Other mutations in this stock |
Total: 89 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930579G24Rik |
A |
G |
3: 79,538,451 (GRCm39) |
T66A |
probably benign |
Het |
5430401F13Rik |
A |
T |
6: 131,529,766 (GRCm39) |
Q120L |
unknown |
Het |
Akirin1 |
A |
G |
4: 123,637,256 (GRCm39) |
S110P |
possibly damaging |
Het |
Ankmy2 |
T |
A |
12: 36,237,668 (GRCm39) |
S256T |
probably benign |
Het |
Areg |
T |
C |
5: 91,291,485 (GRCm39) |
F143L |
probably damaging |
Het |
Arhgap42 |
A |
G |
9: 9,006,585 (GRCm39) |
S604P |
probably damaging |
Het |
Arid1a |
A |
G |
4: 133,416,571 (GRCm39) |
V1068A |
unknown |
Het |
Arid4a |
G |
A |
12: 71,122,112 (GRCm39) |
S509N |
probably benign |
Het |
Atoh1 |
T |
G |
6: 64,706,914 (GRCm39) |
I203S |
possibly damaging |
Het |
Atp5mg |
T |
C |
9: 44,825,957 (GRCm39) |
T69A |
possibly damaging |
Het |
Baz1b |
A |
G |
5: 135,233,965 (GRCm39) |
E164G |
probably damaging |
Het |
Baz2b |
A |
T |
2: 59,743,336 (GRCm39) |
V1545E |
possibly damaging |
Het |
Best1 |
A |
G |
19: 9,970,590 (GRCm39) |
|
probably null |
Het |
Casp8 |
T |
A |
1: 58,883,575 (GRCm39) |
I314N |
probably damaging |
Het |
Ccdc13 |
T |
C |
9: 121,638,208 (GRCm39) |
T26A |
probably damaging |
Het |
Ccr6 |
A |
T |
17: 8,475,049 (GRCm39) |
I85L |
probably damaging |
Het |
Cdh10 |
A |
T |
15: 18,985,152 (GRCm39) |
N272I |
probably benign |
Het |
Cdh10 |
T |
A |
15: 19,013,416 (GRCm39) |
I672K |
probably damaging |
Het |
Cdk17 |
A |
T |
10: 93,057,492 (GRCm39) |
E163V |
probably benign |
Het |
Chsy1 |
T |
C |
7: 65,821,411 (GRCm39) |
F549L |
probably damaging |
Het |
CN725425 |
T |
C |
15: 91,131,124 (GRCm39) |
Y420H |
possibly damaging |
Het |
Cpt1b |
A |
T |
15: 89,306,535 (GRCm39) |
M281K |
possibly damaging |
Het |
Crlf2 |
A |
G |
5: 109,706,669 (GRCm39) |
|
probably null |
Het |
Ctif |
T |
C |
18: 75,770,251 (GRCm39) |
T45A |
probably benign |
Het |
Ddx31 |
T |
C |
2: 28,748,828 (GRCm39) |
F252S |
probably damaging |
Het |
Dennd5b |
A |
G |
6: 148,899,782 (GRCm39) |
F1205S |
probably damaging |
Het |
Dop1a |
T |
C |
9: 86,418,213 (GRCm39) |
S1981P |
probably damaging |
Het |
Dsg1b |
A |
T |
18: 20,532,578 (GRCm39) |
T541S |
probably benign |
Het |
Dst |
T |
A |
1: 34,262,876 (GRCm39) |
|
probably null |
Het |
Dysf |
T |
C |
6: 84,156,697 (GRCm39) |
V1508A |
probably benign |
Het |
Erf |
A |
T |
7: 24,944,731 (GRCm39) |
L200Q |
possibly damaging |
Het |
Erich3 |
A |
G |
3: 154,468,260 (GRCm39) |
|
probably benign |
Het |
Esrrb |
C |
T |
12: 86,561,225 (GRCm39) |
L320F |
probably damaging |
Het |
Fap |
T |
A |
2: 62,349,349 (GRCm39) |
D508V |
probably benign |
Het |
Fdft1 |
A |
C |
14: 63,402,034 (GRCm39) |
N48K |
probably benign |
Het |
Fdps |
A |
G |
3: 89,008,037 (GRCm39) |
V94A |
probably benign |
Het |
Fes |
A |
T |
7: 80,027,686 (GRCm39) |
H819Q |
probably benign |
Het |
Foxd1 |
G |
T |
13: 98,491,347 (GRCm39) |
D74Y |
unknown |
Het |
Gm136 |
A |
T |
4: 34,746,662 (GRCm39) |
|
probably benign |
Het |
Gm5919 |
T |
A |
9: 83,765,338 (GRCm39) |
L58* |
probably null |
Het |
Gm6871 |
C |
T |
7: 41,223,059 (GRCm39) |
V10I |
possibly damaging |
Het |
Isy1 |
T |
C |
6: 87,811,469 (GRCm39) |
R29G |
probably damaging |
Het |
Kif16b |
T |
A |
2: 142,554,873 (GRCm39) |
K653* |
probably null |
Het |
Kif17 |
A |
G |
4: 138,028,569 (GRCm39) |
T706A |
probably benign |
Het |
Kif18b |
G |
T |
11: 102,803,886 (GRCm39) |
P425T |
probably benign |
Het |
Lama1 |
T |
A |
17: 68,098,239 (GRCm39) |
V1812E |
probably benign |
Het |
Lama5 |
A |
G |
2: 179,843,780 (GRCm39) |
V430A |
probably benign |
Het |
Lclat1 |
A |
G |
17: 73,546,776 (GRCm39) |
E231G |
probably damaging |
Het |
Lig4 |
T |
C |
8: 10,021,692 (GRCm39) |
D696G |
probably benign |
Het |
Mylpf |
T |
A |
7: 126,813,309 (GRCm39) |
V151E |
probably damaging |
Het |
Naa16 |
A |
T |
14: 79,624,497 (GRCm39) |
M1K |
probably null |
Het |
Ndufaf6 |
T |
C |
4: 11,070,264 (GRCm39) |
K119R |
probably benign |
Het |
Nt5c1b |
T |
C |
12: 10,420,055 (GRCm39) |
|
probably benign |
Het |
Or14a260 |
G |
A |
7: 85,984,765 (GRCm39) |
P280S |
probably damaging |
Het |
Or4a27 |
A |
G |
2: 88,559,601 (GRCm39) |
V114A |
probably damaging |
Het |
Or5t17 |
T |
C |
2: 86,832,577 (GRCm39) |
V88A |
probably benign |
Het |
Or8k33 |
T |
A |
2: 86,384,204 (GRCm39) |
D88V |
probably damaging |
Het |
Or9i16 |
T |
A |
19: 13,864,954 (GRCm39) |
I207L |
probably benign |
Het |
Otud4 |
A |
G |
8: 80,399,776 (GRCm39) |
N830S |
probably benign |
Het |
Pdcd10 |
A |
C |
3: 75,448,486 (GRCm39) |
M26R |
probably damaging |
Het |
Pitpnc1 |
A |
G |
11: 107,117,071 (GRCm39) |
V223A |
possibly damaging |
Het |
Pkp2 |
A |
G |
16: 16,058,422 (GRCm39) |
D368G |
possibly damaging |
Het |
Pla1a |
A |
T |
16: 38,235,172 (GRCm39) |
M174K |
probably benign |
Het |
Polr2b |
A |
G |
5: 77,474,470 (GRCm39) |
K436E |
possibly damaging |
Het |
Pwwp4a |
G |
T |
X: 72,171,261 (GRCm39) |
G218C |
probably damaging |
Het |
Rdh16 |
A |
G |
10: 127,637,226 (GRCm39) |
M54V |
probably benign |
Het |
Sall2 |
C |
A |
14: 52,551,293 (GRCm39) |
C632F |
probably damaging |
Het |
Sart1 |
T |
A |
19: 5,435,853 (GRCm39) |
I120F |
probably damaging |
Het |
Slco1a1 |
A |
T |
6: 141,881,661 (GRCm39) |
M157K |
probably damaging |
Het |
Snapc4 |
T |
C |
2: 26,266,209 (GRCm39) |
T178A |
probably benign |
Het |
Sox6 |
T |
C |
7: 115,400,654 (GRCm39) |
I63V |
probably benign |
Het |
Spin1 |
T |
A |
13: 51,303,135 (GRCm39) |
Y243N |
probably damaging |
Het |
Stmnd1 |
T |
C |
13: 46,453,097 (GRCm39) |
Y258H |
possibly damaging |
Het |
Tex13b |
A |
T |
X: 139,710,819 (GRCm39) |
N184K |
probably benign |
Het |
Tgm5 |
T |
C |
2: 120,902,025 (GRCm39) |
T215A |
possibly damaging |
Het |
Tnks2 |
A |
G |
19: 36,849,022 (GRCm39) |
T165A |
probably benign |
Het |
Top2a |
A |
T |
11: 98,900,099 (GRCm39) |
F667Y |
probably damaging |
Het |
Tpo |
T |
C |
12: 30,150,567 (GRCm39) |
M438V |
probably benign |
Het |
Tyw1 |
A |
G |
5: 130,298,169 (GRCm39) |
R237G |
probably benign |
Het |
Unc5c |
G |
A |
3: 141,463,598 (GRCm39) |
V240I |
possibly damaging |
Het |
Unc80 |
A |
C |
1: 66,548,467 (GRCm39) |
T580P |
probably damaging |
Het |
Upp2 |
G |
A |
2: 58,680,076 (GRCm39) |
E301K |
probably benign |
Het |
Utp18 |
A |
G |
11: 93,766,879 (GRCm39) |
|
probably null |
Het |
Vmn1r23 |
T |
C |
6: 57,903,046 (GRCm39) |
D244G |
possibly damaging |
Het |
Vps13c |
T |
A |
9: 67,760,985 (GRCm39) |
L51* |
probably null |
Het |
Xpnpep3 |
A |
G |
15: 81,314,968 (GRCm39) |
T223A |
probably benign |
Het |
Zfp28 |
T |
A |
7: 6,397,942 (GRCm39) |
H792Q |
possibly damaging |
Het |
Zfp804a |
A |
G |
2: 82,089,168 (GRCm39) |
K999R |
probably benign |
Het |
Zkscan16 |
G |
A |
4: 58,948,918 (GRCm39) |
V158M |
possibly damaging |
Het |
|
Other mutations in Dennd2d |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00513:Dennd2d
|
APN |
3 |
106,407,861 (GRCm39) |
missense |
possibly damaging |
0.45 |
IGL01397:Dennd2d
|
APN |
3 |
106,394,365 (GRCm39) |
critical splice donor site |
probably null |
0.00 |
IGL01410:Dennd2d
|
APN |
3 |
106,398,542 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02022:Dennd2d
|
APN |
3 |
106,407,220 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02032:Dennd2d
|
APN |
3 |
106,398,543 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02309:Dennd2d
|
APN |
3 |
106,402,284 (GRCm39) |
missense |
probably benign |
|
R0140:Dennd2d
|
UTSW |
3 |
106,399,799 (GRCm39) |
missense |
probably benign |
0.08 |
R0648:Dennd2d
|
UTSW |
3 |
106,407,871 (GRCm39) |
missense |
probably damaging |
0.97 |
R1519:Dennd2d
|
UTSW |
3 |
106,399,875 (GRCm39) |
missense |
probably damaging |
1.00 |
R1539:Dennd2d
|
UTSW |
3 |
106,394,236 (GRCm39) |
missense |
probably benign |
0.00 |
R1652:Dennd2d
|
UTSW |
3 |
106,394,317 (GRCm39) |
missense |
probably benign |
0.00 |
R2179:Dennd2d
|
UTSW |
3 |
106,399,776 (GRCm39) |
missense |
probably benign |
0.00 |
R3731:Dennd2d
|
UTSW |
3 |
106,407,271 (GRCm39) |
missense |
probably damaging |
1.00 |
R4077:Dennd2d
|
UTSW |
3 |
106,389,939 (GRCm39) |
unclassified |
probably benign |
|
R4134:Dennd2d
|
UTSW |
3 |
106,389,977 (GRCm39) |
missense |
probably benign |
0.34 |
R4135:Dennd2d
|
UTSW |
3 |
106,389,977 (GRCm39) |
missense |
probably benign |
0.34 |
R5214:Dennd2d
|
UTSW |
3 |
106,393,637 (GRCm39) |
critical splice donor site |
probably null |
|
R5767:Dennd2d
|
UTSW |
3 |
106,395,131 (GRCm39) |
intron |
probably benign |
|
R6001:Dennd2d
|
UTSW |
3 |
106,399,776 (GRCm39) |
missense |
probably benign |
0.00 |
R6239:Dennd2d
|
UTSW |
3 |
106,402,193 (GRCm39) |
missense |
probably damaging |
1.00 |
R7312:Dennd2d
|
UTSW |
3 |
106,398,579 (GRCm39) |
missense |
probably benign |
0.38 |
R7593:Dennd2d
|
UTSW |
3 |
106,407,244 (GRCm39) |
missense |
probably damaging |
1.00 |
R8841:Dennd2d
|
UTSW |
3 |
106,393,580 (GRCm39) |
missense |
probably benign |
|
R9103:Dennd2d
|
UTSW |
3 |
106,397,684 (GRCm39) |
missense |
|
|
R9341:Dennd2d
|
UTSW |
3 |
106,397,730 (GRCm39) |
critical splice donor site |
probably null |
|
R9343:Dennd2d
|
UTSW |
3 |
106,397,730 (GRCm39) |
critical splice donor site |
probably null |
|
R9388:Dennd2d
|
UTSW |
3 |
106,395,915 (GRCm39) |
missense |
possibly damaging |
0.93 |
Z1088:Dennd2d
|
UTSW |
3 |
106,407,190 (GRCm39) |
nonsense |
probably null |
|
|