Other mutations in this stock |
Total: 45 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca12 |
C |
T |
1: 71,349,047 (GRCm39) |
|
probably null |
Het |
Acsl5 |
A |
G |
19: 55,280,259 (GRCm39) |
T511A |
probably damaging |
Het |
Ankrd35 |
A |
G |
3: 96,589,353 (GRCm39) |
I191V |
probably damaging |
Het |
Apmap |
T |
C |
2: 150,428,385 (GRCm39) |
Q254R |
probably benign |
Het |
Arhgef12 |
A |
T |
9: 42,908,944 (GRCm39) |
L661Q |
possibly damaging |
Het |
Atf7ip2 |
T |
A |
16: 10,055,129 (GRCm39) |
|
probably benign |
Het |
Braf |
T |
C |
6: 39,604,693 (GRCm39) |
H592R |
probably benign |
Het |
Dgcr6 |
T |
C |
16: 17,887,390 (GRCm39) |
|
probably null |
Het |
Efcab12 |
T |
C |
6: 115,791,535 (GRCm39) |
I546V |
probably benign |
Het |
Eya1 |
G |
T |
1: 14,322,672 (GRCm39) |
A268E |
probably damaging |
Het |
Fbxl12 |
C |
A |
9: 20,550,160 (GRCm39) |
R165L |
possibly damaging |
Het |
Gas6 |
T |
C |
8: 13,515,790 (GRCm39) |
I661V |
probably damaging |
Het |
Gipc3 |
T |
A |
10: 81,174,055 (GRCm39) |
M240L |
possibly damaging |
Het |
Gm12689 |
A |
G |
4: 99,184,450 (GRCm39) |
D101G |
unknown |
Het |
Kctd2 |
G |
T |
11: 115,320,310 (GRCm39) |
|
probably benign |
Het |
Kdm5b |
A |
T |
1: 134,533,512 (GRCm39) |
M534L |
possibly damaging |
Het |
Kif14 |
T |
A |
1: 136,396,495 (GRCm39) |
V267D |
possibly damaging |
Het |
Lca5l |
C |
A |
16: 95,960,438 (GRCm39) |
G675C |
probably damaging |
Het |
Lmod1 |
T |
C |
1: 135,292,221 (GRCm39) |
F359L |
possibly damaging |
Het |
Lonrf1 |
G |
T |
8: 36,686,986 (GRCm39) |
N783K |
possibly damaging |
Het |
Megf10 |
T |
C |
18: 57,425,790 (GRCm39) |
S1059P |
probably benign |
Het |
Mmp24 |
A |
G |
2: 155,641,634 (GRCm39) |
E154G |
probably benign |
Het |
Mtus2 |
A |
C |
5: 148,240,408 (GRCm39) |
K85T |
probably damaging |
Het |
Myh11 |
T |
C |
16: 14,048,570 (GRCm39) |
H586R |
probably damaging |
Het |
Noc2l |
A |
G |
4: 156,326,187 (GRCm39) |
T425A |
probably benign |
Het |
Olfm3 |
A |
T |
3: 114,916,196 (GRCm39) |
Q376L |
probably benign |
Het |
Pax5 |
A |
T |
4: 44,570,071 (GRCm39) |
Y272N |
probably damaging |
Het |
Rasgrp1 |
A |
T |
2: 117,168,785 (GRCm39) |
D64E |
probably benign |
Het |
Rb1cc1 |
T |
A |
1: 6,315,099 (GRCm39) |
N417K |
probably damaging |
Het |
Rpl3l |
A |
G |
17: 24,954,754 (GRCm39) |
D369G |
probably damaging |
Het |
Scn3a |
G |
T |
2: 65,327,863 (GRCm39) |
H876N |
probably damaging |
Het |
Slc29a3 |
A |
G |
10: 60,566,401 (GRCm39) |
S111P |
probably damaging |
Het |
Smarca2 |
G |
C |
19: 26,654,187 (GRCm39) |
V791L |
probably damaging |
Het |
Smc4 |
T |
A |
3: 68,940,224 (GRCm39) |
|
probably null |
Het |
Sorbs1 |
G |
C |
19: 40,365,244 (GRCm39) |
R180G |
probably benign |
Het |
Tanc2 |
A |
G |
11: 105,807,834 (GRCm39) |
E1288G |
probably damaging |
Het |
Tex52 |
G |
A |
6: 128,356,828 (GRCm39) |
V174I |
probably benign |
Het |
Tjp2 |
C |
A |
19: 24,088,937 (GRCm39) |
G660W |
probably damaging |
Het |
Tmem121b |
T |
C |
6: 120,469,055 (GRCm39) |
E554G |
probably damaging |
Het |
Tmem209 |
C |
A |
6: 30,497,237 (GRCm39) |
V318F |
probably damaging |
Het |
Tnxb |
A |
G |
17: 34,907,634 (GRCm39) |
E1226G |
probably damaging |
Het |
Traf3ip3 |
T |
A |
1: 192,876,851 (GRCm39) |
I196F |
probably damaging |
Het |
Trpc4ap |
G |
C |
2: 155,534,132 (GRCm39) |
P32R |
unknown |
Het |
Vav3 |
A |
G |
3: 109,410,787 (GRCm39) |
K206R |
probably damaging |
Het |
Zan |
T |
C |
5: 137,433,971 (GRCm39) |
E2254G |
unknown |
Het |
|
Other mutations in Ceacam2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00788:Ceacam2
|
APN |
7 |
25,237,998 (GRCm39) |
critical splice donor site |
probably null |
|
IGL01606:Ceacam2
|
APN |
7 |
25,230,132 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02106:Ceacam2
|
APN |
7 |
25,230,166 (GRCm39) |
missense |
probably benign |
|
IGL02506:Ceacam2
|
APN |
7 |
25,227,379 (GRCm39) |
missense |
probably benign |
0.34 |
IGL02820:Ceacam2
|
APN |
7 |
25,219,411 (GRCm39) |
missense |
probably damaging |
1.00 |
R0514:Ceacam2
|
UTSW |
7 |
25,220,356 (GRCm39) |
missense |
probably benign |
0.43 |
R2146:Ceacam2
|
UTSW |
7 |
25,227,368 (GRCm39) |
nonsense |
probably null |
|
R3854:Ceacam2
|
UTSW |
7 |
25,238,227 (GRCm39) |
missense |
probably benign |
0.06 |
R4887:Ceacam2
|
UTSW |
7 |
25,220,257 (GRCm39) |
missense |
probably benign |
0.00 |
R6480:Ceacam2
|
UTSW |
7 |
25,219,414 (GRCm39) |
missense |
probably damaging |
1.00 |
R6533:Ceacam2
|
UTSW |
7 |
25,230,136 (GRCm39) |
missense |
probably benign |
0.03 |
R6709:Ceacam2
|
UTSW |
7 |
25,229,262 (GRCm39) |
missense |
possibly damaging |
0.95 |
R6711:Ceacam2
|
UTSW |
7 |
25,238,295 (GRCm39) |
missense |
probably benign |
|
R6853:Ceacam2
|
UTSW |
7 |
25,217,561 (GRCm39) |
missense |
possibly damaging |
0.54 |
R7177:Ceacam2
|
UTSW |
7 |
25,220,341 (GRCm39) |
missense |
probably benign |
0.11 |
R7548:Ceacam2
|
UTSW |
7 |
25,229,958 (GRCm39) |
missense |
probably benign |
0.00 |
R7567:Ceacam2
|
UTSW |
7 |
25,227,333 (GRCm39) |
missense |
probably benign |
0.12 |
R7709:Ceacam2
|
UTSW |
7 |
25,238,076 (GRCm39) |
missense |
probably damaging |
0.97 |
R8378:Ceacam2
|
UTSW |
7 |
25,217,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R8878:Ceacam2
|
UTSW |
7 |
25,227,351 (GRCm39) |
missense |
probably benign |
0.06 |
R9186:Ceacam2
|
UTSW |
7 |
25,227,213 (GRCm39) |
missense |
probably damaging |
1.00 |
R9321:Ceacam2
|
UTSW |
7 |
25,230,089 (GRCm39) |
missense |
possibly damaging |
0.84 |
|