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2024-04-25 12:31:21, GGRNA : RefSeq release 60 (20130726)

LOCUS       NR_075080               3950 bp    RNA     linear   PRI 18-JUL-2013
DEFINITION  Homo sapiens leucine zipper transcription factor-like 1 (LZTFL1),
            transcript variant 4, non-coding RNA.
ACCESSION   NR_075080
VERSION     NR_075080.1  GI:444909180
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 3950)
  AUTHORS   Marion,V., Stutzmann,F., Gerard,M., De Melo,C., Schaefer,E.,
            Claussmann,A., Helle,S., Delague,V., Souied,E., Barrey,C.,
            Verloes,A., Stoetzel,C. and Dollfus,H.
  TITLE     Exome sequencing identifies mutations in LZTFL1, a BBSome and
            smoothened trafficking regulator, in a family with Bardet--Biedl
            syndrome with situs inversus and insertional polydactyly
  JOURNAL   J. Med. Genet. 49 (5), 317-321 (2012)
   PUBMED   22510444
  REMARK    GeneRIF: The absence of LZTFL1 leads to a BBS phenotype with
            enhanced developmental abnormalities associated with cellular Shh
            dysfunction. LZTFL1 is a novel BBS gene (BBS17).
REFERENCE   2  (bases 1 to 3950)
  AUTHORS   Seo,S., Zhang,Q., Bugge,K., Breslow,D.K., Searby,C.C., Nachury,M.V.
            and Sheffield,V.C.
  TITLE     A novel protein LZTFL1 regulates ciliary trafficking of the BBSome
            and Smoothened
  JOURNAL   PLoS Genet. 7 (11), E1002358 (2011)
   PUBMED   22072986
  REMARK    GeneRIF: Our findings suggest that LZTFL1 is an important regulator
            of BBSome ciliary trafficking and hedgehog signaling
REFERENCE   3  (bases 1 to 3950)
  AUTHORS   Wei,Q., Zhou,W., Wang,W., Gao,B., Wang,L., Cao,J. and Liu,Z.P.
  TITLE     Tumor-suppressive functions of leucine zipper transcription
            factor-like 1
  JOURNAL   Cancer Res. 70 (7), 2942-2950 (2010)
   PUBMED   20233871
  REMARK    GeneRIF: LZTFL1 may inhibit tumorigenesis by stabilizing
            E-cadherin-mediated adherens junction formation and promoting
            epithelial cell differentiation.
REFERENCE   4  (bases 1 to 3950)
  AUTHORS   Davila,S., Froeling,F.E., Tan,A., Bonnard,C., Boland,G.J.,
            Snippe,H., Hibberd,M.L. and Seielstad,M.
  TITLE     New genetic associations detected in a host response study to
            hepatitis B vaccine
  JOURNAL   Genes Immun. 11 (3), 232-238 (2010)
   PUBMED   20237496
  REMARK    GeneRIF: Observational study of gene-disease association. (HuGE
            Navigator)
REFERENCE   5  (bases 1 to 3950)
  AUTHORS   Kiss,H., Kedra,D., Kiss,C., Kost-Alimova,M., Yang,Y., Klein,G.,
            Imreh,S. and Dumanski,J.P.
  TITLE     The LZTFL1 gene is a part of a transcriptional map covering 250 kb
            within the common eliminated region 1 (C3CER1) in 3p21.3
  JOURNAL   Genomics 73 (1), 10-19 (2001)
   PUBMED   11352561
COMMENT     REVIEWED REFSEQ: This record has been curated by NCBI staff. The
            reference sequence was derived from HY159348.1, DA408809.1,
            AJ297351.1, AC098476.2 and BX112707.1.
            
            Summary: This gene encodes a ubiquitously expressed protein that
            localizes to the cytoplasm. This protein interacts with
            Bardet-Biedl Syndrome (BBS) proteins and, through its interaction
            with BBS protein complexes, regulates protein trafficking to the
            ciliary membrane. Nonsense mutations in this gene cause a form of
            Bardet-Biedl Syndrome; a ciliopathy characterized in part by
            polydactyly, obesity, cognitive impairment, hypogonadism, and
            kidney failure. This gene may also function as a tumor suppressor;
            possibly by interacting with E-cadherin and the actin cytoskeleton
            and thereby regulating the transition of epithelial cells to
            mesenchymal cells. Alternative splicing of this gene results in
            multiple transcript variants. [provided by RefSeq, Feb 2013].
            
            Transcript Variant: This variant (4) lacks an internal exon,
            compared to variant 1. This variant is represented as non-coding
            because the use of the 5'-most translational start codon, as used
            in variant 1, renders the transcript a candidate for
            nonsense-mediated mRNA decay (NMD).
            
            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.
            COMPLETENESS: complete on the 3' end.
PRIMARY     REFSEQ_SPAN         PRIMARY_IDENTIFIER PRIMARY_SPAN        COMP
            1-29                HY159348.1         2-30
            30-675              DA408809.1         1-646
            676-3302            AJ297351.1         758-3384
            3303-3930           AC098476.2         173999-174626       c
            3931-3950           BX112707.1         1-20                c
FEATURES             Location/Qualifiers
     source          1..3950
                     /organism="Homo sapiens"
                     /mol_type="transcribed RNA"
                     /db_xref="taxon:9606"
                     /chromosome="3"
                     /map="3p21.3"
     gene            1..3950
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /note="leucine zipper transcription factor-like 1"
                     /db_xref="GeneID:54585"
                     /db_xref="HGNC:6741"
                     /db_xref="MIM:606568"
     misc_RNA        1..3950
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /product="leucine zipper transcription factor-like 1,
                     transcript variant 4"
                     /db_xref="GeneID:54585"
                     /db_xref="HGNC:6741"
                     /db_xref="MIM:606568"
     exon            1..170
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /inference="alignment:Splign:1.39.8"
     exon            171..365
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /inference="alignment:Splign:1.39.8"
     exon            366..426
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /inference="alignment:Splign:1.39.8"
     exon            427..498
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /inference="alignment:Splign:1.39.8"
     exon            499..564
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /inference="alignment:Splign:1.39.8"
     exon            565..642
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /inference="alignment:Splign:1.39.8"
     exon            643..819
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /inference="alignment:Splign:1.39.8"
     variation       778
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1129183"
     exon            820..923
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /inference="alignment:Splign:1.39.8"
     exon            924..3940
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /inference="alignment:Splign:1.39.8"
     polyA_signal    1272..1277
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     polyA_signal    1327..1332
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     polyA_signal    1382..1387
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     polyA_signal    1684..1689
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     polyA_signal    2323..2328
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     polyA_signal    2727..2732
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     variation       2890..2891
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /replace=""
                     /replace="gtt"
                     /db_xref="dbSNP:3834206"
     polyA_signal    3166..3171
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     polyA_signal    3242..3247
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     polyA_signal    3246..3251
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     polyA_site      3265
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     variation       3742
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
                     /replace="a"
                     /replace="g"
                     /db_xref="dbSNP:1058961"
     polyA_signal    3911..3916
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
     polyA_site      3940
                     /gene="LZTFL1"
                     /gene_synonym="BBS17"
ORIGIN      


ataattgcagtccacgtgcctcggtttccgttagcaaccagaggcttctaaacaacctaccctccttccccattttctgtggtccaactaccctcggcgatcccaggcttggcggggcaccgcctggcctctcccgttcctttaggctgccgccgctgcctgccgccatggctggtggaggacaccttcaccatagatgaagtctctgaagtcctcaatggattacaagctgtggttcatagtgaggtggaatctgagctcatcaacactgcctataccaatgtgttacttctgcgacagctgtttgcacaagctgagaagtggtatcttaagctacagacagacatctctgaacttgaaaaccgagaattattagaacaagttgcagaatttgaaaaagcagagattacatcttcaaacaaaaagcccatcttagatgtcacaaagccaaaacttgctccacttaatgaaggtggaacagcagaactcctaaacaaggaaattttaagacttcaagaagagaatgagaaattgaagtcaaggttgaagaccattgaaatacaggctacaaatgcactggatgaaaagtcaaaactagaaaaagcactgcaagatttacagcttgatcaaggaaatcaaaaggattttataaaggcccaagacttaagtaacttagaaaacactgtcgctgccttaaagagtgagtttcagaagacacttaatgacaagacagaaaaccagaagtcactggaggagaatctggcgacagccaagcacgatctactcagggttcaggagcagctgcacatggctgaaaaggaattagaaaagaaatttcagcaaacagcagcttatcgaaacatgaaagagattcttaccaagaagaatgaccaaatcaaagatctgaggaaaagactggcacaatatgaacctgaagattaaaactgaagatttcctctggaagctaccacatgcaaacatacaagcagtctcacctcaggcatgtattttgaaaagcattttgtcatatcccctctccttatttttctaatatttagactttgaatatttagaactagagttcctattttcagctagttgaaaacagagaaaacctagtgattctgtctggtcatcccacacacctctctactgagtgctccagagtcttagctcacatgcactgagaattctttacagcaaagaagagatttttagagtgggaagaagaggcttatccttctgcattagtataaagagtctgtatttttaataaatgttaaataagctaacaatgtttgtacttatgcattccccatgggtaaaaataaataatagcattgttaaagatagttattaccaaaaaaagagagttattacaaataaatatgtctctttatttttaaaaatgaaatcttaattcatttactctatttgatgataaactataaattcattgaaaatgtgaattctattatgggtagcctttttaccaattataaggaaaatttacagcagtgaacatgaacattcacttagcttcctcagtctctccatcttaaagatcatttatcagaggaggttcagcattttttgcagcataacttttcatgagtctgtattactaatggataagtcaaatccatcctgcacttctacagtttagaaagtatctggactcagaataaatgtaatatttatacttgtttccagaatgttattttacattttatgttcaataagaacactttttaaaagacgtatattcaacataaaatcagctatcagacttcagattagactttatttatgtgggtctataataattgtattttcaagaggttttcactatatttgtattggcctggttttctcagacgattttggacaaatcattagaaactgggcatcatatccacagttatgtaaggcagtgatatactataaggataaacaaagtcaagtccataaagcaataatccctcagaaggaaagtccttacttttcacatattaatatttagtaatttttcctgcttctaaaagtgagagtatcacaccctaaatgaacactgtctactaagagacatcattccatttccacaaatgaagattttattccaagaaacgagtttactgattggagcatagggcttgttgttatttttattcaagcttttagtaatagccttgaatttattatttttcttataggctttttgttaaaatagtgaaggaacaaatgttaaagggtaagataatttccctgcaaaaggacacagaaggcagtcttaagaagatgaatggatgagagaagggagagaataaaatgcaataacgagccagcatttactatgtattttctcctcacctgtctctccatatttaggtcacttaccagtttctgtgcccttttggagcttttgttgagggcttcattctcaccctgtatttctttagccctaaattgacactctctccaaaaatccattccattgtctgtggaccaagatgttctatgtaattcagaagcagaactcttggctaaagggctagtgtggccttcagaaaccattcaattattttctccctacacctttgtcagtttgaaaccagtgaggaaaaaaggtatgttgataagaaacctatattgctaggtagaatttgtacttgttttcttggtagcagttttgaaatattctgtacagtacgttcctattgtttaataataaattcaaaaatatttctaaaaccttaaaaccaactatgccaagcattaagataaacaaatatgatgttctttgacgtaaatcaacgtgatgattctttcacatgtaaacacattttagtgtttctggtttgtcatttttgttgttgttgttgttgttgttatttactctataccctttagcaaaatacagttttaaatttttattgtttttagtagtttcccaactttaagacttatctaatttaactgagaaagaaagcctttttcatatatatatatattggatttctaaggatggtggtttgagccttgattagacttttgatgtgctaagccagacaggcagtctgtacattgatggccatcacaatgcagctttggtttaatttaattcaggcctgctgctgagttatgcacagactttttgttgaccaaaataaaatataaagggttttcttctgtttgacatttgtgttcattttttctctttatgtattacattttaacctatattaaataaatgtttaaatgataatttgcttatgtcttataaaactcagcataagaaaaatactgccctaccttgactgtgtaatcttatttgataaagcctttgctattcattatttccattctgattaactgaaagagatttatagagatgctcaaattttaagcccttggtgcttttagatatatattggttgcaaaagtttggcattaatgatttccctctgcttatgtgtaaatgcctatgttccaaagctttgccactagatattcaaatcataaattgtcatgtaagccagtcttccagaaagaaaagctatttcagcaaaatgatatttcacatttagacaaaacagtagtatttagacaataatattttgacaaaaccattttcaaaactgcttaggaaaaaggggaaatattatacttaaaggtaatgacctctgtcttgaatagaggtgagtgggttggtgacaactggtttggaggcttttgtgggggactgtggtgtcttttggattgtgtcatcagctccttcatcaagtaagcgtgtagctgttattgcctattgtaaaacatgaattgatgtgaacagtactcaatctcttacattatatgaagtataacttcctctcttttttgcctataatacatcctttaacttttacagattaaaaaaccactgttagacaaagcaaaaaaaaaaaaaa
//

Annotations:

ANNOTATIONS from NCBI Entrez Gene (20130726):
            GeneID:54585 -> Molecular function: GO:0005515 [protein binding] evidence: IPI
            GeneID:54585 -> Molecular function: GO:0042802 [identical protein binding] evidence: IPI
            GeneID:54585 -> Biological process: GO:0072594 [establishment of protein localization to organelle] evidence: IEA
            GeneID:54585 -> Cellular component: GO:0005737 [cytoplasm] evidence: IEA

by @meso_cacase at DBCLS
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