Description

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

Synonyms

pejvakin

Location

Chromosome 2: 178,451,436-178,461,390 forward strand.

GRCh38:CM000664.2

About this gene

This gene has 6 transcripts (splice variants), 50 orthologues, 1 paralogue, is a member of 1 Ensembl protein family and is associated with 3 phenotypes.

NameTranscript IDbpProteinTranslation IDBiotypeCCDSUniProtRefSeqFlags
DFNB59-001ENST000004091171531352aaENSP00000386647
 
Protein coding
CCDS42787Q0ZLH3 NM_001042702
NP_001036167
TSL:1GENCODE basicAPPRIS P1
DFNB59-003ENST000003751291202352aaENSP00000364271
 
Protein coding
CCDS42787Q0ZLH3 -TSL:1GENCODE basicAPPRIS P1
DFNB59-005ENST00000442710713156aaENSP00000410776
 
Protein coding
-H7C3A9 -CDS 5' incompleteTSL:5
DFNB59-004ENST00000444615471105aaENSP00000399579
 
Nonsense mediated decay
-H7C1C3 -CDS 5' incompleteTSL:3
DFNB59-006ENST00000605419261No protein-
 
Processed transcript
---TSL:5
DFNB59-002ENST000004370561942No protein-
 
Retained intron
---TSL:1

Gene-based displays