Description

deafness, autosomal recessive 59 [Source:HGNC Symbol;Acc:HGNC:29502]

Synonyms

pejvakin

INSDC coordinates

chromosome:GRCh38:CM000664.2:178451436:178461390:1

Transcripts

This gene has 6 transcripts (splice variants) Show transcript tableHide transcript table

NameTranscript IDLengthProteinBiotypeCCDSUniProtRefSeqFlags
DFNB59-001ENST000004091171531 bp352 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS42787A0PK15 Q0ZLH3 NM_001042702
NP_001036167
GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
DFNB59-003ENST000003751291202 bp352 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
CCDS42787A0PK15 Q0ZLH3 -GENCODE basicThe GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).
DFNB59-005ENST00000442710713 bp156 aa (view)
 
Protein codingGenes and/or transcript that contains an open reading frame (ORF).
---CDS 5' incomplete5' truncation in transcript evidence prevents annotation of the start of the CDS.
DFNB59-004ENST00000444615471 bp105 aa (view)
 
Nonsense mediated decayTranscript is thought to undergo nonsense mediated decay, a process which detects nonsense mutations and prevents the expression of truncated or erroneous proteins.
---CDS 5' incomplete5' truncation in transcript evidence prevents annotation of the start of the CDS.
DFNB59-006ENST00000605419261 bp No protein product
 
Processed transcriptTranscripts that don't contain an open reading frame (ORF) and cannot be placed in one of the other categories.
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DFNB59-002ENST000004370561942 bp No protein product
 
Retained intronAlternatively spliced transcript that is believed to contain intronic sequence relative to other coding transcripts in a given locus.
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Gene-based displays