EMBL-EBI User Survey 2024

Do data resources managed by EMBL-EBI and our collaborators make a difference to your work?

Please take 10 minutes to fill in our annual user survey, and help us make the case for why sustaining open data resources is critical for life sciences research.

Survey link: https://www.surveymonkey.com/r/HJKYKTT?channel=[webpage]

Human (GRCh37.p13)
Description

retinitis pigmentosa 2 (X-linked recessive) [Source:HGNC Symbol;Acc:10274]

Gene Synonyms

DELXp11.3, NM23-H10, NME10, TBCCD2, XRP2

Location
About this transcript

This transcript has 5 exons, is annotated with 10 domains and features, is associated with 12665 variant alleles and maps to 318 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000218340.3RP2-0013803350aaENSP00000218340.3
 
Protein coding
CCDS14270O75695 NM_006915.2Ensembl CanonicalGENCODE basic
Statistics

Exons: 5, Coding exons: 5, Transcript length: 3,803 bps, Translation length: 350 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: O75695

CCDS

This transcript is a member of the Human CCDS set: CCDS14270

Version

ENST00000218340.3

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000056375 (version 1)
GENCODE basic gene

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