GGRNA Home | Help | Advanced search

2024-03-29 17:14:05, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_017849               4593 bp    mRNA    linear   PRI 17-APR-2013
DEFINITION  Homo sapiens transmembrane protein 127 (TMEM127), transcript
            variant 1, mRNA.
ACCESSION   NM_017849
VERSION     NM_017849.3  GI:305682550
KEYWORDS    RefSeq.
SOURCE      Homo sapiens (human)
  ORGANISM  Homo sapiens
            Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi;
            Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini;
            Catarrhini; Hominidae; Homo.
REFERENCE   1  (bases 1 to 4593)
  AUTHORS   Takeichi,N., Midorikawa,S., Watanabe,A., Naing,B.T., Tamura,H.,
            Wakakuri-Kano,T., Ishizaki,A., Sugihara,H., Nissato,S., Saito,Y.,
            Aita,Y., Ishii,K.A., Igarashi,T., Kawakami,Y., Hara,H., Ikeda,T.,
            Shimizu,K., Suzuki,S., Shimano,H., Kawamoto,M., Shimada,T.,
            Watanabe,T., Oikawa,S. and Takekoshi,K.
  TITLE     Identical germline mutations in the TMEM127 gene in two unrelated
            Japanese patients with bilateral pheochromocytoma
  JOURNAL   Clin. Endocrinol. (Oxf) 77 (5), 707-714 (2012)
   PUBMED   22541004
  REMARK    GeneRIF: report shows that TMEM127 mutation plays a pathological
            role in pheochromocytoma in an Asian population.
REFERENCE   2  (bases 1 to 4593)
  AUTHORS   Neumann,H.P., Sullivan,M., Winter,A., Malinoc,A., Hoffmann,M.M.,
            Boedeker,C.C., Bertz,H., Walz,M.K., Moeller,L.C., Schmid,K.W. and
            Eng,C.
  TITLE     Germline mutations of the TMEM127 gene in patients with
            paraganglioma of head and neck and extraadrenal abdominal sites
  JOURNAL   J. Clin. Endocrinol. Metab. 96 (8), E1279-E1282 (2011)
   PUBMED   21613359
  REMARK    GeneRIF: TMEM127 germline mutations confer risks of extraadrenal
            paraganglial tumors in addition to the documented adrenal
            pheochromocytoma.
REFERENCE   3  (bases 1 to 4593)
  AUTHORS   Jiang,S. and Dahia,P.L.
  TITLE     Minireview: the busy road to pheochromocytomas and paragangliomas
            has a new member, TMEM127
  JOURNAL   Endocrinology 152 (6), 2133-2140 (2011)
   PUBMED   21447639
  REMARK    GeneRIF: TMEM127 is a novel pheochromocytoma susceptibility
            gene.[review]
            Review article
REFERENCE   4  (bases 1 to 4593)
  AUTHORS   Burnichon,N., Lepoutre-Lussey,C., Laffaire,J., Gadessaud,N.,
            Molinie,V., Hernigou,A., Plouin,P.F., Jeunemaitre,X., Favier,J. and
            Gimenez-Roqueplo,A.P.
  TITLE     A novel TMEM127 mutation in a patient with familial bilateral
            pheochromocytoma
  JOURNAL   Eur. J. Endocrinol. 164 (1), 141-145 (2011)
   PUBMED   20923864
  REMARK    GeneRIF: Pathological and genomic data demonstrated that a TMEM127
            gene mutation not previously described was causative of a new case
            of familial bilateral pheochromocytoma.
REFERENCE   5  (bases 1 to 4593)
  AUTHORS   Yao,L., Schiavi,F., Cascon,A., Qin,Y., Inglada-Perez,L., King,E.E.,
            Toledo,R.A., Ercolino,T., Rapizzi,E., Ricketts,C.J., Mori,L.,
            Giacche,M., Mendola,A., Taschin,E., Boaretto,F., Loli,P.,
            Iacobone,M., Rossi,G.P., Biondi,B., Lima-Junior,J.V., Kater,C.E.,
            Bex,M., Vikkula,M., Grossman,A.B., Gruber,S.B., Barontini,M.,
            Persu,A., Castellano,M., Toledo,S.P., Maher,E.R., Mannelli,M.,
            Opocher,G., Robledo,M. and Dahia,P.L.
  TITLE     Spectrum and prevalence of FP/TMEM127 gene mutations in
            pheochromocytomas and paragangliomas
  JOURNAL   JAMA 304 (23), 2611-2619 (2010)
   PUBMED   21156949
  REMARK    GeneRIF: Germline mutations of FP/TMEM127 were associated with
            pheochromocytoma but not paraganglioma and occurred in an age group
            frequently excluded from genetic screening algorithms; mutations
            disrupt intracellular distribution of the FP/TMEM127 protein.
REFERENCE   6  (bases 1 to 4593)
  AUTHORS   Qin,Y., Yao,L., King,E.E., Buddavarapu,K., Lenci,R.E.,
            Chocron,E.S., Lechleiter,J.D., Sass,M., Aronin,N., Schiavi,F.,
            Boaretto,F., Opocher,G., Toledo,R.A., Toledo,S.P., Stiles,C.,
            Aguiar,R.C. and Dahia,P.L.
  TITLE     Germline mutations in TMEM127 confer susceptibility to
            pheochromocytoma
  JOURNAL   Nat. Genet. 42 (3), 229-233 (2010)
   PUBMED   20154675
  REMARK    GeneRIF: Germline mutations in TMEM127 confer susceptibility to
            pheochromocytoma and identify TMEM127 as a tumor suppressor gene.
            GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   7  (bases 1 to 4593)
  AUTHORS   Girard,A., Sachidanandam,R., Hannon,G.J. and Carmell,M.A.
  TITLE     A germline-specific class of small RNAs binds mammalian Piwi
            proteins
  JOURNAL   Nature 442 (7099), 199-202 (2006)
   PUBMED   16751776
REFERENCE   8  (bases 1 to 4593)
  AUTHORS   Hillier,L.W., Graves,T.A., Fulton,R.S., Fulton,L.A., Pepin,K.H.,
            Minx,P., Wagner-McPherson,C., Layman,D., Wylie,K., Sekhon,M.,
            Becker,M.C., Fewell,G.A., Delehaunty,K.D., Miner,T.L., Nash,W.E.,
            Kremitzki,C., Oddy,L., Du,H., Sun,H., Bradshaw-Cordum,H., Ali,J.,
            Carter,J., Cordes,M., Harris,A., Isak,A., van Brunt,A., Nguyen,C.,
            Du,F., Courtney,L., Kalicki,J., Ozersky,P., Abbott,S.,
            Armstrong,J., Belter,E.A., Caruso,L., Cedroni,M., Cotton,M.,
            Davidson,T., Desai,A., Elliott,G., Erb,T., Fronick,C., Gaige,T.,
            Haakenson,W., Haglund,K., Holmes,A., Harkins,R., Kim,K.,
            Kruchowski,S.S., Strong,C.M., Grewal,N., Goyea,E., Hou,S., Levy,A.,
            Martinka,S., Mead,K., McLellan,M.D., Meyer,R., Randall-Maher,J.,
            Tomlinson,C., Dauphin-Kohlberg,S., Kozlowicz-Reilly,A., Shah,N.,
            Swearengen-Shahid,S., Snider,J., Strong,J.T., Thompson,J.,
            Yoakum,M., Leonard,S., Pearman,C., Trani,L., Radionenko,M.,
            Waligorski,J.E., Wang,C., Rock,S.M., Tin-Wollam,A.M., Maupin,R.,
            Latreille,P., Wendl,M.C., Yang,S.P., Pohl,C., Wallis,J.W.,
            Spieth,J., Bieri,T.A., Berkowicz,N., Nelson,J.O., Osborne,J.,
            Ding,L., Meyer,R., Sabo,A., Shotland,Y., Sinha,P., Wohldmann,P.E.,
            Cook,L.L., Hickenbotham,M.T., Eldred,J., Williams,D., Jones,T.A.,
            She,X., Ciccarelli,F.D., Izaurralde,E., Taylor,J., Schmutz,J.,
            Myers,R.M., Cox,D.R., Huang,X., McPherson,J.D., Mardis,E.R.,
            Clifton,S.W., Warren,W.C., Chinwalla,A.T., Eddy,S.R., Marra,M.A.,
            Ovcharenko,I., Furey,T.S., Miller,W., Eichler,E.E., Bork,P.,
            Suyama,M., Torrents,D., Waterston,R.H. and Wilson,R.K.
  TITLE     Generation and annotation of the DNA sequences of human chromosomes
            2 and 4
  JOURNAL   Nature 434 (7034), 724-731 (2005)
   PUBMED   15815621
REFERENCE   9  (bases 1 to 4593)
  AUTHORS   Loftus,B.J., Kim,U.J., Sneddon,V.P., Kalush,F., Brandon,R.,
            Fuhrmann,J., Mason,T., Crosby,M.L., Barnstead,M., Cronin,L.,
            Deslattes Mays,A., Cao,Y., Xu,R.X., Kang,H.L., Mitchell,S.,
            Eichler,E.E., Harris,P.C., Venter,J.C. and Adams,M.D.
  TITLE     Genome duplications and other features in 12 Mb of DNA sequence
            from human chromosome 16p and 16q
  JOURNAL   Genomics 60 (3), 295-308 (1999)
   PUBMED   10493829
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from DA212468.1, BC039892.1 and
            AC012307.8.
            This sequence is a reference standard in the RefSeqGene project.
            On Sep 2, 2010 this sequence version replaced gi:300863090.
            
            Summary: This gene encodes a transmembrane protein with 3 predicted
            transmembrane domains. The protein is associated with a
            subpopulation of vesicular organelles corresponding to early
            endosomal structures, with the Golgi, and with lysosomes, and may
            participate in protein trafficking between these structures.
            Mutations in this gene and several other genes cause
            pheochromocytomas. Alternatively spliced transcript variants
            encoding the same protein have been identified. [provided by
            RefSeq, Aug 2010].
            
            Transcript Variant: This variant (1) is the longer transcript. Both
            variants 1 and 2 encode the same protein.
            
            Sequence Note: This RefSeq record was created from transcript and
            genomic sequence data to make the sequence consistent with the
            reference genome assembly. The genomic coordinates used for the
            transcript record were based on transcript alignments.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK000514.1, BC039892.1 [ECO:0000332]
            RNAseq introns              :: single sample supports all introns
                                           ERS025081, ERS025083 [ECO:0000348]
            ##Evidence-Data-END##
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-47                DA212468.1         1-47
            48-1772             BC039892.1         1-1725
            1773-4593           AC012307.8         128546-131366       c
FEATURES             Location/Qualifiers
     source          1..4593
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="2"
                     /map="2q11.2"
     gene            1..4593
                     /gene="TMEM127"
                     /note="transmembrane protein 127"
                     /db_xref="GeneID:55654"
                     /db_xref="HGNC:26038"
                     /db_xref="HPRD:07917"
                     /db_xref="MIM:613403"
     exon            1..145
                     /gene="TMEM127"
                     /inference="alignment:Splign:1.39.8"
     misc_feature    109..111
                     /gene="TMEM127"
                     /note="upstream in-frame stop codon"
     exon            146..520
                     /gene="TMEM127"
                     /inference="alignment:Splign:1.39.8"
     CDS             277..993
                     /gene="TMEM127"
                     /codon_start=1
                     /product="transmembrane protein 127"
                     /protein_id="NP_060319.1"
                     /db_xref="GI:8923466"
                     /db_xref="CCDS:CCDS2018.1"
                     /db_xref="GeneID:55654"
                     /db_xref="HGNC:26038"
                     /db_xref="HPRD:07917"
                     /db_xref="MIM:613403"
                     /translation="
MYAPGGAGLPGGRRRRSPGGSALPKQPERSLASALPGALSITALCTALAEPAWLHIHGGTCSRQELGVSDVLGYVHPDLLKDFCMNPQTVLLLRVIAAFCFLGILCSLSAFLLDVFGPKHPALKITRRYAFAHILTVLQCATVIGFSYWASELILAQQQQHKKYHGSQVYVTFAVSFYLVAGAGGASILATAANLLRHYPTEEEEQALELLSEMEENEPYPAEYEVINQFQPPPAYTP
"
     misc_feature    325..327
                     /gene="TMEM127"
                     /experiment="experimental evidence, no additional details
                     recorded"
                     /note="Phosphoserine; propagated from UniProtKB/Swiss-Prot
                     (O75204.1); phosphorylation site"
     misc_feature    388..864
                     /gene="TMEM127"
                     /note="PMP-22/EMP/MP20/Claudin family; Region:
                     PMP22_Claudin; cl17758"
                     /db_xref="CDD:248312"
     misc_feature    562..624
                     /gene="TMEM127"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O75204.1);
                     transmembrane region"
     misc_feature    664..726
                     /gene="TMEM127"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O75204.1);
                     transmembrane region"
     misc_feature    781..843
                     /gene="TMEM127"
                     /inference="non-experimental evidence, no additional
                     details recorded"
                     /note="propagated from UniProtKB/Swiss-Prot (O75204.1);
                     transmembrane region"
     exon            521..685
                     /gene="TMEM127"
                     /inference="alignment:Splign:1.39.8"
     exon            686..4593
                     /gene="TMEM127"
                     /inference="alignment:Splign:1.39.8"
     variation       1209
                     /gene="TMEM127"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:200462376"
     STS             2185..2319
                     /gene="TMEM127"
                     /standard_name="RH68603"
                     /db_xref="UniSTS:57737"
     variation       2412
                     /gene="TMEM127"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:1061578"
     variation       2574
                     /gene="TMEM127"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:11558941"
     STS             2883..3044
                     /gene="TMEM127"
                     /standard_name="D2S1663E"
                     /db_xref="UniSTS:52675"
     STS             3367..3457
                     /gene="TMEM127"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     variation       3505
                     /gene="TMEM127"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1138984"
     STS             3614..3748
                     /gene="TMEM127"
                     /standard_name="D2S2931"
                     /db_xref="UniSTS:33276"
     STS             4088..4215
                     /gene="TMEM127"
                     /standard_name="SHGC-30679"
                     /db_xref="UniSTS:21283"
     polyA_site      4227
                     /gene="TMEM127"
ORIGIN      
agaggaggaggaagccggaagtgcatcggccccgggtctgtccgggcgttgcgggattggggcctgggaacgctcggcccccggcagccgagaagcccgtgactgggctgagcagcaccatcccagccctggggcctgctgactgcccagtcccggcttcacctgcagcgaacccggagcgttgctatcctccaccggactgtcaggctctgcgcgccccgcggaggtcggcggcgaccagcagcgactgcggagcgacggcgggcggccccgggcatgtacgcccccggaggcgcagggctgcccggcgggcgccggcggaggagcccgggaggcagcgctctgcccaagcagccggagcgtagcctggcctcggccctgcctggcgccctgtctatcacggcgctgtgcactgccctcgccgagcccgcctggttgcacatccacggaggcacctgttcgcgccaggagctgggggtctccgacgtgttgggctatgtgcacccggacctgctgaaagatttctgcatgaatccccagacagtgctgctcctgcgggtcatcgccgccttctgtttcctgggcatcctgtgtagtctctccgctttccttctggatgtctttgggccgaagcatcctgctctgaagatcactcgtcgctatgccttcgcccatatcctaacggttctgcagtgtgccaccgtcattggcttttcttattgggcttctgaactcatcttggcccagcagcagcagcataagaagtaccatggatcccaggtctatgtcaccttcgccgttagcttctacctggtggcaggagctggtggagcctcaatcctggccacggcagccaacctcctgcgccactaccccacagaggaagaggagcaggcgctggagctgctctcagagatggaagagaacgagccctacccggcggaatatgaggtcatcaaccagttccagccaccccctgcttacacaccctaatgccagccctgggctctcttcctcggcagcccctccctcaactctgcagctcctctcgcacccagaggagctcctttccccagcaggcctcactggtaggatcctgaccatcttctccaaaccttccccaggagagactctgcctttagggtcatccaagtatccctgctctcagaaccggaggtccactggttttctataatgtactctttccctcctgccacatcctgcccccttcacattcacgagtcattaccagccagggaaggtcatccaagtttcctccagcatgggcgatatctttgggaccgagactttccttggagagctgctgagagcggacagtcccaaaaacaagtgtcaaagggcccaagggaaaggggactgtgccctggaggctcacttcacagggatcagtgtttgctccacagctgtagctctgggctgacgccccccagaccccttccttctcggagtgacccgcccccaggccacctgctccggggagttctgtgcactttactctttggacttctcctcacgtgtgccctggttttatggggagagggaatcgctgttgggaaggcagagcagttgcaaccctctctgcccttgcttcatgtggctggagcccaggcaaggagagcaggagccagcgtgagactgaggccccctggtgcctatcaaggaccagagtgaaggggactacatctcccagcccttcaccttttaaatatgagtggttttaaaaggaaaaaaatgaaaccaggcaacagcaacaatattctgtttttaaaatagggacaagactgttgtcactttttagacatgtatcccattccttttggctctgcaatatttggggctgtagctccttccaagcccatggtagtccctccccgagtctctcccagtagaatgcagcctcccttccctggccccttccctctcagtgacggtgactccctggggccttctcgtggaacccagaggggctgaggactgtggcctggctggcgggccagcgtggtgctcctcaggactgcagcactgagatggaacctggcctcagtttaggaacaggggccacaacagggcaggaacccaccaccctccacataggaatacaaccagtggggccacatcatgtgaggcatcagacccacactgtcagcccagcaggccgggctgtgtccttcagacccagtgctgccctagactctgactcgggactccagcttgccacgtgccctctcccctcttgaatgtactctggtcttgcagtgtgctgctgggactttcttgctcagccatcactctggtcaccttgtttgctctgggtctggctgaattttctgccctgagatctgggcataaagtggatgaaacttgaaagaccttcagtgtagatccagatggccaacctgtccttgttaagttacttgcttcttgggaatcagtgtcccctgctgagctgaaaaggaaatggattccaatctcttccaacctttaaggtgatagatagtttgagcaagactggagaatggacaacactatgaagctgtggctagaaagggactgtcatgtcccatcctttggccagattgactggggatgtccggacagatgcctgcatgggtggtgagggccacatctgcacacgagccagtggctgcttgcagttcactgctgtgatgccagagtgtgttcaaaggtgactctcctgctcttctggactcttctctcaggcaagaaaggctgcaggctgcctgctatgtgatgcctgagcacaaagccaaggaactgaactaagtctttctgttaagtcctgagtttgtcattggcaggtttacttgtggccagctctctctgcccttgggtgtctgagcaggcagaccagaagaccaggcactggacctgcatgccaaagggactggtcatctcctgaggacctgtaaatgaccctgtggactgttccgcacgatccggaacccactttttattcactccccatgtctttggccttcctcttctttctctttccctctgccatcctgacactgatagtttgtcatataaattccccgggttgtgtttttttttctagaaaaaaattaaaagggaaaacaaaaccaaaaaaaccagaaaccacgaataagaatggaaatgacaatggctgcctgtcatttttctgtcacgattttcctgatttggtttgttccctttgtctcagagaagcaggagatgttgatgaggctgtatttttttttctttttcttgtttttgagacaagagtctcgctctgtcacccgggctggagtgtaacgtggcatgatctcagctcactgcaacctctgcctcctgggttcaagcgattatcctgcctcagcctcctgagtagctgggattacaggcatgcgccactatgcccagataatttttttgtatttttagtagagacagggtttcaccatgttggccaggctggtctggaactcctaacctcaggttatccacccaccttggcctcccaaagtgctgggattataggcatgaaccaccgtgcctggccaaagatgtaatttaaaatagttagaagggacttggcatgggccagctccgtgcatggcattttcacccccagagcttcctaatcctgttttcacacaggaagtttctaggtctttctagaacagctagaaatagtagctgactcccgcccaaggcccaaccttcaaaccctgagctcttcaggctgcatcctctggtgagctatagaggagaacgtggctcctaaactctagccatcctgtgggaggaaatagacttctttgggctgtggcttgcagaacaaactacactttttttccctctattgtttaaattttatttaataatttgtgtgtttttctgtctttattttctgtatttcacgtgttccttcactccctagaaactgcactttctttgaaaccataggtaatgaatcttactaggagaggcatggggatagagacagttctgggagtgtgacctgtaagcctcctgtagggcagtgccaggccttgattgcccacgttctctccgttccttcttccttcatacatttgatcacacagcctacacccagccccgagtgtgcatcacggtaaaagagctgagggctctcttcagggagcagcccatttaggtctcttttgttgttgttagggagaatacacatctttcttggaagctgggagtgtgttctcatttcatgtccattcagacaaagcaccattaggcaccatgaaatatacagtgacggacaggaccctgtctgcaaggattttatgtccttagttcaggagatggacttgtccacagaaaggcagagtgaagtgggcggccggctcggaaaagtcctgtgcccagaagggagccagttctgacctgagtgataatgaaaggcttcctggaggacgcagcttgagccacacttgatgtgggagtgaactgggatagggacactcctgctgagagaatggcaagagcaaaagcacactggtggccaggaggtggtaagagccgaggttagaaaggtgaggggtgctcatttaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:55654 -> Molecular function: GO:0003674 [molecular_function] evidence: ND
            GeneID:55654 -> Biological process: GO:0008285 [negative regulation of cell proliferation] evidence: IMP
            GeneID:55654 -> Biological process: GO:0032007 [negative regulation of TOR signaling cascade] evidence: IMP
            GeneID:55654 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
            GeneID:55654 -> Cellular component: GO:0005886 [plasma membrane] evidence: IDA
            GeneID:55654 -> Cellular component: GO:0016021 [integral to membrane] evidence: IEA

by @meso_cacase at DBCLS
This page is licensed under a Creative Commons Attribution 2.1 Japan License.