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Protein-coding gene in the species Homo sapiens
Peroxisomal membrane protein PEX16 is a protein that in humans is encoded by the PEX16 gene. The protein encoded by this gene is an integral peroxisomal
PEX16
XYYYY) Y <1:1,000,000 males Zellweger syndrome PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, PEX26 recessive 1:50,000-75,000
List_of_genetic_disorders
Congenital disorder of nervous system
mutations in the PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, or PEX26 genes. In almost all cases, patients have mutations that
Zellweger_syndrome
Type of organelle
peroxisomal membrane proteins (PMPs) requires the peroxins PEX19, PEX3, and PEX16. PEX19 is a PMP receptor and chaperone, which binds the PMPs and routes
Peroxisome
Protein families found in peroxisomes
PEX2 PEX3 PEX5 PEX6 PEX7 PEX10 PEX11A, PEX11B, PEX11G PEX12 PEX13 PEX14 PEX16 PEX19 PEX26 Crookes WJ, Olsen LJ (February 1999). "Peroxin puzzles and folded
Peroxin
O00623 11976 PEX13 HGNC:8855; Q92968 11977 PEX14 HGNC:8856; O75381 11978 PEX16 HGNC:8857; Q9Y5Y5 11979 PEX19 HGNC:9713; P40855 11980 PEX26 HGNC:22965;
List of human protein-coding genes 6
List_of_human_protein-coding_genes_6
Protein-coding gene in the species Homo sapiens
shown to interact with: ABCD1, ABCD2, ABCD3, PEX10, PEX11B, PEX12, PEX13, PEX16, and PEX3. GRCh38: Ensembl release 89: ENSG00000162735 – Ensembl, May 2017
PEX19
Canadian cell biologist and academic
are present in oleic acid-grown Yarrowia lipolytica overexpressing the PEX16 gene encoding an intraperoxisomal peripheral membrane peroxin. Journal of
Richard_A._Rachubinski
Protein-coding gene in the species Homo sapiens
reticulum export of the peroxisomal membrane biogenesis factor peroxin 16 (Pex16) in mammalian cells". Proceedings of the National Academy of Sciences of
SEC16B
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