CT45A2

gene
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Also known as CT45-2CT45.2

Summary

CT45A2 (cancer/testis antigen family 45 member A2, HGNC:28400) is a protein-coding gene on chromosome Xq26.3, encoding Cancer/testis antigen family 45 member A2 (Q5DJT8).

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.

Source: NCBI Gene 728911 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 1 total
  • MANE Select transcript: NM_152582

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:28400
Approved symbolCT45A2
Namecancer/testis antigen family 45 member A2
LocationXq26.3
Locus typegene with protein product
StatusApproved
AliasesCT45-2, CT45.2
Ensembl geneENSG00000271449
Ensembl biotypeprotein_coding
OMIM300793
Entrez728911

Gene structure

Transcript identifiers

Ensembl transcripts: 2 — 2 protein_coding

ENST00000605791, ENST00000612907

RefSeq mRNA: 1 — MANE Select: NM_152582 NM_152582

CCDS: CCDS76031

Canonical transcript exons

ENST00000612907 — 5 exons

ExonStartEnd
ENSE00003056746135813454135813547
ENSE00003060881135811668135812231
ENSE00003717108135813928135814176
ENSE00003734388135816097135816271
ENSE00003745200135819774135820012

Expression profiles

Bgee: expression breadth broad, 19 present calls, max score 80.29.

Top tissues by expression

122 total, by Bgee expression score (0-100, higher = more expressed):

TissueAnatomy IDExpression scoreQuality
primordial germ cell in gonadCL:0000670 ∩ UBERON:000099180.29gold quality
male germ line stem cell (sensu Vertebrata) in testisCL:0000089 ∩ UBERON:000047377.62gold quality
granulocyteCL:000009437.28gold quality
colonic epitheliumUBERON:000039737.20gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
prefrontal cortexUBERON:000045132.17gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
bone marrowUBERON:000237131.74gold quality
muscle tissueUBERON:000238531.06gold quality
sural nerveUBERON:001548830.93gold quality
stromal cell of endometriumCL:000225529.87gold quality
duodenumUBERON:000211428.14gold quality
liverUBERON:000210728.04gold quality
lymph nodeUBERON:000002927.57gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.55gold quality
bloodUBERON:000017826.53gold quality
frontal cortexUBERON:000187026.49gold quality
vermiform appendixUBERON:000115426.42gold quality
leukocyteCL:000073826.15gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
urinary bladderUBERON:000125525.72gold quality
monocyteCL:000057625.37gold quality
muscle of legUBERON:000138325.15gold quality

Single-cell (SCXA)

Detected in 1 experiment(s), a significant marker in 0.

ExperimentMarker?Max mean expression
E-ANND-3no0.00

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

18 targeting CT45A2, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):

miRNAMax scoreAvg scoremiRNA target_count
HSA-MIR-6833-3P100.0070.633197
HSA-MIR-4768-5P100.0069.492861
HSA-MIR-4455100.0065.481587
HSA-MIR-314899.9775.066478
HSA-MIR-6845-3P99.9466.881439
HSA-MIR-449399.9066.48977
HSA-MIR-313399.8170.923506
HSA-MIR-4668-5P99.7970.583782
HSA-MIR-58699.6570.402051
HSA-MIR-427999.1966.702437
HSA-MIR-5006-5P98.7966.921246
HSA-MIR-557298.5565.84970
HSA-MIR-6819-5P97.9666.591071
HSA-MIR-3151-3P97.8066.16479
HSA-MIR-6737-5P97.7566.541044
HSA-MIR-6812-5P97.5665.391059
HSA-MIR-367497.0168.861171
HSA-MIR-6747-5P96.1764.99743

Literature-anchored findings (GeneRIF, showing 2)

  • CT45A2 is a novel spliced MLL fusion partner in de novo biphenotypic acute leukemia [case report] (PMID:20920256)
  • Ursolic acid promotes apoptosis and mediates transcriptional suppression of CT45A2 gene expression in non-small-cell lung carcinoma harbouring EGFR T790M mutations. (PMID:31322286)

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
mus_musculusCt45aENSMUSG00000064016
rattus_norvegicusCt45a9ENSRNOG00000048059
drosophila_melanogasterIntS6FBGN0261383
caenorhabditis_elegansWBGENE00000994

Paralogs (11): INTS6 (ENSG00000102786), INTS6L (ENSG00000165359), SAGE1 (ENSG00000181433), CT45A5 (ENSG00000228836), CT45A1 (ENSG00000268940), CT45A3 (ENSG00000269096), CT45A10 (ENSG00000269586), CT45A9 (ENSG00000270946), CT45A7 (ENSG00000273696), CT45A8 (ENSG00000278085), CT45A6 (ENSG00000278289)

Protein

Protein identifiers

Cancer/testis antigen family 45 member A2Q5DJT8 (reviewed: Q5DJT8)

Alternative names: Cancer/testis antigen 45-2, Cancer/testis antigen 45A2

All UniProt accessions (1): Q5DJT8

UniProt curated annotations — full annotation on UniProt →

Tissue specificity. Testis specific. Expressed in cancer cell lines.

Similarity. Belongs to the CT45 family.

RefSeq proteins (1): NP_689795* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR029307INT_SG_DDX_CT_CDomain
IPR051113Integrator_subunit6Family

Pfam: PF15300

UniProt features (4 total): sequence conflict 3, chain 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q5DJT8-F168.890.19

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 3 (showing top): chrXq26, HE_LIM_SUN_FETAL_LUNG_C0_MYOFIBROBLAST_1_CELL, HE_LIM_SUN_FETAL_LUNG_C0_MYOFIBROBLAST_2_CELL

GO Biological Process (0):

GO Molecular Function (0):

GO Cellular Component (0):

Protein interactions and networks

STRING

228 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
CT45A2ZFYVE19Q96K21506
CT45A2MRFAP1L1Q96HT8432
CT45A2ELLP55199379
CT45A2BTBD18B2RXH4370
CT45A2MLLT11Q13015368
CT45A2MPZL3Q6UWV2350
CT45A2VCX2Q9H322348
CT45A2SEPTIN6Q14141344
CT45A2MYO1FO00160339
CT45A2MLLT10P55197321
CT45A2AFF1P51825314
CT45A2VCX3AQ9NNX9310
CT45A2SEPTIN5Q99719305
CT45A2MLLT6P55198300
CT45A2PCDHB11Q9Y5F2296

IntAct

6 interactions, top by confidence:

ABTypeScore
Ppp4r3aTIA1psi-mi:“MI:0914”(association)0.350
MMGT1DERL1psi-mi:“MI:0914”(association)0.350
NCBP3RSL1D1psi-mi:“MI:0914”(association)0.350
NCBP2SEH1Lpsi-mi:“MI:0914”(association)0.350
APOMHLA-Apsi-mi:“MI:0914”(association)0.350

ESM2 similar proteins: A0A097I2D0, A0A1W2PP81, A0A1W2PPE2, A0A1W2PPH5, A0A1W2PPL8, A0A1W2PPW3, A0A1W2PQ09, A0A1W2PR64, A0A1W2PRV1, A6NLC8, F4HR03, O54825, O75461, P0C1H6, P0CV38, P0DMV1, P0DMV2, P0DW11, P0DW12, P0DW13, P0DW14, P40914, P49585, P49906, P81195, Q0MTC0, Q13895, Q15544, Q2N2K6, Q3SZB8, Q5DJT8, Q5RA91, Q5U1X0, Q6CER9, Q6RG77, Q6XL73, Q75DE4, Q7XHR2, Q7Z2G1, Q80WL2

Diamond homologs: A6NJ88, P0DMU7, P0DMU8, P0DMU9, P0DMV0, P0DMV1, P0DMV2, Q2TAF4, Q5DJT8, Q5HYN5, Q5JSJ4, Q5U4W6, Q6PCM2, Q7SYD9, Q8BND4, Q8NHU0, Q9NXZ1, Q9UL03, Q54Z23, Q9W485

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

1 variants total. Per-class counts are floors (≥ shown; pagination cap):

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance1
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

43 predictions. Top by Δscore:

VariantEffectΔscore
X:135812229:CAT:Cacceptor_gain0.9900
X:135812227:TACAT:Tacceptor_gain0.9800
X:135812231:TCTGA:Tacceptor_loss0.9800
X:135812232:C:CCacceptor_gain0.9800
X:135812232:C:CGacceptor_loss0.9800
X:135812233:T:Aacceptor_loss0.9800
X:135812228:ACAT:Aacceptor_gain0.9700
X:135812229:CATC:Cacceptor_gain0.9700
X:135812230:AT:Aacceptor_gain0.9600
X:135812230:A:Tacceptor_gain0.7200
X:135812230:A:Cacceptor_gain0.5700
X:135812234:G:Cacceptor_loss0.5600
X:135814780:G:GTdonor_gain0.5100
X:135814750:G:Tdonor_gain0.4900
X:135812228:ACATC:Aacceptor_gain0.4800
X:135812244:AGACA:Aacceptor_gain0.4600
X:135812230:ATCTG:Aacceptor_gain0.4300
X:135814751:G:GTdonor_gain0.4200
X:135812254:TTAA:Tacceptor_gain0.3400
X:135814776:G:GTdonor_gain0.3300
X:135812231:TCTG:Tacceptor_gain0.3200
X:135812229:CATCT:Cacceptor_gain0.3100
X:135812232:C:Aacceptor_gain0.3000
X:135812645:G:Cacceptor_gain0.3000
X:135812643:C:Gacceptor_gain0.2900
X:135812245:GACAT:Gacceptor_gain0.2800
X:135814735:GAG:Gdonor_gain0.2800
X:135814736:GGA:Gdonor_gain0.2800
X:135812226:A:ACacceptor_gain0.2700
X:135812239:GAAA:Gacceptor_loss0.2600

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 96 via entrez): RS1158059612 (X:135821203 A>AAGAAG,AAGAAGGAAG), RS1175723017 (X:135815478 G>A), RS1252673953 (X:135815517 G>A), RS1255928065 (X:135815906 TAA>T,TA,TAAAA,TAAAAA,TAAAAAA), RS1305263809 (X:135815962 G>T), RS1314336133 (X:135815948 G>C), RS1400787680 (X:135818557 T>A), RS1412382053 (X:135818426 G>A), RS1412951820 (X:135821227 C>A), RS1434689690 (X:135814731 T>C), RS1467476884 (X:135821161 G>A), RS1472413381 (X:135821215 G>A), RS1474276636 (X:135821259 T>C), RS1482826975 (X:135815479 T>C), RS1485008797 (X:135815894 C>T)

Disease associations

OMIM: gene MIM:300793 | disease phenotypes:

GenCC curated gene-disease

Mondo (0):

Orphanet (0):

HPO phenotypes

0 total (0 of 0 shown, HPO-id order):

GWAS associations

0 associations (top):

Drugs & pharmacology

Drug and pharmacology data

Is drug target: no

PharmGKB: 1 entry (VIP=true, CPIC=false)

CTD chemical–gene interactions

3 total (human), top 3 by PubMed support.

ChemicalActions (top 5)PubMed papers
(4-amino-1,4-dihydro-3-(2-pyridyl)-5-thioxo-1,2,4-triazole)copper(II)increases expression1
Cadmiumdecreases expression1
Valproic Acidincreases methylation1

Clinical trials (associated diseases)

0 trials via MONDO — disease-level, not drug-specific.

No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.