Cannabis Ruderalis

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{{PBB_Further_reading
{{PBB_Further_reading
| citations =
| citations =
*{{cite journal | author=Shaw MA, Brunetti-Pierri N, Kádasi L, ''et al.'' |title=Identification of three novel SEDL mutations, including mutation in the rare, non-canonical splice site of exon 4. |journal=Clin. Genet. |volume=64 |issue= 3 |pages= 235-42 |year= 2004 |pmid= 12919139 |doi= }}
*{{cite journal | author=Shaw MA, Brunetti-Pierri N, Kádasi L, ''et al.'' |title=Identification of three novel SEDL mutations, including mutation in the rare, non-canonical splice site of exon 4. |journal=Clin. Genet. |volume=64 |issue= 3 |pages= 235–42 |year= 2004 |pmid= 12919139 |doi= }}
*{{cite journal | author=Adams MD, Soares MB, Kerlavage AR, ''et al.'' |title=Rapid cDNA sequencing (expressed sequence tags) from a directionally cloned human infant brain cDNA library. |journal=Nat. Genet. |volume=4 |issue= 4 |pages= 373-80 |year= 1993 |pmid= 8401585 |doi= 10.1038/ng0893-373 }}
*{{cite journal | author=Adams MD, Soares MB, Kerlavage AR, ''et al.'' |title=Rapid cDNA sequencing (expressed sequence tags) from a directionally cloned human infant brain cDNA library. |journal=Nat. Genet. |volume=4 |issue= 4 |pages= 373–80 |year= 1993 |pmid= 8401585 |doi= 10.1038/ng0893-373 }}
*{{cite journal | author=Bernard LE, Chitayat D, Weksberg R, ''et al.'' |title=Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasia. |journal=J. Med. Genet. |volume=33 |issue= 5 |pages= 432-4 |year= 1996 |pmid= 8733060 |doi= }}
*{{cite journal | author=Bernard LE, Chitayat D, Weksberg R, ''et al.'' |title=Linkage analysis of two Canadian families segregating for X linked spondyloepiphyseal dysplasia. |journal=J. Med. Genet. |volume=33 |issue= 5 |pages= 432–4 |year= 1996 |pmid= 8733060 |doi= }}
*{{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 | 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 | author=Gedeon AK, Colley A, Jamieson R, ''et al.'' |title=Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda. |journal=Nat. Genet. |volume=22 |issue= 4 |pages= 400-4 |year= 1999 |pmid= 10431248 |doi= 10.1038/11976 }}
*{{cite journal | author=Gedeon AK, Colley A, Jamieson R, ''et al.'' |title=Identification of the gene (SEDL) causing X-linked spondyloepiphyseal dysplasia tarda. |journal=Nat. Genet. |volume=22 |issue= 4 |pages= 400–4 |year= 1999 |pmid= 10431248 |doi= 10.1038/11976 }}
*{{cite journal | author=Gécz J, Hillman MA, Gedeon AK, ''et al.'' |title=Gene structure and expression study of the SEDL gene for spondyloepiphyseal dysplasia tarda. |journal=Genomics |volume=69 |issue= 2 |pages= 242-51 |year= 2001 |pmid= 11031107 |doi= 10.1006/geno.2000.6326 }}
*{{cite journal | author=Gécz J, Hillman MA, Gedeon AK, ''et al.'' |title=Gene structure and expression study of the SEDL gene for spondyloepiphyseal dysplasia tarda. |journal=Genomics |volume=69 |issue= 2 |pages= 242–51 |year= 2001 |pmid= 11031107 |doi= 10.1006/geno.2000.6326 }}
*{{cite journal | author=Ghosh AK, Majumder M, Steele R, ''et al.'' |title=A novel 16-kilodalton cellular protein physically interacts with and antagonizes the functional activity of c-myc promoter-binding protein 1. |journal=Mol. Cell. Biol. |volume=21 |issue= 2 |pages= 655-62 |year= 2001 |pmid= 11134351 |doi= 10.1128/MCB.21.2.655-662.2001 }}
*{{cite journal | author=Ghosh AK, Majumder M, Steele R, ''et al.'' |title=A novel 16-kilodalton cellular protein physically interacts with and antagonizes the functional activity of c-myc promoter-binding protein 1. |journal=Mol. Cell. Biol. |volume=21 |issue= 2 |pages= 655–62 |year= 2001 |pmid= 11134351 |doi= 10.1128/MCB.21.2.655-662.2001 }}
*{{cite journal | author=Gedeon AK, Tiller GE, Le Merrer M, ''et al.'' |title=The molecular basis of X-linked spondyloepiphyseal dysplasia tarda. |journal=Am. J. Hum. Genet. |volume=68 |issue= 6 |pages= 1386-97 |year= 2001 |pmid= 11349230 |doi= }}
*{{cite journal | author=Gedeon AK, Tiller GE, Le Merrer M, ''et al.'' |title=The molecular basis of X-linked spondyloepiphyseal dysplasia tarda. |journal=Am. J. Hum. Genet. |volume=68 |issue= 6 |pages= 1386–97 |year= 2001 |pmid= 11349230 |doi= }}
*{{cite journal | author=Grunebaum E, Arpaia E, MacKenzie JJ, ''et al.'' |title=A missense mutation in the SEDL gene results in delayed onset of X linked spondyloepiphyseal dysplasia in a large pedigree. |journal=J. Med. Genet. |volume=38 |issue= 6 |pages= 409-11 |year= 2001 |pmid= 11424925 |doi= }}
*{{cite journal | author=Grunebaum E, Arpaia E, MacKenzie JJ, ''et al.'' |title=A missense mutation in the SEDL gene results in delayed onset of X linked spondyloepiphyseal dysplasia in a large pedigree. |journal=J. Med. Genet. |volume=38 |issue= 6 |pages= 409–11 |year= 2001 |pmid= 11424925 |doi= }}
*{{cite journal | author=Mumm S, Zhang X, Vacca M, ''et al.'' |title=The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site. |journal=Gene |volume=273 |issue= 2 |pages= 285-93 |year= 2001 |pmid= 11595175 |doi= }}
*{{cite journal | author=Mumm S, Zhang X, Vacca M, ''et al.'' |title=The sedlin gene for spondyloepiphyseal dysplasia tarda escapes X-inactivation and contains a non-canonical splice site. |journal=Gene |volume=273 |issue= 2 |pages= 285–93 |year= 2001 |pmid= 11595175 |doi= }}
*{{cite journal | author=Gavin AC, Bösche M, Krause R, ''et al.'' |title=Functional organization of the yeast proteome by systematic analysis of protein complexes. |journal=Nature |volume=415 |issue= 6868 |pages= 141-7 |year= 2002 |pmid= 11805826 |doi= 10.1038/415141a }}
*{{cite journal | author=Gavin AC, Bösche M, Krause R, ''et al.'' |title=Functional organization of the yeast proteome by systematic analysis of protein complexes. |journal=Nature |volume=415 |issue= 6868 |pages= 141–7 |year= 2002 |pmid= 11805826 |doi= 10.1038/415141a }}
*{{cite journal | author=Takahashi T, Takahashi I, Tsuchida S, ''et al.'' |title=An SEDL gene mutation in a Japanese kindred of X-linked spondyloepiphyseal dysplasia tarda. |journal=Clin. Genet. |volume=61 |issue= 4 |pages= 319-20 |year= 2003 |pmid= 12030902 |doi= }}
*{{cite journal | author=Takahashi T, Takahashi I, Tsuchida S, ''et al.'' |title=An SEDL gene mutation in a Japanese kindred of X-linked spondyloepiphyseal dysplasia tarda. |journal=Clin. Genet. |volume=61 |issue= 4 |pages= 319–20 |year= 2003 |pmid= 12030902 |doi= }}
*{{cite journal | author=Fiedler J, Bittner M, Puhl W, Brenner RE |title=Mutations in the X-linked spondyloepiphyseal dysplasia tarda (SEDL) coding sequence are not a common cause of early primary osteoarthritis in men. |journal=Clin. Genet. |volume=62 |issue= 1 |pages= 94-5 |year= 2003 |pmid= 12123495 |doi= }}
*{{cite journal | author=Fiedler J, Bittner M, Puhl W, Brenner RE |title=Mutations in the X-linked spondyloepiphyseal dysplasia tarda (SEDL) coding sequence are not a common cause of early primary osteoarthritis in men. |journal=Clin. Genet. |volume=62 |issue= 1 |pages= 94–5 |year= 2003 |pmid= 12123495 |doi= }}
*{{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 | 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 | author=Gao C, Luo Q, Wang HL, ''et al.'' |title=[Identification of a novel mutation IVS2-2A-->C of SEDL gene in a Chinese family with X-linked spondyloepiphyseal dysplasia tarda] |journal=Zhonghua Yi Xue Yi Chuan Xue Za Zhi |volume=20 |issue= 1 |pages= 15-8 |year= 2003 |pmid= 12579492 |doi= }}
*{{cite journal | author=Gao C, Luo Q, Wang HL, ''et al.'' |title=[Identification of a novel mutation IVS2-2A-->C of SEDL gene in a Chinese family with X-linked spondyloepiphyseal dysplasia tarda] |journal=Zhonghua Yi Xue Yi Chuan Xue Za Zhi |volume=20 |issue= 1 |pages= 15–8 |year= 2003 |pmid= 12579492 |doi= }}
*{{cite journal | author=Xiao C, Zhang S, Wang J, ''et al.'' |title=A single nucleotide deletion of 293delT in SEDL gene causing spondyloepiphyseal dysplasia tarda in a four-generation Chinese family. |journal=Mutat. Res. |volume=525 |issue= 1-2 |pages= 61-5 |year= 2003 |pmid= 12650905 |doi= }}
*{{cite journal | author=Xiao C, Zhang S, Wang J, ''et al.'' |title=A single nucleotide deletion of 293delT in SEDL gene causing spondyloepiphyseal dysplasia tarda in a four-generation Chinese family. |journal=Mutat. Res. |volume=525 |issue= 1-2 |pages= 61–5 |year= 2003 |pmid= 12650905 |doi= }}
*{{cite journal | author=Fan L, Yu W, Zhu X |title=Interaction of Sedlin with chloride intracellular channel proteins. |journal=FEBS Lett. |volume=540 |issue= 1-3 |pages= 77-80 |year= 2003 |pmid= 12681486 |doi= }}
*{{cite journal | author=Fan L, Yu W, Zhu X |title=Interaction of Sedlin with chloride intracellular channel proteins. |journal=FEBS Lett. |volume=540 |issue= 1-3 |pages= 77–80 |year= 2003 |pmid= 12681486 |doi= }}
*{{cite journal | author=Savarirayan R, Thompson E, Gécz J |title=Spondyloepiphyseal dysplasia tarda (SEDL, MIM #313400). |journal=Eur. J. Hum. Genet. |volume=11 |issue= 9 |pages= 639-42 |year= 2004 |pmid= 12939648 |doi= 10.1038/sj.ejhg.5201025 }}
*{{cite journal | author=Savarirayan R, Thompson E, Gécz J |title=Spondyloepiphyseal dysplasia tarda (SEDL, MIM #313400). |journal=Eur. J. Hum. Genet. |volume=11 |issue= 9 |pages= 639–42 |year= 2004 |pmid= 12939648 |doi= 10.1038/sj.ejhg.5201025 }}
*{{cite journal | author=Gécz J, Shaw MA, Bellon JR, de Barros Lopes M |title=Human wild-type SEDL protein functionally complements yeast Trs20p but some naturally occurring SEDL mutants do not. |journal=Gene |volume=320 |issue= |pages= 137-44 |year= 2004 |pmid= 14597397 |doi= }}
*{{cite journal | author=Gécz J, Shaw MA, Bellon JR, de Barros Lopes M |title=Human wild-type SEDL protein functionally complements yeast Trs20p but some naturally occurring SEDL mutants do not. |journal=Gene |volume=320 |issue= |pages= 137–44 |year= 2004 |pmid= 14597397 |doi= }}
}}
}}
{{refend}}
{{refend}}

Revision as of 22:28, 10 June 2008

Template:PBB Controls

TRAPPC2
Identifiers
AliasesTRAPPC2, MIP2A, SEDL, SEDT, TRAPPC2P1, TRS20, ZNF547L, hYP38334, trafficking protein particle complex 2, trafficking protein particle complex subunit 2
External IDsOMIM: 300202; MGI: 1913476; HomoloGene: 5436; GeneCards: TRAPPC2; OMA:TRAPPC2 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

6399

66226

Ensembl

ENSG00000196459

ENSMUSG00000079317

UniProt

P0DI81
P0DI82

Q9CQP2

RefSeq (mRNA)

NM_001011658
NM_001128835
NM_014563

NM_025432
NM_001313722

RefSeq (protein)

NP_001011658
NP_001122307
NP_055378
NP_001011658.1
NP_055378.1

NP_001300651
NP_079708
NP_079595

Location (UCSC)n/aChr X: 165.22 – 165.24 Mb
PubMed search[2][3]
Wikidata
View/Edit HumanView/Edit Mouse

Trafficking protein particle complex 2, also known as TRAPPC2, is a human gene.[4]

Template:PBB Summary

References

  1. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000079317 – Ensembl, May 2017
  2. ^ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  3. ^ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ^ "Entrez Gene: TRAPPC2 trafficking protein particle complex 2".

Further reading

Template:PBB Further reading

source: https://en.wikipedia.org/wiki/Special%3ADiff%2F218498288

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