DPAGT1
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DPAGT1
Summary
DPAGT1 is a gene[1]. DPAGT1 is known by 15 alternative names across languages and contexts.[2]
Key Facts
- DPAGT1's instance of is recorded as gene[3].
- DPAGT1 is a type of protein-coding gene[4].
- DPAGT1's HomoloGene ID is recorded as 1058[5].
- DPAGT1's genomic start is recorded as 118967213[6].
- DPAGT1's genomic start is recorded as 119096025[7].
- DPAGT1's genomic end is recorded as 119108331[8].
- DPAGT1's genomic end is recorded as 118979041[9].
- DPAGT1's ortholog is recorded as Dpagt1[10].
- DPAGT1's ortholog is recorded as ALG7[11].
- DPAGT1's ortholog is recorded as Dpagt1[12].
- DPAGT1's ortholog is recorded as algn-7[13].
- DPAGT1's ortholog is recorded as dpagt1[14].
- DPAGT1's ortholog is recorded as CG5287[15].
- DPAGT1's encodes is recorded as Dolichyl-phosphate N-acetylglucosaminephosphotransferase 1[16].
- DPAGT1's found in taxon is recorded as Homo sapiens[17].
- DPAGT1's chromosome is recorded as human chromosome 11[18].
- DPAGT1's genetic association is recorded as congenital myasthenic syndrome 13[19].
- DPAGT1's genetic association is recorded as congenital myasthenic syndrome[20].
- DPAGT1's strand orientation is recorded as reverse strand[21].
Why It Matters
DPAGT1 is known by 15 alternative names across languages and contexts.[2]