Other mutations in this stock |
Total: 56 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Aass |
T |
C |
6: 23,113,432 (GRCm39) |
N296S |
probably benign |
Het |
Abca13 |
A |
T |
11: 9,244,632 (GRCm39) |
N2165I |
possibly damaging |
Het |
Anpep |
T |
A |
7: 79,491,109 (GRCm39) |
|
probably null |
Het |
Bcl2a1b |
A |
C |
9: 89,089,647 (GRCm39) |
I145L |
probably benign |
Het |
Ccar2 |
G |
A |
14: 70,377,925 (GRCm39) |
L687F |
probably damaging |
Het |
Cd69 |
A |
G |
6: 129,246,537 (GRCm39) |
|
probably null |
Het |
Chchd10 |
A |
C |
10: 75,772,158 (GRCm39) |
Q43P |
probably damaging |
Het |
Ddx55 |
A |
G |
5: 124,704,988 (GRCm39) |
E415G |
probably damaging |
Het |
Defa41 |
A |
G |
8: 21,692,471 (GRCm39) |
|
probably null |
Het |
Dhx40 |
A |
T |
11: 86,676,599 (GRCm39) |
C172S |
possibly damaging |
Het |
Epha1 |
G |
A |
6: 42,341,625 (GRCm39) |
T475I |
probably benign |
Het |
Eri1 |
T |
C |
8: 35,949,687 (GRCm39) |
T91A |
probably damaging |
Het |
Fscn1 |
C |
T |
5: 142,955,783 (GRCm39) |
A158V |
probably benign |
Het |
Gm11437 |
C |
T |
11: 84,055,386 (GRCm39) |
G77R |
probably null |
Het |
Gpat2 |
G |
C |
2: 127,273,838 (GRCm39) |
G294R |
possibly damaging |
Het |
Haus4 |
C |
A |
14: 54,781,268 (GRCm39) |
E269D |
possibly damaging |
Het |
Hyou1 |
T |
C |
9: 44,300,619 (GRCm39) |
M896T |
probably benign |
Het |
Itpr2 |
T |
A |
6: 146,091,978 (GRCm39) |
M2174L |
possibly damaging |
Het |
Kars1 |
T |
C |
8: 112,720,299 (GRCm39) |
|
probably benign |
Het |
Kif1a |
T |
C |
1: 92,949,035 (GRCm39) |
M1488V |
probably benign |
Het |
Lrp2 |
T |
C |
2: 69,270,267 (GRCm39) |
T4106A |
possibly damaging |
Het |
Lrrc20 |
G |
A |
10: 61,318,225 (GRCm39) |
V16I |
possibly damaging |
Het |
Mecr |
T |
A |
4: 131,582,004 (GRCm39) |
V162E |
probably damaging |
Het |
Ms4a4a |
C |
A |
19: 11,363,778 (GRCm39) |
A102E |
probably damaging |
Het |
Mycn |
T |
C |
12: 12,990,051 (GRCm39) |
D115G |
probably damaging |
Het |
Ninj2 |
A |
T |
6: 120,175,750 (GRCm39) |
T138S |
possibly damaging |
Het |
Oasl2 |
G |
A |
5: 115,044,836 (GRCm39) |
V121I |
probably benign |
Het |
Or10s1 |
T |
C |
9: 39,986,239 (GRCm39) |
L216P |
probably damaging |
Het |
Or2r11 |
A |
T |
6: 42,437,309 (GRCm39) |
S215T |
probably benign |
Het |
Or7g19 |
T |
C |
9: 18,856,127 (GRCm39) |
F61S |
probably damaging |
Het |
Pcdha11 |
A |
C |
18: 37,144,235 (GRCm39) |
I109L |
probably benign |
Het |
Pira1 |
T |
A |
7: 3,739,498 (GRCm39) |
K457* |
probably null |
Het |
Pon1 |
A |
G |
6: 5,185,314 (GRCm39) |
L62P |
probably damaging |
Het |
Rp1l1 |
A |
T |
14: 64,269,126 (GRCm39) |
K1571* |
probably null |
Het |
Sec24d |
G |
T |
3: 123,087,412 (GRCm39) |
G193C |
probably damaging |
Het |
Sema3b |
A |
T |
9: 107,476,025 (GRCm39) |
M732K |
probably benign |
Het |
Serpinb8 |
T |
C |
1: 107,525,201 (GRCm39) |
M1T |
probably null |
Het |
Sgip1 |
T |
A |
4: 102,819,676 (GRCm39) |
V594E |
probably damaging |
Het |
Slc3a2 |
T |
C |
19: 8,685,410 (GRCm39) |
S197G |
probably damaging |
Het |
Slc44a5 |
T |
C |
3: 153,964,660 (GRCm39) |
V520A |
possibly damaging |
Het |
Surf6 |
G |
T |
2: 26,792,761 (GRCm39) |
D13E |
possibly damaging |
Het |
Tmem94 |
G |
A |
11: 115,689,112 (GRCm39) |
R1341H |
probably damaging |
Het |
Tns2 |
G |
A |
15: 102,018,994 (GRCm39) |
R395Q |
probably benign |
Het |
Traf7 |
A |
G |
17: 24,728,813 (GRCm39) |
V591A |
possibly damaging |
Het |
Trim72 |
T |
C |
7: 127,609,220 (GRCm39) |
S341P |
probably damaging |
Het |
Trps1 |
A |
G |
15: 50,694,351 (GRCm39) |
V398A |
probably damaging |
Het |
Ube2m |
C |
A |
7: 12,771,617 (GRCm39) |
E14* |
probably null |
Het |
Unc119 |
T |
A |
11: 78,238,046 (GRCm39) |
Y10N |
probably damaging |
Het |
Ush2a |
T |
C |
1: 188,642,995 (GRCm39) |
L4119P |
possibly damaging |
Het |
Vcp |
A |
T |
4: 42,993,826 (GRCm39) |
I102N |
probably damaging |
Het |
Vmn2r4 |
A |
G |
3: 64,296,731 (GRCm39) |
S685P |
probably damaging |
Het |
Vmn2r58 |
T |
C |
7: 41,486,535 (GRCm39) |
M787V |
possibly damaging |
Het |
Vmn2r72 |
T |
C |
7: 85,398,892 (GRCm39) |
H487R |
probably benign |
Het |
Xcr1 |
A |
G |
9: 123,685,309 (GRCm39) |
I151T |
probably benign |
Het |
Zfp658 |
T |
C |
7: 43,216,701 (GRCm39) |
S24P |
possibly damaging |
Het |
Zfyve16 |
T |
C |
13: 92,650,326 (GRCm39) |
D886G |
probably benign |
Het |
|
Other mutations in Golm1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01116:Golm1
|
APN |
13 |
59,797,470 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01327:Golm1
|
APN |
13 |
59,792,958 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL02348:Golm1
|
APN |
13 |
59,786,191 (GRCm39) |
missense |
probably benign |
0.00 |
R0047:Golm1
|
UTSW |
13 |
59,792,914 (GRCm39) |
missense |
probably benign |
0.03 |
R0047:Golm1
|
UTSW |
13 |
59,792,914 (GRCm39) |
missense |
probably benign |
0.03 |
R0458:Golm1
|
UTSW |
13 |
59,812,178 (GRCm39) |
missense |
probably damaging |
0.98 |
R0989:Golm1
|
UTSW |
13 |
59,787,997 (GRCm39) |
missense |
probably benign |
0.01 |
R1301:Golm1
|
UTSW |
13 |
59,786,187 (GRCm39) |
missense |
probably damaging |
0.99 |
R1804:Golm1
|
UTSW |
13 |
59,790,203 (GRCm39) |
critical splice acceptor site |
probably null |
|
R1905:Golm1
|
UTSW |
13 |
59,790,065 (GRCm39) |
missense |
probably benign |
0.04 |
R1940:Golm1
|
UTSW |
13 |
59,790,051 (GRCm39) |
splice site |
probably benign |
|
R2086:Golm1
|
UTSW |
13 |
59,792,999 (GRCm39) |
nonsense |
probably null |
|
R2513:Golm1
|
UTSW |
13 |
59,790,072 (GRCm39) |
missense |
probably benign |
0.01 |
R2887:Golm1
|
UTSW |
13 |
59,788,044 (GRCm39) |
missense |
probably benign |
0.00 |
R3903:Golm1
|
UTSW |
13 |
59,786,154 (GRCm39) |
missense |
probably damaging |
1.00 |
R4154:Golm1
|
UTSW |
13 |
59,790,167 (GRCm39) |
missense |
probably benign |
0.01 |
R5580:Golm1
|
UTSW |
13 |
59,790,179 (GRCm39) |
missense |
probably benign |
0.03 |
R6193:Golm1
|
UTSW |
13 |
59,792,972 (GRCm39) |
missense |
probably benign |
0.00 |
R6418:Golm1
|
UTSW |
13 |
59,813,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R6604:Golm1
|
UTSW |
13 |
59,786,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R6967:Golm1
|
UTSW |
13 |
59,797,390 (GRCm39) |
small deletion |
probably benign |
|
R6968:Golm1
|
UTSW |
13 |
59,797,390 (GRCm39) |
small deletion |
probably benign |
|
R6991:Golm1
|
UTSW |
13 |
59,797,390 (GRCm39) |
small deletion |
probably benign |
|
R6992:Golm1
|
UTSW |
13 |
59,797,390 (GRCm39) |
small deletion |
probably benign |
|
R6993:Golm1
|
UTSW |
13 |
59,797,390 (GRCm39) |
small deletion |
probably benign |
|
R6996:Golm1
|
UTSW |
13 |
59,790,058 (GRCm39) |
missense |
probably benign |
0.00 |
R7576:Golm1
|
UTSW |
13 |
59,792,920 (GRCm39) |
missense |
probably benign |
0.00 |
R7692:Golm1
|
UTSW |
13 |
59,788,071 (GRCm39) |
missense |
probably benign |
0.08 |
R7863:Golm1
|
UTSW |
13 |
59,797,383 (GRCm39) |
missense |
probably damaging |
1.00 |
R7948:Golm1
|
UTSW |
13 |
59,812,011 (GRCm39) |
critical splice donor site |
probably null |
|
R9519:Golm1
|
UTSW |
13 |
59,792,914 (GRCm39) |
missense |
probably benign |
|
R9703:Golm1
|
UTSW |
13 |
59,797,433 (GRCm39) |
missense |
probably benign |
0.39 |
X0026:Golm1
|
UTSW |
13 |
59,786,127 (GRCm39) |
missense |
probably damaging |
1.00 |
|