CT45A7
gene geneOn this page
Summary
CT45A7 (cancer/testis antigen family 45 member A7, HGNC:51260) is a protein-coding gene on chromosome Xq26.3, encoding Cancer/testis antigen family 45 member A7 (P0DMV0).
Located in nucleus.
Source: NCBI Gene 101060211 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_001394668
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:51260 |
| Approved symbol | CT45A7 |
| Name | cancer/testis antigen family 45 member A7 |
| Location | Xq26.3 |
| Locus type | gene with protein product |
| Status | Approved |
| Ensembl gene | ENSG00000273696 |
| Ensembl biotype | protein_coding |
| Entrez | 101060211 |
Gene structure
Transcript identifiers
Ensembl transcripts: 2 — 2 protein_coding
ENST00000610598, ENST00000620885
RefSeq mRNA: 2 — MANE Select: NM_001394668
NM_001291543, NM_001394668
CCDS: CCDS76032
Canonical transcript exons
ENST00000610598 — 5 exons
| Exon | Start | End |
|---|---|---|
| ENSE00003091584 | 135837042 | 135837280 |
| ENSE00003668015 | 135831197 | 135831445 |
| ENSE00003727382 | 135830722 | 135830815 |
| ENSE00003744623 | 135829229 | 135829497 |
| ENSE00003752157 | 135833365 | 135833539 |
Expression profiles
Bgee: expression breadth broad, 48 present calls, max score 82.78.
Top tissues by expression
112 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| primordial germ cell in gonad | CL:0000670 ∩ UBERON:0000991 | 82.78 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 81.05 | gold quality |
| apex of heart | UBERON:0002098 | 42.50 | silver quality |
| sural nerve | UBERON:0015488 | 41.64 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 37.52 | gold quality |
| colonic epithelium | UBERON:0000397 | 37.20 | gold quality |
| ventricular zone | UBERON:0003053 | 36.48 | gold quality |
| cortical plate | UBERON:0005343 | 36.47 | gold quality |
| bone marrow cell | CL:0002092 | 36.16 | gold quality |
| ganglionic eminence | UBERON:0004023 | 35.49 | gold quality |
| prefrontal cortex | UBERON:0000451 | 34.26 | gold quality |
| muscle tissue | UBERON:0002385 | 34.10 | gold quality |
| fundus of stomach | UBERON:0001160 | 33.96 | gold quality |
| urinary bladder | UBERON:0001255 | 33.09 | gold quality |
| bone marrow | UBERON:0002371 | 32.79 | gold quality |
| duodenum | UBERON:0002114 | 32.33 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| monocyte | CL:0000576 | 31.22 | silver quality |
| leukocyte | CL:0000738 | 30.90 | silver quality |
| liver | UBERON:0002107 | 30.63 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| vermiform appendix | UBERON:0001154 | 29.14 | gold quality |
| right lobe of liver | UBERON:0001114 | 29.05 | gold quality |
| frontal cortex | UBERON:0001870 | 28.26 | gold quality |
| blood | UBERON:0000178 | 28.19 | gold quality |
| muscle of leg | UBERON:0001383 | 27.88 | silver quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| gastrocnemius | UBERON:0001388 | 27.14 | silver quality |
| tonsil | UBERON:0002372 | 27.05 | gold quality |
| superior frontal gyrus | UBERON:0002661 | 26.81 | gold quality |
Single-cell (SCXA)
Detected in 3 experiment(s), a significant marker in 2.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-MTAB-6308 | yes | 211.76 |
| E-HCAD-5 | yes | 151.27 |
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
15 targeting CT45A7, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-6833-3P | 100.00 | 70.63 | 3197 |
| HSA-MIR-4768-5P | 100.00 | 69.49 | 2861 |
| HSA-MIR-4455 | 100.00 | 65.48 | 1587 |
| HSA-MIR-6845-3P | 99.94 | 66.88 | 1439 |
| HSA-MIR-4493 | 99.90 | 66.48 | 977 |
| HSA-MIR-3133 | 99.81 | 70.92 | 3506 |
| HSA-MIR-586 | 99.65 | 70.40 | 2051 |
| HSA-MIR-5006-5P | 98.79 | 66.92 | 1246 |
| HSA-MIR-5572 | 98.55 | 65.84 | 970 |
| HSA-MIR-6819-5P | 97.96 | 66.59 | 1071 |
| HSA-MIR-3151-3P | 97.80 | 66.16 | 479 |
| HSA-MIR-6737-5P | 97.75 | 66.54 | 1044 |
| HSA-MIR-6812-5P | 97.56 | 65.39 | 1059 |
| HSA-MIR-3674 | 97.01 | 68.86 | 1171 |
| HSA-MIR-6747-5P | 96.17 | 64.99 | 743 |
Cross-species orthologs
4 orthologs
| Organism | Symbol | Gene ID |
|---|---|---|
| mus_musculus | Ct45a | ENSMUSG00000064016 |
| rattus_norvegicus | Ct45a9 | ENSRNOG00000048059 |
| drosophila_melanogaster | IntS6 | FBGN0261383 |
| caenorhabditis_elegans | WBGENE00000994 |
Paralogs (11): INTS6 (ENSG00000102786), INTS6L (ENSG00000165359), SAGE1 (ENSG00000181433), CT45A5 (ENSG00000228836), CT45A1 (ENSG00000268940), CT45A3 (ENSG00000269096), CT45A10 (ENSG00000269586), CT45A9 (ENSG00000270946), CT45A2 (ENSG00000271449), CT45A8 (ENSG00000278085), CT45A6 (ENSG00000278289)
Protein
Protein identifiers
Cancer/testis antigen family 45 member A7 — P0DMV0 (reviewed: P0DMV0)
Alternative names: Cancer/testis antigen 45A7
All UniProt accessions (1): P0DMV0
UniProt curated annotations — full annotation on UniProt →
Similarity. Belongs to the CT45 family.
RefSeq proteins (2): NP_001278472, NP_001381597* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR029307 | INT_SG_DDX_CT_C | Domain |
| IPR051113 | Integrator_subunit6 | Family |
Pfam: PF15300
UniProt features (4 total): region of interest 2, chain 1, compositionally biased region 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-P0DMV0-F1 | 70.05 | 0.22 |
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
0 interactions, top by confidence (×1000):
IntAct
2 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| CT45A7 | SDCBP2 | psi-mi:“MI:0915”(physical association) | 0.370 |
ESM2 similar proteins: A0FKI7, A2YX04, A5WUN7, A5WV69, A7J1T2, C5DZR8, E9Q555, F4J6F6, O43310, O48767, P0DMS1, P0DMU7, P0DMU8, P0DMU9, P0DMV0, P0DMV1, P0DMV2, Q0V9S3, Q12912, Q14693, Q1LXZ9, Q2NKQ1, Q2PFD7, Q3TEL6, Q502L1, Q5DJT8, Q5R7V3, Q5T8D3, Q5XG73, Q621Z7, Q640U0, Q641E3, Q6IRN6, Q6Z8M8, Q700C2, Q758T8, Q80Y56, Q811D2, Q8AV28, Q8BLN6
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
0 variants total. Per-class counts are floors (≥ shown; pagination cap):
| Classification | Count (floor) |
|---|---|
| Pathogenic | 0 |
| Likely pathogenic | 0 |
| Uncertain significance | 0 |
| Likely benign | 0 |
| Benign | 0 |
Top pathogenic / likely-pathogenic (0)
SpliceAI
819 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| X:135830719:CACCT:C | donor_loss | 1.0000 |
| X:135830720:A:AC | donor_gain | 1.0000 |
| X:135830720:A:AT | donor_loss | 1.0000 |
| X:135830721:C:CC | donor_gain | 1.0000 |
| X:135830721:C:CG | donor_loss | 1.0000 |
| X:135830721:CCTTG:C | donor_gain | 1.0000 |
| X:135830731:T:TA | donor_gain | 1.0000 |
| X:135830811:ATATT:A | acceptor_gain | 1.0000 |
| X:135830812:TATT:T | acceptor_gain | 1.0000 |
| X:135830813:ATT:A | acceptor_gain | 1.0000 |
| X:135830814:TT:T | acceptor_gain | 1.0000 |
| X:135830815:TC:T | acceptor_loss | 1.0000 |
| X:135830816:C:CA | acceptor_loss | 1.0000 |
| X:135830816:C:CC | acceptor_gain | 1.0000 |
| X:135830822:A:AC | acceptor_gain | 1.0000 |
| X:135830822:A:C | acceptor_gain | 1.0000 |
| X:135830825:T:C | acceptor_gain | 1.0000 |
| X:135830825:T:TC | acceptor_gain | 1.0000 |
| X:135831444:CT:C | acceptor_gain | 1.0000 |
| X:135833364:CT:C | donor_gain | 1.0000 |
| X:135830824:G:C | acceptor_gain | 0.9900 |
| X:135830824:G:GC | acceptor_gain | 0.9900 |
| X:135830848:T:TC | acceptor_gain | 0.9900 |
| X:135831441:AAGCT:A | acceptor_gain | 0.9900 |
| X:135831442:AGCT:A | acceptor_gain | 0.9900 |
| X:135831443:GCT:G | acceptor_gain | 0.9900 |
| X:135831443:GCTC:G | acceptor_loss | 0.9900 |
| X:135831443:GCTCT:G | acceptor_gain | 0.9900 |
| X:135831444:CTC:C | acceptor_gain | 0.9900 |
| X:135831445:TCTG:T | acceptor_gain | 0.9900 |
AlphaMissense
1259 scored. Top likely-pathogenic:
| Variant | Protein change | am_pathogenicity |
|---|---|---|
| X:135830729:C:G | A169P | 0.881 |
| X:135830799:G:C | F145L | 0.852 |
| X:135830799:G:T | F145L | 0.852 |
| X:135830801:A:G | F145L | 0.852 |
| X:135831234:T:A | K127N | 0.840 |
| X:135831234:T:G | K127N | 0.840 |
| X:135830777:C:G | G153R | 0.836 |
| X:135830777:C:T | G153R | 0.836 |
| X:135833486:A:C | F16L | 0.835 |
| X:135833486:A:T | F16L | 0.835 |
| X:135833488:A:G | F16L | 0.835 |
| X:135830748:A:C | F162L | 0.823 |
| X:135830748:A:T | F162L | 0.823 |
| X:135830750:A:G | F162L | 0.823 |
| X:135830791:A:T | L148H | 0.766 |
| X:135831246:A:C | N123K | 0.763 |
| X:135831246:A:T | N123K | 0.763 |
| X:135830751:A:C | F161L | 0.762 |
| X:135830751:A:T | F161L | 0.762 |
| X:135830753:A:G | F161L | 0.762 |
| X:135830752:A:G | F161S | 0.730 |
| X:135833444:C:A | R30S | 0.719 |
| X:135833444:C:G | R30S | 0.719 |
| X:135831226:A:G | L130S | 0.713 |
| X:135829479:A:C | F177L | 0.703 |
| X:135829479:A:T | F177L | 0.703 |
| X:135829481:A:G | F177L | 0.703 |
| X:135830744:A:G | S164P | 0.702 |
| X:135829468:A:G | L181P | 0.699 |
| X:135830776:C:T | G153E | 0.698 |
dbSNP variants (sampled 264 via entrez): RS112696531 (X:135838954 A>G), RS1159476873 (X:135835081 G>C), RS1163535156 (X:135836052 A>T), RS1166663895 (X:135836151 A>C), RS1174654523 (X:135829393 C>T), RS1180746038 (X:135835289 G>C), RS1182372781 (X:135834487 A>C), RS1186522071 (X:135835760 A>T), RS1199750847 (X:135828857 G>A), RS1200592531 (X:135828760 A>ACACC), RS1203141885 (X:135834937 T>C), RS1205237826 (X:135828808 T>C), RS1209370400 (X:135834707 G>A), RS1209643029 (X:135835848 A>C,G), RS1227805553 (X:135835861 AT>A)
Disease associations
OMIM: gene `` | 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)
Clinical trials (associated diseases)
0 trials via MONDO — disease-level, not drug-specific.
Related Atlas pages
No linked Atlas pages yet — the cross-entity mesh grows as the corpus expands.