Other mutations in this stock |
Total: 67 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
5031439G07Rik |
A |
T |
15: 84,839,833 (GRCm39) |
|
probably benign |
Het |
Adamts7 |
T |
A |
9: 90,070,823 (GRCm39) |
I648N |
probably damaging |
Het |
Akap13 |
T |
A |
7: 75,385,526 (GRCm39) |
F2252I |
probably damaging |
Het |
Akr1c6 |
A |
T |
13: 4,507,159 (GRCm39) |
H314L |
probably damaging |
Het |
Anxa3 |
T |
A |
5: 96,976,549 (GRCm39) |
|
probably null |
Het |
Apob |
T |
G |
12: 8,036,165 (GRCm39) |
F298V |
probably benign |
Het |
Atp8a2 |
A |
C |
14: 60,097,772 (GRCm39) |
|
probably benign |
Het |
Atp8b5 |
A |
T |
4: 43,334,313 (GRCm39) |
T360S |
probably damaging |
Het |
BC051665 |
A |
T |
13: 60,932,555 (GRCm39) |
N43K |
probably benign |
Het |
Bicral |
T |
A |
17: 47,112,650 (GRCm39) |
H850L |
probably benign |
Het |
C1qtnf1 |
A |
G |
11: 118,339,011 (GRCm39) |
D227G |
probably damaging |
Het |
C8a |
T |
A |
4: 104,685,275 (GRCm39) |
T323S |
possibly damaging |
Het |
Cep89 |
T |
C |
7: 35,117,636 (GRCm39) |
|
probably benign |
Het |
Cercam |
G |
T |
2: 29,770,652 (GRCm39) |
V408L |
probably benign |
Het |
CN725425 |
G |
A |
15: 91,123,158 (GRCm39) |
V76M |
possibly damaging |
Het |
Cops7b |
T |
A |
1: 86,532,835 (GRCm39) |
M231K |
probably benign |
Het |
Cpa2 |
T |
A |
6: 30,544,865 (GRCm39) |
|
probably null |
Het |
Dab2ip |
A |
T |
2: 35,600,268 (GRCm39) |
I287F |
probably damaging |
Het |
Defb10 |
A |
T |
8: 22,348,944 (GRCm39) |
M1L |
probably benign |
Het |
Dscam |
C |
A |
16: 96,409,274 (GRCm39) |
R1883L |
possibly damaging |
Het |
Dsg4 |
T |
A |
18: 20,595,717 (GRCm39) |
I640N |
possibly damaging |
Het |
Duox2 |
G |
C |
2: 122,112,232 (GRCm39) |
P1318R |
probably benign |
Het |
Dzip3 |
T |
C |
16: 48,765,985 (GRCm39) |
D466G |
probably benign |
Het |
E230025N22Rik |
T |
A |
18: 36,824,462 (GRCm39) |
|
probably null |
Het |
E2f3 |
A |
G |
13: 30,102,652 (GRCm39) |
L80P |
probably damaging |
Het |
Eif2b2 |
T |
C |
12: 85,266,360 (GRCm39) |
S9P |
probably benign |
Het |
Etaa1 |
A |
T |
11: 17,897,201 (GRCm39) |
D305E |
probably benign |
Het |
Fads6 |
C |
A |
11: 115,188,235 (GRCm39) |
R23L |
probably benign |
Het |
Flrt2 |
T |
C |
12: 95,746,979 (GRCm39) |
V439A |
probably damaging |
Het |
Gtse1 |
C |
T |
15: 85,744,303 (GRCm39) |
|
probably benign |
Het |
Irf7 |
T |
C |
7: 140,843,935 (GRCm39) |
T246A |
probably damaging |
Het |
Kif28 |
A |
G |
1: 179,532,697 (GRCm39) |
V639A |
possibly damaging |
Het |
Klhdc8a |
G |
A |
1: 132,230,385 (GRCm39) |
A167T |
possibly damaging |
Het |
Lrfn3 |
T |
C |
7: 30,059,469 (GRCm39) |
H252R |
probably benign |
Het |
Lzts1 |
G |
T |
8: 69,591,638 (GRCm39) |
A170E |
probably damaging |
Het |
Mphosph9 |
T |
A |
5: 124,403,461 (GRCm39) |
I856F |
possibly damaging |
Het |
Mroh2a |
C |
T |
1: 88,160,075 (GRCm39) |
|
probably benign |
Het |
Mroh2a |
C |
A |
1: 88,170,142 (GRCm39) |
A685D |
possibly damaging |
Het |
Myh3 |
A |
G |
11: 66,978,103 (GRCm39) |
N392D |
possibly damaging |
Het |
Naalad2 |
T |
C |
9: 18,262,328 (GRCm39) |
|
probably benign |
Het |
Npc1 |
T |
A |
18: 12,328,106 (GRCm39) |
M1068L |
probably benign |
Het |
Nup58 |
T |
A |
14: 60,469,992 (GRCm39) |
|
probably benign |
Het |
Or10c1 |
T |
C |
17: 37,522,595 (GRCm39) |
T50A |
probably benign |
Het |
Or4k40 |
A |
T |
2: 111,250,438 (GRCm39) |
I286N |
probably damaging |
Het |
Or8b1 |
A |
T |
9: 38,399,939 (GRCm39) |
I205F |
probably benign |
Het |
Or8s16 |
T |
C |
15: 98,211,068 (GRCm39) |
Y121C |
probably damaging |
Het |
Parp2 |
T |
G |
14: 51,056,732 (GRCm39) |
|
probably null |
Het |
Ppp4r4 |
T |
C |
12: 103,564,504 (GRCm39) |
V9A |
probably damaging |
Het |
Ptprc |
T |
A |
1: 138,000,050 (GRCm39) |
D856V |
probably damaging |
Het |
Ptpru |
T |
A |
4: 131,535,580 (GRCm39) |
T466S |
probably benign |
Het |
Rhob |
A |
G |
12: 8,549,325 (GRCm39) |
V103A |
possibly damaging |
Het |
Sec23ip |
A |
C |
7: 128,378,510 (GRCm39) |
S775R |
probably benign |
Het |
Slit2 |
T |
G |
5: 48,395,725 (GRCm39) |
D709E |
probably damaging |
Het |
Smok2b |
C |
G |
17: 13,454,390 (GRCm39) |
I183M |
probably damaging |
Het |
Smtnl1 |
T |
A |
2: 84,648,780 (GRCm39) |
D158V |
probably damaging |
Het |
Syne2 |
T |
C |
12: 75,993,489 (GRCm39) |
I2087T |
probably damaging |
Het |
Tada1 |
G |
A |
1: 166,214,319 (GRCm39) |
R106H |
possibly damaging |
Het |
Tecta |
T |
A |
9: 42,243,778 (GRCm39) |
I2025F |
probably damaging |
Het |
Themis |
T |
C |
10: 28,658,131 (GRCm39) |
V386A |
probably damaging |
Het |
Ubr5 |
G |
A |
15: 38,015,168 (GRCm39) |
|
probably benign |
Het |
Vcl |
T |
A |
14: 21,033,446 (GRCm39) |
I134N |
probably damaging |
Het |
Vegfa |
G |
A |
17: 46,336,418 (GRCm39) |
T56I |
possibly damaging |
Het |
Vmn2r108 |
T |
A |
17: 20,692,623 (GRCm39) |
K78* |
probably null |
Het |
Vmn2r82 |
A |
T |
10: 79,215,201 (GRCm39) |
T395S |
probably benign |
Het |
Wbp2nl |
T |
C |
15: 82,198,407 (GRCm39) |
S315P |
probably benign |
Het |
Zfp566 |
T |
C |
7: 29,777,344 (GRCm39) |
Y279C |
probably damaging |
Het |
Zmym2 |
T |
C |
14: 57,180,784 (GRCm39) |
Y899H |
probably damaging |
Het |
|
Other mutations in Galm |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01011:Galm
|
APN |
17 |
80,490,709 (GRCm39) |
missense |
probably benign |
0.03 |
IGL02057:Galm
|
APN |
17 |
80,488,996 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02212:Galm
|
APN |
17 |
80,457,546 (GRCm39) |
missense |
probably benign |
0.09 |
IGL02239:Galm
|
APN |
17 |
80,452,467 (GRCm39) |
missense |
probably damaging |
1.00 |
R1511:Galm
|
UTSW |
17 |
80,490,696 (GRCm39) |
missense |
probably damaging |
1.00 |
R2129:Galm
|
UTSW |
17 |
80,490,647 (GRCm39) |
missense |
probably benign |
|
R2298:Galm
|
UTSW |
17 |
80,489,126 (GRCm39) |
nonsense |
probably null |
|
R3724:Galm
|
UTSW |
17 |
80,490,709 (GRCm39) |
missense |
probably benign |
0.03 |
R5307:Galm
|
UTSW |
17 |
80,452,417 (GRCm39) |
missense |
probably damaging |
1.00 |
R5307:Galm
|
UTSW |
17 |
80,452,416 (GRCm39) |
nonsense |
probably null |
|
R5602:Galm
|
UTSW |
17 |
80,457,568 (GRCm39) |
nonsense |
probably null |
|
R5778:Galm
|
UTSW |
17 |
80,435,146 (GRCm39) |
start codon destroyed |
probably null |
1.00 |
R5873:Galm
|
UTSW |
17 |
80,445,532 (GRCm39) |
missense |
probably benign |
0.19 |
R6801:Galm
|
UTSW |
17 |
80,489,053 (GRCm39) |
missense |
probably benign |
0.01 |
R7454:Galm
|
UTSW |
17 |
80,445,550 (GRCm39) |
missense |
possibly damaging |
0.76 |
R8304:Galm
|
UTSW |
17 |
80,490,766 (GRCm39) |
missense |
probably damaging |
0.98 |
R8812:Galm
|
UTSW |
17 |
80,435,215 (GRCm39) |
missense |
probably damaging |
1.00 |
R8856:Galm
|
UTSW |
17 |
80,490,661 (GRCm39) |
missense |
possibly damaging |
0.95 |
R9474:Galm
|
UTSW |
17 |
80,457,561 (GRCm39) |
missense |
possibly damaging |
0.76 |
R9562:Galm
|
UTSW |
17 |
80,490,859 (GRCm39) |
nonsense |
probably null |
|
Z1176:Galm
|
UTSW |
17 |
80,490,662 (GRCm39) |
missense |
possibly damaging |
0.74 |
|