RSPH1

Radial spoke head 1 homolog (RSPH1), also known as cancer/testis antigen 79 (CT79) or testis-specific gene A2 protein (TSGA2), is a protein that in humans is encoded by the RSPH1 gene.[5]

RSPH1
Identifiers
Aliases	RSPH1, CILD24, RSP44, RSPH10A, TSA2, TSGA2, CT79, radial spoke head 1 homolog, radial spoke head component 1
External IDs	OMIM: 609314 MGI: 1194909 HomoloGene: 11905 GeneCards: RSPH1
Gene location (Human) Chr. Chromosome 21 (human)[1] Band 21q22.3 Start 42,472,486 bp[1] End 42,496,246 bp[1]
Gene location (Mouse) Chr. Chromosome 17 (mouse)[2] Band 17 A3.3|17 15.94 cM Start 31,255,019 bp[2] End 31,277,383 bp[2]
Gene ontology Molecular function • GO:0001948 protein binding Cellular component • cytoplasm • condensed nuclear chromosome • meiotic spindle • outer dense fiber • cytosol • cell projection • motile cilium • sperm flagellum • cilium • cell nucleus Biological process • GO:0007126 meiotic cell cycle • axoneme assembly • spermatid development Sources:Amigo / QuickGO
Orthologs
Species	Human	Mouse
Entrez	89765	22092
Ensembl	ENSG00000160188	ENSMUSG00000024033
UniProt	Q8WYR4	Q8VIG3
RefSeq (mRNA)	NM_001286506 NM_080860	NM_025290 NM_001364916
RefSeq (protein)	NP_001273435 NP_543136	NP_079566 NP_001351845
Location (UCSC)	Chr 21: 42.47 – 42.5 Mb	Chr 17: 31.26 – 31.28 Mb
PubMed search	[3]	[4]
Wikidata
View/Edit Human View/Edit Mouse

Clinical significance

Mutations in RSPH1 are associated to Primary ciliary dyskinesia.[6]

References

1. GRCh38: Ensembl release 89: ENSG00000160188 - Ensembl, May 2017
2. GRCm38: Ensembl release 89: ENSMUSG00000024033 - 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: radial spoke head 1 homolog (Chlamydomonas)".
6. Kott E, Legendre M, Copin B, Papon JF, Dastot-Le Moal F, Montantin G, Duquesnoy P, Piterboth W, Amram D, Bassinet L, Beucher J, Beydon N, Deneuville E, Houdouin V, Journel H, Just J, Nathan N, Tamalet A, Collot N, Jeanson L, Le Gouez M, Vallette B, Vojtek AM, Epaud R, Coste A, Clement A, Housset B, Louis B, Escudier E, Amselem S (September 2013). "Loss-of-function mutations in RSPH1 cause primary ciliary dyskinesia with central-complex and radial-spoke defects". Am. J. Hum. Genet. 93 (3): 561–70. doi:10.1016/j.ajhg.2013.07.013. PMC 3769924. PMID 23993197.

Further reading

• Strausberg RL, Feingold EA, Grouse LH, et al. (2002). "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.
• Shetty J, Klotz KL, Wolkowicz MJ, et al. (2007). "Radial spoke protein 44 (human meichroacidin) is an axonemal alloantigen of sperm and cilia". Gene. 396 (1): 93–107. doi:10.1016/j.gene.2007.02.031. PMC 1935023. PMID 17451891.
• Hu YH, Warnatz HJ, Vanhecke D, et al. (2006). "Cell array-based intracellular localization screening reveals novel functional features of human chromosome 21 proteins". BMC Genomics. 7: 155. doi:10.1186/1471-2164-7-155. PMC 1526728. PMID 16780588.
• Taketo MM, Araki Y, Matsunaga A, et al. (1997). "Mapping of eight testis-specific genes to mouse chromosomes". Genomics. 46 (1): 138–42. doi:10.1006/geno.1997.5014. PMID 9403069.
• 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.
• Tsuchida J, Nishina Y, Wakabayashi N, et al. (1998). "Molecular cloning and characterization of meichroacidin (male meiotic metaphase chromosome-associated acidic protein)". Dev. Biol. 197 (1): 67–76. doi:10.1006/dbio.1998.8885. PMID 9578619.
• 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.