Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca14 |
A |
G |
7: 119,822,850 (GRCm39) |
I321V |
probably benign |
Het |
Adcy7 |
A |
G |
8: 89,051,391 (GRCm39) |
D837G |
probably damaging |
Het |
Aldh1a1 |
T |
A |
19: 20,617,440 (GRCm39) |
Y457* |
probably null |
Het |
Alox5 |
T |
C |
6: 116,397,323 (GRCm39) |
Y287C |
probably benign |
Het |
Ano8 |
T |
C |
8: 71,933,168 (GRCm39) |
|
probably benign |
Het |
Ap3b1 |
A |
G |
13: 94,630,189 (GRCm39) |
K815E |
unknown |
Het |
Atp11a |
A |
T |
8: 12,906,930 (GRCm39) |
|
probably benign |
Het |
Atp6v0a1 |
A |
T |
11: 100,939,341 (GRCm39) |
D702V |
possibly damaging |
Het |
Cacna1b |
T |
A |
2: 24,651,856 (GRCm39) |
N108Y |
probably damaging |
Het |
Ccdc57 |
G |
C |
11: 120,812,637 (GRCm39) |
A39G |
probably benign |
Het |
Cdhr1 |
A |
T |
14: 36,803,333 (GRCm39) |
V581D |
probably benign |
Het |
Cfap20dc |
T |
G |
14: 8,431,667 (GRCm38) |
Y655S |
probably damaging |
Het |
Cyp2b23 |
A |
G |
7: 26,372,304 (GRCm39) |
|
probably benign |
Het |
D430041D05Rik |
G |
C |
2: 103,998,295 (GRCm39) |
P1836R |
probably damaging |
Het |
Ddit4l |
C |
T |
3: 137,330,048 (GRCm39) |
|
probably benign |
Het |
Dnah8 |
A |
T |
17: 30,909,245 (GRCm39) |
I1024F |
probably benign |
Het |
Dync2i1 |
T |
C |
12: 116,221,026 (GRCm39) |
|
probably benign |
Het |
Edc3 |
T |
A |
9: 57,634,621 (GRCm39) |
F213I |
probably damaging |
Het |
Edrf1 |
G |
A |
7: 133,258,774 (GRCm39) |
D717N |
probably damaging |
Het |
Efna5 |
G |
A |
17: 62,958,068 (GRCm39) |
P63S |
probably damaging |
Het |
Elapor2 |
T |
C |
5: 9,484,681 (GRCm39) |
L486P |
probably damaging |
Het |
Entpd3 |
A |
G |
9: 120,387,547 (GRCm39) |
Y248C |
probably damaging |
Het |
Flcn |
G |
A |
11: 59,686,635 (GRCm39) |
Q373* |
probably null |
Het |
Fry |
T |
C |
5: 150,358,241 (GRCm39) |
V1908A |
probably damaging |
Het |
Gabrg3 |
A |
T |
7: 57,031,365 (GRCm39) |
Y58* |
probably null |
Het |
Gabrp |
A |
T |
11: 33,502,614 (GRCm39) |
Y417N |
probably damaging |
Het |
Golga2 |
C |
A |
2: 32,194,964 (GRCm39) |
|
probably null |
Het |
Grip2 |
C |
A |
6: 91,750,773 (GRCm39) |
|
probably null |
Het |
Gsx2 |
A |
G |
5: 75,237,729 (GRCm39) |
Y227C |
probably damaging |
Het |
H2ac1 |
T |
C |
13: 24,118,632 (GRCm39) |
V63A |
probably benign |
Het |
Hif3a |
T |
C |
7: 16,769,793 (GRCm39) |
*665W |
probably null |
Het |
Hsd3b1 |
C |
A |
3: 98,760,089 (GRCm39) |
V301L |
probably damaging |
Het |
Ifitm5 |
T |
C |
7: 140,529,921 (GRCm39) |
|
probably benign |
Het |
Inpp4a |
A |
T |
1: 37,418,067 (GRCm39) |
D498V |
probably damaging |
Het |
Itga1 |
A |
T |
13: 115,128,995 (GRCm39) |
D554E |
probably benign |
Het |
Itk |
G |
A |
11: 46,280,285 (GRCm39) |
|
probably benign |
Het |
Kdm3b |
T |
A |
18: 34,928,716 (GRCm39) |
|
probably benign |
Het |
Klhl6 |
A |
G |
16: 19,766,984 (GRCm39) |
V470A |
probably benign |
Het |
Lamb3 |
T |
A |
1: 193,002,839 (GRCm39) |
W95R |
probably damaging |
Het |
Lbhd2 |
T |
A |
12: 111,376,676 (GRCm39) |
I41N |
probably damaging |
Het |
Lrp4 |
A |
T |
2: 91,321,015 (GRCm39) |
S1014C |
probably damaging |
Het |
Ltbp2 |
C |
T |
12: 84,832,743 (GRCm39) |
|
probably null |
Het |
Map3k19 |
A |
G |
1: 127,749,919 (GRCm39) |
I1144T |
possibly damaging |
Het |
Mfsd10 |
T |
C |
5: 34,792,507 (GRCm39) |
|
probably benign |
Het |
Mocos |
A |
G |
18: 24,799,333 (GRCm39) |
D189G |
probably benign |
Het |
Mvb12a |
T |
A |
8: 71,999,654 (GRCm39) |
F224L |
probably damaging |
Het |
Myo15a |
A |
T |
11: 60,405,723 (GRCm39) |
|
probably null |
Het |
Nos2 |
A |
T |
11: 78,828,428 (GRCm39) |
H249L |
probably damaging |
Het |
Notum |
A |
G |
11: 120,549,160 (GRCm39) |
M184T |
probably benign |
Het |
Nvl |
C |
A |
1: 180,962,395 (GRCm39) |
D192Y |
probably damaging |
Het |
Or10j3 |
A |
G |
1: 173,031,484 (GRCm39) |
K187R |
probably benign |
Het |
Or4f57 |
T |
C |
2: 111,790,839 (GRCm39) |
Y193C |
probably damaging |
Het |
Or5m12 |
T |
A |
2: 85,734,591 (GRCm39) |
N269I |
probably benign |
Het |
Or8k27 |
C |
A |
2: 86,276,303 (GRCm39) |
V8L |
probably benign |
Het |
Osgin1 |
A |
G |
8: 120,172,396 (GRCm39) |
I397V |
possibly damaging |
Het |
Otulin |
A |
G |
15: 27,616,510 (GRCm39) |
V123A |
probably damaging |
Het |
P4ha1 |
A |
G |
10: 59,184,081 (GRCm39) |
Y181C |
probably damaging |
Het |
Pcdhgc5 |
A |
T |
18: 37,954,403 (GRCm39) |
D559V |
probably damaging |
Het |
Phf2 |
T |
C |
13: 48,982,270 (GRCm39) |
N151S |
unknown |
Het |
Plxnc1 |
C |
A |
10: 94,648,991 (GRCm39) |
G1263C |
probably benign |
Het |
Rad51ap1 |
A |
G |
6: 126,901,160 (GRCm39) |
*338Q |
probably null |
Het |
Raver1 |
A |
G |
9: 20,986,955 (GRCm39) |
S676P |
probably benign |
Het |
Rfx8 |
T |
C |
1: 39,727,737 (GRCm39) |
E196G |
possibly damaging |
Het |
Rreb1 |
A |
T |
13: 38,100,131 (GRCm39) |
K187* |
probably null |
Het |
Rxfp1 |
T |
C |
3: 79,574,961 (GRCm39) |
T217A |
probably benign |
Het |
Rxra |
T |
C |
2: 27,642,442 (GRCm39) |
L305P |
probably damaging |
Het |
Sardh |
T |
C |
2: 27,117,078 (GRCm39) |
|
probably benign |
Het |
Skor2 |
A |
T |
18: 76,964,293 (GRCm39) |
E952D |
probably damaging |
Het |
Slc22a29 |
A |
T |
19: 8,147,334 (GRCm39) |
S343T |
probably benign |
Het |
Sorbs2 |
T |
C |
8: 46,238,374 (GRCm39) |
|
probably benign |
Het |
Supt7l |
C |
T |
5: 31,673,262 (GRCm39) |
V329I |
probably benign |
Het |
Taar2 |
G |
A |
10: 23,817,393 (GRCm39) |
R311H |
probably benign |
Het |
Tac1 |
T |
C |
6: 7,559,165 (GRCm39) |
|
probably benign |
Het |
Tcn2 |
A |
T |
11: 3,872,044 (GRCm39) |
V361D |
probably damaging |
Het |
Tm2d3 |
G |
A |
7: 65,347,582 (GRCm39) |
A170T |
possibly damaging |
Het |
Tnks |
G |
A |
8: 35,307,124 (GRCm39) |
R1142* |
probably null |
Het |
Ttll7 |
C |
A |
3: 146,649,915 (GRCm39) |
Y648* |
probably null |
Het |
Umod |
G |
T |
7: 119,065,296 (GRCm39) |
Q578K |
probably benign |
Het |
Upf2 |
G |
A |
2: 6,032,015 (GRCm39) |
|
probably benign |
Het |
Vmn2r92 |
C |
T |
17: 18,388,219 (GRCm39) |
A408V |
probably damaging |
Het |
Washc5 |
A |
G |
15: 59,210,809 (GRCm39) |
I1013T |
probably benign |
Het |
Zfp704 |
C |
A |
3: 9,630,217 (GRCm39) |
R48L |
probably damaging |
Het |
|
Other mutations in Or5ac22 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01771:Or5ac22
|
APN |
16 |
59,134,891 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01915:Or5ac22
|
APN |
16 |
59,135,473 (GRCm39) |
missense |
probably damaging |
1.00 |
R0532:Or5ac22
|
UTSW |
16 |
59,134,964 (GRCm39) |
missense |
probably benign |
0.00 |
R1719:Or5ac22
|
UTSW |
16 |
59,135,069 (GRCm39) |
nonsense |
probably null |
|
R1864:Or5ac22
|
UTSW |
16 |
59,135,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R1889:Or5ac22
|
UTSW |
16 |
59,135,326 (GRCm39) |
missense |
probably damaging |
0.98 |
R1925:Or5ac22
|
UTSW |
16 |
59,135,027 (GRCm39) |
missense |
probably damaging |
1.00 |
R2973:Or5ac22
|
UTSW |
16 |
59,135,767 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R3078:Or5ac22
|
UTSW |
16 |
59,135,089 (GRCm39) |
missense |
probably benign |
|
R3819:Or5ac22
|
UTSW |
16 |
59,135,434 (GRCm39) |
missense |
probably damaging |
1.00 |
R4036:Or5ac22
|
UTSW |
16 |
59,135,113 (GRCm39) |
missense |
probably benign |
|
R4698:Or5ac22
|
UTSW |
16 |
59,135,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R4930:Or5ac22
|
UTSW |
16 |
59,135,236 (GRCm39) |
missense |
probably damaging |
1.00 |
R5457:Or5ac22
|
UTSW |
16 |
59,135,213 (GRCm39) |
missense |
probably benign |
0.12 |
R6597:Or5ac22
|
UTSW |
16 |
59,135,713 (GRCm39) |
missense |
probably benign |
0.00 |
R7341:Or5ac22
|
UTSW |
16 |
59,135,512 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7512:Or5ac22
|
UTSW |
16 |
59,135,390 (GRCm39) |
missense |
probably damaging |
0.99 |
R7702:Or5ac22
|
UTSW |
16 |
59,134,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R8132:Or5ac22
|
UTSW |
16 |
59,134,907 (GRCm39) |
missense |
possibly damaging |
0.55 |
R9642:Or5ac22
|
UTSW |
16 |
59,135,610 (GRCm39) |
missense |
possibly damaging |
0.70 |
|