Gene Gene information from NCBI Gene database.
Entrez ID 85453
Gene name TSPY like 5
Gene symbol TSPYL5
Synonyms (NCBI Gene)
-
Chromosome 8
Chromosome location 8q22.1
miRNA miRNA information provided by mirtarbase database.
356
miRTarBase ID miRNA Experiments Reference
MIRT1460376 hsa-let-7a CLIP-seq
MIRT1460377 hsa-let-7b CLIP-seq
MIRT1460378 hsa-let-7c CLIP-seq
MIRT1460379 hsa-let-7d CLIP-seq
MIRT1460380 hsa-let-7e CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
12
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IBA
GO:0003682 Function Chromatin binding IBA
GO:0005515 Function Protein binding IPI 21170034
GO:0005634 Component Nucleus IBA
GO:0005634 Component Nucleus IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614721 29367 ENSG00000180543
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86VY4
Protein name Testis-specific Y-encoded-like protein 5 (TSPY-like protein 5)
Protein function Involved in modulation of cell growth and cellular response to gamma radiation probably via regulation of the Akt signaling pathway. Involved in regulation of p53/TP53. Suppresses p53/TP53 protein levels and promotes its ubiquitination; the func
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00956 NAP 239 384 Nucleosome assembly protein (NAP) Family
Sequence
MSGRSRGRKSSRAKNRGKGRAKARVRPAPDDAPRDPDPSQYQSLGEDTQAAQVQAGAGWG
GLEAAASAQLLRLGEEAACRLPLDCGLALRARAAGDHGQAAARPGPGKAASLSERLAADT
VFVGTAGTVGRPKNAPRVGNRRGPAGKKAPETCSTAGRGPQVIAGGRQKKGAAGENTSVS
AGEEKKEERDAGSGPPATEGSMDTLENVQLKLENMNAQADRAYLRLSRKFGQLRLQHLER
RNHLIQNIPGFWGQAFQNHPQLASFLNSQEKEVLSYLNSLEVEELGLARLGYKIKFYFDR
NPYFQNKVLIKEYGCGPSGQVVSRSTPIQWLPGHDLQSLSQGNPENNRSFFGWFSNHSSI
ESDKIVEIINEELWPNPLQFYLLS
EGARVEKGKEKEGRQGPGKQPMETTQPGVSQSN
Sequence length 417
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
4
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
BASAL CELL CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
KERATINOCYTE CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MIGRAINE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TOURETTE SYNDROME GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Alternating hemiplegia of childhood Associate 28716051, 31278054
★☆☆☆☆
Found in Text Mining only
Breast Neoplasms Associate 23518928, 24073403
★☆☆☆☆
Found in Text Mining only
Carcinoma Endometrioid Associate 29060924
★☆☆☆☆
Found in Text Mining only
Carcinoma Hepatocellular Associate 26059414, 33237575
★☆☆☆☆
Found in Text Mining only
Colorectal Neoplasms Inhibit 32627024
★☆☆☆☆
Found in Text Mining only
Down Syndrome Associate 26911678
★☆☆☆☆
Found in Text Mining only
Glioblastoma Associate 21156036
★☆☆☆☆
Found in Text Mining only
Glioma Associate 18059362
★☆☆☆☆
Found in Text Mining only
Idiopathic Noncirrhotic Portal Hypertension Associate 33237575
★☆☆☆☆
Found in Text Mining only
Mesothelioma Malignant Associate 28716051
★☆☆☆☆
Found in Text Mining only