Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
C |
6: 121,654,944 (GRCm39) |
S1423P |
possibly damaging |
Het |
Acvr1c |
A |
G |
2: 58,173,399 (GRCm39) |
|
probably null |
Het |
Adgrf5 |
A |
G |
17: 43,761,788 (GRCm39) |
K1161R |
probably damaging |
Het |
Aoc1l3 |
A |
G |
6: 48,967,083 (GRCm39) |
Y677C |
probably damaging |
Het |
Arhgap32 |
T |
G |
9: 32,063,232 (GRCm39) |
D80E |
probably benign |
Het |
Aspg |
T |
C |
12: 112,078,632 (GRCm39) |
V30A |
possibly damaging |
Het |
Bcl2a1d |
T |
C |
9: 88,613,531 (GRCm39) |
D81G |
probably damaging |
Het |
Cep170b |
T |
C |
12: 112,701,601 (GRCm39) |
V160A |
probably benign |
Het |
Ces1c |
T |
C |
8: 93,857,470 (GRCm39) |
Y37C |
probably benign |
Het |
Cntnap5a |
T |
C |
1: 116,017,106 (GRCm39) |
L233P |
probably damaging |
Het |
Crem |
C |
A |
18: 3,273,459 (GRCm39) |
A245S |
possibly damaging |
Het |
Cyp2d12 |
C |
T |
15: 82,442,022 (GRCm39) |
A280V |
probably benign |
Het |
Dnah2 |
C |
T |
11: 69,382,381 (GRCm39) |
G1243D |
probably damaging |
Het |
Emcn |
T |
G |
3: 137,109,752 (GRCm39) |
N131K |
probably damaging |
Het |
Fat3 |
A |
T |
9: 15,908,444 (GRCm39) |
D2519E |
probably damaging |
Het |
Fibin |
T |
A |
2: 110,193,001 (GRCm39) |
D47V |
probably damaging |
Het |
Fsd1 |
G |
A |
17: 56,300,876 (GRCm39) |
R245H |
probably damaging |
Het |
Gimap8 |
C |
A |
6: 48,627,187 (GRCm39) |
L54I |
probably damaging |
Het |
Gm20481 |
A |
G |
17: 35,189,071 (GRCm39) |
Y27C |
unknown |
Het |
Grin1 |
T |
G |
2: 25,203,550 (GRCm39) |
M154L |
probably benign |
Het |
Ighv8-13 |
A |
G |
12: 115,729,197 (GRCm39) |
L20P |
probably damaging |
Het |
Insc |
G |
A |
7: 114,410,850 (GRCm39) |
V236I |
probably benign |
Het |
Lrrk1 |
A |
G |
7: 65,935,027 (GRCm39) |
F1031L |
probably benign |
Het |
Man2a2 |
C |
A |
7: 80,009,499 (GRCm39) |
R785L |
probably benign |
Het |
Mcur1 |
C |
A |
13: 43,697,931 (GRCm39) |
|
probably null |
Het |
Med12l |
A |
C |
3: 59,165,675 (GRCm39) |
R1464S |
probably damaging |
Het |
Mycbp2 |
A |
T |
14: 103,520,115 (GRCm39) |
M767K |
possibly damaging |
Het |
Naalad2 |
T |
C |
9: 18,234,783 (GRCm39) |
I762V |
probably benign |
Het |
Nfkbid |
A |
G |
7: 30,125,681 (GRCm39) |
T357A |
possibly damaging |
Het |
Pcdh17 |
A |
G |
14: 84,770,989 (GRCm39) |
R1156G |
possibly damaging |
Het |
Pcdhb1 |
T |
C |
18: 37,400,445 (GRCm39) |
S799P |
possibly damaging |
Het |
Pde3a |
A |
T |
6: 141,444,472 (GRCm39) |
E1093D |
probably benign |
Het |
Plcg1 |
T |
C |
2: 160,595,846 (GRCm39) |
Y572H |
possibly damaging |
Het |
Plxna4 |
A |
G |
6: 32,494,199 (GRCm39) |
L139P |
probably damaging |
Het |
Psma1 |
A |
G |
7: 113,873,683 (GRCm39) |
Y6H |
probably damaging |
Het |
Psmd2 |
A |
G |
16: 20,471,377 (GRCm39) |
E76G |
probably benign |
Het |
Ptk2 |
G |
A |
15: 73,093,658 (GRCm39) |
P854S |
possibly damaging |
Het |
Pyy |
T |
G |
11: 101,998,099 (GRCm39) |
D27A |
possibly damaging |
Het |
Slc22a2 |
A |
G |
17: 12,803,228 (GRCm39) |
T21A |
probably benign |
Het |
Slc25a2 |
T |
C |
18: 37,771,200 (GRCm39) |
I110V |
probably benign |
Het |
Sult1c2 |
A |
C |
17: 54,145,422 (GRCm39) |
W85G |
probably damaging |
Het |
Syt12 |
C |
T |
19: 4,503,978 (GRCm39) |
D218N |
probably damaging |
Het |
Tln1 |
C |
T |
4: 43,540,616 (GRCm39) |
V1462M |
probably damaging |
Het |
Tor1aip2 |
T |
A |
1: 155,927,722 (GRCm39) |
N33K |
possibly damaging |
Het |
Usp17lb |
C |
A |
7: 104,490,798 (GRCm39) |
W43L |
probably benign |
Het |
Vmn1r76 |
A |
G |
7: 11,664,612 (GRCm39) |
Y201H |
possibly damaging |
Het |
Wnk1 |
C |
A |
6: 120,015,173 (GRCm39) |
|
probably benign |
Het |
Wrnip1 |
A |
G |
13: 32,986,732 (GRCm39) |
D171G |
probably benign |
Het |
Zar1 |
T |
A |
5: 72,738,159 (GRCm39) |
N81I |
probably damaging |
Het |
Zbtb45 |
T |
C |
7: 12,741,083 (GRCm39) |
T392A |
probably benign |
Het |
Zfp445 |
T |
C |
9: 122,683,843 (GRCm39) |
E272G |
probably 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 |
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 |
R8711:Eif1ad19
|
UTSW |
12 |
87,740,130 (GRCm39) |
missense |
unknown |
|
R8966:Eif1ad19
|
UTSW |
12 |
87,740,273 (GRCm39) |
nonsense |
probably null |
|
R9751:Eif1ad19
|
UTSW |
12 |
87,740,526 (GRCm39) |
missense |
possibly damaging |
0.90 |
|