Incidental Mutation 'IGL01352:Myorg'
ID |
75411 |
Institutional Source |
Australian Phenomics Network
(link to record)
|
Gene Symbol |
Myorg
|
Ensembl Gene |
ENSMUSG00000046312 |
Gene Name |
myogenesis regulating glycosidase (putative) |
Synonyms |
NET37, AI464131 |
Accession Numbers |
|
Essential gene? |
Non essential
(E-score: 0.000)
|
Stock # |
IGL01352
|
Quality Score |
|
Status
|
|
Chromosome |
4 |
Chromosomal Location |
41495604-41503076 bp(-) (GRCm39) |
Type of Mutation |
nonsense |
DNA Base Change (assembly) |
T to A
at 41499469 bp (GRCm39)
|
Zygosity |
Heterozygous |
Amino Acid Change |
Arginine to Stop codon
at position 54
(R54*)
|
Ref Sequence |
ENSEMBL: ENSMUSP00000059038
(fasta)
|
Gene Model |
predicted gene model for transcript(s):
[ENSMUST00000054920]
[ENSMUST00000149596]
|
AlphaFold |
Q69ZQ1 |
Predicted Effect |
probably null
Transcript: ENSMUST00000054920
AA Change: R54*
|
SMART Domains |
Protein: ENSMUSP00000059038 Gene: ENSMUSG00000046312 AA Change: R54*
Domain | Start | End | E-Value | Type |
transmembrane domain
|
56 |
78 |
N/A |
INTRINSIC |
Pfam:Glyco_hydro_31
|
311 |
712 |
9.7e-55 |
PFAM |
|
Predicted Effect |
probably benign
Transcript: ENSMUST00000149596
|
Coding Region Coverage |
|
Validation Efficiency |
|
Allele List at MGI |
|
Other mutations in this stock |
Total: 39 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Adamts9 |
T |
C |
6: 92,837,155 (GRCm39) |
I1169V |
probably benign |
Het |
B3gnt5 |
T |
C |
16: 19,587,963 (GRCm39) |
S61P |
probably damaging |
Het |
Bambi |
G |
A |
18: 3,512,071 (GRCm39) |
A152T |
probably damaging |
Het |
Cacna1c |
G |
A |
6: 118,633,518 (GRCm39) |
Q930* |
probably null |
Het |
Ccdc178 |
A |
G |
18: 22,152,031 (GRCm39) |
|
probably benign |
Het |
Chit1 |
C |
T |
1: 134,076,228 (GRCm39) |
T295M |
probably damaging |
Het |
Cntnap5c |
C |
A |
17: 58,600,896 (GRCm39) |
N746K |
probably benign |
Het |
Cyfip2 |
A |
T |
11: 46,156,823 (GRCm39) |
F422I |
probably benign |
Het |
Dsg3 |
A |
G |
18: 20,656,753 (GRCm39) |
M208V |
probably benign |
Het |
Erich6 |
G |
A |
3: 58,529,781 (GRCm39) |
|
probably null |
Het |
Gbf1 |
A |
G |
19: 46,253,654 (GRCm39) |
H574R |
probably damaging |
Het |
Gm17654 |
T |
G |
14: 43,813,331 (GRCm39) |
E186D |
probably damaging |
Het |
Gm8165 |
T |
C |
14: 43,913,573 (GRCm39) |
N97S |
unknown |
Het |
Ilf3 |
C |
T |
9: 21,303,618 (GRCm39) |
L160F |
possibly damaging |
Het |
Krt84 |
T |
A |
15: 101,437,209 (GRCm39) |
Q318L |
probably damaging |
Het |
Lrp2 |
T |
A |
2: 69,333,870 (GRCm39) |
H1457L |
possibly damaging |
Het |
Lrrc37a |
T |
A |
11: 103,390,181 (GRCm39) |
D1748V |
probably benign |
Het |
Mybl1 |
T |
C |
1: 9,741,904 (GRCm39) |
E676G |
probably damaging |
Het |
Myo10 |
C |
A |
15: 25,701,783 (GRCm39) |
R53S |
probably damaging |
Het |
Nrap |
A |
G |
19: 56,368,268 (GRCm39) |
S205P |
probably benign |
Het |
Or4c52 |
A |
G |
2: 89,846,063 (GRCm39) |
D263G |
probably damaging |
Het |
Or52z1 |
A |
T |
7: 103,437,285 (GRCm39) |
Y66* |
probably null |
Het |
Or8b1b |
A |
G |
9: 38,376,030 (GRCm39) |
N231S |
probably benign |
Het |
Pkhd1 |
T |
A |
1: 20,619,939 (GRCm39) |
M894L |
probably benign |
Het |
Ptpn13 |
G |
A |
5: 103,634,641 (GRCm39) |
|
probably null |
Het |
Pycard |
T |
C |
7: 127,592,674 (GRCm39) |
D9G |
probably damaging |
Het |
Rbfox3 |
G |
A |
11: 118,396,439 (GRCm39) |
|
probably benign |
Het |
Rnf122 |
C |
T |
8: 31,614,908 (GRCm39) |
R71* |
probably null |
Het |
Scel |
T |
A |
14: 103,770,774 (GRCm39) |
D69E |
possibly damaging |
Het |
Spag6 |
T |
G |
2: 18,715,284 (GRCm39) |
M21R |
possibly damaging |
Het |
Stat5a |
A |
G |
11: 100,771,898 (GRCm39) |
D650G |
probably damaging |
Het |
Tars3 |
T |
C |
7: 65,308,658 (GRCm39) |
I276T |
possibly damaging |
Het |
Tnfaip2 |
G |
T |
12: 111,412,053 (GRCm39) |
E151D |
probably damaging |
Het |
Trio |
G |
A |
15: 27,901,315 (GRCm39) |
T313I |
probably benign |
Het |
Ubqln4 |
A |
C |
3: 88,471,775 (GRCm39) |
M404L |
probably benign |
Het |
Vps33b |
T |
A |
7: 79,934,807 (GRCm39) |
|
probably null |
Het |
Wdfy3 |
A |
T |
5: 102,091,986 (GRCm39) |
V451D |
probably damaging |
Het |
Zfp341 |
G |
T |
2: 154,470,816 (GRCm39) |
A278S |
probably benign |
Het |
Zp3r |
C |
T |
1: 130,547,093 (GRCm39) |
A28T |
possibly damaging |
Het |
|
Other mutations in Myorg |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL01287:Myorg
|
APN |
4 |
41,498,923 (GRCm39) |
missense |
possibly damaging |
0.68 |
IGL01384:Myorg
|
APN |
4 |
41,498,151 (GRCm39) |
missense |
probably damaging |
0.99 |
IGL02150:Myorg
|
APN |
4 |
41,499,183 (GRCm39) |
missense |
possibly damaging |
0.48 |
IGL02557:Myorg
|
APN |
4 |
41,497,900 (GRCm39) |
missense |
possibly damaging |
0.51 |
R0238:Myorg
|
UTSW |
4 |
41,498,912 (GRCm39) |
missense |
probably benign |
0.11 |
R0238:Myorg
|
UTSW |
4 |
41,498,912 (GRCm39) |
missense |
probably benign |
0.11 |
R0413:Myorg
|
UTSW |
4 |
41,498,585 (GRCm39) |
missense |
probably benign |
0.00 |
R0455:Myorg
|
UTSW |
4 |
41,499,538 (GRCm39) |
nonsense |
probably null |
|
R0511:Myorg
|
UTSW |
4 |
41,498,538 (GRCm39) |
missense |
probably damaging |
0.96 |
R0560:Myorg
|
UTSW |
4 |
41,498,167 (GRCm39) |
missense |
probably damaging |
0.99 |
R0785:Myorg
|
UTSW |
4 |
41,497,539 (GRCm39) |
missense |
probably benign |
0.02 |
R0940:Myorg
|
UTSW |
4 |
41,497,996 (GRCm39) |
missense |
probably damaging |
1.00 |
R1677:Myorg
|
UTSW |
4 |
41,497,947 (GRCm39) |
missense |
probably benign |
0.00 |
R1762:Myorg
|
UTSW |
4 |
41,498,553 (GRCm39) |
missense |
possibly damaging |
0.91 |
R1984:Myorg
|
UTSW |
4 |
41,497,501 (GRCm39) |
missense |
possibly damaging |
0.95 |
R2192:Myorg
|
UTSW |
4 |
41,497,704 (GRCm39) |
missense |
probably damaging |
0.99 |
R2496:Myorg
|
UTSW |
4 |
41,499,165 (GRCm39) |
missense |
probably benign |
0.28 |
R4212:Myorg
|
UTSW |
4 |
41,498,307 (GRCm39) |
missense |
probably benign |
0.01 |
R4321:Myorg
|
UTSW |
4 |
41,498,767 (GRCm39) |
missense |
probably benign |
0.00 |
R4672:Myorg
|
UTSW |
4 |
41,499,061 (GRCm39) |
missense |
probably benign |
0.00 |
R4890:Myorg
|
UTSW |
4 |
41,498,877 (GRCm39) |
missense |
probably benign |
0.00 |
R4954:Myorg
|
UTSW |
4 |
41,498,241 (GRCm39) |
missense |
possibly damaging |
0.89 |
R5177:Myorg
|
UTSW |
4 |
41,498,407 (GRCm39) |
nonsense |
probably null |
|
R5967:Myorg
|
UTSW |
4 |
41,497,830 (GRCm39) |
missense |
probably benign |
0.00 |
R6005:Myorg
|
UTSW |
4 |
41,498,895 (GRCm39) |
missense |
probably benign |
0.31 |
R6128:Myorg
|
UTSW |
4 |
41,498,445 (GRCm39) |
missense |
probably damaging |
1.00 |
R6162:Myorg
|
UTSW |
4 |
41,497,899 (GRCm39) |
missense |
possibly damaging |
0.51 |
R7202:Myorg
|
UTSW |
4 |
41,498,268 (GRCm39) |
missense |
probably damaging |
0.99 |
R7211:Myorg
|
UTSW |
4 |
41,498,028 (GRCm39) |
missense |
probably damaging |
1.00 |
R7311:Myorg
|
UTSW |
4 |
41,498,577 (GRCm39) |
missense |
probably damaging |
1.00 |
R7524:Myorg
|
UTSW |
4 |
41,498,779 (GRCm39) |
missense |
probably benign |
0.03 |
R7680:Myorg
|
UTSW |
4 |
41,497,978 (GRCm39) |
missense |
probably damaging |
1.00 |
R8177:Myorg
|
UTSW |
4 |
41,497,568 (GRCm39) |
nonsense |
probably null |
|
R8809:Myorg
|
UTSW |
4 |
41,498,812 (GRCm39) |
missense |
probably benign |
|
R8981:Myorg
|
UTSW |
4 |
41,498,209 (GRCm39) |
missense |
possibly damaging |
0.56 |
R9257:Myorg
|
UTSW |
4 |
41,499,030 (GRCm39) |
missense |
probably benign |
|
X0024:Myorg
|
UTSW |
4 |
41,498,107 (GRCm39) |
missense |
possibly damaging |
0.92 |
Z1088:Myorg
|
UTSW |
4 |
41,497,557 (GRCm39) |
missense |
probably benign |
0.00 |
|
Posted On |
2013-10-07 |