Nodal homolog

Nodal homolog is a secretory protein that in humans is encoded by the NODAL gene which is located on chromosome 10q22.1. It belongs to the transforming growth factor beta superfamily (TGF-β superfamily). Like many other members of this superfamily it is involved in cell differentiation in early embryogenesis, playing a key role in signal transfer from the primitive node, in the anterior primitive streak, to lateral plate mesoderm (LPM).

NODAL
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesNODAL, HTX5, nodal growth differentiation factor
External IDsOMIM: 601265 MGI: 97359 HomoloGene: 8417 GeneCards: NODAL
Orthologs
SpeciesHumanMouse
Entrez

4838

18119

Ensembl

ENSG00000156574

ENSMUSG00000037171

UniProt

Q96S42

P43021

RefSeq (mRNA)

NM_018055
NM_001329906

NM_013611

RefSeq (protein)

NP_001316835
NP_060525

NP_038639

Location (UCSC)Chr 10: 70.43 – 70.45 MbChr 10: 61.25 – 61.26 Mb
PubMed search
Wikidata
View/Edit HumanView/Edit Mouse

Nodal signaling is important very early in development for mesoderm and endoderm formation and subsequent organization of left-right axial structures. In addition, Nodal seems to have important functions in neural patterning, stem cell maintenance and many other developmental processes, including left/right handedness.

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