Other mutations in this stock |
Total: 38 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ankrd60 |
C |
T |
2: 173,412,996 (GRCm39) |
C164Y |
probably benign |
Het |
Atp13a2 |
C |
T |
4: 140,733,463 (GRCm39) |
A979V |
probably benign |
Het |
Col5a2 |
C |
T |
1: 45,421,393 (GRCm39) |
|
probably benign |
Het |
Col6a6 |
T |
C |
9: 105,658,184 (GRCm39) |
N676S |
probably damaging |
Het |
Cpa1 |
T |
C |
6: 30,641,581 (GRCm39) |
F192L |
possibly damaging |
Het |
Entpd6 |
T |
A |
2: 150,604,286 (GRCm39) |
|
probably null |
Het |
Fam185a |
A |
G |
5: 21,664,171 (GRCm39) |
K302E |
probably damaging |
Het |
Il12rb2 |
T |
C |
6: 67,337,519 (GRCm39) |
K121E |
probably benign |
Het |
Impg2 |
G |
A |
16: 56,041,890 (GRCm39) |
C178Y |
probably damaging |
Het |
Kdm3b |
G |
T |
18: 34,967,289 (GRCm39) |
C1698F |
probably damaging |
Het |
Llgl2 |
A |
G |
11: 115,740,851 (GRCm39) |
D451G |
probably damaging |
Het |
Mgat4b |
T |
A |
11: 50,121,540 (GRCm39) |
L52Q |
probably damaging |
Het |
Mmp9 |
C |
A |
2: 164,792,836 (GRCm39) |
S363R |
probably benign |
Het |
Mtfmt |
A |
G |
9: 65,344,356 (GRCm39) |
Y94C |
probably benign |
Het |
Myo7b |
G |
A |
18: 32,094,953 (GRCm39) |
L1881F |
possibly damaging |
Het |
Or51a10 |
A |
T |
7: 103,699,300 (GRCm39) |
M87K |
probably benign |
Het |
Or6c6 |
G |
T |
10: 129,187,386 (GRCm39) |
|
probably benign |
Het |
Pex5 |
T |
C |
6: 124,375,339 (GRCm39) |
N524S |
probably damaging |
Het |
Plppr1 |
A |
T |
4: 49,319,992 (GRCm39) |
Y206F |
possibly damaging |
Het |
Polr3e |
A |
G |
7: 120,539,519 (GRCm39) |
|
probably benign |
Het |
Rhbdd1 |
A |
G |
1: 82,318,555 (GRCm39) |
|
probably benign |
Het |
Rims4 |
A |
T |
2: 163,707,702 (GRCm39) |
|
probably benign |
Het |
Smarcal1 |
A |
T |
1: 72,655,679 (GRCm39) |
K653* |
probably null |
Het |
Stt3b |
C |
T |
9: 115,105,767 (GRCm39) |
|
probably null |
Het |
Syt8 |
C |
A |
7: 141,993,877 (GRCm39) |
L343M |
probably damaging |
Het |
Tbc1d23 |
G |
A |
16: 57,009,615 (GRCm39) |
|
probably benign |
Het |
Tfec |
T |
C |
6: 16,845,465 (GRCm39) |
I65V |
probably damaging |
Het |
Tmem236 |
A |
T |
2: 14,223,716 (GRCm39) |
Q168H |
probably benign |
Het |
Tmem25 |
G |
A |
9: 44,709,568 (GRCm39) |
R78* |
probably null |
Het |
Tnip2 |
A |
G |
5: 34,654,212 (GRCm39) |
V288A |
probably benign |
Het |
Tubb4b-ps1 |
A |
C |
5: 7,229,843 (GRCm39) |
|
probably benign |
Het |
Tut1 |
T |
C |
19: 8,931,364 (GRCm39) |
C21R |
probably damaging |
Het |
Ubr4 |
C |
A |
4: 139,156,913 (GRCm39) |
Q2313K |
probably damaging |
Het |
Unc5b |
T |
C |
10: 60,615,966 (GRCm39) |
E119G |
probably damaging |
Het |
Vmn1r23 |
T |
A |
6: 57,903,475 (GRCm39) |
Q101L |
probably damaging |
Het |
Vmn2r77 |
A |
G |
7: 86,450,678 (GRCm39) |
D188G |
probably benign |
Het |
Vmn2r79 |
A |
G |
7: 86,686,290 (GRCm39) |
E557G |
possibly damaging |
Het |
Zfp738 |
A |
G |
13: 67,818,096 (GRCm39) |
F632L |
possibly damaging |
Het |
|
Other mutations in Ttc1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01017:Ttc1
|
APN |
11 |
43,621,320 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL01449:Ttc1
|
APN |
11 |
43,629,630 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02414:Ttc1
|
APN |
11 |
43,630,664 (GRCm39) |
splice site |
probably benign |
|
IGL02541:Ttc1
|
APN |
11 |
43,629,648 (GRCm39) |
missense |
probably benign |
|
IGL03006:Ttc1
|
APN |
11 |
43,636,147 (GRCm39) |
missense |
probably benign |
|
IGL03253:Ttc1
|
APN |
11 |
43,629,650 (GRCm39) |
missense |
probably benign |
0.01 |
PIT4434001:Ttc1
|
UTSW |
11 |
43,635,955 (GRCm39) |
missense |
probably damaging |
1.00 |
R0113:Ttc1
|
UTSW |
11 |
43,636,115 (GRCm39) |
missense |
probably benign |
0.25 |
R0391:Ttc1
|
UTSW |
11 |
43,629,635 (GRCm39) |
missense |
probably damaging |
1.00 |
R1037:Ttc1
|
UTSW |
11 |
43,621,326 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4667:Ttc1
|
UTSW |
11 |
43,636,144 (GRCm39) |
missense |
probably benign |
0.01 |
R7493:Ttc1
|
UTSW |
11 |
43,636,189 (GRCm39) |
missense |
probably damaging |
1.00 |
R7956:Ttc1
|
UTSW |
11 |
43,627,240 (GRCm39) |
critical splice donor site |
probably null |
|
R8032:Ttc1
|
UTSW |
11 |
43,628,806 (GRCm39) |
missense |
probably damaging |
0.98 |
R9515:Ttc1
|
UTSW |
11 |
43,621,305 (GRCm39) |
missense |
|
|
|