Other mutations in this stock |
Total: 61 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ahrr |
G |
A |
13: 74,431,143 (GRCm39) |
|
probably benign |
Het |
Antxr2 |
G |
A |
5: 98,086,284 (GRCm39) |
T441I |
possibly damaging |
Het |
Apcs |
A |
G |
1: 172,722,023 (GRCm39) |
Y108H |
probably benign |
Het |
Atad5 |
A |
G |
11: 79,988,840 (GRCm39) |
T666A |
probably benign |
Het |
Atcay |
C |
T |
10: 81,046,353 (GRCm39) |
|
probably null |
Het |
Bahcc1 |
A |
G |
11: 120,159,196 (GRCm39) |
D141G |
probably damaging |
Het |
Ceacam10 |
A |
G |
7: 24,477,689 (GRCm39) |
Y68C |
probably damaging |
Het |
Cfap54 |
T |
A |
10: 92,812,901 (GRCm39) |
Q1344L |
probably benign |
Het |
Cyb5r4 |
A |
G |
9: 86,948,795 (GRCm39) |
|
probably null |
Het |
Cyp2b9 |
G |
T |
7: 25,872,899 (GRCm39) |
S14I |
possibly damaging |
Het |
Dusp12 |
A |
G |
1: 170,708,226 (GRCm39) |
Y164H |
probably damaging |
Het |
Eml2 |
T |
C |
7: 18,930,539 (GRCm39) |
V373A |
possibly damaging |
Het |
Fat1 |
A |
G |
8: 45,479,441 (GRCm39) |
D2829G |
probably damaging |
Het |
Fbxl13 |
T |
C |
5: 21,691,371 (GRCm39) |
T671A |
probably damaging |
Het |
Fbxo28 |
G |
T |
1: 182,153,805 (GRCm39) |
|
probably benign |
Het |
Fbxo44 |
A |
G |
4: 148,243,152 (GRCm39) |
L89P |
probably damaging |
Het |
Fndc3b |
T |
A |
3: 27,610,266 (GRCm39) |
|
probably null |
Het |
Gm9955 |
G |
T |
18: 24,842,209 (GRCm39) |
|
probably benign |
Het |
Gprc6a |
T |
A |
10: 51,491,080 (GRCm39) |
K819* |
probably null |
Het |
Gxylt1 |
A |
T |
15: 93,152,436 (GRCm39) |
|
probably benign |
Het |
Hspa12a |
T |
C |
19: 58,788,056 (GRCm39) |
T589A |
probably benign |
Het |
Idh2 |
A |
G |
7: 79,747,570 (GRCm39) |
S317P |
probably damaging |
Het |
Ifi30 |
T |
C |
8: 71,216,421 (GRCm39) |
|
probably null |
Het |
Ifna16 |
G |
A |
4: 88,594,867 (GRCm39) |
A76V |
probably benign |
Het |
Itpr2 |
C |
T |
6: 146,246,638 (GRCm39) |
E1127K |
probably damaging |
Het |
Kank4 |
A |
G |
4: 98,667,457 (GRCm39) |
V330A |
probably benign |
Het |
Kpna1 |
T |
A |
16: 35,843,611 (GRCm39) |
D328E |
probably damaging |
Het |
Krt71 |
T |
A |
15: 101,646,868 (GRCm39) |
H280L |
possibly damaging |
Het |
Lrrc37 |
G |
A |
11: 103,433,816 (GRCm39) |
P942S |
probably damaging |
Het |
Mapt |
A |
G |
11: 104,196,224 (GRCm39) |
M446V |
probably damaging |
Het |
Med1 |
C |
T |
11: 98,057,081 (GRCm39) |
|
probably null |
Het |
Mif |
T |
A |
10: 75,695,614 (GRCm39) |
H63L |
probably damaging |
Het |
Mycbp2 |
A |
G |
14: 103,461,708 (GRCm39) |
V1447A |
probably benign |
Het |
Myo1b |
A |
T |
1: 51,821,148 (GRCm39) |
I451N |
probably damaging |
Het |
Nme2 |
A |
T |
11: 93,842,756 (GRCm39) |
|
probably null |
Het |
Nubp1 |
A |
G |
16: 10,238,981 (GRCm39) |
T199A |
probably damaging |
Het |
Nup210l |
T |
A |
3: 90,089,212 (GRCm39) |
V1165D |
probably damaging |
Het |
Nup98 |
T |
A |
7: 101,841,241 (GRCm39) |
T122S |
probably damaging |
Het |
Or14a258 |
A |
T |
7: 86,035,715 (GRCm39) |
L51Q |
probably benign |
Het |
Or1n2 |
T |
C |
2: 36,797,470 (GRCm39) |
F171L |
probably damaging |
Het |
Or5j1 |
C |
T |
2: 86,879,548 (GRCm39) |
E11K |
probably damaging |
Het |
Or6c202 |
T |
A |
10: 128,996,608 (GRCm39) |
I82L |
probably benign |
Het |
Pard3b |
A |
T |
1: 62,676,979 (GRCm39) |
Y1170F |
probably damaging |
Het |
Pear1 |
T |
C |
3: 87,661,665 (GRCm39) |
D536G |
probably damaging |
Het |
Phrf1 |
G |
T |
7: 140,823,770 (GRCm39) |
R196L |
probably damaging |
Het |
Plxna2 |
G |
T |
1: 194,326,204 (GRCm39) |
R46L |
probably benign |
Het |
Rbm39 |
G |
A |
2: 155,990,099 (GRCm39) |
T496I |
possibly damaging |
Het |
Rpl14 |
C |
G |
9: 120,401,167 (GRCm39) |
F3L |
possibly damaging |
Het |
Rtf2 |
G |
A |
2: 172,286,616 (GRCm39) |
S40N |
probably damaging |
Het |
Runx2 |
G |
A |
17: 44,919,141 (GRCm39) |
S481L |
possibly damaging |
Het |
Sh3rf1 |
T |
A |
8: 61,782,286 (GRCm39) |
Y143N |
possibly damaging |
Het |
Slc4a8 |
T |
A |
15: 100,687,727 (GRCm39) |
I288N |
probably damaging |
Het |
Ttc38 |
C |
A |
15: 85,725,690 (GRCm39) |
F184L |
probably damaging |
Het |
Vmn1r28 |
T |
C |
6: 58,242,879 (GRCm39) |
Y241H |
probably damaging |
Het |
Vmn2r110 |
A |
T |
17: 20,816,346 (GRCm39) |
V59D |
probably benign |
Het |
Wdpcp |
A |
G |
11: 21,661,638 (GRCm39) |
I303M |
probably damaging |
Het |
Zc3h12d |
G |
A |
10: 7,743,678 (GRCm39) |
A483T |
probably benign |
Het |
Zfp106 |
C |
A |
2: 120,362,094 (GRCm39) |
K1008N |
probably damaging |
Het |
Zfp334 |
A |
G |
2: 165,223,492 (GRCm39) |
Y184H |
probably benign |
Het |
Zfp68 |
G |
A |
5: 138,606,041 (GRCm39) |
T94I |
probably benign |
Het |
Zkscan3 |
A |
T |
13: 21,579,090 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Siglec15 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01743:Siglec15
|
APN |
18 |
78,086,820 (GRCm39) |
unclassified |
probably benign |
|
IGL02472:Siglec15
|
APN |
18 |
78,086,832 (GRCm39) |
missense |
possibly damaging |
0.72 |
IGL02988:Siglec15
|
UTSW |
18 |
78,092,462 (GRCm39) |
missense |
probably damaging |
1.00 |
PIT4377001:Siglec15
|
UTSW |
18 |
78,100,590 (GRCm39) |
start gained |
probably benign |
|
R0607:Siglec15
|
UTSW |
18 |
78,089,352 (GRCm39) |
missense |
probably benign |
0.03 |
R4427:Siglec15
|
UTSW |
18 |
78,086,836 (GRCm39) |
missense |
possibly damaging |
0.53 |
R5023:Siglec15
|
UTSW |
18 |
78,091,890 (GRCm39) |
missense |
probably damaging |
1.00 |
R5994:Siglec15
|
UTSW |
18 |
78,090,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R7052:Siglec15
|
UTSW |
18 |
78,091,946 (GRCm39) |
missense |
probably damaging |
1.00 |
R7807:Siglec15
|
UTSW |
18 |
78,090,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R7827:Siglec15
|
UTSW |
18 |
78,100,445 (GRCm39) |
nonsense |
probably null |
|
R7898:Siglec15
|
UTSW |
18 |
78,086,914 (GRCm39) |
missense |
probably benign |
0.19 |
R8052:Siglec15
|
UTSW |
18 |
78,091,803 (GRCm39) |
missense |
possibly damaging |
0.46 |
R9077:Siglec15
|
UTSW |
18 |
78,091,983 (GRCm39) |
missense |
possibly damaging |
0.68 |
|