Other mutations in this stock |
Total: 50 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4931414P19Rik |
G |
A |
14: 54,828,857 (GRCm39) |
R215* |
probably null |
Het |
Brinp2 |
C |
A |
1: 158,074,416 (GRCm39) |
L568F |
probably damaging |
Het |
Brip1 |
T |
C |
11: 86,043,616 (GRCm39) |
Y316C |
probably damaging |
Het |
Cdk5rap2 |
ATGTG |
ATG |
4: 70,208,214 (GRCm39) |
|
probably null |
Het |
Cfap69 |
G |
T |
5: 5,634,645 (GRCm39) |
|
probably benign |
Het |
Chrnb4 |
T |
C |
9: 54,951,182 (GRCm39) |
E27G |
probably damaging |
Het |
Clec14a |
A |
G |
12: 58,315,430 (GRCm39) |
V64A |
possibly damaging |
Het |
Crygs |
A |
G |
16: 22,625,262 (GRCm39) |
Y60H |
probably damaging |
Het |
Dpp10 |
T |
A |
1: 123,281,216 (GRCm39) |
Q611L |
probably damaging |
Het |
Entpd1 |
T |
C |
19: 40,725,264 (GRCm39) |
L450P |
probably damaging |
Het |
Eogt |
G |
A |
6: 97,097,151 (GRCm39) |
S317L |
probably damaging |
Het |
Exosc10 |
T |
A |
4: 148,657,376 (GRCm39) |
S584T |
probably benign |
Het |
Fam184a |
C |
T |
10: 53,575,157 (GRCm39) |
V151I |
probably damaging |
Het |
Fbxo43 |
A |
G |
15: 36,152,258 (GRCm39) |
V517A |
probably damaging |
Het |
Flii |
T |
C |
11: 60,610,698 (GRCm39) |
T533A |
possibly damaging |
Het |
Frmpd1 |
T |
G |
4: 45,284,093 (GRCm39) |
H971Q |
probably benign |
Het |
Gata3 |
A |
T |
2: 9,867,954 (GRCm39) |
N333K |
probably damaging |
Het |
Ibtk |
A |
G |
9: 85,600,479 (GRCm39) |
I816T |
probably benign |
Het |
Kirrel1 |
C |
T |
3: 86,996,458 (GRCm39) |
M380I |
probably null |
Het |
Krt34 |
T |
C |
11: 99,931,791 (GRCm39) |
T143A |
probably benign |
Het |
Lipn |
G |
T |
19: 34,046,828 (GRCm39) |
M43I |
probably benign |
Het |
Lrp1b |
A |
G |
2: 41,335,206 (GRCm39) |
C779R |
probably damaging |
Het |
Mios |
G |
A |
6: 8,233,189 (GRCm39) |
R779Q |
probably damaging |
Het |
Mme |
A |
T |
3: 63,269,480 (GRCm39) |
|
probably benign |
Het |
Ncstn |
A |
G |
1: 171,897,640 (GRCm39) |
S418P |
probably benign |
Het |
Oprk1 |
T |
A |
1: 5,672,884 (GRCm39) |
C340* |
probably null |
Het |
Or10d1c |
T |
A |
9: 38,894,166 (GRCm39) |
Y58F |
probably damaging |
Het |
Or4c29 |
T |
C |
2: 88,739,952 (GRCm39) |
T262A |
possibly damaging |
Het |
Or4k39 |
T |
C |
2: 111,238,967 (GRCm39) |
V69A |
possibly damaging |
Het |
Or6c210 |
C |
T |
10: 129,496,143 (GRCm39) |
P156L |
probably benign |
Het |
Or6z7 |
G |
A |
7: 6,484,131 (GRCm39) |
A8V |
probably benign |
Het |
Pald1 |
T |
A |
10: 61,183,266 (GRCm39) |
N323Y |
probably damaging |
Het |
Pcdhac1 |
C |
A |
18: 37,224,945 (GRCm39) |
A586E |
probably damaging |
Het |
Pcnx2 |
C |
T |
8: 126,614,897 (GRCm39) |
A185T |
probably benign |
Het |
Pik3r1 |
G |
A |
13: 101,821,465 (GRCm39) |
H430Y |
probably benign |
Het |
Polr3b |
G |
A |
10: 84,556,382 (GRCm39) |
|
probably null |
Het |
Prl8a6 |
A |
T |
13: 27,617,015 (GRCm39) |
L225* |
probably null |
Het |
Psme4 |
T |
C |
11: 30,806,068 (GRCm39) |
S89P |
probably damaging |
Het |
Pygl |
G |
A |
12: 70,248,113 (GRCm39) |
T250I |
probably damaging |
Het |
Rgs13 |
T |
A |
1: 144,016,528 (GRCm39) |
K72* |
probably null |
Het |
Ryr2 |
T |
A |
13: 11,603,045 (GRCm39) |
I4514F |
probably damaging |
Het |
Septin3 |
A |
T |
15: 82,170,002 (GRCm39) |
D32V |
probably damaging |
Het |
Sfrp2 |
C |
T |
3: 83,674,335 (GRCm39) |
P163S |
possibly damaging |
Het |
Spata31 |
A |
G |
13: 65,068,745 (GRCm39) |
T298A |
probably benign |
Het |
Stxbp2 |
T |
C |
8: 3,683,369 (GRCm39) |
|
probably null |
Het |
Syne1 |
A |
T |
10: 5,002,345 (GRCm39) |
M282K |
possibly damaging |
Het |
Timd2 |
T |
C |
11: 46,561,847 (GRCm39) |
|
probably null |
Het |
Tlr11 |
G |
A |
14: 50,600,611 (GRCm39) |
V866I |
probably benign |
Het |
Trappc10 |
T |
C |
10: 78,056,020 (GRCm39) |
|
probably null |
Het |
Zfp512b |
AG |
AGG |
2: 181,230,556 (GRCm39) |
|
probably null |
Het |
|
Other mutations in Hectd1 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00402:Hectd1
|
APN |
12 |
51,806,215 (GRCm39) |
missense |
probably benign |
|
IGL00402:Hectd1
|
APN |
12 |
51,815,891 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL00419:Hectd1
|
APN |
12 |
51,810,818 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00518:Hectd1
|
APN |
12 |
51,823,272 (GRCm39) |
splice site |
probably benign |
|
IGL00565:Hectd1
|
APN |
12 |
51,837,181 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL00574:Hectd1
|
APN |
12 |
51,820,787 (GRCm39) |
missense |
probably benign |
0.17 |
IGL00576:Hectd1
|
APN |
12 |
51,806,092 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00788:Hectd1
|
APN |
12 |
51,795,571 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL00978:Hectd1
|
APN |
12 |
51,838,173 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01328:Hectd1
|
APN |
12 |
51,807,904 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01337:Hectd1
|
APN |
12 |
51,849,057 (GRCm39) |
missense |
possibly damaging |
0.95 |
IGL01634:Hectd1
|
APN |
12 |
51,850,562 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL01731:Hectd1
|
APN |
12 |
51,849,593 (GRCm39) |
missense |
possibly damaging |
0.59 |
IGL01920:Hectd1
|
APN |
12 |
51,829,337 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL01951:Hectd1
|
APN |
12 |
51,841,280 (GRCm39) |
nonsense |
probably null |
|
IGL01994:Hectd1
|
APN |
12 |
51,844,725 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02140:Hectd1
|
APN |
12 |
51,820,920 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02150:Hectd1
|
APN |
12 |
51,815,974 (GRCm39) |
missense |
probably damaging |
0.97 |
IGL02156:Hectd1
|
APN |
12 |
51,800,916 (GRCm39) |
splice site |
probably benign |
|
IGL02177:Hectd1
|
APN |
12 |
51,819,103 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02502:Hectd1
|
APN |
12 |
51,844,635 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL02505:Hectd1
|
APN |
12 |
51,847,496 (GRCm39) |
critical splice donor site |
probably null |
|
IGL02519:Hectd1
|
APN |
12 |
51,815,894 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02624:Hectd1
|
APN |
12 |
51,809,233 (GRCm39) |
missense |
possibly damaging |
0.61 |
IGL02833:Hectd1
|
APN |
12 |
51,810,864 (GRCm39) |
missense |
probably damaging |
0.96 |
IGL02851:Hectd1
|
APN |
12 |
51,814,423 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02866:Hectd1
|
APN |
12 |
51,837,396 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02981:Hectd1
|
APN |
12 |
51,815,670 (GRCm39) |
missense |
possibly damaging |
0.70 |
IGL02987:Hectd1
|
APN |
12 |
51,791,550 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02999:Hectd1
|
APN |
12 |
51,874,205 (GRCm39) |
missense |
possibly damaging |
0.77 |
IGL03071:Hectd1
|
APN |
12 |
51,815,957 (GRCm39) |
missense |
probably benign |
0.00 |
IGL03078:Hectd1
|
APN |
12 |
51,849,019 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL03299:Hectd1
|
APN |
12 |
51,847,671 (GRCm39) |
splice site |
probably benign |
|
3-1:Hectd1
|
UTSW |
12 |
51,800,590 (GRCm39) |
missense |
probably damaging |
0.99 |
R0039:Hectd1
|
UTSW |
12 |
51,800,608 (GRCm39) |
missense |
possibly damaging |
0.83 |
R0238:Hectd1
|
UTSW |
12 |
51,816,101 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0238:Hectd1
|
UTSW |
12 |
51,816,101 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0239:Hectd1
|
UTSW |
12 |
51,816,101 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0239:Hectd1
|
UTSW |
12 |
51,816,101 (GRCm39) |
missense |
possibly damaging |
0.72 |
R0268:Hectd1
|
UTSW |
12 |
51,815,891 (GRCm39) |
missense |
possibly damaging |
0.94 |
R0268:Hectd1
|
UTSW |
12 |
51,815,890 (GRCm39) |
missense |
probably damaging |
0.99 |
R0409:Hectd1
|
UTSW |
12 |
51,829,339 (GRCm39) |
missense |
possibly damaging |
0.59 |
R1019:Hectd1
|
UTSW |
12 |
51,795,440 (GRCm39) |
missense |
probably damaging |
0.99 |
R1072:Hectd1
|
UTSW |
12 |
51,807,855 (GRCm39) |
missense |
probably benign |
0.11 |
R1087:Hectd1
|
UTSW |
12 |
51,823,355 (GRCm39) |
missense |
probably damaging |
0.99 |
R1165:Hectd1
|
UTSW |
12 |
51,810,947 (GRCm39) |
splice site |
probably benign |
|
R1350:Hectd1
|
UTSW |
12 |
51,809,217 (GRCm39) |
missense |
probably benign |
|
R1553:Hectd1
|
UTSW |
12 |
51,820,661 (GRCm39) |
missense |
probably damaging |
0.98 |
R1666:Hectd1
|
UTSW |
12 |
51,800,607 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1676:Hectd1
|
UTSW |
12 |
51,791,571 (GRCm39) |
missense |
probably damaging |
1.00 |
R1694:Hectd1
|
UTSW |
12 |
51,791,375 (GRCm39) |
missense |
probably damaging |
1.00 |
R1778:Hectd1
|
UTSW |
12 |
51,800,590 (GRCm39) |
missense |
probably damaging |
0.99 |
R1856:Hectd1
|
UTSW |
12 |
51,791,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R1859:Hectd1
|
UTSW |
12 |
51,853,350 (GRCm39) |
missense |
probably damaging |
1.00 |
R1884:Hectd1
|
UTSW |
12 |
51,847,738 (GRCm39) |
missense |
probably benign |
0.00 |
R1982:Hectd1
|
UTSW |
12 |
51,832,624 (GRCm39) |
missense |
probably damaging |
0.97 |
R2034:Hectd1
|
UTSW |
12 |
51,803,899 (GRCm39) |
splice site |
probably null |
|
R2061:Hectd1
|
UTSW |
12 |
51,841,227 (GRCm39) |
missense |
probably damaging |
0.99 |
R2078:Hectd1
|
UTSW |
12 |
51,795,325 (GRCm39) |
missense |
probably damaging |
0.99 |
R2176:Hectd1
|
UTSW |
12 |
51,792,277 (GRCm39) |
missense |
probably damaging |
1.00 |
R2210:Hectd1
|
UTSW |
12 |
51,853,245 (GRCm39) |
missense |
probably damaging |
0.99 |
R2248:Hectd1
|
UTSW |
12 |
51,853,254 (GRCm39) |
missense |
probably damaging |
0.99 |
R2282:Hectd1
|
UTSW |
12 |
51,815,791 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2402:Hectd1
|
UTSW |
12 |
51,792,317 (GRCm39) |
missense |
probably benign |
0.01 |
R4027:Hectd1
|
UTSW |
12 |
51,849,219 (GRCm39) |
critical splice acceptor site |
probably null |
|
R4085:Hectd1
|
UTSW |
12 |
51,821,533 (GRCm39) |
missense |
possibly damaging |
0.93 |
R4115:Hectd1
|
UTSW |
12 |
51,815,506 (GRCm39) |
nonsense |
probably null |
|
R4116:Hectd1
|
UTSW |
12 |
51,815,506 (GRCm39) |
nonsense |
probably null |
|
R4169:Hectd1
|
UTSW |
12 |
51,837,008 (GRCm39) |
missense |
probably damaging |
0.97 |
R4434:Hectd1
|
UTSW |
12 |
51,798,835 (GRCm39) |
missense |
probably damaging |
1.00 |
R4507:Hectd1
|
UTSW |
12 |
51,837,276 (GRCm39) |
missense |
probably damaging |
0.97 |
R4578:Hectd1
|
UTSW |
12 |
51,798,715 (GRCm39) |
missense |
probably damaging |
1.00 |
R4579:Hectd1
|
UTSW |
12 |
51,791,356 (GRCm39) |
missense |
probably damaging |
0.97 |
R4709:Hectd1
|
UTSW |
12 |
51,834,695 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4812:Hectd1
|
UTSW |
12 |
51,874,134 (GRCm39) |
critical splice donor site |
probably null |
|
R4883:Hectd1
|
UTSW |
12 |
51,831,030 (GRCm39) |
nonsense |
probably null |
|
R4885:Hectd1
|
UTSW |
12 |
51,847,505 (GRCm39) |
missense |
probably damaging |
0.97 |
R4975:Hectd1
|
UTSW |
12 |
51,809,280 (GRCm39) |
missense |
probably benign |
0.02 |
R4983:Hectd1
|
UTSW |
12 |
51,831,045 (GRCm39) |
missense |
probably benign |
0.01 |
R5007:Hectd1
|
UTSW |
12 |
51,849,443 (GRCm39) |
missense |
possibly damaging |
0.95 |
R5046:Hectd1
|
UTSW |
12 |
51,797,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R5062:Hectd1
|
UTSW |
12 |
51,791,662 (GRCm39) |
missense |
probably damaging |
0.98 |
R5164:Hectd1
|
UTSW |
12 |
51,874,272 (GRCm39) |
start codon destroyed |
probably null |
0.60 |
R5213:Hectd1
|
UTSW |
12 |
51,849,316 (GRCm39) |
critical splice donor site |
probably null |
|
R5535:Hectd1
|
UTSW |
12 |
51,849,109 (GRCm39) |
missense |
probably damaging |
0.98 |
R5776:Hectd1
|
UTSW |
12 |
51,810,897 (GRCm39) |
missense |
possibly damaging |
0.91 |
R5846:Hectd1
|
UTSW |
12 |
51,820,618 (GRCm39) |
missense |
probably damaging |
0.99 |
R5907:Hectd1
|
UTSW |
12 |
51,845,537 (GRCm39) |
missense |
probably damaging |
0.98 |
R5911:Hectd1
|
UTSW |
12 |
51,849,035 (GRCm39) |
missense |
probably damaging |
0.99 |
R5919:Hectd1
|
UTSW |
12 |
51,815,855 (GRCm39) |
missense |
probably damaging |
0.98 |
R6051:Hectd1
|
UTSW |
12 |
51,800,887 (GRCm39) |
missense |
probably benign |
|
R6141:Hectd1
|
UTSW |
12 |
51,792,875 (GRCm39) |
critical splice donor site |
probably null |
|
R6172:Hectd1
|
UTSW |
12 |
51,816,065 (GRCm39) |
missense |
probably damaging |
1.00 |
R6194:Hectd1
|
UTSW |
12 |
51,795,228 (GRCm39) |
missense |
probably damaging |
0.99 |
R6356:Hectd1
|
UTSW |
12 |
51,791,402 (GRCm39) |
missense |
probably damaging |
1.00 |
R6795:Hectd1
|
UTSW |
12 |
51,841,270 (GRCm39) |
missense |
possibly damaging |
0.94 |
R6909:Hectd1
|
UTSW |
12 |
51,810,945 (GRCm39) |
splice site |
probably null |
|
R6971:Hectd1
|
UTSW |
12 |
51,795,526 (GRCm39) |
nonsense |
probably null |
|
R7079:Hectd1
|
UTSW |
12 |
51,834,638 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7104:Hectd1
|
UTSW |
12 |
51,874,134 (GRCm39) |
critical splice donor site |
probably null |
|
R7171:Hectd1
|
UTSW |
12 |
51,806,080 (GRCm39) |
missense |
probably damaging |
0.99 |
R7296:Hectd1
|
UTSW |
12 |
51,832,635 (GRCm39) |
missense |
possibly damaging |
0.73 |
R7346:Hectd1
|
UTSW |
12 |
51,797,104 (GRCm39) |
missense |
probably benign |
|
R7355:Hectd1
|
UTSW |
12 |
51,838,081 (GRCm39) |
missense |
possibly damaging |
0.72 |
R7468:Hectd1
|
UTSW |
12 |
51,791,588 (GRCm39) |
splice site |
probably null |
|
R7531:Hectd1
|
UTSW |
12 |
51,853,150 (GRCm39) |
missense |
probably benign |
0.33 |
R7532:Hectd1
|
UTSW |
12 |
51,837,233 (GRCm39) |
missense |
probably damaging |
0.98 |
R7755:Hectd1
|
UTSW |
12 |
51,849,003 (GRCm39) |
missense |
possibly damaging |
0.86 |
R7807:Hectd1
|
UTSW |
12 |
51,792,171 (GRCm39) |
missense |
probably damaging |
1.00 |
R7842:Hectd1
|
UTSW |
12 |
51,819,343 (GRCm39) |
missense |
probably damaging |
0.99 |
R7922:Hectd1
|
UTSW |
12 |
51,836,978 (GRCm39) |
nonsense |
probably null |
|
R8059:Hectd1
|
UTSW |
12 |
51,837,161 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8085:Hectd1
|
UTSW |
12 |
51,795,679 (GRCm39) |
missense |
probably damaging |
0.97 |
R8145:Hectd1
|
UTSW |
12 |
51,831,016 (GRCm39) |
missense |
possibly damaging |
0.72 |
R8157:Hectd1
|
UTSW |
12 |
51,838,073 (GRCm39) |
missense |
possibly damaging |
0.53 |
R8405:Hectd1
|
UTSW |
12 |
51,874,178 (GRCm39) |
missense |
probably benign |
0.01 |
R8505:Hectd1
|
UTSW |
12 |
51,797,145 (GRCm39) |
missense |
probably damaging |
1.00 |
R8511:Hectd1
|
UTSW |
12 |
51,834,654 (GRCm39) |
missense |
probably benign |
0.01 |
R8697:Hectd1
|
UTSW |
12 |
51,819,320 (GRCm39) |
critical splice donor site |
probably benign |
|
R8725:Hectd1
|
UTSW |
12 |
51,849,000 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8727:Hectd1
|
UTSW |
12 |
51,849,000 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8911:Hectd1
|
UTSW |
12 |
51,795,616 (GRCm39) |
missense |
probably damaging |
0.99 |
R8983:Hectd1
|
UTSW |
12 |
51,791,410 (GRCm39) |
missense |
probably damaging |
0.97 |
R9037:Hectd1
|
UTSW |
12 |
51,832,665 (GRCm39) |
missense |
possibly damaging |
0.85 |
R9219:Hectd1
|
UTSW |
12 |
51,800,612 (GRCm39) |
missense |
probably damaging |
0.99 |
R9413:Hectd1
|
UTSW |
12 |
51,792,880 (GRCm39) |
nonsense |
probably null |
|
R9456:Hectd1
|
UTSW |
12 |
51,832,584 (GRCm39) |
missense |
probably benign |
|
R9513:Hectd1
|
UTSW |
12 |
51,816,079 (GRCm39) |
missense |
possibly damaging |
0.92 |
R9640:Hectd1
|
UTSW |
12 |
51,795,197 (GRCm39) |
nonsense |
probably null |
|
R9641:Hectd1
|
UTSW |
12 |
51,816,047 (GRCm39) |
missense |
probably benign |
0.00 |
R9713:Hectd1
|
UTSW |
12 |
51,823,328 (GRCm39) |
missense |
probably benign |
0.02 |
|