Other mutations in this stock |
Total: 58 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A1cf |
T |
A |
19: 31,895,499 (GRCm39) |
M194K |
probably benign |
Het |
Abcg1 |
T |
C |
17: 31,333,122 (GRCm39) |
S622P |
probably benign |
Het |
Ahnak2 |
A |
T |
12: 112,748,446 (GRCm39) |
V467E |
|
Het |
Ank3 |
G |
A |
10: 69,812,086 (GRCm39) |
|
probably null |
Het |
Bank1 |
A |
T |
3: 135,799,308 (GRCm39) |
N545K |
probably benign |
Het |
C9orf72 |
A |
G |
4: 35,205,883 (GRCm39) |
I247T |
|
Het |
Cep63 |
T |
C |
9: 102,467,723 (GRCm39) |
I548V |
probably benign |
Het |
Col28a1 |
T |
C |
6: 8,175,653 (GRCm39) |
D65G |
unknown |
Het |
Cspg4b |
C |
A |
13: 113,453,710 (GRCm39) |
Q58K |
|
Het |
Cyp2c50 |
A |
G |
19: 40,079,010 (GRCm39) |
N118D |
probably benign |
Het |
Dock10 |
C |
T |
1: 80,510,184 (GRCm39) |
C1549Y |
probably damaging |
Het |
Epg5 |
A |
G |
18: 77,991,435 (GRCm39) |
E44G |
probably benign |
Het |
Ephb4 |
T |
C |
5: 137,361,529 (GRCm39) |
S520P |
probably damaging |
Het |
Eppk1 |
T |
C |
15: 75,993,755 (GRCm39) |
E1042G |
probably benign |
Het |
Fmod |
A |
T |
1: 133,968,589 (GRCm39) |
N210Y |
probably damaging |
Het |
Fpr3 |
A |
G |
17: 18,191,713 (GRCm39) |
D328G |
probably damaging |
Het |
Garem2 |
T |
G |
5: 30,321,989 (GRCm39) |
C783G |
probably benign |
Het |
Gm10542 |
A |
G |
18: 44,337,689 (GRCm39) |
N56D |
probably damaging |
Het |
Gm20939 |
T |
A |
17: 95,184,424 (GRCm39) |
N357K |
probably benign |
Het |
Hr |
A |
G |
14: 70,805,228 (GRCm39) |
H990R |
possibly damaging |
Het |
Il21r |
A |
G |
7: 125,226,163 (GRCm39) |
N53S |
unknown |
Het |
Insrr |
C |
T |
3: 87,721,604 (GRCm39) |
T1170I |
probably damaging |
Het |
Itga11 |
A |
G |
9: 62,638,034 (GRCm39) |
M103V |
probably damaging |
Het |
Izumo3 |
G |
T |
4: 92,035,050 (GRCm39) |
Q56K |
probably damaging |
Het |
Kcnh8 |
T |
C |
17: 53,146,084 (GRCm39) |
V324A |
probably damaging |
Het |
Kcnj2 |
T |
A |
11: 110,963,719 (GRCm39) |
N370K |
probably benign |
Het |
Klf16 |
G |
T |
10: 80,412,688 (GRCm39) |
S116* |
probably null |
Het |
Mettl16 |
T |
C |
11: 74,696,089 (GRCm39) |
V310A |
probably benign |
Het |
Misp3 |
G |
T |
8: 84,737,080 (GRCm39) |
Q105K |
unknown |
Het |
Mmrn2 |
G |
A |
14: 34,097,473 (GRCm39) |
|
probably benign |
Het |
Mtcl1 |
A |
G |
17: 66,645,130 (GRCm39) |
L1888P |
probably damaging |
Het |
Muc5ac |
A |
C |
7: 141,365,429 (GRCm39) |
T1984P |
possibly damaging |
Het |
Myo16 |
G |
T |
8: 10,489,705 (GRCm39) |
|
probably null |
Het |
Nckipsd |
T |
C |
9: 108,691,699 (GRCm39) |
I466T |
possibly damaging |
Het |
Nos1 |
G |
C |
5: 118,017,402 (GRCm39) |
R255P |
probably benign |
Het |
Npffr2 |
A |
G |
5: 89,730,661 (GRCm39) |
H197R |
probably benign |
Het |
Nrap |
T |
A |
19: 56,340,100 (GRCm39) |
M842L |
probably benign |
Het |
Nxpe4 |
G |
A |
9: 48,309,984 (GRCm39) |
A416T |
probably benign |
Het |
Nxt2 |
C |
T |
X: 141,020,747 (GRCm39) |
A118V |
possibly damaging |
Het |
Or51t4 |
T |
C |
7: 102,597,687 (GRCm39) |
V5A |
probably benign |
Het |
Or52n20 |
A |
G |
7: 104,320,742 (GRCm39) |
I278V |
probably damaging |
Het |
Or5p53 |
T |
A |
7: 107,533,019 (GRCm39) |
C97* |
probably null |
Het |
Ppp1r15a |
C |
T |
7: 45,174,035 (GRCm39) |
A258T |
possibly damaging |
Het |
Prss36 |
A |
T |
7: 127,532,570 (GRCm39) |
Y760* |
probably null |
Het |
Psg26 |
T |
A |
7: 18,216,480 (GRCm39) |
T120S |
probably damaging |
Het |
Ptk7 |
A |
T |
17: 46,878,977 (GRCm39) |
L908Q |
probably benign |
Het |
S100a13 |
G |
T |
3: 90,423,170 (GRCm39) |
D54Y |
unknown |
Het |
Slc25a44 |
A |
T |
3: 88,328,025 (GRCm39) |
H155Q |
probably benign |
Het |
Smarcc2 |
A |
G |
10: 128,321,486 (GRCm39) |
T894A |
probably damaging |
Het |
Tle4 |
A |
G |
19: 14,574,149 (GRCm39) |
F39L |
probably damaging |
Het |
Tmem181a |
G |
A |
17: 6,346,048 (GRCm39) |
V181M |
possibly damaging |
Het |
Tmt1b |
A |
G |
10: 128,794,607 (GRCm39) |
M239T |
probably benign |
Het |
Trpm3 |
T |
C |
19: 22,896,004 (GRCm39) |
V947A |
possibly damaging |
Het |
Txndc16 |
G |
A |
14: 45,379,448 (GRCm39) |
T663I |
probably benign |
Het |
Vmn2r45 |
T |
C |
7: 8,474,532 (GRCm39) |
Y832C |
probably damaging |
Het |
Vmn2r9 |
T |
C |
5: 108,996,841 (GRCm39) |
T143A |
probably damaging |
Het |
Vps26b |
T |
C |
9: 26,930,750 (GRCm39) |
N82D |
probably benign |
Het |
Zfp318 |
T |
G |
17: 46,721,892 (GRCm39) |
F1298L |
probably damaging |
Het |
|
Other mutations in Amdhd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01546:Amdhd2
|
APN |
17 |
24,382,574 (GRCm39) |
missense |
probably benign |
0.38 |
IGL01868:Amdhd2
|
APN |
17 |
24,376,504 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02889:Amdhd2
|
APN |
17 |
24,376,761 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03127:Amdhd2
|
APN |
17 |
24,376,712 (GRCm39) |
critical splice donor site |
probably null |
|
R0619:Amdhd2
|
UTSW |
17 |
24,375,562 (GRCm39) |
missense |
possibly damaging |
0.65 |
R0759:Amdhd2
|
UTSW |
17 |
24,380,587 (GRCm39) |
missense |
probably benign |
0.02 |
R0970:Amdhd2
|
UTSW |
17 |
24,375,544 (GRCm39) |
critical splice donor site |
probably null |
|
R1657:Amdhd2
|
UTSW |
17 |
24,375,029 (GRCm39) |
missense |
probably damaging |
1.00 |
R1929:Amdhd2
|
UTSW |
17 |
24,376,860 (GRCm39) |
splice site |
probably null |
|
R2080:Amdhd2
|
UTSW |
17 |
24,375,578 (GRCm39) |
missense |
probably benign |
0.00 |
R2127:Amdhd2
|
UTSW |
17 |
24,377,282 (GRCm39) |
critical splice donor site |
probably null |
|
R2871:Amdhd2
|
UTSW |
17 |
24,376,829 (GRCm39) |
unclassified |
probably benign |
|
R4419:Amdhd2
|
UTSW |
17 |
24,377,652 (GRCm39) |
missense |
probably benign |
0.31 |
R5681:Amdhd2
|
UTSW |
17 |
24,375,014 (GRCm39) |
missense |
probably damaging |
1.00 |
R6315:Amdhd2
|
UTSW |
17 |
24,377,330 (GRCm39) |
missense |
probably benign |
0.00 |
R6413:Amdhd2
|
UTSW |
17 |
24,377,290 (GRCm39) |
missense |
probably damaging |
1.00 |
R7402:Amdhd2
|
UTSW |
17 |
24,380,657 (GRCm39) |
missense |
|
|
R8276:Amdhd2
|
UTSW |
17 |
24,382,574 (GRCm39) |
missense |
probably damaging |
0.98 |
R8831:Amdhd2
|
UTSW |
17 |
24,376,712 (GRCm39) |
critical splice donor site |
probably null |
|
|