Gene Gene information from NCBI Gene database.
Entrez ID 170082
Gene name Transcription elongation factor A N-terminal and central domain containing
Gene symbol TCEANC
Synonyms (NCBI Gene)
TCEANC1
Chromosome X
Chromosome location Xp22.2
miRNA miRNA information provided by mirtarbase database.
27
miRTarBase ID miRNA Experiments Reference
MIRT445343 hsa-miR-302a-5p PAR-CLIP 22100165
MIRT445342 hsa-miR-3928-3p PAR-CLIP 22100165
MIRT445340 hsa-miR-3915 PAR-CLIP 22100165
MIRT445341 hsa-miR-1224-5p PAR-CLIP 22100165
MIRT445339 hsa-miR-4689 PAR-CLIP 22100165
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 32296183, 32814053
GO:0005634 Component Nucleus IBA
GO:0006351 Process DNA-templated transcription IEA
GO:0006357 Process Regulation of transcription by RNA polymerase II IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
301084 28277 ENSG00000176896
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N8B7
Protein name Transcription elongation factor A N-terminal and central domain-containing protein (TFIIS central domain-containing protein 1)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF08711 Med26 28 79 TFIIS helical bundle-like domain Domain
PF07500 TFIIS_M 171 281 Transcription factor S-II (TFIIS), central domain Domain
Sequence
MSDKNQIAARASLIEQLMSKRNFEDLGNHLTELETIYVTKEHLQETDVVRAVYRVLKNCP
SVALKKKAKCLLSKWKAVY
KQTHSKARNSPKLFPVRGNKEENSGPSHDPSQNETLGICSS
NSLSSQDVAKLSEMIVPENRAIQLKPKEEHFGDGDPESTGKRSSELLDPTTPMRTKCIEL
LYAALTSSSTDQPKADLWQNFAREIEEHVFTLYSKNIKKYKTCIRSKVANLKNPRNSHLQ
QNLLSGTTSPREFAEMTVMEMANKELKQLRASYTESCIQEH
YLPQVIDGTQTNKIKCRRC
EKYNCKVTVIDRGTLFLPSWVRNSNPDEQMMTYVICNECGEQWYHSKWVCW
Sequence length 351
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
MALE INFERTILITY WITH AZOOSPERMIA OR OLIGOZOOSPERMIA DUE TO SINGLE GENE MUTATION GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Hereditary Breast and Ovarian Cancer Syndrome Hereditary breast and ovarian cancer syndrome Pubtator 25184681 Associate
★☆☆☆☆
Found in Text Mining only
Hypertensive disease Hypertension BEFREE 27480026
★☆☆☆☆
Found in Text Mining only