Human (GRCh37.p13)
Description

spermatogenesis associated 5-like 1 [Source:HGNC Symbol;Acc:28762]

Gene Synonyms

FLJ12286, MGC5347

Location
About this transcript

This transcript has 8 exons, is annotated with 17 domains and features, is associated with 8843 variant alleles and maps to 478 oligo probes.

Transcript IDNamebpProteinTranslation IDBiotypeCCDSUniProt MatchRefSeqFlags
ENST00000305560.6SPATA5L1-0012570753aaENSP00000305494.6
 
Protein coding
CCDS10123Q9BVQ7 NM_024063.2Ensembl CanonicalGENCODE basic
ENST00000559860.1SPATA5L1-0072023620aaENSP00000453406.1
 
Protein coding
Q9BVQ7 -GENCODE basic
ENST00000531624.1SPATA5L1-004944258aaENSP00000431242.1
 
Protein coding
--CDS 5' incomplete
ENST00000531970.1SPATA5L1-0022464620aaENSP00000436823.1
 
Nonsense mediated decay
Q9BVQ7 --
ENST00000525552.1SPATA5L1-00336219aaENSP00000453091.1
 
Nonsense mediated decay
--CDS 5' incomplete
ENST00000533841.1SPATA5L1-006521No protein-
 
Processed transcript
---
ENST00000533199.1SPATA5L1-005583No protein-
 
Retained intron
---
Statistics

Exons: 8, Coding exons: 8, Transcript length: 2,570 bps, Translation length: 753 residues

Uniprot

This transcript corresponds to the following Uniprot identifiers: Q9BVQ7

CCDS

This transcript is a member of the Human CCDS set: CCDS10123

Version

ENST00000305560.6

Type

Protein coding

Annotation Method

Transcript where the Ensembl genebuild transcript and the Havana manual annotation have the same sequence, for every base pair. See article.

Alternative transcripts

This transcript corresponds to the following database identifiers:

Transcript having exact match between ENSEMBL and HAVANA:
OTTHUMT00000254218 (version 1)
GENCODE basic gene

This transcript is a member of the Gencode basic gene set.