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Human protein-coding gene
naturally occurring mutation of the Agtpbp1 gene are known as pcd mice (Purkinje cell degeneration). Several spontaneous Agtpbp1 alleles have been discovered
AGTPBP1
active at neutral pH. This activity has been linked to proteins such as AGTPBP1 in human. Argarana CE, Barra HS, Caputto R (January 1980). "Tubulinyl-tyrosine
Tubulinyl-Tyr carboxypeptidase
Tubulinyl-Tyr_carboxypeptidase
Protein family
Glucose-6-phosphate isomerase (EC 5.3.1.9) AEBP1; AGBL1; AGBL2; AGBL3; AGBL4; AGBL5; AGTPBP1; CPA1; CPA2; CPA3; CPA4; CPA5; CPA6; CPB1; CPB2; CPD; CPE; CPM; CPN1; CPO;
Zinc_carboxypeptidase
HGNC:329; O00468 448 AGRP HGNC:330; O00253 449 AGT HGNC:333; P01019 450 AGTPBP1 HGNC:17258; Q9UPW5 451 AGTR1 HGNC:336; P30556 452 AGTR2 HGNC:338; P50052
List of human protein-coding genes 1
List_of_human_protein-coding_genes_1
Muscle enzyme involved in glycogen breakdown
PDE4DIP, PPP1R3B, ARID1B, TTN, INTS4, FAM110A, TRIM54, TRIM55, WWP1, AGTPBP1, POMP, and CDC42BPB. McArdle disease (GSD-V, myophosphorylase deficiency)
Myophosphorylase
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AGTPBP1
AGTPBP1
AGTPBP1
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AGTPBP1
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AGTPBP1
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