DNAJC28

DnaJ homolog subfamily C member 28 is a protein that in humans is encoded by the DNAJC28 gene.[5]

DNAJC28
Identifiers
Aliases	DNAJC28, C21orf55, C21orf78, DnaJ heat shock protein family (Hsp40) member C28
External IDs	MGI: 2181053 HomoloGene: 9869 GeneCards: DNAJC28
Gene location (Human) Chr. Chromosome 21 (human)[1] Band 21q22.11 Start 33,485,530 bp[1] End 33,491,720 bp[1]
Gene location (Mouse) Chr. Chromosome 16 (mouse)[2] Band 16|16 C3.3 Start 91,614,254 bp[2] End 91,619,026 bp[2]
RNA expression pattern More reference expression data
Gene ontology Molecular function • GO:0001948 protein binding Cellular component • Golgi transport complex Biological process • retrograde transport, vesicle recycling within Golgi • Golgi vesicle prefusion complex stabilization • retrograde vesicle-mediated transport, Golgi to ER • Golgi organization Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	54943	246738
Ensembl	ENSG00000262911 ENSG00000177692	ENSMUSG00000039763
UniProt	Q9NX36	Q8VCE1
RefSeq (mRNA)	NM_001040192 NM_017833 NM_001320746	NM_001099738 NM_138664
RefSeq (protein)	NP_001035282 NP_001307675 NP_060303	NP_001093208 NP_619605
Location (UCSC)	Chr 21: 33.49 – 33.49 Mb	Chr 16: 91.61 – 91.62 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

References

1. ENSG00000177692 GRCh38: Ensembl release 89: ENSG00000262911, ENSG00000177692 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000039763 - 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.
5. "Entrez Gene: C21orf55 chromosome 21 open reading frame 55".

External links

• Human DNAJC28 genome location and DNAJC28 gene details page in the UCSC Genome Browser.

Further reading

• Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMC 1356129. PMID 16344560.
• 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.
• 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.
• 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. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
• Gardiner K, Slavov D, Bechtel L, Davisson M (2002). "Annotation of human chromosome 21 for relevance to Down syndrome: gene structure and expression analysis". Genomics. 79 (6): 833–43. doi:10.1006/geno.2002.6782. PMID 12036298.
• Hattori M, Fujiyama A, Taylor TD, et al. (2000). "The DNA sequence of human chromosome 21". Nature. 405 (6784): 311–9. doi:10.1038/35012518. PMID 10830953.
• 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.
• 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.