1. Gene
  2. BMP8A - bone morphogenetic protein 8a Gene

BMP8A - bone morphogenetic protein 8a Gene

Homo sapiens

Also known as OP-2

Gene ID: 353500 | Gene type: protein coding

About BMP8A

This gene has 1 transcript (splice variant), 212 orthologues and 31 paralogues. Biased expression in thyroid (RPKM 57.4) and endometrium (RPKM 2.6).

Summary

This gene encodes a secreted ligand of the TGF-beta (transforming growth factor-beta) superfamily of proteins. Ligands of this family bind various TGF-beta receptors leading to recruitment and activation of Smad Family transcription factors that regulate gene expression. The encoded preproprotein is proteolytically processed to generate each subunit of the disulfide-linked homodimer. This protein may play a role in development of the reproductive system. This gene may have arose from a gene duplication event and its gene duplicate is also present on chromosome 1. [provided by RefSeq, Jul 2016]

BMP8A Products(1)

mRNA Protein Name
NM_181809.4 NP_861525.2 bone morphogenetic protein 8A preproprotein

BMP8A Protein Structure

TGFb_propeptide

TGFb_propeptide: TGF-beta propeptide (34 - 251)

TGF_beta

TGF_beta: Transforming growth factor beta like domain (299 - 402)

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

bone morphogenetic protein 8A

BMP-8A

Recombinant BMP8A Proteins

Cat. No. Product Name Accession Purity
HY-P79047 BMP-8a Protein, Human (CHO) AAP74559 (A264-H402) ≥95%
HY-P700031AF Animal-Free BMP-8a Protein, Human (His) AAP74559.1 (A264-H402) ≥95%

Related Diseases

Diseases Alias
Breast Giant Fibroadenoma

Giant Fibroadenoma

Giant Fibroadenoma Of Breast

Granulomatous Endometritis
Tympanosclerosis

Ts - [Tympanosclerosis]

Tympanic Membrane Sclerosis

Tympanic Membrane Disease

Disorder Of Tympanic Membrane

Microphthalmia, Isolated 4

Isolated Microphthalmia 4

MCOP4

Microphthalmia, Isolated, 4

Isolated Clinical Anophthalmia

Microphthalmia, Isolated, Type 4

Brachydactyly, Type A1, C

Brachydactyly Type A1c

BDA1C

Brachydactyly A1, C

Brachydactyly A1c

Brachydactyly Type A1 C

Leber Congenital Amaurosis 17

LCA17

Leber Congenital Amaurosis, Type 17

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
Mus musculus BMP8A MGD MGI:104515
Rattus norvegicus BMP8A RGD RGD:1585858