Other mutations in this stock |
Total: 86 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
9330159F19Rik |
T |
C |
10: 29,097,783 (GRCm39) |
L60P |
probably damaging |
Het |
Acsf2 |
T |
G |
11: 94,450,372 (GRCm39) |
M512L |
probably benign |
Het |
Ahrr |
T |
A |
13: 74,363,885 (GRCm39) |
H312L |
probably benign |
Het |
Akr1c18 |
T |
C |
13: 4,186,717 (GRCm39) |
M244V |
probably benign |
Het |
Aldh3b2 |
A |
G |
19: 4,031,128 (GRCm39) |
Y459C |
probably damaging |
Het |
Arhgap29 |
A |
T |
3: 121,803,607 (GRCm39) |
I796L |
possibly damaging |
Het |
Arrdc4 |
T |
A |
7: 68,391,406 (GRCm39) |
D287V |
probably damaging |
Het |
Astn2 |
A |
T |
4: 65,562,991 (GRCm39) |
I930N |
possibly damaging |
Het |
Bace2 |
T |
A |
16: 97,238,073 (GRCm39) |
L508Q |
probably damaging |
Het |
Baz2a |
G |
T |
10: 127,960,811 (GRCm39) |
C1537F |
possibly damaging |
Het |
Cad |
A |
G |
5: 31,224,030 (GRCm39) |
|
probably null |
Het |
Capn5 |
A |
T |
7: 97,773,126 (GRCm39) |
I626N |
probably benign |
Het |
Car8 |
A |
T |
4: 8,169,685 (GRCm39) |
N274K |
probably damaging |
Het |
Casp14 |
T |
C |
10: 78,550,958 (GRCm39) |
I76V |
probably benign |
Het |
Ccdc88c |
A |
G |
12: 100,882,925 (GRCm39) |
V1649A |
probably benign |
Het |
Cemip |
A |
T |
7: 83,596,488 (GRCm39) |
I1092N |
probably damaging |
Het |
Clspn |
A |
G |
4: 126,453,849 (GRCm39) |
N91D |
probably damaging |
Het |
Cpxm2 |
A |
G |
7: 131,656,574 (GRCm39) |
Y563H |
possibly damaging |
Het |
Csnk1g2 |
T |
C |
10: 80,473,749 (GRCm39) |
V72A |
probably benign |
Het |
Cyp46a1 |
T |
C |
12: 108,318,285 (GRCm39) |
|
probably null |
Het |
Cyp4x1 |
T |
C |
4: 114,978,902 (GRCm39) |
H206R |
probably benign |
Het |
Dapk1 |
T |
A |
13: 60,874,476 (GRCm39) |
|
probably null |
Het |
Ddx1 |
A |
G |
12: 13,290,888 (GRCm39) |
W76R |
probably damaging |
Het |
Dhx29 |
G |
A |
13: 113,083,469 (GRCm39) |
R508H |
unknown |
Het |
Dnah2 |
T |
C |
11: 69,320,183 (GRCm39) |
D3962G |
probably benign |
Het |
Dnajc14 |
T |
A |
10: 128,642,113 (GRCm39) |
C12S |
possibly damaging |
Het |
Dock1 |
T |
C |
7: 134,449,899 (GRCm39) |
I804T |
probably damaging |
Het |
Efs |
G |
T |
14: 55,157,801 (GRCm39) |
S170Y |
probably damaging |
Het |
Eml4 |
G |
T |
17: 83,755,654 (GRCm39) |
W295C |
probably benign |
Het |
Fkbp15 |
A |
G |
4: 62,226,306 (GRCm39) |
S748P |
probably damaging |
Het |
Ghr |
T |
G |
15: 3,349,235 (GRCm39) |
I648L |
possibly damaging |
Het |
Gigyf1 |
T |
A |
5: 137,523,494 (GRCm39) |
I942N |
probably damaging |
Het |
Gpam |
T |
A |
19: 55,064,046 (GRCm39) |
E682D |
probably benign |
Het |
Gsr |
A |
T |
8: 34,183,886 (GRCm39) |
K383* |
probably null |
Het |
Hapln1 |
C |
A |
13: 89,753,579 (GRCm39) |
S248R |
probably benign |
Het |
Haus2 |
G |
T |
2: 120,449,583 (GRCm39) |
R209L |
probably benign |
Het |
Hhatl |
A |
G |
9: 121,618,943 (GRCm39) |
F63S |
probably damaging |
Het |
Hmcn1 |
A |
G |
1: 150,494,816 (GRCm39) |
M4091T |
probably benign |
Het |
Hspb7 |
A |
G |
4: 141,149,896 (GRCm39) |
D94G |
probably damaging |
Het |
Irf6 |
T |
A |
1: 192,849,742 (GRCm39) |
|
probably null |
Het |
Itgb2 |
T |
A |
10: 77,381,878 (GRCm39) |
L60* |
probably null |
Het |
Jmjd1c |
C |
T |
10: 66,993,830 (GRCm39) |
Q104* |
probably null |
Het |
Kcnh1 |
A |
G |
1: 191,959,025 (GRCm39) |
D193G |
probably damaging |
Het |
Klhl25 |
G |
T |
7: 75,516,528 (GRCm39) |
C478F |
probably damaging |
Het |
Klhl3 |
T |
C |
13: 58,178,330 (GRCm39) |
D267G |
probably damaging |
Het |
L3mbtl4 |
T |
G |
17: 68,762,708 (GRCm39) |
H80Q |
probably null |
Het |
Mfsd4a |
T |
C |
1: 131,985,633 (GRCm39) |
N168D |
probably benign |
Het |
Mmp3 |
A |
G |
9: 7,449,881 (GRCm39) |
Q255R |
possibly damaging |
Het |
Mrgprb3 |
C |
A |
7: 48,293,000 (GRCm39) |
G184C |
probably benign |
Het |
Mtpap |
C |
T |
18: 4,396,394 (GRCm39) |
A562V |
possibly damaging |
Het |
Nid1 |
T |
C |
13: 13,681,086 (GRCm39) |
V1072A |
probably benign |
Het |
Nsf |
T |
G |
11: 103,714,595 (GRCm39) |
K728T |
probably damaging |
Het |
Or10ak7 |
T |
C |
4: 118,791,626 (GRCm39) |
N140D |
probably benign |
Het |
Or12j3 |
T |
C |
7: 139,953,328 (GRCm39) |
N65S |
probably damaging |
Het |
Or1e17 |
T |
A |
11: 73,831,641 (GRCm39) |
S190T |
possibly damaging |
Het |
Or2a5 |
T |
C |
6: 42,874,158 (GRCm39) |
Y258H |
probably damaging |
Het |
Or4k15b |
A |
T |
14: 50,272,821 (GRCm39) |
V13E |
probably damaging |
Het |
Pcsk5 |
A |
T |
19: 17,502,631 (GRCm39) |
C894S |
probably damaging |
Het |
Pde2a |
A |
G |
7: 101,143,879 (GRCm39) |
D166G |
probably benign |
Het |
Pfpl |
G |
A |
19: 12,406,618 (GRCm39) |
E290K |
probably benign |
Het |
Pi4kb |
A |
C |
3: 94,906,162 (GRCm39) |
I570L |
probably damaging |
Het |
Plxnb2 |
A |
T |
15: 89,041,622 (GRCm39) |
C1727* |
probably null |
Het |
Poln |
A |
T |
5: 34,286,792 (GRCm39) |
D125E |
possibly damaging |
Het |
Pomgnt1 |
A |
G |
4: 116,011,412 (GRCm39) |
D259G |
possibly damaging |
Het |
Prx |
A |
T |
7: 27,216,152 (GRCm39) |
M218L |
probably benign |
Het |
Pxn |
A |
T |
5: 115,690,001 (GRCm39) |
Q342L |
probably damaging |
Het |
Rhpn2 |
A |
G |
7: 35,033,775 (GRCm39) |
D3G |
possibly damaging |
Het |
Rnase2b |
C |
T |
14: 51,400,174 (GRCm39) |
T85I |
possibly damaging |
Het |
Rnaseh2b |
C |
A |
14: 62,591,075 (GRCm39) |
T142K |
probably damaging |
Het |
Sacs |
T |
C |
14: 61,450,304 (GRCm39) |
S4117P |
probably damaging |
Het |
Sdk2 |
T |
C |
11: 113,745,195 (GRCm39) |
N700S |
probably damaging |
Het |
Sec62 |
A |
C |
3: 30,864,020 (GRCm39) |
K101Q |
unknown |
Het |
Sel1l2 |
A |
C |
2: 140,071,943 (GRCm39) |
L659R |
possibly damaging |
Het |
Septin11 |
A |
G |
5: 93,304,815 (GRCm39) |
I211V |
possibly damaging |
Het |
Slc25a42 |
C |
T |
8: 70,642,107 (GRCm39) |
E112K |
probably damaging |
Het |
Spem2 |
T |
C |
11: 69,708,609 (GRCm39) |
N119D |
probably benign |
Het |
Themis |
G |
A |
10: 28,665,748 (GRCm39) |
E604K |
probably benign |
Het |
Tie1 |
T |
C |
4: 118,343,414 (GRCm39) |
K150E |
probably damaging |
Het |
Top6bl |
A |
G |
19: 4,675,901 (GRCm39) |
|
probably benign |
Het |
Ubap2 |
G |
A |
4: 41,218,333 (GRCm39) |
T258I |
possibly damaging |
Het |
Ushbp1 |
C |
T |
8: 71,838,313 (GRCm39) |
A664T |
probably damaging |
Het |
Vmn1r1 |
T |
C |
1: 181,984,774 (GRCm39) |
N297S |
possibly damaging |
Het |
Vmn1r173 |
A |
C |
7: 23,402,637 (GRCm39) |
I291L |
probably damaging |
Het |
Yy1 |
A |
G |
12: 108,759,972 (GRCm39) |
I212V |
possibly damaging |
Het |
Zfp442 |
A |
T |
2: 150,250,149 (GRCm39) |
F527L |
probably damaging |
Het |
Zyg11b |
T |
A |
4: 108,099,069 (GRCm39) |
H632L |
probably damaging |
Het |
|
Other mutations in Lhcgr |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00468:Lhcgr
|
APN |
17 |
89,049,874 (GRCm39) |
missense |
probably benign |
|
IGL00661:Lhcgr
|
APN |
17 |
89,057,546 (GRCm39) |
missense |
probably benign |
|
IGL00840:Lhcgr
|
APN |
17 |
89,061,164 (GRCm39) |
splice site |
probably benign |
|
IGL01434:Lhcgr
|
APN |
17 |
89,049,865 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL01489:Lhcgr
|
APN |
17 |
89,072,401 (GRCm39) |
splice site |
probably benign |
|
IGL02077:Lhcgr
|
APN |
17 |
89,057,558 (GRCm39) |
missense |
probably benign |
0.06 |
IGL02533:Lhcgr
|
APN |
17 |
89,049,838 (GRCm39) |
missense |
probably benign |
0.00 |
IGL02948:Lhcgr
|
APN |
17 |
89,050,050 (GRCm39) |
missense |
probably damaging |
1.00 |
capybara
|
UTSW |
17 |
89,050,014 (GRCm39) |
nonsense |
probably null |
|
coro
|
UTSW |
17 |
89,049,677 (GRCm39) |
nonsense |
probably null |
|
nutria
|
UTSW |
17 |
89,049,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R0101:Lhcgr
|
UTSW |
17 |
89,072,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R0101:Lhcgr
|
UTSW |
17 |
89,072,598 (GRCm39) |
missense |
probably damaging |
1.00 |
R0556:Lhcgr
|
UTSW |
17 |
89,079,491 (GRCm39) |
missense |
probably damaging |
0.99 |
R1824:Lhcgr
|
UTSW |
17 |
89,057,585 (GRCm39) |
missense |
probably benign |
0.00 |
R1846:Lhcgr
|
UTSW |
17 |
89,072,575 (GRCm39) |
critical splice donor site |
probably null |
|
R1852:Lhcgr
|
UTSW |
17 |
89,072,604 (GRCm39) |
missense |
probably damaging |
0.99 |
R2352:Lhcgr
|
UTSW |
17 |
89,049,727 (GRCm39) |
missense |
possibly damaging |
0.52 |
R3147:Lhcgr
|
UTSW |
17 |
89,065,771 (GRCm39) |
missense |
probably damaging |
0.96 |
R3756:Lhcgr
|
UTSW |
17 |
89,061,284 (GRCm39) |
missense |
possibly damaging |
0.77 |
R4180:Lhcgr
|
UTSW |
17 |
89,049,711 (GRCm39) |
missense |
probably damaging |
1.00 |
R4540:Lhcgr
|
UTSW |
17 |
89,063,036 (GRCm39) |
missense |
probably benign |
|
R4688:Lhcgr
|
UTSW |
17 |
89,072,580 (GRCm39) |
missense |
probably damaging |
0.99 |
R4723:Lhcgr
|
UTSW |
17 |
89,050,030 (GRCm39) |
missense |
probably benign |
0.09 |
R4776:Lhcgr
|
UTSW |
17 |
89,050,125 (GRCm39) |
missense |
probably damaging |
1.00 |
R4903:Lhcgr
|
UTSW |
17 |
89,049,789 (GRCm39) |
missense |
probably damaging |
1.00 |
R5195:Lhcgr
|
UTSW |
17 |
89,050,374 (GRCm39) |
missense |
probably damaging |
1.00 |
R5231:Lhcgr
|
UTSW |
17 |
89,063,039 (GRCm39) |
missense |
probably damaging |
1.00 |
R5361:Lhcgr
|
UTSW |
17 |
89,050,281 (GRCm39) |
missense |
probably damaging |
1.00 |
R5683:Lhcgr
|
UTSW |
17 |
89,079,447 (GRCm39) |
missense |
probably benign |
0.00 |
R5758:Lhcgr
|
UTSW |
17 |
89,049,976 (GRCm39) |
missense |
probably damaging |
0.99 |
R5929:Lhcgr
|
UTSW |
17 |
89,050,436 (GRCm39) |
nonsense |
probably null |
|
R5987:Lhcgr
|
UTSW |
17 |
89,063,006 (GRCm39) |
missense |
probably damaging |
1.00 |
R6268:Lhcgr
|
UTSW |
17 |
89,050,132 (GRCm39) |
missense |
probably damaging |
1.00 |
R6477:Lhcgr
|
UTSW |
17 |
89,049,801 (GRCm39) |
missense |
probably damaging |
1.00 |
R6610:Lhcgr
|
UTSW |
17 |
89,077,307 (GRCm39) |
missense |
possibly damaging |
0.93 |
R7234:Lhcgr
|
UTSW |
17 |
89,099,359 (GRCm39) |
missense |
possibly damaging |
0.96 |
R7282:Lhcgr
|
UTSW |
17 |
89,065,811 (GRCm39) |
missense |
probably benign |
|
R7320:Lhcgr
|
UTSW |
17 |
89,049,506 (GRCm39) |
missense |
probably benign |
|
R7398:Lhcgr
|
UTSW |
17 |
89,079,474 (GRCm39) |
missense |
probably benign |
0.03 |
R7710:Lhcgr
|
UTSW |
17 |
89,050,210 (GRCm39) |
missense |
probably damaging |
1.00 |
R8034:Lhcgr
|
UTSW |
17 |
89,049,784 (GRCm39) |
missense |
probably damaging |
1.00 |
R8108:Lhcgr
|
UTSW |
17 |
89,049,478 (GRCm39) |
nonsense |
probably null |
|
R8150:Lhcgr
|
UTSW |
17 |
89,049,677 (GRCm39) |
nonsense |
probably null |
|
R8151:Lhcgr
|
UTSW |
17 |
89,049,677 (GRCm39) |
nonsense |
probably null |
|
R8236:Lhcgr
|
UTSW |
17 |
89,050,014 (GRCm39) |
nonsense |
probably null |
|
R8901:Lhcgr
|
UTSW |
17 |
89,063,030 (GRCm39) |
missense |
probably damaging |
1.00 |
R8916:Lhcgr
|
UTSW |
17 |
89,061,170 (GRCm39) |
critical splice donor site |
probably null |
|
R9632:Lhcgr
|
UTSW |
17 |
89,049,532 (GRCm39) |
missense |
probably benign |
|
R9716:Lhcgr
|
UTSW |
17 |
89,050,446 (GRCm39) |
missense |
probably damaging |
1.00 |
U24488:Lhcgr
|
UTSW |
17 |
89,079,513 (GRCm39) |
critical splice acceptor site |
probably null |
|
X0028:Lhcgr
|
UTSW |
17 |
89,050,150 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Lhcgr
|
UTSW |
17 |
89,049,698 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1177:Lhcgr
|
UTSW |
17 |
89,072,409 (GRCm39) |
critical splice donor site |
probably null |
|
Z1177:Lhcgr
|
UTSW |
17 |
89,061,333 (GRCm39) |
missense |
probably benign |
0.00 |
|