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 8 exons, is associated with 5927 variant alleles and maps to 164 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000371113.4OCRL-0015162901aaENSP00000360154.4
 
Protein coding
CCDS35393Q01968 NM_000276.3Ensembl CanonicalGENCODE 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: 8, Coding exons: 0, Transcript length: 942 bps,

Version

ENST00000486673.1

Type

Processed transcript

Annotation Method

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

Alternative transcripts

This transcript corresponds to the following database identifiers:

Havana transcript:
OTTHUMT00000058919 (version 1)