Other mutations in this stock |
Total: 32 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1500002C15Rik |
G |
T |
4: 155,818,628 (GRCm39) |
|
probably benign |
Het |
4933430I17Rik |
G |
T |
4: 62,450,858 (GRCm39) |
R107L |
possibly damaging |
Het |
Acvr1 |
A |
T |
2: 58,348,997 (GRCm39) |
D388E |
probably benign |
Het |
Art3 |
T |
C |
5: 92,562,199 (GRCm39) |
S354P |
probably damaging |
Het |
Bpnt1 |
C |
A |
1: 185,077,591 (GRCm39) |
S102* |
probably null |
Het |
Ces1a |
G |
T |
8: 93,771,726 (GRCm39) |
P24T |
probably damaging |
Het |
Cfap65 |
A |
T |
1: 74,950,237 (GRCm39) |
S1171T |
probably damaging |
Het |
Cracd |
T |
A |
5: 77,005,478 (GRCm39) |
M613K |
unknown |
Het |
Csn2 |
T |
C |
5: 87,842,838 (GRCm39) |
H47R |
possibly damaging |
Het |
Gm14496 |
T |
A |
2: 181,637,458 (GRCm39) |
D177E |
probably benign |
Het |
Hmbs |
A |
G |
9: 44,250,845 (GRCm39) |
V126A |
possibly damaging |
Het |
Ica1l |
A |
G |
1: 60,054,916 (GRCm39) |
M105T |
probably damaging |
Het |
Morc2a |
G |
A |
11: 3,600,428 (GRCm39) |
E17K |
probably benign |
Het |
Mroh8 |
T |
C |
2: 157,080,232 (GRCm39) |
|
probably benign |
Het |
Mroh9 |
G |
T |
1: 162,883,172 (GRCm39) |
L436I |
probably damaging |
Het |
Nup54 |
T |
C |
5: 92,565,334 (GRCm39) |
D461G |
probably benign |
Het |
Or10ag2 |
A |
T |
2: 87,249,319 (GRCm39) |
D309V |
probably damaging |
Het |
Or2t45 |
A |
G |
11: 58,669,123 (GRCm39) |
T57A |
probably benign |
Het |
Pcid2 |
G |
A |
8: 13,135,319 (GRCm39) |
|
probably benign |
Het |
Ppp1r3b |
G |
T |
8: 35,851,872 (GRCm39) |
R237L |
probably benign |
Het |
Prdm11 |
A |
G |
2: 92,843,102 (GRCm39) |
V119A |
probably damaging |
Het |
Serpina5 |
T |
A |
12: 104,068,149 (GRCm39) |
V70E |
probably damaging |
Het |
Skap2 |
C |
T |
6: 51,884,894 (GRCm39) |
D249N |
probably benign |
Het |
Slc22a29 |
A |
T |
19: 8,184,542 (GRCm39) |
|
probably benign |
Het |
Slc4a1ap |
C |
A |
5: 31,685,571 (GRCm39) |
T283K |
possibly damaging |
Het |
Slc6a21 |
T |
G |
7: 44,937,220 (GRCm39) |
I575S |
probably damaging |
Het |
Smpd1 |
T |
G |
7: 105,203,982 (GRCm39) |
W82G |
probably benign |
Het |
Snx14 |
T |
A |
9: 88,263,553 (GRCm39) |
M897L |
probably damaging |
Het |
Tjp1 |
A |
G |
7: 64,972,406 (GRCm39) |
V586A |
probably damaging |
Het |
Tmc8 |
T |
C |
11: 117,682,910 (GRCm39) |
|
probably benign |
Het |
Trim34a |
A |
G |
7: 103,909,706 (GRCm39) |
Y298C |
probably damaging |
Het |
Ube3c |
T |
C |
5: 29,872,960 (GRCm39) |
V1000A |
probably damaging |
Het |
|
Other mutations in S100a7l2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00231:S100a7l2
|
APN |
3 |
90,995,665 (GRCm39) |
missense |
probably benign |
0.01 |
IGL01372:S100a7l2
|
APN |
3 |
90,995,616 (GRCm39) |
utr 3 prime |
probably benign |
|
IGL02894:S100a7l2
|
APN |
3 |
90,995,700 (GRCm39) |
missense |
probably benign |
0.18 |
IGL03110:S100a7l2
|
APN |
3 |
90,995,626 (GRCm39) |
missense |
unknown |
|
IGL03250:S100a7l2
|
APN |
3 |
90,997,715 (GRCm39) |
utr 5 prime |
probably benign |
|
R2357:S100a7l2
|
UTSW |
3 |
90,995,733 (GRCm39) |
missense |
probably benign |
0.35 |
R3795:S100a7l2
|
UTSW |
3 |
90,995,730 (GRCm39) |
missense |
possibly damaging |
0.73 |
R5315:S100a7l2
|
UTSW |
3 |
90,997,637 (GRCm39) |
missense |
possibly damaging |
0.56 |
R5495:S100a7l2
|
UTSW |
3 |
90,997,602 (GRCm39) |
missense |
possibly damaging |
0.93 |
R6314:S100a7l2
|
UTSW |
3 |
90,995,683 (GRCm39) |
missense |
possibly damaging |
0.56 |
R8351:S100a7l2
|
UTSW |
3 |
90,995,671 (GRCm39) |
missense |
probably benign |
0.01 |
R8451:S100a7l2
|
UTSW |
3 |
90,995,671 (GRCm39) |
missense |
probably benign |
0.01 |
R9371:S100a7l2
|
UTSW |
3 |
90,997,698 (GRCm39) |
missense |
unknown |
|
Z1177:S100a7l2
|
UTSW |
3 |
90,995,663 (GRCm39) |
missense |
probably benign |
0.01 |
|