Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9230009I02Rik |
A |
G |
11: 50,982,089 (GRCm39) |
|
noncoding transcript |
Het |
Actl7b |
T |
C |
4: 56,740,972 (GRCm39) |
I129V |
probably benign |
Het |
Adipor2 |
A |
G |
6: 119,336,047 (GRCm39) |
L225P |
probably benign |
Het |
Arhgap25 |
A |
G |
6: 87,473,053 (GRCm39) |
F35L |
probably benign |
Het |
Asah2 |
A |
T |
19: 32,030,258 (GRCm39) |
M138K |
probably damaging |
Het |
Asxl1 |
T |
A |
2: 153,243,905 (GRCm39) |
M1486K |
probably damaging |
Het |
B4galt4 |
T |
A |
16: 38,572,658 (GRCm39) |
S114R |
probably benign |
Het |
Brpf3 |
T |
G |
17: 29,040,233 (GRCm39) |
S885A |
probably benign |
Het |
Cacna1g |
G |
T |
11: 94,302,298 (GRCm39) |
H1944N |
possibly damaging |
Het |
Cby2 |
T |
A |
14: 75,820,546 (GRCm39) |
Y393F |
probably damaging |
Het |
Ccdc110 |
G |
A |
8: 46,396,245 (GRCm39) |
C712Y |
probably damaging |
Het |
Ccdc175 |
A |
T |
12: 72,182,822 (GRCm39) |
I399N |
probably damaging |
Het |
Cd109 |
CATTTATTTATTTATTTATTTATTTATTTATTTAT |
CATTTATTTATTTATTTATTTATTTATTTATTTATTTAT |
9: 78,619,782 (GRCm39) |
|
probably benign |
Het |
Copa |
A |
G |
1: 171,932,787 (GRCm39) |
N371D |
probably damaging |
Het |
Cpeb1 |
A |
T |
7: 81,005,695 (GRCm39) |
H381Q |
probably benign |
Het |
Cyp2d40 |
T |
A |
15: 82,645,763 (GRCm39) |
I81F |
possibly damaging |
Het |
Dscc1 |
A |
T |
15: 54,943,654 (GRCm39) |
D405E |
probably benign |
Het |
Ece1 |
A |
G |
4: 137,672,464 (GRCm39) |
D369G |
probably benign |
Het |
Exd2 |
T |
C |
12: 80,522,592 (GRCm39) |
V17A |
possibly damaging |
Het |
Fam111a |
A |
T |
19: 12,565,772 (GRCm39) |
N507I |
possibly damaging |
Het |
Flnc |
T |
C |
6: 29,445,038 (GRCm39) |
V719A |
possibly damaging |
Het |
Fscb |
C |
T |
12: 64,520,464 (GRCm39) |
G334D |
probably damaging |
Het |
Glud1 |
T |
C |
14: 34,043,782 (GRCm39) |
|
probably null |
Het |
Gm8126 |
T |
A |
14: 43,119,072 (GRCm39) |
Y180* |
probably null |
Het |
Grip2 |
G |
A |
6: 91,759,413 (GRCm39) |
P347L |
possibly damaging |
Het |
H1f3 |
T |
C |
13: 23,739,576 (GRCm39) |
S105P |
probably damaging |
Het |
H60b |
C |
T |
10: 22,164,644 (GRCm39) |
|
probably benign |
Het |
Iqca1l |
A |
G |
5: 24,755,596 (GRCm39) |
|
probably null |
Het |
Itga6 |
T |
C |
2: 71,652,788 (GRCm39) |
V217A |
probably benign |
Het |
Kndc1 |
G |
A |
7: 139,503,946 (GRCm39) |
W1083* |
probably null |
Het |
Limch1 |
A |
T |
5: 67,184,850 (GRCm39) |
D613V |
probably damaging |
Het |
Lpl |
T |
A |
8: 69,349,403 (GRCm39) |
C310S |
probably damaging |
Het |
Marchf1 |
T |
A |
8: 66,839,876 (GRCm39) |
C220S |
probably benign |
Het |
Mbd5 |
A |
C |
2: 49,164,623 (GRCm39) |
H308P |
probably damaging |
Het |
Med13 |
T |
C |
11: 86,167,746 (GRCm39) |
D2003G |
probably damaging |
Het |
Mettl16 |
T |
A |
11: 74,708,127 (GRCm39) |
V442D |
possibly damaging |
Het |
Mstn |
A |
T |
1: 53,101,267 (GRCm39) |
T115S |
probably benign |
Het |
Mtcl2 |
G |
T |
2: 156,872,489 (GRCm39) |
Q953K |
probably benign |
Het |
Nfil3 |
A |
G |
13: 53,122,050 (GRCm39) |
S285P |
probably damaging |
Het |
Odad4 |
C |
A |
11: 100,440,742 (GRCm39) |
N74K |
probably benign |
Het |
Or10j3 |
A |
C |
1: 173,031,796 (GRCm39) |
Y291S |
probably damaging |
Het |
Or51a24 |
A |
G |
7: 103,733,502 (GRCm39) |
S262P |
probably damaging |
Het |
Otof |
A |
G |
5: 30,552,026 (GRCm39) |
V321A |
probably benign |
Het |
Pcdha8 |
G |
T |
18: 37,127,626 (GRCm39) |
A703S |
probably damaging |
Het |
Pcdhb18 |
A |
G |
18: 37,623,507 (GRCm39) |
Y279C |
probably damaging |
Het |
Pdgfa |
T |
C |
5: 138,979,051 (GRCm39) |
D51G |
probably benign |
Het |
Pdzd8 |
A |
G |
19: 59,289,292 (GRCm39) |
Y703H |
probably damaging |
Het |
Pecr |
G |
T |
1: 72,306,594 (GRCm39) |
P229Q |
probably damaging |
Het |
Phkg1 |
G |
T |
5: 129,902,114 (GRCm39) |
|
probably null |
Het |
Plxnb2 |
A |
T |
15: 89,051,150 (GRCm39) |
H356Q |
probably benign |
Het |
Polr1b |
T |
C |
2: 128,947,248 (GRCm39) |
I191T |
probably benign |
Het |
Ppp4r3a |
A |
G |
12: 101,049,026 (GRCm39) |
L35P |
possibly damaging |
Het |
Rasa2 |
C |
T |
9: 96,426,470 (GRCm39) |
G792D |
probably benign |
Het |
Rps11-ps4 |
T |
C |
12: 51,344,406 (GRCm39) |
|
noncoding transcript |
Het |
Sema3g |
A |
G |
14: 30,942,666 (GRCm39) |
D89G |
probably benign |
Het |
Shroom3 |
G |
T |
5: 93,090,945 (GRCm39) |
V1151F |
probably damaging |
Het |
Slfn8 |
A |
G |
11: 82,908,219 (GRCm39) |
V108A |
probably damaging |
Het |
Smg9 |
T |
A |
7: 24,107,019 (GRCm39) |
M221K |
possibly damaging |
Het |
Sos1 |
A |
G |
17: 80,705,660 (GRCm39) |
S1304P |
probably damaging |
Het |
Sqle |
C |
A |
15: 59,189,688 (GRCm39) |
A110E |
possibly damaging |
Het |
Stab2 |
G |
A |
10: 86,743,235 (GRCm39) |
Q1154* |
probably null |
Het |
Taf4b |
A |
G |
18: 14,937,577 (GRCm39) |
T217A |
probably benign |
Het |
Tex15 |
T |
C |
8: 34,072,760 (GRCm39) |
V2769A |
probably benign |
Het |
Tmem156 |
A |
T |
5: 65,237,502 (GRCm39) |
C53S |
probably damaging |
Het |
Tmtc3 |
T |
A |
10: 100,293,001 (GRCm39) |
K452N |
possibly damaging |
Het |
Tns2 |
C |
T |
15: 102,017,369 (GRCm39) |
R281C |
probably damaging |
Het |
Tph1 |
T |
C |
7: 46,306,376 (GRCm39) |
E195G |
probably damaging |
Het |
Trpc6 |
T |
A |
9: 8,609,852 (GRCm39) |
Y107N |
possibly damaging |
Het |
Tsga10 |
G |
A |
1: 37,874,606 (GRCm39) |
T93I |
probably damaging |
Het |
Ttn |
T |
A |
2: 76,571,778 (GRCm39) |
N26372Y |
probably damaging |
Het |
Tubd1 |
T |
C |
11: 86,446,128 (GRCm39) |
L256P |
possibly damaging |
Het |
Txnrd2 |
C |
G |
16: 18,259,569 (GRCm39) |
A126G |
probably benign |
Het |
Vmn1r210 |
T |
G |
13: 23,011,374 (GRCm39) |
K304T |
probably benign |
Het |
Vps25 |
T |
C |
11: 101,149,655 (GRCm39) |
S160P |
probably benign |
Het |
Vrk3 |
T |
A |
7: 44,424,900 (GRCm39) |
D438E |
probably benign |
Het |
Vwa5b1 |
A |
G |
4: 138,309,066 (GRCm39) |
L708P |
probably benign |
Het |
Washc3 |
C |
T |
10: 88,055,124 (GRCm39) |
Q105* |
probably null |
Het |
Wdr83os |
T |
A |
8: 85,807,410 (GRCm39) |
|
probably benign |
Het |
Wwc1 |
T |
C |
11: 35,758,123 (GRCm39) |
H741R |
probably benign |
Het |
Zan |
T |
C |
5: 137,434,575 (GRCm39) |
|
probably benign |
Het |
Zdhhc4 |
A |
T |
5: 143,311,931 (GRCm39) |
L14I |
possibly damaging |
Het |
Zfp568 |
T |
A |
7: 29,697,195 (GRCm39) |
D38E |
probably damaging |
Het |
|
Other mutations in Cct8l1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01704:Cct8l1
|
APN |
5 |
25,722,097 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02186:Cct8l1
|
APN |
5 |
25,721,836 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02322:Cct8l1
|
APN |
5 |
25,722,581 (GRCm39) |
missense |
probably benign |
0.00 |
G1citation:Cct8l1
|
UTSW |
5 |
25,722,937 (GRCm39) |
missense |
possibly damaging |
0.95 |
R1478:Cct8l1
|
UTSW |
5 |
25,722,767 (GRCm39) |
missense |
probably benign |
0.09 |
R1764:Cct8l1
|
UTSW |
5 |
25,722,097 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1772:Cct8l1
|
UTSW |
5 |
25,722,697 (GRCm39) |
missense |
probably damaging |
0.99 |
R2680:Cct8l1
|
UTSW |
5 |
25,722,133 (GRCm39) |
missense |
probably benign |
0.24 |
R3153:Cct8l1
|
UTSW |
5 |
25,722,137 (GRCm39) |
missense |
probably damaging |
1.00 |
R4937:Cct8l1
|
UTSW |
5 |
25,721,891 (GRCm39) |
missense |
probably benign |
0.37 |
R5071:Cct8l1
|
UTSW |
5 |
25,721,881 (GRCm39) |
missense |
probably benign |
0.00 |
R5072:Cct8l1
|
UTSW |
5 |
25,721,881 (GRCm39) |
missense |
probably benign |
0.00 |
R5073:Cct8l1
|
UTSW |
5 |
25,721,881 (GRCm39) |
missense |
probably benign |
0.00 |
R5074:Cct8l1
|
UTSW |
5 |
25,721,881 (GRCm39) |
missense |
probably benign |
0.00 |
R5432:Cct8l1
|
UTSW |
5 |
25,721,305 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5507:Cct8l1
|
UTSW |
5 |
25,721,377 (GRCm39) |
missense |
probably benign |
|
R5603:Cct8l1
|
UTSW |
5 |
25,721,497 (GRCm39) |
missense |
probably benign |
0.39 |
R5950:Cct8l1
|
UTSW |
5 |
25,722,741 (GRCm39) |
missense |
probably benign |
|
R6822:Cct8l1
|
UTSW |
5 |
25,722,937 (GRCm39) |
missense |
possibly damaging |
0.95 |
R8171:Cct8l1
|
UTSW |
5 |
25,721,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R8808:Cct8l1
|
UTSW |
5 |
25,722,210 (GRCm39) |
missense |
possibly damaging |
0.71 |
R8902:Cct8l1
|
UTSW |
5 |
25,722,908 (GRCm39) |
missense |
probably benign |
0.00 |
R9368:Cct8l1
|
UTSW |
5 |
25,721,336 (GRCm39) |
missense |
probably benign |
0.09 |
|