AIPL1

AIPL1
Identifiers
Aliases	AIPL1, AIPL2, LCA4, aryl hydrocarbon receptor interacting protein like 1
External IDs	OMIM: 604392 MGI: 2148800 HomoloGene: 22806 GeneCards: AIPL1
showGene location (Human)
Chr.	Chromosome 17 (human)
End	6,435,199 bp
showGene location (Mouse)
Chr.	Chromosome 11 (mouse)
End	71,928,335 bp
showRNA expression pattern
	Top expressed in
	retina; ; retinal pigment epithelium; ; pituitary gland; ; muscle tissue; ; stomach; ; temporal lobe; ; hypothalamus; ; anterior pituitary;
	More reference expression data
	More reference expression data
showGene ontology
Molecular function	unfolded protein binding; GO:0001948 protein binding; farnesylated protein binding; peptidyl-prolyl cis-trans isomerase activity;
Cellular component	photoreceptor inner segment; cytoplasm; nucleus; nucleoplasm; cytosol;
Biological process	retina homeostasis; negative regulation of apoptotic process; protein farnesylation; response to stimulus; visual perception; phototransduction, visible light; regulation of rhodopsin mediated signaling pathway; protein peptidyl-prolyl isomerization;
	Sources:Amigo / QuickGO
Orthologs
	23746
	114230
	ENSG00000129221
	ENSMUSG00000040554
	Q9NZN9
	Q924K1
showNM_014336; NM_001033054; NM_001033055; NM_001285399; NM_001285400;
	NM_001285401; NM_001285402; NM_001285403
	NM_053245
showNP_001028226; NP_001028227; NP_001272328; NP_001272329; NP_001272330;
	NP_001272331; NP_001272332; NP_055151
	NP_444475
	Wikidata
View/Edit Human	View/Edit Mouse

Aryl-hydrocarbon-interacting protein-like 1 is a protein that in humans is encoded by the AIPL1 gene.^[5]^[6]^[7]^[8]

Function[]

Leber congenital amaurosis (LCA) accounts for at least 5% of all inherited retinal disease and is the most severe inherited retinopathy with the earliest age of onset. Individuals affected with LCA are diagnosed at birth or in the first few months of life with severely impaired vision or blindness, nystagmus and an abnormal or flat electroretinogram. The photoreceptor/pineal -expressed gene, AIPL1, encoding aryl-hydrocarbon interacting protein-like 1, was mapped within the LCA4 candidate region. The protein contains three tetratricopeptide motifs, consistent with nuclear transport or chaperone activity. AIPL1 mutations may cause approximately 20% of recessive LCA.^[8]

Interactions[]

AIPL1 has been shown to interact with NUB1.^[9]

References[]

^ Jump up to: ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000129221 - Ensembl, May 2017
^ Jump up to: ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000040554 - 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.
^ Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP (Feb 2000). "Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis". Nat. Genet. 24 (1): 79–83. doi:10.1038/71732. PMC 2581448. PMID 10615133.
^ Ramamurthy V, Roberts M, van den Akker F, Niemi G, Reh TA, Hurley JB (Oct 2003). "AIPL1, a protein implicated in Leber's congenital amaurosis, interacts with and aids in processing of farnesylated proteins". Proc. Natl. Acad. Sci. U.S.A. 100 (22): 12630–5. doi:10.1073/pnas.2134194100. PMC 240669. PMID 14555765.
^ Liu X, Bulgakov OV, Wen XH, Woodruff ML, Pawlyk B, Yang J, Fain GL, Sandberg MA, Makino CL, Li T (Sep 2004). "AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesterase". Proc. Natl. Acad. Sci. U.S.A. 101 (38): 13903–8. doi:10.1073/pnas.0405160101. PMC 518851. PMID 15365173.
^ Jump up to: ^a ^b "Entrez Gene: AIPL1 aryl hydrocarbon receptor interacting protein-like 1".
^ Akey DT, Zhu X, Dyer M, Li A, Sorensen A, Blackshaw S, Fukuda-Kamitani T, Daiger SP, Craft CM, Kamitani T, Sohocki MM (Oct 2002). "The inherited blindness associated protein AIPL1 interacts with the cell cycle regulator protein NUB1". Hum. Mol. Genet. 11 (22): 2723–33. doi:10.1093/hmg/11.22.2723. PMC 2585502. PMID 12374762.

External links[]

Human AIPL1 genome location and AIPL1 gene details page in the UCSC Genome Browser.
GeneReviews/NCBI/NIH/UW entry on Retinitis Pigmentosa Overview

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

[refGRCh38Ensembl-1] Jump up to: ^a ^b ^c GRCh38: Ensembl release 89: ENSG00000129221 - Ensembl, May 2017

[refGRCm38Ensembl-2] Jump up to: ^a ^b ^c GRCm38: Ensembl release 89: ENSMUSG00000040554 - 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.

[pmid10615133-5] Sohocki MM, Bowne SJ, Sullivan LS, Blackshaw S, Cepko CL, Payne AM, Bhattacharya SS, Khaliq S, Qasim Mehdi S, Birch DG, Harrison WR, Elder FF, Heckenlively JR, Daiger SP (Feb 2000). "Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis". Nat. Genet. 24 (1): 79–83. doi:10.1038/71732. PMC 2581448. PMID 10615133.

[pmid14555765-6] Ramamurthy V, Roberts M, van den Akker F, Niemi G, Reh TA, Hurley JB (Oct 2003). "AIPL1, a protein implicated in Leber's congenital amaurosis, interacts with and aids in processing of farnesylated proteins". Proc. Natl. Acad. Sci. U.S.A. 100 (22): 12630–5. doi:10.1073/pnas.2134194100. PMC 240669. PMID 14555765.

[pmid15365173-7] Liu X, Bulgakov OV, Wen XH, Woodruff ML, Pawlyk B, Yang J, Fain GL, Sandberg MA, Makino CL, Li T (Sep 2004). "AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesterase". Proc. Natl. Acad. Sci. U.S.A. 101 (38): 13903–8. doi:10.1073/pnas.0405160101. PMC 518851. PMID 15365173.

[entrez-8] Jump up to: ^a ^b "Entrez Gene: AIPL1 aryl hydrocarbon receptor interacting protein-like 1".

[pmid12374762-9] Akey DT, Zhu X, Dyer M, Li A, Sorensen A, Blackshaw S, Fukuda-Kamitani T, Daiger SP, Craft CM, Kamitani T, Sohocki MM (Oct 2002). "The inherited blindness associated protein AIPL1 interacts with the cell cycle regulator protein NUB1". Hum. Mol. Genet. 11 (22): 2723–33. doi:10.1093/hmg/11.22.2723. PMC 2585502. PMID 12374762.

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AIPL1

Contents

Function[]

Interactions[]

References[]

Further reading[]

External links[]