1. Gene
  2. HEBP1 - heme binding protein 1 Gene

HEBP1 - heme binding protein 1 Gene

Homo sapiens

Also known as HBP; HEBP

Gene ID: 50865 | Gene type: protein coding

About HEBP1

Cytogenetic location: 12p13.1 Genomic coordinates (GRCh38): 12:12,974,870-13,000,265 (from NCBI)

This gene has 5 transcripts (splice variants), 148 orthologues and 1 paralogue. Ubiquitous expression in duodenum (RPKM 103.7), small intestine (RPKM 72.8) and 25 other tissues.

Summary

The full-length protein encoded by this gene is an intracellular tetrapyrrole-binding protein. This protein includes a natural chemoattractant peptide of 21 Amino acids at the N-terminus, which is a natural ligand for formyl peptide receptor-like receptor 2 (FPRL2) and promotes calcium mobilization and chemotaxis in monocytes and dendritic cells. [provided by RefSeq, Jul 2008]

HEBP1 Products(1)

mRNA Protein Name
NM_015987.5 NP_057071.2 heme-binding protein 1

HEBP1 Protein Structure

SOUL

SOUL: SOUL heme-binding protein (13 - 186)

  • 0
  • 100
  • 189 a.a.
Protein Preferred Names Protein Names

heme-binding protein 1

p22HBP

Related Diseases

Diseases Alias
Pica Disease

Pica

Proliferative Vasculopathy And Hydranencephaly-Hydrocephaly Syndrome

Fowler Syndrome

Encephaloclastic Proliferative Vasculopathy

Hydrocephaly/Hydranencephaly Due To Cerebral Vasculopathy

PVHH

Epv

Cerebral Proliferative Glomeruloid Vasculopathy

Hydranencephaly, Fowler Type

Proliferative Vasculopathy And Hydranencephaly/Hydrocephaly

Fowler'S Syndrome

Fowler Christmas Chapple Syndrome

Fowler Vasculopathy

Polycystic Ovaries Urethral Sphincter Dysfunction

Voiding Dysfunction And Polycystic Ovaries

Fowler Vasculopaty

Hydranencephaly Fowler Type

Pgv

Polycystic Ovaries-Urethral Sphincter Dysfunction Syndrome

Folate Malabsorption, Hereditary

Hereditary Folate Malabsorption

Congenital Defect Of Folate Absorption

Congenital Folate Malabsorption

Folic Acid Transport Defect

HFM

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
Rattus norvegicus HEBP1 RGD RGD:1304581
Mus musculus HEBP1 MGD MGI:1333880
Macaca mulatta HEBP1 VGNC VGNC:73184
Felis catus HEBP1 VGNC VGNC:62781
Canis familiaris HEBP1 VGNC VGNC:41639
Others HEBP1 NCBI