Gene Gene information from NCBI Gene database.
Entrez ID 55617
Gene name Taspase 1
Gene symbol TASP1
Synonyms (NCBI Gene)
C20orf13SULEHSdJ585I14.2
Chromosome 20
Chromosome location 20p12.1
Summary This gene encodes an endopeptidase that cleaves specific substrates following aspartate residues. The encoded protein undergoes posttranslational autoproteolytic processing to generate alpha and beta subunits, which reassemble into the active alpha2-beta2
SNPs SNP information provided by dbSNP.
2
SNP ID Visualize variation Clinical significance Consequence
rs904200599 G>A Pathogenic Genic downstream transcript variant, missense variant, non coding transcript variant, coding sequence variant, 3 prime UTR variant
rs1200336864 G>A Pathogenic Stop gained, non coding transcript variant, coding sequence variant, 5 prime UTR variant
miRNA miRNA information provided by mirtarbase database.
176
miRTarBase ID miRNA Experiments Reference
MIRT029922 hsa-miR-26b-5p Microarray 19088304
MIRT446593 hsa-miR-100-3p PAR-CLIP 22100165
MIRT446591 hsa-miR-4503 PAR-CLIP 22100165
MIRT446593 hsa-miR-100-3p PAR-CLIP 22100165
MIRT446591 hsa-miR-4503 PAR-CLIP 22100165
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
14
GO ID Ontology Definition Evidence Reference
GO:0004298 Function Threonine-type endopeptidase activity IBA
GO:0004298 Function Threonine-type endopeptidase activity IEA
GO:0004298 Function Threonine-type endopeptidase activity IMP 14636557
GO:0004298 Function Threonine-type endopeptidase activity TAS
GO:0005737 Component Cytoplasm IBA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
608270 15859 ENSG00000089123
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9H6P5
Protein name Threonine aspartase 1 (Taspase-1) (EC 3.4.25.-) [Cleaved into: Threonine aspartase subunit alpha; Threonine aspartase subunit beta]
Protein function Protease responsible for KMT2A/MLL1 processing and activation (PubMed:14636557). It also activates KMT2D/MLL2 (By similarity). Through substrate activation, it controls the expression of HOXA genes, and the expression of key cell cycle regulator
PDB 2A8I , 2A8J , 2A8L , 2A8M , 6UGK , 6VIN
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF01112 Asparaginase_2 42 358 Asparaginase Domain
Sequence
Sequence length 420
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
24
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)
Causal Diseases associated with Pathogenic or Likely Pathogenic variants in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession Evidence Score
Abnormal facial shape Likely pathogenic rs904200599 RCV000782350
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Global developmental delay Pathogenic; Likely pathogenic rs1200336864, rs904200599 RCV000782139
RCV000782350
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Happy demeanor Likely pathogenic rs904200599 RCV000782350
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Suleiman-El-Hattab syndrome Likely pathogenic; Pathogenic rs2515530219, rs867871906, rs1200336864, rs904200599 RCV002510290
RCV003313813
RCV001250727
RCV001250726
★★★★☆
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
Acute myeloid leukemia Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
ALZHEIMER DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Cervical cancer Benign ClinVar
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
CHRONIC OBSTRUCTIVE PULMONARY DISEASE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Anemia Macrocytic Macrocytic anemia Pubtator 31350873 Associate
★☆☆☆☆
Found in Text Mining only
Anemia, Macrocytic Anemia BEFREE 31350873
★☆☆☆☆
Found in Text Mining only
Anterior segment mesenchymal dysgenesis Anterior segment mesenchymal dysgenesis Pubtator 31350873 Associate
★☆☆☆☆
Found in Text Mining only
Congenital malformation syndrome Congenital Malformation Syndrome BEFREE 29633245
★☆☆☆☆
Found in Text Mining only
Craniofacial Abnormalities Craniofacial abnormalities Pubtator 31350873 Associate
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 1 Diabetes mellitus, type 1 Pubtator 33154504 Associate
★☆☆☆☆
Found in Text Mining only
Global developmental delay Developmental Delay BEFREE 29633245, 31209944
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Global developmental delay Developmental Delay CLINVAR_DG
★★★★☆
ClinVar: Pathogenic / Likely Pathogenic (<5 Variants)
Growth Deficiency and Mental Retardation with Facial Dysmorphism Growth Deficiency And Mental Retardation With Facial Dysmorphism BEFREE 29633245
★☆☆☆☆
Found in Text Mining only
Hematologic Neoplasms Hematologic neoplasm Pubtator 31350873 Associate
★☆☆☆☆
Found in Text Mining only