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    CYFIP1 cytoplasmic FMR1 interacting protein 1 [ Homo sapiens (human) ]

    Gene ID: 23191, updated on 4-Jan-2025

    Summary

    Official Symbol
    CYFIP1provided by HGNC
    Official Full Name
    cytoplasmic FMR1 interacting protein 1provided by HGNC
    Primary source
    HGNC:HGNC:13759
    See related
    Ensembl:ENSG00000273749 MIM:606322; AllianceGenome:HGNC:13759
    Gene type
    protein coding
    RefSeq status
    REVIEWED
    Organism
    Homo sapiens
    Lineage
    Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
    Also known as
    SHYC; SRA1; SRA-1; P140SRA-1
    Summary
    This gene encodes a protein that regulates cytoskeletal dynamics and protein translation. The encoded protein is a component of the WAVE regulatory complex (WRC), which promotes actin polymerization. This protein also interacts with the synaptic functional regulator FMR1 protein and translation initiation factor 4E to inhibit protein translation. A large chromosomal deletion including this gene is associated with increased risk of schizophrenia and epilepsy in human patients. Reduced expression of this gene has been observed in various human cancers and the encoded protein may inhibit tumor invasion. [provided by RefSeq, Mar 2022]
    Expression
    Ubiquitous expression in placenta (RPKM 24.8), esophagus (RPKM 20.9) and 25 other tissues See more
    Orthologs
    NEW
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    Genomic context

    See CYFIP1 in Genome Data Viewer
    Location:
    15q11.2
    Exon count:
    34
    Annotation release Status Assembly Chr Location
    RS_2024_08 current GRCh38.p14 (GCF_000001405.40) 15 NC_000015.10 (22867052..22980898, complement)
    RS_2024_08 current T2T-CHM13v2.0 (GCF_009914755.1) 15 NC_060939.1 (20538904..20652761, complement)
    RS_2024_09 previous assembly GRCh37.p13 (GCF_000001405.25) 15 NC_000015.9 (22892170..23006016)

    Chromosome 15 - NC_000015.10Genomic Context describing neighboring genes Neighboring gene uncharacterized LOC283683 Neighboring gene Sharpr-MPRA regulatory region 3977 Neighboring gene golgin subfamily A member 6-like protein 7 Neighboring gene ReSE screen-validated silencer GRCh37_chr15:23086519-23086752 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6259 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6260 Neighboring gene ATAC-STARR-seq lymphoblastoid silent region 6261 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9154 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:23080143-23080643 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9155 Neighboring gene NIPA magnesium transporter 1 Neighboring gene OCT4-NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:23045427-23046179 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9156 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9157 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9158 Neighboring gene NIPA magnesium transporter 2 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:22999149-22999824 Neighboring gene CDK7 strongly-dependent group 2 enhancer GRCh37_chr15:22990202-22991401 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:22981163-22981662 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:22980661-22981162 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9159 Neighboring gene ATAC-STARR-seq lymphoblastoid active region 9160 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:22925256-22925940 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:22905531-22906030 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:22896003-22896502 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:22895501-22896002 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:22893404-22894371 Neighboring gene H3K27ac-H3K4me1 hESC enhancer GRCh37_chr15:22892435-22893403 Neighboring gene tubulin gamma complex component 5 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:22859095-22860005 Neighboring gene NANOG hESC enhancer GRCh37_chr15:22803142-22803643 Neighboring gene H3K4me1 hESC enhancer GRCh37_chr15:22798435-22798945 Neighboring gene engulfment and cell motility 2 pseudogene 1

    Genomic regions, transcripts, and products

    Expression

    • Project title: Tissue-specific circular RNA induction during human fetal development
    • Description: 35 human fetal samples from 6 tissues (3 - 7 replicates per tissue) collected between 10 and 20 weeks gestational time were sequenced using Illumina TruSeq Stranded Total RNA
    • BioProject: PRJNA270632
    • Publication: PMID 26076956
    • Analysis date: Mon Apr 2 22:54:59 2018

    Bibliography

    GeneRIFs: Gene References Into Functions

    What's a GeneRIF?

    Pathways from PubChem

    Interactions

    Products Interactant Other Gene Complex Source Pubs Description

    General gene information

    Clone Names

    • FLJ45151

    Gene Ontology Provided by GOA

    Function Evidence Code Pubs
    enables RNA 7-methylguanosine cap binding  
    enables actin filament binding  
    enables protein binding PubMed 
    contributes_to small GTPase binding PubMed 
    enables small GTPase binding  
    enables translation repressor activity  
    Items 1 - 25 of 26
    Process Evidence Code Pubs
    involved_in Rac protein signal transduction PubMed 
    involved_in axon extension PubMed 
    involved_in axon guidance  
    involved_in cell morphogenesis  
    involved_in cellular response to insulin stimulus  
    involved_in cognition PubMed 
    involved_in dendrite extension  
    involved_in lamellipodium assembly  
    involved_in lamellipodium assembly  
    involved_in modification of synaptic structure  
    involved_in negative regulation of synaptic vesicle recycling  
    involved_in negative regulation of translation  
    involved_in positive regulation of Arp2/3 complex-mediated actin nucleation PubMed 
    involved_in positive regulation of axon extension  
    involved_in positive regulation of dendrite development  
    involved_in positive regulation of lamellipodium assembly PubMed 
    involved_in positive regulation of neurotrophin TRK receptor signaling pathway  
    involved_in positive regulation of ruffle assembly  
    involved_in regulation of actin filament polymerization  
    involved_in regulation of cell shape  
    involved_in regulation of modification of postsynaptic actin cytoskeleton  
    involved_in regulation of myelination  
    involved_in regulation of translation  
    involved_in regulation of translation at postsynapse, modulating synaptic transmission  
    involved_in response to electrical stimulus  
    involved_in ruffle organization  
    Items 1 - 25 of 26
    Items 1 - 20 of 25
    Component Evidence Code Pubs
    part_of SCAR complex  
    part_of SCAR complex PubMed 
    part_of SCAR complex PubMed 
    located_in axonal growth cone  
    located_in central region of growth cone  
    located_in cytosol  
    located_in dendritic growth cone  
    located_in dendritic spine  
    located_in excitatory synapse  
    located_in extracellular exosome PubMed 
    located_in extracellular region  
    located_in filopodium tip  
    located_in focal adhesion PubMed 
    located_in lamellipodium  
    is_active_in neuron projection  
    located_in neuron projection  
    located_in neuronal cell body  
    located_in perinuclear region of cytoplasm  
    located_in peripheral region of growth cone  
    located_in ruffle  
    located_in secretory granule lumen  
    located_in specific granule lumen  
    is_active_in synapse  
    located_in terminal bouton  
    located_in tertiary granule lumen  
    Items 1 - 20 of 25

    General protein information

    Preferred Names
    cytoplasmic FMR1-interacting protein 1
    Names
    cytoplasmic FMRP interacting protein 1
    selective hybridizing clone
    specifically Rac1-associated protein 1

    NCBI Reference Sequences (RefSeq)

    NEW Try the new Transcript table

    RefSeqs maintained independently of Annotated Genomes

    These reference sequences exist independently of genome builds. Explain

    These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

    Genomic

    1. NG_054889.1 RefSeqGene

      Range
      5539..118855
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    mRNA and Protein(s)

    1. NM_001033028.3NP_001028200.1  cytoplasmic FMR1-interacting protein 1 isoform b

      Status: REVIEWED

      Source sequence(s)
      AC011767, AK024816, AY763579, BC005097, CB250660
      Consensus CDS
      CCDS73695.1
      UniProtKB/Swiss-Prot
      Q7L576
      Related
      ENSP00000480525.1, ENST00000617556.4
      Conserved Domains (1) summary
      pfam05994
      Location:115791
      FragX_IP; Cytoplasmic Fragile-X interacting family
    2. NM_001287810.4NP_001274739.1  cytoplasmic FMR1-interacting protein 1 isoform a

      See identical proteins and their annotated locations for NP_001274739.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (2), as well as variants 1, 3, and 4, encodes isoform a.
      Source sequence(s)
      AC011767, AC090764, CB250660
      Consensus CDS
      CCDS73696.1
      UniProtKB/Swiss-Prot
      A8K6D9, Q14467, Q5IED0, Q6ZSX1, Q7L576, Q9BSD9, Q9BVC7
      UniProtKB/TrEMBL
      X5D2F4
      Related
      ENSP00000478779.1, ENST00000610365.4
      Conserved Domains (1) summary
      pfam05994
      Location:3891222
      FragX_IP; Cytoplasmic Fragile-X interacting family
    3. NM_001324119.2NP_001311048.1  cytoplasmic FMR1-interacting protein 1 isoform c

      Status: REVIEWED

      Description
      Transcript Variant: This variant (5) encodes the longest isoform (c).
      Source sequence(s)
      AC011767, AC090764, CB250660
      UniProtKB/TrEMBL
      X5D2F4
    4. NM_001324120.2NP_001311049.1  cytoplasmic FMR1-interacting protein 1 isoform a

      Status: REVIEWED

      Description
      Transcript Variant: This variant (3), as well as variants 1, 2, and 4, encodes isoform a.
      Source sequence(s)
      AC011767, AC090764, CB250660
      Consensus CDS
      CCDS73696.1
      UniProtKB/Swiss-Prot
      A8K6D9, Q14467, Q5IED0, Q6ZSX1, Q7L576, Q9BSD9, Q9BVC7
      UniProtKB/TrEMBL
      X5D2F4
      Conserved Domains (1) summary
      pfam05994
      Location:3891222
      FragX_IP; Cytoplasmic Fragile-X interacting family
    5. NM_001324122.3NP_001311051.1  cytoplasmic FMR1-interacting protein 1 isoform d

      Status: REVIEWED

      Source sequence(s)
      AC011767, AC090764, CB250660
    6. NM_001324123.3NP_001311052.1  cytoplasmic FMR1-interacting protein 1 isoform a

      Status: REVIEWED

      Description
      Transcript Variant: This variant (4), as well as variants 1-3, encodes isoform a.
      Source sequence(s)
      AC011767, AC090764, CB250660
      Consensus CDS
      CCDS73696.1
      UniProtKB/Swiss-Prot
      A8K6D9, Q14467, Q5IED0, Q6ZSX1, Q7L576, Q9BSD9, Q9BVC7
      UniProtKB/TrEMBL
      X5D2F4
      Conserved Domains (1) summary
      pfam05994
      Location:3891222
      FragX_IP; Cytoplasmic Fragile-X interacting family
    7. NM_001324124.3NP_001311053.1  cytoplasmic FMR1-interacting protein 1 isoform e

      Status: REVIEWED

      Source sequence(s)
      AC011767, AC090764, CB250660
      UniProtKB/TrEMBL
      X5D2F4
    8. NM_001324125.3NP_001311054.1  cytoplasmic FMR1-interacting protein 1 isoform f

      Status: REVIEWED

      Source sequence(s)
      AC011767, AC090764, CB250660
      UniProtKB/TrEMBL
      X5D2F4
    9. NM_001324126.3NP_001311055.1  cytoplasmic FMR1-interacting protein 1 isoform g

      Status: REVIEWED

      Source sequence(s)
      AC011767, AC090764, CB250660
      UniProtKB/TrEMBL
      X5D2F4
    10. NM_014608.6NP_055423.1  cytoplasmic FMR1-interacting protein 1 isoform a

      See identical proteins and their annotated locations for NP_055423.1

      Status: REVIEWED

      Description
      Transcript Variant: This variant (1), as well as variants 2-4, encodes isoform a.
      Source sequence(s)
      AC011767, AC090764, CB250660
      Consensus CDS
      CCDS73696.1
      UniProtKB/Swiss-Prot
      A8K6D9, Q14467, Q5IED0, Q6ZSX1, Q7L576, Q9BSD9, Q9BVC7
      UniProtKB/TrEMBL
      X5D2F4
      Related
      ENSP00000481038.1, ENST00000617928.5
      Conserved Domains (1) summary
      pfam05994
      Location:3891222
      FragX_IP; Cytoplasmic Fragile-X interacting family

    RefSeqs of Annotated Genomes: GCF_000001405.40-RS_2024_08

    The following sections contain reference sequences that belong to a specific genome build. Explain

    Reference GRCh38.p14 Primary Assembly

    Genomic

    1. NC_000015.10 Reference GRCh38.p14 Primary Assembly

      Range
      22867052..22980898 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 PATCHES

    Genomic

    1. NW_021160017.1 Reference GRCh38.p14 PATCHES

      Range
      3761127..3874986 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Reference GRCh38.p14 ALT_REF_LOCI_1

    Genomic

    1. NT_187603.1 Reference GRCh38.p14 ALT_REF_LOCI_1

      Range
      744..77893 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)

    Alternate T2T-CHM13v2.0

    Genomic

    1. NC_060939.1 Alternate T2T-CHM13v2.0

      Range
      20538904..20652761 complement
      Download
      GenBank, FASTA, Sequence Viewer (Graphics)
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