Gene Details | GeDiPNet - Complete Gene Info, Disease Associations & Pathways

Gene Gene SNPs miRNA Gene ontology Other IDs Protein Pathways Associated diseases
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.	6448
Gene name Gene Name - the full gene name approved by the HGNC.	N-sulfoglucosamine sulfohydrolase
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.	SGSH
Synonyms (NCBI Gene) Gene synonyms aliases	HSS, MPS3A, SFMD
Chromosome Chromosome number	17
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.	17q25.3
Summary Summary of gene provided in NCBI Entrez Gene.	This gene encodes the enzyme sulfamidase; one of several enzymes involved in the lysosomal degradation of heparan sulfate. Mutations in this gene are associated with the lysosomal storage disease mucopolysaccaridosis IIIA, also known as Sanfilippo syndrom

Show/Hide all(64)

SNP ID	Visualize variation	Clinical significance	Consequence
rs34520362	G>A,C	Pathogenic, benign, uncertain-significance	Synonymous variant, non coding transcript variant, missense variant, coding sequence variant
rs104894635	C>A,T	Pathogenic, uncertain-significance	Non coding transcript variant, missense variant, coding sequence variant
rs104894636	G>A	Likely-pathogenic, pathogenic-likely-pathogenic, pathogenic	Non coding transcript variant, missense variant, coding sequence variant
rs104894637	G>A,C	Pathogenic	Non coding transcript variant, missense variant, coding sequence variant
rs104894638	C>T	Pathogenic-likely-pathogenic	Non coding transcript variant, missense variant, coding sequence variant
rs104894639	C>T	Pathogenic-likely-pathogenic, pathogenic	Non coding transcript variant, genic downstream transcript variant, downstream transcript variant, coding sequence variant, intron variant, missense variant, 3 prime UTR variant
rs104894640	C>A,G,T	Likely-pathogenic, pathogenic	Stop gained, non coding transcript variant, genic downstream transcript variant, downstream transcript variant, coding sequence variant, intron variant, missense variant, 3 prime UTR variant
rs104894641	C>T	Pathogenic-likely-pathogenic, pathogenic	Non coding transcript variant, genic downstream transcript variant, downstream transcript variant, coding sequence variant, intron variant, missense variant, 3 prime UTR variant
rs104894642	G>A	Pathogenic	Non coding transcript variant, missense variant, coding sequence variant
rs104894643	C>G,T	Likely-pathogenic	Non coding transcript variant, missense variant, coding sequence variant
rs138504221	A>G	Pathogenic	Coding sequence variant, non coding transcript variant, missense variant
rs141153056	G>A	Conflicting-interpretations-of-pathogenicity, uncertain-significance	3 prime UTR variant, intron variant, coding sequence variant, genic downstream transcript variant, downstream transcript variant, synonymous variant, non coding transcript variant
rs143947056	G>A	Pathogenic, pathogenic-likely-pathogenic	Coding sequence variant, non coding transcript variant, missense variant
rs144143780	T>C	Pathogenic	3 prime UTR variant, intron variant, downstream transcript variant, coding sequence variant, genic downstream transcript variant, non coding transcript variant, missense variant
rs144862290	C>G,T	Conflicting-interpretations-of-pathogenicity	3 prime UTR variant, intron variant, downstream transcript variant, coding sequence variant, genic downstream transcript variant, non coding transcript variant, missense variant
rs374621913	G>A,C	Pathogenic-likely-pathogenic, pathogenic, uncertain-significance	Non coding transcript variant, stop gained, coding sequence variant, missense variant
rs398123244	->CGCTGG	Likely-pathogenic, uncertain-significance	Intron variant, downstream transcript variant, genic downstream transcript variant, coding sequence variant, 3 prime UTR variant, non coding transcript variant, inframe insertion
rs529855742	G>A	Pathogenic-likely-pathogenic	Non coding transcript variant, coding sequence variant, missense variant
rs745884647	C>A,G,T	Likely-pathogenic	Coding sequence variant, missense variant, non coding transcript variant
rs746776254	G>A,C	Likely-pathogenic	Coding sequence variant, missense variant, non coding transcript variant
rs752914124	GGAGGTCCTTG>-	Pathogenic, pathogenic-likely-pathogenic	3 prime UTR variant, coding sequence variant, downstream transcript variant, stop gained, intron variant, inframe indel, non coding transcript variant, genic downstream transcript variant
rs753472891	C>T	Pathogenic-likely-pathogenic	Coding sequence variant, missense variant, non coding transcript variant
rs753666460	C>T	Likely-pathogenic	Coding sequence variant, missense variant, non coding transcript variant
rs758756630	T>C	Likely-pathogenic, uncertain-significance	3 prime UTR variant, coding sequence variant, intron variant, missense variant, genic downstream transcript variant, downstream transcript variant, non coding transcript variant
rs761607612	C>T	Pathogenic-likely-pathogenic	Coding sequence variant, missense variant, non coding transcript variant
rs764057581	G>T	Likely-pathogenic	3 prime UTR variant, coding sequence variant, intron variant, missense variant, genic downstream transcript variant, downstream transcript variant, non coding transcript variant
rs766938111	C>T	Conflicting-interpretations-of-pathogenicity, likely-pathogenic	3 prime UTR variant, non coding transcript variant, missense variant, intron variant, downstream transcript variant, genic downstream transcript variant, coding sequence variant
rs770947426	G>-	Pathogenic	Frameshift variant, 3 prime UTR variant, non coding transcript variant, intron variant, downstream transcript variant, genic downstream transcript variant, coding sequence variant
rs772311757	G>A	Pathogenic	3 prime UTR variant, non coding transcript variant, missense variant, intron variant, downstream transcript variant, genic downstream transcript variant, coding sequence variant
rs774010006	C>T	Likely-pathogenic	Missense variant, intron variant, non coding transcript variant, coding sequence variant
rs777267343	G>A	Pathogenic-likely-pathogenic	3 prime UTR variant, non coding transcript variant, missense variant, intron variant, downstream transcript variant, genic downstream transcript variant, coding sequence variant
rs777956287	C>-	Pathogenic	Frameshift variant, 3 prime UTR variant, non coding transcript variant, intron variant, downstream transcript variant, genic downstream transcript variant, coding sequence variant
rs778336949	C>T	Pathogenic-likely-pathogenic	Missense variant, non coding transcript variant, coding sequence variant
rs778700037	->G	Pathogenic	Frameshift variant, 3 prime UTR variant, non coding transcript variant, intron variant, downstream transcript variant, genic downstream transcript variant, coding sequence variant
rs779703983	T>G	Likely-pathogenic	Missense variant, non coding transcript variant, coding sequence variant
rs781572815	C>-	Likely-pathogenic	Frameshift variant, genic downstream transcript variant, coding sequence variant, 3 prime UTR variant, intron variant, non coding transcript variant, downstream transcript variant
rs886041370	C>T	Likely-pathogenic, pathogenic	Coding sequence variant, non coding transcript variant, stop gained
rs1046551417	C>A,G,T	Conflicting-interpretations-of-pathogenicity, uncertain-significance	Missense variant, coding sequence variant, non coding transcript variant
rs1057517927	T>C	Pathogenic	Splice acceptor variant
rs1057521146	C>T	Likely-pathogenic, uncertain-significance	Coding sequence variant, non coding transcript variant, missense variant
rs1057521801	A>G	Likely-pathogenic, pathogenic	Coding sequence variant, non coding transcript variant, missense variant
rs1064794815	C>T	Likely-pathogenic	Intron variant, genic downstream transcript variant, missense variant, coding sequence variant, 3 prime UTR variant, downstream transcript variant, non coding transcript variant
rs1064795109	C>T	Likely-pathogenic	Intron variant, genic downstream transcript variant, missense variant, coding sequence variant, 3 prime UTR variant, downstream transcript variant, non coding transcript variant
rs1131691434	G>C	Likely-pathogenic, uncertain-significance	Coding sequence variant, non coding transcript variant, missense variant
rs1323958195	G>A	Likely-pathogenic	Stop gained, 3 prime UTR variant, coding sequence variant, intron variant, downstream transcript variant, non coding transcript variant, genic downstream transcript variant
rs1369704445	T>C	Pathogenic	Splice acceptor variant
rs1424242431	G>A	Likely-pathogenic	Stop gained, non coding transcript variant, intron variant, genic downstream transcript variant, 3 prime UTR variant, downstream transcript variant, coding sequence variant
rs1555620092	A>-	Likely-pathogenic	Intron variant, coding sequence variant, frameshift variant, 3 prime UTR variant, genic downstream transcript variant, non coding transcript variant, downstream transcript variant
rs1555620141	C>T	Likely-pathogenic	Intron variant, coding sequence variant, 3 prime UTR variant, stop gained, genic downstream transcript variant, non coding transcript variant, downstream transcript variant
rs1555620214	T>C	Pathogenic-likely-pathogenic	Intron variant, coding sequence variant, 3 prime UTR variant, missense variant, genic downstream transcript variant, non coding transcript variant, downstream transcript variant
rs1555620827	G>-	Pathogenic	Frameshift variant, non coding transcript variant, coding sequence variant
rs1555621425	C>A	Likely-pathogenic	Splice acceptor variant
rs1555621659	A>T	Pathogenic	Stop gained, non coding transcript variant, coding sequence variant
rs1555621662	A>G	Pathogenic	Non coding transcript variant, coding sequence variant, missense variant
rs1555621971	->C	Pathogenic	Frameshift variant, non coding transcript variant, coding sequence variant
rs1555621984	C>T	Likely-pathogenic	Splice acceptor variant
rs1555622888	G>-	Likely-pathogenic	Frameshift variant, non coding transcript variant, coding sequence variant
rs1567914459	G>A	Likely-pathogenic	Coding sequence variant, 3 prime UTR variant, genic downstream transcript variant, non coding transcript variant, intron variant, downstream transcript variant, stop gained
rs1598736884	G>A	Likely-pathogenic	Coding sequence variant, 3 prime UTR variant, genic downstream transcript variant, non coding transcript variant, intron variant, missense variant, downstream transcript variant
rs1598738369	G>-	Likely-pathogenic	Frameshift variant, coding sequence variant, 3 prime UTR variant, genic downstream transcript variant, non coding transcript variant, intron variant, downstream transcript variant
rs1598738720	C>-	Likely-pathogenic	Frameshift variant, coding sequence variant, 3 prime UTR variant, genic downstream transcript variant, non coding transcript variant, intron variant, downstream transcript variant
rs1598749661	G>A	Pathogenic	Coding sequence variant, non coding transcript variant, stop gained
rs1598749984	->A	Pathogenic	Coding sequence variant, non coding transcript variant, stop gained
rs1598758001	A>T	Likely-pathogenic	Missense variant, coding sequence variant, non coding transcript variant

Show/Hide all(58)

miRTarBase ID	miRNA	Experiments	Reference
MIRT049918	hsa-miR-30a-3p	CLASH	23622248
MIRT044118	hsa-miR-30e-3p	CLASH	23622248
MIRT036568	hsa-miR-941	CLASH	23622248
MIRT1343837	hsa-miR-1913	CLIP-seq
MIRT1343838	hsa-miR-197	CLIP-seq
MIRT1343839	hsa-miR-198	CLIP-seq
MIRT1343840	hsa-miR-2110	CLIP-seq
MIRT1343841	hsa-miR-324-3p	CLIP-seq
MIRT1343842	hsa-miR-3613-3p	CLIP-seq
MIRT1343843	hsa-miR-3908	CLIP-seq
MIRT1343844	hsa-miR-4271	CLIP-seq
MIRT1343845	hsa-miR-4645-5p	CLIP-seq
MIRT1343846	hsa-miR-4667-5p	CLIP-seq
MIRT1343847	hsa-miR-4673	CLIP-seq
MIRT1343848	hsa-miR-4700-5p	CLIP-seq
MIRT1343849	hsa-miR-4725-3p	CLIP-seq
MIRT1343850	hsa-miR-4727-5p	CLIP-seq
MIRT1343851	hsa-miR-591	CLIP-seq
MIRT1343852	hsa-miR-598	CLIP-seq
MIRT1343853	hsa-miR-767-3p	CLIP-seq
MIRT2101621	hsa-miR-4731-5p	CLIP-seq
MIRT2394330	hsa-miR-1285	CLIP-seq
MIRT2394331	hsa-miR-3184	CLIP-seq
MIRT2394332	hsa-miR-3187-5p	CLIP-seq
MIRT2394333	hsa-miR-423-5p	CLIP-seq
MIRT2394334	hsa-miR-4492	CLIP-seq
MIRT2394335	hsa-miR-4498	CLIP-seq
MIRT2394336	hsa-miR-4505	CLIP-seq
MIRT2394337	hsa-miR-612	CLIP-seq
MIRT2394338	hsa-miR-762	CLIP-seq
MIRT2621692	hsa-miR-1193	CLIP-seq
MIRT2621693	hsa-miR-1252	CLIP-seq
MIRT2621694	hsa-miR-1254	CLIP-seq
MIRT1343840	hsa-miR-2110	CLIP-seq
MIRT2621695	hsa-miR-3116	CLIP-seq
MIRT2621696	hsa-miR-3185	CLIP-seq
MIRT2621697	hsa-miR-3189-3p	CLIP-seq
MIRT2621698	hsa-miR-3675-5p	CLIP-seq
MIRT1343844	hsa-miR-4271	CLIP-seq
MIRT2621699	hsa-miR-4476	CLIP-seq
MIRT2621700	hsa-miR-4533	CLIP-seq
MIRT2621701	hsa-miR-4667-3p	CLIP-seq
MIRT1343846	hsa-miR-4667-5p	CLIP-seq
MIRT1343848	hsa-miR-4700-5p	CLIP-seq
MIRT1343849	hsa-miR-4725-3p	CLIP-seq
MIRT2621702	hsa-miR-486-3p	CLIP-seq
MIRT2621703	hsa-miR-548b-3p	CLIP-seq
MIRT1343851	hsa-miR-591	CLIP-seq
MIRT2621704	hsa-miR-661	CLIP-seq
MIRT2621692	hsa-miR-1193	CLIP-seq
MIRT2690610	hsa-miR-122	CLIP-seq
MIRT2621693	hsa-miR-1252	CLIP-seq
MIRT2621697	hsa-miR-3189-3p	CLIP-seq
MIRT2621699	hsa-miR-4476	CLIP-seq
MIRT2621700	hsa-miR-4533	CLIP-seq
MIRT2621701	hsa-miR-4667-3p	CLIP-seq
MIRT2621703	hsa-miR-548b-3p	CLIP-seq
MIRT2690611	hsa-miR-574-5p	CLIP-seq

Show/Hide all(21)

GO ID	Ontology	Definition	Evidence	Reference
GO:0005515	Function	Protein binding	IPI	15962010, 33961781
GO:0005764	Component	Lysosome	IDA	15146460
GO:0005764	Component	Lysosome	IEA
GO:0006027	Process	Glycosaminoglycan catabolic process	IBA
GO:0006027	Process	Glycosaminoglycan catabolic process	IDA	7493035, 15146460
GO:0008340	Process	Determination of adult lifespan	IEA
GO:0008484	Function	Sulfuric ester hydrolase activity	IEA
GO:0016250	Function	N-sulfoglucosamine sulfohydrolase activity	IBA
GO:0016250	Function	N-sulfoglucosamine sulfohydrolase activity	IDA	7493035, 15146460
GO:0016250	Function	N-sulfoglucosamine sulfohydrolase activity	IEA
GO:0016250	Function	N-sulfoglucosamine sulfohydrolase activity	TAS
GO:0016787	Function	Hydrolase activity	IEA
GO:0030200	Process	Heparan sulfate proteoglycan catabolic process	IBA
GO:0030200	Process	Heparan sulfate proteoglycan catabolic process	IEA
GO:0030200	Process	Heparan sulfate proteoglycan catabolic process	IMP	15146460
GO:0030200	Process	Heparan sulfate proteoglycan catabolic process	TAS
GO:0043202	Component	Lysosomal lumen	IEA
GO:0043202	Component	Lysosomal lumen	TAS
GO:0046872	Function	Metal ion binding	IEA
GO:0061744	Process	Motor behavior	IEA
GO:0070062	Component	Extracellular exosome	HDA	23533145

MIM	HGNC	e!Ensembl
605270	10818	ENSG00000181523

Protein

UniProt ID

P51688

Protein name

N-sulphoglucosamine sulphohydrolase (EC 3.10.1.1) (Sulfoglucosamine sulfamidase) (Sulphamidase)

Protein function

Catalyzes a step in lysosomal heparan sulfate degradation.

PDB

4MHX , 4MIV

Family and domains

Pfam

Accession	ID	Position in sequence	Description	Type
PF00884	Sulfatase	23 → 328	Sulfatase	Family
PF16347	DUF4976	400 → 477	Domain of unknown function (DUF4976)	Family

Sequence

MSCPVPACCALLLVLGLCRARPRNALLLLADDGGFESGAYNNSAIATPHLDALARRSLLF
RNAFTSVSSCSPSRASLLTGLPQHQNGMYGLHQDVHHFNSFDKVRSLPLLLSQAGVRTGI
IGKKHVGPETVYPFDFAYTEENGSVLQVGRNITRIKLLVRKFLQTQDDRPFFLYVAFHDP
HRCGHSQPQYGTFCEKFGNGESGMGRIPDWTPQAYDPLDVLVPYFVPNTPAARADLAAQY
TTVGRMDQGVGLVLQELRDAGVLNDTLVIFTSDNGIPFPSGRTNLYWPGTAEPLLVSSPE
HPKRWGQVSEAYVSLLDLTPTILDWFSIPYPSYAIFGSKTIHLTGRSLLPALEAEPLWAT
VFGSQSHHEVTMSYPMRSVQHRHFRLVHNLNFKMPFPIDQDFYVSPTFQDLLNRTTAGQP
TGWYKDLRHYYYRARWELYDRSRDPHETQNLATDPRFAQLLEMLRDQLAKWQWETHDPWV
CAPDGVLEEKLSPQCQPLHNEL

Sequence length

502

Interactions

View interactions

	KEGG		Reactome
	Glycosaminoglycan degradation Metabolic pathways Lysosome		HS-GAG degradation MPS IIIA - Sanfilippo syndrome A

Show/Hide Causal Diseases (4)

Disease merge term	Disease name	dbSNP ID	References
Causal Diseases caused by PATHOGENIC or LIKELY PATHOGENIC variants from ClinVar only
Mucopolysaccharidosis	Mucopolysaccharidosis, MPS-III-A	rs1323958195, rs1555622888, rs752914124, rs1598749984, rs770947426, rs1555621659, rs1555624111, rs766938111, rs1250300189, rs777267343, rs374621913, rs104894636, rs761607612, rs764057581, rs778700037 View all (39 more)	N/A
sanfilippo syndrome	Sanfilippo syndrome	rs138504221, rs374621913, rs778700037, rs777956287	N/A
mucopolysaccharidosis	Mucopolysaccharidosis	rs138504221, rs770947426, rs104894636, rs144143780	N/A
neurodegeneration	Neurodegeneration	rs138504221	N/A

Show/Hide Unknown Diseases (2)

Disease merge term	Disease name	Evidence	References	Source
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Glioblastoma	Glioblastoma	N/A	N/A	GWAS
Mental retardation	intellectual disability	N/A	N/A	ClinVar

Show/Hide Text Mining Associations (10)

Disease Name	Relationship Type	References
Associations from Text Mining Disease associations identified through Pubtator
Cognitive Dysfunction	Associate	31385193
Diarrhea	Associate	39201540
Dystonic Disorders	Associate	30593151
Glycogen Storage Disease IIIA	Associate	30269021
Hyperkinesis	Associate	31385193
Intellectual Disability	Associate	31385193
Kluver Bucy Syndrome	Associate	27827379
Mucopolysaccharidosis III	Associate	24816101, 30593151, 31385193, 35835061, 39201540, 40020439
Neurodegenerative Diseases	Associate	24816101
Pulmonary Disease Chronic Obstructive	Associate	30760748

SGSH (N-sulfoglucosamine sulfohydrolase)