Details for: SEC23B

Gene ID: 10483

Symbol: SEC23B

Ensembl ID: ENSG00000101310

Description: SEC23 homolog B, COPII coat complex component

Associated with

Other Information

Genular Protein ID: 56003521

Symbol: SC23B_HUMAN

Name: SEC23-related protein B

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 8898360

Title: Cloning and functional characterization of mammalian homologues of the COPII component Sec23.

PubMed ID: 8898360

DOI: 10.1091/mbc.7.10.1535

PubMed ID: 11780052

Title: The DNA sequence and comparative analysis of human chromosome 20.

PubMed ID: 11780052

DOI: 10.1038/414865a

PubMed ID: 15489334

Title: The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).

PubMed ID: 15489334

DOI: 10.1101/gr.2596504

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 22223895

Title: Comparative large-scale characterisation of plant vs. mammal proteins reveals similar and idiosyncratic N-alpha acetylation features.

PubMed ID: 22223895

DOI: 10.1074/mcp.m111.015131

PubMed ID: 22814378

Title: N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.

PubMed ID: 22814378

DOI: 10.1073/pnas.1210303109

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

PubMed ID: 19621418

Title: Congenital dyserythropoietic anemia type II (CDAII) is caused by mutations in the SEC23B gene.

PubMed ID: 19621418

DOI: 10.1002/humu.21077

PubMed ID: 19561605

Title: Mutations affecting the secretory COPII coat component SEC23B cause congenital dyserythropoietic anemia type II.

PubMed ID: 19561605

DOI: 10.1038/ng.405

PubMed ID: 26522472

Title: Germline heterozygous variants in SEC23B are associated with Cowden syndrome and enriched in apparently sporadic thyroid cancer.

PubMed ID: 26522472

DOI: 10.1016/j.ajhg.2015.10.001

PubMed ID: 33159567

Title: Congenital dyserythropoietic anemia types Ib, II, and III: novel variants in the CDIN1 gene and functional study of a novel variant in the KIF23 gene.

PubMed ID: 33159567

DOI: 10.1007/s00277-020-04319-5

Sequence Information:

  • Length: 767
  • Mass: 86479
  • Checksum: 1A00DE39D56B0204
  • Sequence:
  • MATYLEFIQQ NEERDGVRFS WNVWPSSRLE ATRMVVPLAC LLTPLKERPD LPPVQYEPVL 
    CSRPTCKAVL NPLCQVDYRA KLWACNFCFQ RNQFPPAYGG ISEVNQPAEL MPQFSTIEYV 
    IQRGAQSPLI FLYVVDTCLE EDDLQALKES LQMSLSLLPP DALVGLITFG RMVQVHELSC 
    EGISKSYVFR GTKDLTAKQI QDMLGLTKPA MPMQQARPAQ PQEHPFASSR FLQPVHKIDM 
    NLTDLLGELQ RDPWPVTQGK RPLRSTGVAL SIAVGLLEGT FPNTGARIML FTGGPPTQGP 
    GMVVGDELKI PIRSWHDIEK DNARFMKKAT KHYEMLANRT AANGHCIDIY ACALDQTGLL 
    EMKCCANLTG GYMVMGDSFN TSLFKQTFQR IFTKDFNGDF RMAFGATLDV KTSRELKIAG 
    AIGPCVSLNV KGPCVSENEL GVGGTSQWKI CGLDPTSTLG IYFEVVNQHN TPIPQGGRGA 
    IQFVTHYQHS STQRRIRVTT IARNWADVQS QLRHIEAAFD QEAAAVLMAR LGVFRAESEE 
    GPDVLRWLDR QLIRLCQKFG QYNKEDPTSF RLSDSFSLYP QFMFHLRRSP FLQVFNNSPD 
    ESSYYRHHFA RQDLTQSLIM IQPILYSYSF HGPPEPVLLD SSSILADRIL LMDTFFQIVI 
    YLGETIAQWR KAGYQDMPEY ENFKHLLQAP LDDAQEILQA RFPMPRYINT EHGGSQARFL 
    LSKVNPSQTH NNLYAWGQET GAPILTDDVS LQVFMDHLKK LAVSSAC

Genular Protein ID: 1259082467

Symbol: A0A2R8YFH5_HUMAN

Name: N/A

UniProtKB Accession Codes:

Database IDs:

Citations:

PubMed ID: 11780052

Title: The DNA sequence and comparative analysis of human chromosome 20.

PubMed ID: 11780052

DOI: 10.1038/414865a

PubMed ID: 21269460

Title: Initial characterization of the human central proteome.

PubMed ID: 21269460

DOI: 10.1186/1752-0509-5-17

PubMed ID: 22223895

Title: Comparative large-scale characterisation of plant vs. mammal proteins reveals similar and idiosyncratic N-alpha acetylation features.

PubMed ID: 22223895

DOI: 10.1074/mcp.M111.015131

PubMed ID: 22814378

Title: N-terminal acetylome analyses and functional insights of the N-terminal acetyltransferase NatB.

PubMed ID: 22814378

DOI: 10.1073/pnas.1210303109

PubMed ID: 24275569

Title: An enzyme assisted RP-RPLC approach for in-depth analysis of human liver phosphoproteome.

PubMed ID: 24275569

DOI: 10.1016/j.jprot.2013.11.014

Sequence Information:

  • Length: 749
  • Mass: 84473
  • Checksum: 37A5BC41253EA4F6
  • Sequence:
  • MATYLEFIQQ NEERDGVRFS WNVWPSSRLE ATRMVVPLAC LLTPLKERPD LPPVQYEPVL 
    CSRPTCKAVL NPLCQVDYRA KLWACNFCFQ RNQFPPAYGG ISEVNQPAEL MPQFSTIEYV 
    IQEDDLQALK ESLQMSLSLL PPDALVGLIT FGRMVQVHEL SCEGISKSYV FRGTKDLTAK 
    QIQDMLGLTK PAMPMQQARP AQPQEHPFAS SRFLQPVHKI DMNLTDLLGE LQRDPWPVTQ 
    GKRPLRSTGV ALSIAVGLLE GTFPNTGARI MLFTGGPPTQ GPGMVVGDEL KIPIRSWHDI 
    EKDNARFMKK ATKHYEMLAN RTAANGHCID IYACALDQTG LLEMKCCANL TGGYMVMGDS 
    FNTSLFKQTF QRIFTKDFNG DFRMAFGATL DVKTSRELKI AGAIGPCVSL NVKGPCVSEN 
    ELGVGGTSQW KICGLDPTST LGIYFEVVNQ HNTPIPQGGR GAIQFVTHYQ HSSTQRRIRV 
    TTIARNWADV QSQLRHIEAA FDQEAAAVLM ARLGVFRAES EEGPDVLRWL DRQLIRLCQK 
    FGQYNKEDPT SFRLSDSFSL YPQFMFHLRR SPFLQVFNNS PDESSYYRHH FARQDLTQSL 
    IMIQPILYSY SFHGPPEPVL LDSSSILADR ILLMDTFFQI VIYLGETIAQ WRKAGYQDMP 
    EYENFKHLLQ APLDDAQEIL QARFPMPRYI NTEHGGSQAR FLLSKVNPSQ THNNLYAWGQ 
    ETGAPILTDD VSLQVFMDHL KKLAVSSAC

Database document:

This is a preview of the gene's schema. Only a few entries are kept for 'singleCellExpressions,' 'mRNAExpressions,' and other large data arrays for visualization purposes. You can zoom in with the mouse wheel for a closer view, and the text will adjust automatically if necessary. For the full schema, download it here.