Human (GRCh38.p14)
Description

family with sequence similarity 135 member B [Source:HGNC Symbol;Acc:HGNC:28029]

Gene Synonyms

C8ORFK32

Location

Chromosome 8: 138,130,023-138,497,261 reverse strand.

GRCh38:CM000670.2

About this gene

This gene has 11 transcripts (splice variants), 220 orthologues, 1 paralogue and is associated with 69 phenotypes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeq MatchFlags
ENST00000395297.6FAM135B-20474011406aaENSP00000378710.1
 
Protein coding
CCDS6375Q49AJ0-1 NM_015912.4MANE SelectEnsembl CanonicalGENCODE basicAPPRIS P1TSL:5
ENST00000520380.1FAM135B-20968468aaENSP00000428017.1
 
Protein coding
E5RFQ7 -TSL:3CDS 3' incomplete
ENST00000160713.8FAM135B-201558153aaENSP00000160713.4
 
Protein coding
J3QSR3 -TSL:3CDS 3' incomplete
ENST00000482951.6FAM135B-206473443aaENSP00000429874.1
 
Nonsense mediated decay
E5RH68 -TSL:1
ENST00000276737.10FAM135B-20242881141aaENSP00000276737.6
 
Nonsense mediated decay
Q49AJ0-3 -TSL:5
ENST00000520283.1FAM135B-2085067No protein-
 
Protein coding CDS not defined
--TSL:1
ENST00000517849.1FAM135B-207547No protein-
 
Protein coding CDS not defined
--TSL:5
ENST00000523049.1FAM135B-211427No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000520954.1FAM135B-210378No protein-
 
Protein coding CDS not defined
--TSL:3
ENST00000467365.2FAM135B-2051616No protein-
 
Retained intron
--TSL:1
ENST00000395295.2FAM135B-203585No protein-
 
Retained intron
--TSL:4