TAF11L14

gene
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Summary

TAF11L14 (TATA-box binding protein associated factor 11 like 14, HGNC:53857) is a protein-coding gene on chromosome 5p15.1, encoding TATA-box-binding protein-associated factor 11-like protein 14 (A0A1W2PPL8).

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 112488740 — RefSeq curated summary.

At a glance

  • MANE Select transcript: NM_001401687

Identifiers

Gene identifiers

FieldValue
HGNC IDHGNC:53857
Approved symbolTAF11L14
NameTATA-box binding protein associated factor 11 like 14
Location5p15.1
Locus typegene with protein product
StatusApproved
Ensembl geneENSG00000250782
Ensembl biotypeprotein_coding
Entrez112488740

Gene structure

Transcript identifiers

Ensembl transcripts: 1 — 1 protein_coding

ENST00000512227

RefSeq mRNA: 1 — MANE Select: NM_001401687 NM_001401687

CCDS: CCDS93700

Canonical transcript exons

ENST00000512227 — 1 exons

ExonStartEnd
ENSE000020234471763446017635053

Expression profiles

Bgee: expression breadth broad, 11 present calls, max score 37.20.

Top tissues by expression

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

TissueAnatomy IDExpression scoreQuality
colonic epitheliumUBERON:000039737.20gold quality
hindlimb stylopod muscleUBERON:000425237.12gold quality
ventricular zoneUBERON:000305336.48gold quality
cortical plateUBERON:000534336.47gold quality
bone marrow cellCL:000209236.16gold quality
ganglionic eminenceUBERON:000402335.49gold quality
skeletal muscle tissueUBERON:000113433.38gold quality
muscle tissueUBERON:000238533.08gold quality
smooth muscle tissueUBERON:000113531.79gold quality
bone marrowUBERON:000237131.74gold quality
sural nerveUBERON:001548830.93gold quality
stromal cell of endometriumCL:000225529.87gold quality
prefrontal cortexUBERON:000045129.47gold quality
liverUBERON:000210728.34gold quality
duodenumUBERON:000211428.14gold quality
descending thoracic aortaUBERON:000234527.65silver quality
lymph nodeUBERON:000002927.57gold quality
leukocyteCL:000073827.31gold quality
monocyteCL:000057627.28gold quality
tonsilUBERON:000237227.05gold quality
islet of LangerhansUBERON:000000626.55gold quality
vermiform appendixUBERON:000115426.42gold quality
gall bladderUBERON:000211025.98gold quality
bloodUBERON:000017825.91gold quality
olfactory segment of nasal mucosaUBERON:000538625.89gold quality
placentaUBERON:000198725.81gold quality
urinary bladderUBERON:000125525.72gold quality
primary visual cortexUBERON:000243624.61gold quality
frontal cortexUBERON:000187024.30silver quality
gastrocnemiusUBERON:000138824.18gold quality

Single-cell (SCXA)

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

ExperimentMarker?Max mean expression
E-ANND-3no1.00

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), TAF11L11 (ENSG00000283740), TAF11L13 (ENSG00000283776), 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 14A0A1W2PPL8 (reviewed: A0A1W2PPL8)

All UniProt accessions (1): A0A1W2PPL8

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_001388616* (*=MANE)

Domains & families (InterPro)

IDNameType
IPR006809TAFII28_domDomain
IPR009072Histone-foldHomologous_superfamily
IPR045127TAF11-likeFamily

Pfam: PF04719

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

Structure

Experimental structures (PDB)

0 structures.

Predicted structure (AlphaFold)

ModelpLDDTFraction very-high
AF-A0A1W2PPL8-F170.610.40

Function

Pathways and Gene Ontology

Reactome pathways

0 pathways

MSigDB gene sets: 21 (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, ZNF274_TARGET_GENES

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
TAF11L14TAF12Q16514166
TAF11L14TAF10Q12962166
TAF11L14TAF13Q15543166
TAF11L14TAF8Q7Z7C8166
TAF11L14TAF2Q6P1X5166
TAF11L14TAF6P49848166
TAF11L14BTAF1O14981164
TAF11L14C4orf33Q8N1A6161
TAF11L14PRDX4Q13162161
TAF11L14TAF3Q5VWG9157
TAF11L14TAF4O00268138
TAF11L14TAF5LO75529138
TAF11L14TAF6LQ9Y6J9138
TAF11L14TAF7Q15545138
TAF11L14TAF9BQ9HBM6138
TAF11L14TAF5Q15542138
TAF11L14TAF7LQ5H9L4138
TAF11L14TAF9Q16594138
TAF11L14TAF4BQ92750138

IntAct

0 interactions, top by confidence:

ESM2 similar proteins: A0A097I1R9, A0A097I2B5, A0A097I2D0, A0A1W2PP81, A0A1W2PPE2, A0A1W2PPH5, A0A1W2PPL8, A0A1W2PPW3, A0A1W2PQ09, A0A1W2PR64, A0A1W2PRV1, A6NLC8, O04027, O15819, P06898, P06902, P0C1H6, P0DW11, P0DW12, P0DW13, P0DW14, P27795, P27893, P40284, P40285, P40287, P81195, P81196, P81197, P81198, P81199, P81200, P81201, P81202, Q06196, Q27490, Q2N2K6, Q5M8Q2, Q6CER9, Q6VEU3

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

1297 scored. Top likely-pathogenic:

VariantProtein changeam_pathogenicity
5:17634808:T:CF117L0.840
5:17634810:C:AF117L0.840
5:17634810:C:GF117L0.840
5:17635048:T:CF197L0.700
5:17635050:C:AF197L0.700
5:17635050:C:GF197L0.700
5:17635021:T:CF188L0.657
5:17635023:C:AF188L0.657
5:17635023:C:GF188L0.657
5:17634900:G:CK147N0.633
5:17634900:G:TK147N0.633
5:17634824:T:AV122D0.632
5:17634809:T:CF117S0.617
5:17634908:T:AV150D0.602
5:17634924:A:CE155D0.580
5:17634924:A:TE155D0.580
5:17634762:G:AM101I0.579
5:17634762:G:CM101I0.579
5:17634762:G:TM101I0.579
5:17634816:A:CK119N0.571
5:17634816:A:TK119N0.571
5:17634764:C:TS102F0.570

dbSNP variants (sampled 300 via entrez): RS1000148594 (5:17634696 G>A), RS1000187264 (5:17632978 C>G,T), RS1002171346 (5:17633325 A>G,T), RS1003421848 (5:17633935 C>G,T), RS1003883477 (5:17633858 A>G,T), RS1004215387 (5:17634136 G>T), RS1004707083 (5:17634326 C>T), RS1005892093 (5:17634899 A>C,G), RS1006384248 (5:17635110 C>G), RS1006712578 (5:17632964 C>T), RS10076372 (5:17633671 A>C), RS1007890749 (5:17633477 T>A), RS1008913212 (5:17632829 G>T), RS1009270646 (5:17633845 C>T), RS1010225086 (5:17633307 A>G)

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.