Other mutations in this stock |
Total: 48 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931406B18Rik |
G |
T |
7: 43,150,519 (GRCm39) |
Y84* |
probably null |
Het |
Adam5 |
A |
G |
8: 25,302,395 (GRCm39) |
|
probably benign |
Het |
Aipl1 |
T |
C |
11: 71,920,222 (GRCm39) |
E282G |
possibly damaging |
Het |
Akp3 |
A |
G |
1: 87,052,994 (GRCm39) |
D61G |
probably damaging |
Het |
Anpep |
A |
G |
7: 79,488,478 (GRCm39) |
S451P |
probably damaging |
Het |
Csnka2ip |
A |
G |
16: 64,298,675 (GRCm39) |
L119P |
probably damaging |
Het |
Ddx19a |
T |
C |
8: 111,716,241 (GRCm39) |
E53G |
probably benign |
Het |
Ddx50 |
C |
T |
10: 62,452,072 (GRCm39) |
R116Q |
unknown |
Het |
Ddx60 |
A |
T |
8: 62,441,166 (GRCm39) |
E1078D |
probably damaging |
Het |
Dpy19l1 |
T |
C |
9: 24,396,368 (GRCm39) |
D116G |
probably damaging |
Het |
Dsg4 |
A |
G |
18: 20,597,933 (GRCm39) |
T668A |
possibly damaging |
Het |
Dspp |
A |
G |
5: 104,323,843 (GRCm39) |
T329A |
possibly damaging |
Het |
Eftud2 |
T |
C |
11: 102,737,440 (GRCm39) |
T554A |
probably damaging |
Het |
Enpp1 |
T |
C |
10: 24,555,083 (GRCm39) |
|
probably benign |
Het |
Ext2 |
A |
T |
2: 93,537,590 (GRCm39) |
F599I |
probably damaging |
Het |
Fahd1 |
A |
T |
17: 25,068,504 (GRCm39) |
I191N |
probably damaging |
Het |
Fcrl2 |
A |
T |
3: 87,166,694 (GRCm39) |
S100T |
probably benign |
Het |
Fras1 |
T |
A |
5: 96,692,883 (GRCm39) |
C181S |
probably damaging |
Het |
Garre1 |
T |
A |
7: 33,941,834 (GRCm39) |
|
probably benign |
Het |
Gcnt4 |
A |
G |
13: 97,083,741 (GRCm39) |
I346V |
probably benign |
Het |
Gfra1 |
G |
A |
19: 58,441,787 (GRCm39) |
T48I |
probably damaging |
Het |
Kcnma1 |
A |
G |
14: 23,513,224 (GRCm39) |
Y392H |
probably damaging |
Het |
Klc2 |
T |
C |
19: 5,161,696 (GRCm39) |
Y298C |
probably damaging |
Het |
Lamb3 |
G |
A |
1: 193,021,830 (GRCm39) |
V1011I |
probably benign |
Het |
Ldb1 |
T |
C |
19: 46,024,594 (GRCm39) |
|
probably benign |
Het |
Mcph1 |
A |
G |
8: 18,675,609 (GRCm39) |
K11E |
probably damaging |
Het |
Myc |
A |
G |
15: 61,861,513 (GRCm39) |
H374R |
probably damaging |
Het |
Myom1 |
A |
G |
17: 71,391,344 (GRCm39) |
Y853C |
probably damaging |
Het |
Or4k38 |
A |
T |
2: 111,166,147 (GRCm39) |
I92N |
probably damaging |
Het |
Pakap |
C |
T |
4: 57,856,263 (GRCm39) |
P572S |
probably benign |
Het |
Pclo |
A |
G |
5: 14,726,943 (GRCm39) |
|
probably benign |
Het |
Pde3a |
G |
A |
6: 141,350,898 (GRCm39) |
|
probably benign |
Het |
Per1 |
T |
C |
11: 68,997,486 (GRCm39) |
V887A |
probably benign |
Het |
Prokr1 |
G |
A |
6: 87,565,350 (GRCm39) |
|
probably benign |
Het |
Rb1cc1 |
A |
G |
1: 6,319,643 (GRCm39) |
I1021V |
probably benign |
Het |
Ryr1 |
T |
C |
7: 28,810,033 (GRCm39) |
E344G |
probably benign |
Het |
Sec24c |
A |
T |
14: 20,739,710 (GRCm39) |
D529V |
probably damaging |
Het |
Slc1a6 |
T |
C |
10: 78,624,898 (GRCm39) |
V101A |
probably damaging |
Het |
Srrm1 |
G |
A |
4: 135,052,415 (GRCm39) |
P658L |
unknown |
Het |
Tap2 |
G |
A |
17: 34,431,021 (GRCm39) |
V374M |
probably benign |
Het |
Tex15 |
T |
A |
8: 34,061,108 (GRCm39) |
D179E |
probably benign |
Het |
Tmem8b |
T |
C |
4: 43,686,092 (GRCm39) |
L241P |
probably damaging |
Het |
Tmprss11g |
T |
C |
5: 86,640,149 (GRCm39) |
D160G |
probably benign |
Het |
Trim30a |
C |
T |
7: 104,085,120 (GRCm39) |
C30Y |
probably damaging |
Het |
Ttn |
A |
G |
2: 76,601,840 (GRCm39) |
|
probably benign |
Het |
Ush2a |
A |
G |
1: 188,466,882 (GRCm39) |
R2849G |
probably damaging |
Het |
Usp5 |
A |
G |
6: 124,796,389 (GRCm39) |
V570A |
probably damaging |
Het |
Vipr1 |
T |
C |
9: 121,489,349 (GRCm39) |
|
probably benign |
Het |
|
Other mutations in Zc2hc1c |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01763:Zc2hc1c
|
APN |
12 |
85,336,450 (GRCm39) |
missense |
probably benign |
0.03 |
R1053:Zc2hc1c
|
UTSW |
12 |
85,343,330 (GRCm39) |
missense |
probably damaging |
1.00 |
R1696:Zc2hc1c
|
UTSW |
12 |
85,337,555 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1724:Zc2hc1c
|
UTSW |
12 |
85,336,586 (GRCm39) |
missense |
probably benign |
0.00 |
R1905:Zc2hc1c
|
UTSW |
12 |
85,337,288 (GRCm39) |
missense |
probably benign |
0.03 |
R1996:Zc2hc1c
|
UTSW |
12 |
85,343,434 (GRCm39) |
missense |
probably benign |
0.31 |
R4463:Zc2hc1c
|
UTSW |
12 |
85,337,071 (GRCm39) |
missense |
probably damaging |
0.97 |
R4834:Zc2hc1c
|
UTSW |
12 |
85,336,982 (GRCm39) |
missense |
probably damaging |
1.00 |
R5070:Zc2hc1c
|
UTSW |
12 |
85,337,288 (GRCm39) |
missense |
probably benign |
0.03 |
R5943:Zc2hc1c
|
UTSW |
12 |
85,336,483 (GRCm39) |
missense |
probably damaging |
1.00 |
R6184:Zc2hc1c
|
UTSW |
12 |
85,343,218 (GRCm39) |
missense |
probably damaging |
0.96 |
R6701:Zc2hc1c
|
UTSW |
12 |
85,336,446 (GRCm39) |
splice site |
probably null |
|
R6704:Zc2hc1c
|
UTSW |
12 |
85,337,258 (GRCm39) |
missense |
possibly damaging |
0.84 |
R6719:Zc2hc1c
|
UTSW |
12 |
85,337,446 (GRCm39) |
missense |
probably damaging |
1.00 |
R7665:Zc2hc1c
|
UTSW |
12 |
85,343,336 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8125:Zc2hc1c
|
UTSW |
12 |
85,343,386 (GRCm39) |
missense |
probably damaging |
1.00 |
R8154:Zc2hc1c
|
UTSW |
12 |
85,336,946 (GRCm39) |
missense |
probably benign |
0.00 |
R8268:Zc2hc1c
|
UTSW |
12 |
85,336,595 (GRCm39) |
missense |
probably benign |
0.02 |
R8356:Zc2hc1c
|
UTSW |
12 |
85,337,471 (GRCm39) |
missense |
probably damaging |
0.97 |
R8678:Zc2hc1c
|
UTSW |
12 |
85,337,084 (GRCm39) |
missense |
probably benign |
0.07 |
R8875:Zc2hc1c
|
UTSW |
12 |
85,336,549 (GRCm39) |
missense |
possibly damaging |
0.87 |
R9056:Zc2hc1c
|
UTSW |
12 |
85,343,230 (GRCm39) |
small deletion |
probably benign |
|
|