Gene Gene information from NCBI Gene database.
Entrez ID 80177
Gene name MYC target 1
Gene symbol MYCT1
Synonyms (NCBI Gene)
MTLC
Chromosome 6
Chromosome location 6q25.2
miRNA miRNA information provided by mirtarbase database.
103
miRTarBase ID miRNA Experiments Reference
MIRT017315 hsa-miR-335-5p Microarray 18185580
MIRT1167895 hsa-miR-1208 CLIP-seq
MIRT1167896 hsa-miR-135a CLIP-seq
MIRT1167897 hsa-miR-135b CLIP-seq
MIRT1167898 hsa-miR-186 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
5
GO ID Ontology Definition Evidence Reference
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm IBA
GO:0005654 Component Nucleoplasm IDA
GO:0016604 Component Nuclear body IDA
GO:0061484 Process Hematopoietic stem cell homeostasis IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616805 23172 ENSG00000120279
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N699
Protein name Myc target protein 1 (Myc target in myeloid cells protein 1)
Protein function May regulate certain MYC target genes, MYC seems to be a direct upstream transcriptional activator. Does not seem to significantly affect growth cell capacity. Overexpression seems to mediate many of the known phenotypic features associated with
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15179 Myc_target_1 49 234 Myc target protein 1 Family
Tissue specificity TISSUE SPECIFICITY: Down-regulated in gastric cancer tissues.
Sequence
Sequence length 235
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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
UTERINE FIBROID GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinogenesis Associate 21998677, 28485541
★☆☆☆☆
Found in Text Mining only
Cholangiocarcinoma Associate 36868481
★☆☆☆☆
Found in Text Mining only
Laryngeal Neoplasms Associate 22672838, 28485541, 31152622, 32659265
★☆☆☆☆
Found in Text Mining only
Leukemia Myeloid Acute Associate 25331116
★☆☆☆☆
Found in Text Mining only
Lymphatic Metastasis Inhibit 28485541
★☆☆☆☆
Found in Text Mining only
Lymphoma Associate 38172714
★☆☆☆☆
Found in Text Mining only
Lymphoma Large B Cell Diffuse Associate 38172714
★☆☆☆☆
Found in Text Mining only
Neoplasms Inhibit 21998677, 22672838, 38172714
★☆☆☆☆
Found in Text Mining only
Neoplasms Squamous Cell Associate 22672838
★☆☆☆☆
Found in Text Mining only
Neoplasms Squamous Cell Inhibit 22672838
★☆☆☆☆
Found in Text Mining only