Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
81628
Gene name Gene Name - the full gene name approved by the HGNC.
TSC22 domain family member 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
TSC22D4
Synonyms (NCBI Gene) Gene synonyms aliases
SPACDR, THG-1, THG1, TILZ2
Chromosome Chromosome number
7
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
7q22.1
Summary Summary of gene provided in NCBI Entrez Gene.
TSC22D4 is a member of the TSC22 domain family of leucine zipper transcriptional regulators (see TSC22D3; MIM 300506) (Kester et al., 1999 [PubMed 10488076]; Fiorenza et al., 2001 [PubMed 11707329]).[supplied by OMIM, Mar 2008]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT004100 hsa-miR-124-3p Microarray 15685193
MIRT004100 hsa-miR-124-3p Microarray 18668037
MIRT004100 hsa-miR-124-3p Microarray 15685193
MIRT025708 hsa-miR-7-5p Sequencing 20371350
MIRT030651 hsa-miR-22-3p Sequencing 20371350
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 16713569, 19615732, 21516116, 21988832, 25416956, 28514442, 31515488, 32296183, 32814053
GO:0005634 Component Nucleus IEA
GO:0006357 Process Regulation of transcription by RNA polymerase II IEA
GO:0006970 Process Response to osmotic stress IBA 21873635
GO:0045892 Process Negative regulation of transcription, DNA-templated NAS 10488076
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
611914 21696 ENSG00000166925
Protein
UniProt ID Q9Y3Q8
Protein name TSC22 domain family protein 4 (TSC22-related-inducible leucine zipper protein 2)
Protein function Binds DNA and acts as a transcriptional repressor (PubMed:10488076). Involved in the regulation of systematic glucose homeostasis and insulin sensitivity, via transcriptional repression of downstream insulin signaling targets such as OBP2A/LCN13
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01166 TSC22 326 381 TSC-22/dip/bun family Coiled-coil
Tissue specificity TISSUE SPECIFICITY: Expressed in the liver. {ECO:0000269|PubMed:27827363}.
Sequence
MSGGKKKSSFQITSVTTDYEGPGSPGASDPPTPQPPTGPPPRLPNGEPSPDPGGKGTPRN
GSPPPGAPSSRFRVVKLPHGLGEPYRRGRWTCVDVYERDLEPHSFGGLLEGIRGASGGAG
GRSLDSRLELASLGLGAPTPPSGLSQGPTSWLRPPPTSPGPQARSFTGGLGQLVVPSKAK
AEKPPLSASSPQQRPPEPETGESAGTSRAATPLPSLRVEAEAGGSGARTPPLSRRKAVDM
RLRMELGAPEEMGQVPPLDSRPSSPALYFTHDASLVHKSPDPFGAVAAQKFSLAHSMLAI
SGHLDSDDDSGSGSLVGIDNKIEQAMDLVKSHLMFAVREEVEVLKEQIRELAERNAALEQ
ENGLLRALASPEQLAQLPSSG
VPRLGPPAPNGPSV
Sequence length 395
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Breast cancer Malignant neoplasm of breast rs587776547, rs1137887, rs137853007, rs587776650, rs80359351, rs80359714, rs121917783, rs104886456, rs121964878, rs80359874, rs80357868, rs80357508, rs387906843, rs80357569, rs80358158
View all (309 more)
Associations from Text Mining
Disease Name Relationship Type References
Carcinoma Squamous Cell Associate 31864704
Cell Transformation Neoplastic Associate 31864704
Esophageal Squamous Cell Carcinoma Associate 31864704
Leukemia Myeloid Acute Associate 37237254