HOXA10-HOXA9

Chr 7

HOXA10-HOXA9 readthrough

Also known as: HDSP

This locus represents naturally occurring read-through transcription between the neighboring HOXA10 (homeobox A10) and HOXA9 (full description written out) genes on chromosome 7. The read-through transcript is a candidate for nonsense-mediated mRNA decay (NMD), and is unlikely to produce a protein product. [provided by RefSeq, Mar 2011]

0
Active trials
9
Pathogenic / LP
163
ClinVar variants
0
Pubs (1 yr)
Missense Z
LOEUF
Clinical SummaryHOXA10-HOXA9
📋
ClinVar Variants
9 Pathogenic / Likely Pathogenic· 142 VUS of 163 total submissions
Some data sources returned errors (1)

gnomad: Error: Gene not found

Population Genetics & Constraint

Constraint data not available from gnomAD.

ClinVar Variant Classifications

163 submitted variants in ClinVar

Classification Summary

Pathogenic9
VUS142
Likely Benign6
Benign6
9
Pathogenic
142
VUS
6
Likely Benign
6
Benign

Curated Variants Distribution

Classified variants from ClinVar · 5 ACMG categories

ClassificationLoFMissense + InframeNon-codingSynonymousTotal
Pathogenic
0
0
9
0
9
Likely Pathogenic
0
0
0
0
0
VUS
0
141
1
0
142
Likely Benign
0
0
1
5
6
Benign
0
1
1
4
6
Total0142129163

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

View in ClinVar →

HOXA10-HOXA9 · protein map & ClinVar variants

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

Clinical Trials

Active and recruiting trials from ClinicalTrials.gov

No active trials found for this gene.

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Clinical Literature
Landmark / reviewRecent case evidence