Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1110002E22Rik |
T |
A |
3: 137,773,028 (GRCm39) |
L739Q |
probably damaging |
Het |
4933436I01Rik |
A |
T |
X: 66,963,655 (GRCm39) |
Y401* |
probably null |
Het |
Abcg3 |
A |
G |
5: 105,111,504 (GRCm39) |
V321A |
probably benign |
Het |
Acad10 |
C |
A |
5: 121,764,248 (GRCm39) |
V894L |
possibly damaging |
Het |
Adam9 |
A |
G |
8: 25,482,240 (GRCm39) |
I255T |
probably damaging |
Het |
Ago3 |
T |
C |
4: 126,240,544 (GRCm39) |
Y785C |
probably damaging |
Het |
Aif1 |
G |
A |
17: 35,391,127 (GRCm39) |
P44L |
probably benign |
Het |
Akap4 |
A |
G |
X: 6,943,595 (GRCm39) |
S633G |
probably benign |
Het |
Alox15 |
T |
A |
11: 70,240,799 (GRCm39) |
T194S |
probably benign |
Het |
Amh |
T |
C |
10: 80,642,250 (GRCm39) |
S207P |
probably benign |
Het |
Apc |
T |
A |
18: 34,433,057 (GRCm39) |
C415S |
possibly damaging |
Het |
Atg14 |
G |
A |
14: 47,783,298 (GRCm39) |
R346C |
probably damaging |
Het |
Atp5mf |
A |
T |
5: 145,121,389 (GRCm39) |
L64Q |
probably damaging |
Het |
Barhl2 |
C |
G |
5: 106,605,179 (GRCm39) |
E177Q |
probably benign |
Het |
C1qtnf5 |
T |
C |
9: 44,020,072 (GRCm39) |
V232A |
probably damaging |
Het |
Calr |
T |
C |
8: 85,570,786 (GRCm39) |
I290V |
probably benign |
Het |
Cdh19 |
G |
C |
1: 110,817,889 (GRCm39) |
Q618E |
possibly damaging |
Het |
Celsr2 |
G |
T |
3: 108,321,530 (GRCm39) |
D427E |
probably damaging |
Het |
Cep250 |
T |
C |
2: 155,831,424 (GRCm39) |
S1294P |
probably damaging |
Het |
Chrna7 |
T |
A |
7: 62,749,034 (GRCm39) |
T483S |
probably damaging |
Het |
Clmn |
A |
T |
12: 104,758,121 (GRCm39) |
W132R |
probably damaging |
Het |
Cpsf2 |
G |
A |
12: 101,956,306 (GRCm39) |
D370N |
probably benign |
Het |
Crnn |
T |
C |
3: 93,056,594 (GRCm39) |
V460A |
probably benign |
Het |
Daam1 |
T |
A |
12: 72,035,703 (GRCm39) |
I957N |
probably damaging |
Het |
Defb9 |
T |
C |
8: 22,371,905 (GRCm39) |
K36R |
probably benign |
Het |
Dock10 |
T |
A |
1: 80,488,143 (GRCm39) |
I2007F |
possibly damaging |
Het |
Dpm1 |
A |
T |
2: 168,059,667 (GRCm39) |
V143D |
probably damaging |
Het |
Dync1h1 |
T |
C |
12: 110,592,166 (GRCm39) |
V1110A |
possibly damaging |
Het |
Erlec1 |
T |
G |
11: 30,889,604 (GRCm39) |
K373N |
possibly damaging |
Het |
Fbxo40 |
C |
T |
16: 36,790,303 (GRCm39) |
G269E |
probably benign |
Het |
Fbxw7 |
T |
A |
3: 84,862,242 (GRCm39) |
C70S |
possibly damaging |
Het |
Fhip2a |
T |
C |
19: 57,373,809 (GRCm39) |
F690L |
probably damaging |
Het |
Fnbp1 |
G |
T |
2: 30,943,059 (GRCm39) |
R280S |
probably null |
Het |
Gapvd1 |
G |
A |
2: 34,590,853 (GRCm39) |
R940C |
probably damaging |
Het |
Gfod2 |
T |
C |
8: 106,444,142 (GRCm39) |
K134E |
possibly damaging |
Het |
Gpi1 |
A |
T |
7: 33,920,228 (GRCm39) |
|
probably null |
Het |
Grik2 |
A |
T |
10: 49,008,923 (GRCm39) |
N721K |
possibly damaging |
Het |
Hlx |
G |
T |
1: 184,464,184 (GRCm39) |
A52D |
probably damaging |
Het |
Hpse |
A |
G |
5: 100,840,104 (GRCm39) |
S338P |
probably damaging |
Het |
Hyal2 |
T |
C |
9: 107,449,371 (GRCm39) |
C376R |
probably damaging |
Het |
Inf2 |
A |
G |
12: 112,574,771 (GRCm39) |
T781A |
unknown |
Het |
Iscu |
A |
G |
5: 113,915,079 (GRCm39) |
|
probably benign |
Het |
Kcna4 |
G |
A |
2: 107,126,565 (GRCm39) |
G433D |
possibly damaging |
Het |
Kir3dl2 |
T |
A |
X: 135,357,024 (GRCm39) |
N146I |
probably benign |
Het |
Klrg1 |
T |
A |
6: 122,259,721 (GRCm39) |
Q17L |
possibly damaging |
Het |
Krt82 |
T |
G |
15: 101,453,597 (GRCm39) |
Q263P |
probably benign |
Het |
Mfrp |
T |
C |
9: 44,017,669 (GRCm39) |
C554R |
probably damaging |
Het |
Minar1 |
T |
G |
9: 89,483,256 (GRCm39) |
T714P |
probably damaging |
Het |
Mst1r |
T |
C |
9: 107,791,962 (GRCm39) |
Y833H |
probably damaging |
Het |
Mst1r |
T |
A |
9: 107,793,132 (GRCm39) |
|
probably null |
Het |
Nfix |
G |
A |
8: 85,453,155 (GRCm39) |
R300C |
probably damaging |
Het |
Nipal4 |
T |
C |
11: 46,042,210 (GRCm39) |
N157S |
probably damaging |
Het |
Notch2 |
G |
A |
3: 97,980,071 (GRCm39) |
G195D |
probably damaging |
Het |
Nrcam |
A |
T |
12: 44,610,776 (GRCm39) |
H492L |
probably benign |
Het |
Or10aa1 |
A |
T |
1: 173,870,154 (GRCm39) |
I213F |
probably damaging |
Het |
Or4p21 |
A |
T |
2: 88,276,853 (GRCm39) |
I143N |
probably damaging |
Het |
Papln |
G |
A |
12: 83,828,811 (GRCm39) |
R817H |
probably damaging |
Het |
Pcnx2 |
T |
C |
8: 126,614,110 (GRCm39) |
E447G |
probably benign |
Het |
Pdp2 |
T |
C |
8: 105,320,538 (GRCm39) |
V129A |
probably benign |
Het |
Plch2 |
A |
G |
4: 155,069,410 (GRCm39) |
F1072S |
possibly damaging |
Het |
Prag1 |
T |
A |
8: 36,570,081 (GRCm39) |
D221E |
probably damaging |
Het |
Prkg1 |
T |
C |
19: 31,563,095 (GRCm39) |
D102G |
probably damaging |
Het |
Psme4 |
T |
A |
11: 30,769,011 (GRCm39) |
D662E |
probably benign |
Het |
Ptprn |
T |
C |
1: 75,231,464 (GRCm39) |
|
probably null |
Het |
Ptprz1 |
A |
G |
6: 22,986,310 (GRCm39) |
D370G |
probably damaging |
Het |
Qser1 |
A |
G |
2: 104,590,886 (GRCm39) |
S1637P |
probably damaging |
Het |
Sema6a |
T |
A |
18: 47,403,696 (GRCm39) |
H642L |
probably benign |
Het |
Slc30a5 |
A |
T |
13: 100,950,461 (GRCm39) |
F209I |
probably benign |
Het |
Slc4a3 |
G |
T |
1: 75,528,835 (GRCm39) |
E508* |
probably null |
Het |
Stpg2 |
C |
T |
3: 139,014,944 (GRCm39) |
R370* |
probably null |
Het |
Tas2r113 |
T |
A |
6: 132,870,796 (GRCm39) |
F275I |
probably benign |
Het |
Tmem132d |
T |
G |
5: 128,346,263 (GRCm39) |
K86N |
probably damaging |
Het |
Tpgs2 |
A |
T |
18: 25,273,593 (GRCm39) |
F189L |
probably damaging |
Het |
Trmt6 |
A |
G |
2: 132,652,968 (GRCm39) |
S104P |
probably damaging |
Het |
Trpv3 |
T |
C |
11: 73,174,514 (GRCm39) |
S294P |
probably damaging |
Het |
Ugt2b36 |
A |
G |
5: 87,228,727 (GRCm39) |
|
probably null |
Het |
Vmn1r170 |
A |
T |
7: 23,305,906 (GRCm39) |
M103L |
probably benign |
Het |
Vmn2r107 |
T |
A |
17: 20,575,879 (GRCm39) |
|
probably null |
Het |
Vmn2r5 |
C |
T |
3: 64,411,642 (GRCm39) |
E309K |
probably damaging |
Het |
Vmn2r77 |
T |
C |
7: 86,449,964 (GRCm39) |
V70A |
probably benign |
Het |
|
Other mutations in Gsn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00797:Gsn
|
APN |
2 |
35,174,049 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02119:Gsn
|
APN |
2 |
35,192,507 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02512:Gsn
|
APN |
2 |
35,173,962 (GRCm39) |
nonsense |
probably null |
|
IGL02550:Gsn
|
APN |
2 |
35,172,619 (GRCm39) |
intron |
probably benign |
|
IGL02975:Gsn
|
APN |
2 |
35,194,666 (GRCm39) |
missense |
probably benign |
0.25 |
IGL03061:Gsn
|
APN |
2 |
35,172,471 (GRCm39) |
intron |
probably benign |
|
R0321:Gsn
|
UTSW |
2 |
35,180,408 (GRCm39) |
missense |
probably benign |
0.03 |
R0454:Gsn
|
UTSW |
2 |
35,194,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R1446:Gsn
|
UTSW |
2 |
35,196,598 (GRCm39) |
missense |
probably benign |
0.04 |
R1760:Gsn
|
UTSW |
2 |
35,174,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R2258:Gsn
|
UTSW |
2 |
35,180,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R2260:Gsn
|
UTSW |
2 |
35,180,349 (GRCm39) |
missense |
probably damaging |
1.00 |
R2281:Gsn
|
UTSW |
2 |
35,173,930 (GRCm39) |
missense |
probably benign |
0.01 |
R2495:Gsn
|
UTSW |
2 |
35,193,205 (GRCm39) |
missense |
probably damaging |
1.00 |
R2516:Gsn
|
UTSW |
2 |
35,173,965 (GRCm39) |
missense |
probably benign |
|
R3896:Gsn
|
UTSW |
2 |
35,192,650 (GRCm39) |
missense |
possibly damaging |
0.92 |
R4003:Gsn
|
UTSW |
2 |
35,173,995 (GRCm39) |
missense |
probably benign |
0.38 |
R4006:Gsn
|
UTSW |
2 |
35,197,633 (GRCm39) |
nonsense |
probably null |
|
R4281:Gsn
|
UTSW |
2 |
35,188,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R4291:Gsn
|
UTSW |
2 |
35,180,432 (GRCm39) |
missense |
probably benign |
0.14 |
R4692:Gsn
|
UTSW |
2 |
35,188,883 (GRCm39) |
missense |
probably damaging |
1.00 |
R4850:Gsn
|
UTSW |
2 |
35,173,912 (GRCm39) |
splice site |
probably null |
|
R4895:Gsn
|
UTSW |
2 |
35,192,590 (GRCm39) |
missense |
probably damaging |
1.00 |
R5011:Gsn
|
UTSW |
2 |
35,188,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R5013:Gsn
|
UTSW |
2 |
35,188,933 (GRCm39) |
missense |
probably damaging |
1.00 |
R5290:Gsn
|
UTSW |
2 |
35,186,484 (GRCm39) |
missense |
probably benign |
0.01 |
R6472:Gsn
|
UTSW |
2 |
35,180,463 (GRCm39) |
splice site |
probably null |
|
R6764:Gsn
|
UTSW |
2 |
35,174,056 (GRCm39) |
missense |
probably damaging |
1.00 |
R7018:Gsn
|
UTSW |
2 |
35,183,518 (GRCm39) |
missense |
probably benign |
0.03 |
R7036:Gsn
|
UTSW |
2 |
35,182,611 (GRCm39) |
missense |
probably damaging |
1.00 |
R7097:Gsn
|
UTSW |
2 |
35,185,061 (GRCm39) |
nonsense |
probably null |
|
R7122:Gsn
|
UTSW |
2 |
35,185,061 (GRCm39) |
nonsense |
probably null |
|
R7183:Gsn
|
UTSW |
2 |
35,184,960 (GRCm39) |
missense |
probably benign |
0.00 |
R7203:Gsn
|
UTSW |
2 |
35,188,807 (GRCm39) |
missense |
probably benign |
0.00 |
R7456:Gsn
|
UTSW |
2 |
35,172,718 (GRCm39) |
missense |
possibly damaging |
0.84 |
R7488:Gsn
|
UTSW |
2 |
35,186,433 (GRCm39) |
missense |
possibly damaging |
0.65 |
R7880:Gsn
|
UTSW |
2 |
35,173,939 (GRCm39) |
missense |
probably damaging |
1.00 |
R8088:Gsn
|
UTSW |
2 |
35,182,659 (GRCm39) |
missense |
possibly damaging |
0.77 |
R9472:Gsn
|
UTSW |
2 |
35,182,741 (GRCm39) |
missense |
probably damaging |
1.00 |
R9479:Gsn
|
UTSW |
2 |
35,186,227 (GRCm39) |
critical splice donor site |
probably null |
|
R9568:Gsn
|
UTSW |
2 |
35,174,003 (GRCm39) |
missense |
probably benign |
0.02 |
R9777:Gsn
|
UTSW |
2 |
35,194,600 (GRCm39) |
missense |
probably damaging |
1.00 |
|