PTPN14
close
Please copy/paste those URLs into your code to get same results in machine-readable formats:
|
Homo sapiens |
|
PTPN14 is differentially expressed in 248 experiments: 138 organism parts: liver, placenta, ... (136 more);, 189 disease states: normal, acute lymphoblastic leukemia, ... (187 more);, 79 cell types 349 cell lines 29 compound treatments and 69 other conditions. |
| Synonyms |
PEZ |
| Orthologs |
PTPN14
(Bos taurus)
Ptpn14
(Mus musculus)
PTP1
(Saccharomyces cerevisiae)
PTPN14
(Gallus gallus)
Ptpn14
(Rattus norvegicus)
Pez
(Drosophila melanogaster)
ptpn14
(Xenopus laevis)
PTPN14
(Canis familiaris)
(Compare orthologs)
|
| Gene Ontology ID |
GO:0008138, GO:0016311, GO:0016791, GO:0016787, GO:0004725, GO:0005488, GO:0004872, GO:0005737, GO:0005856, GO:0006470, GO:0030971, GO:0001946, GO:0035335 |
| Gene Ontology Term |
phosphatase activity, cytoskeleton, cytoplasm, dephosphorylation, protein tyrosine/serine/threonine phosphatase activity, protein tyrosine phosphatase activity, receptor activity, hydrolase activity, binding, lymphangiogenesis, receptor tyrosine kinase binding, peptidyl-tyrosine dephosphorylation, protein dephosphorylation |
| InterPro ID |
IPR000242, IPR000299, IPR019748, IPR019749, IPR019750, IPR000340, IPR000387, IPR003595, IPR014392, IPR018979, IPR018980 |
| InterPro Term |
Tyr_Pase_cat, FERM_central, Band_41_domain, Dual-sp_phosphatase_cat-dom, Tyr_Pase_rcpt/non-rcpt, FERM_domain, Tyr_Pase_non-rcpt_typ-14/21, Band_41_fam, FERM_N, FERM_PH-like_C, Tyr/Dual-specificity_Pase |
| Ensembl Family Description |
TYROSINE PHOSPHATASE NON RECEPTOR TYPE EC_3.1.3.48 TYROSINE PHOSPHATASE |
| Ensembl Family |
ENSFM00250000001986 |
| EMBL-Bank ID |
AL445305, AL592216, BC104803, AL603838, AL929236, X82676, BC101754, CH471100, HQ116786 |
| RefSeq ID |
NM_005401, NP_005392 |
| UniProt Accession |
Q15678, E2J9M0 |
| HGNC Symbol |
PTPN14 |
| Ensembl Protein ID |
ENSP00000355923, ENSP00000443330 |
| Description |
protein tyrosine phosphatase, non-receptor type 14 [Source:HGNC Symbol;Acc:9647] |
| UniGene ID |
Hs.193557, Hs.688910 |
| Ensembl Gene ID |
ENSG00000152104 |
| Entrez Gene ID |
5784 |
| Ensembl Transcript ID |
ENST00000491277, ENST00000366956, ENST00000543945, ENST00000473261, ENST00000486173 |
| Gene-Disease Assocation |
CHOANAL ATRESIA AND LYMPHEDEMA |
| Design Element |
205503_at, ENST00000486173, Hs.294079.0.A1_3p_at, 801_at, 244533_at, ENST00000491277, g4885566_3p_at, X82676_at, ENST00000366956, 89351_at, ENST00000473261, ENST00000543945 |
| Search EB-eye |
ENSG00000152104
|
Show more
properties
|
|