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Protein-coding gene in the species Homo sapiens
protein that in humans is encoded by the PEX6 gene. PEX6 is an AAA ATPase that localizes to the peroxisome. PEX6 forms a hexamer with PEX1 and is recruited
PEX6
Medical condition
peroxisomal biogenesis factor 1 (PEX1) or peroxisomal biogenesis factor 6 (PEX6) genes. These gene are involved in peroxisome biogenesis. PEX 1 is located
Heimler_syndrome
Medical condition
and retinopathy. PBD-ZSD is most commonly caused by mutations in the PEX1, PEX6, PEX10, PEX12, and PEX26 genes. This results in the over-accumulation of
Peroxisomal_disorder
Congenital disorder of nervous system
peroxisomes. Most commonly, patients have mutations in the PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, or PEX26 genes. In almost all
Zellweger_syndrome
Medical condition
peroxisome assembly. Most commonly, patients have mutations in the PEX1, PEX3, PEX6, PEX12, and PEX26 genes. In almost all cases, patients have mutations that
Infantile_Refsum_disease
Protein-coding gene in the species Homo sapiens
syndrome. PEX1 has been shown to interact with PEX6 and PEX26. Mutations in the genes encoding PEX1, along with PEX6, are the leading causes of peroxisomal biogenesis
PEX1
(49,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
Type of organelle
Genes that encode peroxin proteins include: PEX1, PEX2 (PXMP3), PEX3, PEX5, PEX6, PEX7, PEX9, PEX10, PEX11A, PEX11B, PEX11G, PEX12, PEX13, PEX14, PEX16, PEX19
Peroxisome
Protein family
KATNA1; KATNAL1; KATNAL2; LONP1; LONP2; MDN1; NSF; NVL; ORC1; ORC4; PEX1; PEX6; PSMC1; PSMC2 (Nbla10058); PSMC3; PSMC4; PSMC5; PSMC6; RFC1; RFC2; RFC3;
AAA_proteins
Biological mechanism for routing proteins
an ATP dependent removal involving the cytosolic protein complex pex1 and pex6. The cycle for pex5 mediated import into the peroxisomal matrix is restored
Protein_targeting
Protein-coding gene in the species Homo sapiens
is encoded by the PEX26 gene. PEX26 has been shown to interact with PEX1, PEX6 and SUFU. GRCh38: Ensembl release 89: ENSG00000215193 – Ensembl, May 2017
PEX26
P56589 11967 PEX5 HGNC:9719; P50542 11968 PEX5L HGNC:30024; Q8IYB4 11969 PEX6 HGNC:8859; Q13608 11970 PEX7 HGNC:8860; O00628 11971 PEX10 HGNC:8851; O60683
List of human protein-coding genes 6
List_of_human_protein-coding_genes_6
Protein families found in peroxisomes
proteins, for example Peroxisomal biogenesis factor 11. PEX1 PEX2 PEX3 PEX5 PEX6 PEX7 PEX10 PEX11A, PEX11B, PEX11G PEX12 PEX13 PEX14 PEX16 PEX19 PEX26 Crookes
Peroxin
PEX6
PEX6
PEX6
PEX6
Girl/Female
Indian, Tamil
Golden Smile
Girl/Female
Hindu, Indian
Beautiful Nature
Boy/Male
Hindi
Monkey.
Girl/Female
African, Arabic
Conscious; Pious; Wise; Mature
Girl/Female
Arabic, Kurdish, Muslim, Parsi
Garden; Rose Garden
Boy/Male
Tamil
Another name of Lord Krishna, Sweet like Honey
Female
Egyptian
, the daughter of Heraclius Soter.
Male
Hebrew
(עֵבֶר) Variant spelling of Hebrew Heber, EVER means "the region beyond; on the other side (of a stream or sea)." In the bible, this is the name of many characters, including a great grandson of Shem.
Boy/Male
Indian, Punjabi, Sikh
Meditation of Supreme God
Girl/Female
Indian, Tamil
Skill
PEX6
PEX6
PEX6
PEX6
PEX6