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2024-04-25 10:40:16, GGRNA : RefSeq release 60 (20130726)

LOCUS       NM_001243198            7898 bp    mRNA    linear   PRI 24-JUN-2013
DEFINITION  Homo sapiens huntingtin interacting protein 1 (HIP1), transcript
            variant 2, mRNA.
ACCESSION   NM_001243198
VERSION     NM_001243198.1  GI:342307095
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 7898)
  AUTHORS   Sistani,L., Rodriguez,P.Q., Hultenby,K., Uhlen,M., Betsholtz,C.,
            Jalanko,H., Tryggvason,K., Wernerson,A. and Patrakka,J.
  TITLE     Neuronal proteins are novel components of podocyte major processes
            and their expression in glomerular crescents supports their role in
            crescent formation
  JOURNAL   Kidney Int. 83 (1), 63-71 (2013)
   PUBMED   22913984
  REMARK    GeneRIF: Three neuronal proteins (Huntingtin interacting protein 1,
            neurofascin, and olfactomedin-like 2a) are novel components of
            podocyte major processes and their expression in glomerular
            crescents supports their role in crescent formation.
REFERENCE   2  (bases 1 to 7898)
  AUTHORS   Fontaine,S.N., Bauer,S.P., Lin,X., Poorfarahani,S. and Ybe,J.A.
  TITLE     Replacement of charged and polar residues in the coiled-coiled
            interface of huntingtin-interacting protein 1 (HIP1) causes
            aggregation and cell death
  JOURNAL   FEBS Lett. 586 (19), 3030-3036 (2012)
   PUBMED   22835334
  REMARK    GeneRIF: flexibility of the HIP1 coiled-coil domain is important
            for normal function and may lead to new insights into Huntington's
            disease
REFERENCE   3  (bases 1 to 7898)
  AUTHORS   Martins-de-Souza,D., Guest,P.C., Mann,D.M., Roeber,S., Rahmoune,H.,
            Bauder,C., Kretzschmar,H., Volk,B., Baborie,A. and Bahn,S.
  TITLE     Proteomic analysis identifies dysfunction in cellular transport,
            energy, and protein metabolism in different brain regions of
            atypical frontotemporal lobar degeneration
  JOURNAL   J. Proteome Res. 11 (4), 2533-2543 (2012)
   PUBMED   22360420
  REMARK    GeneRIF: A protein encoded by this locus was found to be
            differentially expressed in postmortem brains from patients with
            atypical frontotemporal lobar degeneration.
REFERENCE   4  (bases 1 to 7898)
  AUTHORS   Ames,H.M., Bichakjian,C.K., Liu,G.Y., Oravecz-Wilson,K.I.,
            Fullen,D.R., Verhaegen,M.E., Johnson,T.M., Dlugosz,A.A. and
            Ross,T.S.
  TITLE     Huntingtin-interacting protein 1: a Merkel cell carcinoma marker
            that interacts with c-Kit
  JOURNAL   J. Invest. Dermatol. 131 (10), 2113-2120 (2011)
   PUBMED   21697888
  REMARK    GeneRIF: Huntingtin-interacting protein 1 is a Merkel cell
            carcinoma marker that interacts with c-Kit
REFERENCE   5  (bases 1 to 7898)
  AUTHORS   Heath,A.C., Whitfield,J.B., Martin,N.G., Pergadia,M.L., Goate,A.M.,
            Lind,P.A., McEvoy,B.P., Schrage,A.J., Grant,J.D., Chou,Y.L.,
            Zhu,R., Henders,A.K., Medland,S.E., Gordon,S.D., Nelson,E.C.,
            Agrawal,A., Nyholt,D.R., Bucholz,K.K., Madden,P.A. and
            Montgomery,G.W.
  TITLE     A quantitative-trait genome-wide association study of alcoholism
            risk in the community: findings and implications
  JOURNAL   Biol. Psychiatry 70 (6), 513-518 (2011)
   PUBMED   21529783
REFERENCE   6  (bases 1 to 7898)
  AUTHORS   Ross,T.S., Bernard,O.A., Berger,R. and Gilliland,D.G.
  TITLE     Fusion of Huntingtin interacting protein 1 to platelet-derived
            growth factor beta receptor (PDGFbetaR) in chronic myelomonocytic
            leukemia with t(5;7)(q33;q11.2)
  JOURNAL   Blood 91 (12), 4419-4426 (1998)
   PUBMED   9616134
REFERENCE   7  (bases 1 to 7898)
  AUTHORS   Wedemeyer,N., Peoples,R., Himmelbauer,H., Lehrach,H., Francke,U.
            and Wanker,E.E.
  TITLE     Localization of the human HIP1 gene close to the elastin (ELN)
            locus on 7q11.23
  JOURNAL   Genomics 46 (2), 313-315 (1997)
   PUBMED   9417924
REFERENCE   8  (bases 1 to 7898)
  AUTHORS   Kalchman,M.A., Koide,H.B., McCutcheon,K., Graham,R.K., Nichol,K.,
            Nishiyama,K., Kazemi-Esfarjani,P., Lynn,F.C., Wellington,C.,
            Metzler,M., Goldberg,Y.P., Kanazawa,I., Gietz,R.D. and Hayden,M.R.
  TITLE     HIP1, a human homologue of S. cerevisiae Sla2p, interacts with
            membrane-associated huntingtin in the brain
  JOURNAL   Nat. Genet. 16 (1), 44-53 (1997)
   PUBMED   9140394
REFERENCE   9  (bases 1 to 7898)
  AUTHORS   Wanker,E.E., Rovira,C., Scherzinger,E., Hasenbank,R., Walter,S.,
            Tait,D., Colicelli,J. and Lehrach,H.
  TITLE     HIP-I: a huntingtin interacting protein isolated by the yeast
            two-hybrid system
  JOURNAL   Hum. Mol. Genet. 6 (3), 487-495 (1997)
   PUBMED   9147654
REFERENCE   10 (bases 1 to 7898)
  AUTHORS   Puigvert,A.
  TITLE     Caliceal urodynamics
  JOURNAL   Urol. Int. 30 (4), 282-296 (1975)
   PUBMED   1189126
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from BP282107.1, U79734.1,
            AK304738.1, AC018720.5 and BE350891.1.
            
            Summary: The product of this gene is a membrane-associated protein
            that colocalizes with huntingtin. This protein has similarities to
            cytoskeleton proteins and its interaction with huntingtin is
            thought to play a functional role in the cell filament network.
            Loss of normal huntingtin-HIP1 interaction in Huntington disease
            may contribute to a defect in membrane-cytoskeletal integrity in
            the brain. This gene could help in the understanding of the normal
            function of huntingtin and also the pathogenesis of Huntington
            disease. It also has been implicated in the pathogenesis of
            hematopoietic malignancies. Two transcript variants encoding
            different isoforms have been found for this gene. [provided by
            RefSeq, Aug 2011].
            
            Transcript Variant: This variant (2) lacks an alternate in-frame
            coding segment compared to variant 1. The resulting isoform (2) has
            the same N- and C-termini but is shorter compared to isoform 1.
            
            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.
            
            Publication Note:  This RefSeq record includes a subset of the
            publications that are available for this gene. Please see the Gene
            record to access additional publications.
            
            ##Evidence-Data-START##
            Transcript exon combination :: AK304738.1 [ECO:0000332]
            RNAseq introns              :: mixed/partial sample support
                                           ERS025081, ERS025082 [ECO:0000350]
            ##Evidence-Data-END##
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-587               BP282107.1         1-587
            588-1116            U79734.1           418-946
            1117-2681           AK304738.1         1093-2657
            2682-3154           U79734.1           2665-3137
            3155-7873           AC018720.5         42019-46737
            7874-7898           BE350891.1         1-25                c
FEATURES             Location/Qualifiers
     source          1..7898
                     /organism="Homo sapiens"
                     /mol_type="mRNA"
                     /db_xref="taxon:9606"
                     /chromosome="7"
                     /map="7q11.23"
     gene            1..7898
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /note="huntingtin interacting protein 1"
                     /db_xref="GeneID:3092"
                     /db_xref="HGNC:4913"
                     /db_xref="MIM:601767"
     exon            1..165
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     CDS             46..3006
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /note="isoform 2 is encoded by transcript variant 2;
                     huntingtin-interacting protein I; HIP-I"
                     /codon_start=1
                     /product="huntingtin-interacting protein 1 isoform 2"
                     /protein_id="NP_001230127.1"
                     /db_xref="GI:342307096"
                     /db_xref="CCDS:CCDS59060.1"
                     /db_xref="GeneID:3092"
                     /db_xref="HGNC:4913"
                     /db_xref="MIM:601767"
                     /translation="
MDRMASSMKQVPNPLPKVLSRRGVGAGLEAAERESFERTQTVSINKAINTQEVAVKEKHARTCILGTHHEKGAQTFWSVVNRLPLSSNAVLCWKFCHVFHKLLRDGHPNVLKDSLRYRNELSDMSRMWGHLSEGYGQLCSIYLKLLRTKMEYHTKNPRFPGNLQMSDRQLDEAGESDVNNFFQLTVEMFDYLECELNLFQTVFNSLDMSRSVSVTAAGQCRLAPLIQVILDCSHLYDYTVKLLFKLHSCLPADTLQGHRDRFMEQFTKLKDLFYRSSNLQYFKRLIQIPQLPENPPNFLRASALSEHISPVVVIPAEASSPDSEPVLEKDDLMDMDASQQNLFDNKFDDIFGSSFSSDPFNFNSQNGVNKDEKDHLIERLYREISGLKAQLENMKTESQRVVLQLKGHVSELEADLAEQQHLRQQAADDCEFLRAELDELRRQREDTEKAQRSLSEIERKAQANEQRYSKLKEKYSELVQNHADLLRKNAEVTKQVSMARQAQVDLEREKKELEDSLERISDQGQRKTQEQLEVLESLKQELATSQRELQVLQGSLETSAQSEANWAAEFAELEKERDSLVSGAAHREEELSALRKELQDTQLKLASTEESMCQLAKDQRKMLLVGSRKAAEQVIQDALNQLEEPPLISCAGSADHLLSTVTSISSCIEQLEKSWSQYLACPEDISGLLHSITLLAHLTSDAIAHGATTCLRAPPEPADSLTEACKQYGRETLAYLASLEEEGSLENADSTAMRNCLSKIKAIGEELLPRGLDIKQEELGDLVDKEMAATSAAIETATARIEGTASPKEFYAKNSRWTEGLISASKAVGWGATVMVDAADLVVQGRGKFEELMVCSHEIAASTAQLVAASKVKADKDSPNLAQLQQASRGVNQATAGVVASTISGKSQIEETDNMDFSSMTLTQIKRQEMDSQVRVLELENELQKERQKLGELRKKHYELAGVAEGWEEGTEASPPTLQEVVTEKE
"
     misc_feature    166..504
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /note="ANTH domain family; composed of adaptor protein 180
                     (AP180), clathrin assembly lymphoid myeloid leukemia
                     protein (CALM) and similar proteins. A set of proteins
                     previously designated as harboring an ENTH domain in fact
                     contains a highly similar, yet...; Region:
                     ANTH_AP180_CALM; cd03564"
                     /db_xref="CDD:48660"
     misc_feature    order(181..183,211..213,217..222)
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /note="PtdIns(4,5)P2-binding site; other site"
                     /db_xref="CDD:48660"
     misc_feature    1213..1977
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /note="Uncharacterized archaeal coiled-coil protein
                     [Function unknown]; Region: COG1340"
                     /db_xref="CDD:31531"
     misc_feature    1393..>1881
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /note="The Bin/Amphiphysin/Rvs (BAR) domain, a
                     dimerization module that binds membranes and detects
                     membrane curvature; Region: BAR; cl12013"
                     /db_xref="CDD:209413"
     misc_feature    <2461..2928
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /note="I/LWEQ domain; Region: ILWEQ; smart00307"
                     /db_xref="CDD:128602"
     misc_feature    2461..2928
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /note="I/LWEQ domain; Region: I_LWEQ; pfam01608"
                     /db_xref="CDD:201885"
     exon            166..229
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     variation       209
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /replace="g"
                     /replace="t"
                     /db_xref="dbSNP:202058558"
     exon            230..372
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            373..429
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            430..510
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            511..587
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            588..649
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            650..790
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            791..848
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            849..924
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     STS             859..1029
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="HIP1"
                     /db_xref="UniSTS:504762"
     exon            925..1065
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            1066..1163
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            1164..1236
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     STS             1165..1264
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="D7S3303"
                     /db_xref="UniSTS:254232"
     exon            1237..1420
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            1421..1509
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            1510..1626
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            1627..1728
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            1729..1872
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            1873..2008
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            2009..2095
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            2096..2203
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     variation       2170
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /replace="a"
                     /replace="c"
                     /db_xref="dbSNP:77320442"
     exon            2204..2340
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            2341..2451
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            2452..2552
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     STS             2475..2601
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="GDB:4585037"
                     /db_xref="UniSTS:62321"
     exon            2553..2658
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            2659..2782
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     variation       2682
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:1167794"
     exon            2783..2844
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            2845..2953
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     exon            2954..7880
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /inference="alignment:Splign:1.39.8"
     STS             3143..3214
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="GDB:4585029"
                     /db_xref="UniSTS:411"
     variation       3992
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:3801476"
     variation       4537
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /replace="c"
                     /replace="g"
                     /db_xref="dbSNP:2599326"
     STS             5234..5350
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="D10S16"
                     /db_xref="UniSTS:155756"
     STS             5343..6489
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="GDB:434012"
                     /db_xref="UniSTS:157204"
     STS             5346..6535
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="G38154"
                     /db_xref="UniSTS:53341"
     STS             5541..6571
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="D11S3114"
                     /db_xref="UniSTS:152207"
     STS             5880..6491
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="L17705"
                     /db_xref="UniSTS:66091"
     variation       6534
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /replace="c"
                     /replace="t"
                     /db_xref="dbSNP:75801816"
     STS             6553..6641
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="D8S2279"
                     /db_xref="UniSTS:473907"
     STS             7162..7230
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
                     /standard_name="GDB:4585453"
                     /db_xref="UniSTS:61651"
     polyA_signal    7859..7864
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
     polyA_site      7880
                     /gene="HIP1"
                     /gene_synonym="ILWEQ"
ORIGIN      
atcccggggcagccgagggcccctgactcggctcctcgcggcgacatggatcggatggccagctccatgaagcaggtgcccaacccactgcccaaggtgctgagccggcgcggggtcggcgctgggctggaggcggcggagcgcgagagcttcgagcggactcagactgtcagcatcaataaggccattaatacgcaggaagtggctgtaaaggaaaaacacgccagaacgtgcatactgggcacccaccatgagaaaggggcacagaccttctggtctgttgtcaaccgcctgcctctgtctagcaacgcagtgctctgctggaagttctgccatgtgttccacaaactcctccgagatggacacccgaacgtcctgaaggactctctgagatacagaaatgaattgagtgacatgagcaggatgtggggccacctgagcgaggggtatggccagctgtgcagcatctacctgaaactgctaagaaccaagatggagtaccacaccaaaaatcccaggttcccaggcaacctgcagatgagtgaccgccagctggacgaggctggagaaagtgacgtgaacaactttttccagttaacagtggagatgtttgactacctggagtgtgaactcaacctcttccaaacagtattcaactccctggacatgtcccgctctgtgtccgtgacggcagcagggcagtgccgcctcgccccgctgatccaggtcatcttggactgcagccacctttatgactacactgtcaagcttctcttcaaactccactcctgcctcccagctgacaccctgcaaggccaccgggaccgcttcatggagcagtttacaaagttgaaagatctgttctaccgctccagcaacctgcagtacttcaagcggctcattcagatcccccagctgcctgagaacccacccaacttcctgcgagcctcagccctgtcagaacatatcagccctgtggtggtgatccctgcagaggcctcatcccccgacagcgagccagtcctagagaaggatgacctcatggacatggatgcctctcagcagaatttatttgacaacaagtttgatgacatctttggcagttcattcagcagtgatcccttcaatttcaacagtcaaaatggtgtgaacaaggatgagaaggaccacttaattgagcgactatacagagagatcagtggattgaaggcacagctagaaaacatgaagactgagagccagcgggttgtgctgcagctgaagggccacgtcagcgagctggaagcagatctggccgagcagcagcacctgcggcagcaggcggccgacgactgtgaattcctgcgggcagaactggacgagctcaggaggcagcgggaggacaccgagaaggctcagcggagcctgtctgagatagaaaggaaagctcaagccaatgaacagcgatatagcaagctaaaggagaagtacagcgagctggttcagaaccacgctgacctgctgcggaagaatgcagaggtgaccaaacaggtgtccatggccagacaagcccaggtagatttggaacgagagaaaaaagagctggaggattcgttggagcgcatcagtgaccagggccagcggaagactcaagaacagctggaagttctagagagcttgaagcaggaacttgccacaagccaacgggagcttcaggttctgcaaggcagcctggaaacttctgcccagtcagaagcaaactgggcagccgagttcgccgagctagagaaggagcgggacagcctggtgagtggcgcagctcatagggaggaggaattatctgctcttcggaaagaactgcaggacactcagctcaaactggccagcacagaggaatctatgtgccagcttgccaaagaccaacgaaaaatgcttctggtggggtccaggaaggctgcggagcaggtgatacaagacgccctgaaccagcttgaagaacctcctctcatcagctgcgctgggtctgcagatcacctcctctccacggtcacatccatttccagctgcatcgagcaactggagaaaagctggagccagtatctggcctgcccagaagacatcagtggacttctccattccataaccctgctggcccacttgaccagcgacgccattgctcatggtgccaccacctgcctcagagccccacctgagcctgccgactcactgaccgaggcctgtaagcagtatggcagggaaaccctcgcctacctggcctccctggaggaagagggaagccttgagaatgccgacagcacagccatgaggaactgcctgagcaagatcaaggccatcggcgaggagctcctgcccaggggactggacatcaagcaggaggagctgggggacctggtggacaaggagatggcggccacttcagctgctattgaaactgccacggccagaatagagggtacagcatcccctaaagagttttatgccaagaactctcgatggacagaaggacttatctcagcctccaaggctgtgggctggggagccactgtcatggtggatgcagctgatctggtggtacaaggcagagggaaatttgaggagctaatggtgtgttctcatgaaattgctgctagcacagcccagcttgtggctgcatccaaggtgaaagctgataaggacagccccaacctagcccagctgcagcaggcctctcggggagtgaaccaggccactgccggcgttgtggcctcaaccatttccggcaaatcacagatcgaagagacagacaacatggacttctcaagcatgacgctgacacagatcaaacgccaagagatggattctcaggttagggtgctagagctagaaaatgaattgcagaaggagcgtcaaaaactgggagagcttcggaaaaagcactacgagcttgctggtgttgctgagggctgggaagaaggaacagaggcatctccacctacactgcaagaagtggtaaccgaaaaagaatagagccaaaccaacaccccatatgtcagtgtaaatccttgttacctatctcgtgtgtgttatttccccagccacaggccaaatccttggagtcccaggggcagccacaccactgccattacccagtgccgaggacatgcatgacacttccaaagactccctccatagcgacaccctttctgtttggacccatggtcatctctgttcttttcccgcctccctagttagcatccaggctggccagtgctgcccatgagcaagcctaggtacgaagaggggtggtggggggcagggccactcaacagagaggaccaacatccagtcctgctgactatttgacccccacaacaatgggtatccttaatagaggagctgcttgttgtttgttgacagcttggaaagggaagatcttatgccttttcttttctgttttcttctcagtcttttcagtttcatcatttgcacaaacttgtgagcatcagagggctgatggattccaaaccaggacactaccctgagatctgcacagtcagaaggacggcaggagtgtcctggctgtgaatgccaaagccattctccccctctttgggcagtgccatggatttccactgcttcttatggtggttggttgggttttttggttttgtttttttttttaagtttcactcacatagccaactctcccaaagggcacacccctggggctgagtctccagggccccccaactgtggtagctccagcgatggtgctgcccaggcctctcggtgctccatctccgcctccacactgaccaagtgctggcccacccagtccatgctccagggtcaggcggagctgctgagtgacagctttcctcaaaaagcagaaggagagtgagtgcctttccctcctaaagctgaatcccggcggaaagcctctgtccgcctttacaagggagaagacaacagaaagagggacaagagggttcacacagcccagttcccgtgacgaggctcaaaaacttgatcacatgcttgaatggagctggtgagatcaacaacactacttccctgccggaatgaactgtccgtgaatggtctctgtcaagcgggccgtctcccttggcccagagacggagtgtgggagtgattcccaactcctttctgcagacgtctgccttggcatcctcttgaataggaagatcgttccaccttctacgcaattgacaaacccggaagatcagatgcaattgctcccatcagggaagaaccctatacttggtttgctacccttagtatttattactaacctcccttaagcagcaacagcctacaaagagatgcttggagcaatcagaacttcaggtgtgactctagcaaggctcatctttctgcccggctacatcagccttcaagaatcagaagaaaggccaaggtgctggactgttactgacttggatcccaaagcaaggagatcatttggagctcttgggtcagagaaaatgagaaaggacagagccagcggctccaactcctttcagccacatgccccaggctctcgctgccctgtggacaggatgaggacagagggcacatgaacagcttgccagggatgggcagcccaacagcacttttcctcttctagatggaccccagcatttaagtgaccttctgatcttggaaaaacagcgtcttccttctttatctatagcaactcattggtggtagccatcaagcacttcccaggatctgctccaacagaatattgctaggttttgctacatgacgggttgtgagacttctgtttgatcactgtgaaccaacccccatctccctagcccacccccctccccaactccctctctgtgcattttctaagtgggacattcaaaaaactctctcccaggacctcggatgaccatactcagacgtgtgacctccatactgggctaaggaagtatcagcactagaaattgggcagtcttaatgttgaatgctgctttctgcttagtatttttttgattcaaggctcagaaggaatggtgcgtggcttccctgtcccagttgtggcaactaaaccaatcggtgtgttcttgatgcgggtcaacatttccaaaagtggctagtcctcacttctagatctcagccattctaactcatatgttcccaattaccaaggggtggccgggcacagtggctcacgcctgtaatcccagcactttgagaggctgaggtggtaggatcacctgaggtcaggagttcaagaccagcctgtccaacatggtgaaacccccatctctactaaaaataccaaaaattagccgagcgtagtgacgggtgcccgtaatcccagctactcaggaggctgagacaggagaatcacctgaaccccagaggcagaggttgcagtgagctgagatcacgccattgtactccagcctgggcaacaagagcaaaactccgtctcaaaaaaaaaaaaaaattacaaatggggcaaacagtctagtgtaatggatcaaattaagattctctgcccagccgggcacagtggcgcatgcctgtaatcccagaactttgggaggccaagacgggatgattgcttgagctcaggagtttgagaccaggctgggcatcatagcaagacctcatctctactaaaattcaaaaacaaaattagccgggcatgatggtgcatgcctgtagtctcagctagttggggagctaaggtgggagaattgcttgagcttgggaagtcgaggctgcagtcagccctgattgtgccagtgcactccggcctgggtgacagagtgagaccctgtctcaaaaaaaaaaagattctgtgtcagagcccagcccaggagtttgaggctgcaatgagccatgatttcccactgcactccagcctgagtgacagagcgagactccatctctttaaaaacaaacaaaaaattatctgaatgatcctgtctctaaaaagaagccacagaaatgtttaaaaacttcatcgacttagcctgagtcataacggttaagaaagcacttaaacagaagcagaggctaattcagtgtcacatgaggaagtagctgtcagatgtcacataattactttcgtaatagctcagattagaatggctaccccattctctagacaaaatcaaattgtcctattgtgactcttctaaaaatgaagatgaagagctatttaatgacacaccttggattaaaacgggaatcacatcttaaagctaaaaatgaacctgcaagccttctaaatgagtcactgagcatcactagtgacaagtctcgggtgagcgtaaatgggtcatgacaagatgggacagcaacaaaatcatggcttaggatcgacaagaagttaaaaaacagctgcatctgttacttaagtttgtaagacagtgccctgagacctctagagaaaagatgtttgtttacataagagaaagaggccagacatggtgtctcacacgtttaatcccagcactttgggaggcaggggcgggtggatcacctgaggtcaggagttcaagactagcctggccaacatggtgaaaccccgtctctactaaaaatacaaaaattagccgggcatggtggcaggcgcctataatcccagctactggggaggctgaggcaggagaatcacttgaacccgggggacagaggttgtagtgagccaagatcgcaccactgcactccagcctgggtcacagagtgagactccatctcaaaaaaaaaaaagagagagagagagaaagaaatagaagagaagagccatcttggcagggttattttatatctgagcaaggagtttaaatgagactagtttagattgtctgctgatgcagccgtccatagcagtacccctaaaatcccaccagaatacgggtccctctaacccagtggctggaagaaccactgtctagagcaacttttcttggaactgtcccagctaccaagtcagacaccaaggtttatgccaccaggtaacacgggaatcacaggtacatgtcgctccggtcagattagttggctttggcccctcgaccctgtgcaggagctagttctcagcttgcagctggaagttccctcttagctccttagtctagaggggtctcctggctccatttgaccctggtctttaataaccggtcagcatcttgctaccttctaccacctttccaaatctctggaaatcctgccagggaaagcctccagttccaacattggctttccaagcaaactggctttgccctctctctgccatccttgtcctccagagactgcaccacctgtagcatagaaaaccaccaccacggacctgccagccattggcgcagcaaaccagccagctgtttgctgccaaattccttcctctcccaggtccagaccaaatacaagatcagcaccacaccgtggtgttgtcaggagccaaagcaacaggaaacaattcaatgctgttgggttcgattctgagagtagatttttccagacatgtctttcaggtgaccctcaactacctcaggtttgaaggccctaaatgaaactgattaccactcatagggacaaaccgagggggttcggttacatcttggtgataatgcagttgtctcaaacttataacagactctttcacatttcagtttgcagggatagggttgggtttgtttttcttctgtttttaacctttcccctgggtttccattagggtagttccttgaaatgaatttcatttttcactgagtgcctaccttcccagggcaggtggccactggcttctgtttccctccaacaatacttttattatggtattaagacctttctttgtataatacattgcatctgtgttttcaatttttcaaataaatatttccgcctggcaaaaaaaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:3092 -> Molecular function: GO:0003779 [actin binding] evidence: IEA
            GeneID:3092 -> Molecular function: GO:0005200 [structural constituent of cytoskeleton] evidence: TAS
            GeneID:3092 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:3092 -> Molecular function: GO:0030276 [clathrin binding] evidence: IDA
            GeneID:3092 -> Molecular function: GO:0035091 [phosphatidylinositol binding] evidence: IDA
            GeneID:3092 -> Biological process: GO:0006351 [transcription, DNA-dependent] evidence: IEA
            GeneID:3092 -> Biological process: GO:0006355 [regulation of transcription, DNA-dependent] evidence: IEA
            GeneID:3092 -> Biological process: GO:0006897 [endocytosis] evidence: IEA
            GeneID:3092 -> Biological process: GO:0006915 [apoptotic process] evidence: IDA
            GeneID:3092 -> Biological process: GO:0006919 [activation of cysteine-type endopeptidase activity involved in apoptotic process] evidence: IDA
            GeneID:3092 -> Biological process: GO:0030154 [cell differentiation] evidence: IEA
            GeneID:3092 -> Biological process: GO:0042981 [regulation of apoptotic process] evidence: IDA
            GeneID:3092 -> Biological process: GO:0048260 [positive regulation of receptor-mediated endocytosis] evidence: IMP
            GeneID:3092 -> Biological process: GO:0048268 [clathrin coat assembly] evidence: IDA
            GeneID:3092 -> Biological process: GO:0097190 [apoptotic signaling pathway] evidence: IDA
            GeneID:3092 -> Cellular component: GO:0005634 [nucleus] evidence: IEA
            GeneID:3092 -> Cellular component: GO:0005737 [cytoplasm] evidence: IDA
            GeneID:3092 -> Cellular component: GO:0005794 [Golgi apparatus] evidence: IDA
            GeneID:3092 -> Cellular component: GO:0005856 [cytoskeleton] evidence: TAS
            GeneID:3092 -> Cellular component: GO:0016020 [membrane] evidence: TAS
            GeneID:3092 -> Cellular component: GO:0030136 [clathrin-coated vesicle] evidence: IDA
            GeneID:3092 -> Cellular component: GO:0030665 [clathrin-coated vesicle membrane] evidence: IEA
            GeneID:3092 -> Cellular component: GO:0043231 [intracellular membrane-bounded organelle] evidence: IDA

by @meso_cacase at DBCLS
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