Other mutations in this stock |
Total: 85 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc4 |
T |
C |
14: 118,790,737 (GRCm39) |
M757V |
probably benign |
Het |
Abitram |
T |
A |
4: 56,805,916 (GRCm39) |
I138N |
probably damaging |
Het |
Acan |
T |
G |
7: 78,750,970 (GRCm39) |
S1914A |
probably benign |
Het |
Axin2 |
T |
A |
11: 108,833,904 (GRCm39) |
V617D |
probably damaging |
Het |
Bhlhe22 |
A |
G |
3: 18,109,975 (GRCm39) |
S342G |
probably benign |
Het |
Cald1 |
AAGAGAGAGAGAGAG |
AAGAGAGAGAGAG |
6: 34,723,108 (GRCm39) |
|
probably null |
Het |
Ccdc34 |
A |
G |
2: 109,862,731 (GRCm39) |
K179E |
possibly damaging |
Het |
Clasp1 |
A |
G |
1: 118,432,629 (GRCm39) |
T208A |
probably damaging |
Het |
Crabp1 |
C |
T |
9: 54,675,752 (GRCm39) |
R112* |
probably null |
Het |
Cstdc1 |
T |
C |
2: 148,624,148 (GRCm39) |
F41L |
probably damaging |
Het |
D130040H23Rik |
A |
G |
8: 69,755,525 (GRCm39) |
N310S |
probably benign |
Het |
Dalrd3 |
T |
C |
9: 108,448,284 (GRCm39) |
I278T |
probably benign |
Het |
Dbp |
C |
A |
7: 45,357,700 (GRCm39) |
D89E |
probably benign |
Het |
Dennd2c |
A |
G |
3: 103,039,005 (GRCm39) |
D51G |
possibly damaging |
Het |
Dido1 |
A |
T |
2: 180,330,974 (GRCm39) |
L158* |
probably null |
Het |
Disp1 |
G |
T |
1: 182,869,767 (GRCm39) |
F884L |
probably damaging |
Het |
Dmrtb1 |
T |
C |
4: 107,540,782 (GRCm39) |
D193G |
probably damaging |
Het |
Dnah8 |
A |
G |
17: 30,950,133 (GRCm39) |
D1984G |
probably damaging |
Het |
Dpf2 |
T |
C |
19: 5,952,781 (GRCm39) |
Y218C |
possibly damaging |
Het |
Dsg4 |
C |
T |
18: 20,599,693 (GRCm39) |
Q770* |
probably null |
Het |
Efemp1 |
A |
T |
11: 28,864,696 (GRCm39) |
Y250F |
possibly damaging |
Het |
Erbin |
A |
T |
13: 103,966,703 (GRCm39) |
I1249N |
probably benign |
Het |
F5 |
A |
G |
1: 164,037,044 (GRCm39) |
K1928E |
probably benign |
Het |
Fhip1b |
A |
G |
7: 105,038,143 (GRCm39) |
V260A |
probably damaging |
Het |
Gdf11 |
T |
A |
10: 128,727,314 (GRCm39) |
I81F |
probably damaging |
Het |
Gm10518 |
T |
A |
1: 179,631,483 (GRCm39) |
|
probably benign |
Het |
Grb10 |
G |
C |
11: 11,920,576 (GRCm39) |
S14* |
probably null |
Het |
Greb1l |
A |
T |
18: 10,515,221 (GRCm39) |
Y562F |
possibly damaging |
Het |
Gtf2ird1 |
T |
C |
5: 134,392,788 (GRCm39) |
E789G |
probably damaging |
Het |
Hook3 |
T |
C |
8: 26,528,126 (GRCm39) |
E588G |
probably damaging |
Het |
Hpx |
A |
G |
7: 105,244,311 (GRCm39) |
S266P |
probably damaging |
Het |
Hs6st3 |
A |
G |
14: 120,106,801 (GRCm39) |
D403G |
probably damaging |
Het |
Igf2bp1 |
A |
G |
11: 95,864,996 (GRCm39) |
V151A |
possibly damaging |
Het |
Itga11 |
C |
T |
9: 62,670,093 (GRCm39) |
T739I |
probably damaging |
Het |
Kalrn |
T |
C |
16: 34,010,106 (GRCm39) |
I702V |
probably damaging |
Het |
Kif2b |
C |
T |
11: 91,468,172 (GRCm39) |
S37N |
probably damaging |
Het |
Kng2 |
T |
A |
16: 22,819,325 (GRCm39) |
D237V |
probably benign |
Het |
Krtap27-1 |
C |
A |
16: 88,468,173 (GRCm39) |
V124L |
possibly damaging |
Het |
Lig4 |
A |
T |
8: 10,022,436 (GRCm39) |
L448Q |
probably damaging |
Het |
Macf1 |
C |
T |
4: 123,265,711 (GRCm39) |
A4821T |
probably damaging |
Het |
Msh5 |
T |
A |
17: 35,251,768 (GRCm39) |
I431F |
possibly damaging |
Het |
Ndufa10 |
A |
G |
1: 92,367,614 (GRCm39) |
Y339H |
probably damaging |
Het |
Nin |
T |
A |
12: 70,076,782 (GRCm39) |
Q1091L |
probably damaging |
Het |
Nom1 |
A |
C |
5: 29,651,849 (GRCm39) |
D729A |
probably damaging |
Het |
Or52e8 |
C |
A |
7: 104,624,451 (GRCm39) |
G247V |
probably benign |
Het |
P2ry14 |
A |
T |
3: 59,022,866 (GRCm39) |
V207E |
probably damaging |
Het |
Pdss2 |
A |
T |
10: 43,269,871 (GRCm39) |
N238I |
possibly damaging |
Het |
Pkn1 |
A |
G |
8: 84,398,007 (GRCm39) |
V795A |
probably damaging |
Het |
Pla2g6 |
A |
C |
15: 79,170,964 (GRCm39) |
L804R |
probably damaging |
Het |
Poglut1 |
A |
T |
16: 38,358,267 (GRCm39) |
|
probably null |
Het |
Prkcz |
A |
T |
4: 155,374,167 (GRCm39) |
V83D |
probably damaging |
Het |
Prss50 |
T |
C |
9: 110,690,328 (GRCm39) |
F157S |
probably benign |
Het |
Psors1c2 |
A |
G |
17: 35,845,099 (GRCm39) |
|
probably benign |
Het |
Ptch1 |
T |
G |
13: 63,672,773 (GRCm39) |
E944A |
probably benign |
Het |
Ptpro |
T |
A |
6: 137,420,592 (GRCm39) |
V1007D |
probably damaging |
Het |
Pwwp4a |
G |
T |
X: 72,171,261 (GRCm39) |
G218C |
probably damaging |
Het |
Rab7 |
G |
A |
6: 87,981,161 (GRCm39) |
L174F |
probably damaging |
Het |
Rapgef4 |
A |
G |
2: 72,073,083 (GRCm39) |
T790A |
probably benign |
Het |
Rb1cc1 |
G |
T |
1: 6,315,533 (GRCm39) |
V503L |
probably damaging |
Het |
Sbf1 |
T |
A |
15: 89,186,933 (GRCm39) |
E815V |
probably damaging |
Het |
Slc39a5 |
A |
T |
10: 128,234,279 (GRCm39) |
L208Q |
probably damaging |
Het |
Slc39a5 |
G |
T |
10: 128,234,280 (GRCm39) |
L208M |
probably damaging |
Het |
Slc3a1 |
T |
G |
17: 85,340,273 (GRCm39) |
Y232D |
probably damaging |
Het |
Slc8a1 |
T |
A |
17: 81,956,541 (GRCm39) |
S166C |
probably damaging |
Het |
Stard9 |
T |
A |
2: 120,532,879 (GRCm39) |
D3045E |
probably benign |
Het |
Stk4 |
C |
A |
2: 163,938,751 (GRCm39) |
D206E |
probably damaging |
Het |
Syn3 |
T |
C |
10: 86,302,846 (GRCm39) |
D103G |
probably damaging |
Het |
Tbc1d30 |
T |
A |
10: 121,115,051 (GRCm39) |
Y369F |
probably benign |
Het |
Tenm2 |
G |
T |
11: 35,938,091 (GRCm39) |
Y1527* |
probably null |
Het |
Tfg |
T |
C |
16: 56,525,988 (GRCm39) |
K85R |
possibly damaging |
Het |
Timp3 |
T |
C |
10: 86,136,749 (GRCm39) |
L11P |
probably damaging |
Het |
Tmem144 |
A |
T |
3: 79,735,018 (GRCm39) |
|
probably null |
Het |
Tmtc4 |
T |
C |
14: 123,158,677 (GRCm39) |
N682S |
probably benign |
Het |
Tnks2 |
C |
T |
19: 36,843,466 (GRCm39) |
L464F |
probably damaging |
Het |
Trank1 |
T |
C |
9: 111,221,107 (GRCm39) |
F2615L |
probably benign |
Het |
Trio |
T |
C |
15: 27,744,223 (GRCm39) |
K2570E |
probably damaging |
Het |
Trio |
T |
A |
15: 27,774,013 (GRCm39) |
D673V |
probably damaging |
Het |
Ublcp1 |
A |
T |
11: 44,356,458 (GRCm39) |
C87S |
probably benign |
Het |
Unc13a |
C |
T |
8: 72,092,412 (GRCm39) |
E1386K |
possibly damaging |
Het |
Wdr41 |
C |
T |
13: 95,155,456 (GRCm39) |
H404Y |
probably damaging |
Het |
Zfp280b |
T |
C |
10: 75,874,328 (GRCm39) |
L69S |
probably damaging |
Het |
Zfp346 |
T |
C |
13: 55,280,121 (GRCm39) |
S282P |
probably damaging |
Het |
Zfp579 |
C |
A |
7: 4,996,520 (GRCm39) |
E464* |
probably null |
Het |
Zfp78 |
T |
A |
7: 6,378,513 (GRCm39) |
|
probably null |
Het |
Zswim9 |
T |
C |
7: 13,003,292 (GRCm39) |
E186G |
probably damaging |
Het |
|
Other mutations in Setd3 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00971:Setd3
|
APN |
12 |
108,126,496 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01365:Setd3
|
APN |
12 |
108,124,165 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02031:Setd3
|
APN |
12 |
108,129,289 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02826:Setd3
|
APN |
12 |
108,078,383 (GRCm39) |
unclassified |
probably benign |
|
IGL02878:Setd3
|
APN |
12 |
108,074,814 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03039:Setd3
|
APN |
12 |
108,129,229 (GRCm39) |
splice site |
probably null |
|
R0332:Setd3
|
UTSW |
12 |
108,073,838 (GRCm39) |
missense |
probably benign |
|
R1644:Setd3
|
UTSW |
12 |
108,079,603 (GRCm39) |
missense |
possibly damaging |
0.88 |
R1776:Setd3
|
UTSW |
12 |
108,131,420 (GRCm39) |
missense |
probably damaging |
1.00 |
R2018:Setd3
|
UTSW |
12 |
108,084,513 (GRCm39) |
missense |
probably damaging |
1.00 |
R2041:Setd3
|
UTSW |
12 |
108,079,651 (GRCm39) |
missense |
possibly damaging |
0.84 |
R2058:Setd3
|
UTSW |
12 |
108,073,600 (GRCm39) |
missense |
probably benign |
0.03 |
R2206:Setd3
|
UTSW |
12 |
108,073,544 (GRCm39) |
missense |
probably benign |
0.11 |
R2207:Setd3
|
UTSW |
12 |
108,073,544 (GRCm39) |
missense |
probably benign |
0.11 |
R3973:Setd3
|
UTSW |
12 |
108,131,417 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3976:Setd3
|
UTSW |
12 |
108,131,417 (GRCm39) |
missense |
possibly damaging |
0.93 |
R3978:Setd3
|
UTSW |
12 |
108,124,201 (GRCm39) |
missense |
possibly damaging |
0.63 |
R4684:Setd3
|
UTSW |
12 |
108,074,949 (GRCm39) |
missense |
probably benign |
0.05 |
R4965:Setd3
|
UTSW |
12 |
108,079,630 (GRCm39) |
missense |
probably benign |
0.29 |
R5691:Setd3
|
UTSW |
12 |
108,126,544 (GRCm39) |
missense |
probably benign |
0.19 |
R5990:Setd3
|
UTSW |
12 |
108,126,594 (GRCm39) |
missense |
probably benign |
|
R6198:Setd3
|
UTSW |
12 |
108,131,427 (GRCm39) |
missense |
possibly damaging |
0.66 |
R6241:Setd3
|
UTSW |
12 |
108,124,114 (GRCm39) |
missense |
probably benign |
0.24 |
R6428:Setd3
|
UTSW |
12 |
108,079,597 (GRCm39) |
missense |
probably damaging |
0.99 |
R7652:Setd3
|
UTSW |
12 |
108,078,548 (GRCm39) |
missense |
probably damaging |
1.00 |
R7913:Setd3
|
UTSW |
12 |
108,073,924 (GRCm39) |
missense |
probably benign |
0.37 |
R8221:Setd3
|
UTSW |
12 |
108,073,612 (GRCm39) |
missense |
possibly damaging |
0.91 |
R9585:Setd3
|
UTSW |
12 |
108,074,814 (GRCm39) |
critical splice donor site |
probably null |
|
X0052:Setd3
|
UTSW |
12 |
108,073,924 (GRCm39) |
missense |
probably benign |
0.37 |
|