Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Abcc6 |
A |
G |
7: 45,999,121 |
L649P |
probably damaging |
Het |
Acad10 |
T |
C |
5: 121,639,255 |
Y371C |
probably damaging |
Het |
Avp |
A |
G |
2: 130,581,178 |
V71A |
probably damaging |
Het |
Bhmt |
C |
T |
13: 93,620,081 |
|
probably null |
Het |
Capn15 |
T |
C |
17: 25,960,764 |
E874G |
probably damaging |
Het |
Capn5 |
A |
G |
7: 98,124,024 |
F591S |
probably damaging |
Het |
Ccne2 |
A |
T |
4: 11,201,348 |
Q292L |
probably benign |
Het |
Cd96 |
T |
G |
16: 46,052,021 |
T406P |
probably damaging |
Het |
Csnk1e |
G |
A |
15: 79,426,366 |
A153V |
probably damaging |
Het |
Dlk1 |
G |
A |
12: 109,454,963 |
V15I |
unknown |
Het |
Dmbt1 |
A |
G |
7: 131,104,867 |
N1372S |
unknown |
Het |
Dntt |
A |
T |
19: 41,029,487 |
R17W |
probably damaging |
Het |
Erich3 |
G |
T |
3: 154,733,500 |
A260S |
probably benign |
Het |
Foxp2 |
C |
T |
6: 15,437,882 |
S669L |
unknown |
Het |
Gm40460 |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
ACCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAGCCACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAGGAACTACAGCCTCCCTTGCAGCCCCCACAG |
7: 142,240,713 |
|
probably benign |
Het |
Gm9268 |
T |
G |
7: 43,048,023 |
C835G |
probably damaging |
Het |
Grid2 |
A |
G |
6: 64,076,941 |
K375E |
possibly damaging |
Het |
Grin2b |
C |
T |
6: 135,772,396 |
G603S |
possibly damaging |
Het |
Hexb |
C |
T |
13: 97,198,173 |
R30Q |
probably benign |
Het |
Homer3 |
A |
T |
8: 70,290,124 |
T162S |
probably benign |
Het |
L3mbtl1 |
A |
G |
2: 162,948,231 |
E15G |
probably benign |
Het |
Manea |
A |
T |
4: 26,327,986 |
F352I |
probably damaging |
Het |
Mcf2l |
T |
A |
8: 12,997,268 |
M210K |
probably benign |
Het |
Morc3 |
T |
C |
16: 93,870,936 |
L734P |
probably damaging |
Het |
Mybpc2 |
A |
G |
7: 44,506,147 |
V894A |
possibly damaging |
Het |
Myh4 |
T |
A |
11: 67,256,395 |
M1622K |
probably damaging |
Het |
Myrf |
A |
G |
19: 10,228,876 |
F59L |
probably benign |
Het |
Ndst3 |
G |
T |
3: 123,557,060 |
|
probably null |
Het |
Nln |
TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC |
TGGTCCAGGTAAAACTGCCCCAGCCAATCAGGTACCTTGGATAGAGGTCCAGGTAGAACTGCCCCAGC |
13: 104,050,416 |
|
probably null |
Het |
Nos3 |
A |
T |
5: 24,381,717 |
D986V |
possibly damaging |
Het |
Nrp1 |
G |
A |
8: 128,431,987 |
A252T |
probably damaging |
Het |
Nup205 |
G |
T |
6: 35,201,999 |
R668L |
probably damaging |
Het |
Olfr313 |
T |
A |
11: 58,817,060 |
D17E |
probably benign |
Het |
Olfr477 |
G |
A |
7: 107,990,475 |
V37I |
probably benign |
Het |
Olfr612 |
T |
C |
7: 103,539,156 |
Y26C |
probably damaging |
Het |
Pcdhga1 |
T |
A |
18: 37,749,682 |
|
probably null |
Het |
Pck1 |
A |
G |
2: 173,157,067 |
I373V |
probably benign |
Het |
Pde8b |
T |
C |
13: 95,086,750 |
N227S |
probably benign |
Het |
Pianp |
T |
G |
6: 124,999,251 |
S8A |
unknown |
Het |
Pkd1l3 |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
GACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCAACAAACATGACATCAGACACACCTGCATCCAGCAGCCCA |
8: 109,624,195 |
|
probably benign |
Het |
Pla2r1 |
A |
T |
2: 60,522,899 |
N239K |
possibly damaging |
Het |
Pls1 |
T |
A |
9: 95,787,087 |
N27I |
probably damaging |
Het |
Prep |
T |
C |
10: 45,158,524 |
*711Q |
probably null |
Het |
Prkag3 |
A |
G |
1: 74,744,735 |
F330L |
probably damaging |
Het |
Prss56 |
A |
G |
1: 87,183,539 |
D16G |
probably benign |
Het |
Rad17 |
A |
T |
13: 100,633,286 |
F255Y |
probably damaging |
Het |
Rap1gap2 |
T |
C |
11: 74,435,722 |
E173G |
probably damaging |
Het |
Retreg3 |
C |
T |
11: 101,106,390 |
R88H |
possibly damaging |
Het |
Rhag |
G |
A |
17: 40,828,395 |
G74R |
probably damaging |
Het |
Rybp |
A |
G |
6: 100,232,259 |
S201P |
possibly damaging |
Het |
S100a10 |
G |
A |
3: 93,564,295 |
C62Y |
probably benign |
Het |
Scgb2b3 |
T |
A |
7: 31,360,248 |
S34C |
possibly damaging |
Het |
Serpind1 |
A |
G |
16: 17,336,675 |
D122G |
probably benign |
Het |
Setdb1 |
A |
G |
3: 95,346,765 |
L242P |
probably damaging |
Het |
Slc14a2 |
T |
A |
18: 78,155,588 |
I776F |
probably damaging |
Het |
Slc9a1 |
A |
G |
4: 133,412,269 |
E266G |
probably damaging |
Het |
Stpg2 |
A |
G |
3: 139,218,337 |
Y167C |
probably damaging |
Het |
Tex264 |
T |
C |
9: 106,659,136 |
E274G |
probably damaging |
Het |
Tigd2 |
G |
A |
6: 59,211,579 |
S477N |
probably benign |
Het |
Urb1 |
A |
G |
16: 90,792,864 |
L343P |
probably damaging |
Het |
Vars2 |
A |
T |
17: 35,664,788 |
C246S |
possibly damaging |
Het |
Vil1 |
G |
A |
1: 74,426,732 |
|
probably null |
Het |
Vmn2r61 |
C |
G |
7: 42,266,781 |
L273V |
not run |
Het |
Zfp37 |
C |
A |
4: 62,191,999 |
G317V |
probably damaging |
Het |
Zfp760 |
A |
G |
17: 21,722,891 |
K349R |
possibly damaging |
Het |
Zyx |
A |
T |
6: 42,350,474 |
E69V |
probably null |
Het |
|