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Skeletal dysplasia

Gene: TNXB

Red List (low evidence)

TNXB (tenascin XB)
EnsemblGeneIds (GRCh38): ENSG00000168477
EnsemblGeneIds (GRCh37): ENSG00000168477
OMIM: 600985, Gene2Phenotype
TNXB is in 11 panels

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History Filter Activity

9 Aug 2016, Gel status: 0

panel promoted to version 1

Sarah Leigh (Genomics England Curator)

Promoted to version 1 9th August 2016

18 May 2016, Gel status: 0

Added New Source

Sarah Leigh (Genomics England Curator)

TNXB was added to Unexplained skeletal dysplasiapanel. Sources: Expert

18 May 2016, Gel status: 0

Created

Sarah Leigh (Genomics England Curator)

TNXB was created by sleigh