Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930432M17Rik |
A |
C |
3: 121,473,095 (GRCm39) |
K83N |
unknown |
Het |
Abca13 |
A |
T |
11: 9,244,649 (GRCm39) |
N2171Y |
probably damaging |
Het |
Abcc8 |
G |
A |
7: 45,754,922 (GRCm39) |
T1532I |
possibly damaging |
Het |
Abtb2 |
A |
T |
2: 103,532,769 (GRCm39) |
|
probably null |
Het |
Actmap |
G |
A |
7: 26,900,548 (GRCm39) |
A176T |
probably damaging |
Het |
Agk |
A |
T |
6: 40,306,451 (GRCm39) |
T7S |
possibly damaging |
Het |
Akap9 |
C |
A |
5: 4,082,696 (GRCm39) |
T1940K |
probably damaging |
Het |
Ccdc8 |
A |
G |
7: 16,729,956 (GRCm39) |
T482A |
unknown |
Het |
Cd2ap |
G |
A |
17: 43,140,904 (GRCm39) |
R212* |
probably null |
Het |
Cenpt |
G |
A |
8: 106,576,536 (GRCm39) |
Q45* |
probably null |
Het |
Cnga1 |
T |
C |
5: 72,762,775 (GRCm39) |
I246M |
probably benign |
Het |
Cnot7 |
A |
G |
8: 40,960,586 (GRCm39) |
I74T |
probably damaging |
Het |
Cog6 |
T |
C |
3: 52,909,928 (GRCm39) |
S275G |
probably benign |
Het |
Csmd2 |
C |
A |
4: 128,422,055 (GRCm39) |
D2797E |
|
Het |
Ddx24 |
A |
G |
12: 103,385,709 (GRCm39) |
M298T |
possibly damaging |
Het |
Eif2b3 |
T |
A |
4: 116,910,019 (GRCm39) |
S185T |
probably benign |
Het |
Ergic2 |
T |
A |
6: 148,089,610 (GRCm39) |
Y249F |
probably damaging |
Het |
Exoc1 |
T |
A |
5: 76,690,006 (GRCm39) |
M182K |
probably damaging |
Het |
Fhdc1 |
T |
C |
3: 84,351,847 (GRCm39) |
E1126G |
probably damaging |
Het |
Gabrr2 |
T |
A |
4: 33,095,284 (GRCm39) |
M391K |
probably benign |
Het |
Gap43 |
T |
C |
16: 42,112,615 (GRCm39) |
K49E |
probably damaging |
Het |
Gata4 |
T |
A |
14: 63,441,191 (GRCm39) |
T276S |
probably damaging |
Het |
Gca |
C |
T |
2: 62,520,320 (GRCm39) |
P160L |
probably benign |
Het |
Ghdc |
C |
T |
11: 100,658,942 (GRCm39) |
V397I |
possibly damaging |
Het |
Gm3409 |
T |
A |
5: 146,476,357 (GRCm39) |
D169E |
probably benign |
Het |
Gtf3c3 |
G |
A |
1: 54,456,867 (GRCm39) |
P511L |
probably benign |
Het |
Hal |
T |
C |
10: 93,328,423 (GRCm39) |
V233A |
probably benign |
Het |
Ighv1-4 |
T |
C |
12: 114,450,908 (GRCm39) |
I67V |
probably benign |
Het |
Itgb8 |
T |
C |
12: 119,166,196 (GRCm39) |
N112D |
probably benign |
Het |
Klhl38 |
G |
A |
15: 58,186,376 (GRCm39) |
R118W |
probably damaging |
Het |
Krtap26-1 |
T |
C |
16: 88,444,132 (GRCm39) |
Y163C |
possibly damaging |
Het |
Kyat1 |
T |
C |
2: 30,082,007 (GRCm39) |
D44G |
probably benign |
Het |
Mob1a |
G |
A |
6: 83,315,431 (GRCm39) |
|
probably null |
Het |
Mst1r |
G |
T |
9: 107,791,989 (GRCm39) |
A842S |
possibly damaging |
Het |
Nhsl1 |
A |
G |
10: 18,403,419 (GRCm39) |
|
probably null |
Het |
Nos1 |
A |
T |
5: 118,005,970 (GRCm39) |
D230V |
possibly damaging |
Het |
Nppb |
T |
C |
4: 148,070,780 (GRCm39) |
S52P |
probably benign |
Het |
Odad2 |
T |
C |
18: 7,222,635 (GRCm39) |
K545E |
probably damaging |
Het |
Olfml3 |
T |
C |
3: 103,643,176 (GRCm39) |
K402E |
probably damaging |
Het |
Or1s2 |
G |
A |
19: 13,758,688 (GRCm39) |
W235* |
probably null |
Het |
Pcdha3 |
G |
A |
18: 37,079,977 (GRCm39) |
E240K |
possibly damaging |
Het |
Podxl |
G |
T |
6: 31,501,371 (GRCm39) |
P395T |
probably damaging |
Het |
Prr5l |
T |
A |
2: 101,547,631 (GRCm39) |
D298V |
probably damaging |
Het |
Ptpro |
G |
A |
6: 137,418,142 (GRCm39) |
|
probably null |
Het |
Rad9b |
A |
G |
5: 122,490,677 (GRCm39) |
V13A |
possibly damaging |
Het |
Ralgps1 |
T |
C |
2: 33,047,885 (GRCm39) |
K365R |
probably benign |
Het |
Reep1 |
A |
T |
6: 71,738,373 (GRCm39) |
I44L |
probably benign |
Het |
Ripor2 |
T |
C |
13: 24,908,984 (GRCm39) |
I1034T |
possibly damaging |
Het |
Rtn4ip1 |
T |
C |
10: 43,812,016 (GRCm39) |
Y338H |
probably damaging |
Het |
Shisa5 |
G |
T |
9: 108,883,952 (GRCm39) |
|
probably benign |
Het |
Snx24 |
G |
T |
18: 53,473,244 (GRCm39) |
V63F |
probably damaging |
Het |
Svep1 |
G |
A |
4: 58,046,587 (GRCm39) |
Q3515* |
probably null |
Het |
Tfap2a |
T |
C |
13: 40,874,784 (GRCm39) |
K276E |
probably damaging |
Het |
Tmem158 |
C |
A |
9: 123,089,366 (GRCm39) |
S82I |
probably damaging |
Het |
Tmem263 |
T |
A |
10: 84,950,261 (GRCm39) |
|
probably null |
Het |
Tmtc3 |
G |
T |
10: 100,283,336 (GRCm39) |
H740N |
not run |
Het |
Tnrc6a |
A |
C |
7: 122,770,136 (GRCm39) |
N642T |
probably benign |
Het |
Top3a |
A |
T |
11: 60,638,974 (GRCm39) |
F559I |
probably damaging |
Het |
Trak1 |
A |
G |
9: 121,280,929 (GRCm39) |
|
probably null |
Het |
Trpc4 |
T |
C |
3: 54,225,048 (GRCm39) |
I799T |
possibly damaging |
Het |
Ttc7 |
T |
C |
17: 87,653,970 (GRCm39) |
I549T |
possibly damaging |
Het |
Tysnd1 |
C |
A |
10: 61,532,328 (GRCm39) |
P327T |
possibly damaging |
Het |
Ulk4 |
T |
A |
9: 120,974,125 (GRCm39) |
D969V |
probably benign |
Het |
Vcan |
T |
A |
13: 89,853,385 (GRCm39) |
Y525F |
probably benign |
Het |
Vmn1r204 |
G |
A |
13: 22,740,975 (GRCm39) |
S202N |
probably damaging |
Het |
Vmn2r107 |
A |
G |
17: 20,565,878 (GRCm39) |
I64M |
probably benign |
Het |
Wrn |
A |
G |
8: 33,782,746 (GRCm39) |
F728S |
probably damaging |
Het |
Zfp280b |
C |
G |
10: 75,874,537 (GRCm39) |
Q139E |
probably damaging |
Het |
Zfp322a |
C |
A |
13: 23,541,313 (GRCm39) |
G143V |
probably damaging |
Het |
Zfp322a |
C |
T |
13: 23,541,314 (GRCm39) |
G143S |
probably benign |
Het |
Zfp418 |
T |
A |
7: 7,185,827 (GRCm39) |
C597S |
possibly damaging |
Het |
Zfp568 |
A |
G |
7: 29,716,669 (GRCm39) |
T190A |
probably benign |
Het |
|
Other mutations in Zfyve26 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00090:Zfyve26
|
APN |
12 |
79,296,234 (GRCm39) |
unclassified |
probably benign |
|
IGL00940:Zfyve26
|
APN |
12 |
79,327,674 (GRCm39) |
missense |
probably benign |
|
IGL01148:Zfyve26
|
APN |
12 |
79,307,644 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01347:Zfyve26
|
APN |
12 |
79,298,957 (GRCm39) |
splice site |
probably null |
|
IGL01472:Zfyve26
|
APN |
12 |
79,323,117 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01490:Zfyve26
|
APN |
12 |
79,291,147 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01516:Zfyve26
|
APN |
12 |
79,334,625 (GRCm39) |
missense |
probably benign |
0.37 |
IGL01642:Zfyve26
|
APN |
12 |
79,308,348 (GRCm39) |
splice site |
probably null |
|
IGL01689:Zfyve26
|
APN |
12 |
79,330,827 (GRCm39) |
missense |
possibly damaging |
0.71 |
IGL01877:Zfyve26
|
APN |
12 |
79,334,218 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01997:Zfyve26
|
APN |
12 |
79,291,174 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02077:Zfyve26
|
APN |
12 |
79,323,169 (GRCm39) |
missense |
possibly damaging |
0.54 |
IGL02437:Zfyve26
|
APN |
12 |
79,315,621 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02933:Zfyve26
|
APN |
12 |
79,326,854 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02937:Zfyve26
|
APN |
12 |
79,285,794 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02982:Zfyve26
|
APN |
12 |
79,310,644 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03064:Zfyve26
|
APN |
12 |
79,308,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03086:Zfyve26
|
APN |
12 |
79,342,338 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03146:Zfyve26
|
APN |
12 |
79,330,846 (GRCm39) |
nonsense |
probably null |
|
challenge
|
UTSW |
12 |
79,317,610 (GRCm39) |
critical splice donor site |
probably null |
|
fourteener
|
UTSW |
12 |
79,302,037 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02799:Zfyve26
|
UTSW |
12 |
79,320,084 (GRCm39) |
missense |
probably benign |
0.28 |
R0318:Zfyve26
|
UTSW |
12 |
79,323,055 (GRCm39) |
missense |
probably damaging |
1.00 |
R0513:Zfyve26
|
UTSW |
12 |
79,291,258 (GRCm39) |
missense |
probably damaging |
1.00 |
R0582:Zfyve26
|
UTSW |
12 |
79,292,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R0586:Zfyve26
|
UTSW |
12 |
79,315,502 (GRCm39) |
missense |
possibly damaging |
0.96 |
R0718:Zfyve26
|
UTSW |
12 |
79,312,576 (GRCm39) |
splice site |
probably benign |
|
R0738:Zfyve26
|
UTSW |
12 |
79,342,308 (GRCm39) |
missense |
probably damaging |
1.00 |
R0781:Zfyve26
|
UTSW |
12 |
79,326,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R0894:Zfyve26
|
UTSW |
12 |
79,320,372 (GRCm39) |
missense |
possibly damaging |
0.80 |
R1109:Zfyve26
|
UTSW |
12 |
79,318,901 (GRCm39) |
missense |
probably damaging |
1.00 |
R1110:Zfyve26
|
UTSW |
12 |
79,326,841 (GRCm39) |
missense |
probably damaging |
0.99 |
R1186:Zfyve26
|
UTSW |
12 |
79,310,723 (GRCm39) |
missense |
probably damaging |
1.00 |
R1295:Zfyve26
|
UTSW |
12 |
79,321,694 (GRCm39) |
missense |
probably damaging |
1.00 |
R1430:Zfyve26
|
UTSW |
12 |
79,329,591 (GRCm39) |
missense |
probably benign |
0.07 |
R1439:Zfyve26
|
UTSW |
12 |
79,298,937 (GRCm39) |
missense |
probably benign |
0.03 |
R1517:Zfyve26
|
UTSW |
12 |
79,298,925 (GRCm39) |
missense |
probably damaging |
0.98 |
R1553:Zfyve26
|
UTSW |
12 |
79,334,535 (GRCm39) |
missense |
probably benign |
0.00 |
R1721:Zfyve26
|
UTSW |
12 |
79,308,573 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1758:Zfyve26
|
UTSW |
12 |
79,285,718 (GRCm39) |
missense |
probably damaging |
1.00 |
R1779:Zfyve26
|
UTSW |
12 |
79,325,237 (GRCm39) |
missense |
probably damaging |
1.00 |
R1785:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1786:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R1826:Zfyve26
|
UTSW |
12 |
79,315,823 (GRCm39) |
missense |
probably damaging |
1.00 |
R1833:Zfyve26
|
UTSW |
12 |
79,333,032 (GRCm39) |
missense |
probably benign |
0.36 |
R1868:Zfyve26
|
UTSW |
12 |
79,308,573 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1900:Zfyve26
|
UTSW |
12 |
79,311,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Zfyve26
|
UTSW |
12 |
79,286,744 (GRCm39) |
nonsense |
probably null |
|
R1982:Zfyve26
|
UTSW |
12 |
79,302,017 (GRCm39) |
missense |
possibly damaging |
0.55 |
R2062:Zfyve26
|
UTSW |
12 |
79,330,806 (GRCm39) |
splice site |
probably null |
|
R2071:Zfyve26
|
UTSW |
12 |
79,334,220 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2130:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2132:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2133:Zfyve26
|
UTSW |
12 |
79,315,208 (GRCm39) |
missense |
possibly damaging |
0.48 |
R2135:Zfyve26
|
UTSW |
12 |
79,292,826 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2207:Zfyve26
|
UTSW |
12 |
79,292,861 (GRCm39) |
missense |
probably damaging |
0.99 |
R2280:Zfyve26
|
UTSW |
12 |
79,321,814 (GRCm39) |
missense |
probably damaging |
1.00 |
R2352:Zfyve26
|
UTSW |
12 |
79,330,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R2398:Zfyve26
|
UTSW |
12 |
79,329,573 (GRCm39) |
splice site |
probably null |
|
R3084:Zfyve26
|
UTSW |
12 |
79,312,457 (GRCm39) |
splice site |
probably benign |
|
R3086:Zfyve26
|
UTSW |
12 |
79,312,457 (GRCm39) |
splice site |
probably benign |
|
R4626:Zfyve26
|
UTSW |
12 |
79,315,844 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4727:Zfyve26
|
UTSW |
12 |
79,291,170 (GRCm39) |
missense |
probably benign |
0.16 |
R4908:Zfyve26
|
UTSW |
12 |
79,296,469 (GRCm39) |
splice site |
probably null |
|
R4926:Zfyve26
|
UTSW |
12 |
79,321,785 (GRCm39) |
missense |
probably benign |
|
R4990:Zfyve26
|
UTSW |
12 |
79,334,607 (GRCm39) |
missense |
probably damaging |
1.00 |
R4999:Zfyve26
|
UTSW |
12 |
79,327,159 (GRCm39) |
nonsense |
probably null |
|
R5029:Zfyve26
|
UTSW |
12 |
79,333,097 (GRCm39) |
missense |
probably damaging |
0.99 |
R5070:Zfyve26
|
UTSW |
12 |
79,302,135 (GRCm39) |
missense |
probably damaging |
1.00 |
R5100:Zfyve26
|
UTSW |
12 |
79,326,832 (GRCm39) |
nonsense |
probably null |
|
R5252:Zfyve26
|
UTSW |
12 |
79,315,756 (GRCm39) |
missense |
probably damaging |
1.00 |
R5318:Zfyve26
|
UTSW |
12 |
79,317,624 (GRCm39) |
missense |
probably benign |
0.35 |
R5509:Zfyve26
|
UTSW |
12 |
79,293,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R5574:Zfyve26
|
UTSW |
12 |
79,286,698 (GRCm39) |
missense |
possibly damaging |
0.63 |
R5735:Zfyve26
|
UTSW |
12 |
79,320,147 (GRCm39) |
missense |
probably damaging |
0.96 |
R5756:Zfyve26
|
UTSW |
12 |
79,311,131 (GRCm39) |
missense |
probably damaging |
1.00 |
R5773:Zfyve26
|
UTSW |
12 |
79,334,511 (GRCm39) |
missense |
probably damaging |
1.00 |
R5834:Zfyve26
|
UTSW |
12 |
79,313,311 (GRCm39) |
missense |
probably benign |
0.30 |
R6075:Zfyve26
|
UTSW |
12 |
79,340,628 (GRCm39) |
missense |
possibly damaging |
0.74 |
R6184:Zfyve26
|
UTSW |
12 |
79,315,501 (GRCm39) |
missense |
probably damaging |
0.98 |
R6235:Zfyve26
|
UTSW |
12 |
79,296,373 (GRCm39) |
missense |
probably damaging |
1.00 |
R6247:Zfyve26
|
UTSW |
12 |
79,329,758 (GRCm39) |
missense |
probably benign |
0.04 |
R6320:Zfyve26
|
UTSW |
12 |
79,286,776 (GRCm39) |
missense |
probably damaging |
0.97 |
R6548:Zfyve26
|
UTSW |
12 |
79,285,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R6887:Zfyve26
|
UTSW |
12 |
79,313,223 (GRCm39) |
missense |
probably damaging |
1.00 |
R7133:Zfyve26
|
UTSW |
12 |
79,330,926 (GRCm39) |
missense |
probably benign |
0.06 |
R7152:Zfyve26
|
UTSW |
12 |
79,325,888 (GRCm39) |
missense |
probably benign |
0.42 |
R7165:Zfyve26
|
UTSW |
12 |
79,327,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R7181:Zfyve26
|
UTSW |
12 |
79,315,182 (GRCm39) |
missense |
probably benign |
0.00 |
R7223:Zfyve26
|
UTSW |
12 |
79,292,945 (GRCm39) |
missense |
probably damaging |
0.99 |
R7296:Zfyve26
|
UTSW |
12 |
79,325,146 (GRCm39) |
splice site |
probably null |
|
R7301:Zfyve26
|
UTSW |
12 |
79,329,758 (GRCm39) |
missense |
probably benign |
0.01 |
R7302:Zfyve26
|
UTSW |
12 |
79,297,942 (GRCm39) |
missense |
probably damaging |
1.00 |
R7355:Zfyve26
|
UTSW |
12 |
79,286,828 (GRCm39) |
missense |
probably damaging |
1.00 |
R7466:Zfyve26
|
UTSW |
12 |
79,334,581 (GRCm39) |
missense |
probably benign |
0.00 |
R7540:Zfyve26
|
UTSW |
12 |
79,315,450 (GRCm39) |
missense |
probably damaging |
0.99 |
R7552:Zfyve26
|
UTSW |
12 |
79,337,731 (GRCm39) |
missense |
probably damaging |
0.97 |
R7762:Zfyve26
|
UTSW |
12 |
79,315,409 (GRCm39) |
missense |
probably benign |
0.02 |
R7806:Zfyve26
|
UTSW |
12 |
79,327,129 (GRCm39) |
critical splice donor site |
probably null |
|
R7821:Zfyve26
|
UTSW |
12 |
79,302,098 (GRCm39) |
missense |
probably damaging |
1.00 |
R8141:Zfyve26
|
UTSW |
12 |
79,315,331 (GRCm39) |
missense |
possibly damaging |
0.79 |
R8190:Zfyve26
|
UTSW |
12 |
79,327,610 (GRCm39) |
missense |
probably benign |
0.00 |
R8207:Zfyve26
|
UTSW |
12 |
79,307,605 (GRCm39) |
missense |
probably damaging |
1.00 |
R8210:Zfyve26
|
UTSW |
12 |
79,302,037 (GRCm39) |
missense |
probably damaging |
1.00 |
R8500:Zfyve26
|
UTSW |
12 |
79,334,454 (GRCm39) |
missense |
probably damaging |
0.99 |
R8686:Zfyve26
|
UTSW |
12 |
79,334,227 (GRCm39) |
missense |
probably benign |
|
R8758:Zfyve26
|
UTSW |
12 |
79,311,083 (GRCm39) |
critical splice donor site |
probably benign |
|
R8826:Zfyve26
|
UTSW |
12 |
79,285,742 (GRCm39) |
missense |
probably benign |
0.05 |
R8877:Zfyve26
|
UTSW |
12 |
79,334,152 (GRCm39) |
missense |
probably benign |
0.05 |
R9067:Zfyve26
|
UTSW |
12 |
79,318,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R9195:Zfyve26
|
UTSW |
12 |
79,311,168 (GRCm39) |
missense |
probably benign |
0.12 |
R9269:Zfyve26
|
UTSW |
12 |
79,323,076 (GRCm39) |
missense |
possibly damaging |
0.73 |
R9273:Zfyve26
|
UTSW |
12 |
79,317,610 (GRCm39) |
critical splice donor site |
probably null |
|
R9340:Zfyve26
|
UTSW |
12 |
79,321,680 (GRCm39) |
nonsense |
probably null |
|
R9348:Zfyve26
|
UTSW |
12 |
79,315,231 (GRCm39) |
missense |
possibly damaging |
0.81 |
R9482:Zfyve26
|
UTSW |
12 |
79,291,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R9536:Zfyve26
|
UTSW |
12 |
79,298,046 (GRCm39) |
missense |
probably benign |
0.32 |
R9653:Zfyve26
|
UTSW |
12 |
79,334,418 (GRCm39) |
missense |
probably benign |
|
R9676:Zfyve26
|
UTSW |
12 |
79,330,959 (GRCm39) |
missense |
probably benign |
0.01 |
R9797:Zfyve26
|
UTSW |
12 |
79,293,006 (GRCm39) |
missense |
probably damaging |
0.98 |
RF010:Zfyve26
|
UTSW |
12 |
79,302,112 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Zfyve26
|
UTSW |
12 |
79,285,779 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Zfyve26
|
UTSW |
12 |
79,315,307 (GRCm39) |
missense |
probably benign |
0.07 |
Z1177:Zfyve26
|
UTSW |
12 |
79,334,149 (GRCm39) |
missense |
probably null |
1.00 |
|