CT47A11
gene geneOn this page
Also known as CT47.11
Summary
CT47A11 (cancer/testis antigen family 47 member A11, HGNC:27397) is a protein-coding gene on chromosome Xq24, encoding Cancer/testis antigen 47A (Q5JQC4).
This locus represents a member of the cancer/testis gene family 47. This family, also known as CT47, is comprised of 13 nearly identical loci clustered at Xq24.
Source: NCBI Gene 255313 — RefSeq curated summary.
At a glance
- MANE Select transcript:
NM_173571
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:27397 |
| Approved symbol | CT47A11 |
| Name | cancer/testis antigen family 47 member A11 |
| Location | Xq24 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | CT47.11 |
| Ensembl gene | ENSG00000226929 |
| Ensembl biotype | protein_coding |
| OMIM | 300592 |
| Entrez | 255313 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 protein_coding
ENST00000457020
RefSeq mRNA: 1 — MANE Select: NM_173571
NM_173571
CCDS: CCDS35381
Canonical transcript exons
ENST00000457020 — 3 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001737067 | 120935119 | 120935274 |
| ENSE00001839061 | 120933840 | 120933980 |
| ENSE00001891561 | 120936162 | 120937158 |
Expression profiles
Bgee: expression breadth broad, 12 present calls, max score 86.47.
Top tissues by expression
127 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 | 86.47 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 75.65 | silver quality |
| right testis | UBERON:0004534 | 54.20 | gold quality |
| testis | UBERON:0000473 | 53.33 | gold quality |
| left testis | UBERON:0004533 | 53.00 | 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 |
| skeletal muscle tissue | UBERON:0001134 | 33.38 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 32.15 | gold quality |
| bone marrow | UBERON:0002371 | 31.74 | gold quality |
| muscle tissue | UBERON:0002385 | 31.06 | gold quality |
| sural nerve | UBERON:0015488 | 30.93 | gold quality |
| stromal cell of endometrium | CL:0002255 | 29.87 | gold quality |
| prefrontal cortex | UBERON:0000451 | 29.19 | gold quality |
| placenta | UBERON:0001987 | 29.10 | gold quality |
| liver | UBERON:0002107 | 28.49 | gold quality |
| duodenum | UBERON:0002114 | 28.14 | gold quality |
| lymph node | UBERON:0000029 | 27.57 | gold quality |
| tonsil | UBERON:0002372 | 27.05 | gold quality |
| islet of Langerhans | UBERON:0000006 | 26.55 | gold quality |
| vermiform appendix | UBERON:0001154 | 26.42 | gold quality |
| leukocyte | CL:0000738 | 26.10 | gold quality |
| gall bladder | UBERON:0002110 | 25.98 | gold quality |
| monocyte | CL:0000576 | 25.95 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 25.89 | gold quality |
| urinary bladder | UBERON:0001255 | 25.72 | gold quality |
| adrenal tissue | UBERON:0018303 | 25.39 | gold quality |
Single-cell (SCXA)
Detected in 3 experiment(s), a significant marker in 2.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-GEOD-36552 | yes | 62.36 |
| E-GEOD-134144 | yes | 31.23 |
| E-ANND-3 | no | 0.00 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
14 targeting CT47A11, 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-5696 | 99.98 | 72.36 | 4487 |
| HSA-MIR-495-3P | 99.96 | 72.81 | 4197 |
| HSA-MIR-5688 | 99.96 | 73.23 | 4504 |
| HSA-MIR-6505-5P | 99.73 | 69.25 | 1595 |
| HSA-MIR-1290 | 99.59 | 69.90 | 2079 |
| HSA-MIR-190A-5P | 99.54 | 71.45 | 933 |
| HSA-MIR-190B-5P | 99.54 | 71.40 | 925 |
| HSA-MIR-12123 | 99.52 | 71.79 | 2990 |
| HSA-MIR-664A-3P | 99.22 | 71.08 | 2696 |
| HSA-MIR-653-3P | 98.31 | 67.71 | 1542 |
| HSA-MIR-6773-3P | 98.17 | 65.51 | 1213 |
| HSA-MIR-6839-5P | 96.74 | 68.29 | 1088 |
| HSA-MIR-378J | 96.44 | 66.20 | 1020 |
| HSA-MIR-6760-3P | 96.35 | 68.31 | 1001 |
Literature-anchored findings (GeneRIF, showing 1)
- CT47 expression was found in approximately 15% of lung cancer and esophageal cancer specimens, but not in colorectal cancer or breast cancer. The putative CT47 protein consists of 288 amino acid, with a C-terminus rich in alanine and glutamic acid. (PMID:16382448)
Cross-species orthologs
0 orthologs
Paralogs (13): CT47A10 (ENSG00000224089), CT47A6 (ENSG00000226023), CT47A9 (ENSG00000226600), CT47A12 (ENSG00000226685), CT47A7 (ENSG00000228517), CT47A8 (ENSG00000230347), CT47A4 (ENSG00000230594), CT47A3 (ENSG00000236126), CT47A1 (ENSG00000236371), CT47B1 (ENSG00000236446), CT47A5 (ENSG00000237957), CT47A2 (ENSG00000242362), CT47C1 (ENSG00000277535)
Protein
Protein identifiers
Cancer/testis antigen 47A — Q5JQC4 (reviewed: Q5JQC4)
Alternative names: Cancer/testis antigen 47
All UniProt accessions (1): Q5JQC4
UniProt curated annotations — full annotation on UniProt →
Tissue specificity. Strongly expressed in testis, low expression in placenta, and very low expression in brain.
RefSeq proteins (1): NP_775842* (*=MANE)
Domains & families (InterPro)
| ID | Name | Type |
|---|---|---|
| IPR028930 | CT47 | Family |
Pfam: PF15623
UniProt features (14 total): compositionally biased region 9, region of interest 2, chain 1, sequence conflict 1, coiled-coil region 1
Structure
Experimental structures (PDB)
0 structures.
Predicted structure (AlphaFold)
| Model | pLDDT | Fraction very-high |
|---|---|---|
| AF-Q5JQC4-F1 | 53.93 | 0.00 |
Function
Pathways and Gene Ontology
Reactome pathways
0 pathways
MSigDB gene sets: 6 (showing top):
chrXq24, MIR5696, MIR12123, MIR664A_3P, FOURATI_BLOOD_TWINRIX_AGE_25_83YO_RESPONDERS_VS_POOR_RESPONDERS_0DY_UP, ZHOU_INFLAMMATORY_RESPONSE_LPS_UP
GO Biological Process (0):
GO Molecular Function (0):
GO Cellular Component (0):
Protein interactions and networks
STRING
350 interactions, top by confidence (×1000):
| Protein A | Protein B | Partner UniProt | Score |
|---|---|---|---|
| CT47A11 | GPHRA | B7ZAQ6 | 952 |
| CT47A11 | TAF11L5 | A0A1W2PP81 | 654 |
| CT47A11 | TAF11L4 | A0A1W2PPE2 | 654 |
| CT47A11 | TAF11L3 | A0A1W2PRV1 | 654 |
| CT47A11 | TAF11L2 | A6NLC8 | 620 |
| CT47A11 | CTAG2 | O75638 | 616 |
| CT47A11 | CT45A1 | Q5HYN5 | 602 |
| CT47A11 | MAGEA1 | P43355 | 584 |
| CT47A11 | A0A1W2PRN6 | A0A1W2PRN6 | 544 |
| CT47A11 | CT55 | Q8WUE5 | 522 |
| CT47A11 | PRR20A | P86496 | 522 |
| CT47A11 | A0A1W2PQG5 | A0A1W2PQG5 | 520 |
| CT47A11 | SPANXA1 | Q9NS26 | 507 |
| CT47A11 | CSAG2 | Q9Y5P2 | 507 |
| CT47A11 | USP17L23 | D6RBM5 | 506 |
IntAct
3 interactions, top by confidence:
| A | B | Type | Score |
|---|---|---|---|
| CSAG2 | CAMK2D | psi-mi:“MI:0914”(association) | 0.350 |
| NXT2 | MYO1G | psi-mi:“MI:0914”(association) | 0.350 |
BioGRID (15): CT47A3 (Positive Genetic), CT47A2 (Positive Genetic), CT47A6 (Positive Genetic), CT47A5 (Positive Genetic), CT47A1 (Positive Genetic), CT47A7 (Positive Genetic), CT47A11 (Positive Genetic), CT47A4 (Positive Genetic), CT47A10 (Positive Genetic), CT47A12 (Positive Genetic), CT47A9 (Positive Genetic), CT47A8 (Positive Genetic), CT47A6 (Negative Genetic), CT47A3 (Negative Genetic), CT47A1 (Affinity Capture-MS)
ESM2 similar proteins: A0A0U1RQG5, A1L429, A6NDE8, A6NER3, A6NGK3, E1AZ71, O08664, O60829, O75459, O76087, P0C2W7, P0CL80, P0CL81, P0CL82, P0DSO3, P0DTW1, P52651, P62521, P86478, P86479, P86480, P86481, P86496, Q13066, Q13069, Q13070, Q17QW4, Q28181, Q2T9P9, Q32PA2, Q4V321, Q4V326, Q5JQC4, Q5U2Y8, Q62100, Q63803, Q64256, Q6NT46, Q6X7S9, Q7Z2X7
Diamond homologs: A0A0U1RQG5, P0C2W7, Q5JQC4
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
643 predictions. Top by Δscore:
| Variant | Effect | Δscore |
|---|---|---|
| X:120933878:A:C | donor_gain | 1.0000 |
| X:120933881:TGA:T | donor_gain | 1.0000 |
| X:120936179:T:TA | donor_gain | 1.0000 |
| X:120933881:TGAAC:T | donor_gain | 0.9900 |
| X:120933896:ACAT:A | donor_gain | 0.9900 |
| X:120933897:CAT:C | donor_gain | 0.9900 |
| X:120933897:CATC:C | donor_gain | 0.9900 |
| X:120933899:T:TA | donor_gain | 0.9900 |
| X:120933925:A:AC | donor_gain | 0.9900 |
| X:120935272:CTT:C | acceptor_gain | 0.9900 |
| X:120935277:T:C | acceptor_gain | 0.9900 |
| X:120935277:T:TC | acceptor_gain | 0.9900 |
| X:120935306:C:CT | acceptor_gain | 0.9900 |
| X:120936160:AC:A | donor_gain | 0.9900 |
| X:120936161:CC:C | donor_gain | 0.9900 |
| X:120936161:CCCT:C | donor_gain | 0.9900 |
| X:120935275:C:CC | acceptor_gain | 0.9800 |
| X:120935276:T:C | acceptor_gain | 0.9800 |
| X:120936156:CCTTA:C | donor_loss | 0.9700 |
| X:120936157:CTTAC:C | donor_loss | 0.9700 |
| X:120936158:TTA:T | donor_loss | 0.9700 |
| X:120936159:TA:T | donor_loss | 0.9700 |
| X:120936160:A:AG | donor_loss | 0.9700 |
| X:120936161:C:CA | donor_loss | 0.9700 |
| X:120933896:A:AC | donor_gain | 0.9600 |
| X:120933897:C:CC | donor_gain | 0.9600 |
| X:120935270:GACTT:G | acceptor_gain | 0.9600 |
| X:120935135:TC:T | donor_gain | 0.9500 |
| X:120935632:T:TG | acceptor_gain | 0.9500 |
| X:120935311:A:C | acceptor_gain | 0.9400 |
AlphaMissense
0 scored. Top likely-pathogenic:
dbSNP variants (sampled 138 via entrez): RS111897421 (X:120933526 C>A), RS112187612 (X:120961549 T>C), RS1161215653 (X:120960524 TGTGGCTGG>T), RS1173923429 (X:120960523 C>A), RS1178078523 (X:120960530 T>C), RS1197669488 (X:120960565 C>T), RS1225955136 (X:120960538 C>G), RS1233264210 (X:120960545 T>C), RS1238535920 (X:120960571 G>A), RS1244521626 (X:120960502 C>A,T), RS1253712605 (X:120960478 G>A), RS1264478689 (X:120960559 C>T), RS1299893650 (X:120960541 C>T), RS1309004824 (X:120960437 G>A), RS1337478774 (X:120960530 TG>T,TGG)
Disease associations
OMIM: gene MIM:300592 | 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
2 total (human), top 2 by PubMed support.
| Chemical | Actions (top 5) | PubMed papers |
|---|---|---|
| butyraldehyde | increases expression | 1 |
| Copper Sulfate | affects expression | 1 |
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.