SUSD3 - sushi domain containing 3 Gene

Homo sapiens

Gene ID: 203328 | Gene type: protein coding

About SUSD3

Cytogenetic location: 9q22.31 Genomic coordinates (GRCh38): 9:93,058,701-93,085,133 (from NCBI)

This gene has 5 transcripts (splice variants), 121 orthologues and 39 paralogues. Biased expression in testis (RPKM 12.2), lymph node (RPKM 7.6) and 12 other tissues.

Summary

Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

SUSD3 Products(5)

mRNA	Protein	Name
NM_001287005.2	NP_001273934.1	sushi domain-containing protein 3 isoform b
NM_001287006.2	NP_001273935.1	sushi domain-containing protein 3 isoform c
NM_001287007.2	NP_001273936.1	sushi domain-containing protein 3 isoform d
NM_001287008.2	NP_001273937.1	sushi domain-containing protein 3 isoform e
NM_145006.4	NP_659443.1	sushi domain-containing protein 3 isoform a

Gene Ontology

Molecular Function
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables protein binding	IPI IPI: Inferred from physical interaction	32296183	GOA

Cellular Component GO Annotation	Evidence	Reference	Source
located in plasma membrane	IDA IDA: Inferred from direct assay	24413080	GOA

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

SUSD3 Protein Structure

Sushi

0
100
200
255 a.a.

Protein Preferred Names

Protein Names

sushi domain-containing protein 3

Related Diseases

Diseases

Alias

Aarskog-Scott Syndrome

Aarskog Syndrome	Faciogenital Dysplasia
Faciodigitogenital Syndrome	AAS
Fgdy	X-Linked Aarskog Syndrome
Intellectual Developmental Disorder, X-Linked, Syndromic 16	Aarskog Syndrome, X-Linked
Intellectual Developmental Disorder, X-Linked Syndromic 16	Greig'S Syndrome
Aarskog Scott Syndrome	Aarskog Disease
Scott Aarskog Syndrome	Facio-Digito-Genital Dysplasia
Faciogenital Dysplasia With Attention Deficit-Hyperactivity Disorder	Aarskog-Scott Syndrome ) Syndrome

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS14048	SUSD3 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Macaca mulatta	SUSD3	VGNC	VGNC:78229
Mus musculus	SUSD3	MGD	MGI:1913579
Canis familiaris	SUSD3	VGNC	VGNC:46999
Rattus norvegicus	SUSD3	RGD	RGD:1310933
Bos taurus	SUSD3	VGNC	VGNC:35488
Felis catus	SUSD3	VGNC	VGNC:102992

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