Other mutations in this stock |
Total: 54 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700020N01Rik |
T |
C |
10: 21,497,571 (GRCm39) |
Y71H |
possibly damaging |
Het |
Acsl6 |
C |
A |
11: 54,242,872 (GRCm39) |
P628T |
probably damaging |
Het |
Ak7 |
A |
G |
12: 105,734,807 (GRCm39) |
D591G |
probably benign |
Het |
Anxa5 |
T |
C |
3: 36,516,130 (GRCm39) |
D66G |
probably damaging |
Het |
Cacna1b |
G |
A |
2: 24,496,721 (GRCm39) |
T2283I |
probably damaging |
Het |
Cand1 |
A |
T |
10: 119,045,919 (GRCm39) |
D995E |
possibly damaging |
Het |
Cblc |
G |
T |
7: 19,530,427 (GRCm39) |
A94E |
probably damaging |
Het |
Cd48 |
G |
A |
1: 171,509,687 (GRCm39) |
C9Y |
probably benign |
Het |
Chd9 |
A |
G |
8: 91,721,224 (GRCm39) |
K1004R |
probably benign |
Het |
Cilk1 |
A |
G |
9: 78,057,919 (GRCm39) |
Y156C |
probably damaging |
Het |
Cldn1 |
T |
C |
16: 26,190,202 (GRCm39) |
T59A |
probably damaging |
Het |
Col11a1 |
G |
A |
3: 113,925,218 (GRCm39) |
G17D |
probably damaging |
Het |
Cpeb1 |
A |
G |
7: 81,085,995 (GRCm39) |
V49A |
probably damaging |
Het |
Cyp4b1 |
G |
T |
4: 115,498,855 (GRCm39) |
P109Q |
probably damaging |
Het |
Dhrs7b |
T |
A |
11: 60,735,082 (GRCm39) |
F23I |
possibly damaging |
Het |
Dnah9 |
C |
A |
11: 65,976,093 (GRCm39) |
A1319S |
probably benign |
Het |
Egf |
A |
T |
3: 129,479,864 (GRCm39) |
V553D |
possibly damaging |
Het |
Fbn1 |
T |
C |
2: 125,183,199 (GRCm39) |
D1760G |
probably damaging |
Het |
Fbxo31 |
A |
G |
8: 122,286,745 (GRCm39) |
F178L |
probably damaging |
Het |
Fstl4 |
C |
A |
11: 52,891,117 (GRCm39) |
S85* |
probably null |
Het |
Gfm1 |
A |
G |
3: 67,345,977 (GRCm39) |
Y225C |
probably damaging |
Het |
Gm10797 |
A |
T |
10: 67,408,453 (GRCm39) |
|
noncoding transcript |
Het |
H3c8 |
G |
A |
13: 23,719,721 (GRCm39) |
V36M |
probably damaging |
Het |
Heatr4 |
T |
A |
12: 84,020,495 (GRCm39) |
I499L |
probably benign |
Het |
Igfn1 |
A |
T |
1: 135,896,705 (GRCm39) |
M1287K |
probably benign |
Het |
Inpp5b |
C |
A |
4: 124,677,696 (GRCm39) |
D385E |
probably damaging |
Het |
Lrrc9 |
A |
G |
12: 72,542,435 (GRCm39) |
|
probably null |
Het |
Ltb4r1 |
A |
G |
14: 56,004,699 (GRCm39) |
M1V |
probably null |
Het |
Macf1 |
T |
C |
4: 123,365,327 (GRCm39) |
I3145V |
probably benign |
Het |
Man2a2 |
T |
C |
7: 80,017,450 (GRCm39) |
N277S |
probably damaging |
Het |
Megf6 |
G |
T |
4: 154,261,578 (GRCm39) |
V68L |
probably benign |
Het |
Mgat4e |
A |
G |
1: 134,469,016 (GRCm39) |
Y343H |
probably benign |
Het |
Noxred1 |
T |
C |
12: 87,268,029 (GRCm39) |
*367W |
probably null |
Het |
Nup58 |
A |
T |
14: 60,480,076 (GRCm39) |
L190* |
probably null |
Het |
Olfml2a |
G |
T |
2: 38,841,275 (GRCm39) |
K270N |
probably damaging |
Het |
Or5c1 |
A |
G |
2: 37,222,774 (GRCm39) |
|
probably null |
Het |
Or7g32 |
A |
G |
9: 19,389,495 (GRCm39) |
L14P |
probably damaging |
Het |
Phgdh |
G |
T |
3: 98,223,725 (GRCm39) |
Q359K |
probably benign |
Het |
Plpp5 |
G |
T |
8: 26,212,604 (GRCm39) |
C200F |
possibly damaging |
Het |
Pole |
A |
C |
5: 110,441,235 (GRCm39) |
I230L |
probably benign |
Het |
Prtg |
A |
T |
9: 72,752,193 (GRCm39) |
D193V |
probably damaging |
Het |
Ptgs2 |
G |
A |
1: 149,979,619 (GRCm39) |
|
probably null |
Het |
Ptprz1 |
A |
T |
6: 23,001,573 (GRCm39) |
Q1221L |
probably benign |
Het |
Rufy2 |
T |
C |
10: 62,831,151 (GRCm39) |
I204T |
probably benign |
Het |
Rybp |
A |
G |
6: 100,209,919 (GRCm39) |
S115P |
possibly damaging |
Het |
Samd13 |
A |
G |
3: 146,368,481 (GRCm39) |
V37A |
probably benign |
Het |
Secisbp2l |
T |
G |
2: 125,617,606 (GRCm39) |
K24Q |
probably damaging |
Het |
Sorbs2 |
A |
G |
8: 46,222,891 (GRCm39) |
Y198C |
probably damaging |
Het |
Svil |
T |
G |
18: 5,117,099 (GRCm39) |
|
probably null |
Het |
Ttn |
C |
T |
2: 76,588,888 (GRCm39) |
V21394M |
probably damaging |
Het |
Tubal3 |
G |
T |
13: 3,982,841 (GRCm39) |
C207F |
probably damaging |
Het |
Vmn2r16 |
A |
T |
5: 109,511,443 (GRCm39) |
D550V |
probably damaging |
Het |
Vmn2r2 |
T |
A |
3: 64,041,921 (GRCm39) |
I265F |
possibly damaging |
Het |
Zfp507 |
T |
C |
7: 35,494,858 (GRCm39) |
K62E |
probably damaging |
Het |
|
Other mutations in Ttc24 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01896:Ttc24
|
APN |
3 |
87,977,720 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03069:Ttc24
|
APN |
3 |
87,977,408 (GRCm39) |
missense |
probably benign |
0.07 |
R0153:Ttc24
|
UTSW |
3 |
87,982,234 (GRCm39) |
unclassified |
probably benign |
|
R1735:Ttc24
|
UTSW |
3 |
87,980,401 (GRCm39) |
splice site |
probably null |
|
R1938:Ttc24
|
UTSW |
3 |
87,982,181 (GRCm39) |
missense |
probably benign |
0.28 |
R4112:Ttc24
|
UTSW |
3 |
87,981,946 (GRCm39) |
missense |
probably damaging |
0.99 |
R4200:Ttc24
|
UTSW |
3 |
87,981,824 (GRCm39) |
missense |
probably benign |
0.01 |
R7600:Ttc24
|
UTSW |
3 |
87,979,320 (GRCm39) |
start codon destroyed |
probably null |
|
R7939:Ttc24
|
UTSW |
3 |
87,981,945 (GRCm39) |
missense |
possibly damaging |
0.83 |
R8432:Ttc24
|
UTSW |
3 |
87,977,366 (GRCm39) |
missense |
probably benign |
0.15 |
R8519:Ttc24
|
UTSW |
3 |
87,980,369 (GRCm39) |
missense |
probably damaging |
1.00 |
R8784:Ttc24
|
UTSW |
3 |
87,980,033 (GRCm39) |
nonsense |
probably null |
|
R9164:Ttc24
|
UTSW |
3 |
87,980,295 (GRCm39) |
nonsense |
probably null |
|
R9370:Ttc24
|
UTSW |
3 |
87,980,136 (GRCm39) |
missense |
probably benign |
0.20 |
R9531:Ttc24
|
UTSW |
3 |
87,978,416 (GRCm39) |
missense |
possibly damaging |
0.79 |
Z1176:Ttc24
|
UTSW |
3 |
87,979,293 (GRCm39) |
missense |
probably benign |
0.06 |
Z1176:Ttc24
|
UTSW |
3 |
87,978,365 (GRCm39) |
frame shift |
probably null |
|
|