TAF11L13

gene
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Summary

TAF11L13 (TATA-box binding protein associated factor 11 like 13, HGNC:53856) is a protein-coding gene on chromosome 5p15.1, encoding TATA-box-binding protein-associated factor 11-like protein 13 (A0A1W2PPH5).

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 112488747 — RefSeq curated summary.

At a glance

  • MANE Select transcript: NM_001401695

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:53856
Approved symbolTAF11L13
NameTATA-box binding protein associated factor 11 like 13
Location5p15.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000283776
Ensembl biotypeprotein_coding
Entrez112488747

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000639073

RefSeq mRNA: 1 — MANE Select: NM_001401695 NM_001401695

CCDS: CCDS93699

Canonical transcript exons

ENST00000639073 — 1 exons

ExonStartEnd
ENSE000038044411763208817632684

Expression profiles

Bgee: expression breadth tissue_specific, 2 present calls, max score 41.73.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
colonic epitheliumUBERON:000039741.73gold quality
sural nerveUBERON:001548839.45gold quality
bone marrow cellCL:000209238.45gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113434.84gold quality
bone marrowUBERON:000237132.91gold quality
hindlimb stylopod muscleUBERON:000425232.15gold quality
muscle tissueUBERON:000238532.13gold quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.04gold quality
liverUBERON:000210728.35gold quality
duodenumUBERON:000211428.14gold quality
lymph nodeUBERON:000002927.57gold quality
urinary bladderUBERON:000125527.23gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.55gold quality
leukocyteCL:000073826.49gold quality
vermiform appendixUBERON:000115426.42gold quality
monocyteCL:000057626.38gold quality
bloodUBERON:000017826.28gold quality
gall bladderUBERON:000211025.98gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
calcaneal tendonUBERON:000370125.72gold quality
muscle of legUBERON:000138325.08gold quality
primary visual cortexUBERON:000243624.61gold quality
superior frontal gyrusUBERON:000266124.08gold quality
pancreasUBERON:000126424.03gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no0.64

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), TAF11L8 (ENSG00000283967), TAF11L9 (ENSG00000283988), TAF11L6 (ENSG00000284042), TAF11L5 (ENSG00000284234), TAF11L4 (ENSG00000284283), TAF11L10 (ENSG00000284356), TAF11L2 (ENSG00000284373), TAF11L3 (ENSG00000284439), TAF11L7 (ENSG00000284465)

Protein

Protein identifiers

TATA-box-binding protein-associated factor 11-like protein 13A0A1W2PPH5 (reviewed: A0A1W2PPH5)

All UniProt accessions (1): A0A1W2PPH5

UniProt curated annotations — full annotation on UniProt →

Tissue specificity. Expressed in fetal brain and testis.

Similarity. Belongs to the TAF11 family.

RefSeq proteins (1): NP_001388624* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR006809TAFII28_domDomain
IPR009072Histone-foldHomologous_superfamily
IPR045127TAF11-likeFamily

Pfam: PF04719

UniProt features (4 total): compositionally biased region 2, chain 1, region of interest 1

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A0A1W2PPH5-F171.400.45

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 20 (showing top): GOBP_DNA_TEMPLATED_TRANSCRIPTION_INITIATION, GOBP_TRANSCRIPTION_INITIATION_AT_RNA_POLYMERASE_II_PROMOTER, GOCC_RNA_POLYMERASE_COMPLEX, GOBP_PROTEIN_DNA_COMPLEX_ORGANIZATION, GOCC_TRANSCRIPTION_FACTOR_TFIID_COMPLEX, GOCC_TRANSFERASE_COMPLEX_TRANSFERRING_PHOSPHORUS_CONTAINING_GROUPS, GOCC_RNA_POLYMERASE_II_TRANSCRIPTION_REGULATOR_COMPLEX, GOCC_TRANSFERASE_COMPLEX, GOCC_TRANSCRIPTION_REGULATOR_COMPLEX, GOMF_PROTEIN_HETERODIMERIZATION_ACTIVITY, GOMF_PROTEIN_DIMERIZATION_ACTIVITY, GOBP_RNA_POLYMERASE_II_PREINITIATION_COMPLEX_ASSEMBLY, GOBP_TRANSCRIPTION_PREINITIATION_COMPLEX_ASSEMBLY, GOMF_GENERAL_TRANSCRIPTION_INITIATION_FACTOR_ACTIVITY, GOCC_NUCLEAR_PROTEIN_CONTAINING_COMPLEX

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

202 interactions, top by confidence (×1000):

Protein AProtein BPartner UniProtScore
TAF11L13TAF12Q16514166
TAF11L13TAF10Q12962166
TAF11L13TAF13Q15543166
TAF11L13TAF8Q7Z7C8166
TAF11L13TAF2Q6P1X5166
TAF11L13TAF6P49848166
TAF11L13BTAF1O14981164
TAF11L13C4orf33Q8N1A6161
TAF11L13PRDX4Q13162161
TAF11L13TAF3Q5VWG9157
TAF11L13TAF4O00268138
TAF11L13TAF5LO75529138
TAF11L13TAF6LQ9Y6J9138
TAF11L13TAF7Q15545138
TAF11L13TAF9BQ9HBM6138
TAF11L13TAF5Q15542138
TAF11L13TAF7LQ5H9L4138
TAF11L13TAF9Q16594138
TAF11L13TAF4BQ92750138

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

1293 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
5:17632436:T:CF117L0.920
5:17632438:C:AF117L0.920
5:17632438:C:GF117L0.920
5:17632528:G:CK147N0.900
5:17632528:G:TK147N0.900
5:17632437:T:CF117S0.859
5:17632611:T:CL175S0.854
5:17632524:C:AA146D0.829
5:17632509:C:AA141D0.823
5:17632390:G:AM101I0.818
5:17632390:G:CM101I0.818
5:17632390:G:TM101I0.818
5:17632437:T:GF117C0.817
5:17632536:T:AV150D0.813
5:17632556:G:CA157P0.813
5:17632552:A:CE155D0.802
5:17632552:A:TE155D0.802
5:17632402:G:CQ105H0.799
5:17632402:G:TQ105H0.799
5:17632679:T:CF198L0.794
5:17632681:C:AF198L0.794
5:17632681:C:GF198L0.794
5:17632392:C:TS102F0.785
5:17632619:G:CA178P0.759
5:17632369:G:AM94I0.743
5:17632369:G:CM94I0.743
5:17632369:G:TM94I0.743
5:17632389:T:CM101T0.738
5:17632514:G:CA143P0.736
5:17632464:T:CM126T0.719

dbSNP variants (sampled 300 via entrez): RS1000187264 (5:17632978 C>G,T), RS1003191749 (5:17630504 C>T), RS1005102839 (5:17630719 C>T), RS1006712578 (5:17632964 C>T), RS1006862313 (5:17631746 A>G), RS1007696282 (5:17632127 C>A,G,T), RS1008913212 (5:17632829 G>T), RS1010277658 (5:17633159 T>A,C), RS1010969568 (5:17631059 AAT>A), RS1011834712 (5:17631307 T>A,G), RS1015179836 (5:17631755 C>T), RS1015479452 (5:17631482 T>G), RS1017264743 (5:17632690 A>C,G), RS1017576316 (5:17632739 T>G), RS1017685947 (5:17632968 G>A,C)

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.