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Human (GRCh37.p13)
Description

fragile X mental retardation, autosomal homolog 2 [Source:HGNC Symbol;Acc:4024]

Gene Synonyms

FMR1L2, FXR2P

Location
About this transcript

This transcript has 3 exons, is associated with 633 variant alleles and maps to 64 oligo probes.

Gene
Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000250113.7FXR2-0012957673aaENSP00000250113.7
 
Protein coding
CCDS45604P51116 NM_004860.3Ensembl CanonicalGENCODE basic
ENST00000571597.1FXR2-002565118aaENSP00000459230.1
 
Protein coding
I3L1Z2 -CDS 3' incomplete
ENST00000573057.1FXR2-006675No protein-
 
Processed transcript
---
ENST00000574490.1FXR2-005743No protein-
 
Retained intron
---
ENST00000573957.1FXR2-004582No protein-
 
Retained intron
---
ENST00000576693.1FXR2-003477No protein-
 
Retained intron
---
ENST00000571079.1FXR2-007462No protein-
 
Retained intron
---
Statistics

Exons: 3, Coding exons: 0, Transcript length: 477 bps,

Version

ENST00000576693.1

Type

Retained intron

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:
OTTHUMT00000441089 (version 1)