1. Gene
  2. DAND5 - DAN domain BMP antagonist family member 5 Gene

DAND5 - DAN domain BMP antagonist family member 5 Gene

中文名称:DAN 结构域 BMP 拮抗因子家族成员 5

种属: Homo sapiens

同用名: SP1; CER2; COCO; CRL2; CERL2; DANTE; GREM3; CKTSF1B3

基因 ID: 199699 | 基因类型: protein coding

关于 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.

功能概要

该基因编码 BMP (骨形态发生蛋白) 拮抗剂家族的成员。与 BMP 一样,BMP 拮抗剂含有胱氨酸结,通常形成同二聚体和异二聚体。该基因所属的 BMP 拮抗剂的 CAN (cerberus 和 dan) 亚家族的特征在于具有八元环的 C 末端胱氨酸结。由该基因编码的分泌蛋白的拮抗作用可能是由于它与 BMP 蛋白直接结合。作为 BMP 的拮抗剂,该基因可能在调节器官发生、身体形态和组织分化中发挥作用。在小鼠中,这种蛋白质已被证明可以结合 Nodal 并抑制影响左/右身体不对称的 Nodal 信号通路。[RefSeq 提供,2008 年 7 月]

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 基因产物(1)

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

DAND5 蛋白结构

DAN

DAN: DAN domain (84 - 186)

  • 0
  • 100
  • 189 a.a.
蛋白主名 其他名称

DAN domain family member 5

DAN domain family member 5, BMP antagonist

关联疾病

疾病名称 别名
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

疾病名称 别名
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

直系同源

种属 基因名 来源 基因 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