Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700012B07Rik |
G |
T |
11: 109,684,980 (GRCm39) |
C172* |
probably null |
Het |
Akap9 |
A |
G |
5: 4,004,410 (GRCm39) |
N108S |
probably benign |
Het |
Ankmy1 |
A |
G |
1: 92,811,480 (GRCm39) |
I636T |
possibly damaging |
Het |
Bbs9 |
T |
A |
9: 22,798,926 (GRCm39) |
D851E |
probably damaging |
Het |
Bicd1 |
T |
A |
6: 149,420,489 (GRCm39) |
L780M |
probably damaging |
Het |
Ccdc175 |
T |
C |
12: 72,227,598 (GRCm39) |
T62A |
possibly damaging |
Het |
Cfhr4 |
T |
A |
1: 139,680,773 (GRCm39) |
K248N |
probably damaging |
Het |
Clcnka |
T |
C |
4: 141,114,601 (GRCm39) |
E615G |
probably null |
Het |
Col1a2 |
G |
A |
6: 4,518,822 (GRCm39) |
|
probably benign |
Het |
Cpxm2 |
C |
T |
7: 131,681,820 (GRCm39) |
M236I |
probably benign |
Het |
Fam131a |
G |
A |
16: 20,514,608 (GRCm39) |
V70M |
probably benign |
Het |
Fat3 |
G |
A |
9: 15,909,567 (GRCm39) |
S2145F |
probably damaging |
Het |
Fbxl15 |
G |
C |
19: 46,317,891 (GRCm39) |
R191P |
possibly damaging |
Het |
Fcrlb |
T |
C |
1: 170,735,183 (GRCm39) |
T315A |
probably benign |
Het |
Fer1l4 |
C |
T |
2: 155,887,603 (GRCm39) |
G531D |
probably damaging |
Het |
Gem |
C |
T |
4: 11,705,965 (GRCm39) |
Q18* |
probably null |
Het |
Hemk1 |
T |
A |
9: 107,214,229 (GRCm39) |
I68F |
probably damaging |
Het |
Herc3 |
C |
A |
6: 58,893,835 (GRCm39) |
H970Q |
probably damaging |
Het |
Ighv5-17 |
C |
A |
12: 113,822,918 (GRCm39) |
A68S |
probably benign |
Het |
Ip6k3 |
T |
C |
17: 27,363,974 (GRCm39) |
H358R |
probably damaging |
Het |
Itpr2 |
T |
C |
6: 146,133,789 (GRCm39) |
|
probably null |
Het |
Kmt2a |
C |
T |
9: 44,731,653 (GRCm39) |
|
probably benign |
Het |
Krt16 |
G |
T |
11: 100,139,566 (GRCm39) |
R51S |
unknown |
Het |
Lamtor1 |
G |
A |
7: 101,560,552 (GRCm39) |
V156I |
probably damaging |
Het |
Lingo4 |
A |
G |
3: 94,309,407 (GRCm39) |
D115G |
probably damaging |
Het |
Lrrc7 |
T |
C |
3: 157,891,130 (GRCm39) |
I346V |
probably benign |
Het |
Maco1 |
C |
T |
4: 134,557,891 (GRCm39) |
M207I |
probably benign |
Het |
Man1c1 |
A |
T |
4: 134,430,662 (GRCm39) |
L40Q |
probably damaging |
Het |
Mgat4c |
A |
G |
10: 102,224,221 (GRCm39) |
N145S |
probably benign |
Het |
Morf4l1 |
A |
G |
9: 89,977,196 (GRCm39) |
S203P |
probably benign |
Het |
Muc5ac |
T |
C |
7: 141,367,471 (GRCm39) |
I2964T |
possibly damaging |
Het |
Naip2 |
T |
A |
13: 100,289,142 (GRCm39) |
Q1196L |
possibly damaging |
Het |
Nbas |
G |
A |
12: 13,532,505 (GRCm39) |
G1738S |
probably damaging |
Het |
Nlrp5 |
A |
G |
7: 23,104,271 (GRCm39) |
E44G |
probably benign |
Het |
Nolc1 |
CCAGCAGCAGCAGCAGCAGCAGCAGC |
CCAGCAGCAGCAGCAGCAGCAGCAGCAGC |
19: 46,069,791 (GRCm39) |
|
probably benign |
Het |
Or4ac1-ps1 |
A |
T |
2: 88,370,700 (GRCm39) |
|
noncoding transcript |
Het |
Or5d18 |
A |
G |
2: 87,864,911 (GRCm39) |
S191P |
possibly damaging |
Het |
Otof |
T |
A |
5: 30,543,843 (GRCm39) |
|
probably null |
Het |
Pcdha2 |
G |
A |
18: 37,072,582 (GRCm39) |
R71H |
probably benign |
Het |
Pcdha2 |
G |
T |
18: 37,074,744 (GRCm39) |
E792* |
probably null |
Het |
Pcnx1 |
A |
G |
12: 81,996,911 (GRCm39) |
T936A |
possibly damaging |
Het |
Pofut2 |
T |
C |
10: 77,096,640 (GRCm39) |
Y122H |
probably damaging |
Het |
Psg16 |
A |
G |
7: 16,824,609 (GRCm39) |
E131G |
probably benign |
Het |
Psmd12 |
T |
G |
11: 107,386,591 (GRCm39) |
D387E |
probably benign |
Het |
Rab6a |
A |
G |
7: 100,257,431 (GRCm39) |
M1V |
probably null |
Het |
Ripk3 |
T |
C |
14: 56,023,725 (GRCm39) |
R29G |
probably benign |
Het |
Robo4 |
A |
T |
9: 37,315,734 (GRCm39) |
D329V |
possibly damaging |
Het |
Ruvbl2 |
A |
G |
7: 45,071,614 (GRCm39) |
V423A |
possibly damaging |
Het |
Rxylt1 |
A |
T |
10: 121,917,514 (GRCm39) |
V333E |
possibly damaging |
Het |
Scgb2b18 |
T |
G |
7: 32,872,563 (GRCm39) |
M81L |
probably benign |
Het |
Slc24a2 |
A |
T |
4: 87,146,021 (GRCm39) |
L11H |
possibly damaging |
Het |
Slc4a1 |
T |
C |
11: 102,248,019 (GRCm39) |
E325G |
probably benign |
Het |
Syt16 |
A |
G |
12: 74,276,172 (GRCm39) |
E212G |
possibly damaging |
Het |
Them6 |
A |
G |
15: 74,593,367 (GRCm39) |
D75G |
probably damaging |
Het |
Tnrc18 |
G |
A |
5: 142,773,029 (GRCm39) |
A417V |
unknown |
Het |
Vmn2r115 |
ATCTTCT |
ATCT |
17: 23,578,962 (GRCm39) |
|
probably benign |
Het |
Zbtb22 |
C |
T |
17: 34,135,920 (GRCm39) |
|
probably benign |
Het |
Zfp235 |
A |
G |
7: 23,840,046 (GRCm39) |
D225G |
probably benign |
Het |
|
Other mutations in Dhrs2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01747:Dhrs2
|
APN |
14 |
55,472,120 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02510:Dhrs2
|
APN |
14 |
55,473,532 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02604:Dhrs2
|
APN |
14 |
55,474,778 (GRCm39) |
missense |
possibly damaging |
0.88 |
IGL02746:Dhrs2
|
APN |
14 |
55,478,628 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03060:Dhrs2
|
APN |
14 |
55,474,775 (GRCm39) |
missense |
probably benign |
0.06 |
R0179:Dhrs2
|
UTSW |
14 |
55,477,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R0358:Dhrs2
|
UTSW |
14 |
55,473,574 (GRCm39) |
missense |
probably damaging |
0.99 |
R0755:Dhrs2
|
UTSW |
14 |
55,472,247 (GRCm39) |
missense |
probably damaging |
1.00 |
R1848:Dhrs2
|
UTSW |
14 |
55,478,298 (GRCm39) |
missense |
probably benign |
|
R1977:Dhrs2
|
UTSW |
14 |
55,472,112 (GRCm39) |
start codon destroyed |
probably null |
0.11 |
R3084:Dhrs2
|
UTSW |
14 |
55,477,301 (GRCm39) |
missense |
probably benign |
0.00 |
R3086:Dhrs2
|
UTSW |
14 |
55,477,301 (GRCm39) |
missense |
probably benign |
0.00 |
R3805:Dhrs2
|
UTSW |
14 |
55,472,205 (GRCm39) |
missense |
probably benign |
0.03 |
R4361:Dhrs2
|
UTSW |
14 |
55,478,646 (GRCm39) |
missense |
probably damaging |
0.99 |
R4754:Dhrs2
|
UTSW |
14 |
55,476,205 (GRCm39) |
missense |
probably damaging |
0.97 |
R4989:Dhrs2
|
UTSW |
14 |
55,474,722 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Dhrs2
|
UTSW |
14 |
55,473,601 (GRCm39) |
missense |
possibly damaging |
0.71 |
R7561:Dhrs2
|
UTSW |
14 |
55,474,698 (GRCm39) |
missense |
probably benign |
|
R8245:Dhrs2
|
UTSW |
14 |
55,478,637 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8296:Dhrs2
|
UTSW |
14 |
55,477,928 (GRCm39) |
missense |
probably damaging |
1.00 |
R8324:Dhrs2
|
UTSW |
14 |
55,476,221 (GRCm39) |
missense |
probably damaging |
1.00 |
R8782:Dhrs2
|
UTSW |
14 |
55,473,538 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8923:Dhrs2
|
UTSW |
14 |
55,478,309 (GRCm39) |
missense |
probably benign |
0.00 |
|