Other mutations in this stock |
Total: 115 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9130230L23Rik |
A |
T |
5: 66,157,560 (GRCm39) |
M1K |
probably null |
Het |
A630073D07Rik |
C |
T |
6: 132,603,457 (GRCm39) |
E100K |
unknown |
Het |
Abcc3 |
T |
G |
11: 94,254,889 (GRCm39) |
D638A |
probably benign |
Het |
Acadm |
T |
C |
3: 153,635,889 (GRCm39) |
I272V |
probably benign |
Het |
Adam2 |
G |
A |
14: 66,315,107 (GRCm39) |
T22I |
probably damaging |
Het |
Aldh3b1 |
G |
A |
19: 3,971,271 (GRCm39) |
|
probably benign |
Het |
Arfgef3 |
A |
T |
10: 18,537,135 (GRCm39) |
I182K |
probably benign |
Het |
Arhgef17 |
A |
G |
7: 100,528,184 (GRCm39) |
S677P |
probably benign |
Het |
Atp2b1 |
T |
C |
10: 98,832,750 (GRCm39) |
V417A |
probably damaging |
Het |
Brca1 |
T |
A |
11: 101,388,839 (GRCm39) |
H1675L |
probably benign |
Het |
Brd10 |
A |
T |
19: 29,720,998 (GRCm39) |
S743T |
probably damaging |
Het |
Btd |
G |
T |
14: 31,389,266 (GRCm39) |
G329V |
probably benign |
Het |
Capsl |
T |
A |
15: 9,461,916 (GRCm39) |
L104* |
probably null |
Het |
Cbx1 |
T |
C |
11: 96,693,554 (GRCm39) |
S107P |
probably benign |
Het |
Cd207 |
G |
T |
6: 83,648,683 (GRCm39) |
Y326* |
probably null |
Het |
Cenpp |
T |
C |
13: 49,794,759 (GRCm39) |
D136G |
probably damaging |
Het |
Chsy3 |
A |
G |
18: 59,309,560 (GRCm39) |
|
probably null |
Het |
Cntrl |
T |
A |
2: 35,019,827 (GRCm39) |
H551Q |
probably benign |
Het |
Col14a1 |
T |
A |
15: 55,310,858 (GRCm39) |
|
probably benign |
Het |
Cybrd1 |
T |
A |
2: 70,967,978 (GRCm39) |
F183Y |
possibly damaging |
Het |
D5Ertd579e |
G |
A |
5: 36,773,771 (GRCm39) |
S208L |
probably damaging |
Het |
Dlg2 |
A |
T |
7: 92,036,160 (GRCm39) |
K719* |
probably null |
Het |
Dppa1 |
A |
T |
11: 46,516,393 (GRCm39) |
|
probably null |
Het |
Dse |
A |
G |
10: 34,029,284 (GRCm39) |
V602A |
possibly damaging |
Het |
Elapor2 |
T |
A |
5: 9,529,251 (GRCm39) |
I1028K |
probably damaging |
Het |
Elmo1 |
C |
T |
13: 20,773,823 (GRCm39) |
A611V |
possibly damaging |
Het |
Ets2 |
T |
C |
16: 95,516,118 (GRCm39) |
S233P |
probably benign |
Het |
Fchsd2 |
G |
A |
7: 100,899,645 (GRCm39) |
|
probably benign |
Het |
Fhip2a |
T |
C |
19: 57,374,737 (GRCm39) |
I704T |
possibly damaging |
Het |
Fkbp4 |
T |
C |
6: 128,409,453 (GRCm39) |
R402G |
probably benign |
Het |
G2e3 |
T |
A |
12: 51,400,412 (GRCm39) |
D21E |
probably benign |
Het |
Gask1a |
A |
G |
9: 121,794,493 (GRCm39) |
T216A |
possibly damaging |
Het |
Gck |
A |
T |
11: 5,852,165 (GRCm39) |
N391K |
probably damaging |
Het |
Gm11077 |
T |
A |
6: 140,675,017 (GRCm39) |
I3N |
unknown |
Het |
Gm6793 |
T |
C |
8: 112,741,088 (GRCm39) |
M185V |
probably benign |
Het |
Gucy2d |
T |
A |
7: 98,103,268 (GRCm39) |
L504H |
probably damaging |
Het |
Hat1 |
T |
A |
2: 71,251,627 (GRCm39) |
Y225* |
probably null |
Het |
Iars2 |
A |
T |
1: 185,050,765 (GRCm39) |
D441E |
probably benign |
Het |
Ido2 |
C |
A |
8: 25,043,776 (GRCm39) |
M92I |
possibly damaging |
Het |
Ifne |
T |
C |
4: 88,797,908 (GRCm39) |
E170G |
probably damaging |
Het |
Ints8 |
C |
A |
4: 11,241,684 (GRCm39) |
C253F |
probably damaging |
Het |
Intu |
G |
T |
3: 40,618,765 (GRCm39) |
G257V |
probably damaging |
Het |
Jakmip3 |
A |
G |
7: 138,609,316 (GRCm39) |
K140R |
probably benign |
Het |
Kcnip3 |
T |
C |
2: 127,301,263 (GRCm39) |
E237G |
probably damaging |
Het |
Ksr2 |
A |
C |
5: 117,643,594 (GRCm39) |
E121A |
probably benign |
Het |
Lars1 |
T |
A |
18: 42,347,902 (GRCm39) |
I974F |
probably benign |
Het |
Lce1b |
A |
G |
3: 92,563,318 (GRCm39) |
S72P |
unknown |
Het |
Lhfpl4 |
T |
A |
6: 113,153,394 (GRCm39) |
D125V |
probably benign |
Het |
Luc7l |
G |
A |
17: 26,499,030 (GRCm39) |
|
probably benign |
Het |
Mei1 |
T |
C |
15: 82,009,154 (GRCm39) |
L833P |
probably damaging |
Het |
Mier2 |
A |
G |
10: 79,384,664 (GRCm39) |
V150A |
probably damaging |
Het |
Muc4 |
C |
T |
16: 32,576,715 (GRCm39) |
R2072C |
unknown |
Het |
Myh3 |
A |
G |
11: 66,975,852 (GRCm39) |
K295E |
probably benign |
Het |
Ndufaf5 |
A |
G |
2: 140,023,509 (GRCm39) |
I115V |
probably benign |
Het |
Neb |
T |
C |
2: 52,216,756 (GRCm39) |
K140E |
probably damaging |
Het |
Niban1 |
A |
G |
1: 151,517,302 (GRCm39) |
S104G |
possibly damaging |
Het |
Ntrk3 |
A |
T |
7: 77,842,352 (GRCm39) |
H825Q |
possibly damaging |
Het |
Nup62 |
T |
A |
7: 44,478,472 (GRCm39) |
S162R |
possibly damaging |
Het |
Or4c108 |
T |
C |
2: 88,804,128 (GRCm39) |
T36A |
possibly damaging |
Het |
Or5g23 |
T |
A |
2: 85,438,409 (GRCm39) |
I282F |
probably damaging |
Het |
Or5t7 |
G |
A |
2: 86,507,629 (GRCm39) |
T16I |
possibly damaging |
Het |
Or8c8 |
A |
G |
9: 38,164,986 (GRCm39) |
E91G |
probably damaging |
Het |
Orc4 |
A |
G |
2: 48,800,305 (GRCm39) |
M281T |
probably benign |
Het |
Osbpl5 |
C |
A |
7: 143,269,510 (GRCm39) |
R22L |
probably damaging |
Het |
Otos |
A |
G |
1: 92,572,185 (GRCm39) |
F47S |
probably damaging |
Het |
Parp11 |
A |
G |
6: 127,447,740 (GRCm39) |
T25A |
probably damaging |
Het |
Pcdhb9 |
A |
C |
18: 37,535,137 (GRCm39) |
D377A |
probably damaging |
Het |
Pdgfra |
C |
T |
5: 75,331,534 (GRCm39) |
S348L |
probably benign |
Het |
Pdlim5 |
C |
A |
3: 142,012,060 (GRCm39) |
|
probably null |
Het |
Peg12 |
T |
C |
7: 62,113,416 (GRCm39) |
H227R |
probably benign |
Het |
Piezo2 |
T |
C |
18: 63,152,415 (GRCm39) |
E2559G |
probably damaging |
Het |
Pnisr |
C |
T |
4: 21,874,086 (GRCm39) |
|
probably benign |
Het |
Ppa2 |
A |
T |
3: 133,053,858 (GRCm39) |
I183F |
probably damaging |
Het |
Pramel48 |
T |
A |
5: 95,630,758 (GRCm39) |
Y212N |
probably benign |
Het |
Prl2a1 |
T |
C |
13: 27,988,923 (GRCm39) |
L16P |
probably damaging |
Het |
Rai14 |
C |
A |
15: 10,633,314 (GRCm39) |
Q25H |
probably damaging |
Het |
Rapgef6 |
TG |
TGG |
11: 54,437,223 (GRCm39) |
|
probably null |
Het |
Rbm34 |
C |
A |
8: 127,697,631 (GRCm39) |
A27S |
probably benign |
Het |
Rchy1 |
T |
C |
5: 92,099,762 (GRCm39) |
D192G |
probably damaging |
Het |
Rexo1 |
T |
C |
10: 80,378,754 (GRCm39) |
D1094G |
probably damaging |
Het |
Rtl1 |
T |
A |
12: 109,556,970 (GRCm39) |
D1623V |
probably damaging |
Het |
Ryr2 |
C |
T |
13: 11,746,586 (GRCm39) |
E1989K |
probably benign |
Het |
Sema6c |
A |
G |
3: 95,078,124 (GRCm39) |
E500G |
probably damaging |
Het |
Slc13a1 |
T |
A |
6: 24,117,999 (GRCm39) |
Y246F |
probably damaging |
Het |
Slc39a9 |
C |
T |
12: 80,726,297 (GRCm39) |
L249F |
probably damaging |
Het |
Slc6a21 |
C |
T |
7: 44,937,252 (GRCm39) |
P261S |
probably benign |
Het |
Slco2b1 |
C |
T |
7: 99,335,243 (GRCm39) |
C179Y |
probably damaging |
Het |
Sox6 |
T |
C |
7: 115,258,773 (GRCm39) |
N252S |
possibly damaging |
Het |
Spr-ps1 |
C |
T |
6: 85,132,885 (GRCm39) |
|
noncoding transcript |
Het |
Sptbn1 |
C |
A |
11: 30,064,781 (GRCm39) |
R1906L |
possibly damaging |
Het |
Stac2 |
T |
C |
11: 97,943,771 (GRCm39) |
D13G |
probably benign |
Het |
Stat5a |
G |
T |
11: 100,764,955 (GRCm39) |
R226L |
probably damaging |
Het |
Suz12 |
A |
G |
11: 79,904,425 (GRCm39) |
|
probably null |
Het |
Tas2r144 |
C |
A |
6: 42,192,936 (GRCm39) |
H225Q |
probably benign |
Het |
Tdo2 |
T |
A |
3: 81,867,853 (GRCm39) |
M331L |
probably benign |
Het |
Tesk1 |
T |
C |
4: 43,447,201 (GRCm39) |
W530R |
probably damaging |
Het |
Tlr6 |
T |
C |
5: 65,112,172 (GRCm39) |
N245S |
probably benign |
Het |
Tnfrsf11a |
G |
T |
1: 105,772,431 (GRCm39) |
A573S |
probably damaging |
Het |
Tpbpb |
A |
T |
13: 61,050,344 (GRCm39) |
|
probably benign |
Het |
Trim24 |
T |
A |
6: 37,928,447 (GRCm39) |
S590T |
probably damaging |
Het |
Ttll3 |
G |
T |
6: 113,369,725 (GRCm39) |
A90S |
possibly damaging |
Het |
Ubr5 |
A |
T |
15: 38,042,090 (GRCm39) |
S169T |
probably benign |
Het |
Usp28 |
T |
C |
9: 48,928,007 (GRCm39) |
V363A |
probably damaging |
Het |
Vcan |
A |
G |
13: 89,838,990 (GRCm39) |
S2185P |
probably benign |
Het |
Vmn1r211 |
T |
C |
13: 23,035,779 (GRCm39) |
H296R |
probably benign |
Het |
Vmn2r3 |
G |
A |
3: 64,166,537 (GRCm39) |
P865S |
probably damaging |
Het |
Wapl |
A |
G |
14: 34,414,415 (GRCm39) |
T426A |
probably benign |
Het |
Wdr37 |
G |
T |
13: 8,886,887 (GRCm39) |
T300K |
probably damaging |
Het |
Wrap53 |
A |
T |
11: 69,452,990 (GRCm39) |
V439E |
probably null |
Het |
Wrn |
A |
G |
8: 33,747,249 (GRCm39) |
S868P |
probably benign |
Het |
Zfhx4 |
A |
G |
3: 5,477,774 (GRCm39) |
E3463G |
probably damaging |
Het |
Zfp189 |
T |
A |
4: 49,529,283 (GRCm39) |
C129S |
possibly damaging |
Het |
Zfp442 |
T |
C |
2: 150,250,100 (GRCm39) |
K544E |
probably damaging |
Het |
Zfp939 |
T |
A |
7: 39,122,728 (GRCm39) |
|
noncoding transcript |
Het |
Zfyve26 |
T |
C |
12: 79,308,573 (GRCm39) |
H228R |
possibly damaging |
Het |
|
Other mutations in Npas2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02560:Npas2
|
APN |
1 |
39,373,042 (GRCm39) |
splice site |
probably benign |
|
IGL02608:Npas2
|
APN |
1 |
39,384,527 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02882:Npas2
|
APN |
1 |
39,352,077 (GRCm39) |
missense |
probably benign |
0.08 |
IGL02976:Npas2
|
APN |
1 |
39,326,565 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03130:Npas2
|
APN |
1 |
39,352,109 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03297:Npas2
|
APN |
1 |
39,331,771 (GRCm39) |
missense |
possibly damaging |
0.71 |
R1263:Npas2
|
UTSW |
1 |
39,373,849 (GRCm39) |
missense |
possibly damaging |
0.51 |
R1514:Npas2
|
UTSW |
1 |
39,350,935 (GRCm39) |
missense |
possibly damaging |
0.82 |
R1618:Npas2
|
UTSW |
1 |
39,339,808 (GRCm39) |
missense |
probably damaging |
1.00 |
R1620:Npas2
|
UTSW |
1 |
39,372,993 (GRCm39) |
missense |
possibly damaging |
0.68 |
R1844:Npas2
|
UTSW |
1 |
39,364,456 (GRCm39) |
missense |
probably damaging |
1.00 |
R1892:Npas2
|
UTSW |
1 |
39,384,503 (GRCm39) |
missense |
probably benign |
0.00 |
R2002:Npas2
|
UTSW |
1 |
39,377,276 (GRCm39) |
missense |
probably benign |
0.10 |
R3157:Npas2
|
UTSW |
1 |
39,386,690 (GRCm39) |
missense |
possibly damaging |
0.92 |
R3551:Npas2
|
UTSW |
1 |
39,326,643 (GRCm39) |
missense |
probably benign |
0.05 |
R4564:Npas2
|
UTSW |
1 |
39,326,647 (GRCm39) |
missense |
probably damaging |
1.00 |
R4907:Npas2
|
UTSW |
1 |
39,401,066 (GRCm39) |
missense |
unknown |
|
R5044:Npas2
|
UTSW |
1 |
39,386,587 (GRCm39) |
nonsense |
probably null |
|
R5621:Npas2
|
UTSW |
1 |
39,398,794 (GRCm39) |
missense |
probably benign |
|
R5779:Npas2
|
UTSW |
1 |
39,326,652 (GRCm39) |
missense |
possibly damaging |
0.48 |
R5822:Npas2
|
UTSW |
1 |
39,386,647 (GRCm39) |
missense |
probably benign |
0.00 |
R6033:Npas2
|
UTSW |
1 |
39,377,261 (GRCm39) |
missense |
probably damaging |
0.99 |
R6033:Npas2
|
UTSW |
1 |
39,377,261 (GRCm39) |
missense |
probably damaging |
0.99 |
R6155:Npas2
|
UTSW |
1 |
39,326,557 (GRCm39) |
missense |
probably damaging |
1.00 |
R6193:Npas2
|
UTSW |
1 |
39,331,843 (GRCm39) |
missense |
probably damaging |
1.00 |
R6220:Npas2
|
UTSW |
1 |
39,375,142 (GRCm39) |
missense |
probably benign |
0.00 |
R6341:Npas2
|
UTSW |
1 |
39,339,768 (GRCm39) |
missense |
probably damaging |
0.98 |
R6656:Npas2
|
UTSW |
1 |
39,401,029 (GRCm39) |
missense |
unknown |
|
R6778:Npas2
|
UTSW |
1 |
39,364,381 (GRCm39) |
missense |
possibly damaging |
0.92 |
R6803:Npas2
|
UTSW |
1 |
39,375,130 (GRCm39) |
missense |
probably benign |
0.35 |
R7165:Npas2
|
UTSW |
1 |
39,331,798 (GRCm39) |
missense |
possibly damaging |
0.79 |
R7250:Npas2
|
UTSW |
1 |
39,377,188 (GRCm39) |
missense |
probably damaging |
1.00 |
R7268:Npas2
|
UTSW |
1 |
39,326,658 (GRCm39) |
missense |
probably damaging |
0.98 |
R7284:Npas2
|
UTSW |
1 |
39,363,548 (GRCm39) |
missense |
probably benign |
0.36 |
R7833:Npas2
|
UTSW |
1 |
39,365,228 (GRCm39) |
missense |
probably damaging |
1.00 |
R7994:Npas2
|
UTSW |
1 |
39,367,418 (GRCm39) |
missense |
possibly damaging |
0.86 |
R8013:Npas2
|
UTSW |
1 |
39,377,146 (GRCm39) |
missense |
probably benign |
|
R8054:Npas2
|
UTSW |
1 |
39,326,652 (GRCm39) |
missense |
possibly damaging |
0.69 |
R8510:Npas2
|
UTSW |
1 |
39,326,553 (GRCm39) |
missense |
probably damaging |
1.00 |
R8683:Npas2
|
UTSW |
1 |
39,386,708 (GRCm39) |
missense |
probably benign |
0.00 |
R8738:Npas2
|
UTSW |
1 |
39,331,797 (GRCm39) |
missense |
possibly damaging |
0.65 |
R8779:Npas2
|
UTSW |
1 |
39,377,267 (GRCm39) |
missense |
probably damaging |
0.99 |
R9283:Npas2
|
UTSW |
1 |
39,326,689 (GRCm39) |
missense |
probably damaging |
1.00 |
R9541:Npas2
|
UTSW |
1 |
39,377,194 (GRCm39) |
missense |
possibly damaging |
0.94 |
R9675:Npas2
|
UTSW |
1 |
39,364,446 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Npas2
|
UTSW |
1 |
39,375,091 (GRCm39) |
missense |
probably benign |
0.03 |
|