Other mutations in this stock |
Total: 40 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aasdh |
A |
T |
5: 77,026,364 (GRCm39) |
C887S |
possibly damaging |
Het |
Adamdec1 |
C |
A |
14: 68,807,605 (GRCm39) |
E352* |
probably null |
Het |
Bglap2 |
A |
T |
3: 88,285,319 (GRCm39) |
|
probably null |
Het |
Bsn |
A |
T |
9: 107,989,745 (GRCm39) |
H2002Q |
probably benign |
Het |
Chtop |
T |
A |
3: 90,409,557 (GRCm39) |
Q165L |
possibly damaging |
Het |
Clcn1 |
A |
T |
6: 42,263,714 (GRCm39) |
|
probably null |
Het |
Ctsr |
T |
C |
13: 61,309,658 (GRCm39) |
T184A |
probably benign |
Het |
Defb36 |
T |
C |
2: 152,446,439 (GRCm39) |
L11P |
unknown |
Het |
Dock8 |
A |
G |
19: 25,165,852 (GRCm39) |
E1912G |
probably damaging |
Het |
Dpp3 |
A |
G |
19: 4,973,756 (GRCm39) |
Y106H |
probably damaging |
Het |
Epas1 |
A |
G |
17: 87,112,710 (GRCm39) |
T103A |
probably damaging |
Het |
Epcam |
A |
T |
17: 87,947,922 (GRCm39) |
T131S |
probably benign |
Het |
Fam169a |
A |
G |
13: 97,230,563 (GRCm39) |
|
probably benign |
Het |
Gh |
T |
A |
11: 106,192,559 (GRCm39) |
|
probably benign |
Het |
Kif20a |
A |
T |
18: 34,761,996 (GRCm39) |
K399* |
probably null |
Het |
Lrp1b |
A |
G |
2: 41,388,227 (GRCm39) |
I466T |
probably damaging |
Het |
Nlk |
A |
G |
11: 78,465,677 (GRCm39) |
V409A |
probably benign |
Het |
Nomo1 |
A |
G |
7: 45,693,731 (GRCm39) |
|
probably null |
Het |
Nr2c1 |
T |
A |
10: 93,992,834 (GRCm39) |
M16K |
probably damaging |
Het |
Nxph2 |
A |
T |
2: 23,289,912 (GRCm39) |
Q88L |
probably benign |
Het |
Or51a39 |
A |
G |
7: 102,363,521 (GRCm39) |
I33T |
possibly damaging |
Het |
Pkdrej |
T |
A |
15: 85,703,895 (GRCm39) |
R680S |
probably benign |
Het |
Pkhd1l1 |
A |
T |
15: 44,404,346 (GRCm39) |
N2325I |
probably benign |
Het |
Pnliprp2 |
T |
C |
19: 58,748,941 (GRCm39) |
|
probably null |
Het |
Ppp1r42 |
T |
A |
1: 10,039,078 (GRCm39) |
K347N |
probably benign |
Het |
Prtg |
T |
C |
9: 72,758,867 (GRCm39) |
V407A |
possibly damaging |
Het |
Psmb8 |
C |
A |
17: 34,419,728 (GRCm39) |
S194* |
probably null |
Het |
Rnf214 |
T |
C |
9: 45,780,772 (GRCm39) |
I406V |
probably benign |
Het |
Rreb1 |
C |
T |
13: 38,077,797 (GRCm39) |
S3L |
probably damaging |
Het |
Sdad1 |
C |
T |
5: 92,437,931 (GRCm39) |
A539T |
probably benign |
Het |
Sema3a |
A |
G |
5: 13,501,128 (GRCm39) |
Y57C |
probably damaging |
Het |
Syngr3 |
T |
C |
17: 24,905,372 (GRCm39) |
T175A |
probably damaging |
Het |
Tcf20 |
T |
A |
15: 82,740,281 (GRCm39) |
Q390L |
probably damaging |
Het |
Tex15 |
A |
G |
8: 34,071,721 (GRCm39) |
T2423A |
possibly damaging |
Het |
Tlr1 |
T |
C |
5: 65,084,469 (GRCm39) |
N36S |
probably benign |
Het |
Uchl4 |
C |
T |
9: 64,142,819 (GRCm39) |
T100M |
probably damaging |
Het |
Uhrf1 |
A |
G |
17: 56,612,129 (GRCm39) |
K11R |
probably benign |
Het |
Vps13b |
T |
A |
15: 35,880,046 (GRCm39) |
D3040E |
probably damaging |
Het |
Wdr62 |
A |
T |
7: 29,941,885 (GRCm39) |
Y640* |
probably null |
Het |
Zkscan17 |
T |
G |
11: 59,394,352 (GRCm39) |
E83A |
probably damaging |
Het |
|
Other mutations in Susd5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01514:Susd5
|
APN |
9 |
113,897,947 (GRCm39) |
splice site |
probably benign |
|
IGL01720:Susd5
|
APN |
9 |
113,893,052 (GRCm39) |
missense |
possibly damaging |
0.85 |
H8441:Susd5
|
UTSW |
9 |
113,925,253 (GRCm39) |
nonsense |
probably null |
|
R0238:Susd5
|
UTSW |
9 |
113,925,977 (GRCm39) |
makesense |
probably null |
|
R0238:Susd5
|
UTSW |
9 |
113,925,977 (GRCm39) |
makesense |
probably null |
|
R0650:Susd5
|
UTSW |
9 |
113,911,603 (GRCm39) |
missense |
possibly damaging |
0.53 |
R0666:Susd5
|
UTSW |
9 |
113,924,852 (GRCm39) |
missense |
possibly damaging |
0.53 |
R1478:Susd5
|
UTSW |
9 |
113,925,752 (GRCm39) |
missense |
probably benign |
|
R1672:Susd5
|
UTSW |
9 |
113,897,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R3416:Susd5
|
UTSW |
9 |
113,924,726 (GRCm39) |
missense |
possibly damaging |
0.85 |
R3965:Susd5
|
UTSW |
9 |
113,925,260 (GRCm39) |
missense |
possibly damaging |
0.72 |
R4182:Susd5
|
UTSW |
9 |
113,925,053 (GRCm39) |
missense |
probably benign |
0.12 |
R4514:Susd5
|
UTSW |
9 |
113,924,992 (GRCm39) |
missense |
probably benign |
0.18 |
R5373:Susd5
|
UTSW |
9 |
113,911,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R5947:Susd5
|
UTSW |
9 |
113,886,659 (GRCm39) |
missense |
possibly damaging |
0.96 |
R6189:Susd5
|
UTSW |
9 |
113,924,726 (GRCm39) |
missense |
probably damaging |
0.98 |
R6349:Susd5
|
UTSW |
9 |
113,924,870 (GRCm39) |
missense |
probably benign |
0.33 |
R7535:Susd5
|
UTSW |
9 |
113,893,108 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8973:Susd5
|
UTSW |
9 |
113,911,572 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9143:Susd5
|
UTSW |
9 |
113,924,879 (GRCm39) |
missense |
possibly damaging |
0.86 |
R9145:Susd5
|
UTSW |
9 |
113,925,289 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Susd5
|
UTSW |
9 |
113,925,208 (GRCm39) |
missense |
probably damaging |
0.98 |
Z1177:Susd5
|
UTSW |
9 |
113,893,135 (GRCm39) |
frame shift |
probably null |
|
|