Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Agtr1b |
G |
T |
3: 20,369,943 (GRCm39) |
A221D |
probably benign |
Het |
Apob |
G |
A |
12: 8,039,194 (GRCm39) |
D475N |
probably benign |
Het |
Bmi1 |
C |
T |
2: 18,689,186 (GRCm39) |
T290I |
probably benign |
Het |
Brd8 |
A |
T |
18: 34,746,292 (GRCm39) |
D139E |
possibly damaging |
Het |
Cacna1e |
C |
A |
1: 154,317,270 (GRCm39) |
V1467F |
possibly damaging |
Het |
Cdh15 |
A |
G |
8: 123,591,086 (GRCm39) |
D445G |
probably benign |
Het |
Ceacam5 |
T |
A |
7: 17,481,123 (GRCm39) |
L290H |
probably damaging |
Het |
Celsr1 |
G |
T |
15: 85,785,160 (GRCm39) |
Q3025K |
probably benign |
Het |
Chi3l1 |
T |
A |
1: 134,109,996 (GRCm39) |
M1K |
probably null |
Het |
Crybg2 |
T |
C |
4: 133,808,737 (GRCm39) |
S1404P |
probably damaging |
Het |
Cubn |
C |
A |
2: 13,285,006 (GRCm39) |
C3470F |
probably damaging |
Het |
Cyp20a1 |
T |
C |
1: 60,391,331 (GRCm39) |
|
probably null |
Het |
Cyp24a1 |
G |
T |
2: 170,328,704 (GRCm39) |
T408K |
probably benign |
Het |
Cyp2a12 |
A |
T |
7: 26,730,577 (GRCm39) |
I181F |
possibly damaging |
Het |
Dnm1l |
A |
T |
16: 16,149,952 (GRCm39) |
I268N |
probably damaging |
Het |
Eif2a |
A |
G |
3: 58,464,517 (GRCm39) |
|
probably null |
Het |
Epg5 |
T |
C |
18: 78,005,613 (GRCm39) |
F701S |
probably damaging |
Het |
Fbxo46 |
T |
C |
7: 18,870,466 (GRCm39) |
S362P |
possibly damaging |
Het |
Fgf22 |
A |
G |
10: 79,592,830 (GRCm39) |
|
probably benign |
Het |
Fhod1 |
A |
C |
8: 106,063,982 (GRCm39) |
|
probably benign |
Het |
Flnc |
T |
A |
6: 29,459,062 (GRCm39) |
V2448D |
probably damaging |
Het |
Gm2696 |
G |
T |
10: 77,671,972 (GRCm39) |
|
probably benign |
Het |
Gmpr |
T |
C |
13: 45,685,874 (GRCm39) |
S214P |
possibly damaging |
Het |
Krt6a |
A |
G |
15: 101,600,744 (GRCm39) |
V308A |
probably damaging |
Het |
Lig3 |
T |
A |
11: 82,684,833 (GRCm39) |
|
probably null |
Het |
Lrrc37a |
T |
A |
11: 103,394,877 (GRCm39) |
N183Y |
probably benign |
Het |
Mapk8ip3 |
C |
A |
17: 25,125,879 (GRCm39) |
G422V |
probably damaging |
Het |
Mks1 |
T |
C |
11: 87,746,325 (GRCm39) |
S97P |
probably benign |
Het |
Mphosph9 |
A |
T |
5: 124,463,024 (GRCm39) |
V7E |
probably damaging |
Het |
Msh5 |
A |
G |
17: 35,248,900 (GRCm39) |
L711P |
probably damaging |
Het |
Naga |
T |
A |
15: 82,216,404 (GRCm39) |
|
probably null |
Het |
Nherf4 |
A |
G |
9: 44,159,980 (GRCm39) |
V380A |
probably benign |
Het |
Nlrp10 |
T |
A |
7: 108,524,953 (GRCm39) |
T176S |
possibly damaging |
Het |
Nqo1 |
T |
C |
8: 108,115,582 (GRCm39) |
N232D |
probably benign |
Het |
Or1j21 |
C |
G |
2: 36,683,585 (GRCm39) |
N112K |
possibly damaging |
Het |
Or2b6 |
T |
A |
13: 21,823,418 (GRCm39) |
I92L |
probably damaging |
Het |
P2ry6 |
A |
G |
7: 100,587,603 (GRCm39) |
F252S |
probably damaging |
Het |
P3h3 |
G |
A |
6: 124,831,835 (GRCm39) |
R317W |
probably benign |
Het |
Pakap |
T |
A |
4: 57,710,173 (GRCm39) |
C373S |
probably damaging |
Het |
Phkb |
T |
A |
8: 86,602,327 (GRCm39) |
D39E |
probably benign |
Het |
Psg16 |
G |
A |
7: 16,822,112 (GRCm39) |
G23D |
probably damaging |
Het |
Ptgr2 |
T |
A |
12: 84,349,111 (GRCm39) |
I150K |
probably benign |
Het |
Ptprf |
A |
G |
4: 118,070,011 (GRCm39) |
V1457A |
probably benign |
Het |
Sart3 |
A |
T |
5: 113,889,301 (GRCm39) |
Y508N |
probably benign |
Het |
Sh3bp1 |
C |
T |
15: 78,795,715 (GRCm39) |
P615S |
probably damaging |
Het |
Ska3 |
A |
T |
14: 58,054,148 (GRCm39) |
N267K |
probably benign |
Het |
Slc26a7 |
A |
G |
4: 14,524,498 (GRCm39) |
I462T |
probably benign |
Het |
Slu7 |
C |
T |
11: 43,332,316 (GRCm39) |
A244V |
probably benign |
Het |
Smarca4 |
C |
T |
9: 21,548,671 (GRCm39) |
P319L |
probably damaging |
Het |
Smg9 |
A |
G |
7: 24,120,286 (GRCm39) |
D420G |
probably benign |
Het |
Strc |
T |
A |
2: 121,205,439 (GRCm39) |
D25V |
probably benign |
Het |
Syne2 |
T |
G |
12: 76,108,424 (GRCm39) |
V936G |
probably damaging |
Het |
Tbc1d7 |
C |
T |
13: 43,306,409 (GRCm39) |
|
probably benign |
Het |
Terb1 |
C |
A |
8: 105,173,831 (GRCm39) |
D751Y |
probably damaging |
Het |
Trpc1 |
A |
G |
9: 95,603,303 (GRCm39) |
Y410H |
probably damaging |
Het |
Ush2a |
A |
G |
1: 188,089,043 (GRCm39) |
N333D |
probably benign |
Het |
Usp34 |
T |
C |
11: 23,402,520 (GRCm39) |
S2438P |
probably damaging |
Het |
Vps35l |
T |
C |
7: 118,353,072 (GRCm39) |
V189A |
probably benign |
Het |
Zbtb17 |
G |
A |
4: 141,190,694 (GRCm39) |
G171S |
probably benign |
Het |
Zfp7 |
G |
A |
15: 76,774,810 (GRCm39) |
G284D |
possibly damaging |
Het |
Zfyve26 |
A |
G |
12: 79,286,776 (GRCm39) |
S2271P |
probably damaging |
Het |
Zscan18 |
G |
A |
7: 12,509,147 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Aldh18a1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01020:Aldh18a1
|
APN |
19 |
40,557,625 (GRCm39) |
splice site |
probably benign |
|
IGL02353:Aldh18a1
|
APN |
19 |
40,566,364 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02360:Aldh18a1
|
APN |
19 |
40,566,364 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02974:Aldh18a1
|
APN |
19 |
40,557,528 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL03295:Aldh18a1
|
APN |
19 |
40,551,386 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4498001:Aldh18a1
|
UTSW |
19 |
40,562,800 (GRCm39) |
missense |
probably benign |
|
R0267:Aldh18a1
|
UTSW |
19 |
40,562,233 (GRCm39) |
missense |
probably benign |
0.25 |
R0498:Aldh18a1
|
UTSW |
19 |
40,562,716 (GRCm39) |
missense |
probably benign |
0.29 |
R1140:Aldh18a1
|
UTSW |
19 |
40,562,729 (GRCm39) |
missense |
probably benign |
0.01 |
R1142:Aldh18a1
|
UTSW |
19 |
40,539,657 (GRCm39) |
missense |
probably damaging |
0.97 |
R1509:Aldh18a1
|
UTSW |
19 |
40,545,927 (GRCm39) |
missense |
probably damaging |
0.98 |
R1640:Aldh18a1
|
UTSW |
19 |
40,573,943 (GRCm39) |
missense |
probably benign |
|
R1721:Aldh18a1
|
UTSW |
19 |
40,553,282 (GRCm39) |
missense |
probably damaging |
1.00 |
R3012:Aldh18a1
|
UTSW |
19 |
40,546,135 (GRCm39) |
nonsense |
probably null |
|
R3085:Aldh18a1
|
UTSW |
19 |
40,562,813 (GRCm39) |
missense |
probably benign |
|
R3815:Aldh18a1
|
UTSW |
19 |
40,558,944 (GRCm39) |
missense |
probably damaging |
1.00 |
R3863:Aldh18a1
|
UTSW |
19 |
40,539,758 (GRCm39) |
missense |
probably damaging |
1.00 |
R4156:Aldh18a1
|
UTSW |
19 |
40,539,725 (GRCm39) |
missense |
probably damaging |
1.00 |
R5116:Aldh18a1
|
UTSW |
19 |
40,541,949 (GRCm39) |
missense |
probably benign |
|
R5135:Aldh18a1
|
UTSW |
19 |
40,543,261 (GRCm39) |
intron |
probably benign |
|
R5393:Aldh18a1
|
UTSW |
19 |
40,574,011 (GRCm39) |
missense |
probably benign |
0.00 |
R5492:Aldh18a1
|
UTSW |
19 |
40,539,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5493:Aldh18a1
|
UTSW |
19 |
40,539,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5494:Aldh18a1
|
UTSW |
19 |
40,539,734 (GRCm39) |
missense |
probably damaging |
1.00 |
R5957:Aldh18a1
|
UTSW |
19 |
40,558,981 (GRCm39) |
nonsense |
probably null |
|
R6255:Aldh18a1
|
UTSW |
19 |
40,568,487 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6358:Aldh18a1
|
UTSW |
19 |
40,566,122 (GRCm39) |
missense |
possibly damaging |
0.83 |
R6379:Aldh18a1
|
UTSW |
19 |
40,566,214 (GRCm39) |
critical splice donor site |
probably null |
|
R6785:Aldh18a1
|
UTSW |
19 |
40,556,788 (GRCm39) |
missense |
probably damaging |
1.00 |
R7334:Aldh18a1
|
UTSW |
19 |
40,539,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R7549:Aldh18a1
|
UTSW |
19 |
40,553,291 (GRCm39) |
missense |
probably damaging |
1.00 |
R7935:Aldh18a1
|
UTSW |
19 |
40,562,226 (GRCm39) |
nonsense |
probably null |
|
R7960:Aldh18a1
|
UTSW |
19 |
40,546,264 (GRCm39) |
missense |
probably benign |
0.03 |
R8152:Aldh18a1
|
UTSW |
19 |
40,553,456 (GRCm39) |
missense |
probably benign |
0.01 |
R8179:Aldh18a1
|
UTSW |
19 |
40,545,952 (GRCm39) |
missense |
probably damaging |
1.00 |
R8181:Aldh18a1
|
UTSW |
19 |
40,545,881 (GRCm39) |
missense |
probably benign |
0.27 |
R8222:Aldh18a1
|
UTSW |
19 |
40,562,296 (GRCm39) |
missense |
probably benign |
0.00 |
R8787:Aldh18a1
|
UTSW |
19 |
40,546,230 (GRCm39) |
missense |
possibly damaging |
0.50 |
|