Gene Gene information from NCBI Gene database.
Entrez ID 27143
Gene name Phosphatase domain containing paladin 1
Gene symbol PALD1
Synonyms (NCBI Gene)
KIAA1274PALD
Chromosome 10
Chromosome location 10q22.1
miRNA miRNA information provided by mirtarbase database.
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miRTarBase ID miRNA Experiments Reference
MIRT020931 hsa-miR-155-5p Other 18262046
MIRT020931 hsa-miR-155-5p Reporter assay;Other 20584899
MIRT052627 hsa-let-7a-5p CLASH 23622248
MIRT052051 hsa-let-7b-5p CLASH 23622248
MIRT048127 hsa-miR-197-3p CLASH 23622248
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
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GO ID Ontology Definition Evidence Reference
GO:0004725 Function Protein tyrosine phosphatase activity IBA
GO:0005515 Function Protein binding IPI 21903422
GO:0005634 Component Nucleus IBA
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
614656 23530 ENSG00000107719
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q9ULE6
Protein name Paladin
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14566 PTPlike_phytase 161 330 Domain
PF14566 PTPlike_phytase 545 679 Domain
Tissue specificity TISSUE SPECIFICITY: Expressed in endothelial cells, and in certain larger vessels, in mural cells. In the brain, possibly expressed in microglia. Expressed in peripheral blood mononuclear cells (at protein level). {ECO:0000269|PubMed:22354871}.
Sequence
MGTTASTAQQTVSAGTPFEGLQGSGTMDSRHSVSIHSFQSTSLHNSKAKSIIPNKVAPVV
ITYNCKEEFQIHDELLKAHYTLGRLSDNTPEHYLVQGRYFLVRDVTEKMDVLGTVGSCGA
PNFRQVQGGLTVFGMGQPSLSGFRRVLQKLQKDGHRECVIFCVREEPVLFLRADEDFVSY
TPRDKQNLHENLQGLGPGVRVESLELAIRKEIHDFAQLSENTYHVYHNTEDLWGEPHAVA
IHGEDDLHVTEEVYKRPLFLQPTYRYHRLPLPEQGSPLEAQLDAFVSVLRETPSLLQLRD
AHGPPPALVFSCQMGVGRTNLGMVLGTLIL
LHRSGTTSQPEAAPTQAKPLPMEQFQVIQS
FLRMVPQGRRMVEEVDRAITACAELHDLKEVVLENQKKLEGIRPESPAQGSGSRHSVWQR
ALWSLERYFYLILFNYYLHEQYPLAFALSFSRWLCAHPELYRLPVTLSSAGPVAPRDLIA
RGSLREDDLVSPDALSTVREMDVANFRRVPRMPIYGTAQPSAKALGSILAYLTDAKRRLR
KVVWVSLREEAVLECDGHTYSLRWPGPPVAPDQLETLEAQLKAHLSEPPPGKEGPLTYRF
QTCLTMQEVFSQHRRACPGLTYHRIPMPDFCAPREEDFDQLLEALRAALSKDPGTGFVFS
CLSGQGRTTTAMVVAVLAF
WHIQGFPEVGEEELVSVPDAKFTKGEFQVVMKVVQLLPDGH
RVKKEVDAALDTVSETMTPMHYHLREIIICTYRQAKAAKEAQEMRRLQLRSLQYLERYVC
LILFNAYLHLEKADSWQRPFSTWMQEVASKAGIYEILNELGFPELESGEDQPFSRLRYRW
QEQSCSLEPSAPEDLL
Sequence length 856
Interactions View interactions
Associated diseases Disease associations from ClinVar categorized as Causal (Pathogenic/Likely Pathogenic) or Unknown.
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Unknown Diseases with uncertain, conflicting, or no pathogenic evidence in ClinVar
Phenotype Name Clinical Significance dbSNP ID RCV Accession
Acute myeloid leukemia Benign rs200131551 RCV005904874
Familial cancer of breast Benign rs200131551 RCV005904873
Gastric cancer Likely benign; Benign rs527946557, rs200131551 RCV005932941
RCV005904876
Lung cancer Benign rs200131551 RCV005904878
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References
Carcinoma Pancreatic Ductal Associate 34313325
Lymphoma Large B Cell Diffuse Associate 26311899
Subarachnoid Hemorrhage Associate 32450902