Other mutations in this stock |
Total: 43 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
C |
T |
3: 137,774,561 (GRCm39) |
T1250M |
probably damaging |
Het |
Actn1 |
C |
T |
12: 80,215,191 (GRCm39) |
A857T |
possibly damaging |
Het |
Adam2 |
C |
T |
14: 66,296,239 (GRCm39) |
V207I |
probably damaging |
Het |
Angpt2 |
T |
C |
8: 18,744,533 (GRCm39) |
T404A |
probably benign |
Het |
Ank3 |
T |
C |
10: 69,827,574 (GRCm39) |
|
probably benign |
Het |
Atosa |
C |
A |
9: 74,930,930 (GRCm39) |
Q958K |
probably damaging |
Het |
B4galt4 |
T |
A |
16: 38,578,184 (GRCm39) |
D210E |
probably benign |
Het |
Brinp3 |
A |
T |
1: 146,777,431 (GRCm39) |
H626L |
possibly damaging |
Het |
Ccna2 |
T |
G |
3: 36,625,112 (GRCm39) |
D68A |
probably damaging |
Het |
Chrm5 |
A |
T |
2: 112,310,825 (GRCm39) |
V97D |
probably benign |
Het |
Dctn5 |
G |
A |
7: 121,734,320 (GRCm39) |
V55I |
probably benign |
Het |
Dnm3 |
A |
T |
1: 162,141,164 (GRCm39) |
I365N |
probably damaging |
Het |
Esyt2 |
A |
G |
12: 116,284,790 (GRCm39) |
D184G |
probably damaging |
Het |
Ifi214 |
C |
A |
1: 173,352,597 (GRCm39) |
K277N |
probably damaging |
Het |
Il11ra1 |
C |
T |
4: 41,765,412 (GRCm39) |
P169L |
probably benign |
Het |
Inhbb |
C |
T |
1: 119,345,069 (GRCm39) |
E407K |
probably damaging |
Het |
Lama2 |
T |
A |
10: 26,907,154 (GRCm39) |
T2336S |
probably damaging |
Het |
Ldhb |
A |
T |
6: 142,439,847 (GRCm39) |
V231E |
possibly damaging |
Het |
Lrit2 |
T |
C |
14: 36,790,767 (GRCm39) |
F149L |
probably damaging |
Het |
Malrd1 |
T |
A |
2: 15,936,500 (GRCm39) |
S1575T |
probably benign |
Het |
Naip5 |
A |
G |
13: 100,358,102 (GRCm39) |
C1045R |
probably benign |
Het |
Nefl |
A |
G |
14: 68,322,034 (GRCm39) |
E208G |
probably damaging |
Het |
Oog4 |
A |
C |
4: 143,164,548 (GRCm39) |
S328A |
probably damaging |
Het |
Or1e1 |
T |
A |
11: 73,245,011 (GRCm39) |
L144Q |
probably damaging |
Het |
Or5p79 |
G |
T |
7: 108,221,713 (GRCm39) |
M231I |
probably benign |
Het |
Or6c216 |
T |
C |
10: 129,678,453 (GRCm39) |
I153V |
probably benign |
Het |
Or7e168 |
A |
G |
9: 19,719,847 (GRCm39) |
I78V |
probably benign |
Het |
Pbrm1 |
A |
G |
14: 30,783,466 (GRCm39) |
N528D |
probably damaging |
Het |
Pls1 |
A |
G |
9: 95,636,798 (GRCm39) |
I558T |
probably damaging |
Het |
Polq |
T |
C |
16: 36,881,189 (GRCm39) |
S839P |
probably benign |
Het |
Psmg1 |
A |
G |
16: 95,789,297 (GRCm39) |
F87L |
probably damaging |
Het |
Ptprt |
A |
G |
2: 161,376,507 (GRCm39) |
M1298T |
probably benign |
Het |
Rbm27 |
T |
A |
18: 42,470,076 (GRCm39) |
W958R |
probably damaging |
Het |
Skint5 |
T |
G |
4: 113,396,552 (GRCm39) |
D1207A |
unknown |
Het |
Stx17 |
T |
A |
4: 48,183,478 (GRCm39) |
|
probably null |
Het |
Tas2r114 |
A |
T |
6: 131,666,099 (GRCm39) |
*310R |
probably null |
Het |
Tmem130 |
T |
A |
5: 144,689,224 (GRCm39) |
N139I |
probably damaging |
Het |
Trpc1 |
T |
C |
9: 95,608,490 (GRCm39) |
E267G |
probably damaging |
Het |
Trrap |
T |
A |
5: 144,793,812 (GRCm39) |
M3398K |
probably damaging |
Het |
Vrtn |
T |
G |
12: 84,697,090 (GRCm39) |
D613E |
probably benign |
Het |
Vsx1 |
G |
T |
2: 150,530,441 (GRCm39) |
T147K |
probably benign |
Het |
Wdr55 |
T |
C |
18: 36,895,231 (GRCm39) |
V103A |
probably benign |
Het |
Zfp712 |
A |
T |
13: 67,200,400 (GRCm39) |
D28E |
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 |
IGL02101:Cd163
|
APN |
6 |
124,284,246 (GRCm39) |
nonsense |
probably null |
|
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 |
|
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 |
|