Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4921528I07Rik |
T |
C |
9: 114,130,770 (GRCm39) |
|
noncoding transcript |
Het |
Apob |
A |
G |
12: 8,056,017 (GRCm39) |
K1500E |
probably benign |
Het |
Atp8b1 |
A |
T |
18: 64,706,333 (GRCm39) |
Y225* |
probably null |
Het |
Cdc25c |
A |
T |
18: 34,882,026 (GRCm39) |
|
probably benign |
Het |
Cntln |
T |
C |
4: 84,914,716 (GRCm39) |
S508P |
probably damaging |
Het |
Defa41 |
T |
A |
8: 21,692,449 (GRCm39) |
F90Y |
probably benign |
Het |
Dhx34 |
A |
G |
7: 15,952,293 (GRCm39) |
S111P |
probably damaging |
Het |
Dst |
A |
G |
1: 34,203,248 (GRCm39) |
E759G |
probably damaging |
Het |
Fis1 |
G |
A |
5: 136,994,000 (GRCm39) |
A28T |
probably damaging |
Het |
Fsd1 |
T |
C |
17: 56,297,542 (GRCm39) |
|
probably null |
Het |
Grk6 |
T |
C |
13: 55,602,340 (GRCm39) |
|
probably null |
Het |
Il23r |
A |
T |
6: 67,450,794 (GRCm39) |
H228Q |
probably benign |
Het |
Kcnh4 |
C |
T |
11: 100,643,164 (GRCm39) |
V368I |
possibly damaging |
Het |
Kdr |
T |
C |
5: 76,116,891 (GRCm39) |
E728G |
probably damaging |
Het |
Krt33a |
T |
A |
11: 99,906,763 (GRCm39) |
M71L |
probably benign |
Het |
Lrrc7 |
T |
G |
3: 157,866,780 (GRCm39) |
D987A |
probably damaging |
Het |
Naalad2 |
C |
T |
9: 18,258,802 (GRCm39) |
R491Q |
probably damaging |
Het |
Nedd4l |
A |
T |
18: 65,300,570 (GRCm39) |
|
probably benign |
Het |
Pramel7 |
A |
G |
2: 87,321,534 (GRCm39) |
L167S |
probably damaging |
Het |
Prkci |
A |
G |
3: 31,104,341 (GRCm39) |
D568G |
probably damaging |
Het |
Psg18 |
G |
A |
7: 18,085,000 (GRCm39) |
T32I |
possibly damaging |
Het |
Ric8b |
T |
A |
10: 84,806,581 (GRCm39) |
|
probably benign |
Het |
Rnf213 |
T |
C |
11: 119,376,824 (GRCm39) |
|
probably benign |
Het |
Rttn |
T |
C |
18: 89,082,373 (GRCm39) |
V1433A |
probably damaging |
Het |
Sbf2 |
A |
T |
7: 109,966,379 (GRCm39) |
|
probably benign |
Het |
Sdk2 |
C |
T |
11: 113,729,472 (GRCm39) |
|
silent |
Het |
Sfta2 |
T |
C |
17: 35,961,019 (GRCm39) |
|
probably benign |
Het |
Slc17a1 |
T |
A |
13: 24,062,433 (GRCm39) |
|
probably benign |
Het |
Slc6a21 |
G |
A |
7: 44,937,626 (GRCm39) |
C314Y |
probably benign |
Het |
Smpd4 |
T |
C |
16: 17,441,833 (GRCm39) |
V35A |
probably damaging |
Het |
Sorl1 |
T |
C |
9: 41,925,786 (GRCm39) |
D1182G |
probably damaging |
Het |
Syne2 |
A |
G |
12: 76,088,809 (GRCm39) |
I5056V |
possibly damaging |
Het |
Tex14 |
T |
C |
11: 87,410,571 (GRCm39) |
|
probably benign |
Het |
Tex44 |
A |
G |
1: 86,354,777 (GRCm39) |
T229A |
probably benign |
Het |
Tfap2b |
T |
A |
1: 19,304,373 (GRCm39) |
C394* |
probably null |
Het |
Ttk |
T |
A |
9: 83,726,202 (GRCm39) |
|
probably benign |
Het |
Vmn2r26 |
G |
A |
6: 124,030,872 (GRCm39) |
V536I |
probably benign |
Het |
Wac |
A |
G |
18: 7,921,916 (GRCm39) |
T553A |
probably damaging |
Het |
Wdcp |
T |
A |
12: 4,900,685 (GRCm39) |
H180Q |
probably damaging |
Het |
Wdr33 |
A |
G |
18: 31,968,514 (GRCm39) |
H235R |
probably benign |
Het |
|
Other mutations in Ceacam15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL03367:Ceacam15
|
APN |
7 |
16,409,512 (GRCm39) |
missense |
possibly damaging |
0.47 |
R0144:Ceacam15
|
UTSW |
7 |
16,407,116 (GRCm39) |
missense |
probably benign |
0.32 |
R0517:Ceacam15
|
UTSW |
7 |
16,407,445 (GRCm39) |
nonsense |
probably null |
|
R0612:Ceacam15
|
UTSW |
7 |
16,407,445 (GRCm39) |
nonsense |
probably null |
|
R0697:Ceacam15
|
UTSW |
7 |
16,407,445 (GRCm39) |
nonsense |
probably null |
|
R1257:Ceacam15
|
UTSW |
7 |
16,405,949 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1389:Ceacam15
|
UTSW |
7 |
16,405,988 (GRCm39) |
missense |
probably damaging |
0.99 |
R4602:Ceacam15
|
UTSW |
7 |
16,405,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R4623:Ceacam15
|
UTSW |
7 |
16,407,391 (GRCm39) |
missense |
probably damaging |
0.97 |
R4674:Ceacam15
|
UTSW |
7 |
16,407,410 (GRCm39) |
missense |
probably benign |
0.09 |
R4675:Ceacam15
|
UTSW |
7 |
16,407,410 (GRCm39) |
missense |
probably benign |
0.09 |
R4745:Ceacam15
|
UTSW |
7 |
16,407,259 (GRCm39) |
missense |
probably benign |
|
R5296:Ceacam15
|
UTSW |
7 |
16,407,121 (GRCm39) |
missense |
probably benign |
0.09 |
R5510:Ceacam15
|
UTSW |
7 |
16,406,024 (GRCm39) |
missense |
probably damaging |
1.00 |
R6210:Ceacam15
|
UTSW |
7 |
16,407,214 (GRCm39) |
missense |
probably damaging |
0.99 |
R7414:Ceacam15
|
UTSW |
7 |
16,407,235 (GRCm39) |
missense |
probably benign |
0.24 |
R8110:Ceacam15
|
UTSW |
7 |
16,407,334 (GRCm39) |
missense |
probably benign |
0.00 |
R8341:Ceacam15
|
UTSW |
7 |
16,405,928 (GRCm39) |
missense |
probably benign |
0.17 |
R9553:Ceacam15
|
UTSW |
7 |
16,407,316 (GRCm39) |
missense |
probably damaging |
1.00 |
X0020:Ceacam15
|
UTSW |
7 |
16,409,531 (GRCm39) |
start codon destroyed |
probably null |
0.00 |
Z1176:Ceacam15
|
UTSW |
7 |
16,409,508 (GRCm39) |
missense |
possibly damaging |
0.83 |
|