Search references for PEX6. Phrases containing PEX6
See searches and references containing PEX6!PEX6
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
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
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
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
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
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
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-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
PEX6
PEX6
PEX6
PEX6
Girl/Female
English French
Medieval male name adopted as a feminine name.
Boy/Male
British, English, German
Surname
Boy/Male
Tamil
Chitrarath | சிதà¯à®°à®°à®¤
The Sun
Boy/Male
Australian, Christian, French, Jamaican
From the Fortified Farm
Boy/Male
Hindu, Indian
Wife of Pandavas; Droupadi
Boy/Male
Muslim/Islamic
Name of a previous chief army guard
Boy/Male
Tamil
Kotijit | கோடீஜித
Conquering millions
Male
Hebrew
(זִמְרִי) Hebrew name ZIMRIY means "celebrated in song." In the bible, this is the name of several characters, including one of the five sons of Zerah. Zimri is the Anglicized form.
Girl/Female
Gujarati, Hindu, Indian, Kannada, Malayalam, Malaysian, Sanskrit, Tamil, Telugu
Place to Live; Home; Lord Vishnu
Boy/Male
Indian, Sanskrit
Owns Ten Chariots
PEX6
PEX6
PEX6
PEX6
PEX6