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Human (GRCh37.p13)
Description

midline 1 (Opitz/BBB syndrome) [Source:HGNC Symbol;Acc:7095]

Gene Synonyms

BBBG1, FXY, GBBB1, MIDIN, OGS1, OS, OSX, RNF59, TRIM18, XPRF, ZNFXY

Location

Chromosome X: 10,413,350-10,851,773 reverse strand.

GRCh37:CM000685.1

About this gene

This gene has 10 transcripts (splice variants), 12 paralogues and is associated with 4 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000317552.4MID1-2016463667aaENSP00000312678.4
 
Protein coding
CCDS14138C9J453 C9JZJ7 O15344
NM_033289.1Ensembl CanonicalGENCODE basic
ENST00000453318.2MID1-2026393667aaENSP00000414521.2
 
Protein coding
CCDS14138C9J453 C9JZJ7 O15344
NM_001098624.2GENCODE basic
ENST00000380780.1MID1-0066195667aaENSP00000370157.1
 
Protein coding
CCDS14138C9J453 C9JZJ7 O15344
-GENCODE basic
ENST00000380785.1MID1-0016092667aaENSP00000370162.1
 
Protein coding
CCDS14138C9J453 C9JZJ7 O15344
-GENCODE basic
ENST00000380779.1MID1-0036044667aaENSP00000370156.1
 
Protein coding
CCDS14138C9J453 C9JZJ7 O15344
NM_001193277.1GENCODE basic
ENST00000380787.1MID1-0055973667aaENSP00000370164.1
 
Protein coding
CCDS14138C9J453 C9JZJ7 O15344
NM_033290.3GENCODE basic
ENST00000380782.2MID1-0073352552aaENSP00000370159.1
 
Protein coding
C9J453 C9JZJ7 O15344
-GENCODE basic
ENST00000413894.1MID1-0041729483aaENSP00000391154.1
 
Protein coding
C9J453 C9JZJ7 -CDS 3' incomplete
ENST00000423614.1MID1-002945197aaENSP00000387771.1
 
Protein coding
C9JZJ7 -CDS 3' incomplete
ENST00000479925.1MID1-008858No protein-
 
Processed transcript
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