Other mutations in this stock |
Total: 65 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adam25 |
G |
C |
8: 41,206,746 (GRCm39) |
R4T |
probably benign |
Het |
Alk |
T |
A |
17: 72,256,820 (GRCm39) |
I680F |
probably benign |
Het |
Best3 |
A |
G |
10: 116,824,572 (GRCm39) |
T13A |
possibly damaging |
Het |
Ccdc7b |
A |
G |
8: 129,872,082 (GRCm39) |
D59G |
|
Het |
Cd300ld2 |
CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG |
CGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGGCAGAACTGTGGATGTCAGAACTGTGGATGTCAGAACTGTGGATGGCACAACTGTGCATGGCAGAACTGTGGATGGCACAACTGTGGATGGCAGAACTGTGG |
11: 114,903,257 (GRCm39) |
|
probably benign |
Het |
Cic |
G |
A |
7: 24,970,631 (GRCm39) |
V121M |
probably damaging |
Het |
Clasp1 |
C |
G |
1: 118,506,705 (GRCm39) |
P1280R |
probably damaging |
Het |
Col6a5 |
A |
T |
9: 105,741,472 (GRCm39) |
N2482K |
possibly damaging |
Het |
Crebbp |
A |
G |
16: 3,902,891 (GRCm39) |
M2116T |
probably benign |
Het |
Ddn |
T |
C |
15: 98,704,794 (GRCm39) |
E166G |
possibly damaging |
Het |
Dennd6a |
C |
T |
14: 26,327,086 (GRCm39) |
T249I |
probably benign |
Het |
Diaph1 |
A |
T |
18: 37,987,590 (GRCm39) |
D1055E |
possibly damaging |
Het |
Dnajc13 |
C |
A |
9: 104,057,360 (GRCm39) |
G1547* |
probably null |
Het |
Dvl1 |
C |
T |
4: 155,942,611 (GRCm39) |
R626C |
possibly damaging |
Het |
Fer1l6 |
A |
C |
15: 58,414,012 (GRCm39) |
K13Q |
possibly damaging |
Het |
Fry |
G |
A |
5: 150,309,472 (GRCm39) |
E639K |
|
Het |
Gm6408 |
G |
T |
5: 146,420,602 (GRCm39) |
V161L |
probably benign |
Het |
Gpatch8 |
A |
T |
11: 102,372,010 (GRCm39) |
N509K |
unknown |
Het |
Hycc2 |
G |
T |
1: 58,595,713 (GRCm39) |
P55Q |
probably damaging |
Het |
Ints13 |
T |
C |
6: 146,457,631 (GRCm39) |
T416A |
probably benign |
Het |
Iqcf6 |
A |
T |
9: 106,504,650 (GRCm39) |
M105L |
probably damaging |
Het |
Magi3 |
C |
A |
3: 103,922,334 (GRCm39) |
R1461L |
probably benign |
Het |
Map3k8 |
A |
T |
18: 4,333,889 (GRCm39) |
L401Q |
|
Het |
Miga2 |
G |
T |
2: 30,273,990 (GRCm39) |
R542L |
probably damaging |
Het |
Mphosph9 |
A |
T |
5: 124,454,209 (GRCm39) |
V96E |
possibly damaging |
Het |
Nek5 |
T |
C |
8: 22,613,595 (GRCm39) |
S28G |
probably benign |
Het |
Niban1 |
A |
G |
1: 151,575,929 (GRCm39) |
E351G |
probably damaging |
Het |
Notch4 |
A |
G |
17: 34,803,962 (GRCm39) |
|
probably benign |
Het |
Npc1 |
A |
G |
18: 12,323,987 (GRCm39) |
L1275P |
probably damaging |
Het |
Nphp4 |
C |
T |
4: 152,590,863 (GRCm39) |
R287C |
probably damaging |
Het |
Or10ak11 |
T |
C |
4: 118,686,821 (GRCm39) |
D271G |
probably damaging |
Het |
Or13a20 |
G |
C |
7: 140,232,326 (GRCm39) |
A145P |
possibly damaging |
Het |
Or1j13 |
G |
A |
2: 36,369,483 (GRCm39) |
R220* |
probably null |
Het |
Or1p1c |
C |
T |
11: 74,160,443 (GRCm39) |
T76I |
probably damaging |
Het |
Parn |
A |
T |
16: 13,446,270 (GRCm39) |
L343* |
probably null |
Het |
Pax5 |
T |
A |
4: 44,691,865 (GRCm39) |
D127V |
probably benign |
Het |
Peak1 |
C |
A |
9: 56,114,427 (GRCm39) |
D1505Y |
probably damaging |
Het |
Perm1 |
C |
T |
4: 156,302,068 (GRCm39) |
T204I |
probably benign |
Het |
Pid1 |
A |
T |
1: 84,093,694 (GRCm39) |
S65T |
unknown |
Het |
Pkn2 |
A |
G |
3: 142,526,401 (GRCm39) |
V392A |
probably benign |
Het |
Plekhh2 |
A |
G |
17: 84,878,479 (GRCm39) |
D578G |
probably benign |
Het |
Ppp4r4 |
T |
A |
12: 103,562,747 (GRCm39) |
L572Q |
probably damaging |
Het |
Pum3 |
G |
A |
19: 27,398,713 (GRCm39) |
T279M |
probably damaging |
Het |
Rasa2 |
A |
G |
9: 96,458,402 (GRCm39) |
V266A |
possibly damaging |
Het |
Sirpb1c |
C |
T |
3: 15,886,584 (GRCm39) |
W264* |
probably null |
Het |
Slk |
T |
A |
19: 47,607,632 (GRCm39) |
H289Q |
|
Het |
Spef2 |
T |
C |
15: 9,668,913 (GRCm39) |
S758G |
probably benign |
Het |
Spon2 |
C |
T |
5: 33,371,841 (GRCm39) |
A322T |
probably benign |
Het |
Spred2 |
T |
C |
11: 19,951,064 (GRCm39) |
L87P |
probably benign |
Het |
Stk10 |
A |
G |
11: 32,539,427 (GRCm39) |
D269G |
|
Het |
Tex48 |
T |
A |
4: 63,530,772 (GRCm39) |
|
probably benign |
Het |
Themis2 |
T |
A |
4: 132,513,509 (GRCm39) |
H239L |
probably damaging |
Het |
Tle4 |
T |
A |
19: 14,493,737 (GRCm39) |
R199* |
probably null |
Het |
Tlr11 |
C |
T |
14: 50,600,182 (GRCm39) |
H723Y |
possibly damaging |
Het |
Trdj2 |
T |
A |
14: 54,374,237 (GRCm39) |
S1T |
|
Het |
Vdac1 |
T |
G |
11: 52,267,230 (GRCm39) |
S44A |
|
Het |
Vill |
C |
T |
9: 118,897,514 (GRCm39) |
T647I |
probably damaging |
Het |
Vmn1r61 |
A |
G |
7: 5,613,817 (GRCm39) |
C166R |
probably damaging |
Het |
Vmn2r114 |
T |
A |
17: 23,528,986 (GRCm39) |
N372I |
probably damaging |
Het |
Vmn2r120 |
T |
A |
17: 57,816,217 (GRCm39) |
M713L |
probably benign |
Het |
Vmn2r61 |
T |
C |
7: 41,950,010 (GRCm39) |
V810A |
probably damaging |
Het |
Vmn2r65 |
A |
T |
7: 84,590,212 (GRCm39) |
L568Q |
probably damaging |
Het |
Wdr7 |
T |
C |
18: 63,872,293 (GRCm39) |
V409A |
probably damaging |
Het |
Ylpm1 |
C |
A |
12: 85,061,672 (GRCm39) |
N524K |
unknown |
Het |
Zfp958 |
A |
C |
8: 4,678,434 (GRCm39) |
H153P |
probably damaging |
Het |
|
Other mutations in Slc35g3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00936:Slc35g3
|
APN |
11 |
69,651,317 (GRCm39) |
splice site |
probably null |
|
IGL03064:Slc35g3
|
APN |
11 |
69,651,895 (GRCm39) |
missense |
possibly damaging |
0.62 |
R1615:Slc35g3
|
UTSW |
11 |
69,651,368 (GRCm39) |
missense |
probably damaging |
0.99 |
R2086:Slc35g3
|
UTSW |
11 |
69,651,772 (GRCm39) |
missense |
probably damaging |
1.00 |
R3796:Slc35g3
|
UTSW |
11 |
69,651,743 (GRCm39) |
missense |
probably benign |
0.02 |
R3797:Slc35g3
|
UTSW |
11 |
69,651,743 (GRCm39) |
missense |
probably benign |
0.02 |
R3798:Slc35g3
|
UTSW |
11 |
69,651,743 (GRCm39) |
missense |
probably benign |
0.02 |
R3799:Slc35g3
|
UTSW |
11 |
69,651,743 (GRCm39) |
missense |
probably benign |
0.02 |
R5014:Slc35g3
|
UTSW |
11 |
69,651,866 (GRCm39) |
nonsense |
probably null |
|
R5727:Slc35g3
|
UTSW |
11 |
69,651,280 (GRCm39) |
missense |
probably benign |
0.00 |
R5774:Slc35g3
|
UTSW |
11 |
69,651,124 (GRCm39) |
missense |
probably damaging |
1.00 |
R5935:Slc35g3
|
UTSW |
11 |
69,652,509 (GRCm39) |
start codon destroyed |
probably null |
|
R6634:Slc35g3
|
UTSW |
11 |
69,651,109 (GRCm39) |
missense |
probably damaging |
1.00 |
R7043:Slc35g3
|
UTSW |
11 |
69,652,476 (GRCm39) |
missense |
probably benign |
0.03 |
R7956:Slc35g3
|
UTSW |
11 |
69,651,623 (GRCm39) |
missense |
probably damaging |
1.00 |
R8547:Slc35g3
|
UTSW |
11 |
69,652,446 (GRCm39) |
missense |
probably benign |
|
X0021:Slc35g3
|
UTSW |
11 |
69,651,563 (GRCm39) |
missense |
probably damaging |
1.00 |
|