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

Configure this page

Share this page

Bookmark this page

.

Gene: Fam185a ENSRNOG00000048371

.

Description

family with sequence similarity 185, member A [Source:RGD Symbol;Acc:1562135]

Gene Synonyms

LOC499979, MGC187429, RGD1562135

Location

Primary_assembly 4: 14,499,869-14,555,167 reverse strand.

GRCr8:CM070394.1

About this gene

This gene has 6 transcripts (splice variants) and 178 orthologues.

Transcripts

Show transcript tableHide transcript table

Transcript ID	Name	bp	Protein	Translation ID	Biotype	UniProt Match	Flags
ENSRNOT00000101027.2	Fam185a-202	2940	378aa	ENSRNOP00000086102.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6A565	A single transcript chosen for a gene which is the most conserved, most highly expressed, has the longest coding sequence and is represented in other key resources, such as NCBI and UniProt. This is defined in detail on http://www.ensembl.org/info/genome/genebuild/canonical.htmlEnsembl Canonical, APPRIS ALT2: For genes in which the APPRIS core modules are unable to choose a clear principal isoform, the ALT1 is the candidate transcript(s) models that appear to be conserved in fewer than three tested species. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS ALT2,
ENSRNOT00000111407.2	Fam185a-204	2847	347aa	ENSRNOP00000094481.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AMA4	-
ENSRNOT00000120183.2	Fam185a-206	2844	346aa	ENSRNOP00000097420.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6ASX3	APPRIS P2: Where the APPRIS core modules are unable to choose a clear principal variant (approximately 25% of human protein coding genes), the database chooses two or more of the CDS variants as "candidates" to be the principal variant. APPRIS is a system to annotate alternatively spliced transcripts based on a range of computational methods to identify the most functionally important transcript(s) of a gene. APPRIS P2,
ENSRNOT00000112320.2	Fam185a-205	2408	218aa	ENSRNOP00000092141.1	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6GJI9	-
ENSRNOT00000107889.2	Fam185a-203	1351	358aa	ENSRNOP00000093591.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	A0A8I6AHV7	-
ENSRNOT00000074662.3	Fam185a-201	905	208aa	ENSRNOP00000067845.2	Gene/transcipt that contains an open reading frame (ORF).Protein coding	B1WBS7	-

.

Summary

.

.