Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
10042
Gene name Gene Name - the full gene name approved by the HGNC.
HMG-box containing 4
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
HMGXB4
Synonyms (NCBI Gene) Gene synonyms aliases
HMG2L1, HMGBCG, P53N, THC211630
Chromosome Chromosome number
22
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
22q12.3
Summary Summary of gene provided in NCBI Entrez Gene.
High mobility group (HMG) proteins are nonhistone chromosomal proteins. See HMG2 (MIM 163906) for additional information on HMG proteins.[supplied by OMIM, Nov 2010]
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT021175 hsa-miR-186-5p Sequencing 20371350
MIRT003368 hsa-miR-221-3p Reporter assay;Microarray 20018759
MIRT047935 hsa-miR-30c-5p CLASH 23622248
MIRT352642 hsa-miR-493-5p HITS-CLIP 21572407
MIRT511496 hsa-miR-1277-5p HITS-CLIP 21572407
Transcription factors
Transcription factor Regulation Reference
SRF Unknown 20511232
SRF Unknown 20511232
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0003677 Function DNA binding IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0008333 Process Endosome to lysosome transport NAS 10329004
GO:0016055 Process Wnt signaling pathway IEA
GO:0016589 Component NURF complex IDA 20850016
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
604702 5003 ENSG00000100281
Protein
UniProt ID Q9UGU5
Protein name HMG domain-containing protein 4 (HMG box-containing protein 4) (High mobility group protein 2-like 1) (Protein HMGBCG)
Protein function Negatively regulates Wnt/beta-catenin signaling during development.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF13775 DUF4171 107 232 Domain of unknown function (DUF4171) Domain
PF00505 HMG_box 407 473 HMG (high mobility group) box Domain
Sequence
MAYDDSVKKEDCFDGDHTFEDIGLAAGRSQREKKRSYKDFLREEEEIAAQVRNSSKKKLK
DSELYFLGTDTHKKKRKHSSDDYYYGDISSLESSQKKKKKSSPQSTDTAMDLLKAITSPL
AAGSKPSKKTGEKSSGSSSHSESKKEHHRKKVSGSSGELPLEDGGSHKSKKMKPLYVNTE
TLTLREPDGLKMKLILSPKEKGSSSVDEESFQYPSQQATVKKSSKKSARDEQ
GALLLGHE
LQSFLKTARKKHKSSSDAHSSPGPEGCGSDASQFAESHSANLDLSGLEPILVESDSSSGG
ELEAGELVIDDSYREIKKKKKSKKSKKKKDKEKHKEKRHSKSKRSLGLSAVPVGEVTVTS
GPPPSIPYAGAAAPPLPLPGLHTDGHSEKKKKKEEKDKERERGEKPKKKNMSAYQVFCKE
YRVTIVADHPGIDFGELSKKLAEVWKQLPEKDKLIWKQKAQYLQHKQNKAEAT
TVKRKAS
SSEGSMKVKASSVGVLSPQKKSPPTTMLLPASPAKAPETEPIDVAAHLQLLGESLSLIGH
RLQETEGMVAVSGSLSVLLDSIICALGPLACLTTQLPELNGCPKQVLSNTLDNIAYIMPG
L
Sequence length 601
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Major affective disorder MAJOR AFFECTIVE DISORDER 2 17671966 ClinVar