Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aacs |
T |
A |
5: 125,583,362 (GRCm39) |
|
probably null |
Het |
Arhgef1 |
A |
G |
7: 24,623,156 (GRCm39) |
I423V |
probably benign |
Het |
Aspm |
T |
C |
1: 139,408,280 (GRCm39) |
L2389P |
probably damaging |
Het |
B4galt1 |
T |
C |
4: 40,812,860 (GRCm39) |
M222V |
probably benign |
Het |
Bsn |
C |
A |
9: 107,985,016 (GRCm39) |
G3013C |
unknown |
Het |
Camsap2 |
T |
C |
1: 136,232,187 (GRCm39) |
H136R |
probably damaging |
Het |
Ccar1 |
A |
G |
10: 62,582,715 (GRCm39) |
V1047A |
unknown |
Het |
Ccdc80 |
A |
G |
16: 44,915,445 (GRCm39) |
E67G |
probably benign |
Het |
Ces3b |
G |
T |
8: 105,819,710 (GRCm39) |
G511V |
probably damaging |
Het |
Cops6 |
T |
A |
5: 138,161,790 (GRCm39) |
H224Q |
probably benign |
Het |
Dnah5 |
A |
T |
15: 28,235,866 (GRCm39) |
D331V |
probably damaging |
Het |
Dusp29 |
T |
C |
14: 21,727,135 (GRCm39) |
D171G |
probably damaging |
Het |
Ehmt2 |
G |
A |
17: 35,130,406 (GRCm39) |
C1017Y |
probably damaging |
Het |
Epb41l5 |
C |
T |
1: 119,536,859 (GRCm39) |
R344Q |
probably damaging |
Het |
Fcgbp |
G |
A |
7: 27,791,477 (GRCm39) |
V913I |
probably benign |
Het |
Foxd4 |
A |
G |
19: 24,877,240 (GRCm39) |
F320S |
probably damaging |
Het |
Frmpd4 |
C |
T |
X: 166,387,579 (GRCm39) |
R133K |
probably damaging |
Het |
Glmp |
A |
G |
3: 88,233,917 (GRCm39) |
Y258C |
probably damaging |
Het |
Gphn |
C |
G |
12: 78,538,955 (GRCm39) |
S200R |
possibly damaging |
Het |
Gvin2 |
G |
A |
7: 105,551,187 (GRCm39) |
Q622* |
probably null |
Het |
H2-Q7 |
T |
G |
17: 35,658,560 (GRCm39) |
M66R |
probably benign |
Het |
Hivep2 |
T |
A |
10: 14,004,058 (GRCm39) |
C219S |
probably damaging |
Het |
Hlcs |
A |
T |
16: 93,942,261 (GRCm39) |
M90K |
possibly damaging |
Het |
Itga8 |
C |
A |
2: 12,160,182 (GRCm39) |
|
probably null |
Het |
Klrk1 |
T |
A |
6: 129,598,203 (GRCm39) |
M1L |
possibly damaging |
Het |
Kmo |
T |
A |
1: 175,485,941 (GRCm39) |
F385I |
probably benign |
Het |
Lrit1 |
G |
C |
14: 36,782,052 (GRCm39) |
V242L |
probably damaging |
Het |
Lrrc3c |
A |
G |
11: 98,490,075 (GRCm39) |
D144G |
probably damaging |
Het |
Lyzl4 |
C |
T |
9: 121,412,047 (GRCm39) |
W123* |
probably null |
Het |
Map3k1 |
A |
G |
13: 111,909,246 (GRCm39) |
S77P |
probably benign |
Het |
Mark1 |
T |
C |
1: 184,630,984 (GRCm39) |
T709A |
probably damaging |
Het |
Nbr1 |
A |
T |
11: 101,468,777 (GRCm39) |
I878F |
probably damaging |
Het |
Nedd1 |
A |
T |
10: 92,547,168 (GRCm39) |
H118Q |
probably damaging |
Het |
Nfatc1 |
C |
T |
18: 80,678,770 (GRCm39) |
G873S |
probably damaging |
Het |
Ngly1 |
T |
G |
14: 16,283,467 (GRCm38) |
N415K |
probably damaging |
Het |
Nol6 |
C |
A |
4: 41,118,962 (GRCm39) |
R677L |
probably damaging |
Het |
Nop9 |
T |
C |
14: 55,990,270 (GRCm39) |
V471A |
probably benign |
Het |
Notch4 |
A |
G |
17: 34,802,577 (GRCm39) |
N1333D |
probably benign |
Het |
Nsun2 |
G |
A |
13: 69,778,152 (GRCm39) |
G478R |
probably damaging |
Het |
Or10x4 |
T |
A |
1: 174,219,407 (GRCm39) |
Y257* |
probably null |
Het |
Or1ad8 |
T |
A |
11: 50,898,153 (GRCm39) |
M118K |
probably damaging |
Het |
Or5m9b |
T |
C |
2: 85,905,264 (GRCm39) |
F60S |
probably damaging |
Het |
Or8g34 |
A |
T |
9: 39,373,159 (GRCm39) |
Y144F |
probably benign |
Het |
Pcp4l1 |
T |
C |
1: 171,002,022 (GRCm39) |
E46G |
possibly damaging |
Het |
Plek2 |
T |
C |
12: 78,936,083 (GRCm39) |
|
probably null |
Het |
Rbl1 |
T |
G |
2: 157,030,206 (GRCm39) |
I434L |
probably benign |
Het |
Ryr2 |
A |
G |
13: 11,581,834 (GRCm39) |
V4777A |
possibly damaging |
Het |
Sgk1 |
T |
C |
10: 21,758,593 (GRCm39) |
F19S |
probably damaging |
Het |
Stard9 |
C |
T |
2: 120,532,677 (GRCm39) |
A2978V |
probably benign |
Het |
Syne1 |
T |
C |
10: 5,033,940 (GRCm39) |
T7711A |
probably benign |
Het |
Taf10 |
G |
A |
7: 105,393,383 (GRCm39) |
T48I |
probably benign |
Het |
Tgfbi |
T |
G |
13: 56,784,989 (GRCm39) |
S649A |
possibly damaging |
Het |
Thbs3 |
T |
C |
3: 89,132,171 (GRCm39) |
V749A |
probably benign |
Het |
Tmem241 |
G |
T |
18: 12,180,641 (GRCm39) |
H218N |
possibly damaging |
Het |
Tmem266 |
C |
T |
9: 55,284,851 (GRCm39) |
|
probably benign |
Het |
Tnc |
T |
C |
4: 63,900,982 (GRCm39) |
I1586M |
probably damaging |
Het |
Ubr4 |
T |
A |
4: 139,164,442 (GRCm39) |
C2676* |
probably null |
Het |
Unc13a |
A |
T |
8: 72,105,021 (GRCm39) |
I747N |
probably damaging |
Het |
Vangl1 |
A |
T |
3: 102,073,097 (GRCm39) |
|
probably benign |
Het |
Vmn1r184 |
C |
T |
7: 25,966,563 (GRCm39) |
T103I |
possibly damaging |
Het |
Vmn1r204 |
T |
C |
13: 22,740,474 (GRCm39) |
V35A |
probably benign |
Het |
Vps13b |
A |
G |
15: 35,448,835 (GRCm39) |
H603R |
possibly damaging |
Het |
Zfp105 |
A |
G |
9: 122,754,303 (GRCm39) |
D44G |
probably benign |
Het |
Zfp11 |
T |
C |
5: 129,735,152 (GRCm39) |
H103R |
probably damaging |
Het |
Zfp335 |
A |
G |
2: 164,736,795 (GRCm39) |
F947L |
possibly damaging |
Het |
|
Other mutations in Echs1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02318:Echs1
|
APN |
7 |
139,691,623 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03342:Echs1
|
APN |
7 |
139,690,026 (GRCm39) |
splice site |
probably benign |
|
geistlische
|
UTSW |
7 |
139,692,982 (GRCm39) |
missense |
possibly damaging |
0.81 |
R2397:Echs1
|
UTSW |
7 |
139,692,390 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4517:Echs1
|
UTSW |
7 |
139,692,409 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4723:Echs1
|
UTSW |
7 |
139,690,561 (GRCm39) |
splice site |
probably benign |
|
R4858:Echs1
|
UTSW |
7 |
139,692,499 (GRCm39) |
unclassified |
probably benign |
|
R5523:Echs1
|
UTSW |
7 |
139,692,426 (GRCm39) |
missense |
probably benign |
0.01 |
R5747:Echs1
|
UTSW |
7 |
139,691,725 (GRCm39) |
unclassified |
probably benign |
|
R6244:Echs1
|
UTSW |
7 |
139,692,982 (GRCm39) |
missense |
possibly damaging |
0.81 |
R6474:Echs1
|
UTSW |
7 |
139,688,055 (GRCm39) |
missense |
probably benign |
0.44 |
R6917:Echs1
|
UTSW |
7 |
139,689,924 (GRCm39) |
missense |
probably benign |
0.00 |
R7761:Echs1
|
UTSW |
7 |
139,692,378 (GRCm39) |
missense |
probably damaging |
1.00 |
R7826:Echs1
|
UTSW |
7 |
139,696,349 (GRCm39) |
intron |
probably benign |
|
R8163:Echs1
|
UTSW |
7 |
139,692,357 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8680:Echs1
|
UTSW |
7 |
139,690,499 (GRCm39) |
missense |
probably damaging |
1.00 |
R8889:Echs1
|
UTSW |
7 |
139,688,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8892:Echs1
|
UTSW |
7 |
139,688,031 (GRCm39) |
missense |
probably damaging |
1.00 |
R8902:Echs1
|
UTSW |
7 |
139,690,499 (GRCm39) |
missense |
probably damaging |
1.00 |
|