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Search references for PEX3. Phrases containing PEX3
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Search references for PEX3. Phrases containing PEX3
See searches and references containing PEX3!PEX3
Protein-coding gene in the species Homo sapiens
biogenesis factor 3 is a protein that in humans is encoded by the PEX3 gene. PEX3 has been shown to interact with PEX19. GRCh38: Ensembl release 89:
PEX3
Type of organelle
insertion of peroxisomal membrane proteins (PMPs) requires the peroxins PEX19, PEX3, and PEX16. PEX19 is a PMP receptor and chaperone, which binds the PMPs and
Peroxisome
Congenital disorder of nervous system
of peroxisomes. Most commonly, patients have mutations in the PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, or PEX26 genes. In
Zellweger_syndrome
syndrome (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
List_of_genetic_disorders
Protein-coding gene in the species Homo sapiens
interact with: ABCD1, ABCD2, ABCD3, PEX10, PEX11B, PEX12, PEX13, PEX16, and PEX3. GRCh38: Ensembl release 89: ENSG00000162735 – Ensembl, May 2017 GRCm38:
PEX19
Medical condition
Name OMIM Gene ICD-10 Zellweger syndrome 214100 PEX1, PEX2, PEX3, PEX5, PEX6, PEX12, PEX14, PEX26 Q87.82 Infantile Refsum disease 266510 PEX1, PEX2, PEX26
Peroxisomal_disorder
Protein families found in peroxisomes
transmembrane proteins, for example Peroxisomal biogenesis factor 11. PEX1 PEX2 PEX3 PEX5 PEX6 PEX7 PEX10 PEX11A, PEX11B, PEX11G PEX12 PEX13 PEX14 PEX16 PEX19
Peroxin
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
Infantile_Refsum_disease
HGNC:40045; Q6UWS5 11964 PEX1 HGNC:8850; O43933 11965 PEX2 HGNC:9717; P28328 11966 PEX3 HGNC:8858; P56589 11967 PEX5 HGNC:9719; P50542 11968 PEX5L HGNC:30024; Q8IYB4
List of human protein-coding genes 6
List_of_human_protein-coding_genes_6
syndrome; 214100; PXF Zellweger syndrome, complementation group G; 214100; PEX3 Zellweger syndrome-1; 214100; PEX1 https://www.ncbi.nlm.nih.gov/Omim/omimfaq
List_of_OMIM_disorder_codes
PEX3
PEX3
PEX3
PEX3
Girl/Female
Teutonic
Hard working.
Girl/Female
Indian
Hopes for the future
Girl/Female
Indian, Sanskrit
The Destroying
Girl/Female
Australian, German, Italian, Latin, Swedish
From Lucania
Surname or Lastname
English
English : habitational name from Cantrell in Devon, recorded as Canterhulle in 1330, from an unexplained first element + Old English hyll ‘hill’.English : from Old French chanterelle ‘small bell’, ‘treble’, hence a metonymic occupational name for a bellmaker or ringer.English : diminutive of Canter.French : nickname for someone who liked to sing.
Surname or Lastname
English
English : habitational name from Worthen in Shropshire or Worthing in Norfolk, both named from Old English worðign ‘the enclosure’.
Female
Hebrew
Variant spelling of Hebrew Elisheva, ELISHEBA means "God is my oath."
Surname or Lastname
English
English : variant of York.
Girl/Female
Indian
Limitless
Boy/Male
Tamil
Dhanajayan | தநாஜாயண
Lord Murugan
PEX3
PEX3
PEX3
PEX3
PEX3