1. Gene
  2. SUPT16H - SPT16 homolog, facilitates chromatin remodeling subunit Gene

SUPT16H - SPT16 homolog, facilitates chromatin remodeling subunit Gene

Homo sapiens

Also known as CDC68; SPT16; NEDDFAC; FACTP140; SPT16/CDC68

Gene ID: 11198 | Gene type: protein coding

About SUPT16H

Cytogenetic location: 14q11.2 Genomic coordinates (GRCh38): 14:21,351,476-21,384,019 (from NCBI)

This gene has 8 transcripts (splice variants), 202 orthologues and is associated with 2 phenotypes. Ubiquitous expression in testis (RPKM 30.8), lymph node (RPKM 27.6) and 25 other tissues.

Summary

Transcription of protein-coding genes can be reconstituted on naked DNA with only the general transcription factors and RNA polymerase II. However, this minimal system cannot transcribe DNA packaged into chromatin, indicating that accessory factors may facilitate access to DNA. One such factor, FACT (facilitates chromatin transcription), interacts specifically with histones H2A/H2B to effect nucleosome disassembly and transcription elongation. FACT is composed of an 80 kDa subunit and a 140 kDa subunit; this gene encodes the 140 kDa subunit. [provided by RefSeq, Feb 2009]

SUPT16H Products(1)

mRNA Protein Name
NM_007192.4 NP_009123.1 FACT complex subunit SPT16

SUPT16H Protein Structure

FACT-Spt16_Nlob

FACT-Spt16_Nlob: FACT complex subunit SPT16 N-terminal lobe domain (5 - 167)

Peptidase_M24

Peptidase_M24: Metallopeptidase family M24 (182 - 411)

SPT16

SPT16: FACT complex subunit (SPT16/CDC68) (529 - 689)

Rtt106

Rtt106: Histone chaperone Rttp106-like (813 - 895)

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  • 1047 a.a.
Protein Preferred Names Protein Names

FACT complex subunit SPT16

FACT 140 kDa subunit

Related Diseases

Diseases Alias
Neurodevelopmental Disorder With Dysmorphic Facies And Thin Corpus Callosum

NEDDFAC

Autism Spectrum Disorder

Asd

Autism Spectrum Disorders

Autistic Continuum

Pervasive Developmental Disorder

Pervasive Development Disorder

Autistic Behavior

Autistic Disorder

Autistic

Autistic Disorder Of Childhood Onset

Infantile Autism

Childhood Autism

Kanner Syndrome

Pervasive Developmental Delay Nos

Pervasive Developmental Disorder, Not Otherwise Specified

Autism

Autistic Disorder

Autism Susceptibility 1

Childhood Autism

Autistic Disorder Of Childhood Onset

Infantile Autism

Kanner'S Syndrome

Autistic

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus SUPT16H VGNC VGNC:65846
Macaca mulatta SUPT16H VGNC VGNC:78054
Bos taurus SUPT16H VGNC VGNC:35478
Rattus norvegicus SUPT16H RGD RGD:1310032
Mus musculus SUPT16H MGD MGI:1890948
Canis familiaris SUPT16H VGNC VGNC:46989