DAND5 - DAN domain BMP antagonist family member 5 Gene

Also Known as SP1; CER2; COCO; CRL2; CERL2; DANTE; GREM3; CKTSF1B3

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 199699

About DAND5

Cytogenetic location: 19p13.13 Genomic coordinates (GRCh38): 19:12,969,576-12,974,760 (from NCBI)

This gene has 2 transcripts (splice variants), 132 orthologues and 1 paralogue. Biased expression in heart (RPKM 2.6), brain (RPKM 0.4) and 1 other tissue.

Summary

This gene encodes a member of the BMP (bone morphogenic protein) antagonist family. Like BMPs, BMP antagonists contain cystine knots and typically form homo- and heterodimers. The CAN (cerberus and dan) subfamily of BMP antagonists, to which this gene belongs, is characterized by a C-terminal cystine knot with an eight-membered ring. The antagonistic effect of the secreted protein encoded by this gene is likely due to its direct binding to BMP proteins. As an antagonist of BMP, this gene may play a role in regulating organogenesis, body patterning, and tissue differentiation. In mouse, this protein has been shown to bind Nodal and to inhibit the Nodal signaling pathway which patterns left/right body asymmetry. [provided by RefSeq, Jul 2008]

DAND5 Products (1)

mRNA Protein Name
NM_152654.3 NP_689867.1 DAN domain family member 5 precursor

DAND5 Protein Structure

DAN

DAN: DAN domain (84 - 186)

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

DAN domain family member 5

  • DAN domain family member 5, BMP antagonist

Related Diseases

Diseases Alias
Situs Inversus
  • Situs Inversus Viscerum

  • Laterality Sequence

  • Complete Transposition

  • Siv

Visceral Heterotaxy
  • Situs Ambiguus

  • Heterotaxia

  • Heterotaxy Syndrome

  • Heterotaxy

  • Lateralization Defect

  • Situs Ambiguous

  • Left Isomerism

  • Htx

  • Ivemark Syndrome

  • Right Isomerism

  • Situs Ambiguus Viscerum

  • Incomplete Situs Inversus

  • Partial Situs Inversus

  • Heterotaxy, Visceral

  • Asplenia Syndrome

  • Bilateral Left-Sidedness

  • Polysplenia Syndrome

  • Moller Syndrome

Sclerosteosis 1
  • SOST1

  • Sost

  • Cortical Hyperostosis With Syndactyly

  • Sclerosteosis

  • Sclerosteosis, Type 1

Marshall-Smith Syndrome
  • MRSHSS

  • Accelerated Skeletal Maturation-Facial Dysmorphism-Failure To Thrive Syndrome

  • Mss

Right Atrial Isomerism
  • Ivemark Syndrome

  • Asplenia With Cardiovascular Anomalies

  • RAI

  • Asplenia Syndrome

  • Asplenia

  • Right Isomerism

  • Splenic Agenesis Syndrome

  • Bilateral Right-Sidedness Sequence

  • Right Sided Atrial Isomerism

  • Isomerism Of Right Atrial Appendage

  • Heterotaxy, Visceroatrial, Autosomal Recessive

  • Polyasplenia

  • Vah, Autosomal Recessive

  • Atrial Isomerism, Right

  • Congenital Absence Of Spleen

  • Bilateral Right-Sidedness

Polycystic Kidney Disease 2 With Or Without Polycystic Liver Disease
  • Polycystic Kidney Disease 2

  • PKD2

  • Polycystic Kidney Disease, Adult, Type Ii

  • Apkd2

  • Polycystic Kidney Disease, Type 2

  • Adpkd2

  • Adult Polycystic Kidney Disease Type 2

  • Autosomal Dominant Polycystic Kidney Disease 2

  • Pkd-2

  • Polycystic Kidney Disease Adult Type Ii

  • Polycystic Kidney Type 2 Autosomal Dominant Disease

  • Kidney Disease, Polycystic, Type 2

Meckel Syndrome, Type 1
  • Meckel-Gruber Syndrome

  • Meckel Syndrome

  • Dysencephalia Splanchnocystica

  • Meckel Syndrome 1

  • MKS1

  • Mks

  • Gruber Syndrome

  • Meckel-Gruber Syndrome, Type 1

  • Mes

  • Dysencephalia Splachnocystica

  • Meckel Gruber Syndrome

  • Meckel Syndrome Type 1

Primary Ciliary Dyskinesia
  • Immotile Cilia Syndrome

  • Kartagener Syndrome

  • Dextrocardia Bronchiectasis And Sinusitis

  • Pcd

  • Ciliary Motility Disorders

  • Ciliary Motility Disorder

  • Immotile Ciliary Syndrome

  • Ciliary Dyskinesia Primary

  • Ics

  • Polynesian Bronchiectasis

  • Dextrocardia-Bronchiectasis-Sinusitis Syndrome

  • Immotile Cilia Syndrome, Kartagener Type

  • Primary Ciliary Dyskinesia And Situs Inversus

  • Primary Ciliary Dyskinesia, Kartagener Type

  • Siewert Syndrome

  • Dyskinesia, Ciliary, Primary

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 DAND5 VGNC VGNC:71735
Canis familiaris DAND5 VGNC VGNC:39767
Felis catus DAND5 VGNC VGNC:102573
Rattus norvegicus DAND5 RGD RGD:1590249
Mus musculus DAND5 MGD MGI:1344365
Others DAND5 NCBI