Other mutations in this stock |
Total: 33 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
C |
A |
6: 23,093,965 (GRCm39) |
V119F |
probably damaging |
Het |
Abcg5 |
T |
C |
17: 84,981,032 (GRCm39) |
I186V |
possibly damaging |
Het |
B4gat1 |
G |
A |
19: 5,089,446 (GRCm39) |
E148K |
probably benign |
Het |
Ccr6 |
A |
T |
17: 8,475,085 (GRCm39) |
T97S |
probably benign |
Het |
Cd209f |
A |
C |
8: 4,154,483 (GRCm39) |
|
probably null |
Het |
Chst1 |
T |
A |
2: 92,443,922 (GRCm39) |
D131E |
possibly damaging |
Het |
Dennd4a |
C |
T |
9: 64,749,843 (GRCm39) |
R145* |
probably null |
Het |
Dnaaf9 |
A |
G |
2: 130,581,385 (GRCm39) |
S546P |
probably damaging |
Het |
Dnah6 |
A |
G |
6: 73,078,881 (GRCm39) |
Y2361H |
probably benign |
Het |
Dpp6 |
C |
T |
5: 27,857,228 (GRCm39) |
T333I |
probably damaging |
Het |
Glt8d1 |
C |
A |
14: 30,730,767 (GRCm39) |
T91K |
probably damaging |
Het |
Gm4952 |
G |
A |
19: 12,604,275 (GRCm39) |
R229Q |
probably damaging |
Het |
Gm5117 |
T |
C |
8: 32,228,254 (GRCm39) |
|
noncoding transcript |
Het |
Gp5 |
T |
C |
16: 30,128,008 (GRCm39) |
E222G |
probably damaging |
Het |
Herc2 |
T |
A |
7: 55,771,470 (GRCm39) |
D1077E |
probably benign |
Het |
Hfe |
T |
C |
13: 23,888,373 (GRCm39) |
E171G |
probably damaging |
Het |
Hsp90b1 |
A |
G |
10: 86,537,678 (GRCm39) |
V209A |
probably damaging |
Het |
Ktn1 |
A |
T |
14: 47,920,835 (GRCm39) |
|
probably benign |
Het |
Med13 |
T |
C |
11: 86,179,765 (GRCm39) |
I1394M |
probably benign |
Het |
Meioc |
T |
G |
11: 102,559,274 (GRCm39) |
S65R |
probably benign |
Het |
Myof |
T |
C |
19: 37,960,661 (GRCm39) |
Y460C |
possibly damaging |
Het |
Or4f53 |
A |
T |
2: 111,087,588 (GRCm39) |
T43S |
probably benign |
Het |
Pms1 |
A |
G |
1: 53,314,324 (GRCm39) |
Y74H |
possibly damaging |
Het |
Ptprn2 |
A |
C |
12: 116,685,724 (GRCm39) |
Q61P |
probably damaging |
Het |
Rab29 |
A |
G |
1: 131,799,880 (GRCm39) |
T152A |
probably benign |
Het |
Rest |
A |
G |
5: 77,423,135 (GRCm39) |
H313R |
probably damaging |
Het |
Slc9a5 |
T |
C |
8: 106,085,091 (GRCm39) |
Y531H |
probably damaging |
Het |
St3gal3 |
T |
C |
4: 117,815,759 (GRCm39) |
T148A |
probably damaging |
Het |
Taf1c |
T |
C |
8: 120,331,019 (GRCm39) |
D33G |
probably damaging |
Het |
Trim38 |
G |
A |
13: 23,972,213 (GRCm39) |
R178Q |
probably damaging |
Het |
Uvssa |
A |
T |
5: 33,572,193 (GRCm39) |
K704N |
probably damaging |
Het |
Vmn1r69 |
G |
A |
7: 10,314,645 (GRCm39) |
Q29* |
probably null |
Het |
Ypel2 |
T |
C |
11: 86,831,429 (GRCm39) |
D119G |
possibly damaging |
Het |
|
Other mutations in Stxbp5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00466:Stxbp5
|
APN |
10 |
9,675,694 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00950:Stxbp5
|
APN |
10 |
9,684,346 (GRCm39) |
splice site |
probably benign |
|
IGL01725:Stxbp5
|
APN |
10 |
9,693,155 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02150:Stxbp5
|
APN |
10 |
9,638,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02697:Stxbp5
|
APN |
10 |
9,638,700 (GRCm39) |
nonsense |
probably null |
|
IGL02720:Stxbp5
|
APN |
10 |
9,665,105 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03155:Stxbp5
|
APN |
10 |
9,692,034 (GRCm39) |
missense |
probably null |
1.00 |
IGL03288:Stxbp5
|
APN |
10 |
9,742,447 (GRCm39) |
splice site |
probably null |
|
Fatty_fish
|
UTSW |
10 |
9,646,295 (GRCm39) |
missense |
probably damaging |
1.00 |
reindeer
|
UTSW |
10 |
9,713,836 (GRCm39) |
missense |
probably damaging |
1.00 |
H8562:Stxbp5
|
UTSW |
10 |
9,645,187 (GRCm39) |
missense |
probably benign |
0.36 |
PIT4544001:Stxbp5
|
UTSW |
10 |
9,693,048 (GRCm39) |
critical splice donor site |
probably null |
|
R0025:Stxbp5
|
UTSW |
10 |
9,638,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R0025:Stxbp5
|
UTSW |
10 |
9,638,492 (GRCm39) |
missense |
probably damaging |
1.00 |
R0219:Stxbp5
|
UTSW |
10 |
9,646,272 (GRCm39) |
missense |
probably benign |
0.36 |
R0226:Stxbp5
|
UTSW |
10 |
9,742,442 (GRCm39) |
splice site |
probably benign |
|
R0631:Stxbp5
|
UTSW |
10 |
9,660,102 (GRCm39) |
missense |
probably benign |
|
R0723:Stxbp5
|
UTSW |
10 |
9,644,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R0833:Stxbp5
|
UTSW |
10 |
9,740,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R0836:Stxbp5
|
UTSW |
10 |
9,740,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R0863:Stxbp5
|
UTSW |
10 |
9,684,784 (GRCm39) |
missense |
possibly damaging |
0.86 |
R1225:Stxbp5
|
UTSW |
10 |
9,688,135 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1271:Stxbp5
|
UTSW |
10 |
9,692,013 (GRCm39) |
missense |
probably damaging |
1.00 |
R1536:Stxbp5
|
UTSW |
10 |
9,713,836 (GRCm39) |
missense |
probably damaging |
1.00 |
R1852:Stxbp5
|
UTSW |
10 |
9,688,042 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1884:Stxbp5
|
UTSW |
10 |
9,688,042 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1902:Stxbp5
|
UTSW |
10 |
9,688,042 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1917:Stxbp5
|
UTSW |
10 |
9,688,042 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1918:Stxbp5
|
UTSW |
10 |
9,688,042 (GRCm39) |
missense |
possibly damaging |
0.94 |
R2174:Stxbp5
|
UTSW |
10 |
9,711,590 (GRCm39) |
missense |
possibly damaging |
0.69 |
R3773:Stxbp5
|
UTSW |
10 |
9,644,671 (GRCm39) |
missense |
probably damaging |
1.00 |
R3901:Stxbp5
|
UTSW |
10 |
9,645,163 (GRCm39) |
missense |
probably damaging |
1.00 |
R3981:Stxbp5
|
UTSW |
10 |
9,665,060 (GRCm39) |
intron |
probably benign |
|
R4572:Stxbp5
|
UTSW |
10 |
9,713,888 (GRCm39) |
missense |
probably damaging |
0.99 |
R4764:Stxbp5
|
UTSW |
10 |
9,646,367 (GRCm39) |
missense |
probably damaging |
1.00 |
R4841:Stxbp5
|
UTSW |
10 |
9,638,635 (GRCm39) |
missense |
probably benign |
0.06 |
R4842:Stxbp5
|
UTSW |
10 |
9,638,635 (GRCm39) |
missense |
probably benign |
0.06 |
R4884:Stxbp5
|
UTSW |
10 |
9,688,085 (GRCm39) |
nonsense |
probably null |
|
R4887:Stxbp5
|
UTSW |
10 |
9,684,844 (GRCm39) |
missense |
probably benign |
|
R4930:Stxbp5
|
UTSW |
10 |
9,636,610 (GRCm39) |
utr 3 prime |
probably benign |
|
R5065:Stxbp5
|
UTSW |
10 |
9,646,295 (GRCm39) |
missense |
probably damaging |
1.00 |
R5285:Stxbp5
|
UTSW |
10 |
9,674,019 (GRCm39) |
critical splice acceptor site |
probably null |
|
R5306:Stxbp5
|
UTSW |
10 |
9,675,735 (GRCm39) |
missense |
probably damaging |
1.00 |
R5455:Stxbp5
|
UTSW |
10 |
9,684,252 (GRCm39) |
missense |
probably benign |
|
R5531:Stxbp5
|
UTSW |
10 |
9,638,668 (GRCm39) |
nonsense |
probably null |
|
R5605:Stxbp5
|
UTSW |
10 |
9,645,490 (GRCm39) |
intron |
probably benign |
|
R5614:Stxbp5
|
UTSW |
10 |
9,636,638 (GRCm39) |
utr 3 prime |
probably benign |
|
R5805:Stxbp5
|
UTSW |
10 |
9,776,330 (GRCm39) |
missense |
probably benign |
|
R5990:Stxbp5
|
UTSW |
10 |
9,711,677 (GRCm39) |
missense |
probably damaging |
1.00 |
R6025:Stxbp5
|
UTSW |
10 |
9,675,772 (GRCm39) |
missense |
probably benign |
0.00 |
R6056:Stxbp5
|
UTSW |
10 |
9,646,430 (GRCm39) |
missense |
probably benign |
0.00 |
R6147:Stxbp5
|
UTSW |
10 |
9,684,216 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6194:Stxbp5
|
UTSW |
10 |
9,693,083 (GRCm39) |
missense |
probably damaging |
0.99 |
R6284:Stxbp5
|
UTSW |
10 |
9,642,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R6284:Stxbp5
|
UTSW |
10 |
9,642,923 (GRCm39) |
missense |
probably benign |
0.32 |
R6394:Stxbp5
|
UTSW |
10 |
9,774,975 (GRCm39) |
nonsense |
probably null |
|
R6427:Stxbp5
|
UTSW |
10 |
9,774,998 (GRCm39) |
missense |
probably damaging |
1.00 |
R6894:Stxbp5
|
UTSW |
10 |
9,660,105 (GRCm39) |
missense |
probably benign |
0.00 |
R7229:Stxbp5
|
UTSW |
10 |
9,673,931 (GRCm39) |
missense |
probably damaging |
1.00 |
R7337:Stxbp5
|
UTSW |
10 |
9,684,874 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7686:Stxbp5
|
UTSW |
10 |
9,645,154 (GRCm39) |
missense |
probably damaging |
0.99 |
R7811:Stxbp5
|
UTSW |
10 |
9,684,248 (GRCm39) |
missense |
probably benign |
|
R7974:Stxbp5
|
UTSW |
10 |
9,646,439 (GRCm39) |
splice site |
probably null |
|
R8009:Stxbp5
|
UTSW |
10 |
9,692,046 (GRCm39) |
missense |
probably damaging |
1.00 |
R8287:Stxbp5
|
UTSW |
10 |
9,660,129 (GRCm39) |
missense |
probably benign |
|
R8353:Stxbp5
|
UTSW |
10 |
9,684,792 (GRCm39) |
missense |
probably benign |
0.30 |
R8360:Stxbp5
|
UTSW |
10 |
9,688,003 (GRCm39) |
critical splice donor site |
probably null |
|
R8453:Stxbp5
|
UTSW |
10 |
9,684,792 (GRCm39) |
missense |
probably benign |
0.30 |
R8487:Stxbp5
|
UTSW |
10 |
9,688,033 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8548:Stxbp5
|
UTSW |
10 |
9,693,050 (GRCm39) |
missense |
probably null |
0.98 |
R8805:Stxbp5
|
UTSW |
10 |
9,713,859 (GRCm39) |
nonsense |
probably null |
|
R9172:Stxbp5
|
UTSW |
10 |
9,645,152 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9472:Stxbp5
|
UTSW |
10 |
9,719,101 (GRCm39) |
missense |
probably damaging |
1.00 |
R9513:Stxbp5
|
UTSW |
10 |
9,687,754 (GRCm39) |
missense |
probably benign |
0.17 |
R9649:Stxbp5
|
UTSW |
10 |
9,774,938 (GRCm39) |
missense |
probably damaging |
0.96 |
X0020:Stxbp5
|
UTSW |
10 |
9,638,634 (GRCm39) |
missense |
possibly damaging |
0.47 |
Z1176:Stxbp5
|
UTSW |
10 |
9,776,289 (GRCm39) |
missense |
possibly damaging |
0.88 |
|