Other mutations in this stock |
Total: 53 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abr |
C |
A |
11: 76,315,815 (GRCm39) |
R583L |
probably damaging |
Het |
Acss1 |
A |
G |
2: 150,509,840 (GRCm39) |
I93T |
probably damaging |
Het |
Ank3 |
C |
T |
10: 69,827,577 (GRCm39) |
|
probably benign |
Het |
Aoah |
A |
G |
13: 21,184,112 (GRCm39) |
Y392C |
probably damaging |
Het |
Atl3 |
A |
T |
19: 7,498,163 (GRCm39) |
E186D |
probably benign |
Het |
Atp4a |
A |
G |
7: 30,411,887 (GRCm39) |
K41E |
probably benign |
Het |
Atp9a |
G |
A |
2: 168,509,933 (GRCm39) |
P500L |
probably damaging |
Het |
Ccdc88b |
A |
T |
19: 6,832,246 (GRCm39) |
V363D |
possibly damaging |
Het |
Cftr |
T |
C |
6: 18,258,235 (GRCm39) |
V532A |
probably damaging |
Het |
Cldn13 |
T |
C |
5: 134,943,769 (GRCm39) |
T139A |
possibly damaging |
Het |
Cnksr3 |
T |
C |
10: 7,076,820 (GRCm39) |
Y124C |
probably benign |
Het |
Cyb5r2 |
T |
C |
7: 107,352,462 (GRCm39) |
K161E |
possibly damaging |
Het |
Epop |
T |
C |
11: 97,519,333 (GRCm39) |
S259G |
possibly damaging |
Het |
Fhl2 |
G |
A |
1: 43,162,813 (GRCm39) |
T234I |
possibly damaging |
Het |
Fnip2 |
T |
C |
3: 79,388,941 (GRCm39) |
T567A |
possibly damaging |
Het |
Frmd4b |
A |
G |
6: 97,464,601 (GRCm39) |
C39R |
probably damaging |
Het |
Grhl3 |
T |
C |
4: 135,284,744 (GRCm39) |
N116S |
possibly damaging |
Het |
Igkv14-111 |
A |
T |
6: 68,233,725 (GRCm39) |
R75S |
probably benign |
Het |
Il16 |
A |
T |
7: 83,371,529 (GRCm39) |
D92E |
probably damaging |
Het |
Il16 |
C |
A |
7: 83,371,536 (GRCm39) |
G90V |
probably damaging |
Het |
Ipo11 |
T |
C |
13: 107,002,277 (GRCm39) |
|
probably null |
Het |
Kng2 |
A |
G |
16: 22,830,865 (GRCm39) |
I148T |
probably damaging |
Het |
Lrrc41 |
T |
C |
4: 115,945,977 (GRCm39) |
S231P |
possibly damaging |
Het |
Mgat4c |
T |
A |
10: 102,220,988 (GRCm39) |
L90Q |
probably damaging |
Het |
Mrps28 |
A |
G |
3: 8,965,040 (GRCm39) |
|
probably null |
Het |
Ncapd3 |
A |
G |
9: 26,963,051 (GRCm39) |
D452G |
probably benign |
Het |
Nefh |
T |
C |
11: 4,889,551 (GRCm39) |
T1023A |
unknown |
Het |
Nipa1 |
A |
G |
7: 55,629,354 (GRCm39) |
V253A |
probably benign |
Het |
Or5ac17 |
C |
T |
16: 59,036,383 (GRCm39) |
V198M |
probably benign |
Het |
Or5b97 |
G |
T |
19: 12,878,369 (GRCm39) |
F258L |
possibly damaging |
Het |
Or5m11 |
G |
T |
2: 85,781,862 (GRCm39) |
G152C |
probably damaging |
Het |
Or8d23 |
A |
G |
9: 38,841,961 (GRCm39) |
S165G |
probably benign |
Het |
Or8k41 |
T |
A |
2: 86,313,573 (GRCm39) |
H171L |
probably benign |
Het |
Pak1 |
A |
G |
7: 97,557,088 (GRCm39) |
D495G |
probably benign |
Het |
Pcm1 |
G |
A |
8: 41,714,073 (GRCm39) |
R213H |
probably damaging |
Het |
Prg4 |
T |
C |
1: 150,330,052 (GRCm39) |
|
probably benign |
Het |
Proser1 |
C |
T |
3: 53,385,750 (GRCm39) |
T544M |
possibly damaging |
Het |
Rftn1 |
T |
C |
17: 50,354,334 (GRCm39) |
M343V |
probably benign |
Het |
Ryr1 |
T |
C |
7: 28,715,079 (GRCm39) |
I4656V |
probably benign |
Het |
Scg2 |
T |
A |
1: 79,414,007 (GRCm39) |
N239Y |
probably damaging |
Het |
Sec16a |
C |
A |
2: 26,313,512 (GRCm39) |
M1949I |
probably benign |
Het |
Sipa1l2 |
A |
G |
8: 126,171,223 (GRCm39) |
|
probably null |
Het |
Slc10a2 |
A |
C |
8: 5,148,581 (GRCm39) |
|
probably null |
Het |
Slc25a16 |
C |
T |
10: 62,773,256 (GRCm39) |
Q164* |
probably null |
Het |
Specc1l |
T |
C |
10: 75,082,001 (GRCm39) |
Y483H |
probably damaging |
Het |
Ston1 |
T |
C |
17: 88,943,896 (GRCm39) |
V434A |
probably benign |
Het |
Tarbp2 |
A |
G |
15: 102,426,914 (GRCm39) |
|
probably benign |
Het |
Trappc8 |
C |
T |
18: 20,969,925 (GRCm39) |
V1022M |
probably benign |
Het |
Tsen54 |
T |
C |
11: 115,712,506 (GRCm39) |
V269A |
probably damaging |
Het |
Vps13a |
A |
T |
19: 16,641,382 (GRCm39) |
M78K |
possibly damaging |
Het |
Vwa5b2 |
A |
G |
16: 20,413,429 (GRCm39) |
T215A |
probably damaging |
Het |
Zc3h7a |
A |
G |
16: 10,971,025 (GRCm39) |
Y335H |
probably damaging |
Het |
Zfp994 |
T |
A |
17: 22,419,527 (GRCm39) |
Q474L |
possibly damaging |
Het |
|
Other mutations in Maneal |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01973:Maneal
|
APN |
4 |
124,752,948 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02119:Maneal
|
APN |
4 |
124,752,960 (GRCm39) |
missense |
probably benign |
0.01 |
IGL02183:Maneal
|
APN |
4 |
124,754,209 (GRCm39) |
missense |
probably benign |
0.25 |
IGL02338:Maneal
|
APN |
4 |
124,754,276 (GRCm39) |
splice site |
probably benign |
|
IGL02450:Maneal
|
APN |
4 |
124,750,928 (GRCm39) |
missense |
probably benign |
0.37 |
IGL02485:Maneal
|
APN |
4 |
124,750,563 (GRCm39) |
missense |
probably damaging |
1.00 |
BB009:Maneal
|
UTSW |
4 |
124,755,638 (GRCm39) |
missense |
probably damaging |
1.00 |
BB019:Maneal
|
UTSW |
4 |
124,755,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R1481:Maneal
|
UTSW |
4 |
124,755,650 (GRCm39) |
missense |
probably damaging |
0.99 |
R5568:Maneal
|
UTSW |
4 |
124,750,937 (GRCm39) |
missense |
possibly damaging |
0.96 |
R5909:Maneal
|
UTSW |
4 |
124,750,966 (GRCm39) |
nonsense |
probably null |
|
R6493:Maneal
|
UTSW |
4 |
124,750,964 (GRCm39) |
missense |
probably damaging |
1.00 |
R7121:Maneal
|
UTSW |
4 |
124,750,905 (GRCm39) |
missense |
probably benign |
0.00 |
R7199:Maneal
|
UTSW |
4 |
124,750,983 (GRCm39) |
missense |
possibly damaging |
0.62 |
R7329:Maneal
|
UTSW |
4 |
124,750,512 (GRCm39) |
missense |
probably benign |
0.04 |
R7406:Maneal
|
UTSW |
4 |
124,754,161 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7456:Maneal
|
UTSW |
4 |
124,750,767 (GRCm39) |
missense |
probably damaging |
1.00 |
R7932:Maneal
|
UTSW |
4 |
124,755,638 (GRCm39) |
missense |
probably damaging |
1.00 |
R8795:Maneal
|
UTSW |
4 |
124,750,483 (GRCm39) |
nonsense |
probably null |
|
R9151:Maneal
|
UTSW |
4 |
124,755,542 (GRCm39) |
missense |
probably benign |
0.25 |
|