Other mutations in this stock |
Total: 82 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2610008E11Rik |
T |
C |
10: 78,903,668 (GRCm39) |
D216G |
probably benign |
Het |
Abcg5 |
A |
T |
17: 84,965,956 (GRCm39) |
I640K |
possibly damaging |
Het |
Acadvl |
T |
C |
11: 69,905,168 (GRCm39) |
K128R |
probably benign |
Het |
Angptl7 |
T |
A |
4: 148,581,018 (GRCm39) |
N259I |
probably damaging |
Het |
Ankrd35 |
A |
G |
3: 96,586,997 (GRCm39) |
K104R |
possibly damaging |
Het |
Antxr1 |
T |
C |
6: 87,165,198 (GRCm39) |
N413S |
probably damaging |
Het |
Arhgap26 |
A |
G |
18: 39,504,177 (GRCm39) |
T376A |
|
Het |
Atf6b |
T |
G |
17: 34,872,949 (GRCm39) |
S622A |
probably damaging |
Het |
Atp5pd |
T |
A |
11: 115,306,851 (GRCm39) |
Y115F |
possibly damaging |
Het |
Axin2 |
T |
C |
11: 108,822,369 (GRCm39) |
L307P |
probably damaging |
Het |
B4galnt4 |
C |
T |
7: 140,644,564 (GRCm39) |
T153M |
possibly damaging |
Het |
Brd8 |
A |
G |
18: 34,740,231 (GRCm39) |
V604A |
probably benign |
Het |
Ccser2 |
T |
C |
14: 36,618,240 (GRCm39) |
Y765C |
probably damaging |
Het |
Cdh26 |
A |
G |
2: 178,110,006 (GRCm39) |
D433G |
probably damaging |
Het |
Cep85l |
T |
G |
10: 53,175,420 (GRCm39) |
|
probably null |
Het |
Ciao3 |
A |
G |
17: 25,996,395 (GRCm39) |
T135A |
probably benign |
Het |
Col23a1 |
T |
A |
11: 51,461,014 (GRCm39) |
|
probably null |
Het |
Col7a1 |
A |
G |
9: 108,804,452 (GRCm39) |
D2261G |
unknown |
Het |
Comp |
C |
A |
8: 70,833,936 (GRCm39) |
N650K |
probably damaging |
Het |
Copb1 |
A |
G |
7: 113,834,202 (GRCm39) |
M476T |
possibly damaging |
Het |
Dapk1 |
T |
A |
13: 60,897,009 (GRCm39) |
S743T |
probably damaging |
Het |
Ddx39a |
A |
G |
8: 84,451,105 (GRCm39) |
|
probably null |
Het |
Dgkb |
A |
G |
12: 38,186,580 (GRCm39) |
H243R |
probably damaging |
Het |
Dsg1c |
T |
G |
18: 20,416,171 (GRCm39) |
Y691D |
probably damaging |
Het |
Duox2 |
C |
T |
2: 122,117,535 (GRCm39) |
S933N |
probably benign |
Het |
Ece1 |
T |
C |
4: 137,641,133 (GRCm39) |
S19P |
probably benign |
Het |
Edem1 |
G |
A |
6: 108,829,524 (GRCm39) |
E548K |
probably damaging |
Het |
Eif4a3l2 |
C |
T |
6: 116,528,468 (GRCm39) |
T115I |
probably damaging |
Het |
Fpr-rs6 |
A |
G |
17: 20,402,839 (GRCm39) |
V174A |
possibly damaging |
Het |
Fyco1 |
A |
T |
9: 123,658,453 (GRCm39) |
N574K |
probably benign |
Het |
Glb1l2 |
T |
A |
9: 26,676,980 (GRCm39) |
M551L |
probably benign |
Het |
Gm7694 |
G |
T |
1: 170,130,284 (GRCm39) |
P38Q |
probably damaging |
Het |
Grip1 |
A |
G |
10: 119,814,440 (GRCm39) |
T324A |
probably benign |
Het |
Htr3b |
A |
G |
9: 48,857,849 (GRCm39) |
V131A |
possibly damaging |
Het |
Igfbp1 |
T |
C |
11: 7,148,106 (GRCm39) |
C50R |
probably damaging |
Het |
Il5ra |
A |
G |
6: 106,692,611 (GRCm39) |
I378T |
possibly damaging |
Het |
Ints11 |
T |
C |
4: 155,972,687 (GRCm39) |
L504P |
possibly damaging |
Het |
Iqca1 |
A |
T |
1: 89,987,330 (GRCm39) |
I74N |
|
Het |
Kbtbd12 |
C |
T |
6: 88,595,663 (GRCm39) |
A56T |
probably damaging |
Het |
Kcnq5 |
T |
C |
1: 21,549,620 (GRCm39) |
N369S |
possibly damaging |
Het |
Kmt5b |
A |
G |
19: 3,865,381 (GRCm39) |
D815G |
probably benign |
Het |
Lnpk |
T |
C |
2: 74,352,599 (GRCm39) |
Q361R |
probably benign |
Het |
Mep1b |
T |
C |
18: 21,222,442 (GRCm39) |
I277T |
possibly damaging |
Het |
Naip6 |
G |
A |
13: 100,437,851 (GRCm39) |
T385I |
probably benign |
Het |
Npepl1 |
A |
T |
2: 173,953,002 (GRCm39) |
I95F |
probably benign |
Het |
Nxpe4 |
T |
C |
9: 48,304,020 (GRCm39) |
F36L |
probably benign |
Het |
Optn |
C |
A |
2: 5,045,013 (GRCm39) |
C243F |
probably damaging |
Het |
Or10al7 |
A |
T |
17: 38,365,903 (GRCm39) |
C185S |
probably damaging |
Het |
Or1e33 |
C |
T |
11: 73,738,735 (GRCm39) |
C72Y |
probably damaging |
Het |
Paqr7 |
T |
C |
4: 134,234,821 (GRCm39) |
V226A |
probably benign |
Het |
Pcdh12 |
T |
A |
18: 38,415,212 (GRCm39) |
I638F |
probably damaging |
Het |
Pfas |
T |
C |
11: 68,883,119 (GRCm39) |
T722A |
probably damaging |
Het |
Pkhd1 |
T |
A |
1: 20,270,981 (GRCm39) |
I3191F |
probably damaging |
Het |
Plxnc1 |
T |
A |
10: 94,706,944 (GRCm39) |
H531L |
probably benign |
Het |
Pom121l2 |
A |
G |
13: 22,166,544 (GRCm39) |
T272A |
probably benign |
Het |
Pparg |
T |
C |
6: 115,450,102 (GRCm39) |
V367A |
possibly damaging |
Het |
Psen2 |
A |
T |
1: 180,068,356 (GRCm39) |
M99K |
probably damaging |
Het |
Ranbp10 |
T |
C |
8: 106,499,179 (GRCm39) |
T536A |
probably benign |
Het |
Rbfox2 |
G |
T |
15: 76,983,654 (GRCm39) |
P284T |
probably damaging |
Het |
Rbmyf9 |
C |
T |
Y: 3,776,675 (GRCm39) |
T104I |
possibly damaging |
Het |
Rere |
G |
A |
4: 150,701,796 (GRCm39) |
R25H |
probably damaging |
Het |
Rhpn1 |
T |
A |
15: 75,581,115 (GRCm39) |
L119Q |
probably null |
Het |
Rlig1 |
C |
A |
10: 100,413,110 (GRCm39) |
V178F |
probably benign |
Het |
Rreb1 |
A |
G |
13: 38,125,677 (GRCm39) |
T1328A |
probably benign |
Het |
Septin11 |
A |
T |
5: 93,309,007 (GRCm39) |
|
probably null |
Het |
Skida1 |
T |
A |
2: 18,052,549 (GRCm39) |
Q201L |
probably benign |
Het |
Sptan1 |
T |
A |
2: 29,910,055 (GRCm39) |
I1805N |
probably damaging |
Het |
Stard13 |
T |
A |
5: 150,970,435 (GRCm39) |
Q853L |
possibly damaging |
Het |
Szt2 |
T |
A |
4: 118,245,061 (GRCm39) |
Q1158H |
possibly damaging |
Het |
Tbcc |
A |
C |
17: 47,202,046 (GRCm39) |
D144A |
probably benign |
Het |
Tsn |
A |
G |
1: 118,232,437 (GRCm39) |
I146T |
probably benign |
Het |
Umad1 |
A |
T |
6: 8,427,121 (GRCm39) |
T99S |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,805,777 (GRCm39) |
E3261V |
probably damaging |
Het |
Vcan |
C |
A |
13: 89,851,439 (GRCm39) |
E1174* |
probably null |
Het |
Vmn2r100 |
C |
A |
17: 19,751,415 (GRCm39) |
|
probably null |
Het |
Vmn2r65 |
A |
G |
7: 84,595,919 (GRCm39) |
I255T |
probably damaging |
Het |
Vps35l |
T |
C |
7: 118,342,855 (GRCm39) |
S47P |
probably benign |
Het |
Wdr70 |
A |
G |
15: 8,006,612 (GRCm39) |
L313P |
possibly damaging |
Het |
Ythdf2 |
C |
A |
4: 131,932,089 (GRCm39) |
R357L |
probably damaging |
Het |
Zfp523 |
T |
C |
17: 28,420,267 (GRCm39) |
C262R |
probably damaging |
Het |
Zfp553 |
T |
C |
7: 126,835,936 (GRCm39) |
V497A |
probably benign |
Het |
Zhx1 |
A |
G |
15: 57,916,662 (GRCm39) |
L528S |
probably benign |
Het |
|
Other mutations in Susd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01630:Susd1
|
APN |
4 |
59,365,817 (GRCm39) |
missense |
possibly damaging |
0.85 |
IGL01705:Susd1
|
APN |
4 |
59,332,931 (GRCm39) |
splice site |
probably benign |
|
IGL01727:Susd1
|
APN |
4 |
59,412,329 (GRCm39) |
splice site |
probably benign |
|
IGL02015:Susd1
|
APN |
4 |
59,315,745 (GRCm39) |
missense |
possibly damaging |
0.86 |
IGL02102:Susd1
|
APN |
4 |
59,369,636 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02351:Susd1
|
APN |
4 |
59,427,985 (GRCm39) |
nonsense |
probably null |
|
IGL02358:Susd1
|
APN |
4 |
59,427,985 (GRCm39) |
nonsense |
probably null |
|
IGL03210:Susd1
|
APN |
4 |
59,333,035 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL03258:Susd1
|
APN |
4 |
59,379,655 (GRCm39) |
missense |
possibly damaging |
0.73 |
R0612:Susd1
|
UTSW |
4 |
59,390,561 (GRCm39) |
splice site |
probably benign |
|
R0719:Susd1
|
UTSW |
4 |
59,329,506 (GRCm39) |
missense |
possibly damaging |
0.56 |
R0722:Susd1
|
UTSW |
4 |
59,379,749 (GRCm39) |
missense |
possibly damaging |
0.73 |
R1355:Susd1
|
UTSW |
4 |
59,424,114 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1672:Susd1
|
UTSW |
4 |
59,411,395 (GRCm39) |
missense |
probably damaging |
0.98 |
R1677:Susd1
|
UTSW |
4 |
59,424,089 (GRCm39) |
missense |
possibly damaging |
0.85 |
R1921:Susd1
|
UTSW |
4 |
59,412,191 (GRCm39) |
missense |
probably benign |
0.03 |
R1933:Susd1
|
UTSW |
4 |
59,351,695 (GRCm39) |
missense |
possibly damaging |
0.72 |
R1998:Susd1
|
UTSW |
4 |
59,349,925 (GRCm39) |
missense |
probably benign |
0.03 |
R2202:Susd1
|
UTSW |
4 |
59,349,843 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2203:Susd1
|
UTSW |
4 |
59,349,843 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2204:Susd1
|
UTSW |
4 |
59,349,843 (GRCm39) |
missense |
possibly damaging |
0.96 |
R2329:Susd1
|
UTSW |
4 |
59,379,715 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2510:Susd1
|
UTSW |
4 |
59,349,855 (GRCm39) |
missense |
possibly damaging |
0.86 |
R4512:Susd1
|
UTSW |
4 |
59,329,491 (GRCm39) |
missense |
possibly damaging |
0.96 |
R4732:Susd1
|
UTSW |
4 |
59,428,029 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4733:Susd1
|
UTSW |
4 |
59,428,029 (GRCm39) |
missense |
possibly damaging |
0.53 |
R4969:Susd1
|
UTSW |
4 |
59,351,679 (GRCm39) |
missense |
probably benign |
0.04 |
R5121:Susd1
|
UTSW |
4 |
59,379,657 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5548:Susd1
|
UTSW |
4 |
59,369,577 (GRCm39) |
missense |
probably benign |
0.05 |
R5747:Susd1
|
UTSW |
4 |
59,424,108 (GRCm39) |
missense |
probably damaging |
0.98 |
R5776:Susd1
|
UTSW |
4 |
59,315,363 (GRCm39) |
utr 3 prime |
probably benign |
|
R5875:Susd1
|
UTSW |
4 |
59,412,203 (GRCm39) |
missense |
possibly damaging |
0.71 |
R6056:Susd1
|
UTSW |
4 |
59,379,687 (GRCm39) |
missense |
possibly damaging |
0.53 |
R6081:Susd1
|
UTSW |
4 |
59,411,359 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7018:Susd1
|
UTSW |
4 |
59,390,627 (GRCm39) |
missense |
probably benign |
0.44 |
R7122:Susd1
|
UTSW |
4 |
59,411,318 (GRCm39) |
nonsense |
probably null |
|
R7161:Susd1
|
UTSW |
4 |
59,329,581 (GRCm39) |
missense |
possibly damaging |
0.85 |
R7172:Susd1
|
UTSW |
4 |
59,315,420 (GRCm39) |
splice site |
probably null |
|
R7891:Susd1
|
UTSW |
4 |
59,349,915 (GRCm39) |
missense |
possibly damaging |
0.85 |
R8299:Susd1
|
UTSW |
4 |
59,315,773 (GRCm39) |
missense |
probably benign |
0.33 |
R8472:Susd1
|
UTSW |
4 |
59,332,985 (GRCm39) |
missense |
possibly damaging |
0.96 |
R8831:Susd1
|
UTSW |
4 |
59,379,594 (GRCm39) |
splice site |
probably benign |
|
R8903:Susd1
|
UTSW |
4 |
59,390,576 (GRCm39) |
missense |
probably benign |
0.02 |
R8981:Susd1
|
UTSW |
4 |
59,380,883 (GRCm39) |
missense |
probably benign |
0.07 |
R9002:Susd1
|
UTSW |
4 |
59,324,882 (GRCm39) |
missense |
probably benign |
0.00 |
R9091:Susd1
|
UTSW |
4 |
59,412,226 (GRCm39) |
missense |
probably benign |
0.44 |
R9270:Susd1
|
UTSW |
4 |
59,412,226 (GRCm39) |
missense |
probably benign |
0.44 |
R9296:Susd1
|
UTSW |
4 |
59,427,865 (GRCm39) |
intron |
probably benign |
|
|