The SLC45A2 gene homepage

General information
Gene symbol SLC45A2
Gene name solute carrier family 45, member 2
Chromosome 5
Chromosomal band p13.3
Imprinted Unknown
Genomic reference NG_011691.1
Transcript reference NM_016180.3
Exon/intron information NM_016180.3 exon/intron table
Associated with diseases OCA4, SHEP5
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) William (Bill) Oetting
Total number of public variants reported 178
Unique public DNA variants reported 104
Individuals with public variants 176
Hidden variants -
Notes This database is one of the ”Eye disease” gene variant databases
Date created July 06, 2012
Date last updated February 26, 2024
Version SLC45A2:240226

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
Reading frame checker The Reading-frame checker generates a prediction of the effect of whole-exon changes. Active for: NM_016180.3.
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
Homepage URL http://www.LOVD.nl/SLC45A2
External URL Albinism Database
HGNC 16472
Entrez Gene 51151
PubMed articles SLC45A2
OMIM - Gene 606202
OMIM - Diseases OCA4 (albinism, oculocutaneous, type IV (OCA-4))
SHEP5 (pigmentation, hair, black/non-black - eyes, dark/light - skin, dark/fair, type 5 (SHEP-5, skin/hair/eye pigmentation))
HGMD SLC45A2
GeneCards SLC45A2
GeneTests SLC45A2
Orphanet SLC45A2


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00019347 5 transcript variant 1 NM_016180.3 NP_057264.3 178


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