Advanced notice of Ensembl Tools maintenance
Please note that due to planned maintenance, Ensembl Tools will be unavailable from Tuesday, September 9, at 08:30 AM BST until Wednesday, September 10, at 08:30 AM BST.
Jobs submitted during the maintenance window will be queued and processed once maintenance is complete. We apologise for the inconvenience.

Human (GRCh38.p14)
Description

FXYD domain containing ion transport regulator 7 [Source:HGNC Symbol;Acc:HGNC:4034]

Location

Chromosome 19: 35,143,148-35,154,302 forward strand.

GRCh38:CM000681.2

About this gene

This gene has 9 transcripts (splice variants), 36 orthologues and 6 paralogues.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000270310.7FXYD7-20170880aaENSP00000270310.2
 
Protein coding
CCDS12446P58549 NM_022006.2MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicAPPRIS P2TSL:1
ENST00000968511.1FXYD7-20782182aaENSP00000638570.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000968512.1FXYD7-20870552aaENSP00000638571.1
 
Protein coding
--GENCODE Basic
ENST00000900287.1FXYD7-20569072aaENSP00000570346.1
 
Protein coding
--GENCODE PrimaryGENCODE BasicAPPRIS ALT1
ENST00000934123.1FXYD7-20664569aaENSP00000604182.1
 
Protein coding
--GENCODE BasicAPPRIS ALT2
ENST00000588265.1FXYD7-204636117aaENSP00000465784.1
 
Protein coding
K7EKU3 -GENCODE PrimaryGENCODE BasicTSL:2
ENST00000968513.1FXYD7-20960652aaENSP00000638572.1
 
Protein coding
--GENCODE PrimaryGENCODE Basic
ENST00000586063.5FXYD7-20345677aaENSP00000466915.1
 
Protein coding
K7ENE8 -GENCODE BasicAPPRIS ALT1TSL:3
ENST00000439441.1FXYD7-2021111No protein-
 
Retained intron
--TSL:2