Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
23270
Gene name Gene Name - the full gene name approved by the HGNC.
TSPY like 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TSPYL4
Synonyms (NCBI Gene) Gene synonyms aliases
dJ486I3.2
Chromosome Chromosome number
6
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
6q22.1
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021145 hsa-miR-186-5p Sequencing 20371350
MIRT486911 hsa-miR-6760-5p PAR-CLIP 20371350
MIRT486909 hsa-miR-4716-3p PAR-CLIP 20371350
MIRT486908 hsa-miR-6794-5p PAR-CLIP 20371350
MIRT486906 hsa-miR-4419a PAR-CLIP 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0000785 Component Chromatin IBA 21873635
GO:0003682 Function Chromatin binding IBA 21873635
GO:0005515 Function Protein binding IPI 25416956, 28514442, 32296183
GO:0005634 Component Nucleus IBA 21873635
GO:0006334 Process Nucleosome assembly IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
619586 21559 ENSG00000187189
Protein
UniProt ID Q9UJ04
Protein name Testis-specific Y-encoded-like protein 4 (TSPY-like protein 4)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00956 NAP 247 388 Nucleosome assembly protein (NAP) Family
Sequence
MSGLDGGNKLPLAQTGGLAAPDHASGDPDRDQCQGLREETEATQVMANTGGGSLETVAEG
GASQDPVDCGPALRVPVAGSRGGAATKAGQEDAPPSTKGLEAASAAEAADSSQKNGCQLG
EPRGPAGQKALEACGAGGLGSQMIPGKKAKEVTTKKRAISAAVEKEGEAGAAMEEKKVVQ
KEKKVAGGVKEETRPRAPKINNCMDSLEAIDQELSNVNAQADRAFLQLERKFGRMRRLHM
QRRSFIIQNIPGFWVTAFRNHPQLSPMISGQDEDMLRYMINLEVEELKHPRAGCKFKFIF
QGNPYFRNEGLVKEYERRSSGRVVSLSTPIRWHRGQDPQAHIHRNREGNTIPSFFNWFSD
HSLLEFDRIAEIIKGELWPNPLQYYLMG
EGPRRGIRGPPRQPVESARSFRFQSG
Sequence length 414
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Melanoma melanoma rs121913315, rs121913323, rs137853080, rs137853081, rs121909232, rs121913388, rs104894094, rs104894095, rs104894097, rs104894098, rs104894099, rs104894109, rs137854599, rs11547328, rs104894340
View all (64 more)
22535842
Associations from Text Mining
Disease Name Relationship Type References
Colorectal Neoplasms Associate 34537824
Death Sudden Associate 15273283
Sudden Infant Death with Dysgenesis of the Testes Syndrome Associate 15273283