STRA6 signaling receptor and transporter of retinol STRA6 [Homo sapiens (human)] - Gene

Summary

Official Symbol: STRA6provided by HGNC
Official Full Name: signaling receptor and transporter of retinol STRA6provided by HGNC
Primary source: HGNC:HGNC:30650
See related: Ensembl:ENSG00000137868 MIM:610745; AllianceGenome:HGNC:30650
Gene type: protein coding
RefSeq status: REVIEWED
Organism: Homo sapiens
Lineage: Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo
Also known as: MCOPS9; MCOPCB8; PP14296
Summary: The protein encoded by this gene is a membrane protein involved in the metabolism of retinol. The encoded protein acts as a receptor for retinol/retinol binding protein complexes. This protein removes the retinol from the complex and transports it across the cell membrane. Defects in this gene are a cause of syndromic microphthalmia type 9 (MCOPS9). Several transcript variants encoding a few different isoforms have been found for this gene. [provided by RefSeq, Dec 2008]
Expression: Biased expression in placenta (RPKM 6.8), endometrium (RPKM 4.0) and 6 other tissues See more
Orthologs: mouse all
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Genomic context

Location:: 15q24.1

Exon count:: 25

Annotation release	Status	Assembly	Chr	Location
RS_2024_08	current	GRCh38.p14 (GCF_000001405.40)	15	NC_000015.10 (74179466..74212259, complement)
RS_2024_08	current	T2T-CHM13v2.0 (GCF_009914755.1)	15	NC_060939.1 (72045386..72078184, complement)
RS_2024_09	previous assembly	GRCh37.p13 (GCF_000001405.25)	15	NC_000015.9 (74471807..74502046, complement)

Chromosome 15 - NC_000015.10 Genomic Context describing neighboring genes

Genomic regions, transcripts, and products

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Go to reference sequence details

Genomic Sequence:

Go to nucleotide: Graphics FASTA GenBank

Bibliography

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GeneRIFs: Gene References Into Functions

What's a GeneRIF?

STRA6 is essential for induction of vascular smooth muscle lineages in human embryonic cardiac outflow tract development.
Title: STRA6 is essential for induction of vascular smooth muscle lineages in human embryonic cardiac outflow tract development.
Up-regulation of STRA6 predicts poor prognosis and contributes to oxaliplatin resistance in colorectal cancer.
Title: Up-regulation of STRA6 predicts poor prognosis and contributes to oxaliplatin resistance in colorectal cancer.
STRA6 regulates tumor immune microenvironment and is a prognostic marker in BRAF-mutant papillary thyroid carcinoma.
Title: STRA6 regulates tumor immune microenvironment and is a prognostic marker in BRAF-mutant papillary thyroid carcinoma.
The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome.
Title: The protective variant rs7173049 at LOXL1 locus impacts on retinoic acid signaling pathway in pseudoexfoliation syndrome.
STRA6 Expression Serves as a Prognostic Biomarker of Gastric Cancer.
Title: STRA6 Expression Serves as a Prognostic Biomarker of Gastric Cancer.
Electronegative low-density lipoprotein of patients with metabolic syndrome induces pathogenesis of aorta through disruption of the stimulated by retinoic acid 6 cascade.
Title: Electronegative low-density lipoprotein of patients with metabolic syndrome induces pathogenesis of aorta through disruption of the stimulated by retinoic acid 6 cascade.
STRA6 is down-regulated by miR-873 and plays an oncogenic role by activating Wnt/beta-catenin signalling in GC.
Title: STRA6 exerts oncogenic role in gastric tumorigenesis by acting as a crucial target of miR-873.
SRC-2 is required for full induction of the retinol transporter, stimulated by retinoic acid 6 (STRA6), which is essential for endometrial stromal cell decidualization.
Title: Retinoid signaling controlled by SRC-2 in decidualization revealed by transcriptomics.
significant association between STRA6 polymorphism and Gestational diabetes mellitus in Chinese Han population
Title: Association of polymorphisms in STRA6 gene with gestational diabetes mellitus in a Chinese Han population.
We demonstrate that mutations in STRA6 are the cause for syndromic anophthalmia in the original Matthew-Wood patient
Title: Novel STRA6 null mutations in the original family described with Matthew-Wood syndrome.

Submit: New GeneRIF Correction See all GeneRIFs (34)

Phenotypes

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Find tests for this gene in the NIH Genetic Testing Registry (GTR)

Review eQTL and phenotype association data in this region using PheGenI

Associated conditions

Description	Tests
Matthew-Wood syndrome MedGen: C1832661 OMIM: 601186 GeneReviews: Not available	Compare labs

Variation

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See variants in ClinVar

See studies and variants in dbVar

See Variation Viewer (GRCh37.p13)

See Variation Viewer (GRCh38)

Interactions

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Products	Interactant	Other Gene	Complex	Source	Pubs	Description

General gene information

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Markers

NoName (e-PCR)
- UniSTS:9484

G30105 (e-PCR)
- UniSTS:36644

D8S2279 (e-PCR)
- UniSTS:473907

RH45099 (e-PCR)
- UniSTS:36697

D11S3114 (e-PCR)
- UniSTS:152207

Gene Ontology Provided by GOA

Function	Evidence Code	Pubs
enables protein binding	IPI Inferred from Physical Interaction more info	PubMed
enables retinal binding	IEA Inferred from Electronic Annotation more info
enables retinol binding	IEA Inferred from Electronic Annotation more info
enables retinol transmembrane transporter activity	IDA Inferred from Direct Assay more info	PubMed
enables signaling receptor activity	IEA Inferred from Electronic Annotation more info

Process	Evidence Code	Pubs
involved_in adrenal gland development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in alveolar primary septum development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in artery morphogenesis	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in blood vessel development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in camera-type eye development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in cognition	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in developmental growth	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in diaphragm development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in digestive tract morphogenesis	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in ductus arteriosus closure	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in ear development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in embryonic camera-type eye formation	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in embryonic digestive tract development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in eyelid development in camera-type eye	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in face morphogenesis	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in feeding behavior	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in female genitalia development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in head development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in head morphogenesis	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in heart development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in kidney development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in learning	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in lung alveolus development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in lung development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in lung vasculature development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in neuromuscular process	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in nose morphogenesis	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in paramesonephric duct development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in positive regulation of behavior	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in pulmonary artery morphogenesis	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in pulmonary valve morphogenesis	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in retinol transport	IDA Inferred from Direct Assay more info	PubMed
involved_in smooth muscle tissue development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in uterus morphogenesis	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in ventricular septum development	IMP Inferred from Mutant Phenotype more info	PubMed
involved_in vitamin A import into cell	IBA Inferred from Biological aspect of Ancestor more info
involved_in vocal learning	IMP Inferred from Mutant Phenotype more info	PubMed

Component	Evidence Code	Pubs
is_active_in plasma membrane	IBA Inferred from Biological aspect of Ancestor more info
located_in plasma membrane	IDA Inferred from Direct Assay more info	PubMed
located_in plasma membrane	TAS Traceable Author Statement more info
part_of protein-containing complex	IDA Inferred from Direct Assay more info

General protein information

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Preferred Names: receptor for retinol uptake STRA6

Names: RBP receptor; retinol binding protein 4 receptor; retinol-binding protein receptor STRA6; stimulated by retinoic acid 6 homolog; stimulated by retinoic acid gene 6 homolog; stimulated by retinoic acid gene 6 protein homolog

NCBI Reference Sequences (RefSeq)

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RefSeqs maintained independently of Annotated Genomes

These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

Genomic

NG_009207.1 RefSeqGene

Range

11244..34565

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GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

NM_001142617.2 → NP_001136089.1 receptor for retinol uptake STRA6 isoform a

See identical proteins and their annotated locations for NP_001136089.1

Status: REVIEWED

Description

Transcript Variant: This variant (1) differs in the 5' UTR and coding sequence compared to variant 8. The resulting isoform (a) is shorter at the N-terminus compared to isoform f. Variants 1, 2, and 3 all encode the same isoform (a).

Source sequence(s)

AF352729, AK056125

Consensus CDS

CCDS10261.1

UniProtKB/Swiss-Prot

A8K7F1, B7Z5M9, B7Z862, D3DW54, F5GYI8, I3L1G8, Q6PJF8, Q71RB9, Q7L9G1, Q7Z3U9, Q8TB21, Q9BX78, Q9BX79, Q9H9U8

UniProtKB/TrEMBL

B3KPB8

Related

ENSP00000326085.5, ENST00000323940.9

Conserved Domains (1) summary

pfam14752
Location:41 → 657

RBP_receptor; Retinol binding protein receptor
NM_001142618.2 → NP_001136090.1 receptor for retinol uptake STRA6 isoform a

See identical proteins and their annotated locations for NP_001136090.1

Status: REVIEWED

Description

Transcript Variant: This variant (3) differs in the 5' UTR and coding sequence compared to variant 8. The resulting isoform (a) is shorter at the N-terminus compared to isoform f. Variants 1, 2, and 3 all encode the same isoform (a).

Source sequence(s)

AF352729, AK056125, AK291966

Consensus CDS

CCDS10261.1

UniProtKB/Swiss-Prot

A8K7F1, B7Z5M9, B7Z862, D3DW54, F5GYI8, I3L1G8, Q6PJF8, Q71RB9, Q7L9G1, Q7Z3U9, Q8TB21, Q9BX78, Q9BX79, Q9H9U8

UniProtKB/TrEMBL

B3KPB8

Related

ENSP00000479112.1, ENST00000616000.4

Conserved Domains (1) summary

pfam14752
Location:41 → 657

RBP_receptor; Retinol binding protein receptor
NM_001142619.2 → NP_001136091.1 receptor for retinol uptake STRA6 isoform b

See identical proteins and their annotated locations for NP_001136091.1

Status: REVIEWED

Description

Transcript Variant: This variant (4) differs in the 5' UTR and coding sequence and uses an alternate splice junction at the 5' end of an exon compared to variant 8. The resulting isoform (b) is shorter at the N-terminus and lacks an internal segment compared to isoform f.

Source sequence(s)

AF352729, AK056125, DA746408

Consensus CDS

CCDS45301.1

UniProtKB/TrEMBL

B3KPB8

Related

ENSP00000413012.2, ENST00000423167.6

Conserved Domains (1) summary

pfam14752
Location:41 → 648

RBP_receptor; Retinol binding protein receptor
NM_001142620.2 → NP_001136092.1 receptor for retinol uptake STRA6 isoform c

See identical proteins and their annotated locations for NP_001136092.1

Status: REVIEWED

Description

Transcript Variant: This variant (5) differs in the 3' UTR and coding sequence compared to variant 8. The resulting isoform (c) has a shorter and distinct C-terminus compared to isoform f.

Source sequence(s)

BC015881, DA746408

Consensus CDS

CCDS45302.1

UniProtKB/Swiss-Prot

Q9BX79

Related

ENSP00000407176.2, ENST00000432245.6

Conserved Domains (1) summary

pfam14752
Location:41 → 134

RBP_receptor; Retinol binding protein receptor
NM_001199040.2 → NP_001185969.1 receptor for retinol uptake STRA6 isoform d

Status: REVIEWED

Description

Transcript Variant: This variant (6) differs in the 5' UTR and coding sequence compared to variant 8. The resulting isoform (d) has a shorter and distinct N-terminus compared to isoform f.

Source sequence(s)

AC023545, AF352728, AF352729, AK299191

Consensus CDS

CCDS55974.1

UniProtKB/TrEMBL

B3KPB8

Related

ENSP00000440238.1, ENST00000535552.5

Conserved Domains (1) summary

pfam14752
Location:78 → 694

RBP_receptor; Retinol binding protein receptor
NM_001199041.2 → NP_001185970.1 receptor for retinol uptake STRA6 isoform e

Status: REVIEWED

Description

Transcript Variant: This variant (7) differs in the 5' UTR and coding sequence compared to variant 8. The resulting isoform (e) has a shorter and distinct N-terminus compared to isoform f.

Source sequence(s)

AC023545, AF352728, AF352729, AK302932

Consensus CDS

CCDS58387.1

UniProtKB/TrEMBL

B3KPB8

Related

ENSP00000458827.1, ENST00000574278.5

Conserved Domains (1) summary

pfam14752
Location:56 → 672

RBP_receptor; Retinol binding protein receptor
NM_001199042.2 → NP_001185971.1 receptor for retinol uptake STRA6 isoform f

Status: REVIEWED

Description

Transcript Variant: This variant (8) represents the longest transcript and encodes the longest isoform (f).

Source sequence(s)

AC023545, AF352728, AF352729, AK309676

Consensus CDS

CCDS55973.1

UniProtKB/TrEMBL

B7Z5G7

Related

ENSP00000456609.1, ENST00000563965.5

Conserved Domains (1) summary

pfam14752
Location:80 → 696

RBP_receptor; Retinol binding protein receptor
NM_022369.4 → NP_071764.3 receptor for retinol uptake STRA6 isoform a

See identical proteins and their annotated locations for NP_071764.3

Status: REVIEWED

Description

Transcript Variant: This variant (2) differs in the 5' UTR and coding sequence compared to variant 8. The resulting isoform (a) is shorter at the N-terminus compared to isoform f. Variants 1, 2, and 3 all encode the same isoform (a).

Source sequence(s)

AF352729, AK056125, BC025256

Consensus CDS

CCDS10261.1

UniProtKB/Swiss-Prot

A8K7F1, B7Z5M9, B7Z862, D3DW54, F5GYI8, I3L1G8, Q6PJF8, Q71RB9, Q7L9G1, Q7Z3U9, Q8TB21, Q9BX78, Q9BX79, Q9H9U8

UniProtKB/TrEMBL

B3KPB8

Related

ENSP00000378537.4, ENST00000395105.9

Conserved Domains (1) summary

pfam14752
Location:41 → 657

RBP_receptor; Retinol binding protein receptor