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Human (GRCh38.p14)
Description

midline 2 [Source:HGNC Symbol;Acc:HGNC:7096]

Gene Synonyms

FXY2, MRX101, RNF60, TRIM1

Location

Chromosome X: 107,825,730-107,931,637 forward strand.

GRCh38:CM000685.2

About this gene

This gene has 7 transcripts (splice variants), 202 orthologues, 80 paralogues and is associated with 3 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000262843.11MID2-2017333735aaENSP00000262843.6
 
Protein coding
CCDS14532Q9UJV3-1 NM_012216.4MANE SelectEnsembl CanonicalGENCODE PrimaryGENCODE BasicTSL:1
ENST00001135151.1MID2-2077469735aaENSP00000803372.1
 
Protein coding
CCDS14532--Ensembl Canonical ExtendedGENCODE Basic
ENST00000443968.3MID2-2027379705aaENSP00000413976.2
 
Protein coding
CCDS14533Q9UJV3-2 -GENCODE BasicAPPRIS P1TSL:1
ENST00000921443.2MID2-2067373703aaENSP00000591502.1
 
Protein coding
--GENCODE Basic
ENST00000898670.2MID2-2057283673aaENSP00000568729.1
 
Protein coding
--GENCODE Basic
ENST00000451923.1MID2-203758218aaENSP00000410730.1
 
Protein coding
A6PVI4 -TSL:3CDS 3' incomplete
ENST00000474517.1MID2-204689No protein-
 
Retained intron
--TSL:3