Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930550C14Rik |
T |
C |
9: 53,323,122 (GRCm39) |
Y53H |
probably damaging |
Het |
Abca8a |
A |
T |
11: 109,920,913 (GRCm39) |
|
probably null |
Het |
Acads |
C |
A |
5: 115,249,057 (GRCm39) |
Q365H |
probably damaging |
Het |
Acsm3 |
A |
G |
7: 119,380,049 (GRCm39) |
D462G |
probably damaging |
Het |
Adam39 |
T |
A |
8: 41,279,000 (GRCm39) |
C464S |
probably damaging |
Het |
Adgra3 |
A |
G |
5: 50,216,116 (GRCm39) |
M1T |
probably null |
Het |
AI182371 |
T |
C |
2: 34,975,371 (GRCm39) |
Y276C |
probably damaging |
Het |
Ank2 |
T |
A |
3: 126,730,277 (GRCm39) |
H719L |
possibly damaging |
Het |
Ano7 |
G |
A |
1: 93,323,057 (GRCm39) |
V466I |
probably benign |
Het |
Art5 |
A |
G |
7: 101,747,377 (GRCm39) |
L134P |
probably damaging |
Het |
Atcay |
A |
G |
10: 81,046,431 (GRCm39) |
Y298H |
possibly damaging |
Het |
Atp1a4 |
A |
T |
1: 172,067,682 (GRCm39) |
F527Y |
possibly damaging |
Het |
Bpifb2 |
A |
T |
2: 153,734,268 (GRCm39) |
M428L |
probably benign |
Het |
Brinp2 |
A |
C |
1: 158,073,913 (GRCm39) |
V736G |
probably benign |
Het |
Cdc5l |
C |
T |
17: 45,722,849 (GRCm39) |
A437T |
probably benign |
Het |
Cdx2 |
G |
A |
5: 147,243,440 (GRCm39) |
P118L |
possibly damaging |
Het |
Chpt1 |
G |
A |
10: 88,311,193 (GRCm39) |
|
probably null |
Het |
Creb3l2 |
T |
A |
6: 37,312,783 (GRCm39) |
E417V |
probably damaging |
Het |
Csnk2a1 |
A |
G |
2: 152,100,614 (GRCm39) |
T129A |
probably benign |
Het |
Dennd6b |
A |
T |
15: 89,070,376 (GRCm39) |
L431Q |
possibly damaging |
Het |
Dgkz |
C |
T |
2: 91,775,180 (GRCm39) |
A260T |
probably benign |
Het |
Dhx34 |
T |
A |
7: 15,949,373 (GRCm39) |
T352S |
probably benign |
Het |
Elp4 |
C |
T |
2: 105,622,652 (GRCm39) |
R349Q |
not run |
Het |
Emsy |
A |
C |
7: 98,240,010 (GRCm39) |
F1228V |
probably damaging |
Het |
Eps8l1 |
T |
A |
7: 4,473,437 (GRCm39) |
|
probably null |
Het |
Faf1 |
T |
A |
4: 109,719,134 (GRCm39) |
D413E |
probably damaging |
Het |
Fat3 |
T |
C |
9: 16,158,283 (GRCm39) |
Y1109C |
probably damaging |
Het |
Fbp1 |
T |
C |
13: 63,012,867 (GRCm39) |
K314E |
probably benign |
Het |
Fbxl20 |
A |
G |
11: 97,981,614 (GRCm39) |
V358A |
probably benign |
Het |
Fbxo34 |
C |
G |
14: 47,767,992 (GRCm39) |
R502G |
probably benign |
Het |
Fxr2 |
G |
A |
11: 69,532,875 (GRCm39) |
C151Y |
possibly damaging |
Het |
Garin5b |
C |
A |
7: 4,760,681 (GRCm39) |
R677L |
|
Het |
Gja8 |
T |
C |
3: 96,827,338 (GRCm39) |
D108G |
probably benign |
Het |
Gm10722 |
C |
A |
9: 3,001,235 (GRCm39) |
L104I |
probably benign |
Het |
Grsf1 |
A |
G |
5: 88,813,666 (GRCm39) |
V361A |
probably benign |
Het |
Gsap |
T |
A |
5: 21,431,785 (GRCm39) |
I228N |
probably damaging |
Het |
Hagh |
T |
C |
17: 25,075,686 (GRCm39) |
I131T |
probably damaging |
Het |
Heca |
A |
T |
10: 17,791,272 (GRCm39) |
Y261* |
probably null |
Het |
Hipk3 |
A |
G |
2: 104,269,696 (GRCm39) |
F498L |
probably damaging |
Het |
Hps4 |
T |
A |
5: 112,523,324 (GRCm39) |
I614N |
possibly damaging |
Het |
Icam1 |
T |
C |
9: 20,938,886 (GRCm39) |
S450P |
probably benign |
Het |
Il22 |
G |
A |
10: 118,041,069 (GRCm39) |
M58I |
possibly damaging |
Het |
Khdrbs2 |
T |
A |
1: 32,372,883 (GRCm39) |
S186T |
not run |
Het |
Kif16b |
A |
G |
2: 142,699,343 (GRCm39) |
F79S |
probably damaging |
Het |
Kntc1 |
C |
A |
5: 123,948,971 (GRCm39) |
F1905L |
probably benign |
Het |
Liat1 |
A |
T |
11: 75,893,833 (GRCm39) |
D70V |
probably damaging |
Het |
Lrp1b |
C |
T |
2: 40,692,929 (GRCm39) |
G3423D |
|
Het |
Lrp5 |
G |
T |
19: 3,643,588 (GRCm39) |
Q1346K |
probably benign |
Het |
Map3k21 |
A |
C |
8: 126,671,717 (GRCm39) |
T1002P |
possibly damaging |
Het |
Mdga2 |
G |
T |
12: 66,615,670 (GRCm39) |
R646S |
probably benign |
Het |
Mex3b |
G |
T |
7: 82,518,073 (GRCm39) |
M129I |
possibly damaging |
Het |
Mfsd10 |
G |
T |
5: 34,793,770 (GRCm39) |
N85K |
probably damaging |
Het |
Mios |
A |
G |
6: 8,216,064 (GRCm39) |
D420G |
probably damaging |
Het |
Mogs |
C |
A |
6: 83,092,613 (GRCm39) |
P18T |
unknown |
Het |
Mrgpre |
A |
G |
7: 143,335,150 (GRCm39) |
C118R |
probably damaging |
Het |
Muc4 |
A |
T |
16: 32,601,285 (GRCm39) |
H1321L |
|
Het |
Nkapl |
T |
C |
13: 21,651,759 (GRCm39) |
K285E |
probably damaging |
Het |
Nphp4 |
C |
T |
4: 152,583,460 (GRCm39) |
P200S |
possibly damaging |
Het |
Piezo1 |
A |
G |
8: 123,228,397 (GRCm39) |
F297L |
|
Het |
Pkhd1 |
T |
G |
1: 20,271,197 (GRCm39) |
S3119R |
probably damaging |
Het |
Pla2g15 |
G |
A |
8: 106,889,576 (GRCm39) |
V283I |
probably benign |
Het |
Ppp1r13l |
T |
A |
7: 19,102,786 (GRCm39) |
|
probably null |
Het |
Prex1 |
A |
G |
2: 166,429,047 (GRCm39) |
Y849H |
probably damaging |
Het |
Psg27 |
C |
A |
7: 18,301,008 (GRCm39) |
W15L |
probably benign |
Het |
Ptar1 |
A |
T |
19: 23,686,334 (GRCm39) |
|
probably null |
Het |
Ptpn6 |
G |
A |
6: 124,705,135 (GRCm39) |
R264C |
probably damaging |
Het |
Ptprb |
A |
G |
10: 116,177,038 (GRCm39) |
I988V |
probably benign |
Het |
Ptpro |
G |
A |
6: 137,376,559 (GRCm39) |
V680I |
possibly damaging |
Het |
Rnf170 |
C |
T |
8: 26,613,876 (GRCm39) |
P28S |
probably benign |
Het |
Rnpepl1 |
A |
G |
1: 92,846,917 (GRCm39) |
S580G |
possibly damaging |
Het |
Rtel1 |
C |
T |
2: 180,972,608 (GRCm39) |
R29* |
probably null |
Het |
Rtkn |
T |
C |
6: 83,128,726 (GRCm39) |
L26P |
probably damaging |
Het |
Sdk2 |
A |
C |
11: 113,729,315 (GRCm39) |
S1087R |
probably damaging |
Het |
Sema7a |
C |
T |
9: 57,860,852 (GRCm39) |
P71L |
probably benign |
Het |
Sgpp1 |
C |
T |
12: 75,763,038 (GRCm39) |
C381Y |
probably damaging |
Het |
Sis |
A |
T |
3: 72,820,625 (GRCm39) |
|
probably null |
Het |
Slc24a5 |
A |
C |
2: 124,910,869 (GRCm39) |
D100A |
probably benign |
Het |
Slc25a23 |
A |
T |
17: 57,360,587 (GRCm39) |
I251K |
probably damaging |
Het |
Slc6a5 |
T |
A |
7: 49,579,804 (GRCm39) |
L394H |
probably damaging |
Het |
Slc7a4 |
A |
T |
16: 17,392,920 (GRCm39) |
M293K |
probably damaging |
Het |
Syne2 |
T |
A |
12: 75,973,263 (GRCm39) |
S1089T |
probably benign |
Het |
Tanc1 |
A |
T |
2: 59,615,670 (GRCm39) |
T226S |
probably damaging |
Het |
Tdrd6 |
T |
C |
17: 43,936,984 (GRCm39) |
T1355A |
probably benign |
Het |
Tmem101 |
A |
G |
11: 102,044,176 (GRCm39) |
M237T |
possibly damaging |
Het |
Ttn |
G |
A |
2: 76,749,359 (GRCm39) |
H3897Y |
possibly damaging |
Het |
Tubb4a |
C |
T |
17: 57,387,698 (GRCm39) |
V443M |
unknown |
Het |
Ucp2 |
G |
A |
7: 100,147,576 (GRCm39) |
R185H |
possibly damaging |
Het |
Vmn1r116 |
G |
T |
7: 20,606,436 (GRCm39) |
E86* |
probably null |
Het |
Vmn2r37 |
T |
C |
7: 9,213,032 (GRCm39) |
E530G |
probably benign |
Het |
Vwa8 |
A |
G |
14: 79,333,125 (GRCm39) |
T1293A |
probably benign |
Het |
Zfc3h1 |
T |
A |
10: 115,260,535 (GRCm39) |
Y1711N |
probably benign |
Het |
Zfp873 |
A |
T |
10: 81,896,805 (GRCm39) |
E512V |
probably damaging |
Het |
Zhx1 |
T |
C |
15: 57,916,561 (GRCm39) |
N562D |
possibly damaging |
Het |
|
Other mutations in Zfyve16 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00481:Zfyve16
|
APN |
13 |
92,653,046 (GRCm39) |
missense |
possibly damaging |
0.56 |
IGL00737:Zfyve16
|
APN |
13 |
92,657,626 (GRCm39) |
nonsense |
probably null |
|
IGL00741:Zfyve16
|
APN |
13 |
92,660,761 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00753:Zfyve16
|
APN |
13 |
92,657,626 (GRCm39) |
nonsense |
probably null |
|
IGL01123:Zfyve16
|
APN |
13 |
92,629,030 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01149:Zfyve16
|
APN |
13 |
92,644,791 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01414:Zfyve16
|
APN |
13 |
92,658,704 (GRCm39) |
missense |
probably benign |
0.04 |
IGL01771:Zfyve16
|
APN |
13 |
92,658,680 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01889:Zfyve16
|
APN |
13 |
92,659,077 (GRCm39) |
missense |
possibly damaging |
0.87 |
IGL01928:Zfyve16
|
APN |
13 |
92,641,006 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02524:Zfyve16
|
APN |
13 |
92,641,022 (GRCm39) |
missense |
probably benign |
0.19 |
IGL03102:Zfyve16
|
APN |
13 |
92,648,325 (GRCm39) |
missense |
possibly damaging |
0.57 |
IGL03192:Zfyve16
|
APN |
13 |
92,657,748 (GRCm39) |
missense |
possibly damaging |
0.94 |
PIT4151001:Zfyve16
|
UTSW |
13 |
92,657,712 (GRCm39) |
missense |
probably damaging |
0.99 |
R0321:Zfyve16
|
UTSW |
13 |
92,629,042 (GRCm39) |
missense |
probably damaging |
0.99 |
R0548:Zfyve16
|
UTSW |
13 |
92,631,452 (GRCm39) |
missense |
probably benign |
0.00 |
R0555:Zfyve16
|
UTSW |
13 |
92,653,028 (GRCm39) |
splice site |
probably benign |
|
R0616:Zfyve16
|
UTSW |
13 |
92,657,637 (GRCm39) |
missense |
probably damaging |
1.00 |
R0727:Zfyve16
|
UTSW |
13 |
92,630,386 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0730:Zfyve16
|
UTSW |
13 |
92,657,985 (GRCm39) |
missense |
probably damaging |
0.98 |
R1221:Zfyve16
|
UTSW |
13 |
92,644,813 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1297:Zfyve16
|
UTSW |
13 |
92,658,840 (GRCm39) |
missense |
probably benign |
0.41 |
R1597:Zfyve16
|
UTSW |
13 |
92,644,755 (GRCm39) |
missense |
probably benign |
0.02 |
R1635:Zfyve16
|
UTSW |
13 |
92,645,528 (GRCm39) |
missense |
probably damaging |
1.00 |
R1803:Zfyve16
|
UTSW |
13 |
92,640,593 (GRCm39) |
missense |
probably damaging |
1.00 |
R1840:Zfyve16
|
UTSW |
13 |
92,648,033 (GRCm39) |
missense |
possibly damaging |
0.79 |
R1962:Zfyve16
|
UTSW |
13 |
92,659,252 (GRCm39) |
missense |
possibly damaging |
0.74 |
R2029:Zfyve16
|
UTSW |
13 |
92,640,985 (GRCm39) |
missense |
probably damaging |
0.98 |
R2083:Zfyve16
|
UTSW |
13 |
92,660,770 (GRCm39) |
missense |
probably damaging |
1.00 |
R2122:Zfyve16
|
UTSW |
13 |
92,655,991 (GRCm39) |
nonsense |
probably null |
|
R2173:Zfyve16
|
UTSW |
13 |
92,631,596 (GRCm39) |
missense |
probably damaging |
0.99 |
R3822:Zfyve16
|
UTSW |
13 |
92,657,769 (GRCm39) |
missense |
probably damaging |
1.00 |
R3857:Zfyve16
|
UTSW |
13 |
92,631,479 (GRCm39) |
missense |
probably damaging |
1.00 |
R4043:Zfyve16
|
UTSW |
13 |
92,650,271 (GRCm39) |
splice site |
probably null |
|
R4056:Zfyve16
|
UTSW |
13 |
92,641,057 (GRCm39) |
missense |
probably damaging |
1.00 |
R4495:Zfyve16
|
UTSW |
13 |
92,625,075 (GRCm39) |
missense |
probably benign |
0.25 |
R4518:Zfyve16
|
UTSW |
13 |
92,657,820 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4835:Zfyve16
|
UTSW |
13 |
92,658,693 (GRCm39) |
missense |
probably benign |
0.18 |
R4862:Zfyve16
|
UTSW |
13 |
92,644,764 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Zfyve16
|
UTSW |
13 |
92,650,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R5117:Zfyve16
|
UTSW |
13 |
92,642,197 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5344:Zfyve16
|
UTSW |
13 |
92,658,096 (GRCm39) |
missense |
possibly damaging |
0.79 |
R5358:Zfyve16
|
UTSW |
13 |
92,644,771 (GRCm39) |
missense |
probably benign |
0.04 |
R5407:Zfyve16
|
UTSW |
13 |
92,636,792 (GRCm39) |
missense |
probably damaging |
1.00 |
R5410:Zfyve16
|
UTSW |
13 |
92,657,739 (GRCm39) |
missense |
probably benign |
0.08 |
R5704:Zfyve16
|
UTSW |
13 |
92,640,979 (GRCm39) |
splice site |
probably null |
|
R5731:Zfyve16
|
UTSW |
13 |
92,644,701 (GRCm39) |
missense |
probably benign |
0.11 |
R5808:Zfyve16
|
UTSW |
13 |
92,631,563 (GRCm39) |
nonsense |
probably null |
|
R5828:Zfyve16
|
UTSW |
13 |
92,650,410 (GRCm39) |
missense |
probably damaging |
1.00 |
R5928:Zfyve16
|
UTSW |
13 |
92,658,625 (GRCm39) |
missense |
probably benign |
0.01 |
R6044:Zfyve16
|
UTSW |
13 |
92,659,174 (GRCm39) |
nonsense |
probably null |
|
R6141:Zfyve16
|
UTSW |
13 |
92,648,105 (GRCm39) |
missense |
probably benign |
0.00 |
R6538:Zfyve16
|
UTSW |
13 |
92,641,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R6594:Zfyve16
|
UTSW |
13 |
92,650,326 (GRCm39) |
missense |
probably benign |
0.23 |
R6767:Zfyve16
|
UTSW |
13 |
92,644,707 (GRCm39) |
missense |
probably damaging |
1.00 |
R6942:Zfyve16
|
UTSW |
13 |
92,653,139 (GRCm39) |
missense |
probably benign |
|
R7011:Zfyve16
|
UTSW |
13 |
92,658,495 (GRCm39) |
missense |
probably benign |
0.00 |
R7531:Zfyve16
|
UTSW |
13 |
92,659,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R7617:Zfyve16
|
UTSW |
13 |
92,641,070 (GRCm39) |
missense |
probably damaging |
1.00 |
R7831:Zfyve16
|
UTSW |
13 |
92,658,836 (GRCm39) |
missense |
probably benign |
0.05 |
R8127:Zfyve16
|
UTSW |
13 |
92,642,185 (GRCm39) |
missense |
probably damaging |
1.00 |
R8382:Zfyve16
|
UTSW |
13 |
92,650,328 (GRCm39) |
missense |
probably benign |
|
R8467:Zfyve16
|
UTSW |
13 |
92,644,790 (GRCm39) |
missense |
probably damaging |
1.00 |
R8765:Zfyve16
|
UTSW |
13 |
92,658,055 (GRCm39) |
missense |
probably benign |
0.15 |
R8792:Zfyve16
|
UTSW |
13 |
92,659,669 (GRCm39) |
missense |
probably benign |
0.08 |
R9112:Zfyve16
|
UTSW |
13 |
92,659,563 (GRCm39) |
missense |
possibly damaging |
0.75 |
R9169:Zfyve16
|
UTSW |
13 |
92,657,871 (GRCm39) |
missense |
probably damaging |
1.00 |
R9599:Zfyve16
|
UTSW |
13 |
92,636,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R9608:Zfyve16
|
UTSW |
13 |
92,636,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R9636:Zfyve16
|
UTSW |
13 |
92,631,456 (GRCm39) |
missense |
probably benign |
0.17 |
R9669:Zfyve16
|
UTSW |
13 |
92,656,007 (GRCm39) |
missense |
probably damaging |
0.99 |
R9685:Zfyve16
|
UTSW |
13 |
92,659,311 (GRCm39) |
missense |
possibly damaging |
0.75 |
Z1176:Zfyve16
|
UTSW |
13 |
92,629,171 (GRCm39) |
missense |
possibly damaging |
0.95 |
Z1177:Zfyve16
|
UTSW |
13 |
92,659,504 (GRCm39) |
missense |
possibly damaging |
0.87 |
|