably benign |
0.23 |
R4396:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4397:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4418:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4512:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R4670:Naip6
|
UTSW |
13 |
100,431,239 (GRCm39) |
critical splice donor site |
probably null |
|
R4671:Naip6
|
UTSW |
13 |
100,431,239 (GRCm39) |
critical splice donor site |
probably null |
|
R4722:Naip6
|
UTSW |
13 |
100,443,580 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4811:Naip6
|
UTSW |
13 |
100,422,299 (GRCm39) |
missense |
probably damaging |
1.00 |
R4900:Naip6
|
UTSW |
13 |
100,433,477 (GRCm39) |
missense |
probably damaging |
0.99 |
R5162:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R5316:Naip6
|
UTSW |
13 |
100,420,290 (GRCm39) |
missense |
probably benign |
0.00 |
R5403:Naip6
|
UTSW |
13 |
100,436,585 (GRCm39) |
missense |
probably benign |
0.12 |
R5437:Naip6
|
UTSW |
13 |
100,439,812 (GRCm39) |
nonsense |
probably null |
|
R5507:Naip6
|
UTSW |
13 |
100,435,423 (GRCm39) |
missense |
probably benign |
0.01 |
R5631:Naip6
|
UTSW |
13 |
100,436,646 (GRCm39) |
missense |
probably benign |
0.02 |
R5657:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R5684:Naip6
|
UTSW |
13 |
100,436,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R5786:Naip6
|
UTSW |
13 |
100,436,724 (GRCm39) |
missense |
probably benign |
|
R5787:Naip6
|
UTSW |
13 |
100,436,724 (GRCm39) |
missense |
probably benign |
|
R5788:Naip6
|
UTSW |
13 |
100,436,724 (GRCm39) |
missense |
probably benign |
|
R5878:Naip6
|
UTSW |
13 |
100,436,181 (GRCm39) |
missense |
probably damaging |
1.00 |
R5898:Naip6
|
UTSW |
13 |
100,435,829 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6113:Naip6
|
UTSW |
13 |
100,435,794 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6141:Naip6
|
UTSW |
13 |
100,444,741 (GRCm39) |
missense |
possibly damaging |
0.91 |
R6199:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R6321:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R6402:Naip6
|
UTSW |
13 |
100,437,226 (GRCm39) |
missense |
probably benign |
0.30 |
R6435:Naip6
|
UTSW |
13 |
100,431,249 (GRCm39) |
missense |
probably benign |
0.04 |
R6477:Naip6
|
UTSW |
13 |
100,452,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6601:Naip6
|
UTSW |
13 |
100,420,266 (GRCm39) |
missense |
probably benign |
|
R6638:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R6639:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R6804:Naip6
|
UTSW |
13 |
100,435,675 (GRCm39) |
missense |
probably benign |
|
R6922:Naip6
|
UTSW |
13 |
100,438,706 (GRCm39) |
missense |
possibly damaging |
0.88 |
R6975:Naip6
|
UTSW |
13 |
100,452,773 (GRCm39) |
missense |
probably damaging |
1.00 |
R7050:Naip6
|
UTSW |
13 |
100,452,007 (GRCm39) |
missense |
probably damaging |
1.00 |
R7135:Naip6
|
UTSW |
13 |
100,436,927 (GRCm39) |
missense |
probably damaging |
1.00 |
R7140:Naip6
|
UTSW |
13 |
100,436,708 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7182:Naip6
|
UTSW |
13 |
100,452,657 (GRCm39) |
missense |
probably benign |
0.23 |
R7196:Naip6
|
UTSW |
13 |
100,436,666 (GRCm39) |
missense |
probably benign |
0.10 |
R7234:Naip6
|
UTSW |
13 |
100,452,011 (GRCm39) |
nonsense |
probably null |
|
R7259:Naip6
|
UTSW |
13 |
100,440,863 (GRCm39) |
missense |
probably damaging |
1.00 |
R7322:Naip6
|
UTSW |
13 |
100,435,896 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7332:Naip6
|
UTSW |
13 |
100,437,209 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7339:Naip6
|
UTSW |
13 |
100,452,527 (GRCm39) |
missense |
probably damaging |
1.00 |
R7353:Naip6
|
UTSW |
13 |
100,436,259 (GRCm39) |
missense |
probably benign |
0.00 |
R7485:Naip6
|
UTSW |
13 |
100,420,359 (GRCm39) |
missense |
probably benign |
0.07 |
R7597:Naip6
|
UTSW |
13 |
100,437,108 (GRCm39) |
missense |
probably benign |
0.08 |
R7835:Naip6
|
UTSW |
13 |
100,452,512 (GRCm39) |
missense |
probably benign |
0.19 |
R7840:Naip6
|
UTSW |
13 |
100,451,979 (GRCm39) |
missense |
probably damaging |
1.00 |
R8082:Naip6
|
UTSW |
13 |
100,436,961 (GRCm39) |
missense |
probably benign |
|
R8082:Naip6
|
UTSW |
13 |
100,436,909 (GRCm39) |
missense |
probably benign |
|
R8103:Naip6
|
UTSW |
13 |
100,437,851 (GRCm39) |
missense |
probably benign |
0.00 |
R8164:Naip6
|
UTSW |
13 |
100,452,797 (GRCm39) |
missense |
probably benign |
0.00 |
R8206:Naip6
|
UTSW |
13 |
100,431,344 (GRCm39) |
nonsense |
probably null |
|
R8258:Naip6
|
UTSW |
13 |
100,452,920 (GRCm39) |
missense |
probably benign |
0.02 |
R8259:Naip6
|
UTSW |
13 |
100,452,920 (GRCm39) |
missense |
probably benign |
0.02 |
R8348:Naip6
|
UTSW |
13 |
100,436,894 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8405:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8406:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8441:Naip6
|
UTSW |
13 |
100,422,265 (GRCm39) |
missense |
possibly damaging |
0.77 |
R8448:Naip6
|
UTSW |
13 |
100,436,894 (GRCm39) |
missense |
possibly damaging |
0.61 |
R8465:Naip6
|
UTSW |
13 |
100,433,423 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8501:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8502:Naip6
|
UTSW |
13 |
100,436,784 (GRCm39) |
missense |
possibly damaging |
0.89 |
R8687:Naip6
|
UTSW |
13 |
100,435,636 (GRCm39) |
missense |
probably benign |
0.10 |
R8806:Naip6
|
UTSW |
13 |
100,437,161 (GRCm39) |
missense |
possibly damaging |
0.93 |
R9186:Naip6
|
UTSW |
13 |
100,436,390 (GRCm39) |
missense |
possibly damaging |
0.89 |
R9340:Naip6
|
UTSW |
13 |
100,452,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R9352:Naip6
|
UTSW |
13 |
100,437,893 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9585:Naip6
|
UTSW |
13 |
100,436,577 (GRCm39) |
missense |
probably damaging |
0.96 |
R9597:Naip6
|
UTSW |
13 |
100,436,646 (GRCm39) |
missense |
probably benign |
0.02 |
R9601:Naip6
|
UTSW |
13 |
100,436,961 (GRCm39) |
missense |
probably benign |
|
X0066:Naip6
|
UTSW |
13 |
100,451,970 (GRCm39) |
nonsense |
probably null |
|
Z1177:Naip6
|
UTSW |
13 |
100,437,308 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Naip6
|
UTSW |
13 |
100,435,925 (GRCm39) |
missense |
probably benign |
0.20 |
Z1177:Naip6
|
UTSW |
13 |
100,452,638 (GRCm39) |
missense |
probably damaging |
1.00 |
|