Human Gene PIEZO2 (ENST00000674853.1) from GENCODE V50
Description: piezo type mechanosensitive ion channel component 2, transcript variant 1 (from RefSeq NM_001378183.1)
Gencode Transcript: ENST00000674853.1
Gencode Gene: ENSG00000154864.15
Transcript (Including UTRs)
Position: hg38 chr18:10,670,247-11,149,569 Size: 479,323 Total Exon Count: 56 Strand: -
Coding Region
Position: hg38 chr18:10,671,527-11,148,588 Size: 477,062 Coding Exon Count: 56
Data last updated at UCSC: 2026-07-12 09:30:09
Sequence and Links to Tools and Databases
Primer design for this transcript
MalaCards Disease Associations
MalaCards Gene Search: PIEZO2
Diseases sorted by gene-association score: marden-walker syndrome * (1739), arthrogryposis, distal, type 3 * (1650), arthrogryposis, distal, type 5 * (1550), arthrogryposis, distal, with impaired proprioception and touch * (1230), arthrogryposis multiple congenita, ophthalmoplegia, ptosis * (400), pseudohypoaldosteronism, type iie * (283), distal arthrogryposis * (200)* = Manually curated disease association
Comparative Toxicogenomics Database (CTD)
RNA-Seq Expression Data from GTEx (53 Tissues, 570 Donors)
Microarray Expression Data
mRNA Secondary Structure of 3' and 5' UTRs
The RNAfold program from the Vienna RNA Package is used to perform the secondary structure predictions and folding calculations. The estimated folding energy is in kcal/mol. The more negative the energy, the more secondary structure the RNA is likely to have.
Orthologous Genes in Other Species
Orthologies between human, mouse, and rat are computed by taking the best BLASTP hit, and filtering out non-syntenic hits. For more distant species reciprocal-best BLASTP hits are used. Note that the absence of an ortholog in the table below may reflect incomplete annotations in the other species rather than a true absence of the orthologous gene.
Descriptions from all associated GenBank mRNAs
JN790819 - Homo sapiens PIEZO2 (PIEZO2) mRNA, complete cds.MG254547 - Homo sapiens PIEZO2 variant 16 (PIEZO2) mRNA, complete cds, alternatively spliced.AK127627 - Homo sapiens cDNA FLJ45725 fis, clone HCHON2009766.AK095053 - Homo sapiens cDNA FLJ37734 fis, clone BRHIP2020842.AK092226 - Homo sapiens cDNA FLJ34907 fis, clone NT2RI2003392.AX747416 - Sequence 941 from Patent EP1308459.AK026797 - Homo sapiens cDNA: FLJ23144 fis, clone LNG09262.AK027056 - Homo sapiens cDNA: FLJ23403 fis, clone HEP18857.JD422964 - Sequence 403988 from Patent EP1572962.JD084586 - Sequence 65610 from Patent EP1572962.AK302764 - Homo sapiens cDNA FLJ55399 complete cds, highly similar to Protein FAM38B.JD164871 - Sequence 145895 from Patent EP1572962.JD315133 - Sequence 296157 from Patent EP1572962.BC148379 - Synthetic construct Homo sapiens clone IMAGE:100015296, MGC:182972 family with sequence similarity 38, member B (FAM38B) mRNA, encodes complete protein.AB527139 - Synthetic construct DNA, clone: pF1KE0043, Homo sapiens FAM38B gene for family with sequence similarity 38, member B, without stop codon, in Flexi system.JD160185 - Sequence 141209 from Patent EP1572962.JD327823 - Sequence 308847 from Patent EP1572962.AK098782 - Homo sapiens cDNA FLJ25916 fis, clone CBR04903.JD110976 - Sequence 92000 from Patent EP1572962.JD347797 - Sequence 328821 from Patent EP1572962.JD039114 - Sequence 20138 from Patent EP1572962.JD528285 - Sequence 509309 from Patent EP1572962.
Other Names for This Gene
Alternate Gene Symbols: A0A2H4UKA7, A0A2H4UKA7_HUMAN, NM_001378183, PIEZO2 , uc288nyw.1UCSC ID: ENST00000674853.1RefSeq Accession: NM_001378183.1
CCDS: CCDS11850.2
Methods, Credits, and Use Restrictions
Click here
for details on how this gene model was made and data restrictions if any.