PTCHD1-AS
gene geneOn this page
Also known as PTCHD1AS1PTCHD1AS2DDX53-AS1
Summary
PTCHD1-AS (PTCHD1 and PHEX antisense RNA, HGNC:37703) is a long non-coding RNA gene on chromosome Xp22.11.
At a glance
- Gene type: non-coding (lncRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:37703 |
| Approved symbol | PTCHD1-AS |
| Name | PTCHD1 and PHEX antisense RNA |
| Location | Xp22.11 |
| Locus type | RNA, long non-coding |
| Status | Approved |
| Aliases | PTCHD1AS1, PTCHD1AS2, DDX53-AS1 |
| Ensembl gene | ENSG00000233067 |
| Ensembl biotype | lncRNA |
| OMIM | 301140 |
| Entrez | 100873065 |
| RNAcentral | URS0000A76DB3 — lncRNA, 3772 nt, 1 organism(s) |
Gene structure
Transcript identifiers
Ensembl transcripts: 13 — 13 lncRNA
ENST00000424650, ENST00000669979, ENST00000687119, ENST00000687248, ENST00000715857, ENST00000796453, ENST00000799269, ENST00000799270, ENST00000819916, ENST00000825156, ENST00000825157, ENST00000825158, ENST00000825159
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000424650 — 5 exons
| Exon | Start | End |
|---|---|---|
| ENSE00001658112 | 22169794 | 22169855 |
| ENSE00001671565 | 22171510 | 22171644 |
| ENSE00001701462 | 22171159 | 22171190 |
| ENSE00001734605 | 22162733 | 22163371 |
| ENSE00001801931 | 22171946 | 22172983 |
Expression profiles
Bgee: expression breadth broad, 75 present calls, max score 69.44.
Top tissues by expression
75 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| bone marrow cell | CL:0002092 | 69.44 | silver quality |
| ganglionic eminence | UBERON:0004023 | 59.09 | gold quality |
| pancreas | UBERON:0001264 | 54.27 | gold quality |
| prefrontal cortex | UBERON:0000451 | 53.65 | gold quality |
| skeletal muscle tissue | UBERON:0001134 | 51.87 | silver quality |
| islet of Langerhans | UBERON:0000006 | 51.22 | gold quality |
| skin of leg | UBERON:0001511 | 51.05 | gold quality |
| cerebellum | UBERON:0002037 | 49.09 | silver quality |
| monocyte | CL:0000576 | 49.08 | silver quality |
| cerebellar cortex | UBERON:0002129 | 48.99 | silver quality |
| cerebellar hemisphere | UBERON:0002245 | 48.83 | silver quality |
| ovary | UBERON:0000992 | 48.58 | silver quality |
| frontal cortex | UBERON:0001870 | 48.52 | gold quality |
| right hemisphere of cerebellum | UBERON:0014890 | 47.49 | silver quality |
| lymph node | UBERON:0000029 | 47.18 | silver quality |
| muscle of leg | UBERON:0001383 | 47.02 | silver quality |
| myometrium | UBERON:0001296 | 46.78 | gold quality |
| duodenum | UBERON:0002114 | 46.74 | silver quality |
| placenta | UBERON:0001987 | 45.92 | silver quality |
| lung | UBERON:0002048 | 45.57 | silver quality |
| blood | UBERON:0000178 | 45.54 | silver quality |
| superior frontal gyrus | UBERON:0002661 | 45.54 | silver quality |
| cerebral cortex | UBERON:0000956 | 45.01 | gold quality |
| urinary bladder | UBERON:0001255 | 44.92 | gold quality |
| olfactory segment of nasal mucosa | UBERON:0005386 | 44.74 | silver quality |
| vagina | UBERON:0000996 | 44.40 | gold quality |
| gastrocnemius | UBERON:0001388 | 44.30 | silver quality |
| stomach | UBERON:0000945 | 44.26 | silver quality |
| brain | UBERON:0000955 | 44.19 | gold quality |
| right lobe of thyroid gland | UBERON:0001119 | 43.90 | silver quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.57 |
Regulation
Is transcription factor: no
Cross-species orthologs
0 orthologs
Protein
Non-coding RNA — no protein product; not a drug target.
Function
No curated pathway, Gene-Ontology, or interaction data.
Disease & clinical
No curated disease, variant, or cancer-driver associations.
Drugs & pharmacology
No drug or pharmacology data — not an established drug target.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): hypophosphatemic rickets, X-linked dominant hypophosphatemic rickets