Other mutations in this stock |
Total: 37 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgrf1 |
T |
A |
17: 43,632,034 (GRCm39) |
|
probably null |
Het |
Ascc3 |
T |
C |
10: 50,725,679 (GRCm39) |
V2134A |
probably benign |
Het |
Cct6b |
T |
G |
11: 82,645,943 (GRCm39) |
I80L |
probably benign |
Het |
Cfap20dc |
A |
T |
14: 8,536,516 (GRCm38) |
|
probably null |
Het |
Crebbp |
C |
A |
16: 3,903,831 (GRCm39) |
V1765L |
probably benign |
Het |
Cul9 |
C |
T |
17: 46,821,772 (GRCm39) |
|
probably null |
Het |
Cyp2c40 |
A |
G |
19: 39,792,236 (GRCm39) |
I236T |
possibly damaging |
Het |
Dbndd2 |
C |
A |
2: 164,332,113 (GRCm39) |
T112K |
possibly damaging |
Het |
Dmrtc2 |
A |
C |
7: 24,571,916 (GRCm39) |
S4R |
probably benign |
Het |
Dnah6 |
C |
T |
6: 73,052,717 (GRCm39) |
V2988I |
probably benign |
Het |
Dnajb12 |
GC |
G |
10: 59,728,574 (GRCm39) |
|
probably null |
Het |
Ercc3 |
T |
C |
18: 32,400,262 (GRCm39) |
S705P |
possibly damaging |
Het |
Gm10306 |
T |
G |
4: 94,445,077 (GRCm39) |
|
probably benign |
Het |
H2-Q6 |
T |
C |
17: 35,643,860 (GRCm39) |
L3P |
unknown |
Het |
Kcnn4 |
T |
C |
7: 24,076,978 (GRCm39) |
S176P |
probably damaging |
Het |
Maml2 |
T |
A |
9: 13,617,039 (GRCm39) |
Y128* |
probably null |
Het |
Map2 |
G |
A |
1: 66,438,550 (GRCm39) |
E25K |
probably damaging |
Het |
Morc2b |
T |
A |
17: 33,357,584 (GRCm39) |
M63L |
probably benign |
Het |
Mthfd1 |
A |
G |
12: 76,348,062 (GRCm39) |
I569V |
probably benign |
Het |
Myh8 |
G |
A |
11: 67,192,244 (GRCm39) |
R1399H |
possibly damaging |
Het |
Nop2 |
T |
C |
6: 125,117,606 (GRCm39) |
I424T |
probably benign |
Het |
Olfm5 |
T |
C |
7: 103,803,669 (GRCm39) |
R265G |
probably damaging |
Het |
Opalin |
T |
C |
19: 41,058,392 (GRCm39) |
T14A |
probably benign |
Het |
Or10j7 |
A |
G |
1: 173,011,818 (GRCm39) |
F61S |
probably damaging |
Het |
Or7a36 |
C |
T |
10: 78,820,371 (GRCm39) |
S249F |
possibly damaging |
Het |
Pced1b |
C |
A |
15: 97,282,274 (GRCm39) |
S104R |
probably benign |
Het |
Pdia2 |
T |
G |
17: 26,416,137 (GRCm39) |
Q310P |
probably null |
Het |
Ppil6 |
A |
G |
10: 41,374,541 (GRCm39) |
T141A |
probably benign |
Het |
Prrc2b |
A |
G |
2: 32,111,355 (GRCm39) |
|
probably null |
Het |
Synpo2l |
C |
A |
14: 20,712,360 (GRCm39) |
A87S |
probably damaging |
Het |
Tor1b |
GGACG |
GG |
2: 30,846,957 (GRCm39) |
|
probably benign |
Het |
Vmn1r89 |
A |
T |
7: 12,954,194 (GRCm39) |
H121L |
probably benign |
Het |
Vmn2r99 |
T |
A |
17: 19,614,408 (GRCm39) |
C709* |
probably null |
Het |
Vstm4 |
A |
G |
14: 32,585,835 (GRCm39) |
H134R |
possibly damaging |
Het |
Zan |
C |
T |
5: 137,452,262 (GRCm39) |
C1569Y |
unknown |
Het |
Zdhhc13 |
A |
G |
7: 48,455,323 (GRCm39) |
T122A |
possibly damaging |
Het |
Zpbp2 |
G |
T |
11: 98,448,429 (GRCm39) |
V249L |
probably benign |
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 |
IGL02339:Stxbp5
|
APN |
10 |
9,692,041 (GRCm39) |
missense |
possibly damaging |
0.89 |
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 |
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 |
|