Other mutations in this stock |
Total: 108 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Ackr3 |
A |
T |
1: 90,141,565 (GRCm39) |
Y8F |
probably benign |
Het |
Acy1 |
T |
C |
9: 106,312,816 (GRCm39) |
E175G |
probably damaging |
Het |
Add2 |
T |
C |
6: 86,075,580 (GRCm39) |
L243P |
probably damaging |
Het |
Adsl |
A |
G |
15: 80,851,863 (GRCm39) |
D407G |
probably damaging |
Het |
Afg3l1 |
T |
G |
8: 124,221,575 (GRCm39) |
I478S |
probably damaging |
Het |
Aoc1l1 |
T |
A |
6: 48,953,473 (GRCm39) |
I466N |
probably damaging |
Het |
Arfrp1 |
T |
C |
2: 181,001,487 (GRCm39) |
T108A |
probably benign |
Het |
Art5 |
A |
G |
7: 101,747,407 (GRCm39) |
L124P |
possibly damaging |
Het |
Asap2 |
A |
T |
12: 21,162,084 (GRCm39) |
T14S |
probably damaging |
Het |
Atp2c2 |
A |
G |
8: 120,482,841 (GRCm39) |
N901S |
probably benign |
Het |
Bbs12 |
G |
T |
3: 37,375,309 (GRCm39) |
E586* |
probably null |
Het |
Bicd2 |
G |
T |
13: 49,533,052 (GRCm39) |
C546F |
probably damaging |
Het |
Bid |
A |
T |
6: 120,877,215 (GRCm39) |
L42Q |
probably damaging |
Het |
Bpifb9a |
A |
G |
2: 154,102,055 (GRCm39) |
K51E |
probably benign |
Het |
Calcr |
G |
T |
6: 3,687,615 (GRCm39) |
T424K |
probably benign |
Het |
Cd46 |
A |
G |
1: 194,744,721 (GRCm39) |
I339T |
probably benign |
Het |
Chek1 |
C |
A |
9: 36,635,279 (GRCm39) |
V35F |
probably damaging |
Het |
Cntn3 |
A |
G |
6: 102,183,498 (GRCm39) |
I719T |
probably damaging |
Het |
Cyb5r1 |
T |
C |
1: 134,337,363 (GRCm39) |
I163T |
possibly damaging |
Het |
Cyp2d26 |
A |
T |
15: 82,676,907 (GRCm39) |
|
probably null |
Het |
Dclk1 |
A |
G |
3: 55,154,633 (GRCm39) |
Y21C |
probably damaging |
Het |
Dgcr2 |
G |
A |
16: 17,709,351 (GRCm39) |
|
probably null |
Het |
Dhx38 |
T |
C |
8: 110,287,306 (GRCm39) |
S221G |
probably benign |
Het |
Dis3l |
T |
A |
9: 64,214,545 (GRCm39) |
N981I |
probably benign |
Het |
Dnah3 |
C |
T |
7: 119,551,236 (GRCm39) |
V3028I |
probably benign |
Het |
Dnah6 |
T |
C |
6: 73,026,149 (GRCm39) |
Y3448C |
probably benign |
Het |
Dok5 |
G |
A |
2: 170,642,816 (GRCm39) |
G38D |
probably damaging |
Het |
Epb41l1 |
A |
G |
2: 156,356,048 (GRCm39) |
D528G |
probably damaging |
Het |
Fat4 |
A |
T |
3: 39,037,544 (GRCm39) |
Y3732F |
probably damaging |
Het |
Fcsk |
T |
A |
8: 111,615,704 (GRCm39) |
T542S |
probably benign |
Het |
Fgfr4 |
A |
T |
13: 55,314,777 (GRCm39) |
Y640F |
probably damaging |
Het |
Foxo6 |
T |
A |
4: 120,125,811 (GRCm39) |
D328V |
probably benign |
Het |
Foxp1 |
A |
G |
6: 98,993,502 (GRCm39) |
L134P |
probably damaging |
Het |
Frem2 |
G |
A |
3: 53,424,450 (GRCm39) |
R2996* |
probably null |
Het |
Garem2 |
T |
C |
5: 30,313,297 (GRCm39) |
S54P |
probably damaging |
Het |
Gcn1 |
T |
A |
5: 115,747,888 (GRCm39) |
I1765N |
probably benign |
Het |
Gm4787 |
T |
A |
12: 81,423,993 (GRCm39) |
I722F |
probably benign |
Het |
Gpc6 |
G |
T |
14: 117,163,504 (GRCm39) |
A53S |
probably benign |
Het |
Gtpbp8 |
A |
G |
16: 44,560,390 (GRCm39) |
|
probably null |
Het |
H2-Q2 |
T |
C |
17: 35,564,252 (GRCm39) |
|
probably null |
Het |
Hapln2 |
C |
A |
3: 87,930,920 (GRCm39) |
R157L |
probably benign |
Het |
Hpse |
T |
A |
5: 100,839,269 (GRCm39) |
K360* |
probably null |
Het |
Iqcj |
A |
T |
3: 67,962,643 (GRCm39) |
E68V |
probably damaging |
Het |
Kat2a |
T |
C |
11: 100,603,172 (GRCm39) |
|
probably benign |
Het |
Kat6b |
A |
T |
14: 21,718,735 (GRCm39) |
H1138L |
probably benign |
Het |
Kcnab1 |
A |
T |
3: 65,278,861 (GRCm39) |
I371F |
probably damaging |
Het |
Klhl30 |
C |
A |
1: 91,285,546 (GRCm39) |
A356D |
probably benign |
Het |
Klra3 |
G |
C |
6: 130,310,107 (GRCm39) |
R138G |
probably benign |
Het |
Micu1 |
G |
T |
10: 59,699,110 (GRCm39) |
M468I |
probably benign |
Het |
Mrc1 |
A |
G |
2: 14,332,675 (GRCm39) |
T1292A |
probably damaging |
Het |
Myh8 |
G |
A |
11: 67,185,295 (GRCm39) |
E849K |
probably damaging |
Het |
Myom3 |
G |
T |
4: 135,530,544 (GRCm39) |
R1152L |
probably benign |
Het |
Nedd4l |
T |
A |
18: 65,343,401 (GRCm39) |
H820Q |
probably damaging |
Het |
Nlrp4g |
T |
A |
9: 124,353,339 (GRCm38) |
|
noncoding transcript |
Het |
Oga |
A |
T |
19: 45,746,461 (GRCm39) |
Y779* |
probably null |
Het |
Or13p5 |
C |
T |
4: 118,592,446 (GRCm39) |
A240V |
possibly damaging |
Het |
Or1m1 |
T |
C |
9: 18,666,391 (GRCm39) |
D180G |
probably damaging |
Het |
Or2a51 |
A |
G |
6: 43,179,003 (GRCm39) |
I142V |
probably benign |
Het |
Or51a39 |
G |
T |
7: 102,362,788 (GRCm39) |
H277Q |
probably benign |
Het |
Or52j3 |
A |
T |
7: 102,835,847 (GRCm39) |
D13V |
probably benign |
Het |
Or8b49 |
G |
T |
9: 38,505,707 (GRCm39) |
L63F |
probably damaging |
Het |
Or8g54 |
A |
T |
9: 39,706,943 (GRCm39) |
I91F |
probably benign |
Het |
Or9s23 |
T |
C |
1: 92,501,630 (GRCm39) |
S246P |
probably damaging |
Het |
Otop1 |
T |
A |
5: 38,460,194 (GRCm39) |
M587K |
probably damaging |
Het |
Pgm5 |
T |
A |
19: 24,812,179 (GRCm39) |
I118F |
probably damaging |
Het |
Phc2 |
A |
G |
4: 128,638,859 (GRCm39) |
*41W |
probably null |
Het |
Phf8-ps |
T |
A |
17: 33,285,908 (GRCm39) |
D298V |
probably damaging |
Het |
Piezo2 |
A |
T |
18: 63,247,112 (GRCm39) |
M532K |
probably damaging |
Het |
Pjvk |
A |
T |
2: 76,488,713 (GRCm39) |
I295F |
probably benign |
Het |
Popdc2 |
A |
G |
16: 38,183,482 (GRCm39) |
N155S |
possibly damaging |
Het |
Ppp4r3a |
G |
T |
12: 101,008,826 (GRCm39) |
N684K |
probably damaging |
Het |
Prpf4b |
T |
A |
13: 35,084,402 (GRCm39) |
M930K |
probably benign |
Het |
Ptpn12 |
C |
A |
5: 21,207,466 (GRCm39) |
Q297H |
probably damaging |
Het |
Ptprz1 |
C |
A |
6: 23,030,670 (GRCm39) |
L1010I |
probably damaging |
Het |
Rabepk |
A |
T |
2: 34,674,562 (GRCm39) |
D232E |
possibly damaging |
Het |
Rad51ap2 |
A |
G |
12: 11,507,986 (GRCm39) |
H636R |
probably benign |
Het |
Rb1 |
T |
C |
14: 73,526,165 (GRCm39) |
T169A |
probably benign |
Het |
Rcc2 |
T |
C |
4: 140,444,428 (GRCm39) |
L373P |
probably damaging |
Het |
Rif1 |
GCCACCA |
GCCA |
2: 52,000,336 (GRCm39) |
|
probably benign |
Het |
Rrbp1 |
A |
G |
2: 143,796,118 (GRCm39) |
L1200P |
possibly damaging |
Het |
Sdk1 |
A |
G |
5: 141,778,699 (GRCm39) |
N226D |
probably damaging |
Het |
Selenbp1 |
G |
A |
3: 94,851,441 (GRCm39) |
R398H |
probably damaging |
Het |
Selenoo |
A |
G |
15: 88,983,485 (GRCm39) |
M509V |
probably benign |
Het |
Sidt2 |
T |
C |
9: 45,856,638 (GRCm39) |
D477G |
probably damaging |
Het |
Slc2a5 |
T |
G |
4: 150,210,095 (GRCm39) |
S27A |
probably damaging |
Het |
Slc30a5 |
A |
T |
13: 100,940,457 (GRCm39) |
H619Q |
probably damaging |
Het |
Slc5a9 |
A |
G |
4: 111,750,420 (GRCm39) |
I146T |
possibly damaging |
Het |
Slc6a1 |
G |
T |
6: 114,284,731 (GRCm39) |
G263V |
probably damaging |
Het |
Slmap |
A |
G |
14: 26,139,402 (GRCm39) |
Y771H |
probably damaging |
Het |
Snx29 |
A |
G |
16: 11,218,707 (GRCm39) |
D181G |
possibly damaging |
Het |
Spata31d1c |
G |
A |
13: 65,181,779 (GRCm39) |
|
probably null |
Het |
Stat5a |
C |
A |
11: 100,764,916 (GRCm39) |
T213N |
probably benign |
Het |
Stt3a |
A |
T |
9: 36,659,292 (GRCm39) |
V349D |
probably damaging |
Het |
Tcf20 |
A |
T |
15: 82,739,803 (GRCm39) |
D549E |
probably damaging |
Het |
Thbs2 |
T |
A |
17: 14,893,471 (GRCm39) |
D903V |
probably damaging |
Het |
Tln2 |
T |
C |
9: 67,209,842 (GRCm39) |
T432A |
probably damaging |
Het |
Tmc1 |
A |
T |
19: 20,834,039 (GRCm39) |
N241K |
probably benign |
Het |
Tmem260 |
G |
T |
14: 48,715,066 (GRCm39) |
R240L |
possibly damaging |
Het |
Tnfaip6 |
A |
T |
2: 51,933,742 (GRCm39) |
E32D |
probably damaging |
Het |
Trpa1 |
A |
T |
1: 14,969,625 (GRCm39) |
H381Q |
probably damaging |
Het |
Tsen2 |
T |
C |
6: 115,524,936 (GRCm39) |
I45T |
possibly damaging |
Het |
Ttc6 |
G |
A |
12: 57,752,338 (GRCm39) |
V1415I |
probably damaging |
Het |
Ttll7 |
G |
T |
3: 146,635,944 (GRCm39) |
R426L |
probably damaging |
Het |
Ttn |
A |
C |
2: 76,570,482 (GRCm39) |
S26804A |
probably damaging |
Het |
Ubqlnl |
A |
T |
7: 103,797,890 (GRCm39) |
C536S |
probably benign |
Het |
Vmn2r73 |
A |
G |
7: 85,506,936 (GRCm39) |
V792A |
probably benign |
Het |
Zfp345 |
T |
C |
2: 150,314,578 (GRCm39) |
T320A |
probably benign |
Het |
Zfp407 |
T |
C |
18: 84,227,774 (GRCm39) |
D1945G |
possibly damaging |
Het |
|
Other mutations in Hemgn |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00843:Hemgn
|
APN |
4 |
46,396,240 (GRCm39) |
missense |
probably benign |
|
IGL00846:Hemgn
|
APN |
4 |
46,396,171 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL00930:Hemgn
|
APN |
4 |
46,396,383 (GRCm39) |
nonsense |
probably null |
|
IGL01875:Hemgn
|
APN |
4 |
46,396,994 (GRCm39) |
missense |
possibly damaging |
0.65 |
IGL01937:Hemgn
|
APN |
4 |
46,396,057 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02217:Hemgn
|
APN |
4 |
46,396,420 (GRCm39) |
missense |
probably damaging |
0.98 |
IGL02325:Hemgn
|
APN |
4 |
46,396,085 (GRCm39) |
missense |
probably benign |
0.05 |
IGL02746:Hemgn
|
APN |
4 |
46,400,740 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL03093:Hemgn
|
APN |
4 |
46,396,504 (GRCm39) |
missense |
probably benign |
0.26 |
IGL03240:Hemgn
|
APN |
4 |
46,400,732 (GRCm39) |
nonsense |
probably null |
|
PIT4504001:Hemgn
|
UTSW |
4 |
46,395,863 (GRCm39) |
missense |
probably benign |
|
R0925:Hemgn
|
UTSW |
4 |
46,397,049 (GRCm39) |
missense |
probably damaging |
0.98 |
R1413:Hemgn
|
UTSW |
4 |
46,396,091 (GRCm39) |
missense |
possibly damaging |
0.94 |
R1795:Hemgn
|
UTSW |
4 |
46,395,958 (GRCm39) |
missense |
probably damaging |
0.97 |
R1844:Hemgn
|
UTSW |
4 |
46,396,655 (GRCm39) |
missense |
possibly damaging |
0.85 |
R2169:Hemgn
|
UTSW |
4 |
46,396,417 (GRCm39) |
missense |
possibly damaging |
0.92 |
R2207:Hemgn
|
UTSW |
4 |
46,396,301 (GRCm39) |
missense |
possibly damaging |
0.66 |
R3742:Hemgn
|
UTSW |
4 |
46,396,421 (GRCm39) |
missense |
possibly damaging |
0.94 |
R4515:Hemgn
|
UTSW |
4 |
46,396,477 (GRCm39) |
missense |
probably damaging |
0.98 |
R5310:Hemgn
|
UTSW |
4 |
46,403,927 (GRCm39) |
missense |
possibly damaging |
0.77 |
R5445:Hemgn
|
UTSW |
4 |
46,400,738 (GRCm39) |
missense |
probably benign |
0.09 |
R5456:Hemgn
|
UTSW |
4 |
46,396,571 (GRCm39) |
missense |
probably damaging |
0.99 |
R6520:Hemgn
|
UTSW |
4 |
46,396,466 (GRCm39) |
missense |
probably damaging |
0.98 |
R6575:Hemgn
|
UTSW |
4 |
46,395,990 (GRCm39) |
missense |
possibly damaging |
0.46 |
R6983:Hemgn
|
UTSW |
4 |
46,395,997 (GRCm39) |
missense |
possibly damaging |
0.92 |
R7204:Hemgn
|
UTSW |
4 |
46,397,054 (GRCm39) |
missense |
possibly damaging |
0.94 |
R7443:Hemgn
|
UTSW |
4 |
46,396,145 (GRCm39) |
missense |
probably damaging |
0.96 |
R7567:Hemgn
|
UTSW |
4 |
46,397,034 (GRCm39) |
missense |
probably damaging |
0.96 |
R7623:Hemgn
|
UTSW |
4 |
46,396,504 (GRCm39) |
missense |
probably benign |
0.07 |
R8181:Hemgn
|
UTSW |
4 |
46,396,504 (GRCm39) |
missense |
possibly damaging |
0.52 |
R8353:Hemgn
|
UTSW |
4 |
46,403,935 (GRCm39) |
missense |
possibly damaging |
0.92 |
R8714:Hemgn
|
UTSW |
4 |
46,395,904 (GRCm39) |
missense |
probably damaging |
1.00 |
R8725:Hemgn
|
UTSW |
4 |
46,394,638 (GRCm39) |
missense |
probably benign |
0.03 |
R8814:Hemgn
|
UTSW |
4 |
46,400,717 (GRCm39) |
missense |
possibly damaging |
0.66 |
R8865:Hemgn
|
UTSW |
4 |
46,396,682 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9164:Hemgn
|
UTSW |
4 |
46,396,106 (GRCm39) |
missense |
probably benign |
0.03 |
R9335:Hemgn
|
UTSW |
4 |
46,394,647 (GRCm39) |
missense |
probably benign |
0.09 |
Z1177:Hemgn
|
UTSW |
4 |
46,400,693 (GRCm39) |
missense |
possibly damaging |
0.92 |
|