DNAJC28

DnaJ homolog subfamily C member 28 is a protein that in humans is encoded by the DNAJC28 gene.[5] It's a member of chaperone DnaJ family. The family is also known as Hsp40 (heat shock protein 40 kDa).

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. "DNAJC28 DnaJ heat shock protein family (Hsp40) member C28 [ Homo sapiens (human) ]".

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. Bibcode:2000Natur.405..311H. 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.