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PHIP pleckstrin homology domain interacting protein [ Macaca mulatta (Rhesus monkey) ]

Gene ID: 716810, updated on 17-Aug-2024

Summary

Official Symbol
PHIPprovided by VGNC
Official Full Name
pleckstrin homology domain interacting proteinprovided by VGNC
Primary source
VGNC:VGNC:75803
See related
Ensembl:ENSMMUG00000017186
Gene type
protein coding
RefSeq status
MODEL
Organism
Macaca mulatta
Lineage
Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Cercopithecidae; Cercopithecinae; Macaca
Orthologs
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Genomic context

See PHIP in Genome Data Viewer
Location:
chromosome: 4
Exon count:
41
Annotation release Status Assembly Chr Location
103 current Mmul_10 (GCF_003339765.1) 4 NC_041757.1 (93985601..94123334)
102 previous assembly Mmul_8.0.1 (GCF_000772875.2) 4 NC_027896.1 (77148607..77292730, complement)

Chromosome 4 - NC_041757.1Genomic Context describing neighboring genes Neighboring gene ADP/ATP translocase 2-like Neighboring gene dnaJ homolog subfamily B member 6-like Neighboring gene high mobility group nucleosomal binding domain 3 Neighboring gene transfer RNA phenylalanine (anticodon GAA) Neighboring gene interleukin 1 receptor associated kinase 1 binding protein 1 Neighboring gene uncharacterized LOC106998005

Genomic regions, transcripts, and products

General gene information

Markers

Gene Ontology Provided by RefSeq

Function Evidence Code Pubs
enables protein binding IEA
Inferred from Electronic Annotation
more info
PubMed 
Process Evidence Code Pubs
involved_in cytoskeleton organization IEA
Inferred from Electronic Annotation
more info
PubMed 
involved_in regulation of cell shape IEA
Inferred from Electronic Annotation
more info
PubMed 
involved_in regulation of transcription by RNA polymerase II IEA
Inferred from Electronic Annotation
more info
PubMed 
Component Evidence Code Pubs
located_in nucleus IEA
Inferred from Electronic Annotation
more info
PubMed 

NCBI Reference Sequences (RefSeq)

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RefSeqs of Annotated Genomes: Macaca mulatta Annotation Release 103 details...Open this link in a new tab

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

Reference Mmul_10 Primary Assembly

Genomic

  1. NC_041757.1 Reference Mmul_10 Primary Assembly

    Range
    93985601..94123334
    Download
    GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

  1. XM_015136812.2XP_014992298.1  PH-interacting protein isoform X1

    UniProtKB/TrEMBL
    A0A1D5R3B0, F7HIM2, H9FWE9
    Related
    ENSMMUP00000054796.2, ENSMMUT00000071177.2
    Conserved Domains (4) summary
    cd05496
    Location:13161434
    Bromo_WDR9_II; Bromodomain; WDR9 repeat II_like subfamily. WDR9 is a human gene located in the Down Syndrome critical region-2 of chromosome 21. It encodes for a nuclear protein containing WD40 repeats and two bromodomains, which may function as a transcriptional ...
    cd05529
    Location:11481263
    Bromo_WDR9_I_like; Bromodomain; WDR9 repeat I_like subfamily. WDR9 is a human gene located in the Down Syndrome critical region-2 of chromosome 21. It encodes for a nuclear protein containing WD40 repeats and two bromodomains, which may function as a transcriptional ...
    cd00200
    Location:175495
    WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
    sd00039
    Location:186223
    7WD40; WD40 repeat [structural motif]
  2. XM_015136813.2XP_014992299.1  PH-interacting protein isoform X2

    UniProtKB/TrEMBL
    F7HIM2
    Conserved Domains (4) summary
    cd05496
    Location:13151433
    Bromo_WDR9_II; Bromodomain; WDR9 repeat II_like subfamily. WDR9 is a human gene located in the Down Syndrome critical region-2 of chromosome 21. It encodes for a nuclear protein containing WD40 repeats and two bromodomains, which may function as a transcriptional ...
    cd05529
    Location:11471262
    Bromo_WDR9_I_like; Bromodomain; WDR9 repeat I_like subfamily. WDR9 is a human gene located in the Down Syndrome critical region-2 of chromosome 21. It encodes for a nuclear protein containing WD40 repeats and two bromodomains, which may function as a transcriptional ...
    cd00200
    Location:175495
    WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
    sd00039
    Location:186223
    7WD40; WD40 repeat [structural motif]
  3. XM_015136814.2XP_014992300.1  PH-interacting protein isoform X3

    UniProtKB/TrEMBL
    F7HIM2
    Conserved Domains (5) summary
    cd05496
    Location:11441262
    Bromo_WDR9_II; Bromodomain; WDR9 repeat II_like subfamily. WDR9 is a human gene located in the Down Syndrome critical region-2 of chromosome 21. It encodes for a nuclear protein containing WD40 repeats and two bromodomains, which may function as a transcriptional ...
    cd05529
    Location:9761091
    Bromo_WDR9_I_like; Bromodomain; WDR9 repeat I_like subfamily. WDR9 is a human gene located in the Down Syndrome critical region-2 of chromosome 21. It encodes for a nuclear protein containing WD40 repeats and two bromodomains, which may function as a transcriptional ...
    COG2319
    Location:6366
    WD40; WD40 repeat [General function prediction only]
    cd00200
    Location:3323
    WD40; WD40 domain, found in a number of eukaryotic proteins that cover a wide variety of functions including adaptor/regulatory modules in signal transduction, pre-mRNA processing and cytoskeleton assembly; typically contains a GH dipeptide 11-24 residues from ...
    sd00039
    Location:1451
    7WD40; WD40 repeat [structural motif]