Other mutations in this stock |
Total: 62 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Acsbg1 |
G |
A |
9: 54,517,083 (GRCm39) |
P577S |
probably damaging |
Het |
Adal |
T |
C |
2: 120,985,236 (GRCm39) |
V269A |
possibly damaging |
Het |
Adam33 |
T |
C |
2: 130,898,250 (GRCm39) |
T155A |
probably benign |
Het |
Adgre1 |
A |
T |
17: 57,752,061 (GRCm39) |
E603V |
possibly damaging |
Het |
Adgrf4 |
T |
C |
17: 42,978,441 (GRCm39) |
T301A |
probably damaging |
Het |
Agtpbp1 |
G |
T |
13: 59,630,385 (GRCm39) |
A782E |
possibly damaging |
Het |
Ank3 |
A |
T |
10: 69,811,925 (GRCm39) |
K1197N |
possibly damaging |
Het |
Anxa9 |
A |
T |
3: 95,213,207 (GRCm39) |
D46E |
probably damaging |
Het |
Atg9a |
T |
C |
1: 75,161,927 (GRCm39) |
T540A |
probably damaging |
Het |
Atg9a |
A |
G |
1: 75,163,009 (GRCm39) |
Y364H |
probably damaging |
Het |
Bltp1 |
A |
C |
3: 37,067,030 (GRCm39) |
E73A |
|
Het |
Cd300c2 |
C |
T |
11: 114,891,634 (GRCm39) |
G80D |
possibly damaging |
Het |
Cebpz |
T |
C |
17: 79,230,685 (GRCm39) |
E844G |
probably benign |
Het |
Celsr1 |
T |
C |
15: 85,863,436 (GRCm39) |
I1199V |
probably benign |
Het |
Cftr |
A |
G |
6: 18,220,696 (GRCm39) |
N189S |
probably damaging |
Het |
Dhrs13 |
G |
T |
11: 77,924,302 (GRCm39) |
R116I |
unknown |
Het |
Dnah10 |
A |
G |
5: 124,827,858 (GRCm39) |
M735V |
probably benign |
Het |
Dnajb8 |
C |
T |
6: 88,199,940 (GRCm39) |
R159C |
possibly damaging |
Het |
E130208F15Rik |
C |
A |
7: 30,021,619 (GRCm39) |
S93* |
probably null |
Het |
E330034G19Rik |
T |
C |
14: 24,346,104 (GRCm39) |
I92T |
|
Het |
Eef1d |
A |
T |
15: 75,768,309 (GRCm39) |
V511D |
probably damaging |
Het |
Efna1 |
T |
G |
3: 89,183,520 (GRCm39) |
E102A |
probably damaging |
Het |
H2-M11 |
C |
A |
17: 36,858,860 (GRCm39) |
F133L |
probably damaging |
Het |
Htr3b |
G |
T |
9: 48,847,343 (GRCm39) |
|
probably null |
Het |
Kcns3 |
A |
G |
12: 11,142,253 (GRCm39) |
S149P |
probably damaging |
Het |
Lrp1 |
C |
T |
10: 127,412,354 (GRCm39) |
V1317M |
probably damaging |
Het |
Mphosph9 |
A |
G |
5: 124,405,174 (GRCm39) |
I799T |
probably damaging |
Het |
Muc1 |
C |
T |
3: 89,138,906 (GRCm39) |
A505V |
probably damaging |
Het |
Muc6 |
C |
A |
7: 141,235,673 (GRCm39) |
|
probably null |
Het |
Mylk |
A |
G |
16: 34,820,721 (GRCm39) |
D1891G |
probably damaging |
Het |
Nfe2l3 |
A |
T |
6: 51,428,065 (GRCm39) |
H209L |
probably benign |
Het |
Nprl2 |
A |
C |
9: 107,421,947 (GRCm39) |
Y241S |
probably damaging |
Het |
Oprm1 |
A |
T |
10: 6,780,442 (GRCm39) |
Q368L |
probably benign |
Het |
Or4g7 |
T |
A |
2: 111,309,753 (GRCm39) |
M208K |
possibly damaging |
Het |
Pcm1 |
C |
T |
8: 41,766,974 (GRCm39) |
R1593C |
probably damaging |
Het |
Pitpnm1 |
T |
C |
19: 4,162,878 (GRCm39) |
|
probably null |
Het |
Pnoc |
A |
G |
14: 65,642,521 (GRCm39) |
S81P |
probably benign |
Het |
Prkg2 |
T |
A |
5: 99,114,393 (GRCm39) |
D585V |
probably damaging |
Het |
Prpf38b |
A |
T |
3: 108,815,148 (GRCm39) |
|
probably benign |
Het |
Ranbp3l |
G |
T |
15: 9,065,059 (GRCm39) |
S482I |
probably benign |
Het |
Rapgef4 |
T |
C |
2: 72,056,364 (GRCm39) |
F651L |
probably benign |
Het |
Rasgrf1 |
A |
G |
9: 89,793,675 (GRCm39) |
T151A |
unknown |
Het |
Rnf215 |
T |
C |
11: 4,085,544 (GRCm39) |
L91P |
possibly damaging |
Het |
Rph3a |
T |
C |
5: 121,099,312 (GRCm39) |
H193R |
probably benign |
Het |
Rps17 |
C |
T |
7: 80,994,750 (GRCm39) |
V4I |
probably benign |
Het |
Sec61a2 |
A |
T |
2: 5,881,728 (GRCm39) |
F234Y |
possibly damaging |
Het |
Serpinb8 |
T |
C |
1: 107,526,736 (GRCm39) |
L92P |
probably damaging |
Het |
Slc1a6 |
A |
T |
10: 78,632,091 (GRCm39) |
I306F |
possibly damaging |
Het |
Slc26a11 |
T |
C |
11: 119,270,692 (GRCm39) |
V538A |
possibly damaging |
Het |
Slc27a1 |
G |
A |
8: 72,032,566 (GRCm39) |
S193N |
probably benign |
Het |
Slc9b1 |
T |
C |
3: 135,097,948 (GRCm39) |
S393P |
probably damaging |
Het |
Slfn3 |
T |
A |
11: 83,105,332 (GRCm39) |
I320K |
possibly damaging |
Het |
Spata31f1a |
T |
A |
4: 42,848,542 (GRCm39) |
M1205L |
probably benign |
Het |
Tgfbr1 |
A |
T |
4: 47,406,924 (GRCm39) |
I420F |
probably benign |
Het |
Tnik |
A |
T |
3: 28,658,482 (GRCm39) |
D589V |
possibly damaging |
Het |
Trappc8 |
A |
C |
18: 21,006,938 (GRCm39) |
|
probably null |
Het |
Ttbk1 |
A |
G |
17: 46,791,087 (GRCm39) |
S66P |
possibly damaging |
Het |
Unc13c |
A |
G |
9: 73,392,220 (GRCm39) |
V2044A |
probably benign |
Het |
Usp53 |
T |
C |
3: 122,741,045 (GRCm39) |
E735G |
probably benign |
Het |
Vmn2r-ps158 |
T |
A |
7: 42,673,462 (GRCm39) |
N180K |
probably benign |
Het |
Zfyve26 |
A |
T |
12: 79,302,037 (GRCm39) |
V1853D |
probably damaging |
Het |
Zkscan17 |
A |
G |
11: 59,394,574 (GRCm39) |
V9A |
probably damaging |
Het |
|
Other mutations in Lhx4 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL02366:Lhx4
|
APN |
1 |
155,580,934 (GRCm39) |
missense |
possibly damaging |
0.90 |
IGL02516:Lhx4
|
APN |
1 |
155,578,003 (GRCm39) |
missense |
probably damaging |
1.00 |
IGL02806:Lhx4
|
APN |
1 |
155,577,975 (GRCm39) |
missense |
probably benign |
0.22 |
IGL03104:Lhx4
|
APN |
1 |
155,580,967 (GRCm39) |
missense |
probably damaging |
1.00 |
R3434:Lhx4
|
UTSW |
1 |
155,578,147 (GRCm39) |
missense |
probably damaging |
0.99 |
R3438:Lhx4
|
UTSW |
1 |
155,578,230 (GRCm39) |
missense |
probably benign |
0.10 |
R4369:Lhx4
|
UTSW |
1 |
155,580,560 (GRCm39) |
missense |
probably benign |
0.01 |
R4392:Lhx4
|
UTSW |
1 |
155,585,880 (GRCm39) |
missense |
probably damaging |
1.00 |
R4873:Lhx4
|
UTSW |
1 |
155,581,013 (GRCm39) |
missense |
possibly damaging |
0.90 |
R4875:Lhx4
|
UTSW |
1 |
155,581,013 (GRCm39) |
missense |
possibly damaging |
0.90 |
R5937:Lhx4
|
UTSW |
1 |
155,586,023 (GRCm39) |
missense |
probably damaging |
1.00 |
R6329:Lhx4
|
UTSW |
1 |
155,578,300 (GRCm39) |
missense |
probably benign |
0.00 |
R6694:Lhx4
|
UTSW |
1 |
155,580,456 (GRCm39) |
missense |
probably benign |
0.05 |
R7212:Lhx4
|
UTSW |
1 |
155,600,699 (GRCm39) |
missense |
probably benign |
0.01 |
R7418:Lhx4
|
UTSW |
1 |
155,586,005 (GRCm39) |
missense |
probably damaging |
1.00 |
R7653:Lhx4
|
UTSW |
1 |
155,580,617 (GRCm39) |
missense |
probably damaging |
1.00 |
R7900:Lhx4
|
UTSW |
1 |
155,617,709 (GRCm39) |
intron |
probably benign |
|
R8510:Lhx4
|
UTSW |
1 |
155,578,047 (GRCm39) |
missense |
probably damaging |
1.00 |
R8889:Lhx4
|
UTSW |
1 |
155,581,013 (GRCm39) |
missense |
possibly damaging |
0.90 |
R8892:Lhx4
|
UTSW |
1 |
155,581,013 (GRCm39) |
missense |
possibly damaging |
0.90 |
R9300:Lhx4
|
UTSW |
1 |
155,580,956 (GRCm39) |
missense |
probably damaging |
1.00 |
R9322:Lhx4
|
UTSW |
1 |
155,578,353 (GRCm39) |
missense |
probably benign |
0.00 |
R9532:Lhx4
|
UTSW |
1 |
155,586,024 (GRCm39) |
missense |
probably damaging |
1.00 |
Z1176:Lhx4
|
UTSW |
1 |
155,581,001 (GRCm39) |
missense |
probably damaging |
1.00 |
|