Other mutations in this stock |
Total: 63 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ak1 |
A |
T |
2: 32,520,391 (GRCm39) |
K79M |
probably benign |
Het |
Amy1 |
T |
C |
3: 113,356,278 (GRCm39) |
K293E |
probably benign |
Het |
Bcl2l10 |
A |
G |
9: 75,255,333 (GRCm39) |
Q50R |
probably benign |
Het |
Bpifa6 |
G |
A |
2: 153,826,740 (GRCm39) |
G35D |
probably benign |
Het |
Cachd1 |
C |
A |
4: 100,634,339 (GRCm39) |
P5Q |
unknown |
Het |
Capn13 |
A |
T |
17: 73,652,191 (GRCm39) |
I266N |
probably damaging |
Het |
Chil3 |
A |
G |
3: 106,063,081 (GRCm39) |
S170P |
possibly damaging |
Het |
Ckap4 |
A |
G |
10: 84,363,350 (GRCm39) |
I571T |
probably damaging |
Het |
Col14a1 |
A |
G |
15: 55,242,964 (GRCm39) |
M371V |
unknown |
Het |
Dag1 |
A |
G |
9: 108,085,467 (GRCm39) |
L558P |
possibly damaging |
Het |
Edem3 |
G |
A |
1: 151,694,270 (GRCm39) |
E868K |
probably benign |
Het |
Eif3k |
T |
C |
7: 28,673,624 (GRCm39) |
Y150C |
probably damaging |
Het |
Farp1 |
T |
C |
14: 121,518,281 (GRCm39) |
I988T |
probably benign |
Het |
Fat3 |
A |
G |
9: 15,910,248 (GRCm39) |
M1918T |
probably benign |
Het |
Gba2 |
A |
G |
4: 43,578,112 (GRCm39) |
I79T |
probably benign |
Het |
Gbp8 |
T |
C |
5: 105,179,169 (GRCm39) |
D110G |
probably damaging |
Het |
Gm57858 |
G |
T |
3: 36,089,428 (GRCm39) |
N165K |
probably benign |
Het |
H2-M2 |
T |
A |
17: 37,793,428 (GRCm39) |
M193L |
probably benign |
Het |
H2-T13 |
A |
G |
17: 36,391,956 (GRCm39) |
V39A |
possibly damaging |
Het |
Ighv7-1 |
T |
A |
12: 113,860,110 (GRCm39) |
D94V |
probably damaging |
Het |
Il2ra |
T |
C |
2: 11,689,202 (GRCm39) |
F244L |
possibly damaging |
Het |
Jag1 |
A |
T |
2: 136,931,764 (GRCm39) |
H602Q |
probably null |
Het |
Kidins220 |
A |
T |
12: 25,036,966 (GRCm39) |
I16F |
possibly damaging |
Het |
Klb |
A |
G |
5: 65,529,368 (GRCm39) |
T299A |
possibly damaging |
Het |
Lama4 |
A |
G |
10: 38,951,444 (GRCm39) |
K1063R |
probably benign |
Het |
Lrit2 |
A |
G |
14: 36,794,550 (GRCm39) |
E538G |
possibly damaging |
Het |
Lrrc7 |
A |
T |
3: 158,059,011 (GRCm39) |
L32* |
probably null |
Het |
Lrrtm3 |
A |
T |
10: 63,765,883 (GRCm39) |
I568N |
probably damaging |
Het |
Myom1 |
A |
G |
17: 71,343,295 (GRCm39) |
D164G |
probably damaging |
Het |
Naaladl2 |
T |
C |
3: 23,900,742 (GRCm39) |
D696G |
probably damaging |
Het |
Nalcn |
A |
T |
14: 123,545,792 (GRCm39) |
L1073* |
probably null |
Het |
Nid2 |
T |
C |
14: 19,853,278 (GRCm39) |
S1166P |
probably damaging |
Het |
Nlrp4c |
T |
C |
7: 6,095,621 (GRCm39) |
V833A |
probably benign |
Het |
Nyap2 |
T |
C |
1: 81,275,712 (GRCm39) |
S619P |
probably damaging |
Het |
Or10d5j |
T |
C |
9: 39,867,878 (GRCm39) |
M118V |
probably damaging |
Het |
Or4a71 |
A |
G |
2: 89,357,987 (GRCm39) |
Y256H |
probably damaging |
Het |
Or8k16 |
C |
A |
2: 85,520,644 (GRCm39) |
Y290* |
probably null |
Het |
P3h2 |
T |
C |
16: 25,923,991 (GRCm39) |
N148S |
probably benign |
Het |
P4htm |
A |
G |
9: 108,460,081 (GRCm39) |
M231T |
probably damaging |
Het |
Pank1 |
T |
A |
19: 34,804,634 (GRCm39) |
K349I |
possibly damaging |
Het |
Pgam5 |
A |
G |
5: 110,413,466 (GRCm39) |
Y210H |
probably benign |
Het |
Prb1b |
T |
C |
6: 132,288,996 (GRCm39) |
H276R |
unknown |
Het |
Prl2a1 |
T |
A |
13: 27,992,535 (GRCm39) |
C220S |
probably damaging |
Het |
Psca |
C |
T |
15: 74,587,932 (GRCm39) |
Q39* |
probably null |
Het |
Rgs20 |
A |
T |
1: 5,091,067 (GRCm39) |
M121K |
possibly damaging |
Het |
S100z |
C |
T |
13: 95,613,883 (GRCm39) |
V76M |
possibly damaging |
Het |
Slc30a10 |
T |
C |
1: 185,195,034 (GRCm39) |
I282T |
probably damaging |
Het |
Slc30a3 |
T |
C |
5: 31,246,088 (GRCm39) |
Y214C |
probably damaging |
Het |
Sox5 |
C |
T |
6: 143,790,570 (GRCm39) |
E497K |
probably benign |
Het |
Spata31g1 |
A |
G |
4: 42,971,519 (GRCm39) |
D284G |
probably benign |
Het |
Sptbn1 |
C |
T |
11: 30,087,551 (GRCm39) |
E963K |
possibly damaging |
Het |
Srl |
T |
C |
16: 4,311,723 (GRCm39) |
E465G |
possibly damaging |
Het |
Tacc2 |
T |
C |
7: 130,228,304 (GRCm39) |
M1663T |
probably benign |
Het |
Tas2r119 |
T |
G |
15: 32,177,932 (GRCm39) |
V166G |
probably benign |
Het |
Tcf7l1 |
A |
G |
6: 72,611,205 (GRCm39) |
V191A |
probably damaging |
Het |
Thap7 |
A |
T |
16: 17,346,901 (GRCm39) |
I92K |
probably damaging |
Het |
Tnfsf10 |
A |
G |
3: 27,371,407 (GRCm39) |
T38A |
possibly damaging |
Het |
Trav7-5 |
C |
G |
14: 53,768,615 (GRCm39) |
A61G |
probably benign |
Het |
Trim30c |
C |
T |
7: 104,031,553 (GRCm39) |
V421I |
probably benign |
Het |
Ugt2b38 |
A |
T |
5: 87,571,729 (GRCm39) |
M101K |
probably benign |
Het |
Vmn1r44 |
T |
A |
6: 89,870,565 (GRCm39) |
C104S |
probably damaging |
Het |
Wdr74 |
T |
A |
19: 8,715,240 (GRCm39) |
V133E |
probably damaging |
Het |
Zfp735 |
A |
T |
11: 73,580,600 (GRCm39) |
Y33F |
possibly damaging |
Het |
|
Other mutations in Or2a20 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00339:Or2a20
|
APN |
6 |
43,194,782 (GRCm39) |
missense |
probably benign |
0.00 |
R0347:Or2a20
|
UTSW |
6 |
43,194,296 (GRCm39) |
missense |
probably benign |
|
R1099:Or2a20
|
UTSW |
6 |
43,194,558 (GRCm39) |
missense |
probably damaging |
1.00 |
R1147:Or2a20
|
UTSW |
6 |
43,194,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R1147:Or2a20
|
UTSW |
6 |
43,194,146 (GRCm39) |
missense |
probably damaging |
0.99 |
R1353:Or2a20
|
UTSW |
6 |
43,194,624 (GRCm39) |
missense |
probably benign |
0.41 |
R1570:Or2a20
|
UTSW |
6 |
43,194,285 (GRCm39) |
missense |
probably benign |
|
R1720:Or2a20
|
UTSW |
6 |
43,194,494 (GRCm39) |
missense |
probably damaging |
1.00 |
R2098:Or2a20
|
UTSW |
6 |
43,194,437 (GRCm39) |
missense |
probably benign |
0.02 |
R4707:Or2a20
|
UTSW |
6 |
43,193,883 (GRCm39) |
missense |
probably benign |
0.27 |
R4942:Or2a20
|
UTSW |
6 |
43,193,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R5008:Or2a20
|
UTSW |
6 |
43,193,991 (GRCm39) |
missense |
probably damaging |
0.98 |
R5084:Or2a20
|
UTSW |
6 |
43,194,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R6472:Or2a20
|
UTSW |
6 |
43,194,293 (GRCm39) |
missense |
probably benign |
|
R7592:Or2a20
|
UTSW |
6 |
43,194,179 (GRCm39) |
missense |
probably damaging |
1.00 |
R7756:Or2a20
|
UTSW |
6 |
43,193,950 (GRCm39) |
nonsense |
probably null |
|
R7784:Or2a20
|
UTSW |
6 |
43,194,322 (GRCm39) |
missense |
possibly damaging |
0.82 |
R8056:Or2a20
|
UTSW |
6 |
43,193,978 (GRCm39) |
missense |
probably damaging |
0.99 |
R9093:Or2a20
|
UTSW |
6 |
43,194,500 (GRCm39) |
missense |
probably benign |
|
R9745:Or2a20
|
UTSW |
6 |
43,194,258 (GRCm39) |
nonsense |
probably null |
|
R9749:Or2a20
|
UTSW |
6 |
43,194,258 (GRCm39) |
nonsense |
probably null |
|
|