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TCEAL1

Chr Xq22.2

transcription elongation factor A like 1

Aliases:
p21, pp21, SIIR, P21, WEX9
MANE:
ENST00000372625.8

Annotations refreshed 9 hours ago.

Predicted protein structure

Clinical relevance (Genomics England PanelApp)

Diagnostic Grade (Green)

  • DDG2P

    X-LINKED: hemizygous mutation in males, biallelic mutations in females
  • Intellectual disability

    X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)

Disease associations (Open Targets)

  • neurodevelopmental disorder with gait disturbance, dysmorphic facies, and behavioral abnormalities, X-linked

    0.68
  • hereditary disease

    0.40
  • neurodegenerative disease

    0.30
  • neurodevelopmental disorder

    0.19
  • melanoma

    0.07
  • neuroblastoma

    0.04
  • neoplasm

    0.03
  • prostate carcinoma

    0.03
  • prostate cancer

    0.03
  • Familial prostate cancer

    0.03

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

Protein function (UniProt)

Transcription elongation factor A protein-like 1

May be involved in transcriptional regulation. Modulates various viral and cellular promoters in a promoter context-dependent manner. For example, transcription from the FOS promoter is increased, while Rous sarcoma virus (RSV) long terminal repeat (LTR) promoter activity is repressed. Does not bind DNA directly

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.