Other mutations in this stock |
Total: 66 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acaca |
T |
A |
11: 84,254,619 (GRCm39) |
S1899T |
probably damaging |
Het |
Accs |
G |
T |
2: 93,672,243 (GRCm39) |
N208K |
probably benign |
Het |
Actn4 |
C |
A |
7: 28,618,178 (GRCm39) |
V22L |
possibly damaging |
Het |
Adam21 |
A |
G |
12: 81,607,064 (GRCm39) |
S233P |
probably damaging |
Het |
Adrm1b |
G |
A |
3: 92,335,730 (GRCm39) |
A324V |
probably damaging |
Het |
Agmat |
C |
T |
4: 141,476,899 (GRCm39) |
R102C |
probably benign |
Het |
Akap8l |
T |
C |
17: 32,540,569 (GRCm39) |
E608G |
possibly damaging |
Het |
Arap2 |
T |
C |
5: 62,834,519 (GRCm39) |
I788V |
probably damaging |
Het |
Arhgef12 |
G |
T |
9: 42,917,167 (GRCm39) |
H391N |
probably damaging |
Het |
Arhgef28 |
G |
T |
13: 98,187,529 (GRCm39) |
H255Q |
possibly damaging |
Het |
Baz1a |
G |
A |
12: 55,022,154 (GRCm39) |
R43* |
probably null |
Het |
Bcas3 |
T |
C |
11: 85,692,769 (GRCm39) |
S862P |
probably damaging |
Het |
Blm |
A |
T |
7: 80,149,595 (GRCm39) |
H671Q |
possibly damaging |
Het |
Bmp8a |
C |
T |
4: 123,218,911 (GRCm39) |
V166I |
probably benign |
Het |
Cep120 |
G |
T |
18: 53,860,707 (GRCm39) |
P241Q |
probably damaging |
Het |
Col14a1 |
G |
A |
15: 55,244,238 (GRCm39) |
G437E |
unknown |
Het |
Cyp2a5 |
T |
C |
7: 26,539,900 (GRCm39) |
L3S |
probably damaging |
Het |
D16Ertd472e |
T |
C |
16: 78,342,155 (GRCm39) |
T242A |
probably benign |
Het |
Dach1 |
A |
G |
14: 98,405,917 (GRCm39) |
|
probably null |
Het |
Ddx20 |
A |
T |
3: 105,587,656 (GRCm39) |
|
probably benign |
Het |
Eif4enif1 |
A |
G |
11: 3,177,476 (GRCm39) |
S185G |
probably damaging |
Het |
Ep400 |
A |
T |
5: 110,841,421 (GRCm39) |
|
probably benign |
Het |
Fam117b |
T |
A |
1: 60,008,219 (GRCm39) |
I351K |
probably damaging |
Het |
Fbxo31 |
T |
C |
8: 122,293,050 (GRCm39) |
I112V |
probably benign |
Het |
Galntl5 |
A |
T |
5: 25,403,476 (GRCm39) |
N149I |
probably damaging |
Het |
Gja8 |
A |
T |
3: 96,827,218 (GRCm39) |
F148Y |
probably damaging |
Het |
Gpatch1 |
A |
T |
7: 34,993,252 (GRCm39) |
L531Q |
possibly damaging |
Het |
Gprin1 |
G |
A |
13: 54,888,046 (GRCm39) |
T76M |
probably damaging |
Het |
Igf1r |
T |
A |
7: 67,814,982 (GRCm39) |
D294E |
probably benign |
Het |
Kdm6b |
G |
A |
11: 69,295,870 (GRCm39) |
P799L |
unknown |
Het |
Lat |
A |
T |
7: 125,967,137 (GRCm39) |
V139E |
probably damaging |
Het |
Lrrc34 |
G |
A |
3: 30,697,678 (GRCm39) |
R51C |
probably benign |
Het |
Map3k1 |
A |
G |
13: 111,892,322 (GRCm39) |
S978P |
probably benign |
Het |
Masp1 |
T |
A |
16: 23,271,271 (GRCm39) |
D659V |
possibly damaging |
Het |
Mcam |
A |
T |
9: 44,051,250 (GRCm39) |
R415* |
probably null |
Het |
Mtmr10 |
A |
G |
7: 63,987,403 (GRCm39) |
T648A |
probably benign |
Het |
Myh2 |
T |
C |
11: 67,082,563 (GRCm39) |
W1378R |
probably benign |
Het |
Nipsnap2 |
A |
G |
5: 129,816,649 (GRCm39) |
E64G |
probably damaging |
Het |
Or4a68 |
T |
C |
2: 89,270,381 (GRCm39) |
M81V |
probably benign |
Het |
Or52n4b |
T |
C |
7: 108,144,095 (GRCm39) |
L119P |
probably damaging |
Het |
Or6c3 |
A |
T |
10: 129,309,289 (GRCm39) |
I243F |
probably damaging |
Het |
Or9s27 |
G |
A |
1: 92,516,708 (GRCm39) |
V219I |
probably benign |
Het |
Pcdhb8 |
T |
G |
18: 37,490,127 (GRCm39) |
S602A |
probably damaging |
Het |
Peg10 |
A |
T |
6: 4,756,918 (GRCm39) |
|
probably benign |
Het |
Pld1 |
A |
T |
3: 28,132,542 (GRCm39) |
I577F |
probably benign |
Het |
Plekhm1 |
A |
T |
11: 103,267,811 (GRCm39) |
I720N |
probably damaging |
Het |
Ppp2r1a |
A |
G |
17: 21,182,005 (GRCm39) |
|
probably null |
Het |
Retreg3 |
G |
T |
11: 101,010,459 (GRCm39) |
Y49* |
probably null |
Het |
Rrp36 |
T |
C |
17: 46,983,746 (GRCm39) |
E22G |
possibly damaging |
Het |
Sec14l2 |
C |
A |
11: 4,059,169 (GRCm39) |
A167S |
probably damaging |
Het |
Sema5b |
A |
G |
16: 35,480,585 (GRCm39) |
T751A |
probably damaging |
Het |
Smarcc1 |
C |
A |
9: 110,066,907 (GRCm39) |
|
probably benign |
Het |
Smox |
T |
C |
2: 131,362,190 (GRCm39) |
|
probably null |
Het |
Spats2l |
A |
T |
1: 57,985,575 (GRCm39) |
T543S |
possibly damaging |
Het |
Sppl2a |
G |
T |
2: 126,769,754 (GRCm39) |
T34K |
probably benign |
Het |
Svep1 |
T |
C |
4: 58,138,602 (GRCm39) |
|
probably benign |
Het |
Tet2 |
T |
A |
3: 133,192,362 (GRCm39) |
I691F |
probably benign |
Het |
Tnxb |
T |
C |
17: 34,923,114 (GRCm39) |
Y2566H |
possibly damaging |
Het |
Ttn |
T |
C |
2: 76,570,853 (GRCm39) |
E26680G |
probably damaging |
Het |
Txlna |
T |
C |
4: 129,533,111 (GRCm39) |
E139G |
possibly damaging |
Het |
Ubap2 |
T |
C |
4: 41,196,483 (GRCm39) |
|
probably null |
Het |
Ubr3 |
A |
T |
2: 69,809,661 (GRCm39) |
|
probably null |
Het |
Usp37 |
A |
C |
1: 74,483,685 (GRCm39) |
F844V |
probably damaging |
Het |
Usp6nl |
A |
G |
2: 6,429,150 (GRCm39) |
D204G |
probably damaging |
Het |
Vmn1r230 |
T |
C |
17: 21,067,684 (GRCm39) |
I291T |
probably benign |
Het |
Zfp229 |
T |
G |
17: 21,965,258 (GRCm39) |
V496G |
possibly damaging |
Het |
|
Other mutations in Htr4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01965:Htr4
|
APN |
18 |
62,570,740 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02822:Htr4
|
APN |
18 |
62,561,255 (GRCm39) |
splice site |
probably benign |
|
IGL03240:Htr4
|
APN |
18 |
62,570,692 (GRCm39) |
missense |
possibly damaging |
0.92 |
P0042:Htr4
|
UTSW |
18 |
62,546,748 (GRCm39) |
missense |
probably damaging |
1.00 |
R0485:Htr4
|
UTSW |
18 |
62,561,225 (GRCm39) |
missense |
probably damaging |
1.00 |
R1137:Htr4
|
UTSW |
18 |
62,570,624 (GRCm39) |
missense |
probably damaging |
1.00 |
R1661:Htr4
|
UTSW |
18 |
62,545,305 (GRCm39) |
missense |
probably damaging |
0.97 |
R1665:Htr4
|
UTSW |
18 |
62,545,305 (GRCm39) |
missense |
probably damaging |
0.97 |
R1682:Htr4
|
UTSW |
18 |
62,561,137 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1903:Htr4
|
UTSW |
18 |
62,561,193 (GRCm39) |
missense |
probably benign |
0.01 |
R2847:Htr4
|
UTSW |
18 |
62,561,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R2848:Htr4
|
UTSW |
18 |
62,561,197 (GRCm39) |
missense |
probably damaging |
1.00 |
R5764:Htr4
|
UTSW |
18 |
62,570,613 (GRCm39) |
missense |
probably damaging |
0.97 |
R5787:Htr4
|
UTSW |
18 |
62,546,693 (GRCm39) |
missense |
probably damaging |
0.98 |
R7184:Htr4
|
UTSW |
18 |
62,570,498 (GRCm39) |
nonsense |
probably null |
|
R7278:Htr4
|
UTSW |
18 |
62,545,247 (GRCm39) |
missense |
probably benign |
0.04 |
R7811:Htr4
|
UTSW |
18 |
62,545,269 (GRCm39) |
missense |
possibly damaging |
0.51 |
R8190:Htr4
|
UTSW |
18 |
62,570,971 (GRCm39) |
missense |
possibly damaging |
0.64 |
R8312:Htr4
|
UTSW |
18 |
62,570,549 (GRCm39) |
missense |
probably damaging |
1.00 |
R8699:Htr4
|
UTSW |
18 |
62,570,763 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Htr4
|
UTSW |
18 |
62,561,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R8727:Htr4
|
UTSW |
18 |
62,561,209 (GRCm39) |
missense |
probably damaging |
1.00 |
R8757:Htr4
|
UTSW |
18 |
62,545,335 (GRCm39) |
missense |
probably damaging |
1.00 |
R8787:Htr4
|
UTSW |
18 |
62,570,853 (GRCm39) |
missense |
possibly damaging |
0.87 |
Z1177:Htr4
|
UTSW |
18 |
62,570,679 (GRCm39) |
missense |
probably benign |
0.29 |
|