Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
5797
Gene name Gene Name - the full gene name approved by the HGNC.
Protein tyrosine phosphatase receptor type M
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
PTPRM
Synonyms (NCBI Gene) Gene synonyms aliases
PTPRL1, R-PTP-MU, RPTPM, RPTPU, hR-PTPu
Chromosome Chromosome number
18
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
18p11.23
Summary Summary of gene provided in NCBI Entrez Gene.
The protein encoded by this gene is a member of the protein tyrosine phosphatase (PTP) family. PTPs are known to be signaling molecules that regulate a variety of cellular processes including cell growth, differentiation, mitotic cycle, and oncogenic tran
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT018602 hsa-miR-335-5p Microarray 18185580
MIRT054104 hsa-miR-205-5p Immunohistochemistry, Luciferase reporter assay, Microarray, QRTPCR 23497265
MIRT654619 hsa-miR-1264 HITS-CLIP 23824327
MIRT654618 hsa-miR-4461 HITS-CLIP 23824327
MIRT654617 hsa-miR-130b-5p HITS-CLIP 23824327
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001937 Process Negative regulation of endothelial cell proliferation IMP 18566238
GO:0004725 Function Protein tyrosine phosphatase activity IBA 21873635
GO:0004725 Function Protein tyrosine phosphatase activity IDA 8393854, 17965016, 18566238
GO:0005001 Function Transmembrane receptor protein tyrosine phosphatase activity IDA 10809770
GO:0005515 Function Protein binding IPI 9531566, 11278757, 16380380
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
176888 9675 ENSG00000173482
Protein
UniProt ID P28827
Protein name Receptor-type tyrosine-protein phosphatase mu (Protein-tyrosine phosphatase mu) (R-PTP-mu) (EC 3.1.3.48)
Protein function Receptor protein-tyrosine phosphatase that mediates homotypic cell-cell interactions and plays a role in adipogenic differentiation via modulation of p120 catenin/CTNND1 phosphorylation (PubMed:10753936, PubMed:17761881). Promotes CTNND1 dephosp
PDB 1RPM , 2C9A , 2V5Y , 8A16 , 8A17
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF00629 MAM 27 183 MAM domain, meprin/A5/mu Domain
PF00047 ig 189 274 Immunoglobulin domain Domain
PF00041 fn3 283 366 Fibronectin type III domain Domain
PF00041 fn3 488 575 Fibronectin type III domain Domain
PF18861 PTP_tm 611 768 Transmembrane domain of protein tyrosine phosphatase, receptor type J Family
PF00102 Y_phosphatase 923 1153 Protein-tyrosine phosphatase Domain
PF00102 Y_phosphatase 1213 1447 Protein-tyrosine phosphatase Domain
Sequence
MRGLGTCLATLAGLLLTAAGETFSGGCLFDEPYSTCGYSQSEGDDFNWEQVNTLTKPTSD
PWMPSGSFMLVNASGRPEGQRAHLLLPQLKENDTHCIDFHYFVSSKSNSPPGLLNVYVKV
NNGPLGNPIWNISGDPTRTWNRAELAISTFWPNFYQVIFEVITSGHQGYLAIDEVKVLGH
PCT
RTPHFLRIQNVEVNAGQFATFQCSAIGRTVAGDRLWLQGIDVRDAPLKEIKVTSSRR
FIASFNVVNTTKRDAGKYRCMIRTEGGVGISNYA
ELVVKEPPVPIAPPQLASVGATYLWI
QLNANSINGDGPIVAREVEYCTASGSWNDRQPVDSTSYKIGHLDPDTEYEISVLLTRPGE
GGTGSP
GPALRTRTKCADPMRGPRKLEVVEVKSRQITIRWEPFGYNVTRCHSYNLTVHYC
YQVGGQEQVREEVSWDTENSHPQHTITNLSPYTNVSVKLILMNPEGRKESQELIVQTDED
LPGAVPTESIQGSTFEEKIFLQWREPTQTYGVITLYEITYKAVSSFDPEIDLSNQSGRVS
KLGNETHFLFFGLYPGTTYSFTIRASTAKGFGPPA
TNQFTTKISAPSMPAYELETPLNQT
DNTVTVMLKPAHSRGAPVSVYQIVVEEERPRRTKKTTEILKCYPVPIHFQNASLLNSQYY
FAAEFPADSLQAAQPFTIGDNKTYNGYWNTPLLPYKSYRIYFQAASRANGETKIDCVQVA
TKGAATPKPVPEPEKQTDHTVKIAGVIAGILLFVIIFLGVVLVMKKRK
LAKKRKETMSST
RQEMTVMVNSMDKSYAEQGTNCDEAFSFMDTHNLNGRSVSSPSSFTMKTNTLSTSVPNSY
YPDETHTMASDTSSLVQSHTYKKREPADVPYQTGQLHPAIRVADLLQHITQMKCAEGYGF
KEEYESFFEGQSAPWDSAKKDENRMKNRYGNIIAYDHSRVRLQTIEGDTNSDYINGNYID
GYHRPNHYIATQGPMQETIYDFWRMVWHENTASIIMVTNLVEVGRVKCCKYWPDDTEIYK
DIKVTLIETELLAEYVIRTFAVEKRGVHEIREIRQFHFTGWPDHGVPYHATGLLGFVRQV
KSKSPPSAGPLVVHCSAGAGRTGCFIVIDIMLDMAEREGVVDIYNCVRELRSRRVNMVQT
EEQYVFIHDAILE
ACLCGDTSVPASQVRSLYYDMNKLDPQTNSSQIKEEFRTLNMVTPTL
RVEDCSIALLPRNHEKNRCMDILPPDRCLPFLITIDGESSNYINAALMDSYKQPSAFIVT
QHPLPNTVKDFWRLVLDYHCTSVVMLNDVDPAQLCPQYWPENGVHRHGPIQVEFVSADLE
EDIISRIFRIYNAARPQDGYRMVQQFQFLGWPMYRDTPVSKRSFLKLIRQVDKWQEEYNG
GEGRTVVHCLNGGGRSGTFCAISIVCEMLRHQRTVDVFHAVKTLRNNKPNMVDLLDQYKF
CYEVALE
YLNSG
Sequence length 1452
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Unknown
Disease term Disease name Evidence References Source
Huntington Disease Huntington Disease GWAS
Metabolic Syndrome Metabolic Syndrome GWAS
Oligodendroglioma Oligodendroglioma GWAS
Parkinson disease Parkinson disease GWAS
Associations from Text Mining
Disease Name Relationship Type References
Adenocarcinoma Associate 26683690
Astrocytoma Associate 27586084
Breast Neoplasms Inhibit 23185569
Carcinogenesis Associate 22968929, 25910225
Carcinoma Ovarian Epithelial Inhibit 37403117
Colonic Neoplasms Inhibit 25910225
Colorectal Neoplasms Associate 22968929, 25910225
Glioblastoma Associate 27586084, 34225581
Leukemia Myeloid Acute Associate 27784745
Lupus Erythematosus Systemic Associate 30685201