Other mutations in this stock |
Total: 81 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
2810006K23Rik |
G |
T |
5: 124,340,774 (GRCm38) |
E153* |
probably null |
Het |
4930412O13Rik |
T |
C |
2: 9,882,827 (GRCm38) |
|
probably benign |
Het |
7530416G11Rik |
A |
T |
15: 85,494,109 (GRCm38) |
I111N |
unknown |
Het |
Adgb |
C |
T |
10: 10,395,352 (GRCm38) |
R849H |
probably damaging |
Het |
Ahnak |
T |
C |
19: 9,015,161 (GRCm38) |
V4603A |
possibly damaging |
Het |
AI464131 |
T |
A |
4: 41,498,895 (GRCm38) |
H245L |
probably benign |
Het |
Ank1 |
A |
G |
8: 23,132,202 (GRCm38) |
D1589G |
probably damaging |
Het |
Ankrd2 |
A |
G |
19: 42,040,115 (GRCm38) |
D70G |
probably damaging |
Het |
Arid2 |
T |
C |
15: 96,370,972 (GRCm38) |
S989P |
probably benign |
Het |
Bbs1 |
A |
T |
19: 4,903,795 (GRCm38) |
Y113* |
probably null |
Het |
Bfsp2 |
T |
G |
9: 103,448,550 (GRCm38) |
K298T |
probably damaging |
Het |
Bpi |
G |
A |
2: 158,262,480 (GRCm38) |
V168I |
possibly damaging |
Het |
Cacna2d1 |
T |
C |
5: 16,361,821 (GRCm38) |
S921P |
probably damaging |
Het |
Clec4d |
A |
C |
6: 123,267,159 (GRCm38) |
T76P |
probably damaging |
Het |
Coq8b |
C |
T |
7: 27,257,325 (GRCm38) |
Q468* |
probably null |
Het |
Dennd6b |
T |
C |
15: 89,188,168 (GRCm38) |
E248G |
possibly damaging |
Het |
Ednra |
A |
G |
8: 77,674,927 (GRCm38) |
S245P |
possibly damaging |
Het |
Epb41l4a |
C |
T |
18: 33,828,143 (GRCm38) |
C446Y |
probably benign |
Het |
Fam221a |
A |
G |
6: 49,367,822 (GRCm38) |
|
probably benign |
Het |
Fam229a |
T |
C |
4: 129,491,503 (GRCm38) |
S76P |
probably benign |
Het |
Fryl |
C |
T |
5: 73,083,295 (GRCm38) |
D1321N |
probably damaging |
Het |
Gli2 |
C |
T |
1: 118,842,064 (GRCm38) |
R586H |
probably damaging |
Het |
Gm13089 |
T |
A |
4: 143,698,432 (GRCm38) |
H147L |
probably benign |
Het |
Gm94 |
C |
T |
18: 43,792,797 (GRCm38) |
A16T |
possibly damaging |
Het |
Gorasp2 |
T |
C |
2: 70,690,751 (GRCm38) |
V355A |
probably benign |
Het |
Grid1 |
C |
A |
14: 35,323,412 (GRCm38) |
T404N |
probably damaging |
Het |
Gtf2i |
C |
A |
5: 134,255,958 (GRCm38) |
E475* |
probably null |
Het |
Gucy1a2 |
T |
C |
9: 3,865,518 (GRCm38) |
|
probably null |
Het |
Il11ra1 |
T |
C |
4: 41,763,887 (GRCm38) |
|
probably null |
Het |
Ireb2 |
G |
A |
9: 54,908,805 (GRCm38) |
G887S |
probably damaging |
Het |
Kdsr |
T |
C |
1: 106,734,581 (GRCm38) |
E248G |
probably benign |
Het |
Lemd2 |
C |
G |
17: 27,190,785 (GRCm38) |
R464P |
probably damaging |
Het |
Lrrfip1 |
T |
C |
1: 91,114,611 (GRCm38) |
V246A |
probably damaging |
Het |
Macf1 |
T |
A |
4: 123,474,275 (GRCm38) |
D2231V |
possibly damaging |
Het |
Map2k5 |
C |
T |
9: 63,281,019 (GRCm38) |
D283N |
probably damaging |
Het |
Mfsd5 |
A |
G |
15: 102,281,492 (GRCm38) |
D433G |
possibly damaging |
Het |
Mir700 |
C |
A |
4: 135,412,307 (GRCm38) |
|
probably null |
Het |
Mroh9 |
A |
T |
1: 163,075,677 (GRCm38) |
F52L |
probably damaging |
Het |
Mycbp2 |
A |
C |
14: 103,156,723 (GRCm38) |
S2691A |
probably benign |
Het |
Nktr |
T |
A |
9: 121,748,394 (GRCm38) |
|
probably benign |
Het |
Obsl1 |
C |
A |
1: 75,492,215 (GRCm38) |
|
probably null |
Het |
Olfr1130 |
A |
T |
2: 87,608,080 (GRCm38) |
I231F |
probably damaging |
Het |
Olfr251 |
T |
C |
9: 38,378,309 (GRCm38) |
S137P |
probably damaging |
Het |
Olfr259 |
A |
G |
2: 87,108,063 (GRCm38) |
V108A |
probably benign |
Het |
Olfr582 |
A |
T |
7: 103,041,646 (GRCm38) |
I51F |
probably damaging |
Het |
Olfr855 |
C |
T |
9: 19,584,885 (GRCm38) |
T116I |
probably benign |
Het |
Pcdhb22 |
T |
A |
18: 37,519,736 (GRCm38) |
I162N |
possibly damaging |
Het |
Pde1c |
A |
T |
6: 56,479,202 (GRCm38) |
|
probably null |
Het |
Pds5b |
A |
G |
5: 150,769,776 (GRCm38) |
|
probably null |
Het |
Pkd1l1 |
A |
C |
11: 8,857,113 (GRCm38) |
W1568G |
probably damaging |
Het |
Polr3c |
A |
T |
3: 96,719,468 (GRCm38) |
M258K |
possibly damaging |
Het |
Prss12 |
A |
T |
3: 123,482,768 (GRCm38) |
I349F |
probably benign |
Het |
Ptpn21 |
A |
G |
12: 98,678,552 (GRCm38) |
*1177Q |
probably null |
Het |
Rgs22 |
T |
A |
15: 36,010,567 (GRCm38) |
K1125M |
probably benign |
Het |
Rnf182 |
A |
G |
13: 43,668,035 (GRCm38) |
K21E |
probably damaging |
Het |
Rpl6 |
G |
A |
5: 121,205,514 (GRCm38) |
|
probably benign |
Het |
Samsn1 |
C |
T |
16: 75,873,514 (GRCm38) |
V234I |
probably benign |
Het |
Scrib |
A |
G |
15: 76,057,751 (GRCm38) |
I1089T |
probably damaging |
Het |
Sec31a |
T |
C |
5: 100,363,878 (GRCm38) |
T1092A |
probably damaging |
Het |
Sh3bp2 |
G |
T |
5: 34,562,465 (GRCm38) |
R606L |
possibly damaging |
Het |
Sipa1 |
A |
G |
19: 5,656,201 (GRCm38) |
V367A |
probably damaging |
Het |
Slc25a44 |
C |
T |
3: 88,412,846 (GRCm38) |
E269K |
probably damaging |
Het |
Slc44a4 |
T |
A |
17: 34,923,454 (GRCm38) |
M353K |
possibly damaging |
Het |
Sorcs2 |
A |
G |
5: 36,019,384 (GRCm38) |
S1142P |
probably damaging |
Het |
Sptbn4 |
A |
G |
7: 27,418,599 (GRCm38) |
F352L |
probably damaging |
Het |
Synj1 |
A |
T |
16: 90,969,286 (GRCm38) |
N541K |
probably damaging |
Het |
Tas2r113 |
G |
A |
6: 132,893,696 (GRCm38) |
R229K |
probably benign |
Het |
Tcaf3 |
A |
T |
6: 42,589,971 (GRCm38) |
I728K |
probably benign |
Het |
Tcea1 |
A |
G |
1: 4,890,773 (GRCm38) |
E167G |
probably benign |
Het |
Timeless |
G |
A |
10: 128,244,200 (GRCm38) |
R406H |
probably damaging |
Het |
Traf6 |
C |
T |
2: 101,696,684 (GRCm38) |
R260* |
probably null |
Het |
Traj31 |
C |
T |
14: 54,187,931 (GRCm38) |
|
probably benign |
Het |
Ttn |
A |
T |
2: 76,769,563 (GRCm38) |
V19089D |
probably damaging |
Het |
Unc80 |
C |
T |
1: 66,627,257 (GRCm38) |
S1868L |
possibly damaging |
Het |
Wdr38 |
A |
T |
2: 39,001,321 (GRCm38) |
I287F |
possibly damaging |
Het |
Wnt2 |
G |
A |
6: 18,030,323 (GRCm38) |
|
probably benign |
Het |
Wnt5b |
G |
A |
6: 119,433,654 (GRCm38) |
P288L |
probably benign |
Het |
Xkr5 |
G |
T |
8: 18,934,505 (GRCm38) |
N174K |
probably benign |
Het |
Zbtb6 |
C |
T |
2: 37,428,965 (GRCm38) |
R317Q |
probably damaging |
Het |
Zcchc7 |
AGGGG |
AGGG |
4: 44,931,218 (GRCm38) |
|
probably null |
Het |
Zfp647 |
G |
A |
15: 76,912,085 (GRCm38) |
P125L |
probably damaging |
Het |
|
Other mutations in Hs3st5 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00507:Hs3st5
|
APN |
10 |
36,832,922 (GRCm38) |
missense |
probably benign |
0.02 |
IGL00913:Hs3st5
|
APN |
10 |
36,832,850 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01407:Hs3st5
|
APN |
10 |
36,833,408 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01516:Hs3st5
|
APN |
10 |
36,833,051 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02396:Hs3st5
|
APN |
10 |
36,828,703 (GRCm38) |
start codon destroyed |
probably benign |
0.08 |
IGL03351:Hs3st5
|
APN |
10 |
36,833,323 (GRCm38) |
missense |
probably damaging |
1.00 |
R0606:Hs3st5
|
UTSW |
10 |
36,832,588 (GRCm38) |
missense |
probably benign |
0.00 |
R1412:Hs3st5
|
UTSW |
10 |
36,832,676 (GRCm38) |
missense |
probably benign |
0.02 |
R1443:Hs3st5
|
UTSW |
10 |
36,833,414 (GRCm38) |
missense |
probably benign |
0.35 |
R1493:Hs3st5
|
UTSW |
10 |
36,832,874 (GRCm38) |
missense |
probably damaging |
1.00 |
R1768:Hs3st5
|
UTSW |
10 |
36,833,169 (GRCm38) |
missense |
probably benign |
0.01 |
R1792:Hs3st5
|
UTSW |
10 |
36,832,724 (GRCm38) |
missense |
probably benign |
|
R1991:Hs3st5
|
UTSW |
10 |
36,832,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R1992:Hs3st5
|
UTSW |
10 |
36,832,886 (GRCm38) |
missense |
probably damaging |
1.00 |
R4330:Hs3st5
|
UTSW |
10 |
36,832,730 (GRCm38) |
missense |
probably benign |
0.06 |
R4610:Hs3st5
|
UTSW |
10 |
36,828,806 (GRCm38) |
missense |
probably benign |
0.26 |
R5459:Hs3st5
|
UTSW |
10 |
36,828,746 (GRCm38) |
missense |
possibly damaging |
0.85 |
R5561:Hs3st5
|
UTSW |
10 |
36,833,429 (GRCm38) |
missense |
probably damaging |
1.00 |
R7082:Hs3st5
|
UTSW |
10 |
36,832,837 (GRCm38) |
missense |
probably benign |
0.01 |
R7326:Hs3st5
|
UTSW |
10 |
36,833,194 (GRCm38) |
missense |
probably damaging |
1.00 |
R7507:Hs3st5
|
UTSW |
10 |
36,833,015 (GRCm38) |
missense |
probably damaging |
1.00 |
R7885:Hs3st5
|
UTSW |
10 |
36,828,780 (GRCm38) |
nonsense |
probably null |
|
R9147:Hs3st5
|
UTSW |
10 |
36,832,921 (GRCm38) |
missense |
probably damaging |
0.96 |
R9372:Hs3st5
|
UTSW |
10 |
36,832,702 (GRCm38) |
nonsense |
probably null |
|
R9497:Hs3st5
|
UTSW |
10 |
36,833,374 (GRCm38) |
missense |
probably benign |
0.00 |
|