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PTPRH

PTPRH
Identifiers
Aliases PTPRH, R-PTP-H, SAP1, protein tyrosine phosphatase, receptor type H
External IDs MGI: 3026877 HomoloGene: 37693 GeneCards: PTPRH
Gene location (Human)
Chromosome 19 (human)
Chr. Chromosome 19 (human)
Chromosome 19 (human)
Genomic location for PTPRH
Genomic location for PTPRH
Band 19q13.42 Start 55,181,248 bp
End 55,209,506 bp
RNA expression pattern
PBB GE PTPRH 208300 at fs.png
More reference expression data
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001161440
NM_002842

NM_207270

RefSeq (protein)

n/a

NP_997153

Location (UCSC) Chr 19: 55.18 – 55.21 Mb Chr 7: 4.55 – 4.6 Mb
PubMed search

NM_001161440
NM_002842

NM_207270

n/a

NP_997153

Receptor-type tyrosine-protein phosphatase H is an enzyme that in humans is encoded by the PTPRH 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 transformation. This PTP possesses an extracellular region, a single transmembrane region, and a single intracytoplasmic catalytic domain, and thus represents a receptor-type PTP. The extracellular region contains eight fibronectin type III-like repeats and multiple N-glycosylation sites. The gene was shown to be expressed primarily in brain and liver, and at a lower level in heart and stomach. It was also found to be expressed in several cancer cell lines, but not in the corresponding normal tissues.




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