Other mutations in this stock |
Total: 55 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610021A01Rik |
T |
C |
7: 41,275,667 (GRCm39) |
S457P |
probably damaging |
Het |
Aak1 |
A |
G |
6: 86,964,234 (GRCm39) |
N945S |
unknown |
Het |
Actr1a |
C |
A |
19: 46,369,438 (GRCm39) |
R192L |
possibly damaging |
Het |
Adgrl2 |
T |
A |
3: 148,534,119 (GRCm39) |
N1036I |
probably damaging |
Het |
Ak5 |
A |
G |
3: 152,361,511 (GRCm39) |
V137A |
probably damaging |
Het |
Aldh1a2 |
T |
C |
9: 71,169,055 (GRCm39) |
V179A |
probably damaging |
Het |
Ap2b1 |
A |
T |
11: 83,237,579 (GRCm39) |
I548F |
probably damaging |
Het |
Arhgef10l |
A |
G |
4: 140,292,550 (GRCm39) |
Y352H |
probably damaging |
Het |
Atad5 |
C |
T |
11: 79,986,524 (GRCm39) |
T537M |
possibly damaging |
Het |
Atoh7 |
A |
G |
10: 62,935,938 (GRCm39) |
K2E |
possibly damaging |
Het |
BC061237 |
A |
G |
14: 44,741,658 (GRCm39) |
I134V |
probably benign |
Het |
Cadm1 |
T |
C |
9: 47,701,136 (GRCm39) |
I141T |
probably damaging |
Het |
Capn10 |
T |
C |
1: 92,871,454 (GRCm39) |
S351P |
probably damaging |
Het |
Cd19 |
T |
C |
7: 126,011,330 (GRCm39) |
T284A |
probably benign |
Het |
Cfap53 |
A |
G |
18: 74,432,253 (GRCm39) |
Y47C |
probably damaging |
Het |
Cldn18 |
T |
C |
9: 99,578,162 (GRCm39) |
M194V |
probably benign |
Het |
Dgkb |
T |
A |
12: 38,652,777 (GRCm39) |
Y721N |
probably damaging |
Het |
Dmbt1 |
A |
G |
7: 130,721,372 (GRCm39) |
Q1880R |
possibly damaging |
Het |
Dock2 |
T |
C |
11: 34,599,646 (GRCm39) |
N311S |
possibly damaging |
Het |
Dpysl5 |
G |
T |
5: 30,935,375 (GRCm39) |
M159I |
probably benign |
Het |
Eif2b3 |
G |
A |
4: 116,901,778 (GRCm39) |
G147E |
probably damaging |
Het |
Fam193a |
A |
G |
5: 34,597,796 (GRCm39) |
D531G |
probably benign |
Het |
Fndc3b |
T |
C |
3: 27,555,329 (GRCm39) |
|
probably benign |
Het |
Foxe3 |
C |
A |
4: 114,782,523 (GRCm39) |
A230S |
unknown |
Het |
Gm5591 |
A |
T |
7: 38,219,727 (GRCm39) |
V382E |
probably benign |
Het |
Gm7995 |
A |
T |
14: 42,132,228 (GRCm39) |
N21I |
probably damaging |
Het |
Ipo8 |
G |
A |
6: 148,676,547 (GRCm39) |
P981S |
probably benign |
Het |
Kcnh8 |
A |
G |
17: 53,104,486 (GRCm39) |
D161G |
probably benign |
Het |
Krt71 |
A |
G |
15: 101,645,180 (GRCm39) |
I377T |
possibly damaging |
Het |
Krt75 |
A |
T |
15: 101,476,767 (GRCm39) |
M374K |
probably benign |
Het |
Krt9 |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
TCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCCCCCACTTCCTCCTCCATAGCTGCC |
11: 100,079,903 (GRCm39) |
|
probably benign |
Het |
Lpcat1 |
A |
G |
13: 73,662,029 (GRCm39) |
T409A |
probably benign |
Het |
Lrch1 |
A |
T |
14: 75,032,808 (GRCm39) |
I514K |
probably benign |
Het |
Mc4r |
A |
C |
18: 66,993,110 (GRCm39) |
M1R |
probably null |
Het |
Mthfd1l |
A |
T |
10: 3,978,466 (GRCm39) |
H442L |
probably damaging |
Het |
Or5d38 |
T |
A |
2: 87,954,718 (GRCm39) |
I204F |
probably damaging |
Het |
Pdcd1lg2 |
T |
C |
19: 29,423,553 (GRCm39) |
M199T |
probably benign |
Het |
Pigg |
G |
A |
5: 108,484,066 (GRCm39) |
V438M |
probably damaging |
Het |
Pira12 |
T |
C |
7: 3,898,365 (GRCm39) |
E319G |
probably benign |
Het |
Ppfibp1 |
T |
A |
6: 146,920,681 (GRCm39) |
|
probably null |
Het |
Rbm15 |
T |
A |
3: 107,239,372 (GRCm39) |
Y342F |
possibly damaging |
Het |
Rhbdl1 |
A |
T |
17: 26,054,116 (GRCm39) |
V278E |
probably damaging |
Het |
Ryr3 |
T |
C |
2: 112,465,669 (GRCm39) |
N4781S |
probably damaging |
Het |
Scn7a |
A |
T |
2: 66,525,206 (GRCm39) |
|
silent |
Het |
Sfswap |
A |
G |
5: 129,581,168 (GRCm39) |
R114G |
probably damaging |
Het |
Sohlh2 |
C |
A |
3: 55,104,282 (GRCm39) |
A258D |
possibly damaging |
Het |
Sstr4 |
T |
A |
2: 148,237,782 (GRCm39) |
V131D |
possibly damaging |
Het |
Tenm2 |
T |
C |
11: 36,834,861 (GRCm39) |
T45A |
probably damaging |
Het |
Tmem131l |
A |
T |
3: 83,831,479 (GRCm39) |
F818I |
probably damaging |
Het |
Trappc6b |
A |
G |
12: 59,097,149 (GRCm39) |
F58L |
probably damaging |
Het |
Vmn1r229 |
A |
T |
17: 21,035,418 (GRCm39) |
H221L |
possibly damaging |
Het |
Vmn1r33 |
T |
A |
6: 66,588,783 (GRCm39) |
Y257F |
probably damaging |
Het |
Wdfy3 |
T |
C |
5: 101,993,231 (GRCm39) |
|
probably benign |
Het |
Zfp446 |
C |
T |
7: 12,713,564 (GRCm39) |
Q177* |
probably null |
Het |
Zup1 |
A |
G |
10: 33,795,301 (GRCm39) |
*552Q |
probably null |
Het |
|
Other mutations in Cct6b |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02227:Cct6b
|
APN |
11 |
82,632,217 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02606:Cct6b
|
APN |
11 |
82,627,271 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02707:Cct6b
|
APN |
11 |
82,645,780 (GRCm39) |
splice site |
probably benign |
|
IGL03081:Cct6b
|
APN |
11 |
82,654,995 (GRCm39) |
nonsense |
probably null |
|
R0032:Cct6b
|
UTSW |
11 |
82,644,469 (GRCm39) |
missense |
possibly damaging |
0.87 |
R0395:Cct6b
|
UTSW |
11 |
82,630,506 (GRCm39) |
missense |
probably benign |
|
R0556:Cct6b
|
UTSW |
11 |
82,610,270 (GRCm39) |
splice site |
probably benign |
|
R0631:Cct6b
|
UTSW |
11 |
82,627,914 (GRCm39) |
splice site |
probably null |
|
R1456:Cct6b
|
UTSW |
11 |
82,644,446 (GRCm39) |
splice site |
probably benign |
|
R3713:Cct6b
|
UTSW |
11 |
82,651,183 (GRCm39) |
missense |
probably damaging |
1.00 |
R4791:Cct6b
|
UTSW |
11 |
82,632,830 (GRCm39) |
splice site |
probably null |
|
R5154:Cct6b
|
UTSW |
11 |
82,630,521 (GRCm39) |
missense |
probably damaging |
1.00 |
R5256:Cct6b
|
UTSW |
11 |
82,655,046 (GRCm39) |
missense |
probably damaging |
0.98 |
R5338:Cct6b
|
UTSW |
11 |
82,653,015 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5455:Cct6b
|
UTSW |
11 |
82,645,943 (GRCm39) |
missense |
probably benign |
0.04 |
R5560:Cct6b
|
UTSW |
11 |
82,632,239 (GRCm39) |
missense |
probably damaging |
1.00 |
R5616:Cct6b
|
UTSW |
11 |
82,632,175 (GRCm39) |
missense |
probably damaging |
1.00 |
R5644:Cct6b
|
UTSW |
11 |
82,613,281 (GRCm39) |
missense |
probably benign |
0.02 |
R6862:Cct6b
|
UTSW |
11 |
82,610,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R7960:Cct6b
|
UTSW |
11 |
82,632,221 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8240:Cct6b
|
UTSW |
11 |
82,614,650 (GRCm39) |
missense |
probably damaging |
1.00 |
R8785:Cct6b
|
UTSW |
11 |
82,632,157 (GRCm39) |
missense |
probably damaging |
1.00 |
R9527:Cct6b
|
UTSW |
11 |
82,630,447 (GRCm39) |
critical splice donor site |
probably null |
|
R9674:Cct6b
|
UTSW |
11 |
82,645,838 (GRCm39) |
missense |
probably damaging |
1.00 |
X0060:Cct6b
|
UTSW |
11 |
82,632,136 (GRCm39) |
missense |
probably benign |
0.00 |
Z1176:Cct6b
|
UTSW |
11 |
82,654,891 (GRCm39) |
start gained |
probably benign |
|
Z1176:Cct6b
|
UTSW |
11 |
82,614,765 (GRCm39) |
missense |
probably damaging |
1.00 |
|