TAF11L5

gene
On this page

Summary

TAF11L5 (TATA-box binding protein associated factor 11 like 5, HGNC:53848) is a protein-coding gene on chromosome 5p15.1, encoding TATA-box-binding protein-associated factor 11-like protein 5 (A0A1W2PP81).

Predicted to enable protein heterodimerization activity. Predicted to contribute to RNA polymerase II general transcription initiation factor activity. Predicted to be involved in RNA polymerase II preinitiation complex assembly. Predicted to be located in nucleus. Predicted to be part of transcription factor TFIID complex.

Source: NCBI Gene 646066 — RefSeq curated summary.

At a glance

  • MANE Select transcript: NM_001401699

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:53848
Approved symbolTAF11L5
NameTATA-box binding protein associated factor 11 like 5
Location5p15.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000284234
Ensembl biotypeprotein_coding
Entrez646066

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000638483

RefSeq mRNA: 29 — MANE Select: NM_001401699 NM_001401699, NM_001421810, NM_001421811, NM_001421812, NM_001421819, NM_001421828, NM_001421829, NM_001421831, NM_001421834, NM_001421835, NM_001421836, NM_001421837, NM_001421840, NM_001421841, NM_001421842, NM_001421843, NM_001421844, NM_001421845, NM_001421846, NM_001421847, NM_001421848, NM_001421849, NM_001421850, NM_001421851, NM_001421852, NM_001421853, NM_001421854, NM_001421855, NM_001421856

CCDS: CCDS93691

Canonical transcript exons

ENST00000638483 — 1 exons

ExonStartEnd
ENSE000038109801752523517525831

Expression profiles

Bgee: expression breadth broad, 19 present calls, max score 48.13.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
sural nerveUBERON:001548848.13gold quality
left testisUBERON:000453342.46gold quality
testisUBERON:000047341.32gold quality
right testisUBERON:000453440.54gold quality
colonic epitheliumUBERON:000039737.20gold quality
ganglionic eminenceUBERON:000402337.14gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
monocyteCL:000057636.14gold quality
leukocyteCL:000073835.37gold quality
hindlimb stylopod muscleUBERON:000425235.27gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
bloodUBERON:000017832.33gold quality
bone marrowUBERON:000237131.74gold quality
muscle tissueUBERON:000238531.06gold quality
prefrontal cortexUBERON:000045129.95gold quality
stromal cell of endometriumCL:000225529.87gold quality
cortex of kidneyUBERON:000122528.83gold quality
liverUBERON:000210728.31gold quality
duodenumUBERON:000211428.14gold quality
lymph nodeUBERON:000002927.57gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.90gold quality
superior frontal gyrusUBERON:000266126.72gold quality
vermiform appendixUBERON:000115426.42gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
urinary bladderUBERON:000125525.72gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.10

Regulation

Is transcription factor: no

Cross-species orthologs

4 orthologs

OrganismSymbolGene ID
danio_reriotaf11ENSDARG00000037855
drosophila_melanogasterTaf11FBGN0011291
caenorhabditis_elegansWBGENE00006393
caenorhabditis_eleganstaf-11.2WBGENE00006394

Paralogs (14): TAF11 (ENSG00000064995), TAF11L12 (ENSG00000249156), LINC02218 (ENSG00000249662), TAF11L14 (ENSG00000250782), TAF11L11 (ENSG00000283740), TAF11L13 (ENSG00000283776), TAF11L8 (ENSG00000283967), TAF11L9 (ENSG00000283988), TAF11L6 (ENSG00000284042), TAF11L4 (ENSG00000284283), TAF11L10 (ENSG00000284356), TAF11L2 (ENSG00000284373), TAF11L3 (ENSG00000284439), TAF11L7 (ENSG00000284465)

Protein

Protein identifiers

TATA-box-binding protein-associated factor 11-like protein 5A0A1W2PP81 (reviewed: A0A1W2PP81)

All UniProt accessions (1): A0A1W2PP81

UniProt curated annotations — full annotation on UniProt →

Tissue specificity. Expressed in fetal brain and testis.

Similarity. Belongs to the TAF11 family.

RefSeq proteins (29): NP_001388628, NP_001408739, NP_001408740, NP_001408741, NP_001408748, NP_001408757, NP_001408758, NP_001408760, NP_001408763, NP_001408764, NP_001408765, NP_001408766, NP_001408769, NP_001408770, NP_001408771, NP_001408772, NP_001408773, NP_001408774, NP_001408775, NP_001408776, NP_001408777, NP_001408778, NP_001408779, NP_001408780, NP_001408781, NP_001408782, NP_001408783, NP_001408784, NP_001408785 (=MANE)

Domains & families (InterPro)

IDNameType
IPR006809TAFII28_domDomain
IPR009072Histone-foldHomologous_superfamily
IPR045127TAF11-likeFamily

Pfam: PF04719

UniProt features (5 total): compositionally biased region 3, chain 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A0A1W2PP81-F172.420.47

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 1 (showing top): chr5p15

GO Biological Process (2): RNA polymerase II preinitiation complex assembly (GO:0051123), transcription initiation at RNA polymerase II promoter (GO:0006367)

GO Molecular Function (2): protein heterodimerization activity (GO:0046982), RNA polymerase II general transcription initiation factor activity (GO:0016251)

GO Cellular Component (2): transcription factor TFIID complex (GO:0005669), nucleus (GO:0005634)

GO top-level categories

Rollup of top GO terms by namespace:

CategoryTerms
transcription by RNA polymerase II2
transcription initiation at RNA polymerase II promoter1
transcription preinitiation complex assembly1
DNA-templated transcription initiation1
protein dimerization activity1
general transcription initiation factor activity1
RNA polymerase II, holoenzyme1
RNA polymerase II transcription regulator complex1
intracellular membrane-bounded organelle1

Protein interactions and networks

STRING

210 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TAF11L5CT47A11Q5JQC4654
TAF11L5TMEM106AQ96A25644
TAF11L5DUX4L2P0CJ85228
TAF11L5C4BPAP04003202
TAF11L5TAF12Q16514166
TAF11L5TAF10Q12962166
TAF11L5TAF13Q15543166
TAF11L5TAF8Q7Z7C8166
TAF11L5TAF2Q6P1X5166
TAF11L5TAF6P49848166
TAF11L5BTAF1O14981164
TAF11L5C4orf33Q8N1A6161
TAF11L5PRDX4Q13162161
TAF11L5TAF3Q5VWG9157
TAF11L5TAF4O00268138
TAF11L5TAF5LO75529138

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A097I2B5, A0A097I2D0, A0A1W2PP81, A0A1W2PPE2, A0A1W2PPH5, A0A1W2PR64, A0A1W2PRV1, A6NLC8, O75367, O93327, P02276, P06898, P0DW11, P0DW12, P0DW13, P0DW14, P25469, P35066, P35067, P40284, P40287, P61830, P61831, P61833, P61836, P81196, P81198, P81201, P81202, P93354, Q00715, Q02874, Q06196, Q0U1A0, Q2HU65, Q43213, Q54LP8, Q54WG6, Q6C0C4, Q757N1

Diamond homologs: A0A1W2PP81, A0A1W2PPE2, A0A1W2PPH5, A0A1W2PPL8, A0A1W2PPW3, A0A1W2PQ09, A0A1W2PR64, A0A1W2PRV1, A6NLC8, F4HR03, P0DW11, P0DW12, P0DW13, P0DW14, P49906, Q15544, Q54XM9, Q5RA91, Q5U1X0, Q99JX1, Q9M565, Q9US54, Q04226

SIGNOR signaling

0 interactions.

Disease & clinical

Clinical variants and AI predictions

ClinVar

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

ClassificationCount (floor)
Pathogenic0
Likely pathogenic0
Uncertain significance0
Likely benign0
Benign0

Top pathogenic / likely-pathogenic (0)

SpliceAI

0 predictions. Top by Δscore:

AlphaMissense

0 scored. Top likely-pathogenic:

dbSNP variants (sampled 300 via entrez): RS111729073 (5:17525180 A>C), RS113339882 (5:17525832 G>T), RS1156414827 (5:17524260 T>C,G), RS1156681107 (5:17526262 G>A), RS1158169609 (5:17523845 A>T), RS1158363734 (5:17524736 G>C), RS1159300910 (5:17523724 G>A,C,T), RS1159425475 (5:17524607 A>C,G,T), RS1161227686 (5:17523452 C>T), RS1162339375 (5:17524178 A>G,T), RS1162475510 (5:17526055 G>A), RS1162885850 (5:17523557 T>C), RS1163330567 (5:17525817 A>T), RS1163347414 (5:17524056 C>G), RS1164538098 (5:17524772 C>G,T)

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.

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