Other mutations in this stock |
Total: 77 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcb4 |
T |
G |
5: 8,984,203 (GRCm39) |
S644R |
probably benign |
Het |
Adra2a |
A |
G |
19: 54,034,659 (GRCm39) |
E5G |
probably benign |
Het |
Ankrd1 |
A |
T |
19: 36,092,922 (GRCm39) |
V201D |
possibly damaging |
Het |
Ano9 |
A |
T |
7: 140,683,114 (GRCm39) |
V598E |
probably damaging |
Het |
Apob |
T |
A |
12: 8,051,885 (GRCm39) |
M1150K |
possibly damaging |
Het |
BC005624 |
A |
T |
2: 30,864,032 (GRCm39) |
I187N |
probably damaging |
Het |
Bltp3b |
C |
T |
10: 89,651,968 (GRCm39) |
T1381I |
probably benign |
Het |
Ccl9 |
T |
C |
11: 83,467,257 (GRCm39) |
E31G |
probably benign |
Het |
Cnnm4 |
T |
A |
1: 36,511,019 (GRCm39) |
D82E |
probably benign |
Het |
Coq10b |
T |
C |
1: 55,092,013 (GRCm39) |
|
probably benign |
Het |
Cplane1 |
T |
G |
15: 8,233,241 (GRCm39) |
F1189V |
probably damaging |
Het |
Cyb561 |
T |
C |
11: 105,830,935 (GRCm39) |
N50S |
probably benign |
Het |
Dctn4 |
G |
T |
18: 60,679,348 (GRCm39) |
A223S |
probably benign |
Het |
Dysf |
A |
G |
6: 84,114,380 (GRCm39) |
Y1223C |
probably damaging |
Het |
Eed |
C |
T |
7: 89,630,022 (GRCm39) |
|
probably benign |
Het |
Eef1g |
T |
A |
19: 8,954,738 (GRCm39) |
V305E |
probably benign |
Het |
Eif4ebp2 |
C |
A |
10: 61,270,772 (GRCm39) |
A86S |
probably benign |
Het |
Ermp1 |
T |
C |
19: 29,609,788 (GRCm39) |
|
probably null |
Het |
Hid1 |
T |
C |
11: 115,249,821 (GRCm39) |
Y198C |
probably damaging |
Het |
Hoxd1 |
C |
A |
2: 74,593,816 (GRCm39) |
A124E |
probably benign |
Het |
Hyal5 |
G |
A |
6: 24,891,347 (GRCm39) |
C387Y |
probably damaging |
Het |
Il11 |
A |
G |
7: 4,778,999 (GRCm39) |
S103P |
probably damaging |
Het |
Lgalsl2 |
A |
T |
7: 5,362,507 (GRCm39) |
K46M |
probably damaging |
Het |
Lmtk3 |
A |
C |
7: 45,436,327 (GRCm39) |
I128L |
possibly damaging |
Het |
Lrrc4b |
G |
T |
7: 44,094,316 (GRCm39) |
|
probably benign |
Het |
Magel2 |
T |
A |
7: 62,028,116 (GRCm39) |
I340N |
possibly damaging |
Het |
Mfsd14a |
A |
T |
3: 116,442,200 (GRCm39) |
F71I |
possibly damaging |
Het |
Mgarp |
A |
G |
3: 51,296,487 (GRCm39) |
S172P |
probably benign |
Het |
Mug1 |
T |
C |
6: 121,847,611 (GRCm39) |
|
probably null |
Het |
Naa15 |
G |
T |
3: 51,370,688 (GRCm39) |
E651* |
probably null |
Het |
Ndfip2 |
T |
C |
14: 105,529,675 (GRCm39) |
V168A |
probably benign |
Het |
Neb |
C |
A |
2: 52,113,373 (GRCm39) |
|
probably null |
Het |
Nfil3 |
A |
G |
13: 53,121,968 (GRCm39) |
V312A |
possibly damaging |
Het |
Ntrk1 |
T |
A |
3: 87,687,041 (GRCm39) |
K706* |
probably null |
Het |
Nuf2 |
A |
T |
1: 169,352,898 (GRCm39) |
F36I |
probably benign |
Het |
Or51h7 |
T |
A |
7: 102,591,125 (GRCm39) |
T220S |
possibly damaging |
Het |
Or5aq7 |
T |
C |
2: 86,937,861 (GRCm39) |
Y290C |
probably damaging |
Het |
Pcdh8 |
T |
G |
14: 80,006,101 (GRCm39) |
T821P |
possibly damaging |
Het |
Ppl |
C |
T |
16: 4,906,725 (GRCm39) |
R1190H |
probably damaging |
Het |
Ptch2 |
C |
A |
4: 116,962,224 (GRCm39) |
|
probably null |
Het |
Ptdss1 |
A |
G |
13: 67,081,719 (GRCm39) |
I50V |
probably benign |
Het |
Pth2r |
G |
T |
1: 65,390,722 (GRCm39) |
W292L |
probably damaging |
Het |
Ptprd |
G |
A |
4: 75,900,881 (GRCm39) |
T825M |
probably damaging |
Het |
Ptprk |
T |
C |
10: 28,449,385 (GRCm39) |
Y987H |
probably damaging |
Het |
Qser1 |
T |
C |
2: 104,606,579 (GRCm39) |
E1470G |
probably damaging |
Het |
Rab11fip3 |
T |
C |
17: 26,287,232 (GRCm39) |
E307G |
possibly damaging |
Het |
Rims2 |
A |
G |
15: 39,544,475 (GRCm39) |
Y1484C |
probably damaging |
Het |
Rock1 |
A |
T |
18: 10,097,651 (GRCm39) |
|
probably null |
Het |
Slc15a1 |
T |
A |
14: 121,718,145 (GRCm39) |
K245* |
probably null |
Het |
Snx11 |
T |
A |
11: 96,660,032 (GRCm39) |
E219V |
possibly damaging |
Het |
Sox21 |
C |
A |
14: 118,472,729 (GRCm39) |
E107* |
probably null |
Het |
Spink5 |
T |
A |
18: 44,132,888 (GRCm39) |
H501Q |
probably benign |
Het |
Stard5 |
C |
T |
7: 83,285,984 (GRCm39) |
T103M |
probably damaging |
Het |
Stfa2l1 |
A |
T |
16: 35,977,203 (GRCm39) |
|
probably benign |
Het |
Sult1c2 |
A |
C |
17: 54,271,076 (GRCm39) |
V185G |
probably damaging |
Het |
Svs5 |
A |
G |
2: 164,079,500 (GRCm39) |
S136P |
possibly damaging |
Het |
Sytl3 |
T |
A |
17: 6,982,774 (GRCm39) |
|
probably null |
Het |
Tc2n |
C |
T |
12: 101,619,112 (GRCm39) |
V349I |
possibly damaging |
Het |
Tln1 |
A |
G |
4: 43,554,309 (GRCm39) |
V271A |
probably benign |
Het |
Tmem260 |
T |
A |
14: 48,746,519 (GRCm39) |
S446R |
probably benign |
Het |
Trim30a |
T |
C |
7: 104,084,802 (GRCm39) |
D136G |
probably benign |
Het |
Ulk4 |
A |
T |
9: 120,873,885 (GRCm39) |
I1182N |
possibly damaging |
Het |
Unc50 |
T |
G |
1: 37,476,377 (GRCm39) |
I179S |
possibly damaging |
Het |
Upb1 |
T |
A |
10: 75,248,667 (GRCm39) |
Y57* |
probably null |
Het |
Usp34 |
C |
T |
11: 23,396,614 (GRCm39) |
T2349I |
|
Het |
Vmn1r71 |
A |
G |
7: 10,482,277 (GRCm39) |
V137A |
possibly damaging |
Het |
Vmn1r85 |
T |
C |
7: 12,818,698 (GRCm39) |
I149V |
probably benign |
Het |
Vmn2r118 |
A |
G |
17: 55,900,242 (GRCm39) |
L554P |
probably damaging |
Het |
Wdr4 |
C |
G |
17: 31,718,782 (GRCm39) |
|
probably null |
Het |
Zbbx |
A |
T |
3: 74,985,781 (GRCm39) |
S424T |
possibly damaging |
Het |
Zfp207 |
C |
G |
11: 80,282,726 (GRCm39) |
P246A |
probably damaging |
Het |
Zfp414 |
T |
A |
17: 33,848,962 (GRCm39) |
Y65* |
probably null |
Het |
Zfp600 |
T |
A |
4: 146,133,523 (GRCm39) |
N730K |
probably benign |
Het |
Zfp827 |
T |
C |
8: 79,912,979 (GRCm39) |
L1073P |
probably damaging |
Het |
Zfp986 |
A |
G |
4: 145,625,691 (GRCm39) |
K117R |
possibly damaging |
Het |
Zgrf1 |
T |
A |
3: 127,357,080 (GRCm39) |
Y769N |
probably damaging |
Het |
Zup1 |
A |
T |
10: 33,795,315 (GRCm39) |
I547N |
unknown |
Het |
|
Other mutations in Nrap |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00500:Nrap
|
APN |
19 |
56,361,341 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL00570:Nrap
|
APN |
19 |
56,326,545 (GRCm39) |
missense |
probably benign |
0.10 |
IGL00946:Nrap
|
APN |
19 |
56,329,058 (GRCm39) |
splice site |
probably null |
|
IGL01070:Nrap
|
APN |
19 |
56,317,516 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01111:Nrap
|
APN |
19 |
56,333,990 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01138:Nrap
|
APN |
19 |
56,343,970 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01290:Nrap
|
APN |
19 |
56,350,180 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01352:Nrap
|
APN |
19 |
56,368,268 (GRCm39) |
missense |
probably benign |
0.00 |
IGL01372:Nrap
|
APN |
19 |
56,317,534 (GRCm39) |
critical splice acceptor site |
probably null |
|
IGL01395:Nrap
|
APN |
19 |
56,350,225 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01413:Nrap
|
APN |
19 |
56,377,823 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01734:Nrap
|
APN |
19 |
56,338,741 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01933:Nrap
|
APN |
19 |
56,377,250 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02156:Nrap
|
APN |
19 |
56,309,432 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02415:Nrap
|
APN |
19 |
56,370,741 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02447:Nrap
|
APN |
19 |
56,333,951 (GRCm39) |
nonsense |
probably null |
|
IGL02864:Nrap
|
APN |
19 |
56,338,806 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02993:Nrap
|
APN |
19 |
56,333,965 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03003:Nrap
|
APN |
19 |
56,310,384 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03006:Nrap
|
APN |
19 |
56,335,596 (GRCm39) |
missense |
probably benign |
0.02 |
IGL03084:Nrap
|
APN |
19 |
56,353,886 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL03136:Nrap
|
APN |
19 |
56,330,687 (GRCm39) |
missense |
possibly damaging |
0.69 |
IGL03272:Nrap
|
APN |
19 |
56,334,000 (GRCm39) |
intron |
probably benign |
|
IGL03389:Nrap
|
APN |
19 |
56,340,148 (GRCm39) |
missense |
probably benign |
0.10 |
R0116:Nrap
|
UTSW |
19 |
56,343,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R0374:Nrap
|
UTSW |
19 |
56,340,054 (GRCm39) |
missense |
probably damaging |
1.00 |
R0715:Nrap
|
UTSW |
19 |
56,345,757 (GRCm39) |
missense |
probably damaging |
0.98 |
R0828:Nrap
|
UTSW |
19 |
56,333,990 (GRCm39) |
missense |
probably damaging |
1.00 |
R0883:Nrap
|
UTSW |
19 |
56,333,906 (GRCm39) |
missense |
probably damaging |
1.00 |
R1416:Nrap
|
UTSW |
19 |
56,315,725 (GRCm39) |
missense |
possibly damaging |
0.60 |
R1459:Nrap
|
UTSW |
19 |
56,372,562 (GRCm39) |
missense |
probably benign |
0.00 |
R1616:Nrap
|
UTSW |
19 |
56,378,255 (GRCm39) |
missense |
probably damaging |
1.00 |
R1676:Nrap
|
UTSW |
19 |
56,323,687 (GRCm39) |
missense |
probably damaging |
1.00 |
R1687:Nrap
|
UTSW |
19 |
56,343,961 (GRCm39) |
missense |
probably damaging |
0.99 |
R1766:Nrap
|
UTSW |
19 |
56,323,474 (GRCm39) |
missense |
probably damaging |
0.99 |
R1792:Nrap
|
UTSW |
19 |
56,367,590 (GRCm39) |
missense |
probably benign |
0.00 |
R1817:Nrap
|
UTSW |
19 |
56,372,487 (GRCm39) |
unclassified |
probably benign |
|
R1972:Nrap
|
UTSW |
19 |
56,345,785 (GRCm39) |
missense |
probably damaging |
1.00 |
R1982:Nrap
|
UTSW |
19 |
56,372,537 (GRCm39) |
missense |
probably damaging |
0.99 |
R2258:Nrap
|
UTSW |
19 |
56,310,394 (GRCm39) |
missense |
possibly damaging |
0.80 |
R2448:Nrap
|
UTSW |
19 |
56,310,462 (GRCm39) |
missense |
possibly damaging |
0.90 |
R3034:Nrap
|
UTSW |
19 |
56,352,437 (GRCm39) |
missense |
probably damaging |
1.00 |
R3801:Nrap
|
UTSW |
19 |
56,310,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R3804:Nrap
|
UTSW |
19 |
56,310,211 (GRCm39) |
missense |
probably damaging |
1.00 |
R3923:Nrap
|
UTSW |
19 |
56,368,688 (GRCm39) |
missense |
probably damaging |
0.99 |
R3964:Nrap
|
UTSW |
19 |
56,330,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R3965:Nrap
|
UTSW |
19 |
56,330,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R3966:Nrap
|
UTSW |
19 |
56,330,576 (GRCm39) |
missense |
probably damaging |
1.00 |
R3980:Nrap
|
UTSW |
19 |
56,369,984 (GRCm39) |
missense |
probably benign |
0.01 |
R4182:Nrap
|
UTSW |
19 |
56,338,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R4499:Nrap
|
UTSW |
19 |
56,339,913 (GRCm39) |
missense |
probably damaging |
0.97 |
R4573:Nrap
|
UTSW |
19 |
56,330,770 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4603:Nrap
|
UTSW |
19 |
56,323,456 (GRCm39) |
critical splice donor site |
probably null |
|
R4689:Nrap
|
UTSW |
19 |
56,374,458 (GRCm39) |
missense |
probably damaging |
0.97 |
R4749:Nrap
|
UTSW |
19 |
56,368,669 (GRCm39) |
missense |
probably damaging |
0.96 |
R4845:Nrap
|
UTSW |
19 |
56,339,902 (GRCm39) |
missense |
probably benign |
0.16 |
R4937:Nrap
|
UTSW |
19 |
56,335,652 (GRCm39) |
missense |
probably damaging |
1.00 |
R4962:Nrap
|
UTSW |
19 |
56,366,575 (GRCm39) |
missense |
probably damaging |
1.00 |
R5156:Nrap
|
UTSW |
19 |
56,360,277 (GRCm39) |
missense |
possibly damaging |
0.94 |
R5181:Nrap
|
UTSW |
19 |
56,333,960 (GRCm39) |
missense |
possibly damaging |
0.85 |
R5202:Nrap
|
UTSW |
19 |
56,323,583 (GRCm39) |
missense |
probably damaging |
1.00 |
R5262:Nrap
|
UTSW |
19 |
56,308,655 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5301:Nrap
|
UTSW |
19 |
56,367,541 (GRCm39) |
missense |
probably damaging |
1.00 |
R5380:Nrap
|
UTSW |
19 |
56,370,035 (GRCm39) |
missense |
probably damaging |
1.00 |
R5576:Nrap
|
UTSW |
19 |
56,310,414 (GRCm39) |
missense |
probably damaging |
0.99 |
R5631:Nrap
|
UTSW |
19 |
56,342,553 (GRCm39) |
missense |
probably benign |
0.19 |
R5754:Nrap
|
UTSW |
19 |
56,377,916 (GRCm39) |
missense |
possibly damaging |
0.55 |
R5799:Nrap
|
UTSW |
19 |
56,330,601 (GRCm39) |
nonsense |
probably null |
|
R5899:Nrap
|
UTSW |
19 |
56,329,006 (GRCm39) |
missense |
possibly damaging |
0.80 |
R5910:Nrap
|
UTSW |
19 |
56,330,743 (GRCm39) |
missense |
probably benign |
0.00 |
R5994:Nrap
|
UTSW |
19 |
56,340,031 (GRCm39) |
nonsense |
probably null |
|
R6124:Nrap
|
UTSW |
19 |
56,374,458 (GRCm39) |
missense |
probably damaging |
0.97 |
R6149:Nrap
|
UTSW |
19 |
56,377,885 (GRCm39) |
missense |
possibly damaging |
0.79 |
R6182:Nrap
|
UTSW |
19 |
56,350,130 (GRCm39) |
missense |
probably benign |
|
R6245:Nrap
|
UTSW |
19 |
56,368,307 (GRCm39) |
missense |
possibly damaging |
0.80 |
R6245:Nrap
|
UTSW |
19 |
56,342,653 (GRCm39) |
missense |
probably damaging |
1.00 |
R6270:Nrap
|
UTSW |
19 |
56,308,630 (GRCm39) |
missense |
probably benign |
0.00 |
R6274:Nrap
|
UTSW |
19 |
56,350,153 (GRCm39) |
missense |
probably benign |
0.21 |
R6340:Nrap
|
UTSW |
19 |
56,335,616 (GRCm39) |
missense |
probably damaging |
1.00 |
R6547:Nrap
|
UTSW |
19 |
56,339,998 (GRCm39) |
missense |
probably benign |
0.00 |
R6734:Nrap
|
UTSW |
19 |
56,333,941 (GRCm39) |
missense |
probably damaging |
0.99 |
R6770:Nrap
|
UTSW |
19 |
56,370,969 (GRCm39) |
splice site |
probably null |
|
R6812:Nrap
|
UTSW |
19 |
56,340,108 (GRCm39) |
missense |
probably damaging |
1.00 |
R6843:Nrap
|
UTSW |
19 |
56,368,651 (GRCm39) |
missense |
probably damaging |
1.00 |
R7207:Nrap
|
UTSW |
19 |
56,333,953 (GRCm39) |
missense |
probably damaging |
1.00 |
R7214:Nrap
|
UTSW |
19 |
56,366,567 (GRCm39) |
missense |
probably benign |
0.09 |
R7313:Nrap
|
UTSW |
19 |
56,330,700 (GRCm39) |
missense |
probably damaging |
0.97 |
R7515:Nrap
|
UTSW |
19 |
56,354,859 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7662:Nrap
|
UTSW |
19 |
56,308,715 (GRCm39) |
missense |
probably benign |
0.00 |
R7819:Nrap
|
UTSW |
19 |
56,323,720 (GRCm39) |
missense |
probably benign |
|
R7895:Nrap
|
UTSW |
19 |
56,342,584 (GRCm39) |
missense |
probably benign |
0.00 |
R8041:Nrap
|
UTSW |
19 |
56,352,768 (GRCm39) |
nonsense |
probably null |
|
R8046:Nrap
|
UTSW |
19 |
56,308,683 (GRCm39) |
missense |
possibly damaging |
0.46 |
R8066:Nrap
|
UTSW |
19 |
56,342,562 (GRCm39) |
missense |
possibly damaging |
0.94 |
R8129:Nrap
|
UTSW |
19 |
56,355,068 (GRCm39) |
splice site |
probably null |
|
R8188:Nrap
|
UTSW |
19 |
56,325,010 (GRCm39) |
nonsense |
probably null |
|
R8323:Nrap
|
UTSW |
19 |
56,378,255 (GRCm39) |
missense |
probably benign |
0.00 |
R8353:Nrap
|
UTSW |
19 |
56,312,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R8453:Nrap
|
UTSW |
19 |
56,312,352 (GRCm39) |
missense |
probably damaging |
1.00 |
R8693:Nrap
|
UTSW |
19 |
56,310,384 (GRCm39) |
missense |
probably damaging |
1.00 |
R8703:Nrap
|
UTSW |
19 |
56,323,703 (GRCm39) |
missense |
probably damaging |
1.00 |
R8810:Nrap
|
UTSW |
19 |
56,352,843 (GRCm39) |
critical splice acceptor site |
probably benign |
|
R8872:Nrap
|
UTSW |
19 |
56,308,627 (GRCm39) |
makesense |
probably null |
|
R8980:Nrap
|
UTSW |
19 |
56,343,970 (GRCm39) |
missense |
probably damaging |
1.00 |
R9201:Nrap
|
UTSW |
19 |
56,340,093 (GRCm39) |
missense |
probably damaging |
1.00 |
R9229:Nrap
|
UTSW |
19 |
56,310,339 (GRCm39) |
missense |
probably benign |
0.01 |
R9235:Nrap
|
UTSW |
19 |
56,330,760 (GRCm39) |
nonsense |
probably null |
|
R9323:Nrap
|
UTSW |
19 |
56,378,255 (GRCm39) |
missense |
probably benign |
0.00 |
R9327:Nrap
|
UTSW |
19 |
56,340,100 (GRCm39) |
missense |
probably benign |
0.25 |
R9329:Nrap
|
UTSW |
19 |
56,350,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R9468:Nrap
|
UTSW |
19 |
56,330,632 (GRCm39) |
missense |
possibly damaging |
0.52 |
R9517:Nrap
|
UTSW |
19 |
56,360,277 (GRCm39) |
missense |
probably benign |
0.00 |
R9639:Nrap
|
UTSW |
19 |
56,333,948 (GRCm39) |
missense |
possibly damaging |
0.63 |
R9657:Nrap
|
UTSW |
19 |
56,352,377 (GRCm39) |
missense |
probably benign |
0.27 |
R9709:Nrap
|
UTSW |
19 |
56,317,453 (GRCm39) |
missense |
probably benign |
0.08 |
R9709:Nrap
|
UTSW |
19 |
56,317,452 (GRCm39) |
missense |
probably damaging |
0.98 |
X0028:Nrap
|
UTSW |
19 |
56,323,652 (GRCm39) |
nonsense |
probably null |
|
Z1176:Nrap
|
UTSW |
19 |
56,333,949 (GRCm39) |
frame shift |
probably null |
|
Z1177:Nrap
|
UTSW |
19 |
56,333,196 (GRCm39) |
missense |
probably benign |
0.01 |
Z1177:Nrap
|
UTSW |
19 |
56,326,524 (GRCm39) |
missense |
probably damaging |
1.00 |
|