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Protein-coding gene in the species Homo sapiens
membrane protein PEX13 is a protein that in humans is encoded by the PEX13 gene. It located on chromosome 2 next to KIAA1841 PEX13 has been shown to
PEX13
Congenital disorder of nervous system
patients have mutations in the PEX1, PEX2, PEX3, PEX5, PEX6, PEX10, PEX12, PEX13, PEX14, PEX16, PEX19, or PEX26 genes. In almost all cases, patients have
Zellweger_syndrome
Topics referred to by the same term
Server Zero-width space ZWS, the magic cookie for Adobe Flash format SWF PEX13, also called ZWS, the gene for encoding peroxisomal membrane protein 13
ZWS
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
Protein-coding gene in the species Homo sapiens
adrenoleukodystrophy and Zellweger syndrome. PEX5 has been shown to interact with PEX12, PEX13 and PEX14. ENSG00000288217 GRCh38: Ensembl release 89: ENSG00000139197,
PEX5
Topics referred to by the same term
adrenoleukodystrophy Non-alcoholic liver disease PEX10, peroxisome gene PEX13, peroxisome gene This disambiguation page lists articles associated with
NALD
Medical condition
PEX2, PEX26 E80.3 Neonatal adrenoleukodystrophy 202370 PEX5, PEX1, PEX10, PEX13, PEX26 E71.331 RCDP Type 1 215100 PEX7 Q77.3 Heimler syndrome 234580 PEX1
Peroxisomal_disorder
Medical condition
KIAA1841, Uncharacterized protein KIAA1841 PAPOLG, Poly(A) polymerase gamma PEX13, Peroxisomal membrane protein Peroxin-13 PUS10, Pseudouridylate synthase
2p15-16.1 microdeletion syndrome
2p15-16.1_microdeletion_syndrome
Type of organelle
(PXMP3), PEX3, PEX5, PEX6, PEX7, PEX9, PEX10, PEX11A, PEX11B, PEX11G, PEX12, PEX13, PEX14, PEX16, PEX19, PEX26, PEX28, PEX30, and PEX31. Between organisms
Peroxisome
Adrenoleukodystrophy, neonatal; 202370; PEX10 Adrenoleukodystrophy, neonatal; 202370; PEX13 Adrenoleukodystrophy, neonatal; 202370; PEX26 Adrenoleukodystrophy, neonatal;
List_of_OMIM_disorder_codes
O96011 11974 PEX11G HGNC:20208; Q96HA9 11975 PEX12 HGNC:8854; O00623 11976 PEX13 HGNC:8855; Q92968 11977 PEX14 HGNC:8856; O75381 11978 PEX16 HGNC:8857; Q9Y5Y5
List of human protein-coding genes 6
List_of_human_protein-coding_genes_6
Protein families found in peroxisomes
factor 11. PEX1 PEX2 PEX3 PEX5 PEX6 PEX7 PEX10 PEX11A, PEX11B, PEX11G PEX12 PEX13 PEX14 PEX16 PEX19 PEX26 Crookes WJ, Olsen LJ (February 1999). "Peroxin puzzles
Peroxin
Medical condition
(2006). "Identification of novel mutations in PEX2, PEX6, PEX10, PEX12, and PEX13 in Zellweger spectrum patients". Human Mutation. 27 (11): 1157. doi:10.1002/humu
Infantile_Refsum_disease
Protein-coding gene in the species Homo sapiens
Zellweger syndrome. PEX14 has been shown to interact with PEX5, PEX7, and PEX13. GRCh38: Ensembl release 89: ENSG00000142655 – Ensembl, May 2017 GRCm38:
PEX14
Protein-coding gene in humans
Mano S, Nakamori C, Nito K, et al. (2007). "The Arabidopsis pex12 and pex13 mutants are defective in both PTS1- and PTS2-dependent protein transport
PEX12
Protein-coding gene in the species Homo sapiens
up of 4292 base pairs and the protein sequence of 718 amino acids. Genes PEX13 and C2orf74 neighbor KIAA1841 on chromosome 2. KIAA1841 is highly expressed
KIAA1841
Protein-coding gene in the species Homo sapiens
been shown to interact with: ABCD1, ABCD2, ABCD3, PEX10, PEX11B, PEX12, PEX13, PEX16, and PEX3. GRCh38: Ensembl release 89: ENSG00000162735 – Ensembl
PEX19
PEX13
PEX13
PEX13
PEX13
Girl/Female
Australian, Hebrew
The Lord is Gracious; Female Version of John
Girl/Female
Hindu, Indian, Marathi
Bestowing Fortune; Given by Goddess Lakshmi
Surname or Lastname
English
English : habitational name from any of various places called Brownell, for example in Yorkshire, Cheshire, and Staffordshire, from Old English brūn ‘brown’ + hyll ‘hill’.Thomas Brownell came from England to Little Compton, RI, in about 1650.
Boy/Male
Tamil
Brilliant, Ruler, Illuminating
Boy/Male
British, English
From the Pointed Hill
Girl/Female
Assamese, Bengali, Hindu, Indian, Kannada, Malayalam, Marathi, Sanskrit, Tamil, Telugu
Smiling; Sweet Smile
Surname or Lastname
English
English : habitational name from any of various places so named. Those in Cheshire, Herefordshire, Shropshire, and Warwickshire are named from an Old English wilig ‘willow’ + Old English lēah ‘wood’, ‘clearing’; one in Devon probably has Old English wīðig ‘willow’ as the first element, while one in Surrey has Old English wēoh ‘(pre-Christian) temple’.English : variant spelling of Willy 2.English : Isaac Willey is recorded in Boston, MA, in 1640, and went on to be one of the founders of New London, CT. His descendent Samuel Hopkins Willey (1821–1914) was one of the founders of the College of California at Berkeley in 1860.
Surname or Lastname
English (East Anglia)
English (East Anglia) : metonymic occupational name for a cobbler, or perhaps a metonymic occupational name for a maker of cobblers’ lasts (see Laster).German and Jewish (Ashkenazic) : metonymic occupational name for a porter, from Middle High German last; German Last or Yiddish last ‘burden’, ‘load’.Dutch : metonymic occupational name as in 2, from Middle Dutch last ‘load’, ‘burden’; or a nickname for an awkward character, from Dutch last ‘trouble’, ‘nuisance’.French : habitational name from a place so named in Puy-de-Dôme.
Male
Finnish
Pet form of Finnish Aarne, AAKE means "eagle."
Boy/Male
Tamil
Happy
PEX13
PEX13
PEX13
PEX13
PEX13