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2025-05-09 17:23:39, GGRNA : RefSeq release 60 (20130726)
LOCUS NM_001198915 5807 bp mRNA linear PRI 17-APR-2013
DEFINITION Homo sapiens PTPRF interacting protein, binding protein 1 (liprin
beta 1) (PPFIBP1), transcript variant 3, mRNA.
ACCESSION NM_001198915
VERSION NM_001198915.1 GI:312032470
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 5807)
AUTHORS Wei,Z., Zheng,S., Spangler,S.A., Yu,C., Hoogenraad,C.C. and
Zhang,M.
TITLE Liprin-mediated large signaling complex organization revealed by
the liprin-alpha/CASK and liprin-alpha/liprin-beta complex
structures
JOURNAL Mol. Cell 43 (4), 586-598 (2011)
PUBMED 21855798
REMARK GeneRIF: Liprins can mediate assembly of target proteins into large
protein complexes capable of regulating numerous cellular
activities.
REFERENCE 2 (bases 1 to 5807)
AUTHORS Takeuchi,K., Soda,M., Togashi,Y., Sugawara,E., Hatano,S., Asaka,R.,
Okumura,S., Nakagawa,K., Mano,H. and Ishikawa,Y.
TITLE Pulmonary inflammatory myofibroblastic tumor expressing a novel
fusion, PPFIBP1-ALK: reappraisal of anti-ALK immunohistochemistry
as a tool for novel ALK fusion identification
JOURNAL Clin. Cancer Res. 17 (10), 3341-3348 (2011)
PUBMED 21430068
REMARK GeneRIF: Novel ALK fusions are being identified in various tumors
in addition to inflammatory myofibroblastic tumor.
REFERENCE 3 (bases 1 to 5807)
AUTHORS Norrmen,C., Vandevelde,W., Ny,A., Saharinen,P., Gentile,M.,
Haraldsen,G., Puolakkainen,P., Lukanidin,E., Dewerchin,M.,
Alitalo,K. and Petrova,T.V.
TITLE Liprin (beta)1 is highly expressed in lymphatic vasculature and is
important for lymphatic vessel integrity
JOURNAL Blood 115 (4), 906-909 (2010)
PUBMED 19965622
REMARK GeneRIF: liprin beta1, a member of the family of LAR transmembrane
tyrosine phosphatase-interacting proteins, as highly expressed in
intestinal lymphatic endothelial cells in vitro and lymphatic
vasculature in vivo
REFERENCE 4 (bases 1 to 5807)
AUTHORS Jin,J., Smith,F.D., Stark,C., Wells,C.D., Fawcett,J.P.,
Kulkarni,S., Metalnikov,P., O'Donnell,P., Taylor,P., Taylor,L.,
Zougman,A., Woodgett,J.R., Langeberg,L.K., Scott,J.D. and Pawson,T.
TITLE Proteomic, functional, and domain-based analysis of in vivo 14-3-3
binding proteins involved in cytoskeletal regulation and cellular
organization
JOURNAL Curr. Biol. 14 (16), 1436-1450 (2004)
PUBMED 15324660
REFERENCE 5 (bases 1 to 5807)
AUTHORS Kriajevska,M., Fischer-Larsen,M., Moertz,E., Vorm,O.,
Tulchinsky,E., Grigorian,M., Ambartsumian,N. and Lukanidin,E.
TITLE Liprin beta 1, a member of the family of LAR transmembrane tyrosine
phosphatase-interacting proteins, is a new target for the
metastasis-associated protein S100A4 (Mts1)
JOURNAL J. Biol. Chem. 277 (7), 5229-5235 (2002)
PUBMED 11836260
REMARK GeneRIF: new molecular target of the S100A4 protein, liprin beta1
REFERENCE 6 (bases 1 to 5807)
AUTHORS Serra-Pages,C., Medley,Q.G., Tang,M., Hart,A. and Streuli,M.
TITLE Liprins, a family of LAR transmembrane protein-tyrosine
phosphatase-interacting proteins
JOURNAL J. Biol. Chem. 273 (25), 15611-15620 (1998)
PUBMED 9624153
COMMENT REVIEWED REFSEQ: This record has been curated by NCBI staff. The
reference sequence was derived from BQ777042.1, AB033056.2,
AC087257.13 and CA442440.1.
Summary: The protein encoded by this gene is a member of the LAR
protein-tyrosine phosphatase-interacting protein (liprin) family.
Liprins interact with members of LAR family of transmembrane
protein tyrosine phosphatases, which are known to be important for
axon guidance and mammary gland development. It has been proposed
that liprins are multivalent proteins that form complex structures
and act as scaffolds for the recruitment and anchoring of LAR
family of tyrosine phosphatases. This protein was found to interact
with S100A4, a calcium-binding protein related to tumor
invasiveness and metastasis. In vitro experiment demonstrated that
the interaction inhibited the phosphorylation of this protein by
protein kinase C and protein kinase CK2. Alternatively spliced
transcript variants encoding distinct isoforms have been reported.
[provided by RefSeq, Jul 2008].
Transcript Variant: This variant (3) differs in the 5' UTR and
coding sequence compared to variant 2. The resulting isoform (3) is
shorter at the N-terminus compared to isoform 2.
##Evidence-Data-START##
Transcript exon combination :: AB033056.2 [ECO:0000332]
RNAseq introns :: single sample supports all introns
ERS025082, ERS025083 [ECO:0000348]
##Evidence-Data-END##
COMPLETENESS: complete on the 3' end.
PRIMARY REFSEQ_SPAN PRIMARY_IDENTIFIER PRIMARY_SPAN COMP
1-70 BQ777042.1 11-80
71-329 AB033056.2 1-259
330-330 AC087257.13 145419-145419
331-5360 AB033056.2 261-5290
5361-5807 CA442440.1 1-447 c
FEATURES Location/Qualifiers
source 1..5807
/organism="Homo sapiens"
/mol_type="mRNA"
/db_xref="taxon:9606"
/chromosome="12"
/map="12p12.1"
gene 1..5807
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/note="PTPRF interacting protein, binding protein 1
(liprin beta 1)"
/db_xref="GeneID:8496"
/db_xref="HGNC:9249"
/db_xref="MIM:603141"
exon 1..254
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 43
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:2289710"
variation 85
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:372353307"
variation 212
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:12314684"
variation 250
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:374737096"
variation 251
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:147297613"
exon 255..342
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 283
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:114441949"
misc_feature 307..309
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/note="upstream in-frame stop codon"
variation 330
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:4448724"
exon 343..429
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 351
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:373440206"
variation 356
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:73294067"
variation 360
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:370021875"
variation 367
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138904548"
variation 375
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374249871"
variation 376
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373923026"
variation 395
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142823290"
variation 410
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:147402814"
variation 419
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:199985476"
variation 421
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139120224"
variation 425
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201234208"
exon 430..543
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 430
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:148602928"
variation 434
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144532770"
variation 435
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146644142"
variation 436
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140176051"
variation 475
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:143847599"
variation 504
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:376729598"
variation 507
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:151288073"
variation 514
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:2194816"
variation 523
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369134316"
CDS 532..3108
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/note="isoform 3 is encoded by transcript variant 3;
liprin-beta 1; liprin related protein; protein-tyrosine
phosphatase receptor-type f polypeptide-interacting
protein-binding protein 1; liprin-beta-1;
PTPRF-interacting protein-binding protein 1; protein
tyrosine phosphatase receptor type f
polypeptide-interacting protein-binding protein 1"
/codon_start=1
/product="liprin-beta-1 isoform 3"
/protein_id="NP_001185844.1"
/db_xref="GI:312032471"
/db_xref="CCDS:CCDS55814.1"
/db_xref="GeneID:8496"
/db_xref="HGNC:9249"
/db_xref="MIM:603141"
/translation="
MLQQELLSRTSLETQKLDLMAEISNLKLKLTAVEKDRLDYEDKFRDTEGLIQEINDLRLKVSEMDSERLQYEKKLKSTKSLMAKLSSMKIKVGQMQYEKQRMEQKWESLKDELASLKEQLEEKESEVKRLQEKLVCKMKGEGVEIVDRDIEVQKMKKAVESLMAANEEKDRKIEDLRQCLNRYKKMQDTVVLAQGKDGEYEELLNSSSISSLLDAQGFSDLEKSPSPTPVMGSPSCDPFNTSVPEEFHTTILQVSIPSLLPATVSMETSEKSKLTPKPETSFEENDGNIILGATVDTQLCDKLLTSSLQKSSSLGNLKKETSDGEKETIQKTSEDRAPAESRPFGTLPPRPPGQDTSMDDNPFGTRKVRSSFGRGFFKIKSNKRTASAPNLAETEKETAEHLDLAGASSRPKDSQRNSPFQIPPPSPDSKKKSRGIMKLFGKLRRSQSTTFNPDDMSEPEFKRGGTRATAGPRLGWSRDLGQSNSDLDMPFAKWTKEQVCNWLMEQGLGSYLNSGKHWIASGQTLLQASQQDLEKELGIKHSLHRKKLQLALQALGSEEETNHGKLDFNWVTRWLDDIGLPQYKTQFDEGRVDGRMLHYMTVDDLLSLKVVSVLHHLSIKRAIQVLRINNFEPNCLRRRPSDENTIAPSEVQKWTNHRVMEWLRSVDLAEYAPNLRGSGVHGGLMVLEPRFNVETMAQLLNIPPNKTLLRRHLATHFNLLIGAEAQHQKRDAMELPDYVLLTATAKVKPKKLAFSNFGNLRKKKQEDGEEYVCPMELGQASGSASKKGFKPGLDMRLYEEDDLDRLEQMEDSEGTVRQIGAFSEGINNLTHMLKEDDMFKDFAARSPSASITDEDSNV
"
misc_feature 2002..2196
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/note="Sterile alpha motif; Region: SAM; smart00454"
/db_xref="CDD:197735"
misc_feature 2002..2193
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/note="SAM domain of liprin-beta1,2 proteins repeat 1;
Region: SAM_liprin-beta1,2_repeat1; cd09563"
/db_xref="CDD:188962"
misc_feature 2224..2412
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/note="SAM (Sterile alpha motif ); Region:
SAM_superfamily; cl15755"
/db_xref="CDD:210155"
misc_feature 2230..>2334
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/note="Sterile alpha motif; Region: SAM; smart00454"
/db_xref="CDD:197735"
misc_feature 2479..2694
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/note="SAM domain of liprin-beta proteins repeat 3;
Region: SAM_liprin-beta1,2_repeat3; cd09569"
/db_xref="CDD:188968"
misc_feature 2491..2694
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/note="SAM domain (Sterile alpha motif); Region: SAM_2;
pfam07647"
/db_xref="CDD:203706"
variation 533
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200914061"
variation 537
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:73294079"
exon 544..675
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 576
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:145205395"
variation 604
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374026427"
variation 643
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:377169543"
variation 646
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:186690420"
variation 655
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:370323116"
variation 664
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142355778"
exon 676..768
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 695
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202028953"
exon 769..861
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 792
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145263806"
variation 795
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200359000"
variation 832
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:181574182"
exon 862..976
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 904
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:375385877"
variation 908
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:369414467"
variation 930
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:146333349"
variation 939
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:371497886"
exon 977..1038
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 979
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138974239"
variation 997
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376597954"
exon 1039..1114
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 1061
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370141265"
variation 1083
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61748361"
variation 1097
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142893025"
exon 1115..1269
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 1124
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:143554172"
variation 1140
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:185263684"
variation 1180
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:148024203"
variation 1235
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:371077704"
exon 1270..1385
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 1290
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141690857"
variation 1345
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:200687061"
variation 1358
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:150528906"
exon 1386..1442
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 1414
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:113710428"
variation 1420
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:200945345"
variation 1429
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:35670331"
variation 1433
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:76499984"
exon 1443..1503
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 1445
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:377752142"
variation 1448
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:371336714"
variation 1489
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:374468566"
exon 1504..1533
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
exon 1534..1705
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 1542
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:35150305"
variation 1544
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372834652"
variation 1545
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/replace="g"
/db_xref="dbSNP:146181524"
variation 1553
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:375725857"
variation 1557
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202174851"
variation 1566
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140182450"
variation 1625
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:201179220"
variation 1628
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376929898"
variation 1652
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376591163"
variation 1662
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:143859582"
variation 1666
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:200910244"
variation 1685
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373605140"
exon 1706..1856
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 1744
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201187783"
variation 1760
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200486013"
variation 1781
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142910651"
variation 1782
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:187660139"
variation 1800
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:370509537"
exon 1857..1985
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 1857
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61739753"
variation 1911
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368610595"
variation 1940
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:372542352"
variation 1949
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:377120565"
variation 1959
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201006068"
variation 1961
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369476664"
variation 1963
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:151071761"
variation 1964
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:142422262"
variation 1968
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:372089803"
exon 1986..2136
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 1994
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200645200"
variation 2061
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:35291896"
variation 2102
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:201195756"
variation 2109
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:113931583"
variation 2111
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:147864879"
variation 2124
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367649651"
exon 2137..2248
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 2137
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373637167"
variation 2143
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:200119939"
variation 2157
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:141451946"
variation 2162
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150367272"
variation 2165
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:367618122"
variation 2203
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:138046370"
variation 2220..2221
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace=""
/replace="g"
/db_xref="dbSNP:34022369"
variation 2235
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:372355893"
variation 2238
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:149093315"
exon 2249..2337
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 2288
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:202011004"
variation 2329
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:143124134"
variation 2335
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:202193926"
exon 2338..2460
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 2440
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:138624973"
variation 2444..2445
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace=""
/replace="c"
/db_xref="dbSNP:34220354"
variation 2457
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:373465725"
exon 2461..2586
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 2470
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:376329180"
variation 2472
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:61917497"
variation 2490
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:138941072"
variation 2503
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146185523"
variation 2522
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369668351"
variation 2536
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:137864595"
variation 2541
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373149305"
exon 2587..2775
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 2659
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:373264878"
variation 2660
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201325210"
variation 2691
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61730962"
variation 2698
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:192927833"
variation 2702
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:147160498"
variation 2711
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:150045915"
exon 2776..2955
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 2805
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201810502"
variation 2843
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:368511222"
variation 2857
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:140823525"
variation 2869
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:200511262"
variation 2909
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:113985648"
variation 2917
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:144681794"
variation 2918
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:61757741"
variation 2945
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:201126471"
exon 2956..3021
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 3020
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:375535195"
variation 3021
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:369788968"
exon 3022..5790
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/inference="alignment:Splign:1.39.8"
variation 3025
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:142730346"
variation 3054
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:370440817"
variation 3065
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:371325602"
variation 3082
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:199801908"
variation 3102
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:55923847"
variation 3111
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:374114077"
variation 3124
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:367971027"
variation 3155
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:371421286"
variation 3175
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:372609088"
variation 3194
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:144504690"
variation 3217
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:3764010"
variation 3231
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:148395830"
variation 3258
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:183102078"
variation 3411
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:7309005"
variation 3520
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:56856599"
variation 3584
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:368935895"
variation 3684
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:142526071"
variation 3685
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:187768966"
variation 3708
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:16932296"
variation 3822
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:76599957"
STS 3972..5627
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/standard_name="L18426"
/db_xref="UniSTS:34648"
variation 4023
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:11049095"
variation 4029
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:111818593"
variation 4093
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:193300307"
variation 4123
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:185140996"
variation 4223..4224
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace=""
/replace="t"
/db_xref="dbSNP:200249833"
variation 4233
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:78218603"
variation 4240
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:190382759"
variation 4265
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:151006610"
STS 4345..5385
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/standard_name="L18506"
/db_xref="UniSTS:54024"
variation 4367
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:114845811"
variation 4385
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:115719991"
STS 4504..5385
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/standard_name="L18506"
/db_xref="UniSTS:54024"
variation 4510
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:139994391"
variation 4513
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:143369313"
variation 4755
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:74074224"
variation 4770
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146711132"
variation 4787
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:140345118"
variation 4797
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:368687919"
variation 4834
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:74074225"
variation 4837
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="c"
/db_xref="dbSNP:192629982"
variation 4862
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:150209760"
variation 5066
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:184250045"
variation 5067
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:188143172"
variation 5084
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:116652155"
variation 5205
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:74462176"
variation 5289
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:180903040"
variation 5328
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:373193073"
variation 5345..5346
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace=""
/replace="a"
/db_xref="dbSNP:201424178"
variation 5346..5348
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace=""
/replace="t"
/db_xref="dbSNP:57935514"
variation 5347
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="t"
/db_xref="dbSNP:74663411"
variation 5361
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="g"
/replace="t"
/db_xref="dbSNP:201472128"
variation 5365
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:145772097"
variation 5379
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:148923051"
variation 5381
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:186290546"
variation 5382
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:190370936"
variation 5413
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:12315453"
variation 5457
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:376952306"
STS 5521..5623
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/standard_name="D11S3114"
/db_xref="UniSTS:152207"
variation 5523
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace=""
/replace="t"
/db_xref="dbSNP:369436228"
variation 5594
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:143674494"
variation 5598
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="g"
/db_xref="dbSNP:182557126"
variation 5626
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:186682610"
variation 5634
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:148164406"
variation 5636
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="a"
/replace="g"
/db_xref="dbSNP:144049521"
variation 5637
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:146907125"
variation 5641
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
/replace="c"
/replace="t"
/db_xref="dbSNP:369225674"
polyA_signal 5765..5770
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
polyA_site 5790
/gene="PPFIBP1"
/gene_synonym="hSGT2; hSgt2p; L2; SGT2"
ORIGIN
gattcctgcagggagggaggagagaagggcggcagtgggagggggaggtacctggaactgggagtgatgtcagctcccagctcggtgcctgcccggattcctgacatggtgtagtgcaggcagggtggggaaaggacggggaaggactcgtgtgctgcgagctggcggccgggccggagtgctggggctttgaactccgagaggaggtggaccagaacttttggaactagtgccggcggctctccaccccccagtataaaagaacgtgtggatcactttgctgagtacatccaagatttgaagaactgaaataaatcagctttaaacctgctttttaaaaatacaaatggacacctaccagggaacggagatgtgtatcaagaaaggctggcacgtttagaaaatgataaagaatccctcgttcttcaggtaagtgtgttaacagaccaggtggaggctcagggagagaagattcgagatttggagttttgtcttgaagagcacagagagaagttgaatgccacagaagaaatgctgcagcaggagcttctaagtaggacatccttagaaactcagaagttggatctgatggctgaaatatctaacttgaagttgaaactgacagctgtagagaaggacagattggattatgaagataagttcagagacacagaggggctgattcaggagatcaatgatttgaggttaaaagttagtgaaatggacagtgagagacttcagtatgaaaaaaagcttaaatcaaccaaatctttaatggccaaactttctagcatgaaaatcaaggtgggtcagatgcagtatgaaaagcagcggatggaacaaaaatgggagtcactgaaggatgaactggcatctttaaaagaacaactagaagaaaaggaatctgaagtaaaaaggctacaagaaaaattggtttgcaagatgaaaggagaaggggttgaaattgttgatagagacatcgaagtacaaaaaatgaaaaaagctgtggagtccttgatggcagcaaatgaagaaaaggatcggaaaatagaagatcttcgacagtgcctgaacaggtacaagaaaatgcaagacacggtggtactggcccaaggcaaagatggagaatatgaagagctgctcaattccagttccatctcctctttgctggatgcacagggtttcagtgatctggagaaaagtccatcacccactccagtaatgggatctcccagttgtgacccatttaacacaagtgttcccgaagagttccatactaccatcttgcaagtttccatcccttcattattgccagcaactgtaagcatggaaacttctgaaaaatcaaagttgactcctaagccagagacttcatttgaagaaaatgatggaaacataatccttggtgccactgttgatacccaactgtgtgataaacttttaacttcaagtctgcagaagtccagcagcctgggcaatctgaagaaagagacatctgatggggaaaaggaaactattcagaagacttcagaggacagagctccggcagaaagcaggccatttgggacccttcctcccaggcccccagggcaggacacctccatggatgacaaccccttcggcactcgaaaagtcagatcttcctttggccggggcttttttaaaatcaaaagtaacaagagaacagcaagtgcaccaaacttagctgaaacagaaaaagagacagcagagcacctagatctggctggtgcttcttctcggccaaaagattcacagaggaacagtcccttccagataccgcctccatctccagattccaaaaagaaatccagaggtatcatgaaactctttggaaaacttaggagaagtcaatcaactacattcaacccagatgacatgtctgagcctgaattcaaaagaggagggacaagggcaaccgcggggccccgattaggttggtctcgagacttgggacagtctaacagtgacttggatatgccatttgccaagtggaccaaggagcaggtttgcaattggctgatggaacagggcttgggctcgtacctgaattctggcaagcactggattgcatctggccaaacgcttttgcaggcttctcaacaagatctagagaaggaacttggaatcaagcattcacttcatcgaaagaaactccagctagcactccaagccctgggatctgaagaagaaaccaatcatgggaagctggatttcaactgggtcactagatggttggatgacattggcctccctcaatataagacccagtttgatgaaggacgggttgatggtcgaatgctacattacatgactgttgatgacttactgtctctgaaggttgtaagtgtgctacaccatctcagtatcaaaagggccatccaggtcctgaggatcaataactttgaaccaaactgtctacggaggcggccatctgatgagaataccatcgccccatcagaagttcagaagtggactaaccatcgagtgatggagtggctgcgctccgtggacttggcagaatatgcgcccaatctcagaggcagtggtgtccatggtgggctcatggttctagagcctcgttttaacgtagaaacaatggctcagttattgaacatcccacccaataagactttgctgcgaagacatttggccactcatttcaaccttctgattggggctgaggcacagcaccagaagcgagatgccatggagctgccggattatgtacttctaacagctactgccaaagtgaagccaaagaaacttgcctttagcaattttgggaatttgagaaagaagaaacaggaagatggtgaagaatatgtttgtccaatggaattgggacaggcatcaggaagtgcatctaagaaaggatttaaacctggtttggatatgcgcctgtatgaggaagatgatttggaccggttagagcagatggaagattcagaagggacagtgagacagataggtgcattctctgaaggcatcaacaatctgacgcacatgttaaaagaagatgacatgtttaaagattttgctgcccgttcccccagtgccagcattacagatgaagactcaaacgtttgaccgtagcacctggatgaacattaggagtgcttagtcttttttctacttgcttttccaaacactcacagtatatacaacaggcagcggattgtctattgtttgttgttccaacttctgctgtcgagaagtttaaacagaaagcaggagtaatgtgccgattctgaagttgccacaaaaaataagacactggtgaatgagagtataattgtttttcttctatttaatgtaaaaatctgtgatatattatatttaaagtgttgcatttaagatgagtattttaccagagtgtttccattcatatccgcggtatggaggatttgaggaacagtaaccaggatgtgaatgattttgttacatcagtgttcactgtagccacctaagtaggacattatatgatttcagaatcaatatgtggaacttctttaagcattcagtgtgcccactaaatgccagccacacctccacttgcctcttattgtcttatttttatatatttttctaaatatatgtatatatacagtacatagaaaatagaacttttattttgtgacctaaggacgatggtgaaaagatcacgttttcaaaacaatctggtgatcagaatgttcatataccagctggtttctgaagaggtcagaatgatctttctccatactgacttttaacaatgttgatcattgaggctaaattaatatatatgaaatattcctttttgatgacaccacaaaattgttgaacagtttaagaatttcaaccttaatcttggatccctttacctcatatggaagaacttgagggacattagtatacttttttttaagatggagtcttgctctgtcacccaggttggagtgccatggcatgatcttggctcactgcaacctccacctcctgggtcaagccattctgcttcagccccaagtaggtgggactccaggcatgcaccaccatgcctggctaatttttgcatttttagtagagacagggtttcaccatattggccaggctgggactcgaactcctgaccttgtgatctgcccgcctcagcctcccaaagtactgggattataggcatgagccaccacgcccagcctgttatttttttattattattgtttttttttagtgacagagtctcattctgttgcccatgctggagtgcagtggcgtgatcatagctcactgcagccttgaattcctaggctccagtgatcctctcacctcagcttccctaatagctaggattacaggtgtgtggcctcccaccccaccccacccttcacacctggctgatttttcaaaaagtttttttgtagaaacagggtctcaccatgttgtccagcctggtctcaaactcctgtcctcaagtgatcctcccacctcagcctttcaaagtgctggaattacaggtgtgagccactctgcctggcctaccactaacttgaatacattcagaatcacctcctctccccaaaatttgtagaaatagtttttgaggaagccaaaagcaaagcagaaacctttacagtattgtttcttttctctttgttaactgtgtcattacagcaaaatactagcagtctgcctaaacatgttcattgtacatttctcaggctatcaatgaatggaggtttttaaaaagttgaatatttgtctgaacattttatttcaaagttcaaaaaaacagaggctgcaaaattcattttataatggctattttgtgacgataagatgtagttcatgtttttctgtagcactgggcccaaatattctttgtaaagaaaatcgctgcagcaaaaactgttactgtgtttattatatttgtagaagtattagaaaaatattctattttttattcagtgctgcgtaattacccatggtagccaaccctacaaaagacaggttttcacaaattgaggtggaggtgggcggttcagtatctgccactggacttgattataaactgtatttgaatatcagtggtattatcttttaagttgtcagcaagttaccaaggtattcattaaagaacttgtaatatcaaattactatttattcataacaattgatttgatgctaataataattttctttaaactctaccattcattatgtggtaactgtattgaacttactttatttggattttattttaatgtgactagatgtcaccacttcaaaaaatcaatttgttcttagaacctggttgaaaataccaggaaactgttacagacgccattttttttttttttgagacggagtcttgctctgttgcccaggctggagtgcagtggcacaatctcagctcactgcaagctccgcctcctgggttcacgccattctcccacctcagcttcccaagcagctgggactacaggtacctgccaccacgcctggctaattttgtttttgtatttttagtagagacggggtttcaccgtgttagccaggaaggtctcaatctcctgacctcgtgaatcgcccccctcggtctcccaaagtgctgggattacaggcgtgagccaccatgcccggcccaaatattttttattcaggatggtataacctaactgataataggtaataaggttaaatttttttatgacgtattttatttacaaatatcatacactgctggtgttaccatatgaaaggaaataaagtcaattgataattgcctcaaaaaaaaaaaaaaaaaa
//
ANNOTATIONS from NCBI Entrez Gene (20130726):
GeneID:8496 -> Biological process: GO:0007155 [cell adhesion] evidence: TAS
GeneID:8496 -> Cellular component: GO:0005886 [plasma membrane] evidence: NAS
by
@meso_cacase at
DBCLS
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