Other mutations in this stock |
Total: 109 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
4930533L02Rik |
A |
G |
7: 124,917,815 (GRCm39) |
K69R |
unknown |
Het |
Abca13 |
A |
C |
11: 9,244,701 (GRCm39) |
D2188A |
probably benign |
Het |
Acad11 |
T |
C |
9: 104,001,224 (GRCm39) |
M708T |
probably damaging |
Het |
Adam7 |
T |
C |
14: 68,748,306 (GRCm39) |
|
probably null |
Het |
Adgre1 |
T |
A |
17: 57,751,060 (GRCm39) |
I578N |
probably benign |
Het |
Agbl4 |
T |
C |
4: 111,474,419 (GRCm39) |
S403P |
probably damaging |
Het |
Ak3 |
A |
G |
19: 29,025,192 (GRCm39) |
M13T |
possibly damaging |
Het |
Ap2s1 |
T |
C |
7: 16,481,305 (GRCm39) |
|
probably benign |
Het |
Arhgef1 |
A |
T |
7: 24,623,224 (GRCm39) |
|
probably benign |
Het |
Arsk |
T |
C |
13: 76,223,051 (GRCm39) |
N182S |
probably benign |
Het |
Aspscr1 |
G |
A |
11: 120,569,246 (GRCm39) |
V15I |
probably damaging |
Het |
Asxl2 |
A |
G |
12: 3,492,487 (GRCm39) |
Y24C |
probably damaging |
Het |
Atp8b1 |
A |
G |
18: 64,701,323 (GRCm39) |
F345S |
possibly damaging |
Het |
Atp8b3 |
T |
C |
10: 80,362,743 (GRCm39) |
K672E |
probably benign |
Het |
Bltp1 |
T |
A |
3: 36,997,331 (GRCm39) |
C1129* |
probably null |
Het |
Bmp2k |
A |
G |
5: 97,235,682 (GRCm39) |
|
probably benign |
Het |
Casp6 |
T |
A |
3: 129,704,172 (GRCm39) |
V86E |
probably benign |
Het |
Cdca5 |
A |
G |
19: 6,140,742 (GRCm39) |
E260G |
unknown |
Het |
Cpb2 |
T |
A |
14: 75,502,898 (GRCm39) |
V159D |
probably damaging |
Het |
Cylc2 |
T |
A |
4: 51,228,477 (GRCm39) |
S183T |
unknown |
Het |
Dhtkd1 |
T |
A |
2: 5,919,699 (GRCm39) |
M561L |
probably benign |
Het |
Dync2h1 |
T |
C |
9: 7,129,046 (GRCm39) |
D1823G |
probably benign |
Het |
Efcab5 |
G |
A |
11: 77,031,749 (GRCm39) |
R42W |
probably damaging |
Het |
Erc1 |
T |
C |
6: 119,597,289 (GRCm39) |
K1003E |
probably damaging |
Het |
Ezr |
G |
A |
17: 7,022,164 (GRCm39) |
Q105* |
probably null |
Het |
Fam83d |
T |
A |
2: 158,627,467 (GRCm39) |
D385E |
probably benign |
Het |
Fbn2 |
A |
G |
18: 58,178,389 (GRCm39) |
C1950R |
probably damaging |
Het |
Fbxo32 |
A |
T |
15: 58,047,605 (GRCm39) |
I236N |
probably damaging |
Het |
Fcgbp |
G |
T |
7: 27,784,918 (GRCm39) |
|
probably null |
Het |
Foxe3 |
T |
C |
4: 114,782,805 (GRCm39) |
N136D |
probably damaging |
Het |
Fscn2 |
A |
T |
11: 120,258,837 (GRCm39) |
I461F |
probably damaging |
Het |
Gldc |
A |
G |
19: 30,093,851 (GRCm39) |
I722T |
possibly damaging |
Het |
Gm10717 |
T |
G |
9: 3,025,619 (GRCm39) |
V68G |
possibly damaging |
Het |
Gm4841 |
A |
G |
18: 60,403,718 (GRCm39) |
L125S |
possibly damaging |
Het |
Gnl3 |
A |
C |
14: 30,735,384 (GRCm39) |
|
probably null |
Het |
Gsto1 |
A |
T |
19: 47,846,416 (GRCm39) |
I88F |
probably damaging |
Het |
Gucy1b1 |
T |
A |
3: 81,945,463 (GRCm39) |
|
probably null |
Het |
Hhla1 |
C |
A |
15: 65,820,352 (GRCm39) |
V133F |
probably benign |
Het |
Hipk3 |
T |
A |
2: 104,271,593 (GRCm39) |
L446F |
probably damaging |
Het |
Hscb |
T |
C |
5: 110,982,556 (GRCm39) |
E177G |
possibly damaging |
Het |
Hsd17b6 |
T |
C |
10: 127,827,274 (GRCm39) |
D266G |
probably benign |
Het |
Ipo4 |
T |
C |
14: 55,869,572 (GRCm39) |
S363G |
probably benign |
Het |
Kcnip3 |
A |
G |
2: 127,301,899 (GRCm39) |
|
probably benign |
Het |
Klhl41 |
A |
G |
2: 69,501,640 (GRCm39) |
Y367C |
probably damaging |
Het |
Klk1b4 |
C |
G |
7: 43,861,053 (GRCm39) |
P232R |
possibly damaging |
Het |
Llgl2 |
A |
G |
11: 115,741,546 (GRCm39) |
K559E |
probably damaging |
Het |
Lrrc59 |
A |
C |
11: 94,534,248 (GRCm39) |
T269P |
probably damaging |
Het |
Mark1 |
A |
G |
1: 184,677,149 (GRCm39) |
S34P |
possibly damaging |
Het |
Megf11 |
G |
A |
9: 64,598,632 (GRCm39) |
|
probably null |
Het |
Mplkip |
A |
G |
13: 17,871,565 (GRCm39) |
I159V |
possibly damaging |
Het |
Muc4 |
C |
A |
16: 32,755,690 (GRCm38) |
|
probably benign |
Het |
Myo18b |
A |
G |
5: 112,841,213 (GRCm39) |
|
probably benign |
Het |
Myo9b |
T |
C |
8: 71,808,596 (GRCm39) |
|
probably benign |
Het |
Napg |
C |
T |
18: 63,120,034 (GRCm39) |
R149C |
probably damaging |
Het |
Ndrg3 |
A |
G |
2: 156,776,855 (GRCm39) |
|
probably benign |
Het |
Nfe2l3 |
T |
A |
6: 51,434,448 (GRCm39) |
M336K |
probably benign |
Het |
Nrxn1 |
A |
C |
17: 91,008,170 (GRCm39) |
|
probably null |
Het |
Nsun3 |
A |
T |
16: 62,597,007 (GRCm39) |
|
probably benign |
Het |
Nuak1 |
T |
C |
10: 84,210,315 (GRCm39) |
E591G |
probably benign |
Het |
Or10g1b |
T |
C |
14: 52,627,846 (GRCm39) |
Y128C |
probably damaging |
Het |
Or10s1 |
G |
A |
9: 39,986,010 (GRCm39) |
V140I |
probably benign |
Het |
Or1e17 |
A |
T |
11: 73,831,773 (GRCm39) |
I234F |
probably benign |
Het |
Or4k2 |
T |
C |
14: 50,423,789 (GRCm39) |
N296S |
probably null |
Het |
Or6c70 |
T |
A |
10: 129,709,936 (GRCm39) |
Q230L |
probably damaging |
Het |
Or6d15 |
A |
T |
6: 116,559,562 (GRCm39) |
V115E |
probably damaging |
Het |
Or6z6 |
T |
A |
7: 6,491,433 (GRCm39) |
M147L |
probably benign |
Het |
Orc4 |
A |
T |
2: 48,827,479 (GRCm39) |
V38E |
possibly damaging |
Het |
Ovgp1 |
T |
C |
3: 105,887,208 (GRCm39) |
|
probably benign |
Het |
Palm3 |
T |
A |
8: 84,755,349 (GRCm39) |
V287D |
probably damaging |
Het |
Pde4dip |
T |
A |
3: 97,751,028 (GRCm39) |
H62L |
probably benign |
Het |
Pdk4 |
G |
T |
6: 5,491,620 (GRCm39) |
P100Q |
probably damaging |
Het |
Pdss2 |
T |
A |
10: 43,248,172 (GRCm39) |
H225Q |
probably benign |
Het |
Pkhd1 |
A |
T |
1: 20,345,762 (GRCm39) |
D2755E |
probably benign |
Het |
Prune2 |
A |
T |
19: 17,098,753 (GRCm39) |
D1419V |
probably damaging |
Het |
Pth2r |
A |
C |
1: 65,427,775 (GRCm39) |
I483L |
probably benign |
Het |
Qrsl1 |
A |
G |
10: 43,772,003 (GRCm39) |
|
probably null |
Het |
Rab11fip4 |
A |
G |
11: 79,577,455 (GRCm39) |
H403R |
possibly damaging |
Het |
Ralgapa1 |
A |
T |
12: 55,724,023 (GRCm39) |
I1548N |
probably damaging |
Het |
Ric8a |
T |
G |
7: 140,437,813 (GRCm39) |
|
probably benign |
Het |
Rsbn1 |
T |
C |
3: 103,821,897 (GRCm39) |
F44S |
possibly damaging |
Het |
Serpinc1 |
T |
A |
1: 160,817,272 (GRCm39) |
M1K |
probably null |
Het |
Sf3b1 |
T |
C |
1: 55,058,416 (GRCm39) |
I58V |
probably damaging |
Het |
Sh3d19 |
T |
A |
3: 86,033,978 (GRCm39) |
M777K |
probably benign |
Het |
Sipa1 |
A |
T |
19: 5,704,093 (GRCm39) |
M743K |
probably benign |
Het |
Skint5 |
T |
C |
4: 113,794,818 (GRCm39) |
H255R |
probably benign |
Het |
Slco6b1 |
A |
T |
1: 96,916,398 (GRCm39) |
|
noncoding transcript |
Het |
Slfn4 |
A |
T |
11: 83,077,777 (GRCm39) |
R188S |
probably damaging |
Het |
Sort1 |
T |
C |
3: 108,231,908 (GRCm39) |
|
probably benign |
Het |
Spg21 |
A |
T |
9: 65,372,629 (GRCm39) |
K20N |
possibly damaging |
Het |
Sptbn2 |
A |
T |
19: 4,795,173 (GRCm39) |
I1544F |
probably benign |
Het |
Srf |
T |
C |
17: 46,860,415 (GRCm39) |
T456A |
possibly damaging |
Het |
Ssbp2 |
T |
A |
13: 91,712,715 (GRCm39) |
|
probably benign |
Het |
Stx2 |
C |
T |
5: 129,065,967 (GRCm39) |
V230I |
probably benign |
Het |
Sv2b |
A |
T |
7: 74,856,187 (GRCm39) |
D34E |
possibly damaging |
Het |
Synpo2l |
A |
G |
14: 20,711,856 (GRCm39) |
S255P |
probably damaging |
Het |
Tbx15 |
C |
T |
3: 99,259,707 (GRCm39) |
P526L |
probably damaging |
Het |
Tenm4 |
C |
A |
7: 96,344,157 (GRCm39) |
P250Q |
possibly damaging |
Het |
Tgm1 |
C |
A |
14: 55,948,384 (GRCm39) |
|
probably benign |
Het |
Tgm1 |
T |
C |
14: 55,950,109 (GRCm39) |
|
probably benign |
Het |
Thsd7b |
A |
G |
1: 130,123,000 (GRCm39) |
I1540V |
probably benign |
Het |
Tnrc6c |
A |
G |
11: 117,630,707 (GRCm39) |
K1023E |
probably damaging |
Het |
Ube2l6 |
A |
T |
2: 84,636,771 (GRCm39) |
|
probably null |
Het |
Uty |
T |
A |
Y: 1,169,979 (GRCm39) |
I326F |
probably damaging |
Het |
Wdfy4 |
T |
C |
14: 32,805,742 (GRCm39) |
D1735G |
possibly damaging |
Het |
Wnt11 |
A |
G |
7: 98,496,590 (GRCm39) |
K177E |
probably damaging |
Het |
Wnt5a |
A |
T |
14: 28,235,225 (GRCm39) |
M70L |
possibly damaging |
Het |
Wwc1 |
T |
A |
11: 35,743,175 (GRCm39) |
E882V |
probably damaging |
Het |
Zfp455 |
G |
T |
13: 67,346,728 (GRCm39) |
|
probably null |
Het |
Zmpste24 |
A |
G |
4: 120,940,050 (GRCm39) |
Y199H |
probably damaging |
Het |
|
Other mutations in Lcp2 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01451:Lcp2
|
APN |
11 |
33,997,345 (GRCm39) |
start gained |
probably benign |
|
IGL01730:Lcp2
|
APN |
11 |
34,000,943 (GRCm39) |
missense |
possibly damaging |
0.91 |
IGL02174:Lcp2
|
APN |
11 |
34,000,966 (GRCm39) |
splice site |
probably benign |
|
IGL02228:Lcp2
|
APN |
11 |
33,997,424 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02814:Lcp2
|
APN |
11 |
34,021,033 (GRCm39) |
missense |
probably damaging |
1.00 |
R0142:Lcp2
|
UTSW |
11 |
34,032,418 (GRCm39) |
missense |
probably damaging |
0.97 |
R0281:Lcp2
|
UTSW |
11 |
34,019,854 (GRCm39) |
splice site |
probably benign |
|
R0323:Lcp2
|
UTSW |
11 |
34,004,322 (GRCm39) |
missense |
probably damaging |
1.00 |
R0437:Lcp2
|
UTSW |
11 |
34,037,229 (GRCm39) |
missense |
probably benign |
0.00 |
R0632:Lcp2
|
UTSW |
11 |
34,032,426 (GRCm39) |
missense |
possibly damaging |
0.87 |
R1479:Lcp2
|
UTSW |
11 |
34,025,068 (GRCm39) |
missense |
probably benign |
0.01 |
R1570:Lcp2
|
UTSW |
11 |
34,039,601 (GRCm39) |
missense |
probably benign |
0.07 |
R1744:Lcp2
|
UTSW |
11 |
34,019,911 (GRCm39) |
splice site |
probably null |
|
R2212:Lcp2
|
UTSW |
11 |
34,020,995 (GRCm39) |
missense |
probably benign |
0.14 |
R2910:Lcp2
|
UTSW |
11 |
34,018,970 (GRCm39) |
splice site |
probably null |
|
R2911:Lcp2
|
UTSW |
11 |
34,018,970 (GRCm39) |
splice site |
probably null |
|
R3196:Lcp2
|
UTSW |
11 |
34,040,670 (GRCm39) |
missense |
probably benign |
0.05 |
R4012:Lcp2
|
UTSW |
11 |
34,018,439 (GRCm39) |
missense |
probably damaging |
1.00 |
R4411:Lcp2
|
UTSW |
11 |
34,037,173 (GRCm39) |
unclassified |
probably benign |
|
R4417:Lcp2
|
UTSW |
11 |
34,000,917 (GRCm39) |
missense |
probably benign |
0.27 |
R4423:Lcp2
|
UTSW |
11 |
34,028,226 (GRCm39) |
intron |
probably benign |
|
R4718:Lcp2
|
UTSW |
11 |
34,020,992 (GRCm39) |
missense |
probably benign |
0.09 |
R5090:Lcp2
|
UTSW |
11 |
34,039,725 (GRCm39) |
nonsense |
probably null |
|
R6347:Lcp2
|
UTSW |
11 |
34,032,501 (GRCm39) |
missense |
probably benign |
0.10 |
R7315:Lcp2
|
UTSW |
11 |
34,019,906 (GRCm39) |
critical splice donor site |
probably null |
|
R7694:Lcp2
|
UTSW |
11 |
34,000,924 (GRCm39) |
missense |
probably benign |
0.16 |
R7910:Lcp2
|
UTSW |
11 |
34,038,061 (GRCm39) |
missense |
probably damaging |
1.00 |
R8325:Lcp2
|
UTSW |
11 |
34,032,394 (GRCm39) |
missense |
probably benign |
0.34 |
R8435:Lcp2
|
UTSW |
11 |
34,004,316 (GRCm39) |
missense |
probably damaging |
1.00 |
R8709:Lcp2
|
UTSW |
11 |
34,004,354 (GRCm39) |
critical splice donor site |
probably benign |
|
R9091:Lcp2
|
UTSW |
11 |
34,039,688 (GRCm39) |
missense |
|
|
R9270:Lcp2
|
UTSW |
11 |
34,039,688 (GRCm39) |
missense |
|
|
R9566:Lcp2
|
UTSW |
11 |
34,000,944 (GRCm39) |
missense |
|
|
|