HOMER1 - homer scaffold protein 1 Gene

Also Known as HOMER; SYN47; Ves-1; HOMER1A; HOMER1B; HOMER1C

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 9456

About HOMER1

Cytogenetic location: 5q14.1 Genomic coordinates (GRCh38): 5:79,372,636-79,514,134 (from NCBI)

This gene has 5 transcripts (splice variants), 268 orthologues and 2 paralogues. Broad expression in brain (RPKM 8.6), thyroid (RPKM 5.8) and 14 other tissues.

Summary

This gene encodes a member of the homer family of dendritic proteins. Members of this family regulate group 1 metabotrophic glutamate receptor function. [provided by RefSeq, Jul 2008]

HOMER1 Products (3)

mRNA Protein Name
NM_001277077.1 NP_001264006.1 homer protein homolog 1 isoform 2
NM_001277078.1 NP_001264007.1 homer protein homolog 1 isoform 3
NM_004272.5 NP_004263.1 homer protein homolog 1 isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 GOA
enables transmembrane transporter binding IPI
IPI: Inferred from physical interaction
14505576 GOA
Biological Process GO Annotation Evidence References Source
involved in response to calcium ion IDA
IDA: Inferred from direct assay
14505576 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

HOMER1 Protein Structure

WH1

WH1: WH1 domain (4 - 106)

  • 0
  • 100
  • 200
  • 300
  • 354 a.a.
Protein Preferred Names Protein Names

homer protein homolog 1

  • homer homolog 1

HOMER1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
HOMER1 Q86YM7 ABI1 Homo sapiens Q8IZP0-5 32296183
Intra
HOMER1 Q86YM7 ABI1 Homo sapiens Q8IZP0-5 32296183
Intra
HOMER1 Q86YM7 ABI1 Homo sapiens Q8IZP0-5 32296183
Intra
HOMER1 Q86YM7 SYCE2 Homo sapiens Q6PIF2 32296183
Intra
HOMER1 Q86YM7 SYCE2 Homo sapiens Q6PIF2 32296183
Intra
HOMER1 Q86YM7 SHANK2 Homo sapiens Q9UPX8-4 32296183
Intra
HOMER1 Q86YM7 SHANK2 Homo sapiens Q9UPX8-4 32296183
Intra
HOMER1 Q86YM7 SHANK2 Homo sapiens Q9UPX8-4 32296183
Intra
HOMER1 Q86YM7 INADL Homo sapiens A5PKX9 32296183
Intra
HOMER1 Q86YM7 INADL Homo sapiens A5PKX9 32296183
Intra
HOMER1 Q86YM7 AIMP1 Homo sapiens Q12904-2 32296183
Intra
HOMER1 Q86YM7 AIMP1 Homo sapiens Q12904-2 32296183
Intra
HOMER1 Q86YM7 ZMYM5 Homo sapiens Q9UJ78-2 32296183
Intra
HOMER1 Q86YM7 ZMYM5 Homo sapiens Q9UJ78-2 32296183
Intra
HOMER1 Q86YM7 ZMYM5 Homo sapiens Q9UJ78-2 32296183
Intra
HOMER1 Q86YM7 SARG Homo sapiens Q9BW04 32296183
Intra
HOMER1 Q86YM7 SARG Homo sapiens Q9BW04 32296183
Intra
HOMER1 Q86YM7 SARG Homo sapiens Q9BW04 19447967
Intra
HOMER1 Q86YM7 SARG Homo sapiens Q9BW04 32296183
Intra
HOMER1 Q86YM7 SARG Homo sapiens Q9BW04 25416956
Intra
HOMER1 Q86YM7 CENPQ Homo sapiens Q7L2Z9 32296183
Intra
HOMER1 Q86YM7 CENPQ Homo sapiens Q7L2Z9 32296183
Intra
HOMER1 Q86YM7 RASAL3 Homo sapiens Q86YV0 32296183
Intra
HOMER1 Q86YM7 RASAL3 Homo sapiens Q86YV0 32296183
Intra
HOMER1 Q86YM7 RASAL3 Homo sapiens Q86YV0 32296183
Intra
HOMER1 Q86YM7 PIAS2 Homo sapiens O75928-2 32296183
Intra
HOMER1 Q86YM7 PIAS2 Homo sapiens O75928-2 32296183
Intra
HOMER1 Q86YM7 TRAF5 Homo sapiens O00463 28514442
Intra
HOMER1 Q86YM7 TRAF5 Homo sapiens O00463 33961781
Intra
HOMER1 Q86YM7 BRME1 Homo sapiens Q0VDD7 25416956
Intra
HOMER1 Q86YM7 ABI3 Homo sapiens Q9P2A4 32296183
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 35271311
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 25416956
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 32296183
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 25416956
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 32296183
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 25416956
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 32296183
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 32296183
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 25416956
Intra
HOMER1 Q86YM7 HOMER3 Homo sapiens Q9NSC5 25416956
Intra
HOMER1 Q86YM7 FAM9A Homo sapiens Q8IZU1 32296183
Intra
HOMER1 Q86YM7 FAM9A Homo sapiens Q8IZU1 32296183
Intra
HOMER1 Q86YM7 FAM9A Homo sapiens Q8IZU1 32296183
Intra
HOMER1 Q86YM7 RAD54L2 Homo sapiens Q9Y4B4 32296183
Intra
HOMER1 Q86YM7 RAD54L2 Homo sapiens Q9Y4B4 32296183
Intra
HOMER1 Q86YM7 RAD54L2 Homo sapiens Q9Y4B4 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

HOMER1 Antibodies

Cat. No. Product Name Application Reactivity
HY-P83290 Homer1 Antibody (YA3035) WB, IP Mouse, Rat
HY-P83290A Homer1 Antibody (YA3035)(PBS only) WB, IP Mouse, Rat
HY-P86909 Homer1 Antibody (YA6602) WB, IHC-P, IHC-F Mouse, Rat

Related Diseases

Diseases Alias
Fragile X Syndrome
  • FXS

  • Martin-Bell Syndrome

  • Fraxa Syndrome

  • Marker X Syndrome

  • X-Linked Mental Retardation And Macroorchidism

  • Fragile X Mental Retardation Syndrome

  • Fra Syndrome

  • Mental Retardation, X-Linked, Associated With Marxq28

  • X-Linked Intellectual Disability And Macroorchidism

  • Frax Syndrome

  • Symptomatic Form Of Fragile X Syndrome In Female Carriers

  • Fragile-X Syndrome

  • Fraxe Syndrome

Deafness, Autosomal Dominant 68
  • DFNA68

  • Autosomal Dominant Nonsyndromic Deafness 68

  • Autosomal Dominant Deafness 68

  • Deafness, Autosomal Dominant, 68

Autism
  • Autistic Disorder

  • Autism Susceptibility 1

  • Childhood Autism

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Kanner'S Syndrome

  • Autistic

Ogden Syndrome
  • OGDNS

  • N-Terminal Acetyltransferase Deficiency

  • NATD

  • N-Alpha-Acetyltransferase

  • X-Linked Malformation And Infantile Lethality Syndrome

  • Premature Aging Appearance-Developmental Delay-Cardiac Arrhythmia Syndrome

Phelan-Mcdermid Syndrome
  • Chromosome 22q13.3 Deletion Syndrome

  • 22q13.3 Deletion Syndrome

  • Telomeric 22q13 Monosomy Syndrome

  • PHMDS

  • Deletion 22q13 Syndrome

  • 22q13.3 Deletion

  • Deletion 22q13.3 Syndrome

  • Monosomy 22q13

  • Monosomy 22q13.3

  • 22q13 Deletion Syndrome

  • Monosomy 22q13 Syndrome

  • 22q13 Deletion

  • Chromosome Deletion

Autism Spectrum Disorder
  • Asd

  • Autism Spectrum Disorders

  • Autistic Continuum

  • Pervasive Developmental Disorder

  • Pervasive Development Disorder

  • Autistic Behavior

  • Autistic Disorder

  • Autistic

  • Autistic Disorder Of Childhood Onset

  • Infantile Autism

  • Childhood Autism

  • Kanner Syndrome

  • Pervasive Developmental Delay Nos

  • Pervasive Developmental Disorder, Not Otherwise Specified

Bipolar Disorder
  • Bipolar Depression

  • Manic Disorder

  • Depression, Bipolar

  • Bipolar Disorder Manic Phase

  • Depressive-Manic Psych.

  • Manic Bipolar Affective Disorder

  • Manic Bipolar I Disorder

  • Manic Depression

  • Manic Depressive Disorder

  • Mixed Bipolar Disorder

  • Bipolar Affective Disorder

  • Bipolar Affective Psychosis

  • Bipolar Spectrum Disorder

  • Manic Depressive Illness

  • Depression Bipolar

  • Bipolar Disorder, Mixed

  • Major Affective Disorder

  • Major Affective Disorder 1

  • Major Affective Disorder 2

Pervasive Developmental Disorder
  • Pervasive Development Disorder

  • Pervasive Developmental Disorders

  • Pervasive Child Development Disorders

  • Autistic Behavior

  • Autism Spectrum Disorders

Schizophrenia
  • SCZD

  • Schizophrenia With Or Without An Affective Disorder

  • Schizophrenia 12

  • Schizophrenia, Susceptibility To

  • Schizophrenia-1

  • Dementia Praecox

  • Schizophrenia 1

Attention Deficit-Hyperactivity Disorder
  • Attention Deficit Hyperactivity Disorder

  • ADHD

  • Attention Deficit Disorder

  • Attention Deficit-Hyperactivity Disorder, Susceptibility To

  • Attention Deficit Disorder With Hyperactivity

  • Hyperkinetic Disorder

  • Hyperactivity Of Childhood

  • Attention-Deficit/Hyperactivity Disorder

  • Add

  • Addh

  • Attention Deficit

  • Attention Deficit Disorder Of Childhood With Hyperactivity

  • Attention Deficit Disorder With Hyperactivity Syndrome

  • Hyperkinetic Syndrome

  • Attention-Deficit Hyperactivity Disorder

  • Attention-Deficit/Hyperactivity Disorder, Predominantly Inattentive Type

  • Disturbance Of Activity And Attention

  • Disorder Of Activity And Attention

  • Adhd - [Attention Deficit Hyperactivity Disorder]

  • Hyperkinetic Disorders

  • Disorder Of Activity And Attention With Hyperkinesia

  • Attention Deficit Syndrome With Hyperactivity

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Macaca mulatta HOMER1 VGNC VGNC:73405
Mus musculus HOMER1 MGD MGI:1347345
Felis catus HOMER1 VGNC VGNC:62830
Canis familiaris HOMER1 VGNC VGNC:41737
Rattus norvegicus HOMER1 RGD RGD:628725
Bos taurus HOMER1 VGNC VGNC:29901
Others HOMER1 NCBI