LRRC48

DRC3
Identifiers
Aliases	DRC3 , LRRC48, CFAP134, dynein regulatory complex subunit 3
External IDs	MGI: 1921915 HomoloGene: 12581 GeneCards: DRC3
Gene location (Human)
Chr.	Chromosome 17 (human)
End	18,016,889 bp
Gene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	60,285,167 bp
RNA expression pattern
	Top expressed in
	right uterine tube; ; bronchial epithelial cell; ; anterior pituitary; ; caput epididymis; ; right lobe of thyroid gland; ; left lobe of thyroid gland; ; canal of the cervix; ; right lung; ; left uterine tube; ; sural nerve;
	Top expressed in
	spermatocyte; ; spermatid; ; seminiferous tubule; ; interventricular septum; ; respiratory epithelium; ; olfactory epithelium; ; utricle; ; right lung lobe; ; left lung; ; visual cortex;
	More reference expression data
	More reference expression data
Orthologs
	83450
	74665
	ENSG00000171962
	ENSMUSG00000056598
	Q9H069
	Q9D5E4
	NM_001130090 ; NM_001130091 ; NM_001130092 ; NM_031294
	NM_029044
	NP_001123562 ; NP_001123563 ; NP_001123564 ; NP_112584
	NP_083320
	Wikidata
View/Edit Human	View/Edit Mouse

Last updated October 14, 2022

Leucine-rich repeat-containing protein 48 is a protein that in humans is encoded by the LRRC48 gene.^[5]^[6]^[7]

Related Research Articles

Bardet–Biedl syndrome 5 protein is a protein that in humans is encoded by the BBS5 gene.

39S ribosomal protein L15, mitochondrial is a protein that in humans is encoded by the MRPL15 gene.

Mitochondrial dynamic protein MID51 (MID51) also known as mitochondrial elongation factor 1 (MIEF1) or Smith-Magenis syndrome chromosome region candidate gene 7 protein-like (SMCR7L) is a protein that in humans is encoded by the SMCR7L gene.

PH domain and leucine rich repeat protein phosphatase-like, also known as PHLPPL, is an enzyme which in humans is encoded by the PHLPPL gene.

AP-1 complex-associated regulatory protein is a protein that in humans is encoded by the AP1AR gene.

SPATS2-like protein or DNAPTP6 is a protein that in humans is encoded by the SPATS2L gene.

Ectoderm-neural cortex protein 2 is a protein that in humans is encoded by the KLHL25 gene.

Polycomb group RING finger protein 5 is a protein that in humans is encoded by the PCGF5 gene.

Leucine-rich repeat-containing protein 39 is a protein that in humans is encoded by the LRRC39 gene.

Transmembrane and TPR repeat-containing protein 2 is a protein that in humans is encoded by the TMTC2 gene.

Protein FAM32A is a protein that in humans is encoded by the FAM32A gene.

KATNBL1 is a protein that in humans is encoded by the KATNBL1 gene.

Transmembrane protein 22 is a protein that in humans is encoded by the TMEM22 gene.

Tudor domain-containing protein 3 is a protein that in humans is encoded by the TDRD3 gene. It contains a Tudor domain and UBA protein domain and has three distinct Protein isoforms.

Coiled-coil domain-containing protein 3 is a protein that in humans is encoded by the CCDC3 gene.

Protein FAM57B is a protein that in humans is encoded by the FAM57B gene.

UPF0528 protein FAM172A is a protein that in humans is encoded by the FAM172A gene.

Protein FAM186B is a protein that in humans is encoded by the FAM186B gene.

Transmembrane protein 117 is a protein that in humans is encoded by the TMEM117 gene.

NudC domain-containing protein 2 is a protein that in humans is encoded by the NUDCD2 gene.

References

1 2 3 GRCh38: Ensembl release 89: ENSG00000171962 - Ensembl, May 2017
1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000056598 - 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.
↑ Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Bocher M, Blocker H, Bauersachs S, Blum H, Lauber J, Dusterhoft A, Beyer A, Kohrer K, Strack N, Mewes HW, Ottenwalder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A (Mar 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072 . PMID 11230166.
↑ Bi W, Yan J, Stankiewicz P, Park SS, Walz K, Boerkoel CF, Potocki L, Shaffer LG, Devriendt K, Nowaczyk MJ, Inoue K, Lupski JR (May 2002). "Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse". Genome Res. 12 (5): 713–28. doi:10.1101/gr.73702. PMC 186594 . PMID 11997338.
↑ "Entrez Gene: LRRC48 leucine rich repeat containing 48".

Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination". Genome Res. 10 (11): 1788–95. doi:10.1101/gr.143000. PMC 310948 . PMID 11076863.
Simpson JC, Wellenreuther R, Poustka A, et al. (2001). "Systematic subcellular localization of novel proteins identified by large-scale cDNA sequencing". EMBO Rep. 1 (3): 287–92. doi:10.1093/embo-reports/kvd058. PMC 1083732 . PMID 11256614.
Lucas RE, Vlangos CN, Das P, et al. (2002). "Genomic organisation of the approximately 1.5 Mb Smith-Magenis syndrome critical interval: transcription map, genomic contig, and candidate gene analysis". Eur. J. Hum. Genet. 9 (12): 892–902. doi: 10.1038/sj.ejhg.5200734 . PMID 11840190.
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.
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.
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.
Wiemann S, Arlt D, Huber W, et al. (2004). "From ORFeome to biology: a functional genomics pipeline". Genome Res. 14 (10B): 2136–44. doi:10.1101/gr.2576704. PMC 528930 . PMID 15489336.
Mehrle A, Rosenfelder H, Schupp I, et al. (2006). "The LIFEdb database in 2006". Nucleic Acids Res. 34 (Database issue): D415–8. doi:10.1093/nar/gkj139. PMC 1347501 . PMID 16381901.

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

This page is based on this Wikipedia article
Text is available under the CC BY-SA 4.0 license; additional terms may apply.
Images, videos and audio are available under their respective licenses.

[refGRCh38Ensembl-1] 1 2 3 GRCh38: Ensembl release 89: ENSG00000171962 - Ensembl, May 2017

[refGRCm38Ensembl-2] 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000056598 - 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.

[pmid11230166-5] Wiemann S, Weil B, Wellenreuther R, Gassenhuber J, Glassl S, Ansorge W, Bocher M, Blocker H, Bauersachs S, Blum H, Lauber J, Dusterhoft A, Beyer A, Kohrer K, Strack N, Mewes HW, Ottenwalder B, Obermaier B, Tampe J, Heubner D, Wambutt R, Korn B, Klein M, Poustka A (Mar 2001). "Toward a catalog of human genes and proteins: sequencing and analysis of 500 novel complete protein coding human cDNAs". Genome Res. 11 (3): 422–35. doi:10.1101/gr.GR1547R. PMC 311072 . PMID 11230166.

[pmid11997338-6] Bi W, Yan J, Stankiewicz P, Park SS, Walz K, Boerkoel CF, Potocki L, Shaffer LG, Devriendt K, Nowaczyk MJ, Inoue K, Lupski JR (May 2002). "Genes in a refined Smith-Magenis syndrome critical deletion interval on chromosome 17p11.2 and the syntenic region of the mouse". Genome Res. 12 (5): 713–28. doi:10.1101/gr.73702. PMC 186594 . PMID 11997338.

[entrez-7] "Entrez Gene: LRRC48 leucine rich repeat containing 48".

[1]

[2]

[3]

[4]

[5]

[6]

[7]

LRRC48

Related Research Articles

References

Further reading