Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca8b |
T |
C |
11: 109,862,640 (GRCm39) |
K375R |
possibly damaging |
Het |
Adrb2 |
T |
C |
18: 62,311,871 (GRCm39) |
N318S |
probably damaging |
Het |
Akap5 |
A |
C |
12: 76,376,036 (GRCm39) |
E489D |
possibly damaging |
Het |
Aldh7a1 |
T |
A |
18: 56,665,133 (GRCm39) |
I385F |
probably damaging |
Het |
Astn1 |
T |
A |
1: 158,407,146 (GRCm39) |
|
probably benign |
Het |
Atp7b |
T |
A |
8: 22,487,374 (GRCm39) |
T1314S |
probably damaging |
Het |
Bhmt2 |
C |
A |
13: 93,798,847 (GRCm39) |
G325C |
probably damaging |
Het |
Brpf1 |
T |
A |
6: 113,296,050 (GRCm39) |
V781E |
probably benign |
Het |
Cacna1c |
T |
A |
6: 118,575,720 (GRCm39) |
Y1860F |
probably benign |
Het |
Ccdc7a |
T |
C |
8: 129,788,162 (GRCm39) |
T56A |
probably damaging |
Het |
Cep78 |
A |
G |
19: 15,937,027 (GRCm39) |
S560P |
probably damaging |
Het |
Cnot1 |
G |
A |
8: 96,469,841 (GRCm39) |
T1343I |
probably benign |
Het |
Coq10b |
T |
C |
1: 55,103,416 (GRCm39) |
S65P |
probably damaging |
Het |
Creld1 |
T |
A |
6: 113,466,745 (GRCm39) |
C243S |
probably damaging |
Het |
Cst12 |
A |
T |
2: 148,635,172 (GRCm39) |
I121F |
possibly damaging |
Het |
Cyp26a1 |
A |
C |
19: 37,687,308 (GRCm39) |
E165A |
probably benign |
Het |
Cyp2d12 |
T |
G |
15: 82,442,337 (GRCm39) |
M273R |
probably damaging |
Het |
Dnajb7 |
T |
A |
15: 81,291,657 (GRCm39) |
S227C |
probably damaging |
Het |
Evc |
T |
A |
5: 37,476,379 (GRCm39) |
Q390L |
probably damaging |
Het |
F830016B08Rik |
T |
A |
18: 60,433,970 (GRCm39) |
L351* |
probably null |
Het |
Fga |
T |
C |
3: 82,939,145 (GRCm39) |
S507P |
probably benign |
Het |
Gba1 |
A |
T |
3: 89,113,455 (GRCm39) |
Y239F |
probably damaging |
Het |
Golga2 |
C |
A |
2: 32,195,996 (GRCm39) |
Y843* |
probably null |
Het |
Gria4 |
C |
A |
9: 4,793,865 (GRCm39) |
L64F |
probably damaging |
Het |
Hectd3 |
A |
G |
4: 116,860,191 (GRCm39) |
Y803C |
probably damaging |
Het |
Hmcn1 |
T |
C |
1: 150,545,172 (GRCm39) |
K2812E |
probably damaging |
Het |
Il17b |
T |
G |
18: 61,823,316 (GRCm39) |
V50G |
probably damaging |
Het |
Itga2b |
A |
T |
11: 102,357,151 (GRCm39) |
L243* |
probably null |
Het |
Kank4 |
C |
A |
4: 98,667,266 (GRCm39) |
V394L |
possibly damaging |
Het |
Kat14 |
T |
A |
2: 144,215,711 (GRCm39) |
D65E |
probably benign |
Het |
Kcnh3 |
T |
C |
15: 99,136,090 (GRCm39) |
Y696H |
probably damaging |
Het |
Kctd19 |
C |
A |
8: 106,122,008 (GRCm39) |
D180Y |
probably damaging |
Het |
Klra8 |
A |
C |
6: 130,092,603 (GRCm39) |
S233A |
probably benign |
Het |
Masp2 |
A |
T |
4: 148,696,563 (GRCm39) |
T387S |
possibly damaging |
Het |
Midn |
C |
A |
10: 79,989,957 (GRCm39) |
T275N |
probably damaging |
Het |
Mis18bp1 |
A |
G |
12: 65,180,587 (GRCm39) |
F965L |
probably benign |
Het |
Myo3a |
G |
T |
2: 22,287,445 (GRCm39) |
V186L |
probably damaging |
Het |
Ncoa2 |
T |
A |
1: 13,235,281 (GRCm39) |
N884I |
probably benign |
Het |
Or10d4 |
T |
C |
9: 39,581,016 (GRCm39) |
I221T |
probably damaging |
Het |
Or13c25 |
A |
T |
4: 52,911,502 (GRCm39) |
C97* |
probably null |
Het |
Or8k35 |
T |
A |
2: 86,424,948 (GRCm39) |
T75S |
probably damaging |
Het |
Osr2 |
T |
C |
15: 35,300,813 (GRCm39) |
V123A |
probably benign |
Het |
P4ha2 |
A |
G |
11: 54,008,471 (GRCm39) |
H226R |
probably benign |
Het |
Pcdhb16 |
T |
A |
18: 37,611,151 (GRCm39) |
V37E |
probably benign |
Het |
Pcdhb18 |
T |
A |
18: 37,622,673 (GRCm39) |
M1K |
probably null |
Het |
Pcsk1 |
T |
A |
13: 75,246,166 (GRCm39) |
Y181* |
probably null |
Het |
Pros1 |
G |
T |
16: 62,705,875 (GRCm39) |
C63F |
probably damaging |
Het |
Ranbp3l |
T |
A |
15: 9,065,081 (GRCm39) |
C353* |
probably null |
Het |
Rev3l |
T |
C |
10: 39,714,439 (GRCm39) |
Y2388H |
probably benign |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rpl12-ps1 |
G |
T |
1: 36,997,458 (GRCm39) |
|
noncoding transcript |
Het |
Rttn |
T |
C |
18: 89,131,474 (GRCm39) |
V1951A |
probably benign |
Het |
Scn9a |
G |
A |
2: 66,335,371 (GRCm39) |
|
probably benign |
Het |
Sdk1 |
T |
C |
5: 142,113,591 (GRCm39) |
F1546S |
probably damaging |
Het |
Sh3glb2 |
C |
T |
2: 30,244,987 (GRCm39) |
R71Q |
probably damaging |
Het |
Slc30a6 |
T |
C |
17: 74,715,842 (GRCm39) |
F101L |
probably benign |
Het |
Snrpd1 |
T |
C |
18: 10,626,913 (GRCm39) |
I60T |
probably damaging |
Het |
Sox10 |
T |
A |
15: 79,043,378 (GRCm39) |
E218D |
probably benign |
Het |
Tekt3 |
C |
A |
11: 62,961,316 (GRCm39) |
H162N |
probably damaging |
Het |
Tnfsf13 |
T |
C |
11: 69,575,564 (GRCm39) |
S246G |
possibly damaging |
Het |
Trim10 |
T |
A |
17: 37,183,346 (GRCm39) |
I214N |
probably damaging |
Het |
Trp63 |
C |
A |
16: 25,708,003 (GRCm39) |
D566E |
probably damaging |
Het |
Uck2 |
T |
C |
1: 167,062,293 (GRCm39) |
D156G |
probably damaging |
Het |
Zfp386 |
T |
A |
12: 116,023,225 (GRCm39) |
S314R |
possibly damaging |
Het |
Zfp467 |
C |
T |
6: 48,415,170 (GRCm39) |
R494H |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,601,470 (GRCm39) |
D138V |
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 |
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 |
|
R7299:Zfyve26
|
UTSW |
12 |
79,329,758 (GRCm39) |
missense |
probably benign |
0.01 |
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 |
|