Other mutations in this stock |
Total: 72 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
1700003E16Rik |
T |
G |
6: 83,133,556 (GRCm39) |
M1R |
probably null |
Het |
Acap2 |
T |
C |
16: 30,946,238 (GRCm39) |
D235G |
probably damaging |
Het |
Adgrv1 |
C |
A |
13: 81,647,241 (GRCm39) |
V3100F |
probably damaging |
Het |
Aff4 |
A |
G |
11: 53,288,686 (GRCm39) |
T401A |
probably damaging |
Het |
Apcs |
T |
C |
1: 172,722,391 (GRCm39) |
T22A |
probably benign |
Het |
Atf7ip2 |
T |
C |
16: 10,059,738 (GRCm39) |
V426A |
possibly damaging |
Het |
Bach2 |
A |
G |
4: 32,562,175 (GRCm39) |
D214G |
possibly damaging |
Het |
Baz2a |
C |
T |
10: 127,960,925 (GRCm39) |
A1578V |
possibly damaging |
Het |
Camk1d |
T |
C |
2: 5,449,954 (GRCm39) |
I76V |
probably benign |
Het |
Ccdc182 |
A |
T |
11: 88,185,324 (GRCm39) |
M135L |
probably benign |
Het |
Cd47 |
C |
T |
16: 49,716,731 (GRCm39) |
T201I |
|
Het |
Chodl |
T |
C |
16: 78,746,030 (GRCm39) |
S290P |
possibly damaging |
Het |
Chst15 |
A |
G |
7: 131,868,520 (GRCm39) |
L300P |
possibly damaging |
Het |
Ciita |
T |
C |
16: 10,324,571 (GRCm39) |
S168P |
probably damaging |
Het |
Cntn2 |
C |
T |
1: 132,456,678 (GRCm39) |
V123I |
probably benign |
Het |
Cyld |
T |
A |
8: 89,457,348 (GRCm39) |
L527Q |
probably benign |
Het |
Dbn1 |
T |
A |
13: 55,631,241 (GRCm39) |
Y34F |
probably damaging |
Het |
Enc1 |
C |
A |
13: 97,383,018 (GRCm39) |
Y509* |
probably null |
Het |
Ermard |
A |
T |
17: 15,273,643 (GRCm39) |
E409D |
probably benign |
Het |
Extl3 |
T |
C |
14: 65,314,765 (GRCm39) |
E139G |
possibly damaging |
Het |
Fa2h |
A |
T |
8: 112,082,115 (GRCm39) |
V177E |
possibly damaging |
Het |
Flot2 |
T |
C |
11: 77,949,772 (GRCm39) |
I367T |
probably damaging |
Het |
Fras1 |
T |
C |
5: 96,884,813 (GRCm39) |
Y2564H |
probably damaging |
Het |
Fxyd3 |
A |
G |
7: 30,773,018 (GRCm39) |
V10A |
probably benign |
Het |
Gfra3 |
A |
G |
18: 34,837,560 (GRCm39) |
L146P |
probably damaging |
Het |
Gm49359 |
T |
C |
13: 62,602,448 (GRCm39) |
N251D |
probably benign |
Het |
Hps6 |
A |
G |
19: 45,992,542 (GRCm39) |
S160G |
probably benign |
Het |
Hsd17b7 |
C |
A |
1: 169,794,875 (GRCm39) |
A55S |
probably damaging |
Het |
Hspa12a |
T |
C |
19: 58,789,298 (GRCm39) |
D446G |
probably benign |
Het |
Htt |
G |
A |
5: 34,989,957 (GRCm39) |
R1163Q |
possibly damaging |
Het |
Ift81 |
T |
C |
5: 122,697,833 (GRCm39) |
|
probably null |
Het |
Ighv5-15 |
T |
G |
12: 113,790,395 (GRCm39) |
Y75S |
probably benign |
Het |
Kcnd2 |
T |
A |
6: 21,725,981 (GRCm39) |
H491Q |
probably damaging |
Het |
Lamb3 |
C |
A |
1: 193,014,665 (GRCm39) |
T608K |
probably benign |
Het |
Lrtm2 |
T |
A |
6: 119,297,412 (GRCm39) |
K210* |
probably null |
Het |
Med13 |
G |
T |
11: 86,189,283 (GRCm39) |
P1209T |
probably benign |
Het |
Mtus1 |
G |
A |
8: 41,537,239 (GRCm39) |
T159I |
probably damaging |
Het |
Myt1l |
A |
G |
12: 29,901,659 (GRCm39) |
M805V |
unknown |
Het |
Neb |
G |
T |
2: 52,160,231 (GRCm39) |
L2261I |
probably benign |
Het |
Nlrp4c |
G |
A |
7: 6,068,498 (GRCm39) |
R133H |
probably benign |
Het |
Nol11 |
A |
T |
11: 107,071,765 (GRCm39) |
L276Q |
probably damaging |
Het |
Or13c9 |
G |
A |
4: 52,936,211 (GRCm39) |
T24M |
probably damaging |
Het |
Or52p1 |
A |
G |
7: 104,267,705 (GRCm39) |
H273R |
probably damaging |
Het |
Pou2f3 |
A |
G |
9: 43,040,224 (GRCm39) |
S355P |
probably damaging |
Het |
Ppm1l |
C |
A |
3: 69,460,453 (GRCm39) |
N343K |
probably damaging |
Het |
Prh1 |
A |
T |
6: 132,548,573 (GRCm39) |
I27F |
unknown |
Het |
Prkrip1 |
A |
T |
5: 136,223,203 (GRCm39) |
L85Q |
probably damaging |
Het |
Pycr3 |
C |
T |
15: 75,790,563 (GRCm39) |
V99I |
probably benign |
Het |
R3hdm4 |
T |
A |
10: 79,749,393 (GRCm39) |
N72I |
probably damaging |
Het |
Rab11fip3 |
G |
T |
17: 26,231,032 (GRCm39) |
H738N |
probably benign |
Het |
Rtl1 |
G |
A |
12: 109,556,673 (GRCm39) |
A1722V |
possibly damaging |
Het |
Sell |
A |
G |
1: 163,893,122 (GRCm39) |
N113D |
probably damaging |
Het |
Smarcal1 |
T |
C |
1: 72,665,697 (GRCm39) |
S732P |
probably damaging |
Het |
Smurf2 |
A |
T |
11: 106,743,424 (GRCm39) |
D207E |
probably benign |
Het |
Spata31h1 |
G |
A |
10: 82,121,439 (GRCm39) |
S3857L |
probably benign |
Het |
Tat |
C |
T |
8: 110,723,510 (GRCm39) |
R333C |
probably benign |
Het |
Tmem121b |
A |
T |
6: 120,469,234 (GRCm39) |
F494L |
probably damaging |
Het |
Tmem198 |
C |
A |
1: 75,456,522 (GRCm39) |
P89Q |
probably damaging |
Het |
Tnks2 |
T |
G |
19: 36,835,284 (GRCm39) |
C2G |
probably damaging |
Het |
Trappc9 |
T |
C |
15: 72,673,202 (GRCm39) |
E869G |
unknown |
Het |
Trim42 |
T |
A |
9: 97,251,584 (GRCm39) |
K105M |
probably benign |
Het |
Ttll3 |
T |
C |
6: 113,369,635 (GRCm39) |
S60P |
probably benign |
Het |
Ttll4 |
T |
A |
1: 74,725,121 (GRCm39) |
I625N |
possibly damaging |
Het |
Tubgcp5 |
T |
A |
7: 55,479,181 (GRCm39) |
|
probably null |
Het |
Txlnb |
A |
T |
10: 17,682,594 (GRCm39) |
Y172F |
probably damaging |
Het |
Ube2e3 |
A |
T |
2: 78,744,035 (GRCm39) |
D88V |
possibly damaging |
Het |
Vmn1r189 |
T |
A |
13: 22,286,430 (GRCm39) |
I136L |
probably benign |
Het |
Vmn2r71 |
A |
G |
7: 85,267,950 (GRCm39) |
I135V |
probably benign |
Het |
Vmn2r73 |
T |
A |
7: 85,519,073 (GRCm39) |
R516S |
probably benign |
Het |
Wrn |
C |
T |
8: 33,731,006 (GRCm39) |
E1352K |
probably benign |
Het |
Zfp318 |
T |
C |
17: 46,722,139 (GRCm39) |
S1381P |
probably damaging |
Het |
Zfp747 |
A |
T |
7: 126,973,655 (GRCm39) |
Y172N |
probably damaging |
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 |
|
R7836:Nrap
|
UTSW |
19 |
56,338,729 (GRCm39) |
missense |
probably benign |
0.00 |
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 |
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 |
|