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GPNMB

Chr 7p15.3

glycoprotein nmb

Aliases:
NMB, HGFIN
MANE:
ENST00000258733.9

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • Pigmentary skin disorders

    BIALLELIC, autosomal or pseudoautosomal

Disease associations (Open Targets)

  • familial primary localized cutaneous amyloidosis

    0.70
  • Parkinson disease

    0.50
  • amyloidosis cutis dyschromia

    0.46
  • primary cutaneous amyloidosis

    0.37
  • lymphoma

    0.37
  • endometriosis

    0.36
  • temporomandibular joint disorder

    0.31
  • type 2 diabetes mellitus

    0.27
  • response to antihypertensive drug

    0.23
  • hereditary disease

    0.20

Score is the Open Targets composite evidence score (0-1). Higher = stronger gene-disease association.

Protein function (UniProt)

Transmembrane glycoprotein NMB

Could be a melanogenic enzyme

Data sources: HGNC (CC BY 4.0), AlphaFold (CC BY 4.0, Jumper et al. Nature 2021), Genomics England PanelApp (CC BY 4.0), ClinGen, Open Targets (CC0), UniProt.

Not for sole clinical decision-making. Always verify against primary sources.