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Protein-coding gene in the species Homo sapiens
Alpha-1,2-mannosyltransferase ALG9 is an enzyme that in humans is encoded by the ALG9 gene. GRCh38: Ensembl release 89: ENSG00000086848 – Ensembl, May
ALG9
Index of enzymes associated with the same name
ALG9 alpha1,2 mannosyltransferase, or ALG9 mannosyltransferase, may refer to: Dolichyl-P-Man:Man6GlcNAc2-PP-dolichol alpha-1,2-mannosyltransferase
ALG9 alpha1,2 mannosyltransferase
ALG9_alpha1,2_mannosyltransferase
Topics referred to by the same term
Dolichylphosphomannose-dependent ALG9 mannosyltransferase may refer to: Dolichyl-P-Man:Man6GlcNAc2-PP-dolichol alpha-1,2-mannosyltransferase, an enzyme
Dolichylphosphomannose-dependent ALG9 mannosyltransferase
Dolichylphosphomannose-dependent_ALG9_mannosyltransferase
Class of enzymes
2-mannosyltransferase (EC 2.4.1.261, ALG9, ALG9 alpha1,2 mannosyltransferase, dolichylphosphomannose-dependent ALG9 mannosyltransferase, ALG9 mannosyltransferase,
Dolichyl-P-Man:Man8GlcNAc2-PP-dolichol alpha-1,2-mannosyltransferase
Dolichyl-P-Man:Man8GlcNAc2-PP-dolichol_alpha-1,2-mannosyltransferase
Class of enzymes
2-mannosyltransferase (EC 2.4.1.259, ALG9, ALG9 alpha1,2 mannosyltransferase, dolichylphosphomannose-dependent ALG9 mannosyltransferase, ALG9 mannosyltransferase,
Dolichyl-P-Man:Man6GlcNAc2-PP-dolichol alpha-1,2-mannosyltransferase
Dolichyl-P-Man:Man6GlcNAc2-PP-dolichol_alpha-1,2-mannosyltransferase
Medical condition
2004). "Identification and functional analysis of a defect in the human ALG9 gene: definition of congenital disorder of glycosylation type IL". American
Congenital disorder of glycosylation
Congenital_disorder_of_glycosylation
HGNC:20266; Q9Y673 569 ALG6 HGNC:23157; Q9Y672 570 ALG8 HGNC:23161; Q9BVK2 571 ALG9 HGNC:15672; Q9H6U8 572 ALG10 HGNC:23162; Q5BKT4 573 ALG10B HGNC:31088; Q5I7T1
List of human protein-coding genes 1
List_of_human_protein-coding_genes_1
Protein-coding gene in the species Homo sapiens
Experimental evidence shows potential interaction between C15orf32 and PKD2, ALG9, DISP1, NPC1, FZD2, FAM69A, ATP6V1G2, ASIC1, DPY19L4, SPPL2B, and HGSNAT
Uncharacterized protein C15orf32
Uncharacterized_protein_C15orf32
Protein-coding gene in the species Homo sapiens
C11orf1 is located on chromosome 11 and is neighbored by: FDXACB1-201 ALG9-201 ALG9-202 AP001781.5-201 This protein is part of the UPF0686 superfamily.
C11orf1
Ik; 608540; ALG1 Congenital disorder of glycosylation, type Il; 608776; ALG9 Congenital disorder of glycosylation, type Im; 610768; TMEM15 Congenital
List_of_OMIM_disorder_codes
ALG9
ALG9
ALG9
ALG9
Boy/Male
Greek
Son of Daedalus.
Boy/Male
Arabic, Muslim
Arising; Appearance; Manifestation
Boy/Male
Greek
Worships well; pious.
Surname or Lastname
English
English : of uncertain origin; probably a habitational name from a place that has not been identified, perhaps a reduced form of Emberton.
Boy/Male
Tamil
Gulmohar | கà¯à®²à®®à¯‹à®¹à®°Â
Red and yellow flowering tree
Girl/Female
Arabic, Muslim
Princess
Girl/Female
English
which is a.
Boy/Male
Hindu
Five eyed, Name of Lord Shiva
Male
English
Pet form of English Job, JOBY means "hated, oppressed."
Boy/Male
Hindu
ALG9
ALG9
ALG9
ALG9
ALG9