Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110032F04Rik |
C |
T |
3: 68,777,402 (GRCm39) |
P121L |
probably damaging |
Het |
2310002L09Rik |
C |
A |
4: 73,868,934 (GRCm39) |
M1I |
probably null |
Het |
2510039O18Rik |
T |
A |
4: 148,029,873 (GRCm39) |
Y614* |
probably null |
Het |
4930562C15Rik |
A |
T |
16: 4,667,418 (GRCm39) |
S270C |
unknown |
Het |
Ak9 |
A |
C |
10: 41,203,627 (GRCm39) |
T173P |
|
Het |
Cfc1 |
T |
C |
1: 34,575,560 (GRCm39) |
L78P |
probably benign |
Het |
Chrd |
T |
G |
16: 20,552,378 (GRCm39) |
C82W |
probably damaging |
Het |
Cln6 |
T |
C |
9: 62,758,111 (GRCm39) |
V290A |
probably damaging |
Het |
Cps1 |
A |
G |
1: 67,196,975 (GRCm39) |
D342G |
possibly damaging |
Het |
Cracd |
A |
G |
5: 77,004,617 (GRCm39) |
D326G |
unknown |
Het |
Cryzl2 |
G |
A |
1: 157,289,578 (GRCm39) |
R72H |
probably benign |
Het |
Cyp2j6 |
A |
T |
4: 96,414,085 (GRCm39) |
H393Q |
probably benign |
Het |
Eefsec |
T |
C |
6: 88,274,681 (GRCm39) |
T428A |
probably benign |
Het |
Ergic1 |
G |
A |
17: 26,827,619 (GRCm39) |
G25S |
probably damaging |
Het |
Esf1 |
T |
C |
2: 140,001,714 (GRCm39) |
I378V |
probably benign |
Het |
Fndc1 |
T |
A |
17: 7,990,313 (GRCm39) |
T1128S |
unknown |
Het |
Gabrp |
A |
T |
11: 33,504,342 (GRCm39) |
Y324* |
probably null |
Het |
Hadha |
G |
A |
5: 30,339,165 (GRCm39) |
T270M |
possibly damaging |
Het |
Hdac1-ps |
T |
C |
17: 78,799,114 (GRCm39) |
I35T |
probably damaging |
Het |
Ino80d |
G |
A |
1: 63,101,342 (GRCm39) |
T428M |
probably damaging |
Het |
Itgae |
T |
C |
11: 73,011,171 (GRCm39) |
F647S |
possibly damaging |
Het |
Kank4 |
T |
C |
4: 98,653,732 (GRCm39) |
R899G |
possibly damaging |
Het |
Kcna4 |
T |
A |
2: 107,126,374 (GRCm39) |
N369K |
probably benign |
Het |
Kcnip3 |
G |
T |
2: 127,352,812 (GRCm39) |
P69Q |
probably benign |
Het |
Mcf2l |
A |
G |
8: 13,034,320 (GRCm39) |
|
probably benign |
Het |
Mtmr2 |
T |
C |
9: 13,707,315 (GRCm39) |
V289A |
probably benign |
Het |
Muc21 |
GGGGTGGGCATAGATCCTGAGGCAGAGCTGGATGCAGTGGTGGTCAGGGTGGG |
GGGGTGGG |
17: 35,932,935 (GRCm39) |
|
probably benign |
Het |
Nxph1 |
T |
G |
6: 9,247,108 (GRCm39) |
N26K |
probably benign |
Het |
Obox1 |
A |
G |
7: 15,289,624 (GRCm39) |
I138V |
possibly damaging |
Het |
Or4c35 |
A |
T |
2: 89,808,343 (GRCm39) |
T74S |
probably benign |
Het |
Or7e176 |
G |
A |
9: 20,171,639 (GRCm39) |
V168M |
possibly damaging |
Het |
P2ry14 |
T |
A |
3: 59,023,251 (GRCm39) |
M70L |
probably damaging |
Het |
Pcare |
T |
A |
17: 72,057,817 (GRCm39) |
Y620F |
probably damaging |
Het |
Pcnt |
A |
G |
10: 76,188,794 (GRCm39) |
Y2869H |
probably damaging |
Het |
Pkd1l1 |
T |
C |
11: 8,911,420 (GRCm39) |
R286G |
|
Het |
Pygb |
C |
T |
2: 150,657,008 (GRCm39) |
R320W |
|
Het |
Rsf1 |
G |
GACGGCGGCC |
7: 97,229,116 (GRCm39) |
|
probably benign |
Het |
Slc15a5 |
A |
T |
6: 138,032,779 (GRCm39) |
S192T |
possibly damaging |
Het |
Tex15 |
A |
G |
8: 34,062,397 (GRCm39) |
H609R |
probably benign |
Het |
Tmem256 |
T |
A |
11: 69,730,210 (GRCm39) |
S73T |
possibly damaging |
Het |
Tpr |
G |
T |
1: 150,321,979 (GRCm39) |
A2338S |
possibly damaging |
Het |
Trub2 |
A |
T |
2: 29,673,346 (GRCm39) |
M119K |
probably benign |
Het |
Vmn1r228 |
T |
C |
17: 20,997,045 (GRCm39) |
M158V |
probably benign |
Het |
Vmn2r100 |
A |
T |
17: 19,742,583 (GRCm39) |
H319L |
probably damaging |
Het |
Vmn2r3 |
T |
A |
3: 64,178,724 (GRCm39) |
I514F |
probably damaging |
Het |
Wnt16 |
T |
A |
6: 22,297,891 (GRCm39) |
Y252* |
probably null |
Het |
Wnt16 |
G |
T |
6: 22,297,892 (GRCm39) |
E253* |
probably null |
Het |
Xkr4 |
A |
T |
1: 3,741,201 (GRCm39) |
V124E |
probably damaging |
Het |
Zc3h13 |
G |
T |
14: 75,567,542 (GRCm39) |
R945L |
|
Het |
Zfp445 |
T |
C |
9: 122,685,788 (GRCm39) |
N251D |
probably damaging |
Het |
Zfp683 |
A |
T |
4: 133,782,965 (GRCm39) |
D143V |
probably benign |
Het |
|
Other mutations in Or4m1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01140:Or4m1
|
APN |
14 |
50,557,732 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01285:Or4m1
|
APN |
14 |
50,557,713 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02106:Or4m1
|
APN |
14 |
50,557,617 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02313:Or4m1
|
APN |
14 |
50,557,473 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03125:Or4m1
|
APN |
14 |
50,558,149 (GRCm39) |
missense |
probably benign |
0.01 |
R0276:Or4m1
|
UTSW |
14 |
50,557,636 (GRCm39) |
missense |
probably benign |
0.23 |
R0547:Or4m1
|
UTSW |
14 |
50,557,575 (GRCm39) |
missense |
probably benign |
0.06 |
R0567:Or4m1
|
UTSW |
14 |
50,558,115 (GRCm39) |
missense |
probably damaging |
0.99 |
R0927:Or4m1
|
UTSW |
14 |
50,558,186 (GRCm39) |
nonsense |
probably null |
|
R1506:Or4m1
|
UTSW |
14 |
50,557,941 (GRCm39) |
missense |
probably benign |
0.00 |
R4032:Or4m1
|
UTSW |
14 |
50,557,767 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5179:Or4m1
|
UTSW |
14 |
50,557,993 (GRCm39) |
nonsense |
probably null |
|
R5401:Or4m1
|
UTSW |
14 |
50,557,566 (GRCm39) |
missense |
probably damaging |
1.00 |
R6240:Or4m1
|
UTSW |
14 |
50,558,043 (GRCm39) |
missense |
probably benign |
0.00 |
R7752:Or4m1
|
UTSW |
14 |
50,557,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R7901:Or4m1
|
UTSW |
14 |
50,557,573 (GRCm39) |
missense |
probably damaging |
1.00 |
R8034:Or4m1
|
UTSW |
14 |
50,558,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R8260:Or4m1
|
UTSW |
14 |
50,557,615 (GRCm39) |
missense |
probably benign |
0.09 |
R8420:Or4m1
|
UTSW |
14 |
50,558,233 (GRCm39) |
missense |
probably benign |
|
R9056:Or4m1
|
UTSW |
14 |
50,557,999 (GRCm39) |
missense |
probably damaging |
0.98 |
R9128:Or4m1
|
UTSW |
14 |
50,558,214 (GRCm39) |
missense |
probably benign |
0.08 |
R9659:Or4m1
|
UTSW |
14 |
50,558,181 (GRCm39) |
missense |
probably benign |
0.10 |
R9788:Or4m1
|
UTSW |
14 |
50,558,181 (GRCm39) |
missense |
probably benign |
0.10 |
X0064:Or4m1
|
UTSW |
14 |
50,557,511 (GRCm39) |
nonsense |
probably null |
|
|