Other mutations in this stock |
Total: 27 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ces2g |
A |
G |
8: 105,691,769 (GRCm39) |
|
probably null |
Het |
Ckap5 |
T |
C |
2: 91,402,885 (GRCm39) |
|
probably benign |
Het |
Cmtm7 |
T |
C |
9: 114,592,336 (GRCm39) |
H87R |
probably damaging |
Het |
Dennd3 |
A |
G |
15: 73,399,794 (GRCm39) |
D220G |
possibly damaging |
Het |
Dpp10 |
T |
C |
1: 123,339,555 (GRCm39) |
Y324C |
probably damaging |
Het |
Dsc3 |
C |
T |
18: 20,134,963 (GRCm39) |
R7Q |
probably benign |
Het |
Ezh1 |
T |
C |
11: 101,086,392 (GRCm39) |
K598E |
possibly damaging |
Het |
Ighv7-3 |
A |
G |
12: 114,117,045 (GRCm39) |
L39P |
probably damaging |
Het |
Il1rap |
T |
A |
16: 26,442,932 (GRCm39) |
S9R |
possibly damaging |
Het |
Mrgpra3 |
A |
G |
7: 47,239,300 (GRCm39) |
C209R |
probably damaging |
Het |
Oc90 |
G |
T |
15: 65,769,638 (GRCm39) |
P73Q |
probably damaging |
Het |
Or2m12 |
T |
C |
16: 19,105,363 (GRCm39) |
I43M |
probably benign |
Het |
Or3a1b |
G |
A |
11: 74,012,571 (GRCm39) |
W152* |
probably null |
Het |
Pccb |
A |
G |
9: 100,869,894 (GRCm39) |
F346L |
possibly damaging |
Het |
Pdxdc1 |
A |
G |
16: 13,687,720 (GRCm39) |
I225T |
probably damaging |
Het |
Pold3 |
A |
T |
7: 99,749,703 (GRCm39) |
M154K |
probably damaging |
Het |
Polr1a |
T |
G |
6: 71,927,786 (GRCm39) |
C846G |
probably benign |
Het |
Ppip5k1 |
C |
A |
2: 121,162,089 (GRCm39) |
R978L |
possibly damaging |
Het |
Ptpn4 |
A |
G |
1: 119,615,408 (GRCm39) |
V582A |
probably damaging |
Het |
Sez6l |
G |
T |
5: 112,620,612 (GRCm39) |
Q323K |
probably damaging |
Het |
Slc27a5 |
A |
T |
7: 12,727,270 (GRCm39) |
I384N |
possibly damaging |
Het |
Slc39a10 |
G |
A |
1: 46,857,288 (GRCm39) |
A696V |
probably damaging |
Het |
Slc7a2 |
T |
C |
8: 41,355,631 (GRCm39) |
F227L |
probably benign |
Het |
Smad4 |
C |
A |
18: 73,791,723 (GRCm39) |
A273S |
probably benign |
Het |
Spata17 |
T |
C |
1: 186,849,657 (GRCm39) |
I84V |
probably benign |
Het |
Sphkap |
T |
C |
1: 83,268,708 (GRCm39) |
T95A |
probably damaging |
Het |
Tie1 |
T |
C |
4: 118,329,995 (GRCm39) |
D1076G |
probably benign |
Het |
|
Other mutations in Cd163 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00232:Cd163
|
APN |
6 |
124,306,060 (GRCm39) |
splice site |
probably benign |
|
IGL00755:Cd163
|
APN |
6 |
124,295,616 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL01690:Cd163
|
APN |
6 |
124,284,277 (GRCm39) |
missense |
possibly damaging |
0.89 |
IGL02733:Cd163
|
APN |
6 |
124,302,300 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02801:Cd163
|
APN |
6 |
124,297,488 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02897:Cd163
|
APN |
6 |
124,302,486 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03074:Cd163
|
APN |
6 |
124,294,945 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03283:Cd163
|
APN |
6 |
124,286,158 (GRCm39) |
missense |
possibly damaging |
0.49 |
compass
|
UTSW |
6 |
124,306,045 (GRCm39) |
makesense |
probably null |
|
hottish
|
UTSW |
6 |
124,286,167 (GRCm39) |
missense |
probably damaging |
1.00 |
protractor
|
UTSW |
6 |
124,288,525 (GRCm39) |
missense |
probably damaging |
1.00 |
t-square
|
UTSW |
6 |
124,302,247 (GRCm39) |
missense |
probably damaging |
0.97 |
R0494:Cd163
|
UTSW |
6 |
124,288,408 (GRCm39) |
missense |
probably damaging |
1.00 |
R0554:Cd163
|
UTSW |
6 |
124,289,619 (GRCm39) |
missense |
probably benign |
0.03 |
R0622:Cd163
|
UTSW |
6 |
124,294,311 (GRCm39) |
missense |
probably damaging |
1.00 |
R1004:Cd163
|
UTSW |
6 |
124,302,306 (GRCm39) |
missense |
probably damaging |
1.00 |
R1061:Cd163
|
UTSW |
6 |
124,286,128 (GRCm39) |
missense |
probably benign |
0.00 |
R1132:Cd163
|
UTSW |
6 |
124,286,055 (GRCm39) |
nonsense |
probably null |
|
R1195:Cd163
|
UTSW |
6 |
124,302,209 (GRCm39) |
splice site |
probably benign |
|
R1195:Cd163
|
UTSW |
6 |
124,302,209 (GRCm39) |
splice site |
probably benign |
|
R1436:Cd163
|
UTSW |
6 |
124,304,890 (GRCm39) |
missense |
possibly damaging |
0.47 |
R1463:Cd163
|
UTSW |
6 |
124,288,406 (GRCm39) |
missense |
probably damaging |
1.00 |
R1532:Cd163
|
UTSW |
6 |
124,289,689 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1541:Cd163
|
UTSW |
6 |
124,304,920 (GRCm39) |
missense |
probably benign |
|
R1654:Cd163
|
UTSW |
6 |
124,294,540 (GRCm39) |
missense |
probably damaging |
1.00 |
R1717:Cd163
|
UTSW |
6 |
124,306,547 (GRCm39) |
utr 3 prime |
probably benign |
|
R1744:Cd163
|
UTSW |
6 |
124,283,987 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2014:Cd163
|
UTSW |
6 |
124,302,457 (GRCm39) |
missense |
probably damaging |
0.99 |
R2035:Cd163
|
UTSW |
6 |
124,297,588 (GRCm39) |
missense |
probably damaging |
0.97 |
R2095:Cd163
|
UTSW |
6 |
124,294,781 (GRCm39) |
missense |
probably damaging |
1.00 |
R2124:Cd163
|
UTSW |
6 |
124,295,815 (GRCm39) |
missense |
probably damaging |
1.00 |
R2146:Cd163
|
UTSW |
6 |
124,286,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R2353:Cd163
|
UTSW |
6 |
124,296,115 (GRCm39) |
nonsense |
probably null |
|
R3854:Cd163
|
UTSW |
6 |
124,288,525 (GRCm39) |
missense |
probably damaging |
1.00 |
R4425:Cd163
|
UTSW |
6 |
124,304,862 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4631:Cd163
|
UTSW |
6 |
124,306,045 (GRCm39) |
makesense |
probably null |
|
R4647:Cd163
|
UTSW |
6 |
124,297,580 (GRCm39) |
missense |
probably damaging |
1.00 |
R4713:Cd163
|
UTSW |
6 |
124,294,577 (GRCm39) |
critical splice donor site |
probably null |
|
R4803:Cd163
|
UTSW |
6 |
124,289,389 (GRCm39) |
missense |
probably damaging |
0.99 |
R4996:Cd163
|
UTSW |
6 |
124,296,106 (GRCm39) |
missense |
probably benign |
0.00 |
R5022:Cd163
|
UTSW |
6 |
124,302,247 (GRCm39) |
missense |
probably damaging |
0.97 |
R5023:Cd163
|
UTSW |
6 |
124,302,247 (GRCm39) |
missense |
probably damaging |
0.97 |
R5032:Cd163
|
UTSW |
6 |
124,288,628 (GRCm39) |
missense |
probably damaging |
1.00 |
R5057:Cd163
|
UTSW |
6 |
124,302,247 (GRCm39) |
missense |
probably damaging |
0.97 |
R5121:Cd163
|
UTSW |
6 |
124,294,948 (GRCm39) |
missense |
probably damaging |
1.00 |
R5436:Cd163
|
UTSW |
6 |
124,304,923 (GRCm39) |
missense |
probably benign |
|
R5453:Cd163
|
UTSW |
6 |
124,289,500 (GRCm39) |
missense |
probably damaging |
1.00 |
R5723:Cd163
|
UTSW |
6 |
124,296,022 (GRCm39) |
missense |
probably benign |
0.00 |
R5929:Cd163
|
UTSW |
6 |
124,303,568 (GRCm39) |
critical splice donor site |
probably null |
|
R5943:Cd163
|
UTSW |
6 |
124,306,561 (GRCm39) |
makesense |
probably null |
|
R5964:Cd163
|
UTSW |
6 |
124,303,531 (GRCm39) |
missense |
probably benign |
0.01 |
R5966:Cd163
|
UTSW |
6 |
124,297,595 (GRCm39) |
nonsense |
probably null |
|
R6279:Cd163
|
UTSW |
6 |
124,294,950 (GRCm39) |
nonsense |
probably null |
|
R6300:Cd163
|
UTSW |
6 |
124,294,950 (GRCm39) |
nonsense |
probably null |
|
R6499:Cd163
|
UTSW |
6 |
124,281,703 (GRCm39) |
missense |
probably benign |
0.00 |
R6602:Cd163
|
UTSW |
6 |
124,288,594 (GRCm39) |
missense |
probably damaging |
1.00 |
R6708:Cd163
|
UTSW |
6 |
124,286,167 (GRCm39) |
missense |
probably damaging |
1.00 |
R6767:Cd163
|
UTSW |
6 |
124,281,738 (GRCm39) |
missense |
possibly damaging |
0.56 |
R6979:Cd163
|
UTSW |
6 |
124,294,945 (GRCm39) |
missense |
probably benign |
0.00 |
R6993:Cd163
|
UTSW |
6 |
124,294,673 (GRCm39) |
missense |
probably damaging |
1.00 |
R7345:Cd163
|
UTSW |
6 |
124,295,897 (GRCm39) |
missense |
possibly damaging |
0.52 |
R7382:Cd163
|
UTSW |
6 |
124,288,271 (GRCm39) |
splice site |
probably null |
|
R7552:Cd163
|
UTSW |
6 |
124,284,187 (GRCm39) |
missense |
probably benign |
0.08 |
R7829:Cd163
|
UTSW |
6 |
124,281,738 (GRCm39) |
missense |
probably benign |
0.04 |
R8354:Cd163
|
UTSW |
6 |
124,305,924 (GRCm39) |
missense |
probably benign |
0.43 |
R8454:Cd163
|
UTSW |
6 |
124,305,924 (GRCm39) |
missense |
probably benign |
0.43 |
R8530:Cd163
|
UTSW |
6 |
124,295,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R8560:Cd163
|
UTSW |
6 |
124,294,360 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8878:Cd163
|
UTSW |
6 |
124,297,469 (GRCm39) |
missense |
probably damaging |
0.99 |
R8930:Cd163
|
UTSW |
6 |
124,294,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R8932:Cd163
|
UTSW |
6 |
124,294,882 (GRCm39) |
missense |
probably damaging |
1.00 |
R9074:Cd163
|
UTSW |
6 |
124,285,947 (GRCm39) |
nonsense |
probably null |
|
R9408:Cd163
|
UTSW |
6 |
124,297,497 (GRCm39) |
missense |
probably benign |
0.39 |
R9530:Cd163
|
UTSW |
6 |
124,294,491 (GRCm39) |
nonsense |
probably null |
|
R9558:Cd163
|
UTSW |
6 |
124,297,471 (GRCm39) |
missense |
probably benign |
0.01 |
R9608:Cd163
|
UTSW |
6 |
124,286,163 (GRCm39) |
missense |
possibly damaging |
0.79 |
R9685:Cd163
|
UTSW |
6 |
124,288,384 (GRCm39) |
missense |
possibly damaging |
0.77 |
Z1177:Cd163
|
UTSW |
6 |
124,294,344 (GRCm39) |
missense |
probably benign |
0.34 |
|