Human (GRCh37.p13)
Description

FCH and double SH3 domains 2 [Source:HGNC Symbol;Acc:29114]

Gene Synonyms

KIAA0769, NWK, SH3MD3

Location

Chromosome 11: 72,547,790-72,853,306 reverse strand.

GRCh37:CM000673.1

About this gene

This gene has 9 transcripts (splice variants) and 1 paralogue.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000409418.4FCHSD2-0023154740aaENSP00000386722.4
 
Protein coding
CCDS8218C9JM66 O94868 NM_014824.2Ensembl CanonicalGENCODE Basic
ENST00000409314.1FCHSD2-0034509764aaENSP00000386987.1
 
Protein coding
C9JM66 E7ENZ2 E9PG19
-GENCODE Basic
ENST00000311172.7FCHSD2-0014340684aaENSP00000308978.7
 
Protein coding
O94868 -GENCODE Basic
ENST00000458644.2FCHSD2-0082215604aaENSP00000402972.2
 
Protein coding
E7ENZ2 -GENCODE Basic
ENST00000409853.1FCHSD2-0041867515aaENSP00000386314.1
 
Protein coding
O94868 -GENCODE Basic
ENST00000409263.1FCHSD2-007932101aaENSP00000386903.1
 
Protein coding
B8ZZW8 -GENCODE Basic
ENST00000422375.1FCHSD2-005587140aaENSP00000408706.1
 
Protein coding
C9JM66 -CDS 3' incomplete
ENST00000543644.1FCHSD2-01032185aaENSP00000441616.1
 
Protein coding
--CDS 5' incomplete
ENST00000432043.2FCHSD2-009578117aaENSP00000406420.2
 
Nonsense mediated decay
--CDS 5' incomplete
Stable ID

ENSG00000137478.10

Status

Current

Latest Version

ENSG00000137478.10

Release: 113 (current)

Assembly: GRCh37

Database: homo_sapiens_core_113_37

Associated archived IDs for this stable ID version

No associated IDs found