CT45A5

protein-coding

cancer/testis antigen family 45 member A5, the group of CT antigen family 45

Gene summary

This gene represents one of a cluster of several similar genes located on the q arm of chromosome X. The genes in this cluster encode members of the cancer/testis (CT) family of antigens, and are distinct from other CT antigens. These antigens are thought to be novel therapeutic targets for human cancers. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Apr 2014]

MANE transcript

NM_001007551.6

Inheritance

—

ClinVar variants

U:6

Top phenotype

—

Max pathogenic AF

—

Genomic locus

chrX:135,775,852-135,785,503

External References & Databases

Transcript & Mutation Effects

hg38 • Region Span ~9.7 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 CT45A5 variants in ClinVar

1 Conditions Cataloged
not specifiedTotal: 3

ClinVar Variants & Pathogenicity by Type

Statistics based on transcript NM_001007551.6. 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
5
clinvar
5
nonsense
0
start loss
0
frameshift
0
splice donor/acceptor (+/-2bp)
1
clinvar
1
Total006006
Loading ClinVar variants...

Transcript Catalog

Annotated transcript isoforms across RefSeq and Ensembl databases

Showing 4 of 6 transcripts
Transcript IDSourceProtein IDCoding ExonsMANE Status
NM_001007551.6RefSeqNP_001007552.24MANE Select
ENST00000698999.1EnsemblENSP00000514077.14MANE Select
NM_001172288.2RefSeqNP_001165759.24Standard
ENST00000487941.6EnsemblENSP00000427342.24Standard

Gene Ontology (GO) Annotations & Pathways

Biological processes, molecular functions, cellular components and pathways

Biological Process

  • snRNA 3'-end processing

Cellular Component

  • integrator complex

dbNSFP Gene Annotations

Source: dbNSFP

Essentials

Essential (CRISPR)
N
Essential (gene trap)
N
Indispensability pred.
N
Indispensability score
0.000149

Gene Damage Prediction

AllRecessiveDominant
MendelianMediumMediumMedium
Primary ImmunodeficiencyMediumMediumMedium
CancerMediumMediumMedium
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