TCEAL8

gene
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Also known as MGC45400WEX3

Summary

TCEAL8 (transcription elongation factor A like 8, HGNC:28683) is a protein-coding gene on chromosome Xq22.1, encoding Transcription elongation factor A protein-like 8 (Q8IYN2). May be involved in transcriptional regulation.

This gene encodes a member of the transcription elongation factor A (SII)-like (TCEAL) gene family. Members of this family contain TFA domains and may function as nuclear phosphoproteins that modulate transcription in a promoter context-dependent manner. Multiple family members are located on the X chromosome. Alternative splicing results in multiple transcript variants encoding a single isoform.

Source: NCBI Gene 90843 — RefSeq curated summary.

At a glance

  • Clinical variants (ClinVar): 17 total
  • MANE Select transcript: NM_153333

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:28683
Approved symbolTCEAL8
Nametranscription elongation factor A like 8
LocationXq22.1
Locus typegene with protein product
StatusApproved
AliasesMGC45400, WEX3
Ensembl geneENSG00000180964
Ensembl biotypeprotein_coding
OMIM301157
Entrez90843

Gene structure

Transcript identifiers

Ensembl transcripts: 15 — 15 protein_coding

ENST00000360000, ENST00000372685, ENST00000451678, ENST00000866567, ENST00000866568, ENST00000866569, ENST00000866570, ENST00000866571, ENST00000918610, ENST00000918611, ENST00000918612, ENST00000918613, ENST00000918614, ENST00000918615, ENST00000918616

RefSeq mRNA: 2 — MANE Select: NM_153333 NM_001006684, NM_153333

CCDS: CCDS14504

Canonical transcript exons

ENST00000372685 — 3 exons

ExonStartEnd
ENSE00001263715103254605103254677
ENSE00001419203103252995103254017
ENSE00001815787103255078103255155

Expression profiles

Bgee: expression breadth ubiquitous, 252 present calls, max score 97.57.

FANTOM5 (CAGE): breadth ubiquitous, TPM avg 67.0269 / max 1706.3043, expressed in 1743 samples.

FANTOM5 promoters (3 alternative TSS)

Promoter IDTPM avgSamples expressed
19998164.16441738
1999831.7746970
1999821.0879751

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
calcaneal tendonUBERON:000370197.57gold quality
islet of LangerhansUBERON:000000697.56gold quality
corpus epididymisUBERON:000435997.40gold quality
adrenal tissueUBERON:001830397.26gold quality
smooth muscle tissueUBERON:000113596.86gold quality
gall bladderUBERON:000211096.60gold quality
cardiac muscle of right atriumUBERON:000337996.39gold quality
descending thoracic aortaUBERON:000234596.30gold quality
caput epididymisUBERON:000435895.96gold quality
left ventricle myocardiumUBERON:000656695.87gold quality
stromal cell of endometriumCL:000225595.81gold quality
Brodmann (1909) area 9UBERON:001354095.74gold quality
thoracic aortaUBERON:000151595.63gold quality
ascending aortaUBERON:000149695.58gold quality
adenohypophysisUBERON:000219695.58gold quality
prefrontal cortexUBERON:000045195.51gold quality
olfactory segment of nasal mucosaUBERON:000538695.46gold quality
ganglionic eminenceUBERON:000402395.43gold quality
rectumUBERON:000105295.38gold quality
C1 segment of cervical spinal cordUBERON:000646995.33gold quality
right coronary arteryUBERON:000162595.28gold quality
cauda epididymisUBERON:000436095.24gold quality
anterior cingulate cortexUBERON:000983595.19gold quality
aortaUBERON:000094794.97gold quality
left coronary arteryUBERON:000162694.89gold quality
ventricular zoneUBERON:000305394.88gold quality
right atrium auricular regionUBERON:000663194.83gold quality
dorsolateral prefrontal cortexUBERON:000983494.81gold quality
right adrenal gland cortexUBERON:003582794.74gold quality
right adrenal glandUBERON:000123394.73gold quality

Single-cell (SCXA)

Detected in 2 experiment(s), a significant marker in 1.

ExperimentMarker?Max mean expression
E-CURD-112no2.59
E-ANND-3no0.00

Regulation

Is transcription factor: no

miRNA regulators (miRDB)

85 targeting TCEAL8, 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-4668-3P100.0068.742635
HSA-MIR-8485100.0077.574731
HSA-MIR-6867-5P100.0082.213464
HSA-MIR-548N99.9871.944170
HSA-MIR-1213699.9872.815713
HSA-MIR-548P99.9872.253784
HSA-MIR-570-3P99.9672.414910
HSA-MIR-548AB99.9571.313488
HSA-MIR-55999.9572.283609
HSA-MIR-548A-5P99.9471.273482
HSA-MIR-548AD-5P99.9471.233502
HSA-MIR-548AE-5P99.9471.233502
HSA-MIR-548AK99.9471.243488
HSA-MIR-548AM-5P99.9471.243488
HSA-MIR-548AP-5P99.9471.143489
HSA-MIR-548AQ-5P99.9471.343426
HSA-MIR-548AR-5P99.9471.283515
HSA-MIR-548AS-5P99.9471.223482
HSA-MIR-548AU-5P99.9471.243488
HSA-MIR-548AY-5P99.9471.233502
HSA-MIR-548B-5P99.9471.233502
HSA-MIR-548BB-5P99.9471.273509
HSA-MIR-548C-5P99.9471.243488
HSA-MIR-548D-5P99.9471.233502
HSA-MIR-548H-5P99.9471.243488
HSA-MIR-548I99.9471.253481
HSA-MIR-548J-5P99.9471.143489
HSA-MIR-548O-5P99.9471.243488
HSA-MIR-548W99.9471.243488
HSA-MIR-548Y99.9471.283514

Literature-anchored findings (GeneRIF, showing 1)

  • Characterizes TCEAL1, another member of the human TCEAL gene family. (PMID:10051408)

Cross-species orthologs

2 orthologs

OrganismSymbolGene ID
mus_musculusTceal8ENSMUSG00000051579
rattus_norvegicusTceal8ENSRNOG00000028585

Paralogs (8): TCEAL4 (ENSG00000133142), TCEAL1 (ENSG00000172465), TCEAL7 (ENSG00000182916), TCEAL2 (ENSG00000184905), TCEAL9 (ENSG00000185222), TCEAL3 (ENSG00000196507), TCEAL5 (ENSG00000204065), TCEAL6 (ENSG00000204071)

Protein

Protein identifiers

Transcription elongation factor A protein-like 8Q8IYN2 (reviewed: Q8IYN2)

Alternative names: Transcription elongation factor S-II protein-like 8

All UniProt accessions (2): Q8IYN2, Q5H9L1

UniProt curated annotations — full annotation on UniProt →

Function. May be involved in transcriptional regulation.

Subcellular location. Nucleus.

Similarity. Belongs to the TFS-II family. TFA subfamily.

RefSeq proteins (2): NP_001006685, NP_699164* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR021156TF_A-like/BEXFamily

Pfam: PF04538

UniProt features (5 total): compositionally biased region 2, chain 1, region of interest 1, coiled-coil region 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-Q8IYN2-F166.960.16

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 106 (showing top): BENPORATH_ES_WITH_H3K27ME3, STARK_PREFRONTAL_CORTEX_22Q11_DELETION_DN, KOYAMA_SEMA3B_TARGETS_UP, SHETH_LIVER_CANCER_VS_TXNIP_LOSS_PAM2, AACTTT_UNKNOWN, PIT1_Q6, GTAAACC_MIR2995P, WANG_SMARCE1_TARGETS_UP, TCANNTGAY_SREBP1_01, MIKKELSEN_ES_ICP_WITH_H3K4ME3, MIKKELSEN_NPC_ICP_WITH_H3K4ME3, THILLAINADESAN_ZNF217_TARGETS_DN, chrXq22, PASINI_SUZ12_TARGETS_DN, RAO_BOUND_BY_SALL4_ISOFORM_B

GO Biological Process (0):

GO Molecular Function (1): protein binding (GO:0005515)

GO Cellular Component (1): nucleus (GO:0005634)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
binding1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

224 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TCEAL8TCEAL5Q5H9L2678
TCEAL8BEX3Q00994530
TCEAL8TCEAL3Q969E4521
TCEAL8TCEAL2Q9H3H9490
TCEAL8TCEAL4Q96EI5464
TCEAL8BEX2Q9BXY8426
TCEAL8BEX1Q9HBH7424
TCEAL8TCEANC2Q96MN5392
TCEAL8SPMIP5Q8WW14371
TCEAL8TMEM234Q8WY98370
TCEAL8RPP21Q9H633349
TCEAL8TACO1Q9BSH4344
TCEAL8TCEA1P23193336
TCEAL8SUPT5HO00267316
TCEAL8MRPL16Q9NX20308

IntAct

42 interactions, top by confidence:

ABTypeScore
KRT31HGSpsi-mi:“MI:0914”(association)0.780
TCEAL8CCDC24psi-mi:“MI:0915”(physical association)0.560
TCEAL8COMMD1psi-mi:“MI:0915”(physical association)0.560
TCEAL8CD209psi-mi:“MI:0915”(physical association)0.560
GRNTCEAL8psi-mi:“MI:0915”(physical association)0.560
TCEAL8HSPB1psi-mi:“MI:0915”(physical association)0.560
TCEAL8WFS1psi-mi:“MI:0915”(physical association)0.560
TCEAL8YARS1psi-mi:“MI:0915”(physical association)0.560
KIF1BTCEAL8psi-mi:“MI:0915”(physical association)0.560
RNF11TCEAL8psi-mi:“MI:0915”(physical association)0.560
TCEAL8SPRED1psi-mi:“MI:0915”(physical association)0.560
MAGEA4MAGEB16psi-mi:“MI:0914”(association)0.530
MAGEA4MAGEA8psi-mi:“MI:0914”(association)0.530
S100A2PLEKHG3psi-mi:“MI:0914”(association)0.350
S100PPLEKHG3psi-mi:“MI:0914”(association)0.350
MAGEA9CIBAR1psi-mi:“MI:0914”(association)0.350

BioGRID (19): TCEAL8 (Affinity Capture-RNA), TCEAL8 (Two-hybrid), TCEAL8 (Two-hybrid), TCEAL8 (Two-hybrid), TCEAL8 (Affinity Capture-MS), TCEAL8 (Affinity Capture-MS), TCEAL8 (Affinity Capture-MS), TCEAL8 (Affinity Capture-MS), TCEAL8 (Affinity Capture-MS), TCEAL8 (Affinity Capture-MS), TCEAL8 (Affinity Capture-MS), TCEAL8 (Affinity Capture-MS), TCEAL8 (Affinity Capture-MS), TCEAL8 (Proximity Label-MS), TCEAL8 (Affinity Capture-MS)

ESM2 similar proteins: A1L429, A6NDE8, A6NER3, A6NGK3, O41801, O55777, O60829, O75459, O76087, P03204, P04611, P06937, P0CL80, P0CL81, P0CL82, P0DSO3, P0DTW1, P18804, P22421, P86478, P86479, P86480, P86481, P86496, Q13066, Q13069, Q13070, Q2T9P9, Q3KST0, Q4V321, Q4V326, Q5JRK9, Q5JUK9, Q6AY45, Q6I7R5, Q6IPX3, Q6NT46, Q7Z2X7, Q8AIH8, Q8CCT4

Diamond homologs: A1YEW9, A2D4U8, A2D5N1, A2D671, A2T6K9, Q15170, Q2KIJ9, Q3T020, Q5PPP3, Q6I7R5, Q8IYN2, Q921P9, Q9CZY2, Q9DD24, Q9UHQ7, A3KGA4, D3ZT37, Q9BRU2

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance14
Likely benign1
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

271 predictions. Top by Δscore:

VariantEffectΔscore
X:103255074:TAA:Tdonor_loss0.9900
X:103255075:AACCT:Adonor_loss0.9900
X:103255076:A:AGdonor_loss0.9900
X:103254013:TAATC:Tacceptor_gain0.9800
X:103254018:C:CAacceptor_loss0.9800
X:103254018:C:CCacceptor_gain0.9800
X:103254019:T:Aacceptor_loss0.9800
X:103255076:A:ACdonor_gain0.9800
X:103255077:C:CCdonor_gain0.9800
X:103254016:TC:Tacceptor_gain0.9600
X:103254017:CC:Cacceptor_gain0.9600
X:103254015:ATC:Aacceptor_gain0.9300
X:103254676:TC:Tacceptor_gain0.9100
X:103254677:CC:Cacceptor_gain0.9100
X:103254015:ATCCT:Aacceptor_gain0.8900
X:103254014:AATC:Aacceptor_gain0.8800
X:103254676:TCCT:Tacceptor_loss0.8400
X:103254678:C:Aacceptor_loss0.8400
X:103254678:C:CCacceptor_gain0.8400
X:103254679:TG:Tacceptor_loss0.8400
X:103254680:G:Cacceptor_loss0.8400
X:103254685:CAGA:Cacceptor_loss0.8400
X:103254688:A:Cacceptor_loss0.8400
X:103254674:TATC:Tacceptor_gain0.8300
X:103254955:T:TAdonor_gain0.8300
X:103254600:CTGA:Cdonor_loss0.8000
X:103254601:TGACC:Tdonor_loss0.8000
X:103254602:GA:Gdonor_loss0.8000
X:103254016:TCCT:Tacceptor_gain0.7900
X:103254597:AAACT:Adonor_loss0.7900

AlphaMissense

780 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
X:103253701:T:AR93S0.996
X:103253701:T:GR93S0.996
X:103253695:C:AK95N0.993
X:103253695:C:GK95N0.993
X:103253702:C:AR93I0.993
X:103253692:A:CF96L0.992
X:103253692:A:TF96L0.992
X:103253694:A:GF96L0.992
X:103253702:C:GR93T0.992
X:103253674:C:AK102N0.986
X:103253674:C:GK102N0.986
X:103253693:A:GF96S0.986
X:103253677:C:AW101C0.983
X:103253677:C:GW101C0.983
X:103253710:T:AR90S0.983
X:103253710:T:GR90S0.983
X:103253696:T:AK95M0.982
X:103253697:T:CK95E0.982
X:103253717:T:AE88V0.981
X:103253718:C:TE88K0.977
X:103253635:A:CF115L0.975
X:103253635:A:TF115L0.975
X:103253637:A:GF115L0.975
X:103253679:A:GW101R0.973
X:103253679:A:TW101R0.973
X:103253693:A:CF96C0.973
X:103253675:T:GK102T0.972
X:103253697:T:GK95Q0.972
X:103253722:C:AR86S0.970
X:103253722:C:GR86S0.970

dbSNP variants (sampled 300 via entrez): RS1004376515 (X:103253967 A>C), RS1006805737 (X:103253577 T>A,G), RS1007443776 (X:103254380 C>G), RS1008484324 (X:103256630 TGAGA>T), RS1008944785 (X:103256597 C>A), RS1012544284 (X:103257060 C>T), RS1013047769 (X:103255786 T>G), RS1013796191 (X:103254914 T>C), RS1015022073 (X:103256640 C>A,G), RS1015359020 (X:103254464 G>A), RS1016553581 (X:103255109 C>T), RS1016850245 (X:103255821 A>G), RS1017238250 (X:103256654 A>G), RS1020407154 (X:103254479 C>T), RS1020853345 (X:103253848 C>T)

Disease associations

OMIM: gene MIM:301157 | 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

44 total (human), top 30 by PubMed support.

ChemicalActions (top 5)PubMed papers
sodium arseniteincreases methylation, decreases expression, increases expression3
Acetaminophendecreases expression2
Valproic Acidaffects expression, decreases expression2
bisphenol Faffects cotreatment, increases expression1
dicrotophosdecreases expression1
propionaldehydeincreases expression1
bisphenol Aaffects expression1
beta-lapachonedecreases expression1
tris(1,3-dichloro-2-propyl)phosphatedecreases expression1
butyraldehydeincreases expression1
manganese chlorideincreases abundance, increases expression1
potassium chromate(VI)affects cotreatment, decreases expression1
S-(1,2-dichlorovinyl)cysteineaffects response to substance, increases expression1
beta-methylcholineaffects expression1
epigallocatechin gallatedecreases expression, affects cotreatment1
di-n-butylphosphoric acidaffects expression1
perfluorooctane sulfonic acidincreases expression1
CGP 52608affects binding, increases reaction1
2-palmitoylglycerolincreases expression1
K 7174decreases expression1
ICG 001decreases expression1
abrinedecreases expression1
jinfukangaffects cotreatment, increases expression1
Temozolomidedecreases expression1
Air Pollutantsincreases abundance, decreases expression1
Benzo(a)pyreneaffects methylation1
Cisplatinaffects cotreatment, increases expression1
Dexamethasoneaffects cotreatment, increases expression1
Doxorubicinincreases expression1
Estradioldecreases expression1

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.