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Human (GRCh38.p14)
Description

patched 2 [Source:HGNC Symbol;Acc:HGNC:9586]

Location
About this transcript

This transcript has 22 exons, is annotated with 54 domains and features, is associated with 12412 variant alleles and maps to 589 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000372192.4PTCH2-20144101203aaENSP00000361266.3
 
Protein coding
CCDS516Q9Y6C5-1 NM_003738.5MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P2TSL:1
ENST00000447098.7PTCH2-20349881146aaENSP00000389703.2
 
Protein coding
CCDS53312Q9Y6C5-2 -GENCODE PrimaryGENCODE BasicAPPRIS ALT2TSL:1
ENST00000438067.5PTCH2-202111088aaENSP00000413169.1
 
Protein coding
H0Y7J2 -TSL:3CDS 5' incomplete
Statistics

Exons: 22, Coding exons: 22, Transcript length: 4,410 bps, Translation length: 1,203 residues

MANE

This MANE Select transcript contains ENSP00000361266 and matches to NM_003738.5 and NP_003729.3

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9Y6C5

CCDS

This transcript is a member of the Human CCDS set: CCDS516

Transcript Support Level (TSL)

TSL:1

Version

ENST00000372192.4

Type

Protein coding

Annotation Method

Manual annotation (determined on a case-by-case basis) from the Havana project.

GENCODE basic gene

This transcript is a member of the Gencode basic gene set.

GENCODE primary gene

This transcript is a member of the Gencode Primary gene set.