Other mutations in this stock |
Total: 46 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd28 |
A |
T |
14: 31,437,331 (GRCm39) |
V578E |
possibly damaging |
Het |
Arhgap35 |
A |
T |
7: 16,296,132 (GRCm39) |
C978S |
probably benign |
Het |
Asph |
A |
T |
4: 9,517,697 (GRCm39) |
V475E |
probably damaging |
Het |
Atf7ip2 |
T |
A |
16: 10,059,399 (GRCm39) |
|
probably null |
Het |
Bace1 |
A |
T |
9: 45,771,559 (GRCm39) |
D491V |
probably benign |
Het |
Birc2 |
A |
G |
9: 7,819,424 (GRCm39) |
I496T |
probably benign |
Het |
Cacna2d4 |
C |
T |
6: 119,248,882 (GRCm39) |
R448C |
probably benign |
Het |
Ccdc181 |
T |
C |
1: 164,107,989 (GRCm39) |
F224S |
probably damaging |
Het |
Cdan1 |
C |
T |
2: 120,558,405 (GRCm39) |
R469Q |
probably damaging |
Het |
Ddx21 |
G |
A |
10: 62,424,569 (GRCm39) |
P544L |
probably damaging |
Het |
Epas1 |
C |
A |
17: 87,138,526 (GRCm39) |
T874N |
possibly damaging |
Het |
Fam13b |
A |
T |
18: 34,627,660 (GRCm39) |
D180E |
probably damaging |
Het |
Fcgbp |
G |
A |
7: 27,784,794 (GRCm39) |
V285M |
probably damaging |
Het |
Gcn1 |
T |
G |
5: 115,757,755 (GRCm39) |
L2487V |
probably benign |
Het |
Gm19410 |
C |
T |
8: 36,240,772 (GRCm39) |
A216V |
possibly damaging |
Het |
Gm4871 |
G |
T |
5: 144,969,430 (GRCm39) |
R30S |
probably damaging |
Het |
Gtf2ird1 |
T |
C |
5: 134,391,379 (GRCm39) |
D899G |
probably benign |
Het |
Hipk3 |
T |
C |
2: 104,265,059 (GRCm39) |
T674A |
probably benign |
Het |
Hnrnph3 |
A |
G |
10: 62,854,674 (GRCm39) |
L39S |
unknown |
Het |
Ift122 |
T |
C |
6: 115,867,543 (GRCm39) |
V431A |
probably benign |
Het |
Il36b |
A |
G |
2: 24,049,890 (GRCm39) |
H167R |
probably benign |
Het |
Lce3e |
T |
A |
3: 92,875,142 (GRCm39) |
C33S |
unknown |
Het |
Lrrc26 |
T |
C |
2: 25,180,545 (GRCm39) |
I182T |
probably benign |
Het |
Magi1 |
T |
C |
6: 93,685,189 (GRCm39) |
R730G |
probably damaging |
Het |
Meis3 |
G |
T |
7: 15,911,743 (GRCm39) |
V102F |
probably damaging |
Het |
Mpp7 |
G |
A |
18: 7,440,183 (GRCm39) |
Q263* |
probably null |
Het |
Myo7b |
A |
T |
18: 32,146,320 (GRCm39) |
I155N |
probably damaging |
Het |
Nrip1 |
A |
T |
16: 76,088,072 (GRCm39) |
*1162K |
probably null |
Het |
Or3a1b |
T |
A |
11: 74,012,335 (GRCm39) |
D73E |
probably damaging |
Het |
Or4k50-ps1 |
T |
C |
2: 111,522,444 (GRCm39) |
F194L |
unknown |
Het |
Or8i2 |
A |
C |
2: 86,852,486 (GRCm39) |
V134G |
probably benign |
Het |
Pdik1l |
T |
A |
4: 134,005,736 (GRCm39) |
E326V |
possibly damaging |
Het |
Phrf1 |
T |
C |
7: 140,836,523 (GRCm39) |
M265T |
unknown |
Het |
Piezo2 |
A |
T |
18: 63,215,996 (GRCm39) |
N1222K |
possibly damaging |
Het |
Pkd1 |
G |
A |
17: 24,799,393 (GRCm39) |
V2871M |
probably damaging |
Het |
Pon2 |
T |
G |
6: 5,268,997 (GRCm39) |
N226H |
possibly damaging |
Het |
Rftn2 |
G |
T |
1: 55,234,708 (GRCm39) |
D338E |
probably damaging |
Het |
Rnf123 |
A |
T |
9: 107,947,473 (GRCm39) |
Y171* |
probably null |
Het |
Serpinb6c |
T |
A |
13: 34,079,278 (GRCm39) |
N138I |
probably damaging |
Het |
Smco1 |
A |
T |
16: 32,092,785 (GRCm39) |
H152L |
possibly damaging |
Het |
Tgm3 |
T |
G |
2: 129,883,684 (GRCm39) |
S447R |
probably benign |
Het |
Topbp1 |
A |
G |
9: 103,209,932 (GRCm39) |
K860E |
possibly damaging |
Het |
Uba7 |
C |
A |
9: 107,853,897 (GRCm39) |
|
probably benign |
Het |
Ucp3 |
A |
G |
7: 100,131,089 (GRCm39) |
N181D |
probably damaging |
Het |
Unc13b |
C |
A |
4: 43,215,765 (GRCm39) |
S21R |
probably benign |
Het |
Usp34 |
T |
A |
11: 23,396,968 (GRCm39) |
S2395R |
|
Het |
|
Other mutations in Ror2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00159:Ror2
|
APN |
13 |
53,267,118 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01523:Ror2
|
APN |
13 |
53,272,999 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01599:Ror2
|
APN |
13 |
53,265,653 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01669:Ror2
|
APN |
13 |
53,265,124 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02016:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02138:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02139:Ror2
|
APN |
13 |
53,265,200 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02172:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02173:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02176:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02177:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02178:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02179:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02182:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02189:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02190:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02203:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02230:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02231:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02234:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02423:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02424:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02478:Ror2
|
APN |
13 |
53,275,703 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02479:Ror2
|
APN |
13 |
53,285,968 (GRCm39) |
missense |
possibly damaging |
0.62 |
IGL02517:Ror2
|
APN |
13 |
53,272,876 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02554:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02618:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02619:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02622:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02623:Ror2
|
APN |
13 |
53,264,764 (GRCm39) |
missense |
probably damaging |
1.00 |
lavage
|
UTSW |
13 |
53,273,018 (GRCm39) |
missense |
probably damaging |
1.00 |
tendrils
|
UTSW |
13 |
53,265,487 (GRCm39) |
missense |
probably damaging |
0.96 |
willowy
|
UTSW |
13 |
53,285,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0076:Ror2
|
UTSW |
13 |
53,267,110 (GRCm39) |
missense |
probably benign |
0.02 |
R0375:Ror2
|
UTSW |
13 |
53,286,040 (GRCm39) |
missense |
probably damaging |
1.00 |
R0826:Ror2
|
UTSW |
13 |
53,267,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R1823:Ror2
|
UTSW |
13 |
53,264,341 (GRCm39) |
missense |
probably benign |
0.07 |
R1895:Ror2
|
UTSW |
13 |
53,285,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R1946:Ror2
|
UTSW |
13 |
53,285,885 (GRCm39) |
missense |
probably damaging |
1.00 |
R1983:Ror2
|
UTSW |
13 |
53,264,444 (GRCm39) |
missense |
probably benign |
0.01 |
R2031:Ror2
|
UTSW |
13 |
53,271,366 (GRCm39) |
missense |
probably benign |
0.01 |
R2197:Ror2
|
UTSW |
13 |
53,439,816 (GRCm39) |
critical splice donor site |
probably null |
|
R2246:Ror2
|
UTSW |
13 |
53,265,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R2405:Ror2
|
UTSW |
13 |
53,284,980 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2411:Ror2
|
UTSW |
13 |
53,284,980 (GRCm39) |
missense |
possibly damaging |
0.67 |
R2905:Ror2
|
UTSW |
13 |
53,286,031 (GRCm39) |
missense |
probably benign |
0.01 |
R3156:Ror2
|
UTSW |
13 |
53,271,400 (GRCm39) |
missense |
probably damaging |
0.98 |
R4198:Ror2
|
UTSW |
13 |
53,264,680 (GRCm39) |
missense |
probably benign |
0.08 |
R4408:Ror2
|
UTSW |
13 |
53,272,997 (GRCm39) |
missense |
probably damaging |
1.00 |
R4469:Ror2
|
UTSW |
13 |
53,286,016 (GRCm39) |
missense |
possibly damaging |
0.87 |
R4648:Ror2
|
UTSW |
13 |
53,439,536 (GRCm39) |
nonsense |
probably null |
|
R4705:Ror2
|
UTSW |
13 |
53,271,333 (GRCm39) |
missense |
probably benign |
0.00 |
R4824:Ror2
|
UTSW |
13 |
53,264,719 (GRCm39) |
missense |
probably benign |
0.10 |
R4831:Ror2
|
UTSW |
13 |
53,272,880 (GRCm39) |
missense |
probably damaging |
0.97 |
R4951:Ror2
|
UTSW |
13 |
53,271,183 (GRCm39) |
missense |
probably benign |
0.00 |
R4975:Ror2
|
UTSW |
13 |
53,285,954 (GRCm39) |
missense |
probably damaging |
1.00 |
R5380:Ror2
|
UTSW |
13 |
53,271,185 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5469:Ror2
|
UTSW |
13 |
53,271,375 (GRCm39) |
missense |
probably benign |
0.00 |
R5604:Ror2
|
UTSW |
13 |
53,271,201 (GRCm39) |
missense |
probably benign |
0.01 |
R6188:Ror2
|
UTSW |
13 |
53,265,347 (GRCm39) |
missense |
probably damaging |
0.98 |
R6221:Ror2
|
UTSW |
13 |
53,267,253 (GRCm39) |
missense |
probably damaging |
1.00 |
R6243:Ror2
|
UTSW |
13 |
53,267,116 (GRCm39) |
missense |
probably benign |
|
R6255:Ror2
|
UTSW |
13 |
53,264,578 (GRCm39) |
missense |
probably damaging |
1.00 |
R6497:Ror2
|
UTSW |
13 |
53,285,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R6717:Ror2
|
UTSW |
13 |
53,273,018 (GRCm39) |
missense |
probably damaging |
1.00 |
R6918:Ror2
|
UTSW |
13 |
53,265,487 (GRCm39) |
missense |
probably damaging |
0.96 |
R7092:Ror2
|
UTSW |
13 |
53,264,272 (GRCm39) |
missense |
probably benign |
|
R7134:Ror2
|
UTSW |
13 |
53,300,742 (GRCm39) |
missense |
probably benign |
0.00 |
R7254:Ror2
|
UTSW |
13 |
53,272,756 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7560:Ror2
|
UTSW |
13 |
53,264,849 (GRCm39) |
missense |
probably benign |
0.05 |
R7746:Ror2
|
UTSW |
13 |
53,271,261 (GRCm39) |
missense |
probably damaging |
1.00 |
R8031:Ror2
|
UTSW |
13 |
53,267,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R8479:Ror2
|
UTSW |
13 |
53,271,400 (GRCm39) |
missense |
probably damaging |
0.98 |
R8684:Ror2
|
UTSW |
13 |
53,264,302 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8834:Ror2
|
UTSW |
13 |
53,264,338 (GRCm39) |
small deletion |
probably benign |
|
R8948:Ror2
|
UTSW |
13 |
53,286,032 (GRCm39) |
missense |
possibly damaging |
0.67 |
R9233:Ror2
|
UTSW |
13 |
53,265,590 (GRCm39) |
missense |
probably benign |
|
R9234:Ror2
|
UTSW |
13 |
53,265,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R9573:Ror2
|
UTSW |
13 |
53,265,467 (GRCm39) |
missense |
probably benign |
|
R9665:Ror2
|
UTSW |
13 |
53,439,561 (GRCm39) |
start codon destroyed |
probably null |
|
|