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) question?
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*

DomainStartEndE-ValueType
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
GeneRefVarChr/LocMutationPredicted EffectZygosity
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
AlleleSourceChrCoordTypePredicted EffectPPH 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