DOSEN PROFIL LENGKAP

VIPAS39
Identifiers
Aliases	VIPAS39, C14orf133, SPE-39, SPE39, VIPAR, VPS16B, hSPE-39, VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog
External IDs	OMIM: 613401; MGI: 2144805; HomoloGene: 41464; GeneCards: VIPAS39; OMA:VIPAS39 - orthologs
Gene location (Human)
Chr.	Chromosome 14 (human)
End	77,457,952 bp
Gene location (Mouse)
Chr.	Chromosome 12 (mouse)
End	87,313,030 bp
RNA expression pattern
	Top expressed in
	ganglionic eminence; ; gonad; ; tendon of biceps brachii; ; gastric mucosa; ; testicle; ; Achilles tendon; ; popliteal artery; ; tibial arteries; ; stromal cell of endometrium; ; Descending thoracic aorta;
	Top expressed in
	saccule; ; otic vesicle; ; otic placode; ; granulocyte; ; spermatocyte; ; ventricular zone; ; ganglionic eminence; ; medial ganglionic eminence; ; right kidney; ; neural layer of retina;
	More reference expression data
	More reference expression data
Gene ontology
Molecular function	protein binding; protein-containing complex binding;
Cellular component	HOPS complex; endosome; cytoplasmic vesicle; early endosome; cytoplasm; late endosome; recycling endosome; Golgi apparatus;
Biological process	protein transport; cell differentiation; autophagosome maturation; regulation of transcription, DNA-templated; transcription, DNA-templated; spermatogenesis; endosome to lysosome transport; intracellular protein transport; collagen fibril organization; post-translational protein modification; peptidyl-lysine hydroxylation; collagen metabolic process;
	Sources:Amigo / QuickGO
Orthologs
	63894
	104799
	ENSG00000151445
	ENSMUSG00000021038
	Q9H9C1
	Q8BGQ1
	NM_001193314; NM_001193315; NM_001193316; NM_001193317; NM_022067
	NM_001142580; NM_001142581; NM_134044
	NP_001180243; NP_001180244; NP_001180245; NP_001180246; NP_071350
	NP_001136052; NP_001136053; NP_598805
	Wikidata
View/Edit Human	View/Edit Mouse

Spermatogenesis-defective protein 39 homolog is a protein that in humans is encoded by the VIPAS39 gene. This protein is involved in the sorting of lysosomal proteins. Mutations in this gene are associated with ARCS2 (arthrogryposis, renal dysfunction, and cholestasis-2). Alternative splicing results in multiple transcript variants. ^[5]

References

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000151445 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000021038 – Ensembl, May 2017
^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
^ "Entrez Gene: VIPAS39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog".

External links

Human VIPAS39 genome location and VIPAS39 gene details page in the UCSC Genome Browser.

Maruyama K, Sugano S (1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. 138 (1–2): 171–4. doi:10.1016/0378-1119(94)90802-8. PMID 8125298.
Suzuki Y, Yoshitomo-Nakagawa K, Maruyama K, et al. (1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. 200 (1–2): 149–56. doi:10.1016/S0378-1119(97)00411-3. PMID 9373149.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Heilig R, Eckenberg R, Petit JL, et al. (2003). "The DNA sequence and analysis of human chromosome 14". Nature. 421 (6923): 601–7. Bibcode:2003Natur.421..601H. doi:10.1038/nature01348. PMID 12508121.
Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039.
Ballif BA, Villén J, Beausoleil SA, et al. (2005). "Phosphoproteomic analysis of the developing mouse brain". Mol. Cell. Proteomics. 3 (11): 1093–101. doi:10.1074/mcp.M400085-MCP200. PMID 15345747.
Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC)". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMC 528928. PMID 15489334.
Rush J, Moritz A, Lee KA, et al. (2005). "Immunoaffinity profiling of tyrosine phosphorylation in cancer cells". Nat. Biotechnol. 23 (1): 94–101. doi:10.1038/nbt1046. PMID 15592455. S2CID 7200157.
Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network". Nature. 437 (7062): 1173–8. Bibcode:2005Natur.437.1173R. doi:10.1038/nature04209. PMID 16189514. S2CID 4427026.

This article on a gene on human chromosome 14 is a stub. You can help Wikipedia by adding missing information.

[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000151445 – Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000021038 – Ensembl, May 2017

[3] "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[4] "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.

[entrez-5] "Entrez Gene: VIPAS39 VPS33B interacting protein, apical-basolateral polarity regulator, spe-39 homolog".

[1]

[2]

[3]

[4]

[5]

DOSEN PROFIL LENGKAP

VIPAS39

References

External links

Further reading

Content Disclaimer