1. Genes and Genomic Entities
  2. LINC01578

LINC01578

long intergenic non-protein coding RNA 1578
Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber LINC01578 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.181
Latest signed off version: v6.0 (30 Apr 2025)

review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Sources
  • Expert Review Amber
Phenotypes
  • Neurodevelopmental disorder with dysmorphic facies, absent speech and ambulation, and brain abnormalities, OMIM:621012
Tags
  • new-gene-name
Green LINC01578 in Intellectual disability


Level 2: Developmental disorders
Version 9.346
Latest signed off version: v9.0 (30 Apr 2025)

Component of the following Super Panels:

  • Childhood onset leukodystrophy
  • Hypotonic infant
  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
    Sources
    • Expert Review Green
    • NHS GMS
    • Literature
    Phenotypes
    • Neurodevelopmental disorder with dysmorphic facies, absent speech and ambulation, and brain abnormalities, OMIM:621012
    Tags
    • new-gene-name
    • locus-type-rna-long-non-coding
    • gene-checked