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{{Infobox_gene}}
{{PBB_Controls
'''Aryl-hydrocarbon-interacting protein-like 1''' is a [[protein]] that in humans is encoded by the ''AIPL1'' [[gene]].<ref name="pmid10615133">{{cite journal | vauthors = 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 | title = Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis | journal = Nat. Genet. | volume = 24 | issue = 1 | pages = 79–83  | date = Feb 2000 | pmid = 10615133 | pmc = 2581448 | doi = 10.1038/71732 }}</ref><ref name="pmid14555765">{{cite journal | vauthors = Ramamurthy V, Roberts M, van den Akker F, Niemi G, Reh TA, Hurley JB | title = AIPL1, a protein implicated in Leber's congenital amaurosis, interacts with and aids in processing of farnesylated proteins | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 100 | issue = 22 | pages = 12630–5  | date = Oct 2003 | pmid = 14555765 | pmc = 240669 | doi = 10.1073/pnas.2134194100 }}</ref><ref name="pmid15365173">{{cite journal | vauthors = Liu X, Bulgakov OV, Wen XH, Woodruff ML, Pawlyk B, Yang J, Fain GL, Sandberg MA, Makino CL, Li T | title = AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesterase | journal = Proc. Natl. Acad. Sci. U.S.A. | volume = 101 | issue = 38 | pages = 13903–8  | date = Sep 2004 | pmid = 15365173 | pmc = 518851 | doi = 10.1073/pnas.0405160101 }}</ref><ref name="entrez">{{cite web | title = Entrez Gene: AIPL1 aryl hydrocarbon receptor interacting protein-like 1| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=23746| accessdate = }}</ref>
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<!-- The GNF_Protein_box is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
== Function ==
{{GNF_Protein_box
| image =
| image_source =
| PDB =
| Name = Aryl hydrocarbon receptor interacting protein-like 1
| HGNCid = 359
| Symbol = AIPL1
| AltSymbols =; AIPL2; LCA4
| OMIM = 604392
| ECnumber = 
| Homologene = 22806
| MGIid = 2148800
| GeneAtlas_image1 = PBB_GE_AIPL1_219977_at_tn.png
| Function = {{GNF_GO|id=GO:0001918 |text = farnesylated protein binding}} {{GNF_GO|id=GO:0004872 |text = receptor activity}} {{GNF_GO|id=GO:0005488 |text = binding}} {{GNF_GO|id=GO:0051082 |text = unfolded protein binding}}
| Component = {{GNF_GO|id=GO:0001917 |text = photoreceptor inner segment}} {{GNF_GO|id=GO:0005634 |text = nucleus}} {{GNF_GO|id=GO:0005737 |text = cytoplasm}}
| Process = {{GNF_GO|id=GO:0001895 |text = retinal homeostasis}} {{GNF_GO|id=GO:0006457 |text = protein folding}} {{GNF_GO|id=GO:0007601 |text = visual perception}} {{GNF_GO|id=GO:0007603 |text = phototransduction, visible light}} {{GNF_GO|id=GO:0018343 |text = protein farnesylation}} {{GNF_GO|id=GO:0030823 |text = regulation of cGMP metabolic process}} {{GNF_GO|id=GO:0043066 |text = negative regulation of apoptosis}} {{GNF_GO|id=GO:0050896 |text = response to stimulus}}
| Orthologs = {{GNF_Ortholog_box
    | Hs_EntrezGene = 23746
    | Hs_Ensembl = ENSG00000129221
    | Hs_RefseqProtein = NP_001028226
    | Hs_RefseqmRNA = NM_001033054
    | Hs_GenLoc_db = 
    | Hs_GenLoc_chr = 17
    | Hs_GenLoc_start = 6267781
    | Hs_GenLoc_end = 6279243
    | Hs_Uniprot = Q9NZN9
    | Mm_EntrezGene = 114230
    | Mm_Ensembl = ENSMUSG00000040554
    | Mm_RefseqmRNA = NM_053245
    | Mm_RefseqProtein = NP_444475
    | Mm_GenLoc_db = 
    | Mm_GenLoc_chr = 11
    | Mm_GenLoc_start = 71845360
    | Mm_GenLoc_end = 71853653
    | Mm_Uniprot = Q5RI54
  }}
}}
'''Aryl hydrocarbon receptor interacting protein-like 1''', also known as '''AIPL1''', is a human [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: AIPL1 aryl hydrocarbon receptor interacting protein-like 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=23746| accessdate = }}</ref>


<!-- The PBB_Summary template is automatically maintained by Protein Box Bot.  See Template:PBB_Controls to Stop updates. -->
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.<ref name="entrez" />
{{PBB_Summary
| section_title =
| summary_text = 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.<ref name="entrez">{{cite web | title = Entrez Gene: AIPL1 aryl hydrocarbon receptor interacting protein-like 1| url = http://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=23746| accessdate = }}</ref>
}}


==References==
== Interactions ==
{{reflist|2}}
 
==Further reading==
AIPL1 has been shown to [[Protein-protein interaction|interact]] with [[NUB1]].<ref name=pmid12374762>{{cite journal | vauthors = Akey DT, Zhu X, Dyer M, Li A, Sorensen A, Blackshaw S, Fukuda-Kamitani T, Daiger SP, Craft CM, Kamitani T, Sohocki MM | title = The inherited blindness associated protein AIPL1 interacts with the cell cycle regulator protein NUB1 | journal = Hum. Mol. Genet. | volume = 11 | issue = 22 | pages = 2723–33  | date = Oct 2002 | pmid = 12374762 | pmc = 2585502 | doi = 10.1093/hmg/11.22.2723 }}</ref>
 
== References ==
{{reflist}}
 
== Further reading ==
{{refbegin | 2}}
{{refbegin | 2}}
{{PBB_Further_reading
* {{cite journal | vauthors = Bonaldo MF, Lennon G, Soares MB | title = Normalization and subtraction: two approaches to facilitate gene discovery | journal = Genome Res. | volume = 6 | issue = 9 | pages = 791–806 | year = 1996 | pmid = 8889548 | doi = 10.1101/gr.6.9.791 }}
| citations =
* {{cite journal | vauthors = Sohocki MM, Malone KA, Sullivan LS, Daiger SP | title = Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disorders | journal = Genomics | volume = 58 | issue = 1 | pages = 29–33 | year = 1999 | pmid = 10331942 | doi = 10.1006/geno.1999.5810 }}
*{{cite journal | author=Bonaldo MF, Lennon G, Soares MB |title=Normalization and subtraction: two approaches to facilitate gene discovery. |journal=Genome Res. |volume=6 |issue= 9 |pages= 791-806 |year= 1997 |pmid= 8889548 |doi= }}
* {{cite journal | vauthors = Damji KF, Sohocki MM, Khan R, Gupta SK, Rahim M, Loyer M, Hussein N, Karim N, Ladak SS, Jamal A, Bulman D, Koenekoop RK | title = Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p | journal = Can. J. Ophthalmol. | volume = 36 | issue = 5 | pages = 252–9 | year = 2001 | pmid = 11548141 | doi = 10.1016/s0008-4182(01)80018-1 }}
*{{cite journal | author=Sohocki MM, Malone KA, Sullivan LS, Daiger SP |title=Localization of retina/pineal-expressed sequences: identification of novel candidate genes for inherited retinal disorders. |journal=Genomics |volume=58 |issue= 1 |pages= 29-33 |year= 1999 |pmid= 10331942 |doi= 10.1006/geno.1999.5810 }}
* {{cite journal | vauthors = van der Spuy J, Chapple JP, Clark BJ, Luthert PJ, Sethi CS, Cheetham ME | title = The Leber congenital amaurosis gene product AIPL1 is localized exclusively in rod photoreceptors of the adult human retina | journal = Hum. Mol. Genet. | volume = 11 | issue = 7 | pages = 823–31 | year = 2002 | pmid = 11929855 | doi = 10.1093/hmg/11.7.823 }}
*{{cite journal | author=Sohocki MM, Bowne SJ, Sullivan LS, ''et al.'' |title=Mutations in a new photoreceptor-pineal gene on 17p cause Leber congenital amaurosis. |journal=Nat. Genet. |volume=24 |issue= 1 |pages= 79-83 |year= 2000 |pmid= 10615133 |doi= 10.1038/71732 }}
* {{cite journal | vauthors = Akey DT, Zhu X, Dyer M, Li A, Sorensen A, Blackshaw S, Fukuda-Kamitani T, Daiger SP, Craft CM, Kamitani T, Sohocki MM | title = The inherited blindness associated protein AIPL1 interacts with the cell cycle regulator protein NUB1 | journal = Hum. Mol. Genet. | volume = 11 | issue = 22 | pages = 2723–33 | year = 2002 | pmid = 12374762 | pmc = 2585502 | doi = 10.1093/hmg/11.22.2723 }}
*{{cite journal  | author=Damji KF, Sohocki MM, Khan R, ''et al.'' |title=Leber's congenital amaurosis with anterior keratoconus in Pakistani families is caused by the Trp278X mutation in the AIPL1 gene on 17p. |journal=Can. J. Ophthalmol. |volume=36 |issue= 5 |pages= 252-9 |year= 2002 |pmid= 11548141 |doi= }}
* {{cite journal | vauthors = Kanaya K, Sohocki MM, Kamitani T | title = Abolished interaction of NUB1 with mutant AIPL1 involved in Leber congenital amaurosis | journal = Biochem. Biophys. Res. Commun. | volume = 317 | issue = 3 | pages = 768–73 | year = 2004 | pmid = 15081406 | doi = 10.1016/j.bbrc.2004.03.108 }}
*{{cite journal | author=van der Spuy J, Chapple JP, Clark BJ, ''et al.'' |title=The Leber congenital amaurosis gene product AIPL1 is localized exclusively in rod photoreceptors of the adult human retina. |journal=Hum. Mol. Genet. |volume=11 |issue= 7 |pages= 823-31 |year= 2002 |pmid= 11929855 |doi= }}
* {{cite journal | vauthors = Akey DT, Zhu X, Dyer M, Li A, Sorensen A, Fukada-Kamitani T, Daiger SP, Craft C, Kamitani T, Sohocki MM | title = Functional studies of AIPL1: potential role of AIPL1 in cell cycle exit and/or differentiation of photoreceptors | journal = Adv. Exp. Med. Biol. | volume = 533 | issue =  | pages = 287–95 | year = 2003 | pmid = 15180275 | doi = 10.1007/978-1-4615-0067-4_35 }}
*{{cite journal | author=Akey DT, Zhu X, Dyer M, ''et al.'' |title=The inherited blindness associated protein AIPL1 interacts with the cell cycle regulator protein NUB1. |journal=Hum. Mol. Genet. |volume=11 |issue= 22 |pages= 2723-33 |year= 2003 |pmid= 12374762 |doi=  }}
* {{cite journal | vauthors = Dharmaraj S, Leroy BP, Sohocki MM, Koenekoop RK, Perrault I, Anwar K, Khaliq S, Devi RS, Birch DG, De Pool E, Izquierdo N, Van Maldergem L, Ismail M, Payne AM, Holder GE, Bhattacharya SS, Bird AC, Kaplan J, Maumenee IH | title = The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations | journal = Arch. Ophthalmol. | volume = 122 | issue = 7 | pages = 1029–37 | year = 2004 | pmid = 15249368 | doi = 10.1001/archopht.122.7.1029 }}
*{{cite journal  | author=Strausberg RL, Feingold EA, Grouse LH, ''et al.'' |title=Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=99 |issue= 26 |pages= 16899-903 |year= 2003 |pmid= 12477932 |doi= 10.1073/pnas.242603899 }}
* {{cite journal | vauthors = van der Spuy J, Cheetham ME | title = The Leber congenital amaurosis protein AIPL1 modulates the nuclear translocation of NUB1 and suppresses inclusion formation by NUB1 fragments | journal = J. Biol. Chem. | volume = 279 | issue = 46 | pages = 48038–47 | year = 2004 | pmid = 15347646 | doi = 10.1074/jbc.M407871200 }}
*{{cite journal  | author=Ramamurthy V, Roberts M, van den Akker F, ''et al.'' |title=AIPL1, a protein implicated in Leber's congenital amaurosis, interacts with and aids in processing of farnesylated proteins. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=100 |issue= 22 |pages= 12630-5 |year= 2004 |pmid= 14555765 |doi= 10.1073/pnas.2134194100 }}
* {{cite journal | vauthors = Gallon VA, Wilkie SE, Deery EC, Newbold RJ, Sohocki MM, Bhattacharya SS, Hunt DM, Warren MJ | title = Purification, characterisation and intracellular localisation of aryl hydrocarbon interacting protein-like 1 (AIPL1) and effects of mutations associated with inherited retinal dystrophies | journal = Biochim. Biophys. Acta | volume = 1690 | issue = 2 | pages = 141–9 | year = 2004 | pmid = 15469903 | doi = 10.1016/j.bbadis.2004.06.012 }}
*{{cite journal | author=Ota T, Suzuki Y, Nishikawa T, ''et al.'' |title=Complete sequencing and characterization of 21,243 full-length human cDNAs. |journal=Nat. Genet. |volume=36 |issue= 1 |pages= 40-5 |year= 2004 |pmid= 14702039 |doi= 10.1038/ng1285 }}
* {{cite journal | vauthors = Booij JC, Florijn RJ, ten Brink JB, Loves W, Meire F, van Schooneveld MJ, de Jong PT, Bergen AA | title = Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa | journal = J. Med. Genet. | volume = 42 | issue = 11 | pages = e67 | year = 2005 | pmid = 16272259 | pmc = 1735944 | doi = 10.1136/jmg.2005.035121 }}
*{{cite journal  | author=Kanaya K, Sohocki MM, Kamitani T |title=Abolished interaction of NUB1 with mutant AIPL1 involved in Leber congenital amaurosis. |journal=Biochem. Biophys. Res. Commun. |volume=317 |issue= 3 |pages= 768-73 |year= 2004 |pmid= 15081406 |doi= 10.1016/j.bbrc.2004.03.108 }}
*{{cite journal | author=Akey DT, Zhu X, Dyer M, ''et al.'' |title=Functional studies of AIPL1: potential role of AIPL1 in cell cycle exit and/or differentiation of photoreceptors. |journal=Adv. Exp. Med. Biol. |volume=533 |issue=  |pages= 287-95 |year= 2004 |pmid= 15180275 |doi= }}
*{{cite journal | author=Dharmaraj S, Leroy BP, Sohocki MM, ''et al.'' |title=The phenotype of Leber congenital amaurosis in patients with AIPL1 mutations. |journal=Arch. Ophthalmol. |volume=122 |issue= 7 |pages= 1029-37 |year= 2004 |pmid= 15249368 |doi= 10.1001/archopht.122.7.1029 }}
*{{cite journal | author=van der Spuy J, Cheetham ME |title=The Leber congenital amaurosis protein AIPL1 modulates the nuclear translocation of NUB1 and suppresses inclusion formation by NUB1 fragments. |journal=J. Biol. Chem. |volume=279 |issue= 46 |pages= 48038-47 |year= 2005 |pmid= 15347646 |doi= 10.1074/jbc.M407871200 }}
*{{cite journal | author=Liu X, Bulgakov OV, Wen XH, ''et al.'' |title=AIPL1, the protein that is defective in Leber congenital amaurosis, is essential for the biosynthesis of retinal rod cGMP phosphodiesterase. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=101 |issue= 38 |pages= 13903-8 |year= 2004 |pmid= 15365173 |doi= 10.1073/pnas.0405160101 }}
*{{cite journal  | author=Gallon VA, Wilkie SE, Deery EC, ''et al.'' |title=Purification, characterisation and intracellular localisation of aryl hydrocarbon interacting protein-like 1 (AIPL1) and effects of mutations associated with inherited retinal dystrophies. |journal=Biochim. Biophys. Acta |volume=1690 |issue= 2 |pages= 141-9 |year= 2004 |pmid= 15469903 |doi= 10.1016/j.bbadis.2004.06.012 }}
*{{cite journal | author=Gerhard DS, Wagner L, Feingold EA, ''et al.'' |title=The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC). |journal=Genome Res. |volume=14 |issue= 10B |pages= 2121-7 |year= 2004 |pmid= 15489334 |doi= 10.1101/gr.2596504 }}
*{{cite journal  | author=Booij JC, Florijn RJ, ten Brink JB, ''et al.'' |title=Identification of mutations in the AIPL1, CRB1, GUCY2D, RPE65, and RPGRIP1 genes in patients with juvenile retinitis pigmentosa. |journal=J. Med. Genet. |volume=42 |issue= 11 |pages= e67 |year= 2006 |pmid= 16272259 |doi= 10.1136/jmg.2005.035121 }}
}}
{{refend}}
{{refend}}


{{protein-stub}}
== External links ==
{{WikiDoc Sources}}
* {{UCSC gene info|AIPL1}}
* [https://www.ncbi.nlm.nih.gov/books/NBK1417/  GeneReviews/NCBI/NIH/UW entry on Retinitis Pigmentosa Overview]
 
 
{{gene-17-stub}}

Latest revision as of 17:54, 29 August 2017

VALUE_ERROR (nil)
Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez

n/a

n/a

Ensembl

n/a

n/a

UniProt

n/a

n/a

RefSeq (mRNA)

n/a

n/a

RefSeq (protein)

n/a

n/a

Location (UCSC)n/an/a
PubMed searchn/an/a
Wikidata
View/Edit Human

Aryl-hydrocarbon-interacting protein-like 1 is a protein that in humans is encoded by the AIPL1 gene.[1][2][3][4]

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.[4]

Interactions

AIPL1 has been shown to interact with NUB1.[5]

References

  1. ↑ 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.
  2. ↑ 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.
  3. ↑ 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.
  4. ↑ 4.0 4.1 "Entrez Gene: AIPL1 aryl hydrocarbon receptor interacting protein-like 1".
  5. ↑ 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.

Further reading

External links


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