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

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Gene: FAM98B ENSG00000171262

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Description

family with sequence similarity 98, member B [Source:HGNC Symbol;Acc:26773]

Gene Synonyms

FLJ38426

Location

Chromosome 15: 38,746,328-38,779,911 forward strand.

GRCh37:CM000677.1

About this gene

This gene has 4 transcripts (splice variants) and 2 paralogues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	CCDS	UniProt Match	RefSeq	Flags
ENST00000397609.2	FAM98B-001	4388	433aa	ENSP00000380734.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS10047	Q52LJ0	NM_173611.2	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000491535.1	FAM98B-002	3111	330aa	ENSP00000453166.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	CCDS42015	Q52LJ0	NM_001042429.1	The GENCODE set is the gene set for human and mouse. GENCODE Basic is a subset of representative transcripts (splice variants).GENCODE basic,
ENST00000559431.1	FAM98B-004	305	101aa	ENSP00000453926.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding		H0YNA1	-	5' and 3' truncations in transcript evidence prevent annotation of the start and the end of the CDS.CDS 5' and 3' incomplete,
ENST00000305752.4	FAM98B-003	600	No protein	-	An alternatively spliced transcript believed to contain intronic sequence relative to other, coding, transcripts of the same gene.Retained intron		-	-	-

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Summary

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