Other mutations in this stock |
Total: 71 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
A |
G |
11: 84,282,356 (GRCm39) |
T2158A |
probably benign |
Het |
Apeh |
G |
A |
9: 107,969,878 (GRCm39) |
H186Y |
probably damaging |
Het |
Apol7a |
T |
C |
15: 77,277,520 (GRCm39) |
|
probably null |
Het |
Bicdl1 |
C |
T |
5: 115,810,202 (GRCm39) |
|
probably null |
Het |
Bop1 |
T |
A |
15: 76,339,183 (GRCm39) |
Q362L |
probably damaging |
Het |
C4b |
T |
C |
17: 34,949,930 (GRCm39) |
D1418G |
probably benign |
Het |
Cdh23 |
A |
G |
10: 60,214,650 (GRCm39) |
V1455A |
possibly damaging |
Het |
Cecr2 |
T |
G |
6: 120,711,503 (GRCm39) |
|
probably null |
Het |
Cer1 |
T |
C |
4: 82,801,052 (GRCm39) |
S204G |
probably benign |
Het |
Cers3 |
G |
C |
7: 66,413,968 (GRCm39) |
W15C |
probably damaging |
Het |
Csn1s2a |
A |
T |
5: 87,929,731 (GRCm39) |
H110L |
probably benign |
Het |
Dnah10 |
T |
G |
5: 124,867,064 (GRCm39) |
|
probably null |
Het |
Dync2h1 |
T |
C |
9: 7,041,718 (GRCm39) |
N3315S |
probably benign |
Het |
Dynlrb2 |
T |
C |
8: 117,234,299 (GRCm39) |
M21T |
probably benign |
Het |
Emilin1 |
T |
A |
5: 31,072,871 (GRCm39) |
F103I |
probably benign |
Het |
Esrra |
T |
A |
19: 6,889,142 (GRCm39) |
M416L |
probably benign |
Het |
Etaa1 |
C |
A |
11: 17,902,680 (GRCm39) |
V86L |
probably benign |
Het |
Extl3 |
A |
G |
14: 65,314,211 (GRCm39) |
S324P |
probably damaging |
Het |
Fam90a1a |
T |
C |
8: 22,453,368 (GRCm39) |
V241A |
probably benign |
Het |
Fat4 |
C |
A |
3: 39,036,589 (GRCm39) |
Q3414K |
probably benign |
Het |
Gpr162 |
C |
T |
6: 124,838,164 (GRCm39) |
R162H |
probably damaging |
Het |
Gpr21 |
T |
A |
2: 37,407,974 (GRCm39) |
Y173* |
probably null |
Het |
Gprc6a |
G |
A |
10: 51,502,841 (GRCm39) |
Q341* |
probably null |
Het |
Herc2 |
T |
A |
7: 55,814,670 (GRCm39) |
S2674R |
probably damaging |
Het |
Hnrnpdl |
A |
T |
5: 100,186,995 (GRCm39) |
H9Q |
probably null |
Het |
Hps1 |
A |
G |
19: 42,759,217 (GRCm39) |
V125A |
possibly damaging |
Het |
Iba57 |
G |
T |
11: 59,049,440 (GRCm39) |
P243H |
probably damaging |
Het |
Incenp |
G |
T |
19: 9,855,120 (GRCm39) |
A597E |
unknown |
Het |
Kat6a |
T |
A |
8: 23,430,384 (GRCm39) |
M1913K |
unknown |
Het |
Klb |
G |
A |
5: 65,536,877 (GRCm39) |
V736M |
probably damaging |
Het |
Krt33a |
T |
A |
11: 99,903,209 (GRCm39) |
T278S |
possibly damaging |
Het |
Krt73 |
T |
G |
15: 101,704,842 (GRCm39) |
E348A |
probably damaging |
Het |
Lig3 |
T |
A |
11: 82,674,577 (GRCm39) |
D134E |
probably benign |
Het |
Limd2 |
T |
C |
11: 106,049,771 (GRCm39) |
T73A |
probably benign |
Het |
Lrpprc |
A |
G |
17: 85,056,531 (GRCm39) |
S787P |
possibly damaging |
Het |
Macf1 |
A |
G |
4: 123,268,208 (GRCm39) |
M6735T |
probably damaging |
Het |
Mapkbp1 |
C |
A |
2: 119,851,640 (GRCm39) |
Q861K |
probably damaging |
Het |
Mc4r |
T |
A |
18: 66,992,927 (GRCm39) |
N62I |
probably damaging |
Het |
Metap1d |
G |
A |
2: 71,341,858 (GRCm39) |
V151I |
probably damaging |
Het |
Nek2 |
T |
C |
1: 191,554,729 (GRCm39) |
V147A |
probably damaging |
Het |
Nlrp1b |
A |
T |
11: 71,108,530 (GRCm39) |
W324R |
probably damaging |
Het |
Nol4l |
G |
T |
2: 153,325,746 (GRCm39) |
S113* |
probably null |
Het |
Oc90 |
T |
A |
15: 65,761,463 (GRCm39) |
D185V |
probably damaging |
Het |
Or2a52 |
T |
C |
6: 43,144,172 (GRCm39) |
F60S |
probably damaging |
Het |
Or2v1 |
G |
A |
11: 49,025,805 (GRCm39) |
R262K |
probably damaging |
Het |
Or4a71 |
G |
A |
2: 89,357,932 (GRCm39) |
T274M |
probably damaging |
Het |
Or5p51 |
T |
A |
7: 107,444,797 (GRCm39) |
T48S |
possibly damaging |
Het |
Or8g50 |
A |
T |
9: 39,648,914 (GRCm39) |
K268* |
probably null |
Het |
Pcdha8 |
A |
G |
18: 37,127,401 (GRCm39) |
T628A |
probably damaging |
Het |
Pcsk5 |
A |
T |
19: 17,549,986 (GRCm39) |
|
probably null |
Het |
Pdgfrb |
T |
C |
18: 61,211,721 (GRCm39) |
|
probably null |
Het |
Pgm3 |
A |
T |
9: 86,438,555 (GRCm39) |
|
probably null |
Het |
Pin1rt1 |
T |
A |
2: 104,545,063 (GRCm39) |
Y23F |
probably benign |
Het |
Poli |
T |
A |
18: 70,663,222 (GRCm39) |
|
probably null |
Het |
Pom121 |
C |
A |
5: 135,409,978 (GRCm39) |
|
probably benign |
Het |
Ppp2r5c |
A |
G |
12: 110,535,456 (GRCm39) |
D407G |
possibly damaging |
Het |
Pramel28 |
A |
G |
4: 143,691,581 (GRCm39) |
S381P |
probably damaging |
Het |
Rgs12 |
A |
G |
5: 35,180,515 (GRCm39) |
D116G |
probably null |
Het |
Serpina3b |
A |
T |
12: 104,099,251 (GRCm39) |
E255D |
probably benign |
Het |
Sft2d1rt |
T |
C |
11: 45,942,859 (GRCm39) |
Q88R |
probably damaging |
Het |
Slc46a1 |
A |
G |
11: 78,357,790 (GRCm39) |
H281R |
probably damaging |
Het |
Spata6 |
T |
C |
4: 111,642,012 (GRCm39) |
I294T |
probably benign |
Het |
Srgap1 |
T |
A |
10: 121,664,631 (GRCm39) |
|
probably null |
Het |
Stag1 |
C |
T |
9: 100,826,903 (GRCm39) |
R957C |
probably damaging |
Het |
Stk35 |
G |
A |
2: 129,643,573 (GRCm39) |
E186K |
probably damaging |
Het |
Tenm4 |
G |
A |
7: 96,202,703 (GRCm39) |
R106H |
probably benign |
Het |
Tenm4 |
G |
A |
7: 96,544,478 (GRCm39) |
V2165I |
probably damaging |
Het |
Tmem53 |
T |
C |
4: 117,125,528 (GRCm39) |
S207P |
probably benign |
Het |
Ugt2a3 |
A |
G |
5: 87,484,617 (GRCm39) |
F136L |
probably benign |
Het |
Unc13d |
T |
C |
11: 115,957,577 (GRCm39) |
K795E |
probably damaging |
Het |
Zbtb11 |
C |
A |
16: 55,810,865 (GRCm39) |
T341K |
probably benign |
Het |
|
Other mutations in Or5m13 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01660:Or5m13
|
APN |
2 |
85,748,908 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02881:Or5m13
|
APN |
2 |
85,748,460 (GRCm39) |
missense |
probably benign |
0.00 |
R0097:Or5m13
|
UTSW |
2 |
85,749,184 (GRCm39) |
missense |
probably benign |
0.00 |
R0097:Or5m13
|
UTSW |
2 |
85,749,184 (GRCm39) |
missense |
probably benign |
0.00 |
R0324:Or5m13
|
UTSW |
2 |
85,748,295 (GRCm39) |
missense |
probably benign |
0.22 |
R0392:Or5m13
|
UTSW |
2 |
85,749,106 (GRCm39) |
missense |
possibly damaging |
0.81 |
R0765:Or5m13
|
UTSW |
2 |
85,749,049 (GRCm39) |
missense |
probably damaging |
0.99 |
R1199:Or5m13
|
UTSW |
2 |
85,748,379 (GRCm39) |
missense |
probably benign |
0.00 |
R1894:Or5m13
|
UTSW |
2 |
85,748,599 (GRCm39) |
missense |
probably benign |
0.28 |
R2027:Or5m13
|
UTSW |
2 |
85,749,114 (GRCm39) |
missense |
probably damaging |
0.99 |
R2141:Or5m13
|
UTSW |
2 |
85,749,171 (GRCm39) |
missense |
probably null |
|
R3871:Or5m13
|
UTSW |
2 |
85,748,926 (GRCm39) |
splice site |
probably null |
|
R4837:Or5m13
|
UTSW |
2 |
85,748,748 (GRCm39) |
missense |
probably benign |
0.00 |
R4945:Or5m13
|
UTSW |
2 |
85,748,917 (GRCm39) |
missense |
possibly damaging |
0.81 |
R5056:Or5m13
|
UTSW |
2 |
85,748,480 (GRCm39) |
missense |
probably damaging |
1.00 |
R5441:Or5m13
|
UTSW |
2 |
85,748,934 (GRCm39) |
missense |
probably benign |
0.01 |
R5960:Or5m13
|
UTSW |
2 |
85,749,069 (GRCm39) |
missense |
probably benign |
0.07 |
R7320:Or5m13
|
UTSW |
2 |
85,748,718 (GRCm39) |
missense |
probably benign |
0.00 |
R8523:Or5m13
|
UTSW |
2 |
85,748,407 (GRCm39) |
missense |
probably damaging |
0.97 |
R8715:Or5m13
|
UTSW |
2 |
85,748,273 (GRCm39) |
start codon destroyed |
probably null |
0.81 |
R8734:Or5m13
|
UTSW |
2 |
85,748,993 (GRCm39) |
nonsense |
probably null |
|
R9275:Or5m13
|
UTSW |
2 |
85,749,046 (GRCm39) |
missense |
probably benign |
0.17 |
R9427:Or5m13
|
UTSW |
2 |
85,748,704 (GRCm39) |
missense |
probably benign |
0.00 |
R9728:Or5m13
|
UTSW |
2 |
85,748,887 (GRCm39) |
missense |
possibly damaging |
0.72 |
V1662:Or5m13
|
UTSW |
2 |
85,748,938 (GRCm39) |
missense |
probably benign |
0.10 |
Z1176:Or5m13
|
UTSW |
2 |
85,748,845 (GRCm39) |
missense |
probably damaging |
0.99 |
|