VMA21

Summary

VMA21 is a gene^[1].

Key Facts

• VMA21's instance of is recorded as gene^[2].
• VMA21's subclass of is recorded as protein-coding gene^[3].
• VMA21's Entrez Gene ID is recorded as 203547^[4].
• VMA21's HGNC gene symbol is recorded as VMA21^[5].
• VMA21's HGNC ID is recorded as 22082^[6].
• VMA21's OMIM ID is recorded as 300913^[7].
• VMA21's HomoloGene ID is recorded as 134275^[8].
• VMA21's Ensembl gene ID is recorded as ENSG00000160131^[9].
• VMA21's RefSeq RNA ID is recorded as NM_001017980^[10].
• VMA21's RefSeq RNA ID is recorded as NM_001363810^[11].
• VMA21's genomic start is recorded as 151396515^[12].
• VMA21's genomic start is recorded as 150564987^[13].
• VMA21's genomic end is recorded as 151409364^[14].
• VMA21's genomic end is recorded as 150577836^[15].
• VMA21's ortholog is recorded as Vma21^[16].
• VMA21's ortholog is recorded as Vma21^[17].
• VMA21's ortholog is recorded as vma21^[18].
• VMA21's encodes is recorded as Vacuolar ATPase assembly factor VMA21^[19].
• VMA21's found in taxon is recorded as Homo sapiens^[20].
• VMA21's Ensembl transcript ID is recorded as ENST00000477649^[21].
• VMA21's Ensembl transcript ID is recorded as ENST00000330374^[22].
• VMA21's Ensembl transcript ID is recorded as ENST00000370361^[23].
• VMA21's chromosome is recorded as human X chromosome^[24].
• VMA21's genetic association is recorded as X-linked myopathy with excessive autophagy^[25].
• VMA21's strand orientation is recorded as forward strand^[26].