ID FER3L_HUMAN Reviewed; 166 AA. AC Q96RJ6; Q495K0; DT 08-APR-2008, integrated into UniProtKB/Swiss-Prot. DT 01-DEC-2001, sequence version 1. DT 02-OCT-2024, entry version 163. DE RecName: Full=Fer3-like protein; DE AltName: Full=Basic helix-loop-helix protein N-twist; DE AltName: Full=Class A basic helix-loop-helix protein 31; DE Short=bHLHa31; DE AltName: Full=Nephew of atonal 3; DE AltName: Full=Neuronal twist; GN Name=FERD3L; Synonyms=BHLHA31, NATO3, NTWIST; OS Homo sapiens (Human). OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; OC Homo. OX NCBI_TaxID=9606; RN [1] RP NUCLEOTIDE SEQUENCE [GENOMIC DNA]. RX PubMed=11472856; DOI=10.1016/s0925-4773(01)00437-3; RA Segev E., Halachmi N., Salzberg A., Ben-Arie N.; RT "Nato3 is an evolutionarily conserved bHLH transcription factor expressed RT in the CNS of Drosophila and mouse."; RL Mech. Dev. 106:197-202(2001). RN [2] RP NUCLEOTIDE SEQUENCE [MRNA]. RX PubMed=12217327; DOI=10.1006/dbio.2002.0753; RA Verzi M.P., Anderson J.P., Dodou E., Kelly K.K., Greene S.B., North B.J., RA Cripps R.M., Black B.L.; RT "N-twist, an evolutionarily conserved bHLH protein expressed in the RT developing CNS, functions as a transcriptional inhibitor."; RL Dev. Biol. 249:174-190(2002). RN [3] RP NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. RX PubMed=12690205; DOI=10.1126/science.1083423; RA Scherer S.W., Cheung J., MacDonald J.R., Osborne L.R., Nakabayashi K., RA Herbrick J.-A., Carson A.R., Parker-Katiraee L., Skaug J., Khaja R., RA Zhang J., Hudek A.K., Li M., Haddad M., Duggan G.E., Fernandez B.A., RA Kanematsu E., Gentles S., Christopoulos C.C., Choufani S., Kwasnicka D., RA Zheng X.H., Lai Z., Nusskern D.R., Zhang Q., Gu Z., Lu F., Zeesman S., RA Nowaczyk M.J., Teshima I., Chitayat D., Shuman C., Weksberg R., RA Zackai E.H., Grebe T.A., Cox S.R., Kirkpatrick S.J., Rahman N., RA Friedman J.M., Heng H.H.Q., Pelicci P.G., Lo-Coco F., Belloni E., RA Shaffer L.G., Pober B., Morton C.C., Gusella J.F., Bruns G.A.P., Korf B.R., RA Quade B.J., Ligon A.H., Ferguson H., Higgins A.W., Leach N.T., RA Herrick S.R., Lemyre E., Farra C.G., Kim H.-G., Summers A.M., Gripp K.W., RA Roberts W., Szatmari P., Winsor E.J.T., Grzeschik K.-H., Teebi A., RA Minassian B.A., Kere J., Armengol L., Pujana M.A., Estivill X., RA Wilson M.D., Koop B.F., Tosi S., Moore G.E., Boright A.P., Zlotorynski E., RA Kerem B., Kroisel P.M., Petek E., Oscier D.G., Mould S.J., Doehner H., RA Doehner K., Rommens J.M., Vincent J.B., Venter J.C., Li P.W., Mural R.J., RA Adams M.D., Tsui L.-C.; RT "Human chromosome 7: DNA sequence and biology."; RL Science 300:767-772(2003). RN [4] RP NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA]. RA Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M., RA Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J., RA Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S., RA Turner R., Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H., RA Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K., RA Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D., RA Hunkapiller M.W., Myers E.W., Venter J.C.; RL Submitted (JUL-2005) to the EMBL/GenBank/DDBJ databases. RN [5] RP NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA]. RX PubMed=15489334; DOI=10.1101/gr.2596504; RG The MGC Project Team; RT "The status, quality, and expansion of the NIH full-length cDNA project: RT the Mammalian Gene Collection (MGC)."; RL Genome Res. 14:2121-2127(2004). RN [6] RP VARIANT [LARGE SCALE ANALYSIS] ARG-36. RX PubMed=16959974; DOI=10.1126/science.1133427; RA Sjoeblom T., Jones S., Wood L.D., Parsons D.W., Lin J., Barber T.D., RA Mandelker D., Leary R.J., Ptak J., Silliman N., Szabo S., Buckhaults P., RA Farrell C., Meeh P., Markowitz S.D., Willis J., Dawson D., Willson J.K.V., RA Gazdar A.F., Hartigan J., Wu L., Liu C., Parmigiani G., Park B.H., RA Bachman K.E., Papadopoulos N., Vogelstein B., Kinzler K.W., RA Velculescu V.E.; RT "The consensus coding sequences of human breast and colorectal cancers."; RL Science 314:268-274(2006). CC -!- FUNCTION: Transcription factor that binds to the E-box and functions as CC inhibitor of transcription. DNA binding requires dimerization with an E CC protein. Inhibits transcription activation by ASCL1/MASH1 by CC sequestering E proteins (By similarity). {ECO:0000250}. CC -!- SUBUNIT: Heterodimer with TCF3/E12. Interacts with the bHLH domain of CC TCF3/E12 (By similarity). {ECO:0000250}. CC -!- INTERACTION: CC Q96RJ6; Q8IZU0: FAM9B; NbExp=4; IntAct=EBI-10183007, EBI-10175124; CC Q96RJ6; O15481: MAGEB4; NbExp=3; IntAct=EBI-10183007, EBI-751857; CC Q96RJ6; O43765: SGTA; NbExp=3; IntAct=EBI-10183007, EBI-347996; CC Q96RJ6; P15884: TCF4; NbExp=5; IntAct=EBI-10183007, EBI-533224; CC -!- SUBCELLULAR LOCATION: Nucleus {ECO:0000255|PROSITE-ProRule:PRU00981}. CC --------------------------------------------------------------------------- CC Copyrighted by the UniProt Consortium, see https://www.uniprot.org/terms CC Distributed under the Creative Commons Attribution (CC BY 4.0) License CC --------------------------------------------------------------------------- DR EMBL; AF369897; AAK72956.1; -; Genomic_DNA. DR EMBL; AF517122; AAN04086.1; -; mRNA. DR EMBL; CH236948; EAL24278.1; -; Genomic_DNA. DR EMBL; CH471073; EAW93712.1; -; Genomic_DNA. DR EMBL; BC069147; AAH69147.1; -; mRNA. DR EMBL; BC101135; AAI01136.1; -; mRNA. DR EMBL; BC101136; AAI01137.1; -; mRNA. DR EMBL; BC101137; AAI01138.1; -; mRNA. DR EMBL; BC101138; AAI01139.1; -; mRNA. DR CCDS; CCDS5368.1; -. DR RefSeq; NP_690862.1; NM_152898.2. DR AlphaFoldDB; Q96RJ6; -. DR SMR; Q96RJ6; -. DR BioGRID; 128819; 16. DR IntAct; Q96RJ6; 11. DR STRING; 9606.ENSP00000275461; -. DR PhosphoSitePlus; Q96RJ6; -. DR BioMuta; FERD3L; -. DR DMDM; 74752106; -. DR MassIVE; Q96RJ6; -. DR PaxDb; 9606-ENSP00000275461; -. DR PeptideAtlas; Q96RJ6; -. DR Antibodypedia; 11904; 104 antibodies from 20 providers. DR DNASU; 222894; -. DR Ensembl; ENST00000275461.3; ENSP00000275461.3; ENSG00000146618.3. DR GeneID; 222894; -. DR KEGG; hsa:222894; -. DR MANE-Select; ENST00000275461.3; ENSP00000275461.3; NM_152898.2; NP_690862.1. DR UCSC; uc003suo.1; human. DR AGR; HGNC:16660; -. DR CTD; 222894; -. DR DisGeNET; 222894; -. DR GeneCards; FERD3L; -. DR HGNC; HGNC:16660; FERD3L. DR HPA; ENSG00000146618; Not detected. DR MIM; 617578; gene. DR neXtProt; NX_Q96RJ6; -. DR OpenTargets; ENSG00000146618; -. DR PharmGKB; PA134973730; -. DR VEuPathDB; HostDB:ENSG00000146618; -. DR eggNOG; KOG4029; Eukaryota. DR GeneTree; ENSGT00940000161409; -. DR HOGENOM; CLU_148882_0_0_1; -. DR InParanoid; Q96RJ6; -. DR OMA; LDGCSRQ; -. DR OrthoDB; 5315240at2759; -. DR PhylomeDB; Q96RJ6; -. DR PathwayCommons; Q96RJ6; -. DR SignaLink; Q96RJ6; -. DR BioGRID-ORCS; 222894; 10 hits in 1159 CRISPR screens. DR GenomeRNAi; 222894; -. DR Pharos; Q96RJ6; Tbio. DR PRO; PR:Q96RJ6; -. DR Proteomes; UP000005640; Chromosome 7. DR RNAct; Q96RJ6; protein. DR Bgee; ENSG00000146618; Expressed in sural nerve and 23 other cell types or tissues. DR GO; GO:0000785; C:chromatin; ISA:NTNU_SB. DR GO; GO:0005634; C:nucleus; ISS:UniProtKB. DR GO; GO:0000981; F:DNA-binding transcription factor activity, RNA polymerase II-specific; ISA:NTNU_SB. DR GO; GO:0001227; F:DNA-binding transcription repressor activity, RNA polymerase II-specific; IEA:Ensembl. DR GO; GO:0046983; F:protein dimerization activity; IEA:InterPro. DR GO; GO:0000977; F:RNA polymerase II transcription regulatory region sequence-specific DNA binding; IBA:GO_Central. DR GO; GO:1990837; F:sequence-specific double-stranded DNA binding; IDA:ARUK-UCL. DR GO; GO:0048468; P:cell development; IEA:Ensembl. DR GO; GO:0032502; P:developmental process; IBA:GO_Central. DR GO; GO:0033504; P:floor plate development; IEA:Ensembl. DR GO; GO:0045892; P:negative regulation of DNA-templated transcription; ISS:UniProtKB. DR GO; GO:1904338; P:regulation of dopaminergic neuron differentiation; IEA:Ensembl. DR GO; GO:0050767; P:regulation of neurogenesis; IEA:Ensembl. DR GO; GO:0006357; P:regulation of transcription by RNA polymerase II; IBA:GO_Central. DR CDD; cd11415; bHLH_TS_FERD3L_NATO3; 1. DR Gene3D; 4.10.280.10; Helix-loop-helix DNA-binding domain; 1. DR InterPro; IPR011598; bHLH_dom. DR InterPro; IPR050283; E-box_TF_Regulators. DR InterPro; IPR036638; HLH_DNA-bd_sf. DR PANTHER; PTHR23349; BASIC HELIX-LOOP-HELIX TRANSCRIPTION FACTOR, TWIST; 1. DR PANTHER; PTHR23349:SF63; FER3-LIKE PROTEIN; 1. DR Pfam; PF00010; HLH; 1. DR SMART; SM00353; HLH; 1. DR SUPFAM; SSF47459; HLH, helix-loop-helix DNA-binding domain; 1. DR PROSITE; PS50888; BHLH; 1. PE 1: Evidence at protein level; KW DNA-binding; Nucleus; Reference proteome; Repressor; Transcription; KW Transcription regulation. FT CHAIN 1..166 FT /note="Fer3-like protein" FT /id="PRO_0000328682" FT DOMAIN 101..153 FT /note="bHLH" FT /evidence="ECO:0000255|PROSITE-ProRule:PRU00981" FT REGION 57..88 FT /note="Disordered" FT /evidence="ECO:0000256|SAM:MobiDB-lite" FT COMPBIAS 61..80 FT /note="Acidic residues" FT /evidence="ECO:0000256|SAM:MobiDB-lite" FT VARIANT 36 FT /note="G -> R (in a colorectal cancer sample; somatic FT mutation; dbSNP:rs775679607)" FT /evidence="ECO:0000269|PubMed:16959974" FT /id="VAR_042439" FT CONFLICT 74 FT /note="G -> GE (in Ref. 5; AAI01136/AAI01137)" FT /evidence="ECO:0000305" SQ SEQUENCE 166 AA; 19017 MW; 206F6EDE1F54C79C CRC64; MAAYPESCVD TTVLDFVADL SLASPRRPLL CDFAPGVSLG DPALALREGR PRRMARFEEG DPEEEECEVD QGDGEEEEEE ERGRGVSLLG RPKRKRVITY AQRQAANIRE RKRMFNLNEA FDQLRRKVPT FAYEKRLSRI ETLRLAIVYI SFMTELLESC EKKESG //