Other mutations in this stock |
Total: 74 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aadat |
T |
A |
8: 60,969,120 (GRCm39) |
S122T |
probably benign |
Het |
Abcb11 |
G |
A |
2: 69,095,856 (GRCm39) |
T828I |
probably damaging |
Het |
Atp5f1b |
T |
A |
10: 127,921,369 (GRCm39) |
N222K |
probably damaging |
Het |
C1qbp |
T |
C |
11: 70,869,313 (GRCm39) |
T211A |
probably benign |
Het |
Ccdc85a |
A |
T |
11: 28,384,146 (GRCm39) |
S410T |
possibly damaging |
Het |
Chd4 |
T |
A |
6: 125,100,485 (GRCm39) |
|
probably benign |
Het |
Col10a1 |
G |
T |
10: 34,270,824 (GRCm39) |
K265N |
probably damaging |
Het |
Cyp2j5 |
A |
T |
4: 96,529,660 (GRCm39) |
M237K |
possibly damaging |
Het |
Cyp4f40 |
T |
C |
17: 32,894,962 (GRCm39) |
|
probably benign |
Het |
Cytip |
A |
T |
2: 58,041,135 (GRCm39) |
F90L |
probably damaging |
Het |
Dnah7b |
A |
G |
1: 46,214,598 (GRCm39) |
D1121G |
probably damaging |
Het |
Dohh |
G |
T |
10: 81,221,859 (GRCm39) |
E84D |
probably benign |
Het |
Efcab3 |
A |
G |
11: 104,743,371 (GRCm39) |
I2187V |
probably benign |
Het |
Eif4g2 |
T |
C |
7: 110,673,127 (GRCm39) |
Y855C |
probably damaging |
Het |
Ell |
T |
A |
8: 71,034,331 (GRCm39) |
|
probably benign |
Het |
Ermap |
T |
C |
4: 119,044,355 (GRCm39) |
Y147C |
probably damaging |
Het |
Fasn |
T |
C |
11: 120,709,944 (GRCm39) |
D371G |
possibly damaging |
Het |
Fat2 |
A |
G |
11: 55,159,129 (GRCm39) |
S3348P |
probably benign |
Het |
Fhad1 |
T |
A |
4: 141,684,924 (GRCm39) |
N472Y |
probably benign |
Het |
Flad1 |
A |
G |
3: 89,316,415 (GRCm39) |
V49A |
probably damaging |
Het |
Fpr-rs3 |
T |
C |
17: 20,844,554 (GRCm39) |
T196A |
probably benign |
Het |
Fsip2 |
A |
G |
2: 82,815,246 (GRCm39) |
N3660D |
possibly damaging |
Het |
Gabrp |
T |
A |
11: 33,505,023 (GRCm39) |
L259F |
probably damaging |
Het |
Gm16686 |
A |
T |
4: 88,673,473 (GRCm39) |
W119R |
unknown |
Het |
Gng2 |
C |
T |
14: 19,941,438 (GRCm39) |
M1I |
probably null |
Het |
Hmgxb3 |
T |
C |
18: 61,290,721 (GRCm39) |
N384S |
probably benign |
Het |
Ibtk |
T |
C |
9: 85,606,208 (GRCm39) |
I440V |
probably benign |
Het |
Il11ra1 |
A |
G |
4: 41,767,539 (GRCm39) |
D297G |
probably damaging |
Het |
Irf2bpl |
T |
C |
12: 86,928,496 (GRCm39) |
I726V |
probably benign |
Het |
Klk1b5 |
A |
G |
7: 43,867,996 (GRCm39) |
N56S |
probably benign |
Het |
Laptm4b |
T |
A |
15: 34,277,648 (GRCm39) |
V193E |
probably damaging |
Het |
Lrrc37a |
A |
T |
11: 103,388,350 (GRCm39) |
C2358* |
probably null |
Het |
Ltbp2 |
C |
T |
12: 84,900,515 (GRCm39) |
S269N |
probably benign |
Het |
Morc2a |
T |
G |
11: 3,630,013 (GRCm39) |
Y450D |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,407,430 (GRCm39) |
I2740K |
probably benign |
Het |
Naif1 |
T |
A |
2: 32,344,848 (GRCm39) |
V184E |
probably damaging |
Het |
Neurl1b |
T |
C |
17: 26,660,747 (GRCm39) |
V540A |
probably damaging |
Het |
Nt5c1b |
T |
A |
12: 10,431,450 (GRCm39) |
F451Y |
probably damaging |
Het |
Obox3 |
A |
G |
7: 15,360,148 (GRCm39) |
S174P |
probably benign |
Het |
Obscn |
T |
C |
11: 58,951,894 (GRCm39) |
E3953G |
probably damaging |
Het |
Or4a74 |
A |
C |
2: 89,440,291 (GRCm39) |
S52A |
probably benign |
Het |
Or4p19 |
A |
T |
2: 88,242,595 (GRCm39) |
C136S |
probably damaging |
Het |
Pkd1l1 |
G |
A |
11: 8,815,550 (GRCm39) |
H1904Y |
|
Het |
Plec |
C |
T |
15: 76,059,531 (GRCm39) |
D3469N |
probably benign |
Het |
Polr1b |
A |
G |
2: 128,943,064 (GRCm39) |
T20A |
probably damaging |
Het |
Ppp1r16b |
G |
A |
2: 158,603,286 (GRCm39) |
E404K |
possibly damaging |
Het |
Prkce |
T |
A |
17: 86,795,625 (GRCm39) |
N287K |
probably damaging |
Het |
Rchy1 |
C |
A |
5: 92,105,397 (GRCm39) |
C108F |
probably damaging |
Het |
Scpppq1 |
G |
A |
5: 104,219,956 (GRCm39) |
T78I |
unknown |
Het |
Sema6d |
A |
G |
2: 124,502,232 (GRCm39) |
Y572C |
possibly damaging |
Het |
Sh3rf1 |
T |
A |
8: 61,783,030 (GRCm39) |
I248K |
probably damaging |
Het |
Sin3b |
T |
C |
8: 73,450,026 (GRCm39) |
L30P |
probably damaging |
Het |
Slc25a47 |
G |
A |
12: 108,820,313 (GRCm39) |
G106S |
probably damaging |
Het |
Slc43a2 |
A |
C |
11: 75,457,879 (GRCm39) |
M385L |
probably benign |
Het |
Slc43a3 |
A |
G |
2: 84,768,671 (GRCm39) |
T97A |
probably damaging |
Het |
Slc9b2 |
T |
A |
3: 135,030,351 (GRCm39) |
S223T |
probably benign |
Het |
Smc5 |
A |
T |
19: 23,243,058 (GRCm39) |
C118S |
probably damaging |
Het |
Smpdl3b |
T |
C |
4: 132,472,491 (GRCm39) |
D94G |
probably damaging |
Het |
Spred3 |
A |
G |
7: 28,866,086 (GRCm39) |
V71A |
possibly damaging |
Het |
Srsf5 |
T |
A |
12: 80,994,328 (GRCm39) |
S86T |
possibly damaging |
Het |
Sycp2 |
A |
G |
2: 177,990,088 (GRCm39) |
V1386A |
probably benign |
Het |
Syne2 |
T |
C |
12: 76,104,258 (GRCm39) |
L743P |
probably damaging |
Het |
Synj1 |
A |
G |
16: 90,806,971 (GRCm39) |
V62A |
probably damaging |
Het |
Tbc1d9b |
T |
C |
11: 50,047,578 (GRCm39) |
L637P |
probably damaging |
Het |
Tcf12 |
T |
G |
9: 71,757,097 (GRCm39) |
S697R |
possibly damaging |
Het |
Tnfrsf11b |
T |
A |
15: 54,123,508 (GRCm39) |
Y31F |
possibly damaging |
Het |
Trav5n-4 |
T |
C |
14: 53,550,362 (GRCm39) |
M1T |
probably null |
Het |
Trbv13-2 |
A |
G |
6: 41,098,716 (GRCm39) |
E97G |
probably benign |
Het |
Trpa1 |
G |
A |
1: 14,980,998 (GRCm39) |
P135S |
probably damaging |
Het |
Ugt1a6a |
A |
C |
1: 88,066,590 (GRCm39) |
D132A |
possibly damaging |
Het |
Vmn2r8 |
A |
T |
5: 108,945,962 (GRCm39) |
D548E |
possibly damaging |
Het |
Zbtb39 |
A |
T |
10: 127,578,815 (GRCm39) |
D463V |
probably damaging |
Het |
Zc3h12c |
C |
T |
9: 52,037,858 (GRCm39) |
|
probably benign |
Het |
Zfp952 |
C |
T |
17: 33,222,004 (GRCm39) |
P161L |
possibly damaging |
Het |
|
Other mutations in Eif1ad19 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01118:Eif1ad19
|
APN |
12 |
87,740,212 (GRCm39) |
missense |
probably damaging |
1.00 |
R0089:Eif1ad19
|
UTSW |
12 |
87,740,283 (GRCm39) |
missense |
probably damaging |
1.00 |
R0559:Eif1ad19
|
UTSW |
12 |
87,740,223 (GRCm39) |
missense |
probably benign |
|
R1185:Eif1ad19
|
UTSW |
12 |
87,740,478 (GRCm39) |
missense |
probably benign |
0.14 |
R1185:Eif1ad19
|
UTSW |
12 |
87,740,478 (GRCm39) |
missense |
probably benign |
0.14 |
R1185:Eif1ad19
|
UTSW |
12 |
87,740,478 (GRCm39) |
missense |
probably benign |
0.14 |
R3800:Eif1ad19
|
UTSW |
12 |
87,740,491 (GRCm39) |
missense |
possibly damaging |
0.95 |
R4531:Eif1ad19
|
UTSW |
12 |
87,740,314 (GRCm39) |
nonsense |
probably null |
|
R5013:Eif1ad19
|
UTSW |
12 |
87,740,512 (GRCm39) |
nonsense |
probably null |
|
R5817:Eif1ad19
|
UTSW |
12 |
87,740,201 (GRCm39) |
missense |
probably benign |
0.01 |
R7137:Eif1ad19
|
UTSW |
12 |
87,740,316 (GRCm39) |
missense |
possibly damaging |
0.90 |
R7187:Eif1ad19
|
UTSW |
12 |
87,740,708 (GRCm39) |
start gained |
probably benign |
|
R7403:Eif1ad19
|
UTSW |
12 |
87,740,314 (GRCm39) |
missense |
probably benign |
0.10 |
R7505:Eif1ad19
|
UTSW |
12 |
87,740,270 (GRCm39) |
missense |
probably benign |
0.20 |
R8966:Eif1ad19
|
UTSW |
12 |
87,740,273 (GRCm39) |
nonsense |
probably null |
|
R9751:Eif1ad19
|
UTSW |
12 |
87,740,526 (GRCm39) |
missense |
possibly damaging |
0.90 |
|