PICALM: Difference between revisions

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{{Infobox_gene}}
{{Infobox_gene}}
'''Phosphatidylinositol binding clathrin assembly protein''', also known as '''PICALM''', is a [[protein]] which in humans is encoded by the ''PICALM'' [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: PICALM phosphatidylinositol binding clathrin assembly protein| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8301| accessdate = }}</ref>
'''Phosphatidylinositol binding clathrin assembly protein''', also known as '''PICALM''', is a [[protein]] which in humans is encoded by the ''PICALM'' [[gene]].<ref name="entrez">{{cite web | title = Entrez Gene: PICALM phosphatidylinositol binding clathrin assembly protein| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8301| accessdate = }}</ref>
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== Interactions ==
== Interactions ==
PICALM has been shown to [[Protein-protein interaction|interact]] with [[CLTC]].<ref name=pmid10436022>{{cite journal |last=Tebar |first=F |authorlink= |author2=Bohlander S K |author3=Sorkin A  |date=Aug 1999 |title=Clathrin assembly lymphoid myeloid leukemia (CALM) protein: localization in endocytic-coated pits, interactions with clathrin, and the impact of overexpression on clathrin-mediated traffic |journal=Mol. Biol. Cell |volume=10 |issue=8 |pages=2687–702 |publisher= |location = UNITED STATES| issn = 1059-1524| pmid = 10436022 | bibcode = | oclc =| id = | url = | language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pmc=25500 | doi=10.1091/mbc.10.8.2687}}</ref>
PICALM has been shown to [[Protein-protein interaction|interact]] with [[CLTC]].<ref name=pmid10436022>{{cite journal |last=Tebar |first=F |authorlink= |author2=Bohlander S K |author3=Sorkin A  |date=Aug 1999 |title=Clathrin assembly lymphoid myeloid leukemia (CALM) protein: localization in endocytic-coated pits, interactions with clathrin, and the impact of overexpression on clathrin-mediated traffic |journal=Mol. Biol. Cell |volume=10 |issue=8 |pages=2687–702 |publisher= |location = UNITED STATES| issn = 1059-1524| pmid = 10436022 | bibcode = | oclc =| id = | url = http://diposit.ub.edu/dspace/bitstream/2445/25184/1/566402.pdf| language = | format = | accessdate = | laysummary = | laysource = | laydate = | quote = |pmc=25500 | doi=10.1091/mbc.10.8.2687}}</ref>


== Clinical significance ==
== Clinical significance ==
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| citations =  
| citations =  
*{{cite journal |vauthors=Ron D, Habener JF |title=CHOP, a novel developmentally regulated nuclear protein that dimerizes with transcription factors C/EBP and LAP and functions as a dominant-negative inhibitor of gene transcription. |journal=Genes Dev. |volume=6 |issue= 3 |pages= 439–53 |year= 1992 |pmid= 1547942 |doi=10.1101/gad.6.3.439 }}
*{{cite journal |vauthors=Ron D, Habener JF |title=CHOP, a novel developmentally regulated nuclear protein that dimerizes with transcription factors C/EBP and LAP and functions as a dominant-negative inhibitor of gene transcription. |journal=Genes Dev. |volume=6 |issue= 3 |pages= 439–53 |year= 1992 |pmid= 1547942 |doi=10.1101/gad.6.3.439 }}
*{{cite journal  |vauthors=Dreyling MH, Martinez-Climent JA, Zheng M, etal |title=The t(10;11)(p13;q14) in the U937 cell line results in the fusion of the AF10 gene and CALM, encoding a new member of the AP-3 clathrin assembly protein family. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=93 |issue= 10 |pages= 4804–9 |year= 1996 |pmid= 8643484 |doi= 10.1073/pnas.93.10.4804| pmc=39360 }}
*{{cite journal  |vauthors=Dreyling MH, Martinez-Climent JA, Zheng M, etal |title=The t(10;11)(p13;q14) in the U937 cell line results in the fusion of the AF10 gene and CALM, encoding a new member of the AP-3 clathrin assembly protein family. |journal=Proc. Natl. Acad. Sci. U.S.A. |volume=93 |issue= 10 |pages= 4804–9 |year= 1996 |pmid= 8643484 |doi= 10.1073/pnas.93.10.4804| pmc=39360 |bibcode=1996PNAS...93.4804D }}
*{{cite journal  |vauthors=Silliman CC, McGavran L, Wei Q, etal |title=Alternative splicing in wild-type AF10 and CALM cDNAs and in AF10-CALM and CALM-AF10 fusion cDNAs produced by the t(10;11)(p13-14;q14-q21) suggests a potential role for truncated AF10 polypeptides. |journal=Leukemia |volume=12 |issue= 9 |pages= 1404–10 |year= 1998 |pmid= 9737689 |doi=10.1038/sj.leu.2401109 }}
*{{cite journal  |vauthors=Silliman CC, McGavran L, Wei Q, etal |title=Alternative splicing in wild-type AF10 and CALM cDNAs and in AF10-CALM and CALM-AF10 fusion cDNAs produced by the t(10;11)(p13-14;q14-q21) suggests a potential role for truncated AF10 polypeptides. |journal=Leukemia |volume=12 |issue= 9 |pages= 1404–10 |year= 1998 |pmid= 9737689 |doi=10.1038/sj.leu.2401109 }}
*{{cite journal |vauthors=Tebar F, Bohlander SK, Sorkin A |title=Clathrin assembly lymphoid myeloid leukemia (CALM) protein: localization in endocytic-coated pits, interactions with clathrin, and the impact of overexpression on clathrin-mediated traffic. |journal=Mol. Biol. Cell |volume=10 |issue= 8 |pages= 2687–702 |year= 1999 |pmid= 10436022 |doi= 10.1091/mbc.10.8.2687| pmc=25500 }}
*{{cite journal |vauthors=Tebar F, Bohlander SK, Sorkin A |title=Clathrin assembly lymphoid myeloid leukemia (CALM) protein: localization in endocytic-coated pits, interactions with clathrin, and the impact of overexpression on clathrin-mediated traffic. |journal=Mol. Biol. Cell |volume=10 |issue= 8 |pages= 2687–702 |year= 1999 |pmid= 10436022 |doi= 10.1091/mbc.10.8.2687| pmc=25500 }}
*{{cite journal  |vauthors=Kim JA, Kim SR, Jung YK, etal |title=Properties of GST-CALM expressed in E. coli. |journal=Exp. Mol. Med. |volume=32 |issue= 2 |pages= 93–9 |year= 2000 |pmid= 10926122 |doi= }}
*{{cite journal  |vauthors=Kim JA, Kim SR, Jung YK, etal |title=Properties of GST-CALM expressed in E. coli. |journal=Exp. Mol. Med. |volume=32 |issue= 2 |pages= 93–9 |year= 2000 |pmid= 10926122 |doi= }}
*{{cite journal  |vauthors=Wechsler DS, Engstrom LD, Alexander BM, etal |title=A novel chromosomal inversion at 11q23 in infant acute myeloid leukemia fuses MLL to CALM, a gene that encodes a clathrin assembly protein. |journal=Genes Chromosomes Cancer |volume=36 |issue= 1 |pages= 26–36 |year= 2003 |pmid= 12461747 |doi= 10.1002/gcc.10136 }}
*{{cite journal  |vauthors=Wechsler DS, Engstrom LD, Alexander BM, etal |title=A novel chromosomal inversion at 11q23 in infant acute myeloid leukemia fuses MLL to CALM, a gene that encodes a clathrin assembly protein. |journal=Genes Chromosomes Cancer |volume=36 |issue= 1 |pages= 26–36 |year= 2003 |pmid= 12461747 |doi= 10.1002/gcc.10136 }}
*{{cite journal  |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |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 | pmc=139241 }}
*{{cite journal  |vauthors=Strausberg RL, Feingold EA, Grouse LH, etal |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 | pmc=139241 |bibcode=2002PNAS...9916899M }}
*{{cite journal  |vauthors=Ota T, Suzuki Y, Nishikawa T, etal |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=Ota T, Suzuki Y, Nishikawa T, etal |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=Brandenberger R, Wei H, Zhang S, etal |title=Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation. |journal=Nat. Biotechnol. |volume=22 |issue= 6 |pages= 707–16 |year= 2005 |pmid= 15146197 |doi= 10.1038/nbt971 }}
*{{cite journal  |vauthors=Brandenberger R, Wei H, Zhang S, etal |title=Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation. |journal=Nat. Biotechnol. |volume=22 |issue= 6 |pages= 707–16 |year= 2005 |pmid= 15146197 |doi= 10.1038/nbt971 }}

Latest revision as of 15:15, 4 November 2018

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Identifiers
Aliases
External IDsGeneCards: [1]
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

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RefSeq (protein)

n/a

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

Phosphatidylinositol binding clathrin assembly protein, also known as PICALM, is a protein which in humans is encoded by the PICALM gene.[1]

Interactions

PICALM has been shown to interact with CLTC.[2]

Clinical significance

In humans, certain alleles of this gene have been statistically associated with an increased risk of developing late-onset Alzheimer's disease.[3]

References

  1. "Entrez Gene: PICALM phosphatidylinositol binding clathrin assembly protein".
  2. Tebar, F; Bohlander S K; Sorkin A (Aug 1999). "Clathrin assembly lymphoid myeloid leukemia (CALM) protein: localization in endocytic-coated pits, interactions with clathrin, and the impact of overexpression on clathrin-mediated traffic" (PDF). Mol. Biol. Cell. UNITED STATES. 10 (8): 2687–702. doi:10.1091/mbc.10.8.2687. ISSN 1059-1524. PMC 25500. PMID 10436022.
  3. Harold D, Abraham R, Hollingworth P, et al. (September 2009). "Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease". Nat. Genet. 41 (10): 1088–93. doi:10.1038/ng.440. PMC 2845877. PMID 19734902. Lay summaryTIME Magazine (2009-09-06).

Further reading