Other mutations in this stock |
Total: 47 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700029H14Rik |
T |
G |
8: 13,607,704 (GRCm39) |
|
probably null |
Het |
Acp3 |
T |
C |
9: 104,197,204 (GRCm39) |
E145G |
possibly damaging |
Het |
Ankrd28 |
T |
A |
14: 31,477,743 (GRCm39) |
K42* |
probably null |
Het |
Arsg |
A |
T |
11: 109,454,082 (GRCm39) |
K429N |
probably damaging |
Het |
Bsn |
G |
A |
9: 107,991,462 (GRCm39) |
T1430I |
probably damaging |
Het |
Calu |
A |
G |
6: 29,356,582 (GRCm39) |
D36G |
possibly damaging |
Het |
Ccdc18 |
T |
C |
5: 108,376,767 (GRCm39) |
S1403P |
probably damaging |
Het |
Cdca2 |
A |
G |
14: 67,952,385 (GRCm39) |
|
probably benign |
Het |
Cfh |
C |
A |
1: 140,026,793 (GRCm39) |
|
probably benign |
Het |
Cyp2c69 |
C |
T |
19: 39,869,537 (GRCm39) |
G161S |
probably benign |
Het |
Dennd4c |
C |
A |
4: 86,692,674 (GRCm39) |
Y61* |
probably null |
Het |
Diaph3 |
A |
G |
14: 87,009,555 (GRCm39) |
S1075P |
probably damaging |
Het |
Dpp7 |
T |
A |
2: 25,245,735 (GRCm39) |
|
probably null |
Het |
Dtd1 |
T |
A |
2: 144,588,981 (GRCm39) |
|
probably benign |
Het |
Dtl |
C |
A |
1: 191,289,008 (GRCm39) |
|
probably benign |
Het |
Exoc3l4 |
A |
G |
12: 111,390,457 (GRCm39) |
D344G |
probably damaging |
Het |
Hsp90ab1 |
A |
T |
17: 45,879,954 (GRCm39) |
C159S |
possibly damaging |
Het |
Kcnip2 |
T |
C |
19: 45,784,710 (GRCm39) |
|
probably benign |
Het |
Krba1 |
A |
G |
6: 48,391,483 (GRCm39) |
T755A |
possibly damaging |
Het |
L2hgdh |
C |
T |
12: 69,739,173 (GRCm39) |
V433I |
probably benign |
Het |
Lamc1 |
A |
T |
1: 153,115,127 (GRCm39) |
L1050I |
probably damaging |
Het |
Lgals4 |
A |
T |
7: 28,540,343 (GRCm39) |
I213L |
probably benign |
Het |
Lysmd1 |
A |
G |
3: 95,044,945 (GRCm39) |
I64V |
probably damaging |
Het |
Mfsd4b4 |
A |
C |
10: 39,768,311 (GRCm39) |
C261G |
probably benign |
Het |
Mrgprb3 |
T |
A |
7: 48,293,198 (GRCm39) |
I118F |
possibly damaging |
Het |
Mtmr2 |
T |
A |
9: 13,704,501 (GRCm39) |
Y137* |
probably null |
Het |
Ofcc1 |
A |
T |
13: 40,226,140 (GRCm39) |
H797Q |
probably benign |
Het |
Omd |
A |
T |
13: 49,745,870 (GRCm39) |
|
probably benign |
Het |
Or5d46 |
C |
T |
2: 88,170,643 (GRCm39) |
|
probably null |
Het |
Or8g21 |
A |
T |
9: 38,906,728 (GRCm39) |
M1K |
probably null |
Het |
Polr3a |
T |
A |
14: 24,511,808 (GRCm39) |
D916V |
probably damaging |
Het |
Prpf38a |
T |
C |
4: 108,432,628 (GRCm39) |
Y117C |
probably damaging |
Het |
Scn11a |
C |
T |
9: 119,619,029 (GRCm39) |
G771D |
probably benign |
Het |
Smarca4 |
C |
T |
9: 21,547,132 (GRCm39) |
T219I |
probably benign |
Het |
Snx1 |
T |
A |
9: 66,001,906 (GRCm39) |
I306F |
probably benign |
Het |
Snx31 |
T |
A |
15: 36,525,749 (GRCm39) |
R317* |
probably null |
Het |
Sorl1 |
T |
C |
9: 41,902,722 (GRCm39) |
T1612A |
probably benign |
Het |
Spag1 |
G |
T |
15: 36,224,245 (GRCm39) |
|
probably benign |
Het |
Stambp |
A |
G |
6: 83,538,914 (GRCm39) |
F162S |
probably damaging |
Het |
Tkfc |
T |
A |
19: 10,576,518 (GRCm39) |
M122L |
probably benign |
Het |
Tnni3k |
T |
A |
3: 154,647,242 (GRCm39) |
|
probably null |
Het |
Trim56 |
T |
C |
5: 137,142,616 (GRCm39) |
Q300R |
probably damaging |
Het |
Xirp2 |
A |
T |
2: 67,339,876 (GRCm39) |
T706S |
possibly damaging |
Het |
Yipf5 |
T |
A |
18: 40,339,290 (GRCm39) |
|
probably benign |
Het |
Zfp202 |
T |
C |
9: 40,122,695 (GRCm39) |
S486P |
probably damaging |
Het |
Zfp407 |
A |
G |
18: 84,369,100 (GRCm39) |
S1676P |
probably damaging |
Het |
Znrd2 |
G |
T |
19: 5,780,450 (GRCm39) |
L183I |
possibly 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 |
|
R0153:Ttc24
|
UTSW |
3 |
87,982,234 (GRCm39) |
unclassified |
probably benign |
|
R1626:Ttc24
|
UTSW |
3 |
87,977,366 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
|
|