Other mutations in this stock |
Total: 69 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
3300002I08Rik |
A |
T |
2: 150,186,564 (GRCm39) |
D40E |
possibly damaging |
Het |
4921517D22Rik |
C |
T |
13: 59,837,347 (GRCm39) |
R246H |
probably damaging |
Het |
Agbl1 |
A |
G |
7: 76,069,832 (GRCm39) |
T203A |
probably benign |
Het |
Alms1 |
T |
A |
6: 85,600,056 (GRCm39) |
D2096E |
probably damaging |
Het |
Ankrd53 |
T |
C |
6: 83,739,639 (GRCm39) |
|
probably benign |
Het |
Arap3 |
C |
A |
18: 38,118,486 (GRCm39) |
G814C |
probably damaging |
Het |
Armc9 |
T |
G |
1: 86,172,301 (GRCm39) |
I5S |
probably benign |
Het |
Catsperg1 |
T |
C |
7: 28,910,120 (GRCm39) |
T74A |
probably damaging |
Het |
Cdca7l |
T |
A |
12: 117,837,446 (GRCm39) |
|
probably null |
Het |
Cfhr2 |
T |
A |
1: 139,733,153 (GRCm39) |
|
probably benign |
Het |
Chpt1 |
A |
G |
10: 88,288,955 (GRCm39) |
|
probably benign |
Het |
Cntrl |
A |
C |
2: 35,055,745 (GRCm39) |
D1213A |
possibly damaging |
Het |
Col7a1 |
C |
T |
9: 108,803,148 (GRCm39) |
R2149C |
unknown |
Het |
Cpa4 |
T |
C |
6: 30,585,082 (GRCm39) |
S289P |
probably damaging |
Het |
Cpsf3 |
G |
A |
12: 21,356,887 (GRCm39) |
|
probably null |
Het |
Creb3l1 |
T |
C |
2: 91,822,350 (GRCm39) |
H212R |
possibly damaging |
Het |
Cybb |
C |
G |
X: 9,316,989 (GRCm39) |
D246H |
probably benign |
Het |
Cyp2c29 |
A |
G |
19: 39,310,053 (GRCm39) |
D254G |
possibly damaging |
Het |
Dennd1b |
A |
G |
1: 139,008,993 (GRCm39) |
H232R |
probably damaging |
Het |
Dhx29 |
T |
C |
13: 113,101,105 (GRCm39) |
L1216P |
probably damaging |
Het |
Dsg1b |
T |
C |
18: 20,529,476 (GRCm39) |
I307T |
possibly damaging |
Het |
Ep300 |
A |
G |
15: 81,485,435 (GRCm39) |
S141G |
unknown |
Het |
Evl |
A |
C |
12: 108,619,290 (GRCm39) |
K101T |
probably damaging |
Het |
Exph5 |
G |
A |
9: 53,284,328 (GRCm39) |
G470R |
probably benign |
Het |
Flg |
A |
T |
3: 93,190,515 (GRCm39) |
|
probably benign |
Het |
Gm45704 |
T |
A |
8: 73,510,920 (GRCm39) |
|
|
Het |
Grm1 |
T |
C |
10: 10,955,640 (GRCm39) |
M215V |
probably benign |
Het |
Hadha |
T |
C |
5: 30,345,994 (GRCm39) |
D210G |
probably benign |
Het |
Hmcn1 |
T |
C |
1: 150,598,175 (GRCm39) |
Y1709C |
probably damaging |
Het |
Hrc |
A |
T |
7: 44,986,157 (GRCm39) |
H436L |
possibly damaging |
Het |
Hycc1 |
T |
C |
5: 24,171,367 (GRCm39) |
S352G |
possibly damaging |
Het |
Ido1 |
T |
A |
8: 25,075,306 (GRCm39) |
T259S |
possibly damaging |
Het |
Itgb7 |
C |
A |
15: 102,131,917 (GRCm39) |
R222L |
probably benign |
Het |
Khnyn |
T |
C |
14: 56,125,296 (GRCm39) |
V485A |
probably damaging |
Het |
Kifc5b |
T |
C |
17: 27,140,826 (GRCm39) |
V100A |
probably benign |
Het |
Lsm10 |
T |
C |
4: 125,991,794 (GRCm39) |
M50T |
probably damaging |
Het |
Map3k6 |
T |
G |
4: 132,972,986 (GRCm39) |
W382G |
probably damaging |
Het |
Mink1 |
T |
A |
11: 70,501,478 (GRCm39) |
F922I |
possibly damaging |
Het |
Mrap2 |
T |
C |
9: 87,057,871 (GRCm39) |
V53A |
probably damaging |
Het |
Mrps7 |
C |
A |
11: 115,495,000 (GRCm39) |
A5E |
probably benign |
Het |
Muc4 |
A |
G |
16: 32,587,298 (GRCm39) |
N2713S |
possibly damaging |
Het |
Nckipsd |
T |
C |
9: 108,689,585 (GRCm39) |
S249P |
probably damaging |
Het |
Neil3 |
T |
C |
8: 54,052,447 (GRCm39) |
T384A |
probably benign |
Het |
Noc3l |
A |
T |
19: 38,787,399 (GRCm39) |
I504K |
probably damaging |
Het |
Nudt13 |
A |
G |
14: 20,357,839 (GRCm39) |
N107S |
probably benign |
Het |
Or11h4b |
C |
A |
14: 50,918,392 (GRCm39) |
R233L |
probably benign |
Het |
Or2n1 |
T |
A |
17: 38,486,116 (GRCm39) |
L47H |
probably damaging |
Het |
Otub1 |
G |
T |
19: 7,176,518 (GRCm39) |
Y205* |
probably null |
Het |
Pals1 |
T |
C |
12: 78,871,563 (GRCm39) |
V381A |
possibly damaging |
Het |
Pierce2 |
C |
A |
9: 72,887,270 (GRCm39) |
C79F |
probably damaging |
Het |
Plpp7 |
T |
A |
2: 31,986,100 (GRCm39) |
S93T |
probably damaging |
Het |
Pxk |
T |
G |
14: 8,138,011 (GRCm38) |
Y188D |
probably damaging |
Het |
Rigi |
T |
C |
4: 40,229,551 (GRCm39) |
I78V |
probably benign |
Het |
Rnd2 |
C |
T |
11: 101,359,825 (GRCm39) |
L57F |
probably damaging |
Het |
Rpap1 |
A |
T |
2: 119,603,128 (GRCm39) |
C602* |
probably null |
Het |
Sbds |
T |
C |
5: 130,275,185 (GRCm39) |
K248E |
probably benign |
Het |
Serpina10 |
A |
T |
12: 103,595,092 (GRCm39) |
N42K |
probably benign |
Het |
Slc7a8 |
A |
G |
14: 54,966,797 (GRCm39) |
L368P |
probably damaging |
Het |
Srrm1 |
T |
C |
4: 135,065,184 (GRCm39) |
|
probably benign |
Het |
Sun2 |
C |
T |
15: 79,614,533 (GRCm39) |
V288I |
probably benign |
Het |
Tas2r107 |
C |
A |
6: 131,636,966 (GRCm39) |
A28S |
possibly damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,037,155 (GRCm39) |
I268T |
probably benign |
Het |
Tjp2 |
A |
G |
19: 24,097,437 (GRCm39) |
F495L |
probably damaging |
Het |
Top2b |
T |
C |
14: 16,423,740 (GRCm38) |
L1434P |
possibly damaging |
Het |
Top3b |
A |
G |
16: 16,697,005 (GRCm39) |
|
probably null |
Het |
Trdv2-2 |
A |
T |
14: 54,198,761 (GRCm39) |
E17V |
possibly damaging |
Het |
Ttc6 |
T |
A |
12: 57,719,886 (GRCm39) |
L819Q |
possibly damaging |
Het |
Txlnb |
A |
G |
10: 17,718,914 (GRCm39) |
T582A |
probably benign |
Het |
Zfp788 |
T |
C |
7: 41,299,193 (GRCm39) |
S558P |
probably damaging |
Het |
|
Other mutations in Or5c1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01597:Or5c1
|
APN |
2 |
37,222,023 (GRCm39) |
missense |
possibly damaging |
0.60 |
IGL02955:Or5c1
|
APN |
2 |
37,222,013 (GRCm39) |
missense |
probably benign |
0.07 |
IGL03028:Or5c1
|
APN |
2 |
37,221,968 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03084:Or5c1
|
APN |
2 |
37,222,413 (GRCm39) |
missense |
probably damaging |
1.00 |
R1626:Or5c1
|
UTSW |
2 |
37,222,774 (GRCm39) |
splice site |
probably null |
|
R1655:Or5c1
|
UTSW |
2 |
37,221,951 (GRCm39) |
missense |
probably damaging |
1.00 |
R1771:Or5c1
|
UTSW |
2 |
37,222,430 (GRCm39) |
missense |
probably benign |
0.23 |
R1937:Or5c1
|
UTSW |
2 |
37,221,896 (GRCm39) |
missense |
probably damaging |
1.00 |
R2297:Or5c1
|
UTSW |
2 |
37,222,155 (GRCm39) |
missense |
probably benign |
0.04 |
R4354:Or5c1
|
UTSW |
2 |
37,221,888 (GRCm39) |
missense |
probably damaging |
1.00 |
R4888:Or5c1
|
UTSW |
2 |
37,222,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R4974:Or5c1
|
UTSW |
2 |
37,222,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R5121:Or5c1
|
UTSW |
2 |
37,222,601 (GRCm39) |
missense |
probably damaging |
1.00 |
R6449:Or5c1
|
UTSW |
2 |
37,221,837 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7670:Or5c1
|
UTSW |
2 |
37,221,771 (GRCm39) |
missense |
probably benign |
0.10 |
R8049:Or5c1
|
UTSW |
2 |
37,222,346 (GRCm39) |
missense |
probably damaging |
1.00 |
R8486:Or5c1
|
UTSW |
2 |
37,222,662 (GRCm39) |
missense |
probably damaging |
1.00 |
R8893:Or5c1
|
UTSW |
2 |
37,222,388 (GRCm39) |
missense |
probably damaging |
1.00 |
R9147:Or5c1
|
UTSW |
2 |
37,222,017 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9148:Or5c1
|
UTSW |
2 |
37,222,017 (GRCm39) |
missense |
possibly damaging |
0.68 |
R9401:Or5c1
|
UTSW |
2 |
37,222,293 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9574:Or5c1
|
UTSW |
2 |
37,222,148 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1177:Or5c1
|
UTSW |
2 |
37,222,016 (GRCm39) |
missense |
probably damaging |
1.00 |
|