Other mutations in this stock |
Total: 80 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adgb |
T |
C |
10: 10,225,321 (GRCm39) |
Y1415C |
probably damaging |
Het |
Adgrf1 |
T |
C |
17: 43,614,563 (GRCm39) |
S216P |
probably damaging |
Het |
Ankrd12 |
T |
C |
17: 66,338,428 (GRCm39) |
D197G |
probably damaging |
Het |
Aoc3 |
C |
A |
11: 101,222,488 (GRCm39) |
H198Q |
probably damaging |
Het |
Aox1 |
C |
A |
1: 58,143,640 (GRCm39) |
H1253N |
probably benign |
Het |
Arg1 |
T |
A |
10: 24,798,536 (GRCm39) |
E38V |
possibly damaging |
Het |
Baz2b |
T |
A |
2: 59,738,087 (GRCm39) |
M1741L |
probably benign |
Het |
Bend4 |
T |
C |
5: 67,574,915 (GRCm39) |
E322G |
probably damaging |
Het |
Brpf1 |
T |
C |
6: 113,294,639 (GRCm39) |
V661A |
possibly damaging |
Het |
C2cd3 |
A |
T |
7: 100,104,160 (GRCm39) |
T2058S |
probably damaging |
Het |
Camk4 |
T |
C |
18: 33,309,266 (GRCm39) |
V223A |
probably damaging |
Het |
Casp1 |
C |
T |
9: 5,306,742 (GRCm39) |
R395C |
probably damaging |
Het |
Ccdc180 |
T |
G |
4: 45,923,244 (GRCm39) |
I1066S |
probably damaging |
Het |
Ccne1 |
A |
G |
7: 37,798,744 (GRCm39) |
F292L |
probably damaging |
Het |
Ccz1 |
A |
T |
5: 143,949,628 (GRCm39) |
M100K |
probably damaging |
Het |
Cep128 |
T |
C |
12: 91,226,936 (GRCm39) |
T678A |
probably benign |
Het |
Cep290 |
G |
A |
10: 100,330,773 (GRCm39) |
R151Q |
probably benign |
Het |
Crip3 |
A |
G |
17: 46,741,673 (GRCm39) |
|
probably benign |
Het |
Ddx60 |
A |
G |
8: 62,474,348 (GRCm39) |
M1479V |
possibly damaging |
Het |
Defb40 |
T |
A |
8: 19,025,093 (GRCm39) |
I38F |
probably benign |
Het |
Dnajb2 |
C |
T |
1: 75,220,198 (GRCm39) |
T221I |
possibly damaging |
Het |
Dpysl3 |
T |
C |
18: 43,467,079 (GRCm39) |
I279V |
probably damaging |
Het |
Echs1 |
G |
A |
7: 139,692,499 (GRCm39) |
|
probably benign |
Het |
Efl1 |
T |
A |
7: 82,320,835 (GRCm39) |
N89K |
probably damaging |
Het |
Extl3 |
T |
C |
14: 65,313,443 (GRCm39) |
T580A |
probably benign |
Het |
Fam171a2 |
C |
T |
11: 102,330,982 (GRCm39) |
G193E |
probably damaging |
Het |
Fam234a |
A |
T |
17: 26,435,591 (GRCm39) |
D264E |
probably benign |
Het |
Fbxw20 |
A |
T |
9: 109,063,763 (GRCm39) |
V3D |
possibly damaging |
Het |
Fig4 |
G |
A |
10: 41,109,586 (GRCm39) |
P637L |
probably benign |
Het |
Fnbp1l |
G |
A |
3: 122,339,964 (GRCm39) |
T496I |
probably benign |
Het |
Fry |
T |
C |
5: 150,325,108 (GRCm39) |
V1175A |
possibly damaging |
Het |
Gm5617 |
C |
T |
9: 48,406,968 (GRCm39) |
A34V |
possibly damaging |
Het |
Gnai1 |
A |
T |
5: 18,496,596 (GRCm39) |
V109E |
probably benign |
Het |
H2-K2 |
A |
T |
17: 34,216,298 (GRCm39) |
Y283N |
probably benign |
Het |
Hsdl2 |
T |
C |
4: 59,612,812 (GRCm39) |
|
probably null |
Het |
Igkv3-1 |
T |
C |
6: 70,681,028 (GRCm39) |
S76P |
probably damaging |
Het |
Krt15 |
A |
T |
11: 100,022,897 (GRCm39) |
S439R |
probably benign |
Het |
Lama2 |
TTTGCGCATT |
TTT |
10: 26,919,639 (GRCm39) |
|
probably null |
Het |
Lima1 |
G |
A |
15: 99,717,457 (GRCm39) |
T23I |
probably benign |
Het |
Map4k1 |
C |
A |
7: 28,688,195 (GRCm39) |
H248Q |
probably damaging |
Het |
Mcf2l |
C |
A |
8: 13,063,972 (GRCm39) |
T1004K |
probably damaging |
Het |
Meak7 |
T |
G |
8: 120,499,262 (GRCm39) |
T77P |
probably benign |
Het |
Micall1 |
T |
A |
15: 79,007,146 (GRCm39) |
|
probably benign |
Het |
Ms4a14 |
A |
G |
19: 11,278,976 (GRCm39) |
I1194T |
probably benign |
Het |
Mtor |
T |
C |
4: 148,539,273 (GRCm39) |
*257Q |
probably null |
Het |
Mucl3 |
G |
A |
17: 35,948,468 (GRCm39) |
T377I |
possibly damaging |
Het |
Ncan |
T |
A |
8: 70,556,705 (GRCm39) |
T961S |
probably benign |
Het |
Odad4 |
A |
G |
11: 100,441,147 (GRCm39) |
N126S |
probably damaging |
Het |
Or10z1 |
A |
T |
1: 174,078,262 (GRCm39) |
I77N |
probably damaging |
Het |
Or1e29 |
T |
A |
11: 73,667,372 (GRCm39) |
L260F |
probably benign |
Het |
Or1f19 |
T |
C |
16: 3,410,706 (GRCm39) |
S149P |
probably damaging |
Het |
Or2t49 |
T |
A |
11: 58,392,735 (GRCm39) |
I216F |
probably damaging |
Het |
Or8h10 |
T |
G |
2: 86,808,693 (GRCm39) |
Y149S |
probably damaging |
Het |
Or9e1 |
T |
A |
11: 58,732,033 (GRCm39) |
L31H |
possibly damaging |
Het |
Pcdhgb2 |
A |
G |
18: 37,825,153 (GRCm39) |
R715G |
probably benign |
Het |
Pik3c3 |
T |
C |
18: 30,477,131 (GRCm39) |
|
probably null |
Het |
Pkhd1l1 |
A |
T |
15: 44,354,497 (GRCm39) |
D296V |
probably damaging |
Het |
Plekhh2 |
A |
G |
17: 84,908,125 (GRCm39) |
I1189V |
probably damaging |
Het |
Psg18 |
A |
T |
7: 18,087,409 (GRCm39) |
L83Q |
possibly damaging |
Het |
Rps6kc1 |
A |
G |
1: 190,532,515 (GRCm39) |
W496R |
probably damaging |
Het |
Setd5 |
C |
T |
6: 113,126,527 (GRCm39) |
T1188I |
probably damaging |
Het |
Slc4a3 |
T |
C |
1: 75,531,729 (GRCm39) |
F899L |
probably damaging |
Het |
Slitrk6 |
T |
C |
14: 110,989,315 (GRCm39) |
T131A |
probably damaging |
Het |
Speg |
G |
T |
1: 75,398,379 (GRCm39) |
R1942L |
probably damaging |
Het |
Sulf2 |
C |
A |
2: 165,923,524 (GRCm39) |
R565L |
probably benign |
Het |
Tcerg1 |
T |
C |
18: 42,657,046 (GRCm39) |
M176T |
unknown |
Het |
Tfcp2l1 |
T |
C |
1: 118,597,239 (GRCm39) |
I440T |
possibly damaging |
Het |
Tgm7 |
A |
T |
2: 120,929,445 (GRCm39) |
|
probably null |
Het |
Tjp2 |
C |
A |
19: 24,099,484 (GRCm39) |
G433V |
probably damaging |
Het |
Tmc7 |
C |
T |
7: 118,142,565 (GRCm39) |
G608R |
probably damaging |
Het |
Tmed4 |
A |
G |
11: 6,224,456 (GRCm39) |
F68S |
possibly damaging |
Het |
Tmem30b |
G |
A |
12: 73,592,686 (GRCm39) |
P143L |
probably damaging |
Het |
Tnfrsf23 |
C |
T |
7: 143,235,217 (GRCm39) |
C49Y |
probably damaging |
Het |
Tnni3k |
A |
T |
3: 154,492,445 (GRCm39) |
|
probably null |
Het |
Trav12-2 |
G |
T |
14: 53,854,150 (GRCm39) |
M41I |
probably benign |
Het |
Trim6 |
T |
A |
7: 103,881,692 (GRCm39) |
Y314* |
probably null |
Het |
Utp25 |
A |
G |
1: 192,796,072 (GRCm39) |
Y686H |
probably damaging |
Het |
Vmn2r118 |
A |
G |
17: 55,899,894 (GRCm39) |
V670A |
probably damaging |
Het |
Zfp438 |
A |
T |
18: 5,213,154 (GRCm39) |
D601E |
probably benign |
Het |
Zfp606 |
T |
A |
7: 12,226,983 (GRCm39) |
I310N |
possibly damaging |
Het |
|
Other mutations in Hectd2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00515:Hectd2
|
APN |
19 |
36,562,336 (GRCm39) |
missense |
probably benign |
|
IGL01024:Hectd2
|
APN |
19 |
36,583,793 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01111:Hectd2
|
APN |
19 |
36,574,520 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01301:Hectd2
|
APN |
19 |
36,546,770 (GRCm39) |
splice site |
probably benign |
|
IGL02019:Hectd2
|
APN |
19 |
36,592,916 (GRCm39) |
missense |
possibly damaging |
0.94 |
IGL02410:Hectd2
|
APN |
19 |
36,572,613 (GRCm39) |
nonsense |
probably null |
|
IGL02793:Hectd2
|
APN |
19 |
36,564,821 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03010:Hectd2
|
APN |
19 |
36,593,002 (GRCm39) |
missense |
probably benign |
0.01 |
IGL03115:Hectd2
|
APN |
19 |
36,577,121 (GRCm39) |
critical splice donor site |
probably null |
|
IGL03251:Hectd2
|
APN |
19 |
36,562,926 (GRCm39) |
missense |
probably damaging |
1.00 |
chopstix1
|
UTSW |
19 |
36,586,816 (GRCm39) |
missense |
possibly damaging |
0.75 |
Chopstix3
|
UTSW |
19 |
36,592,908 (GRCm39) |
nonsense |
probably null |
|
R0402:Hectd2
|
UTSW |
19 |
36,578,929 (GRCm39) |
critical splice donor site |
probably null |
|
R0415:Hectd2
|
UTSW |
19 |
36,562,284 (GRCm39) |
unclassified |
probably benign |
|
R0576:Hectd2
|
UTSW |
19 |
36,562,897 (GRCm39) |
missense |
probably benign |
|
R0685:Hectd2
|
UTSW |
19 |
36,546,831 (GRCm39) |
missense |
probably damaging |
0.99 |
R1460:Hectd2
|
UTSW |
19 |
36,592,908 (GRCm39) |
nonsense |
probably null |
|
R1791:Hectd2
|
UTSW |
19 |
36,586,816 (GRCm39) |
missense |
possibly damaging |
0.75 |
R1895:Hectd2
|
UTSW |
19 |
36,591,860 (GRCm39) |
missense |
probably damaging |
1.00 |
R1928:Hectd2
|
UTSW |
19 |
36,589,719 (GRCm39) |
missense |
probably damaging |
1.00 |
R2116:Hectd2
|
UTSW |
19 |
36,591,824 (GRCm39) |
missense |
probably damaging |
0.99 |
R2520:Hectd2
|
UTSW |
19 |
36,589,633 (GRCm39) |
critical splice donor site |
probably null |
|
R4693:Hectd2
|
UTSW |
19 |
36,591,738 (GRCm39) |
splice site |
probably benign |
|
R4943:Hectd2
|
UTSW |
19 |
36,581,647 (GRCm39) |
splice site |
probably null |
|
R5031:Hectd2
|
UTSW |
19 |
36,577,004 (GRCm39) |
missense |
probably damaging |
1.00 |
R5408:Hectd2
|
UTSW |
19 |
36,532,296 (GRCm39) |
missense |
possibly damaging |
0.46 |
R5621:Hectd2
|
UTSW |
19 |
36,596,151 (GRCm39) |
missense |
probably damaging |
1.00 |
R5652:Hectd2
|
UTSW |
19 |
36,581,720 (GRCm39) |
missense |
probably damaging |
1.00 |
R5704:Hectd2
|
UTSW |
19 |
36,576,291 (GRCm39) |
missense |
possibly damaging |
0.93 |
R5950:Hectd2
|
UTSW |
19 |
36,574,639 (GRCm39) |
intron |
probably benign |
|
R6414:Hectd2
|
UTSW |
19 |
36,596,186 (GRCm39) |
missense |
probably benign |
0.21 |
R6438:Hectd2
|
UTSW |
19 |
36,596,242 (GRCm39) |
makesense |
probably null |
|
R6544:Hectd2
|
UTSW |
19 |
36,589,728 (GRCm39) |
missense |
probably damaging |
1.00 |
R6545:Hectd2
|
UTSW |
19 |
36,564,778 (GRCm39) |
missense |
probably benign |
0.35 |
R6629:Hectd2
|
UTSW |
19 |
36,592,938 (GRCm39) |
missense |
probably damaging |
1.00 |
R6672:Hectd2
|
UTSW |
19 |
36,564,780 (GRCm39) |
missense |
probably damaging |
1.00 |
R6741:Hectd2
|
UTSW |
19 |
36,589,759 (GRCm39) |
missense |
probably damaging |
1.00 |
R7117:Hectd2
|
UTSW |
19 |
36,577,055 (GRCm39) |
missense |
probably benign |
0.29 |
R7238:Hectd2
|
UTSW |
19 |
36,574,478 (GRCm39) |
missense |
probably damaging |
0.98 |
R7555:Hectd2
|
UTSW |
19 |
36,589,803 (GRCm39) |
missense |
probably damaging |
1.00 |
R8184:Hectd2
|
UTSW |
19 |
36,581,754 (GRCm39) |
missense |
possibly damaging |
0.83 |
R9069:Hectd2
|
UTSW |
19 |
36,562,862 (GRCm39) |
missense |
probably benign |
0.00 |
R9149:Hectd2
|
UTSW |
19 |
36,576,402 (GRCm39) |
missense |
probably damaging |
0.99 |
R9418:Hectd2
|
UTSW |
19 |
36,589,574 (GRCm39) |
missense |
probably benign |
0.01 |
R9514:Hectd2
|
UTSW |
19 |
36,582,689 (GRCm39) |
missense |
possibly damaging |
0.67 |
|