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Human (GRCh38.p14)
Description

RP9 pseudogene [Source:HGNC Symbol;Acc:HGNC:33969]

Location
About this transcript

This transcript has 6 exons, is associated with 11764 variant alleles and maps to 424 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSRefSeq MatchFlags
ENST00000381639.3RP9P-2021303No protein-
 
lncRNA
-Ensembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00000702940.1RP9P-2041263No protein-
 
lncRNA
-GENCODE Basic
ENST00000685019.1RP9P-2031145No protein-
 
lncRNA
--
ENST00000826634.1RP9P-2061118No protein-
 
lncRNA
--
ENST00000826633.1RP9P-2051051No protein-
 
lncRNA
--
ENST00000826635.1RP9P-207518No protein-
 
lncRNA
--
Statistics

Exons: 6, Coding exons: 0, Transcript length: 1,303 bps,

Transcript Support Level (TSL)

TSL:1

Version

ENST00000381639.3

Type

LncRNA

Annotation Method

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

Annotation Attributes

overlaps pseudogene [Definitions]

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.