H2BC6

Chr 6

H2B clustered histone 6

Also known as: H2B.h, H2B/h, H2BC10, H2BC4, H2BC7, H2BC8, H2BFH, HIST1H2BE

Histones are basic nuclear proteins that are responsible for the nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. The protein has antibacterial and antifungal antimicrobial activity. This gene is intronless and encodes a replication-dependent histone that is a member of the histone H2B family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6. [provided by RefSeq, Aug 2015]

46
ClinVar variants
5
Pathogenic / LP
pLI score
0
Active trials
Clinical SummaryH2BC6
📋
ClinVar Variants
5 Pathogenic / Likely Pathogenic· 39 VUS of 46 total submissions
Some data sources returned errors (2)

gnomad: Error: Gene not found

omim: Error: OMIM fetch failed: 429

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

46 submitted variants in ClinVar

Classification Summary

Pathogenic4
Likely Pathogenic1
VUS39
Likely Benign2
4
Pathogenic
1
Likely Pathogenic
39
VUS
2
Likely Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
4
0
4
Likely Pathogenic
0
0
1
0
1
VUS
0
27
12
0
39
Likely Benign
0
0
2
0
2
Benign
0
0
0
0
0
Total02719046

LoF = frameshift, stop gained/lost, canonical splice · Counts from ClinVar esearch · Updated hourly

View in ClinVar →

Protein Context — Lollipop Plot

H2BC6 · protein map & ClinVar variants

Showing all ClinVar variants across the protein. Search a specific variant to highlight its position.

OMIM — Genotype-Phenotype

No OMIM entries found.