Other mutations in this stock |
Total: 42 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abca7 |
G |
A |
10: 79,842,089 (GRCm39) |
D1049N |
probably benign |
Het |
Ankdd1a |
A |
T |
9: 65,411,421 (GRCm39) |
L362Q |
probably damaging |
Het |
Ankib1 |
A |
T |
5: 3,822,594 (GRCm39) |
N37K |
probably damaging |
Het |
Ankrd55 |
T |
A |
13: 112,459,677 (GRCm39) |
D90E |
probably damaging |
Het |
Atp1a2 |
T |
C |
1: 172,106,510 (GRCm39) |
R831G |
probably damaging |
Het |
Bcar3 |
A |
G |
3: 122,316,943 (GRCm39) |
D638G |
probably damaging |
Het |
Cabp4 |
T |
A |
19: 4,189,322 (GRCm39) |
E78D |
probably benign |
Het |
Cmtm8 |
A |
G |
9: 114,619,755 (GRCm39) |
V130A |
possibly damaging |
Het |
Cyth3 |
A |
G |
5: 143,678,393 (GRCm39) |
T66A |
possibly damaging |
Het |
Dmbt1 |
A |
T |
7: 130,705,409 (GRCm39) |
I1171F |
possibly damaging |
Het |
Dnah10 |
G |
A |
5: 124,856,218 (GRCm39) |
G2060D |
probably damaging |
Het |
Dnah11 |
T |
C |
12: 118,156,134 (GRCm39) |
H172R |
probably damaging |
Het |
Dnah5 |
C |
T |
15: 28,230,636 (GRCm39) |
A178V |
probably benign |
Het |
Efcab6 |
T |
G |
15: 83,928,505 (GRCm39) |
M30L |
possibly damaging |
Het |
Ehbp1l1 |
T |
C |
19: 5,765,817 (GRCm39) |
|
probably benign |
Het |
Eps15 |
G |
A |
4: 109,179,303 (GRCm39) |
E230K |
probably damaging |
Het |
Fam91a1 |
A |
G |
15: 58,301,911 (GRCm39) |
I258M |
probably damaging |
Het |
Gm5581 |
G |
A |
6: 131,145,366 (GRCm39) |
|
noncoding transcript |
Het |
Hrh1 |
G |
A |
6: 114,456,958 (GRCm39) |
V80I |
probably damaging |
Het |
Ldhd |
G |
A |
8: 112,355,032 (GRCm39) |
H290Y |
probably benign |
Het |
Lepr |
G |
A |
4: 101,592,774 (GRCm39) |
E130K |
possibly damaging |
Het |
Mycbpap |
T |
C |
11: 94,397,282 (GRCm39) |
I40V |
possibly damaging |
Het |
Nrap |
T |
A |
19: 56,317,534 (GRCm39) |
|
probably null |
Het |
Opn5 |
T |
A |
17: 42,891,435 (GRCm39) |
|
probably null |
Het |
Or1j14 |
T |
A |
2: 36,417,463 (GRCm39) |
I13N |
probably benign |
Het |
Or5ac24 |
A |
G |
16: 59,165,524 (GRCm39) |
I180T |
probably damaging |
Het |
Otop3 |
A |
T |
11: 115,235,930 (GRCm39) |
T521S |
possibly damaging |
Het |
Pcsk5 |
T |
G |
19: 17,595,108 (GRCm39) |
T409P |
probably damaging |
Het |
Pde9a |
T |
A |
17: 31,680,685 (GRCm39) |
F322Y |
probably benign |
Het |
Pgm5 |
T |
A |
19: 24,710,985 (GRCm39) |
I406F |
probably damaging |
Het |
Prrc2b |
T |
C |
2: 32,113,942 (GRCm39) |
S1998P |
probably damaging |
Het |
Prune2 |
T |
C |
19: 17,102,433 (GRCm39) |
Y2531H |
probably damaging |
Het |
Ptprk |
T |
C |
10: 28,445,923 (GRCm39) |
V932A |
probably benign |
Het |
Rapgef6 |
T |
A |
11: 54,559,437 (GRCm39) |
|
probably benign |
Het |
Rgsl1 |
T |
A |
1: 153,701,887 (GRCm39) |
Y224F |
probably damaging |
Het |
Rps6kl1 |
A |
T |
12: 85,193,663 (GRCm39) |
C143S |
probably damaging |
Het |
Slc5a5 |
G |
A |
8: 71,343,020 (GRCm39) |
|
probably benign |
Het |
Tfb2m |
A |
G |
1: 179,369,878 (GRCm39) |
S182P |
probably damaging |
Het |
Tmc3 |
A |
G |
7: 83,261,746 (GRCm39) |
H608R |
probably damaging |
Het |
Trim37 |
T |
A |
11: 87,075,772 (GRCm39) |
H459Q |
probably benign |
Het |
Vmn2r71 |
A |
T |
7: 85,270,022 (GRCm39) |
|
probably benign |
Het |
Xirp2 |
T |
C |
2: 67,344,334 (GRCm39) |
S2192P |
possibly 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 |
IGL01526:S100a7l2
|
APN |
3 |
90,995,612 (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 |
|