Other mutations in this stock |
Total: 57 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930433I11Rik |
C |
T |
7: 40,642,880 (GRCm39) |
T183I |
possibly damaging |
Het |
Abca13 |
T |
A |
11: 9,241,886 (GRCm39) |
S1250T |
probably damaging |
Het |
Adamts12 |
T |
A |
15: 11,336,446 (GRCm39) |
S1510R |
probably benign |
Het |
Adcy5 |
T |
A |
16: 35,089,364 (GRCm39) |
C520* |
probably null |
Het |
Arhgap21 |
A |
T |
2: 20,858,983 (GRCm39) |
M1237K |
probably null |
Het |
Atp8b4 |
T |
A |
2: 126,225,607 (GRCm39) |
N541I |
probably damaging |
Het |
Bbs12 |
G |
T |
3: 37,375,223 (GRCm39) |
R557L |
probably damaging |
Het |
Bcl7c |
T |
C |
7: 127,266,200 (GRCm39) |
T183A |
probably benign |
Het |
Brd7 |
A |
G |
8: 89,081,274 (GRCm39) |
S192P |
probably damaging |
Het |
Ccdc113 |
A |
G |
8: 96,263,101 (GRCm39) |
N37S |
probably damaging |
Het |
Cdh5 |
T |
G |
8: 104,867,337 (GRCm39) |
V538G |
probably damaging |
Het |
Cfap43 |
T |
C |
19: 47,726,293 (GRCm39) |
E1639G |
possibly damaging |
Het |
Clca3a2 |
C |
T |
3: 144,796,599 (GRCm39) |
V203I |
probably benign |
Het |
Clstn2 |
A |
G |
9: 97,414,815 (GRCm39) |
F360L |
probably damaging |
Het |
Cnst |
GTGACACGCTTG |
GTG |
1: 179,407,039 (GRCm39) |
|
probably benign |
Het |
Cog2 |
T |
C |
8: 125,260,058 (GRCm39) |
Y234H |
probably damaging |
Het |
Ddhd2 |
T |
C |
8: 26,244,495 (GRCm39) |
S44G |
probably benign |
Het |
Dync2i2 |
G |
T |
2: 29,922,211 (GRCm39) |
H417N |
probably benign |
Het |
Farp1 |
A |
G |
14: 121,492,988 (GRCm39) |
E530G |
probably damaging |
Het |
Fhad1 |
C |
T |
4: 141,646,058 (GRCm39) |
|
probably null |
Het |
Foxj3 |
T |
A |
4: 119,477,538 (GRCm39) |
C449* |
probably null |
Het |
Fsbp |
G |
C |
4: 11,584,005 (GRCm39) |
V235L |
probably benign |
Het |
Fuom |
T |
C |
7: 139,681,252 (GRCm39) |
E73G |
probably benign |
Het |
Gm5134 |
A |
G |
10: 75,844,645 (GRCm39) |
H667R |
probably damaging |
Het |
Igsf21 |
A |
G |
4: 139,756,028 (GRCm39) |
I361T |
probably damaging |
Het |
Iws1 |
G |
A |
18: 32,213,213 (GRCm39) |
E214K |
possibly damaging |
Het |
Kmt2d |
A |
T |
15: 98,749,896 (GRCm39) |
V2599E |
unknown |
Het |
Lama1 |
T |
A |
17: 68,111,514 (GRCm39) |
M2255K |
|
Het |
Litafd |
C |
A |
16: 8,501,647 (GRCm39) |
P50T |
|
Het |
Lrrc32 |
A |
G |
7: 98,148,234 (GRCm39) |
H338R |
probably benign |
Het |
Map1b |
C |
A |
13: 99,571,914 (GRCm39) |
R269L |
probably damaging |
Het |
Ms4a5 |
T |
A |
19: 11,256,733 (GRCm39) |
I55F |
probably damaging |
Het |
Muc5b |
G |
C |
7: 141,411,939 (GRCm39) |
L1628F |
unknown |
Het |
Myo6 |
A |
G |
9: 80,195,384 (GRCm39) |
Q918R |
unknown |
Het |
Or1e25 |
T |
A |
11: 73,493,877 (GRCm39) |
M157K |
probably benign |
Het |
Or2t48 |
A |
G |
11: 58,420,161 (GRCm39) |
V217A |
possibly damaging |
Het |
Or5m11b |
T |
A |
2: 85,805,884 (GRCm39) |
I99N |
possibly damaging |
Het |
Or9i1b |
T |
G |
19: 13,896,967 (GRCm39) |
N194K |
probably benign |
Het |
Pals2 |
A |
G |
6: 50,157,219 (GRCm39) |
R296G |
probably damaging |
Het |
Plin5 |
A |
G |
17: 56,419,462 (GRCm39) |
V320A |
probably damaging |
Het |
Ptx4 |
A |
T |
17: 25,342,257 (GRCm39) |
Q244L |
possibly damaging |
Het |
Rab3gap1 |
A |
G |
1: 127,858,495 (GRCm39) |
T535A |
probably benign |
Het |
Ranbp2 |
T |
C |
10: 58,313,117 (GRCm39) |
F1279S |
probably damaging |
Het |
Rgl1 |
T |
C |
1: 152,428,362 (GRCm39) |
H254R |
probably damaging |
Het |
Rida |
C |
T |
15: 34,487,909 (GRCm39) |
A69T |
probably damaging |
Het |
Scn2a |
T |
C |
2: 65,511,346 (GRCm39) |
F131L |
probably benign |
Het |
Septin1 |
T |
C |
7: 126,816,092 (GRCm39) |
I141V |
probably benign |
Het |
Slc10a6 |
A |
G |
5: 103,765,571 (GRCm39) |
S171P |
probably damaging |
Het |
Slc18a1 |
A |
G |
8: 69,519,790 (GRCm39) |
|
probably null |
Het |
Slc38a6 |
T |
C |
12: 73,388,526 (GRCm39) |
S247P |
possibly damaging |
Het |
Tet2 |
A |
T |
3: 133,187,147 (GRCm39) |
I1094K |
possibly damaging |
Het |
Tmem234 |
C |
T |
4: 129,501,333 (GRCm39) |
S138L |
probably benign |
Het |
Trpv1 |
T |
A |
11: 73,145,148 (GRCm39) |
|
probably null |
Het |
Vmn2r60 |
T |
A |
7: 41,844,935 (GRCm39) |
M766K |
probably damaging |
Het |
Vmn2r84 |
T |
C |
10: 130,226,843 (GRCm39) |
N332D |
probably benign |
Het |
Zfp292 |
A |
T |
4: 34,819,563 (GRCm39) |
I258N |
probably damaging |
Het |
Zxdc |
A |
G |
6: 90,375,773 (GRCm39) |
K750E |
probably damaging |
Het |
|
Other mutations in Calhm3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
FR4304:Calhm3
|
UTSW |
19 |
47,140,335 (GRCm39) |
frame shift |
probably null |
|
R1203:Calhm3
|
UTSW |
19 |
47,143,839 (GRCm39) |
missense |
probably damaging |
1.00 |
R1863:Calhm3
|
UTSW |
19 |
47,140,539 (GRCm39) |
missense |
probably damaging |
1.00 |
R1911:Calhm3
|
UTSW |
19 |
47,143,908 (GRCm39) |
missense |
possibly damaging |
0.74 |
R1951:Calhm3
|
UTSW |
19 |
47,140,256 (GRCm39) |
missense |
probably benign |
0.00 |
R2089:Calhm3
|
UTSW |
19 |
47,140,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Calhm3
|
UTSW |
19 |
47,140,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R2091:Calhm3
|
UTSW |
19 |
47,140,430 (GRCm39) |
missense |
probably damaging |
1.00 |
R2273:Calhm3
|
UTSW |
19 |
47,145,986 (GRCm39) |
missense |
probably damaging |
0.96 |
R2274:Calhm3
|
UTSW |
19 |
47,145,986 (GRCm39) |
missense |
probably damaging |
0.96 |
R2436:Calhm3
|
UTSW |
19 |
47,140,404 (GRCm39) |
missense |
probably damaging |
1.00 |
R3702:Calhm3
|
UTSW |
19 |
47,140,187 (GRCm39) |
missense |
possibly damaging |
0.88 |
R5758:Calhm3
|
UTSW |
19 |
47,140,190 (GRCm39) |
missense |
probably damaging |
0.99 |
R5901:Calhm3
|
UTSW |
19 |
47,146,052 (GRCm39) |
missense |
probably damaging |
1.00 |
R5938:Calhm3
|
UTSW |
19 |
47,140,516 (GRCm39) |
missense |
probably damaging |
1.00 |
R6948:Calhm3
|
UTSW |
19 |
47,140,344 (GRCm39) |
missense |
probably damaging |
0.99 |
|