Other mutations in this stock |
Total: 106 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsm1 |
A |
T |
7: 119,257,538 (GRCm39) |
T435S |
probably damaging |
Het |
Agtpbp1 |
G |
A |
13: 59,648,014 (GRCm39) |
T602I |
probably benign |
Het |
Ahnak2 |
T |
A |
12: 112,749,154 (GRCm39) |
D231V |
probably damaging |
Het |
Ampd3 |
G |
A |
7: 110,392,876 (GRCm39) |
D215N |
probably benign |
Het |
Ankrd17 |
T |
C |
5: 90,398,264 (GRCm39) |
D1762G |
probably damaging |
Het |
Asb8 |
C |
T |
15: 98,040,552 (GRCm39) |
V37I |
possibly damaging |
Het |
Bicra |
T |
C |
7: 15,721,436 (GRCm39) |
T694A |
possibly damaging |
Het |
Btnl6 |
A |
T |
17: 34,733,273 (GRCm39) |
M234K |
probably benign |
Het |
Ccnb1 |
A |
T |
13: 100,916,289 (GRCm39) |
V336D |
probably damaging |
Het |
Cdca8 |
A |
T |
4: 124,815,047 (GRCm39) |
L190Q |
possibly damaging |
Het |
Cep290 |
A |
T |
10: 100,373,693 (GRCm39) |
L1324F |
probably damaging |
Het |
Ces1f |
T |
C |
8: 93,998,513 (GRCm39) |
E161G |
probably benign |
Het |
Ces2g |
A |
G |
8: 105,692,628 (GRCm39) |
|
probably benign |
Het |
Cfap74 |
C |
T |
4: 155,510,572 (GRCm39) |
R386C |
probably benign |
Het |
Clec3b |
A |
G |
9: 122,986,090 (GRCm39) |
T163A |
probably benign |
Het |
Cntnap4 |
T |
G |
8: 113,529,796 (GRCm39) |
L668R |
probably damaging |
Het |
Col27a1 |
A |
G |
4: 63,194,214 (GRCm39) |
D857G |
probably damaging |
Het |
Csf1 |
A |
G |
3: 107,655,960 (GRCm39) |
V245A |
probably benign |
Het |
Ctss |
A |
G |
3: 95,457,448 (GRCm39) |
Y302C |
probably damaging |
Het |
Cyb5d1 |
A |
G |
11: 69,285,792 (GRCm39) |
|
probably null |
Het |
Cyp1a2 |
A |
G |
9: 57,589,344 (GRCm39) |
S157P |
probably damaging |
Het |
Cyp2b9 |
A |
T |
7: 25,900,238 (GRCm39) |
T349S |
probably benign |
Het |
Dennd6b |
T |
C |
15: 89,070,386 (GRCm39) |
I428V |
probably benign |
Het |
Denr |
A |
G |
5: 124,065,298 (GRCm39) |
|
probably benign |
Het |
Dnah9 |
G |
A |
11: 65,860,781 (GRCm39) |
|
probably benign |
Het |
Dock3 |
G |
T |
9: 106,790,467 (GRCm39) |
Q1419K |
possibly damaging |
Het |
Dph3b-ps |
A |
T |
13: 106,683,375 (GRCm39) |
|
noncoding transcript |
Het |
Emc7 |
G |
T |
2: 112,289,830 (GRCm39) |
D87Y |
probably damaging |
Het |
Enah |
T |
C |
1: 181,740,938 (GRCm39) |
E462G |
possibly damaging |
Het |
Eno1b |
T |
C |
18: 48,180,806 (GRCm39) |
I328T |
probably benign |
Het |
Enpp6 |
A |
G |
8: 47,519,035 (GRCm39) |
K268E |
probably damaging |
Het |
Eps15l1 |
T |
G |
8: 73,135,341 (GRCm39) |
|
probably benign |
Het |
Fam151a |
T |
C |
4: 106,605,371 (GRCm39) |
Y578H |
probably benign |
Het |
Fmn2 |
T |
C |
1: 174,618,880 (GRCm39) |
V1512A |
probably damaging |
Het |
Focad |
C |
A |
4: 88,327,196 (GRCm39) |
N168K |
probably benign |
Het |
Fyco1 |
A |
G |
9: 123,658,074 (GRCm39) |
C701R |
probably damaging |
Het |
Gabbr1 |
G |
T |
17: 37,378,102 (GRCm39) |
|
probably benign |
Het |
Golga7b |
A |
T |
19: 42,255,278 (GRCm39) |
E76V |
probably damaging |
Het |
Gucy2d |
A |
G |
7: 98,116,959 (GRCm39) |
D924G |
probably benign |
Het |
H2-M9 |
A |
G |
17: 36,952,647 (GRCm39) |
F133S |
probably damaging |
Het |
Hc |
A |
G |
2: 34,876,304 (GRCm39) |
Y1581H |
probably damaging |
Het |
Herc3 |
C |
T |
6: 58,851,293 (GRCm39) |
P514L |
probably damaging |
Het |
Hormad1 |
T |
C |
3: 95,492,436 (GRCm39) |
|
probably benign |
Het |
Iigp1 |
T |
A |
18: 60,523,859 (GRCm39) |
S326T |
possibly damaging |
Het |
Itga2 |
G |
A |
13: 115,007,032 (GRCm39) |
S432L |
possibly damaging |
Het |
Kcnk7 |
T |
G |
19: 5,757,042 (GRCm39) |
*344G |
probably null |
Het |
Kif13a |
A |
G |
13: 46,939,987 (GRCm39) |
|
probably null |
Het |
Kif1a |
A |
C |
1: 92,970,080 (GRCm39) |
I1027S |
probably damaging |
Het |
Kif2c |
G |
T |
4: 117,022,714 (GRCm39) |
H416Q |
probably damaging |
Het |
Liat1 |
AGAGGAGGAGGAGGAGG |
AGAGGAGGAGGAGG |
11: 75,890,941 (GRCm39) |
|
probably benign |
Het |
Map3k1 |
A |
G |
13: 111,892,663 (GRCm39) |
V864A |
probably benign |
Het |
Mark2 |
T |
C |
19: 7,263,287 (GRCm39) |
D160G |
probably damaging |
Het |
Mbd4 |
A |
G |
6: 115,821,529 (GRCm39) |
|
probably null |
Het |
Micu1 |
A |
G |
10: 59,624,699 (GRCm39) |
|
probably null |
Het |
Mink1 |
T |
C |
11: 70,503,868 (GRCm39) |
W1263R |
probably damaging |
Het |
Mov10 |
A |
C |
3: 104,711,919 (GRCm39) |
L224R |
probably damaging |
Het |
Ndel1 |
T |
C |
11: 68,726,999 (GRCm39) |
E226G |
probably damaging |
Het |
Neb |
A |
T |
2: 52,112,786 (GRCm39) |
V4336E |
probably damaging |
Het |
Nln |
T |
A |
13: 104,173,399 (GRCm39) |
K602N |
probably damaging |
Het |
Nlrp14 |
A |
T |
7: 106,780,465 (GRCm39) |
|
probably benign |
Het |
Nmd3 |
A |
T |
3: 69,655,654 (GRCm39) |
D445V |
probably damaging |
Het |
Nop14 |
T |
C |
5: 34,801,297 (GRCm39) |
I625V |
probably benign |
Het |
Notch1 |
T |
C |
2: 26,360,943 (GRCm39) |
Q1134R |
probably damaging |
Het |
Nr4a2 |
T |
C |
2: 56,998,627 (GRCm39) |
I392M |
probably benign |
Het |
Or13n4 |
A |
G |
7: 106,422,963 (GRCm39) |
F257L |
possibly damaging |
Het |
Or4f6 |
T |
A |
2: 111,839,365 (GRCm39) |
L55F |
probably damaging |
Het |
Or8b57 |
A |
G |
9: 40,003,549 (GRCm39) |
S234P |
probably damaging |
Het |
Osbp |
T |
C |
19: 11,961,322 (GRCm39) |
Y454H |
probably damaging |
Het |
Pak4 |
G |
A |
7: 28,263,708 (GRCm39) |
R343C |
probably damaging |
Het |
Pak5 |
T |
C |
2: 135,942,704 (GRCm39) |
K479E |
possibly damaging |
Het |
Pard3 |
C |
A |
8: 127,888,058 (GRCm39) |
D73E |
probably damaging |
Het |
Pcdh10 |
T |
C |
3: 45,334,934 (GRCm39) |
V416A |
possibly damaging |
Het |
Plek |
A |
C |
11: 16,935,594 (GRCm39) |
W261G |
probably damaging |
Het |
Pmp22 |
A |
T |
11: 63,049,076 (GRCm39) |
|
probably null |
Het |
Prph2 |
A |
C |
17: 47,230,697 (GRCm39) |
K197Q |
probably benign |
Het |
Prss45 |
T |
A |
9: 110,669,962 (GRCm39) |
L257Q |
probably damaging |
Het |
Psmb6 |
C |
A |
11: 70,417,171 (GRCm39) |
H73Q |
probably benign |
Het |
Rin2 |
T |
C |
2: 145,720,752 (GRCm39) |
|
probably benign |
Het |
Rps6kb1 |
A |
T |
11: 86,402,413 (GRCm39) |
|
probably null |
Het |
Scn10a |
C |
A |
9: 119,499,550 (GRCm39) |
D248Y |
probably damaging |
Het |
Scn4a |
C |
T |
11: 106,215,386 (GRCm39) |
V1197I |
probably benign |
Het |
Siglecf |
A |
T |
7: 43,001,349 (GRCm39) |
I106F |
probably benign |
Het |
Sik1 |
A |
G |
17: 32,066,249 (GRCm39) |
|
probably benign |
Het |
Slc22a21 |
T |
G |
11: 53,870,514 (GRCm39) |
N57T |
probably damaging |
Het |
Slc36a2 |
A |
G |
11: 55,053,621 (GRCm39) |
L339P |
probably damaging |
Het |
Slc4a9 |
G |
T |
18: 36,664,719 (GRCm39) |
|
probably benign |
Het |
Smg1 |
G |
A |
7: 117,811,666 (GRCm39) |
T104I |
possibly damaging |
Het |
Stc2 |
A |
T |
11: 31,315,559 (GRCm39) |
|
probably null |
Het |
Stx18 |
T |
A |
5: 38,249,908 (GRCm39) |
Y74N |
probably damaging |
Het |
Stxbp5 |
A |
T |
10: 9,638,492 (GRCm39) |
H1102Q |
probably damaging |
Het |
Tnfaip8l2 |
G |
A |
3: 95,047,339 (GRCm39) |
L175F |
probably damaging |
Het |
Tom1l2 |
T |
C |
11: 60,120,960 (GRCm39) |
K450E |
probably damaging |
Het |
Tpo |
T |
C |
12: 30,150,389 (GRCm39) |
Q497R |
probably benign |
Het |
Tprg1l |
G |
T |
4: 154,244,802 (GRCm39) |
|
probably benign |
Het |
Triml2 |
A |
G |
8: 43,638,469 (GRCm39) |
M146V |
probably benign |
Het |
Tsc2 |
A |
G |
17: 24,849,978 (GRCm39) |
|
probably benign |
Het |
Tut7 |
A |
T |
13: 59,953,142 (GRCm39) |
D99E |
probably benign |
Het |
Vit |
G |
A |
17: 78,907,264 (GRCm39) |
G229R |
probably benign |
Het |
Vmn2r19 |
C |
T |
6: 123,308,506 (GRCm39) |
L528F |
probably benign |
Het |
Vwf |
T |
A |
6: 125,659,775 (GRCm39) |
I2658N |
probably benign |
Het |
Wdfy3 |
T |
C |
5: 101,992,912 (GRCm39) |
D3341G |
probably damaging |
Het |
Wdr36 |
T |
A |
18: 32,992,360 (GRCm39) |
D632E |
probably damaging |
Het |
Wdr47 |
G |
T |
3: 108,545,307 (GRCm39) |
A733S |
probably damaging |
Het |
Zfp654 |
A |
G |
16: 64,605,181 (GRCm39) |
V466A |
probably benign |
Het |
Zfp804b |
T |
C |
5: 6,821,665 (GRCm39) |
E466G |
probably damaging |
Het |
Zfp941 |
T |
C |
7: 140,393,185 (GRCm39) |
D58G |
probably benign |
Het |
|
Other mutations in Zfp458 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01672:Zfp458
|
APN |
13 |
67,405,300 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01989:Zfp458
|
APN |
13 |
67,407,691 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02168:Zfp458
|
APN |
13 |
67,406,098 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02620:Zfp458
|
APN |
13 |
67,406,058 (GRCm39) |
missense |
probably damaging |
1.00 |
R0014:Zfp458
|
UTSW |
13 |
67,406,154 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0014:Zfp458
|
UTSW |
13 |
67,406,154 (GRCm39) |
missense |
possibly damaging |
0.71 |
R0066:Zfp458
|
UTSW |
13 |
67,407,673 (GRCm39) |
nonsense |
probably null |
|
R0257:Zfp458
|
UTSW |
13 |
67,407,706 (GRCm39) |
nonsense |
probably null |
|
R1218:Zfp458
|
UTSW |
13 |
67,404,273 (GRCm39) |
missense |
probably damaging |
0.99 |
R1292:Zfp458
|
UTSW |
13 |
67,404,754 (GRCm39) |
missense |
probably damaging |
1.00 |
R1490:Zfp458
|
UTSW |
13 |
67,405,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R1664:Zfp458
|
UTSW |
13 |
67,406,144 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2169:Zfp458
|
UTSW |
13 |
67,405,113 (GRCm39) |
missense |
probably damaging |
1.00 |
R3769:Zfp458
|
UTSW |
13 |
67,405,546 (GRCm39) |
missense |
probably damaging |
1.00 |
R5305:Zfp458
|
UTSW |
13 |
67,404,382 (GRCm39) |
missense |
probably benign |
0.31 |
R5364:Zfp458
|
UTSW |
13 |
67,406,012 (GRCm39) |
nonsense |
probably null |
|
R5426:Zfp458
|
UTSW |
13 |
67,405,256 (GRCm39) |
nonsense |
probably null |
|
R5760:Zfp458
|
UTSW |
13 |
67,405,853 (GRCm39) |
missense |
probably damaging |
1.00 |
R6151:Zfp458
|
UTSW |
13 |
67,405,662 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6186:Zfp458
|
UTSW |
13 |
67,405,701 (GRCm39) |
missense |
probably damaging |
1.00 |
R6298:Zfp458
|
UTSW |
13 |
67,404,870 (GRCm39) |
missense |
probably damaging |
1.00 |
R7368:Zfp458
|
UTSW |
13 |
67,405,300 (GRCm39) |
missense |
probably benign |
0.01 |
R7483:Zfp458
|
UTSW |
13 |
67,404,978 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7711:Zfp458
|
UTSW |
13 |
67,407,664 (GRCm39) |
missense |
possibly damaging |
0.95 |
R7921:Zfp458
|
UTSW |
13 |
67,404,180 (GRCm39) |
makesense |
probably null |
|
R7993:Zfp458
|
UTSW |
13 |
67,405,234 (GRCm39) |
missense |
probably damaging |
1.00 |
R8240:Zfp458
|
UTSW |
13 |
67,406,190 (GRCm39) |
missense |
probably damaging |
1.00 |
R8429:Zfp458
|
UTSW |
13 |
67,406,152 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9084:Zfp458
|
UTSW |
13 |
67,407,633 (GRCm39) |
missense |
probably benign |
0.09 |
R9099:Zfp458
|
UTSW |
13 |
67,405,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R9217:Zfp458
|
UTSW |
13 |
67,408,298 (GRCm39) |
missense |
probably damaging |
0.99 |
R9249:Zfp458
|
UTSW |
13 |
67,405,218 (GRCm39) |
missense |
probably damaging |
1.00 |
R9765:Zfp458
|
UTSW |
13 |
67,408,217 (GRCm39) |
missense |
probably damaging |
1.00 |
|