Other mutations in this stock |
Total: 93 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aatk |
T |
C |
11: 119,900,562 (GRCm39) |
T1195A |
probably benign |
Het |
Abca12 |
A |
T |
1: 71,283,930 (GRCm39) |
N2547K |
probably benign |
Het |
Abca16 |
A |
C |
7: 120,139,868 (GRCm39) |
E1510A |
probably damaging |
Het |
Akna |
G |
A |
4: 63,313,397 (GRCm39) |
P242L |
probably benign |
Het |
Akr1b7 |
G |
A |
6: 34,395,929 (GRCm39) |
A144T |
possibly damaging |
Het |
Ankhd1 |
T |
A |
18: 36,767,361 (GRCm39) |
S1167T |
probably damaging |
Het |
Arf5 |
C |
T |
6: 28,424,783 (GRCm39) |
Q71* |
probably null |
Het |
Ark2n |
T |
C |
18: 77,762,168 (GRCm39) |
D48G |
possibly damaging |
Het |
Arl15 |
C |
T |
13: 114,104,196 (GRCm39) |
S111F |
probably damaging |
Het |
Atxn1l |
C |
T |
8: 110,459,240 (GRCm39) |
A341T |
probably benign |
Het |
Birc7 |
C |
A |
2: 180,572,642 (GRCm39) |
Q138K |
possibly damaging |
Het |
Blvra |
G |
T |
2: 126,927,989 (GRCm39) |
E80* |
probably null |
Het |
Ccdc148 |
T |
C |
2: 58,892,128 (GRCm39) |
E188G |
probably damaging |
Het |
Chad |
C |
T |
11: 94,459,052 (GRCm39) |
A318V |
probably benign |
Het |
Cntfr |
A |
G |
4: 41,663,534 (GRCm39) |
|
probably null |
Het |
Dnah17 |
C |
T |
11: 118,010,628 (GRCm39) |
C230Y |
probably benign |
Het |
Dnmt3l |
C |
A |
10: 77,899,130 (GRCm39) |
L110I |
probably damaging |
Het |
Dusp11 |
T |
C |
6: 85,935,651 (GRCm39) |
D74G |
probably damaging |
Het |
Duxf4 |
T |
C |
10: 58,072,073 (GRCm39) |
D47G |
possibly damaging |
Het |
Eif3m |
T |
C |
2: 104,837,141 (GRCm39) |
T61A |
probably damaging |
Het |
Esyt1 |
T |
A |
10: 128,357,973 (GRCm39) |
D212V |
probably damaging |
Het |
Exoc4 |
T |
A |
6: 33,324,760 (GRCm39) |
N351K |
possibly damaging |
Het |
F13a1 |
A |
T |
13: 37,172,831 (GRCm39) |
I183N |
probably damaging |
Het |
Fam83f |
T |
G |
15: 80,576,468 (GRCm39) |
V373G |
possibly damaging |
Het |
Fam83h |
A |
T |
15: 75,874,146 (GRCm39) |
Y1064N |
probably damaging |
Het |
Flrt3 |
G |
T |
2: 140,503,423 (GRCm39) |
N68K |
probably damaging |
Het |
Fut7 |
C |
A |
2: 25,315,343 (GRCm39) |
Y153* |
probably null |
Het |
Gm10277 |
TC |
T |
11: 77,676,828 (GRCm39) |
|
probably null |
Het |
Gm1527 |
T |
C |
3: 28,972,098 (GRCm39) |
L405P |
probably benign |
Het |
Heatr6 |
T |
A |
11: 83,648,281 (GRCm39) |
|
probably benign |
Het |
Herc2 |
T |
C |
7: 55,835,576 (GRCm39) |
|
probably benign |
Het |
Ints14 |
T |
G |
9: 64,887,077 (GRCm39) |
L336R |
probably damaging |
Het |
Irak1 |
G |
T |
X: 73,066,218 (GRCm39) |
P197Q |
possibly damaging |
Het |
Kat7 |
C |
T |
11: 95,194,120 (GRCm39) |
R60Q |
probably benign |
Het |
Katnal2 |
T |
C |
18: 77,067,787 (GRCm39) |
R385G |
probably damaging |
Het |
Kcnt2 |
G |
T |
1: 140,480,701 (GRCm39) |
L755F |
probably damaging |
Het |
Kif4 |
A |
G |
X: 99,709,323 (GRCm39) |
S315G |
probably benign |
Het |
Kifc3 |
A |
G |
8: 95,835,341 (GRCm39) |
Y178H |
probably damaging |
Het |
Krit1 |
A |
T |
5: 3,872,108 (GRCm39) |
R378* |
probably null |
Het |
L3mbtl1 |
T |
A |
2: 162,801,990 (GRCm39) |
|
probably null |
Het |
Lama3 |
C |
A |
18: 12,535,906 (GRCm39) |
T204N |
possibly damaging |
Het |
Lama5 |
A |
G |
2: 179,828,678 (GRCm39) |
C2090R |
probably damaging |
Het |
Mb |
G |
T |
15: 76,906,759 (GRCm39) |
Q9K |
probably benign |
Het |
Mipep |
T |
C |
14: 61,024,829 (GRCm39) |
V90A |
probably damaging |
Het |
Myo3a |
A |
T |
2: 22,250,342 (GRCm39) |
I70F |
probably damaging |
Het |
Napa |
A |
G |
7: 15,848,134 (GRCm39) |
D217G |
possibly damaging |
Het |
Nectin2 |
T |
C |
7: 19,451,489 (GRCm39) |
D515G |
probably damaging |
Het |
Nkx2-6 |
T |
A |
14: 69,409,288 (GRCm39) |
V13E |
probably damaging |
Het |
Nmi |
T |
C |
2: 51,838,719 (GRCm39) |
T272A |
probably benign |
Het |
Nptx2 |
G |
C |
5: 144,492,216 (GRCm39) |
G331A |
probably damaging |
Het |
Or2q1 |
A |
G |
6: 42,794,431 (GRCm39) |
T9A |
possibly damaging |
Het |
Or4c122 |
T |
C |
2: 89,079,874 (GRCm39) |
I55V |
probably damaging |
Het |
Or5h17 |
T |
C |
16: 58,820,783 (GRCm39) |
L245P |
possibly damaging |
Het |
Or7g34 |
T |
C |
9: 19,478,618 (GRCm39) |
T18A |
probably benign |
Het |
Parp14 |
T |
C |
16: 35,678,904 (GRCm39) |
T355A |
probably benign |
Het |
Pcdh12 |
T |
C |
18: 38,417,039 (GRCm39) |
T29A |
probably damaging |
Het |
Pced1b |
T |
A |
15: 97,282,505 (GRCm39) |
C181* |
probably null |
Het |
Phka1 |
C |
T |
X: 101,653,807 (GRCm39) |
R290H |
probably damaging |
Het |
Pick1 |
T |
A |
15: 79,139,781 (GRCm39) |
|
probably benign |
Het |
Pitrm1 |
A |
T |
13: 6,607,809 (GRCm39) |
Y268F |
probably damaging |
Het |
Polr2h |
T |
C |
16: 20,537,737 (GRCm39) |
|
probably benign |
Het |
Ppfia2 |
A |
T |
10: 106,597,972 (GRCm39) |
K178N |
probably damaging |
Het |
Prkag1 |
T |
C |
15: 98,712,433 (GRCm39) |
Y133C |
probably damaging |
Het |
Ptk2 |
A |
G |
15: 73,114,255 (GRCm39) |
V701A |
possibly damaging |
Het |
Ptpra |
G |
T |
2: 130,381,655 (GRCm39) |
R372L |
probably damaging |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Qrich2 |
A |
G |
11: 116,337,982 (GRCm39) |
V1887A |
probably damaging |
Het |
Ralgapa1 |
T |
C |
12: 55,833,134 (GRCm39) |
|
probably null |
Het |
Rassf9 |
A |
G |
10: 102,380,806 (GRCm39) |
T63A |
probably benign |
Het |
Rdh11 |
G |
T |
12: 79,222,996 (GRCm39) |
Q292K |
probably benign |
Het |
Rere |
C |
A |
4: 150,697,018 (GRCm39) |
|
probably benign |
Het |
Rgs18 |
G |
T |
1: 144,629,629 (GRCm39) |
T210K |
possibly damaging |
Het |
Rnf213 |
A |
G |
11: 119,318,839 (GRCm39) |
N1099S |
probably benign |
Het |
Ros1 |
T |
C |
10: 52,004,651 (GRCm39) |
I969V |
probably benign |
Het |
Rrh |
T |
C |
3: 129,604,336 (GRCm39) |
I288M |
probably damaging |
Het |
Rrp12 |
C |
T |
19: 41,879,533 (GRCm39) |
V174I |
probably benign |
Het |
Rtf1 |
T |
A |
2: 119,535,999 (GRCm39) |
H184Q |
probably benign |
Het |
Sbk3 |
A |
G |
7: 4,970,415 (GRCm39) |
L318S |
possibly damaging |
Het |
Scn9a |
T |
C |
2: 66,314,396 (GRCm39) |
E1774G |
probably damaging |
Het |
Sec11c |
A |
T |
18: 65,933,720 (GRCm39) |
T9S |
probably benign |
Het |
Sec23ip |
G |
A |
7: 128,364,185 (GRCm39) |
V488I |
probably benign |
Het |
Serpine3 |
T |
C |
14: 62,910,459 (GRCm39) |
L184P |
probably damaging |
Het |
Slc26a2 |
T |
C |
18: 61,331,896 (GRCm39) |
T512A |
possibly damaging |
Het |
Slc49a4 |
T |
C |
16: 35,518,309 (GRCm39) |
D468G |
probably benign |
Het |
Smpd4 |
T |
C |
16: 17,444,729 (GRCm39) |
Y118H |
probably benign |
Het |
Tcof1 |
T |
C |
18: 60,965,857 (GRCm39) |
E415G |
possibly damaging |
Het |
Ttc33 |
G |
A |
15: 5,241,534 (GRCm39) |
V120I |
probably benign |
Het |
Usp20 |
T |
A |
2: 30,906,317 (GRCm39) |
C562S |
probably damaging |
Het |
Utp20 |
T |
C |
10: 88,621,865 (GRCm39) |
D1136G |
probably benign |
Het |
Vgll1 |
A |
C |
X: 56,137,790 (GRCm39) |
K53T |
probably damaging |
Het |
Yars1 |
T |
G |
4: 129,101,716 (GRCm39) |
|
probably null |
Het |
Zfp472 |
A |
G |
17: 33,196,988 (GRCm39) |
I354M |
possibly damaging |
Het |
Zfp786 |
A |
G |
6: 47,803,931 (GRCm39) |
V37A |
probably damaging |
Het |
|
Other mutations in Adam5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00823:Adam5
|
APN |
8 |
25,308,758 (GRCm39) |
missense |
probably benign |
0.18 |
IGL01285:Adam5
|
APN |
8 |
25,271,610 (GRCm39) |
missense |
probably benign |
0.02 |
IGL01310:Adam5
|
APN |
8 |
25,232,150 (GRCm39) |
intron |
probably benign |
|
IGL01510:Adam5
|
APN |
8 |
25,294,481 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01570:Adam5
|
APN |
8 |
25,300,839 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02017:Adam5
|
APN |
8 |
25,271,775 (GRCm39) |
missense |
probably benign |
0.38 |
IGL02191:Adam5
|
APN |
8 |
25,302,439 (GRCm39) |
nonsense |
probably null |
|
IGL02397:Adam5
|
APN |
8 |
25,234,149 (GRCm39) |
intron |
probably benign |
|
IGL02488:Adam5
|
APN |
8 |
25,282,022 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02490:Adam5
|
APN |
8 |
25,271,720 (GRCm39) |
nonsense |
probably null |
|
IGL02499:Adam5
|
APN |
8 |
25,271,581 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02539:Adam5
|
APN |
8 |
25,276,229 (GRCm39) |
nonsense |
probably null |
|
IGL02590:Adam5
|
APN |
8 |
25,234,151 (GRCm39) |
intron |
probably benign |
|
IGL02677:Adam5
|
APN |
8 |
25,302,395 (GRCm39) |
splice site |
probably benign |
|
IGL02679:Adam5
|
APN |
8 |
25,296,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02982:Adam5
|
APN |
8 |
25,294,447 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03146:Adam5
|
APN |
8 |
25,294,519 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03162:Adam5
|
APN |
8 |
25,271,620 (GRCm39) |
missense |
probably benign |
0.30 |
IGL03284:Adam5
|
APN |
8 |
25,276,354 (GRCm39) |
splice site |
probably benign |
|
R0081:Adam5
|
UTSW |
8 |
25,271,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R0377:Adam5
|
UTSW |
8 |
25,237,557 (GRCm39) |
missense |
probably benign |
0.08 |
R0398:Adam5
|
UTSW |
8 |
25,303,448 (GRCm39) |
missense |
probably benign |
0.17 |
R0771:Adam5
|
UTSW |
8 |
25,276,315 (GRCm39) |
missense |
probably benign |
0.04 |
R0925:Adam5
|
UTSW |
8 |
25,302,441 (GRCm39) |
missense |
probably benign |
0.09 |
R1547:Adam5
|
UTSW |
8 |
25,300,729 (GRCm39) |
missense |
probably benign |
0.10 |
R1985:Adam5
|
UTSW |
8 |
25,236,755 (GRCm39) |
missense |
probably benign |
0.01 |
R2125:Adam5
|
UTSW |
8 |
25,305,134 (GRCm39) |
missense |
probably damaging |
1.00 |
R2144:Adam5
|
UTSW |
8 |
25,305,496 (GRCm39) |
missense |
probably benign |
0.14 |
R3151:Adam5
|
UTSW |
8 |
25,271,647 (GRCm39) |
missense |
probably damaging |
0.99 |
R3612:Adam5
|
UTSW |
8 |
25,308,105 (GRCm39) |
splice site |
probably benign |
|
R3844:Adam5
|
UTSW |
8 |
25,303,426 (GRCm39) |
missense |
probably benign |
0.12 |
R3873:Adam5
|
UTSW |
8 |
25,305,125 (GRCm39) |
missense |
probably benign |
0.02 |
R4514:Adam5
|
UTSW |
8 |
25,308,152 (GRCm39) |
missense |
probably damaging |
1.00 |
R4843:Adam5
|
UTSW |
8 |
25,303,552 (GRCm39) |
missense |
probably damaging |
1.00 |
R4866:Adam5
|
UTSW |
8 |
25,271,619 (GRCm39) |
missense |
probably damaging |
0.98 |
R4866:Adam5
|
UTSW |
8 |
25,232,172 (GRCm39) |
splice site |
probably null |
|
R4900:Adam5
|
UTSW |
8 |
25,232,172 (GRCm39) |
splice site |
probably null |
|
R4900:Adam5
|
UTSW |
8 |
25,271,619 (GRCm39) |
missense |
probably damaging |
0.98 |
R4903:Adam5
|
UTSW |
8 |
25,276,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R4936:Adam5
|
UTSW |
8 |
25,276,287 (GRCm39) |
missense |
probably damaging |
1.00 |
R4964:Adam5
|
UTSW |
8 |
25,276,248 (GRCm39) |
missense |
probably damaging |
1.00 |
R5259:Adam5
|
UTSW |
8 |
25,300,850 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5293:Adam5
|
UTSW |
8 |
25,300,722 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5724:Adam5
|
UTSW |
8 |
25,294,511 (GRCm39) |
nonsense |
probably null |
|
R5859:Adam5
|
UTSW |
8 |
25,303,477 (GRCm39) |
missense |
probably benign |
|
R6004:Adam5
|
UTSW |
8 |
25,271,685 (GRCm39) |
missense |
probably benign |
0.04 |
R6175:Adam5
|
UTSW |
8 |
25,276,167 (GRCm39) |
missense |
probably benign |
0.00 |
R6539:Adam5
|
UTSW |
8 |
25,272,616 (GRCm39) |
missense |
possibly damaging |
0.85 |
R6994:Adam5
|
UTSW |
8 |
25,276,262 (GRCm39) |
nonsense |
probably null |
|
R6996:Adam5
|
UTSW |
8 |
25,296,517 (GRCm39) |
missense |
probably damaging |
1.00 |
R7009:Adam5
|
UTSW |
8 |
25,296,454 (GRCm39) |
missense |
probably benign |
0.00 |
R7115:Adam5
|
UTSW |
8 |
25,271,712 (GRCm39) |
missense |
possibly damaging |
0.69 |
R7127:Adam5
|
UTSW |
8 |
25,300,797 (GRCm39) |
missense |
probably damaging |
1.00 |
R7469:Adam5
|
UTSW |
8 |
25,305,541 (GRCm39) |
missense |
probably benign |
0.45 |
R7780:Adam5
|
UTSW |
8 |
25,294,432 (GRCm39) |
missense |
possibly damaging |
0.49 |
R8027:Adam5
|
UTSW |
8 |
25,272,574 (GRCm39) |
missense |
probably damaging |
1.00 |
R8069:Adam5
|
UTSW |
8 |
25,303,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R8138:Adam5
|
UTSW |
8 |
25,271,778 (GRCm39) |
missense |
probably damaging |
1.00 |
R8305:Adam5
|
UTSW |
8 |
25,300,719 (GRCm39) |
missense |
possibly damaging |
0.93 |
R8359:Adam5
|
UTSW |
8 |
25,296,502 (GRCm39) |
missense |
probably damaging |
1.00 |
R8480:Adam5
|
UTSW |
8 |
25,294,475 (GRCm39) |
nonsense |
probably null |
|
R8743:Adam5
|
UTSW |
8 |
25,276,264 (GRCm39) |
missense |
probably damaging |
1.00 |
R9000:Adam5
|
UTSW |
8 |
25,294,372 (GRCm39) |
critical splice donor site |
probably null |
|
R9442:Adam5
|
UTSW |
8 |
25,296,510 (GRCm39) |
missense |
probably damaging |
0.96 |
R9474:Adam5
|
UTSW |
8 |
25,237,540 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9602:Adam5
|
UTSW |
8 |
25,303,402 (GRCm39) |
missense |
probably damaging |
0.96 |
R9748:Adam5
|
UTSW |
8 |
25,301,068 (GRCm39) |
missense |
probably benign |
0.23 |
X0019:Adam5
|
UTSW |
8 |
25,302,459 (GRCm39) |
missense |
probably benign |
0.00 |
X0022:Adam5
|
UTSW |
8 |
25,303,579 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0027:Adam5
|
UTSW |
8 |
25,308,788 (GRCm39) |
missense |
probably damaging |
1.00 |
|