Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
11075
Gene name Gene Name - the full gene name approved by the HGNC.
Stathmin 2
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
STMN2
Synonyms (NCBI Gene) Gene synonyms aliases
SCG10, SCGN10
Chromosome Chromosome number
8
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
8q21.13
Summary Summary of gene provided in NCBI Entrez Gene.
This gene encodes a member of the stathmin family of phosphoproteins. Stathmin proteins function in microtubule dynamics and signal transduction. The encoded protein plays a regulatory role in neuronal growth and is also thought to be involved in osteogen
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT1398827 hsa-miR-2681 CLIP-seq
MIRT1398828 hsa-miR-3674 CLIP-seq
MIRT1398829 hsa-miR-4642 CLIP-seq
MIRT1398830 hsa-miR-4705 CLIP-seq
MIRT1398831 hsa-miR-665 CLIP-seq
Transcription factors
Transcription factor Regulation Reference
CTNNBIP1 Unknown 16712787
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, 18452648, 25416956, 31515488, 32296183
GO:0005737 Component Cytoplasm IBA 21873635
GO:0005737 Component Cytoplasm IDA 21215777
GO:0005768 Component Endosome IEA
GO:0005794 Component Golgi apparatus IEA
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
600621 10577 ENSG00000104435
Protein
UniProt ID Q93045
Protein name Stathmin-2 (Superior cervical ganglion-10 protein) (Protein SCG10)
Protein function Regulator of microtubule stability. When phosphorylated by MAPK8, stabilizes microtubules and consequently controls neurite length in cortical neurons. In the developing brain, negatively regulates the rate of exit from multipolar stage and reta
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00836 Stathmin 39 174 Stathmin family Family
Tissue specificity TISSUE SPECIFICITY: Neuron specific.
Sequence
Sequence length 179
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Arthritis Degenerative polyarthritis rs1594890601, rs1594882933, rs184370809, rs776489319, rs1594883470 22763110
Unknown
Disease term Disease name Evidence References Source
Mental depression Major Depressive Disorder 25897834 ClinVar
Associations from Text Mining
Disease Name Relationship Type References
Alzheimer Disease Associate 38175301
Amyotrophic Lateral Sclerosis Associate 30643292, 34496257, 35034660, 38175301, 39486415
Amyotrophic Lateral Sclerosis Inhibit 30643298
Budd Chiari Syndrome Stimulate 16162682
Creutzfeldt Jakob Syndrome Associate 19081515
Deafness Autosomal Dominant 43 Associate 32790644, 35879741
Frontotemporal Dementia Associate 32790644, 38175301
Frontotemporal Dementia Stimulate 37466726
Frontotemporal Lobar Degeneration Associate 33074248, 40478310
Liver Cirrhosis Associate 15661146