FAM134C

RETREG3
Identifiers
Aliases	RETREG3, FAM134C, reticulophagy regulator family member 3
External IDs	OMIM: 616498 MGI: 1915248 HomoloGene: 23585 GeneCards: RETREG3
Gene location (Human)
Chr.	Chromosome 17 (human)
End	42,610,623 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	101,010,719 bp
RNA expression pattern
	Top expressed in
	parotid gland; ; nipple; ; periodontal fiber; ; pylorus; ; body of pancreas; ; thymus; ; superior surface of tongue; ; lactiferous duct; ; human penis; ; trachea;
	Top expressed in
	lip; ; spermatid; ; lens; ; thymus; ; cerebellar cortex; ; esophagus; ; seminal vesicula; ; duodenum; ; seminiferous tubule; ; left colon;
	More reference expression data
	n/a
Gene ontology
Molecular function	protein binding;
Cellular component	membrane; integral component of membrane; protein-containing complex;
Biological process	positive regulation of neuron projection development;
	Sources:Amigo / QuickGO
Orthologs
	162427
	67998
	ENSG00000141699
	ENSMUSG00000017802
	Q86VR2
	Q9CQV4
	NM_178126
	NM_026501; NM_028933; NM_001361583
	NP_835227
	NP_080777; NP_083209; NP_001348512
	Wikidata
View/Edit Human	View/Edit Mouse

Protein FAM134C is a protein that in humans is encoded by the FAM134C (family with sequence similarity 134, member C) gene.^[5]

References edit

^ ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000141699 – Ensembl, May 2017
^ ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000017802 – 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: family with sequence similarity 134, member C". Retrieved 2011-08-30.

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.
Rommens JM, Durocher F, McArthur J, et al. (1995). "Generation of a transcription map at the HSD17B locus centromeric to BRCA1 at 17q21". Genomics. 28 (3): 530–42. doi:10.1006/geno.1995.1185. PMID 7490091.

This article on a gene on human chromosome 17 is a stub. You can help Wikipedia by expanding it.