TMEM276-ZFTRAF1

protein-coding

TMEM276-ZFTRAF1 readthrough

Gene summary

This locus represents naturally occurring read-through transcription between the neighboring LOC84773 and cysteine and histidine rich 1 (CYHR1). It encodes a fusion protein that shares sequence identity with proteins encoded by both independent genes. [provided by RefSeq, Feb 2022]

MANE transcript

N/A

Inheritance

—

ClinVar variants

P:3U:4

Top phenotype

Inborn genetic diseases

Max pathogenic AF

—

Genomic locus

chr8:144,449,582-144,465,430

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~15.8 kb
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GenCC Phenotypes & Disease Associations

Curated gene-disease validity assertions and inheritance patterns

No GenCC data available for this gene.

ClinVar Associated Diseases & Phenotypes

Reported disease conditions connected to TMEM276-ZFTRAF1 variants in ClinVar

3 Conditions Cataloged
Inborn genetic diseasesTotal: 4
Neurodevelopmental disorder with hypotonia and gross motor and speech delayTotal: 3
Autosomal recessive non-syndromic intellectual disabilityTotal: 1

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript . Only rare variants are included.

We include only reliable ClinVar variants with their consequences to MANE Select, MANE Plus Clinical transcripts, or transcripts with TSL equal to 1. Click a count to filter the variants table below.

Slight differences between displayed counts and ClinVar may occur due to a different transcript/consequence chosen by our variant effect predictor, or because we classify Benign/Likely benign as Likely benign and Pathogenic/Likely pathogenic as Likely pathogenic.

EffectPLPVUSLBBSum
synonymous
0
missense
4
clinvar
4
nonsense
0
start loss
0
frameshift
1
clinvar
1
clinvar
2
splice donor/acceptor (+/-2bp)
1
clinvar
1
Total214007
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 4 of 20 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_001408008.1RefSeqNP_001394937.15Standard
NM_001408009.1RefSeqNP_001394938.15Standard
NM_001408010.1RefSeqNP_001394939.15Standard
NM_001408011.1RefSeqNP_001394940.14Standard
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