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Summary
- Splice variants
- Transcript comparison
- Gene alleles
Sequence
- Secondary Structure
Comparative Genomics
- Paralogues
- Genomic alignments
- Gene tree
- Gene gain/loss tree
- Orthologues
Ontologies
- GO: Cellular component
- GO: Molecular function
- GO: Biological process
Phenotypes
Genetic Variation
Gene expression
Pathway
Molecular interactions
Regulation
External references
Supporting evidence
ID History
- Gene history

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Gene: MANSC1 ENSG00000111261

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Description

MANSC domain containing 1 [Source:HGNC Symbol;Acc:25505]

Gene Synonyms

9130403P13Rik, FLJ10298, LOH12CR3

Location

Chromosome 12: 12,482,198-12,503,475 reverse strand.

GRCh37:CM000674.1

About this gene

This gene has 4 transcripts (splice variants).

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000535902.1	MANSC1-001	2623	431aa	ENSP00000438205.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS8648	F5H3M3 F5H6G8 Q9H8J5	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000396349.3	MANSC1-002	2220	397aa	ENSP00000379638.3	Gene/transcipt that contains an open reading frame (ORF).Protein coding		F5H3M3 Q9NW60	NM_018050.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000545735.1	MANSC1-004	1501	350aa	ENSP00000445303.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		F5H3M3	-	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000543314.1	MANSC1-005	496	57aa	ENSP00000437624.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		F5H6G8	-	3' truncation in transcript evidence prevents annotation of the end of the CDS.CDS 3' incomplete,

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Summary

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