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Gene Gene information from NCBI Gene database.
Entrez ID 158248
Gene name Tetratricopeptide repeat domain 16
Gene symbol TTC16
Synonyms (NCBI Gene)
-
Chromosome 9
Chromosome location 9q34.11
miRNA miRNA information provided by mirtarbase database.
26 Show/Hide all (26)
miRTarBase ID miRNA Experiments Reference
MIRT2462580 hsa-miR-1207-3p CLIP-seq
MIRT2462581 hsa-miR-2861 CLIP-seq
MIRT2462582 hsa-miR-3614-5p CLIP-seq
MIRT2462583 hsa-miR-3649 CLIP-seq
MIRT2462584 hsa-miR-369-3p CLIP-seq
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8NEE8
Protein name Tetratricopeptide repeat protein 16 (TPR repeat protein 16)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00515 TPR_1 367 → 398 Tetratricopeptide repeat Repeat
PF13432 TPR_16 256 → 318 Family
PF13432 TPR_16 65 → 128 Family
Sequence
MTDSDEDALKVDQGPSRDIPKPWVIPAPKGILQHIFGTSHVFQSICDVKPKVTGLTVPLK
VREYYSRGQQCLEQADWETAVLLFSRALHLDPQLVDFYALRAEAYLQLCDFSSAAQNLRR
AYSLQQDN
CKHLERLTFVLYLQGQCLFEQCAFLDALNVFSHAAELQPEKPCFRYRCMACL
LALKQHQACLTLITNELKQDTTNADVYIFRARLYNFLQKPHLCYRDLHSALLLNPKHPQA
RMLLQKMVAQAQQARQDAGILAVQGKLQHALQRINRAIENNPLDPSLFLFRGTMYRRLQE
FDGAVEDFLKVLDMVTED
QEDMVRQAQRQLLLTYNDFAVHCYRQGAYQEGVLLLNKALRD
EQQEKGLYINRGDCFFQLGNLAFAEADYQQALALSPQDEGANTRMGLLQEKMGFCEQRRK
QFQKAENHFSTAIRHNPQKAQYYLYRAKSRQLLQNIFGARQDVATVLLLNPKQPKLSLLM
TNLFPGMSVEEVLSTQIAHLARLQLEQMVEGSLQAGSPQGIVGMLKRHELERQKALALQH
SWKQGEPLIATSEELKATPEIPQVKPGSSEGEAEAPEEEEEKEKEKKEEKKSELIPSKVA
SLSDSYLDQTSSASSMSFRTTGTSETEMSAICQEYRSTSATAVTFSDSSLLKTQSSDSGN
NREALSHGPRKIKATQGQRQSLSKTEPTQSQRRNSSKTKATIHKRNSSKTKATQSQRRNS
SKTRATQGQGQSSSKTEATQGQRQSSSEIEATQGPRQEPSKTKTTRSPRQRPRKVKAARG
RSWRPSKVDATQGRSRGLLRSSTKTEAFYDSNWSLSKTEYAQGQGQRSSKAEGAQGKSQG
MSSTSSKAESTWGPSPSLSKTEVDQDLTYYEAV
Sequence length 873
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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 Reference Evidence Score
Gastric cancer Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Premature ovarian insufficiency Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations