Human (GRCh37.p13)
Description

oculocerebrorenal syndrome of Lowe [Source:HGNC Symbol;Acc:8108]

Gene Synonyms

INPP5F, LOCR, NPHL2, OCRL-1, OCRL1

About this transcript

This transcript has 23 exons, is annotated with 14 domains and features, is associated with 15697 variant alleles and maps to 736 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000371113.4OCRL-0015162901aaENSP00000360154.4
 
Protein coding
CCDS35393Q01968 NM_000276.3GENCODE basic
ENST00000357121.5OCRL-0025138893aaENSP00000349635.5
 
Protein coding
CCDS35394Q01968 NM_001587.3GENCODE basic
ENST00000486673.1OCRL-003942No protein-
 
Processed transcript
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ENST00000463271.1OCRL-005856No protein-
 
Processed transcript
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Statistics

Exons: 23, Coding exons: 23, Transcript length: 5,138 bps, Translation length: 893 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q01968

CCDS

This transcript is a member of the Human CCDS set: CCDS35394

Version

ENST00000357121.5

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:
OTTHUMT00000058918 (version 1)
GENCODE basic gene

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