RecName: Full=Nucleotide sugar transporter SLC35D1; AltName: Full=Solu - Protein

Run BLAST
Find regions of similarity between this sequence and other sequences using BLAST.
Identify Conserved Domains
View conserved domains detected in this protein sequence using CD-search.
Highlight Sequence Features
Opens the Highlight Feature Bar and highlights feature annotations from the FEATURES table of the record. The Highlight Feature Bar can be used to navigate to and highlight other features and provides links to display the highlighted region separately. Links in the FEATURES table will also highlight the corresponding region of the sequence. More...
Find in this Sequence
Finds sub-sequences or patterns in the sequence and highlights the matching regions. The tool works with standard single letter nucleotide or protein codes including ambiguities and can match Prosite patterns in protein sequences. More...

A novel SLC35D1 variant causing milder phenotype of Schneckenbecken dysplasia in a large pedigree. [Am J Med Genet A. 2022]
A novel SLC35D1 variant causing milder phenotype of Schneckenbecken dysplasia in a large pedigree.
Özer L, Aktuna S, Unsal E, Ünal MA, Sahin G, Baltaci V. Am J Med Genet A. 2022 Oct; 188(10):3078-3083. Epub 2022 Aug 7.
A hypomorphic allele of SLC35D1 results in Schneckenbecken-like dysplasia. [Hum Mol Genet. 2019]
A hypomorphic allele of SLC35D1 results in Schneckenbecken-like dysplasia.
Rautengarten C, Quarrell OW, Stals K, Caswell RC, De Franco E, Baple E, Burgess N, Jokhi R, Heazlewood JL, Offiah AC, et al. Hum Mol Genet. 2019 Nov 1; 28(21):3543-3551.
Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases. [J Med Genet. 2009]
Identification of loss-of-function mutations of SLC35D1 in patients with Schneckenbecken dysplasia, but not with other severe spondylodysplastic dysplasias group diseases.
Furuichi T, Kayserili H, Hiraoka S, Nishimura G, Ohashi H, Alanay Y, Lerena JC, Aslanger AD, Koseki H, Cohn DH, et al. J Med Genet. 2009 Aug; 46(8):562-8. Epub 2009 Jun 8.

RefSeq genomic sequence
See the genomic reference sequence for the SLC35D1 gene (NG_012933.1).
RefSeq protein isoforms
See 15 reference sequence protein isoforms for the SLC35D1 gene.

PubMed
PubMed articles cited by protein sequence record
Taxonomy
Taxonomy sequences associated with protein record
BioSystems
BioSystems
CDD Search Results
Display conserved domains within a protein
Conserved Domains (Concise)
Link to a concise list of conserved domains in a protein
Conserved Domains (Full)
Link to conserved domains within a protein
Domain Relatives
Display proteins with similar conserved domain architecture
Full text in PMC
Free full text articles in PMC
Gene
Link to related Genes
OMIM
OMIM records associated with protein sequence
Protein (RefSeq)
Protein gi (UniProtKB) to protein gi (refseq)
PubMed (Weighted)
Links to pubmed

Q9NTN3 [Domain Mapping of Disease Mut...]
Q9NTN3
Domain Mapping of Disease Mutations
Transcript/Protein Information [PANTHER Classification System]
Transcript/Protein Information
PANTHER Classification System
Reactome [Reactome]
Reactome
reagents [ExactAntigen/Labome]
reagents
ExactAntigen/Labome

RecName: Full=Nucleotide sugar transporter SLC35D1; AltName: Full=Solute carrier...
RecName: Full=Nucleotide sugar transporter SLC35D1; AltName: Full=Solute carrier family 35 member D1; AltName: Full=UDP-galactose transporter-related protein 7; Short=UGTrel7; AltName: Full=UDP-glucuronic acid/UDP-N-acetylgalactosamine transporter; Short=UDP-GlcA/UDP-GalNAc transporter
gi|20140875|sp|Q9NTN3.1|S35D1_HUMAN

Protein

Your browsing activity is empty.

Activity recording is turned off.

Protein