Other mutations in this stock |
Total: 100 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
A2m |
T |
C |
6: 121,626,792 (GRCm39) |
L548P |
probably damaging |
Het |
Abca6 |
A |
G |
11: 110,100,909 (GRCm39) |
|
probably null |
Het |
Abcb5 |
A |
G |
12: 118,871,235 (GRCm39) |
|
probably null |
Het |
Acacb |
G |
A |
5: 114,336,343 (GRCm39) |
A686T |
probably benign |
Het |
Acot6 |
T |
C |
12: 84,153,367 (GRCm39) |
V203A |
probably benign |
Het |
Adam25 |
A |
T |
8: 41,207,922 (GRCm39) |
Y396F |
probably benign |
Het |
Adamts9 |
A |
G |
6: 92,920,102 (GRCm39) |
L12P |
possibly damaging |
Het |
Adamtsl2 |
A |
T |
2: 26,979,605 (GRCm39) |
D258V |
probably damaging |
Het |
Aox4 |
G |
A |
1: 58,285,095 (GRCm39) |
V616I |
probably benign |
Het |
Ap1m1 |
A |
G |
8: 73,009,637 (GRCm39) |
I382V |
probably damaging |
Het |
Arhgef2 |
G |
A |
3: 88,537,098 (GRCm39) |
R8Q |
probably damaging |
Het |
Arhgef37 |
T |
G |
18: 61,657,014 (GRCm39) |
E17A |
probably benign |
Het |
Arhgef7 |
C |
A |
8: 11,858,713 (GRCm39) |
|
probably null |
Het |
Arih1 |
T |
C |
9: 59,302,215 (GRCm39) |
D431G |
probably damaging |
Het |
Astn2 |
C |
T |
4: 65,353,426 (GRCm39) |
V1115M |
probably damaging |
Het |
Atg7 |
T |
A |
6: 114,678,196 (GRCm39) |
M280K |
probably damaging |
Het |
Birc2 |
T |
C |
9: 7,854,500 (GRCm39) |
T397A |
possibly damaging |
Het |
Ccdc110 |
A |
G |
8: 46,396,287 (GRCm39) |
N726S |
probably damaging |
Het |
Cdadc1 |
A |
T |
14: 59,827,309 (GRCm39) |
S121T |
possibly damaging |
Het |
Cdh16 |
A |
G |
8: 105,344,595 (GRCm39) |
V7A |
possibly damaging |
Het |
Cenpb |
A |
G |
2: 131,021,184 (GRCm39) |
S205P |
probably benign |
Het |
Chsy1 |
T |
C |
7: 65,821,991 (GRCm39) |
V742A |
probably damaging |
Het |
Col12a1 |
G |
A |
9: 79,511,804 (GRCm39) |
R133* |
probably null |
Het |
Col18a1 |
A |
C |
10: 76,948,578 (GRCm39) |
S311R |
possibly damaging |
Het |
Col9a3 |
G |
A |
2: 180,248,927 (GRCm39) |
V260M |
probably damaging |
Het |
Coq2 |
T |
A |
5: 100,809,731 (GRCm39) |
R17S |
probably damaging |
Het |
Ctf1 |
A |
G |
7: 127,311,936 (GRCm39) |
R4G |
probably damaging |
Het |
Cwc27 |
T |
C |
13: 104,768,184 (GRCm39) |
D437G |
probably benign |
Het |
Cyp4f14 |
T |
C |
17: 33,125,289 (GRCm39) |
N430D |
probably damaging |
Het |
Dars2 |
A |
G |
1: 160,890,811 (GRCm39) |
|
probably null |
Het |
Dnhd1 |
T |
G |
7: 105,357,789 (GRCm39) |
V3208G |
probably benign |
Het |
Dsg1b |
A |
G |
18: 20,528,963 (GRCm39) |
Y233C |
probably damaging |
Het |
Edem3 |
A |
T |
1: 151,680,034 (GRCm39) |
D460V |
probably damaging |
Het |
Ednra |
A |
G |
8: 78,415,747 (GRCm39) |
S167P |
possibly damaging |
Het |
Eif3m |
A |
T |
2: 104,831,624 (GRCm39) |
V180D |
probably damaging |
Het |
Fam217a |
T |
A |
13: 35,094,864 (GRCm39) |
R207S |
probably damaging |
Het |
Fcgbp |
G |
A |
7: 27,806,518 (GRCm39) |
G2162D |
probably damaging |
Het |
Fhod3 |
A |
T |
18: 25,223,335 (GRCm39) |
I894F |
probably benign |
Het |
Fpgs |
A |
T |
2: 32,577,993 (GRCm39) |
I143N |
probably damaging |
Het |
Fpr-rs6 |
A |
G |
17: 20,403,152 (GRCm39) |
S70P |
probably benign |
Het |
Frs2 |
T |
C |
10: 116,914,806 (GRCm39) |
M38V |
probably damaging |
Het |
Fsip2 |
A |
G |
2: 82,810,902 (GRCm39) |
N2407S |
possibly damaging |
Het |
Gabrg2 |
T |
A |
11: 41,811,297 (GRCm39) |
T283S |
probably benign |
Het |
Gas2l1 |
T |
A |
11: 5,011,408 (GRCm39) |
T474S |
probably benign |
Het |
Gli1 |
A |
T |
10: 127,167,108 (GRCm39) |
M715K |
possibly damaging |
Het |
Glra3 |
G |
T |
8: 56,393,942 (GRCm39) |
A18S |
probably benign |
Het |
Gm5800 |
T |
A |
14: 51,949,396 (GRCm39) |
N183I |
possibly damaging |
Het |
Gm8674 |
T |
A |
13: 50,055,471 (GRCm39) |
|
noncoding transcript |
Het |
Gnat3 |
A |
T |
5: 18,224,508 (GRCm39) |
I303F |
possibly damaging |
Het |
Grin2d |
C |
T |
7: 45,506,251 (GRCm39) |
V547M |
probably damaging |
Het |
Grpr |
C |
A |
X: 162,332,137 (GRCm39) |
V53L |
probably benign |
Het |
Heatr5b |
T |
C |
17: 79,103,347 (GRCm39) |
I1169V |
possibly damaging |
Het |
Icam5 |
A |
G |
9: 20,946,082 (GRCm39) |
T305A |
probably benign |
Het |
Itga11 |
T |
A |
9: 62,651,796 (GRCm39) |
N309K |
probably damaging |
Het |
Itgb6 |
T |
C |
2: 60,499,493 (GRCm39) |
D100G |
probably benign |
Het |
Kdm3b |
A |
G |
18: 34,946,597 (GRCm39) |
K862R |
probably benign |
Het |
Kif7 |
T |
C |
7: 79,361,286 (GRCm39) |
D135G |
probably benign |
Het |
Lrp4 |
A |
G |
2: 91,310,777 (GRCm39) |
D606G |
probably damaging |
Het |
Lrrtm1 |
A |
T |
6: 77,221,949 (GRCm39) |
|
probably null |
Het |
Metap1d |
A |
T |
2: 71,352,927 (GRCm39) |
H252L |
possibly damaging |
Het |
Mfhas1 |
A |
G |
8: 36,058,251 (GRCm39) |
K909E |
possibly damaging |
Het |
Mrgprh |
C |
T |
17: 13,095,838 (GRCm39) |
T26I |
probably damaging |
Het |
Myo15b |
T |
C |
11: 115,754,310 (GRCm39) |
S937P |
probably benign |
Het |
Neto2 |
A |
T |
8: 86,397,033 (GRCm39) |
I73N |
possibly damaging |
Het |
Nod2 |
T |
C |
8: 89,390,347 (GRCm39) |
I196T |
probably benign |
Het |
Nvl |
T |
G |
1: 180,926,693 (GRCm39) |
T788P |
probably damaging |
Het |
Or13a25 |
C |
A |
7: 140,247,951 (GRCm39) |
C243* |
probably null |
Het |
Or2h2 |
A |
T |
17: 37,396,906 (GRCm39) |
D50E |
possibly damaging |
Het |
Pax3 |
G |
A |
1: 78,080,117 (GRCm39) |
T423I |
possibly damaging |
Het |
Pde4dip |
A |
G |
3: 97,600,007 (GRCm39) |
V2403A |
possibly damaging |
Het |
Phip |
C |
T |
9: 82,785,235 (GRCm39) |
V827I |
probably benign |
Het |
Plcb3 |
A |
G |
19: 6,941,977 (GRCm39) |
F285L |
probably damaging |
Het |
Pnp2 |
A |
G |
14: 51,193,675 (GRCm39) |
I16V |
probably benign |
Het |
Pola2 |
A |
G |
19: 6,003,769 (GRCm39) |
L202P |
probably damaging |
Het |
Ppfia1 |
A |
T |
7: 144,058,847 (GRCm39) |
N651K |
probably benign |
Het |
Prss53 |
T |
C |
7: 127,485,920 (GRCm39) |
|
probably null |
Het |
Rasgrf1 |
G |
T |
9: 89,835,966 (GRCm39) |
Q231H |
probably damaging |
Het |
Rasgrf2 |
A |
T |
13: 92,131,825 (GRCm39) |
|
probably null |
Het |
Rccd1 |
T |
A |
7: 79,970,272 (GRCm39) |
N115I |
possibly damaging |
Het |
Rpgrip1 |
A |
T |
14: 52,352,101 (GRCm39) |
T26S |
possibly damaging |
Het |
Rpn1 |
T |
A |
6: 88,070,841 (GRCm39) |
V237E |
probably damaging |
Het |
Sema4f |
G |
T |
6: 82,907,908 (GRCm39) |
P180Q |
probably damaging |
Het |
Slc36a4 |
T |
C |
9: 15,632,085 (GRCm39) |
V87A |
probably damaging |
Het |
Slc5a4b |
A |
T |
10: 75,917,307 (GRCm39) |
V243E |
possibly damaging |
Het |
Sos2 |
T |
G |
12: 69,695,315 (GRCm39) |
I141L |
probably damaging |
Het |
Srbd1 |
A |
G |
17: 86,410,321 (GRCm39) |
V537A |
probably damaging |
Het |
Sugp1 |
A |
G |
8: 70,509,225 (GRCm39) |
E166G |
possibly damaging |
Het |
Tktl2 |
G |
A |
8: 66,964,999 (GRCm39) |
V186M |
probably damaging |
Het |
Tshr |
T |
C |
12: 91,503,955 (GRCm39) |
S298P |
probably damaging |
Het |
Tspan14 |
T |
C |
14: 40,656,209 (GRCm39) |
Y6C |
probably damaging |
Het |
Ttn |
A |
T |
2: 76,577,384 (GRCm39) |
V24503E |
probably damaging |
Het |
Vcan |
T |
A |
13: 89,851,045 (GRCm39) |
N1305I |
probably damaging |
Het |
Vmn2r81 |
A |
G |
10: 79,083,628 (GRCm39) |
M1V |
probably null |
Het |
Vps39 |
A |
T |
2: 120,148,558 (GRCm39) |
V873E |
probably damaging |
Het |
Vstm2a |
A |
T |
11: 16,359,734 (GRCm39) |
D270V |
unknown |
Het |
Wdr24 |
A |
T |
17: 26,043,240 (GRCm39) |
M21L |
possibly damaging |
Het |
Wee1 |
A |
G |
7: 109,721,698 (GRCm39) |
T48A |
probably benign |
Het |
Zfp369 |
T |
C |
13: 65,444,965 (GRCm39) |
C703R |
probably damaging |
Het |
Zfp532 |
A |
T |
18: 65,818,682 (GRCm39) |
D1114V |
probably damaging |
Het |
Zfp758 |
A |
G |
17: 22,592,633 (GRCm39) |
T46A |
probably damaging |
Het |
|
Other mutations in Dgkz |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01680:Dgkz
|
APN |
2 |
91,766,210 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01995:Dgkz
|
APN |
2 |
91,764,395 (GRCm39) |
splice site |
probably benign |
|
IGL02247:Dgkz
|
APN |
2 |
91,767,805 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02573:Dgkz
|
APN |
2 |
91,764,542 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02627:Dgkz
|
APN |
2 |
91,769,055 (GRCm39) |
splice site |
probably benign |
|
IGL02903:Dgkz
|
APN |
2 |
91,770,307 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL03106:Dgkz
|
APN |
2 |
91,771,204 (GRCm39) |
missense |
probably damaging |
0.99 |
R0103:Dgkz
|
UTSW |
2 |
91,764,550 (GRCm39) |
missense |
probably benign |
|
R0312:Dgkz
|
UTSW |
2 |
91,768,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R0761:Dgkz
|
UTSW |
2 |
91,775,696 (GRCm39) |
missense |
probably benign |
0.00 |
R0839:Dgkz
|
UTSW |
2 |
91,765,456 (GRCm39) |
missense |
probably benign |
0.00 |
R1162:Dgkz
|
UTSW |
2 |
91,774,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R1223:Dgkz
|
UTSW |
2 |
91,769,660 (GRCm39) |
splice site |
probably benign |
|
R1539:Dgkz
|
UTSW |
2 |
91,768,405 (GRCm39) |
missense |
probably damaging |
1.00 |
R1936:Dgkz
|
UTSW |
2 |
91,768,323 (GRCm39) |
missense |
possibly damaging |
0.94 |
R3438:Dgkz
|
UTSW |
2 |
91,764,395 (GRCm39) |
splice site |
probably benign |
|
R3804:Dgkz
|
UTSW |
2 |
91,769,975 (GRCm39) |
missense |
probably benign |
0.06 |
R4675:Dgkz
|
UTSW |
2 |
91,768,691 (GRCm39) |
nonsense |
probably null |
|
R4731:Dgkz
|
UTSW |
2 |
91,768,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4732:Dgkz
|
UTSW |
2 |
91,768,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4733:Dgkz
|
UTSW |
2 |
91,768,684 (GRCm39) |
missense |
probably damaging |
1.00 |
R4901:Dgkz
|
UTSW |
2 |
91,767,076 (GRCm39) |
missense |
probably benign |
|
R4972:Dgkz
|
UTSW |
2 |
91,776,047 (GRCm39) |
missense |
probably benign |
0.00 |
R5027:Dgkz
|
UTSW |
2 |
91,775,888 (GRCm39) |
missense |
probably benign |
0.02 |
R5128:Dgkz
|
UTSW |
2 |
91,773,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R5408:Dgkz
|
UTSW |
2 |
91,766,168 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5494:Dgkz
|
UTSW |
2 |
91,771,394 (GRCm39) |
splice site |
probably null |
|
R5728:Dgkz
|
UTSW |
2 |
91,776,132 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5813:Dgkz
|
UTSW |
2 |
91,769,733 (GRCm39) |
missense |
possibly damaging |
0.50 |
R6025:Dgkz
|
UTSW |
2 |
91,776,255 (GRCm39) |
missense |
possibly damaging |
0.75 |
R6043:Dgkz
|
UTSW |
2 |
91,766,234 (GRCm39) |
missense |
probably benign |
0.03 |
R6328:Dgkz
|
UTSW |
2 |
91,772,980 (GRCm39) |
missense |
probably benign |
0.04 |
R6335:Dgkz
|
UTSW |
2 |
91,774,724 (GRCm39) |
missense |
probably benign |
0.16 |
R7381:Dgkz
|
UTSW |
2 |
91,775,180 (GRCm39) |
missense |
probably benign |
0.02 |
R7541:Dgkz
|
UTSW |
2 |
91,773,020 (GRCm39) |
missense |
probably damaging |
1.00 |
R7560:Dgkz
|
UTSW |
2 |
91,773,160 (GRCm39) |
unclassified |
probably benign |
|
R7608:Dgkz
|
UTSW |
2 |
91,764,399 (GRCm39) |
critical splice donor site |
probably null |
|
R7624:Dgkz
|
UTSW |
2 |
91,773,019 (GRCm39) |
missense |
probably damaging |
1.00 |
R7709:Dgkz
|
UTSW |
2 |
91,767,404 (GRCm39) |
missense |
probably benign |
0.02 |
R7938:Dgkz
|
UTSW |
2 |
91,795,817 (GRCm39) |
missense |
probably damaging |
0.96 |
R8183:Dgkz
|
UTSW |
2 |
91,769,937 (GRCm39) |
missense |
probably damaging |
1.00 |
R8233:Dgkz
|
UTSW |
2 |
91,769,994 (GRCm39) |
missense |
probably damaging |
1.00 |
R8415:Dgkz
|
UTSW |
2 |
91,770,649 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8416:Dgkz
|
UTSW |
2 |
91,770,649 (GRCm39) |
missense |
possibly damaging |
0.80 |
R8757:Dgkz
|
UTSW |
2 |
91,775,922 (GRCm39) |
missense |
probably benign |
|
R8759:Dgkz
|
UTSW |
2 |
91,775,922 (GRCm39) |
missense |
probably benign |
|
R8930:Dgkz
|
UTSW |
2 |
91,769,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R8932:Dgkz
|
UTSW |
2 |
91,769,915 (GRCm39) |
missense |
probably damaging |
0.99 |
R9005:Dgkz
|
UTSW |
2 |
91,769,090 (GRCm39) |
missense |
probably benign |
0.34 |
R9120:Dgkz
|
UTSW |
2 |
91,768,545 (GRCm39) |
missense |
probably benign |
0.00 |
R9205:Dgkz
|
UTSW |
2 |
91,764,144 (GRCm39) |
missense |
probably benign |
0.31 |
R9719:Dgkz
|
UTSW |
2 |
91,768,911 (GRCm39) |
critical splice acceptor site |
probably null |
|
RF001:Dgkz
|
UTSW |
2 |
91,770,286 (GRCm39) |
missense |
possibly damaging |
0.83 |
X0002:Dgkz
|
UTSW |
2 |
91,766,907 (GRCm39) |
missense |
probably damaging |
0.97 |
X0021:Dgkz
|
UTSW |
2 |
91,767,464 (GRCm39) |
missense |
possibly damaging |
0.91 |
Z1177:Dgkz
|
UTSW |
2 |
91,772,679 (GRCm39) |
missense |
probably damaging |
1.00 |
|