Details for: FERMT1
Associated with
Other Information
Genular Protein ID: 1749420737
Symbol: FERM1_HUMAN
Name: Fermitin family homolog 1
UniProtKB Accession Codes:
Database IDs:
Citations:
PubMed ID: 12697302
Title: URP1: a member of a novel family of PH and FERM domain-containing membrane-associated proteins is significantly over-expressed in lung and colon carcinomas.
PubMed ID: 12697302
PubMed ID: 12789646
Title: Loss of kindlin-1, a human homolog of the Caenorhabditis elegans actin-extracellular-matrix linker protein UNC-112, causes Kindler syndrome.
PubMed ID: 12789646
DOI: 10.1086/376609
PubMed ID: 14702039
Title: Complete sequencing and characterization of 21,243 full-length human cDNAs.
PubMed ID: 14702039
DOI: 10.1038/ng1285
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: 12668616
Title: Identification of mutations in a new gene encoding a FERM family protein with a pleckstrin homology domain in Kindler syndrome.
PubMed ID: 12668616
DOI: 10.1093/hmg/ddg097
PubMed ID: 14634021
Title: The Kindler syndrome protein is regulated by transforming growth factor-beta and involved in integrin-mediated adhesion.
PubMed ID: 14634021
PubMed ID: 17012746
Title: Kindlin-1 is a phosphoprotein involved in regulation of polarity, proliferation, and motility of epidermal keratinocytes.
PubMed ID: 17012746
PubMed ID: 18669648
Title: A quantitative atlas of mitotic phosphorylation.
PubMed ID: 18669648
PubMed ID: 19804783
Title: The structure of the N-terminus of kindlin-1: a domain important for alphaIIbbeta3 integrin activation.
PubMed ID: 19804783
PubMed ID: 20068231
Title: Quantitative phosphoproteomics reveals widespread full phosphorylation site occupancy during mitosis.
PubMed ID: 20068231
PubMed ID: 21269460
Title: Initial characterization of the human central proteome.
PubMed ID: 21269460
PubMed ID: 23186163
Title: Toward a comprehensive characterization of a human cancer cell phosphoproteome.
PubMed ID: 23186163
DOI: 10.1021/pr300630k
PubMed ID: 21936020
Title: Kindler syndrome: extension of FERMT1 mutational spectrum and natural history.
PubMed ID: 21936020
DOI: 10.1002/humu.21576
Sequence Information:
- Length: 677
- Mass: 77437
- Checksum: 7354DCD84C516F90
- Sequence:
MLSSTDFTFA SWELVVRVDH PNEEQQKDVT LRVSGDLHVG GVMLKLVEQI NISQDWSDFA LWWEQKHCWL LKTHWTLDKY GVQADAKLLF TPQHKMLRLR LPNLKMVRLR VSFSAVVFKA VSDICKILNI RRSEELSLLK PSGDYFKKKK KKDKNNKEPI IEDILNLESS PTASGSSVSP GLYSKTMTPI YDPINGTPAS STMTWFSDSP LTEQNCSILA FSQPPQSPEA LADMYQPRSL VDKAKLNAGW LDSSRSLMEQ GIQEDEQLLL RFKYYSFFDL NPKYDAVRIN QLYEQARWAI LLEEIDCTEE EMLIFAALQY HISKLSLSAE TQDFAGESEV DEIEAALSNL EVTLEGGKAD SLLEDITDIP KLADNLKLFR PKKLLPKAFK QYWFIFKDTS IAYFKNKELE QGEPLEKLNL RGCEVVPDVN VAGRKFGIKL LIPVADGMNE MYLRCDHENQ YAQWMAACML ASKGKTMADS SYQPEVLNIL SFLRMKNRNS ASQVASSLEN MDMNPECFVS PRCAKRHKSK QLAARILEAH QNVAQMPLVE AKLRFIQAWQ SLPEFGLTYY LVRFKGSKKD DILGVSYNRL IKIDAATGIP VTTWRFTNIK QWNVNWETRQ VVIEFDQNVF TAFTCLSADC KIVHEYIGGY IFLSTRSKDQ NETLDEDLFH KLTGGQD
Genular Protein ID: 374679554
Symbol: Q54A15_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Sequence Information:
- Length: 677
- Mass: 77409
- Checksum: 40A17D514C49FE13
- Sequence:
MLSSTDFTFA SWELVVRVDH PNEEQQKDVT LRVSGDLHVG GVMLKLVEQI NISQDWSDFA LWWEQKHCWL LKTHWTLDKY GVQADAKLLF TPQHKMLRLR LPNLKMVRLR VSFSAVVFKA VSDICKILNI RRSEELSLLK PSGDYFKKKK KKDKNNKEPI IEDILNLESS PTASGSSVSP GLYSKTMTPI YDPINGTPAS STMTWFSDSP LTEQNCSILA FSQPPQSPEA LADMYQPRSL VDKAKLNAGW LDSSRSLMEQ GIQEDEQLLL RFKYYSFFDL NPKYDAVRIN QLYEQARWAI LLEEIDCTEE EMLIFAALQY HISKLSLSAE TQDFAGESEV DEIEAALSNL EVTLEGGKAD SLLEDITDIP KLADNLKLFR PKKLLPKAFK QYWFIFKDTS IAYFKNKELE QGEPLEKLNL RGCEVVPDVN VAGRKFGIKL LIPVADGMNE MYLRCDHENQ YAQWMAACML ASKGKTMADS SYQPEVLNIL SFLRMKNRNS ASQVASSLEN MDMNPECFVS PRCAKKHKSK QLAARILEAH QNVAQMPLVE AKLRFIQAWQ SLPEFGLTYY LVRFKGSKKD DILGVSYNRL IKIDAATGIP VTTWRFTNIK QWNVNWETRQ VVIEFDQNVF TAFTCLSADC KIVHEYIGGY IFLSTRSKDQ NETLDEDLFH KLTGGQD
Genular Protein ID: 3737641797
Symbol: Q49AC8_HUMAN
Name: N/A
UniProtKB Accession Codes:
Database IDs:
Citations:
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
Sequence Information:
- Length: 420
- Mass: 48267
- Checksum: 378D0F836A3BA1AA
- Sequence:
MEQGIKEDEQ LLLRFKYYSF FDLNPKYDAV QINQLYEQAR WAILLEEIDC TEEEMLIFAA LQYHISKLSL SAETQDFAGE SEVDEIEAAL SNLEVTLEGG KADSLLEDIT DIPKLADNLK LFRPKKLLPK AFKQYWFIFK DTSIAYFKNK ELEQGEPLEK LNLRGCEVVP DVNVAGRKFG IKLLIPVADG MNEMYLRCDH ENQYAQWMAA CMLASKGKTM ADSSYQPEVL NILSFLRMKN RNSASQVASS LENMDMNPEC FVSPRCAKRH KSKQLAARIL EAHQNVAQMP LVEAKLRFIQ AWQSLPEFGL TYYLVRFKGS KKDDILGVSY NRLIKIDAAT GIPVTTWRFT NIKQWNVNWE TRQVVIEFDQ NVFTAFTCLS ADCKIVHEYI GGYIFLSTRS KDQNETLDED LFHKLTGGQD
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.