The SPATA31C1 gene homepage

General information
Gene symbol SPATA31C1
Gene name SPATA31 subfamily C member 1
Chromosome 9
Chromosomal band q22.1
Imprinted Unknown
Genomic reference NC_000009.11
Transcript reference NM_001145124.1
Exon/intron information NM_001145124.1 exon/intron table
Associated with diseases -
Citation reference(s) -
Refseq URL Genomic reference sequence
Curators (1) Global Variome, with Curator vacancy
Total number of public variants reported 4
Unique public DNA variants reported 4
Individuals with public variants 2
Hidden variants 1
Download all this gene's data Download all data
Notes Establishment of this gene variant database (LSDB) was supported by the Leiden University Medical Center (LUMC), Leiden, Nederland.
Date created August 09, 2017
Date last updated May 09, 2022
Version SPATA31C1:220509

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_001145124.1.
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 https://www.LOVD.nl/SPATA31C1
HGNC HGNC:27846
Entrez Gene 441452
PubMed articles SPATA31C1
HGMD SPATA31C1
GeneCards SPATA31C1
NIH Genetic Testing Registry SPATA31C1
Orphanet SPATA31C1


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00025079 9 SPATA31 subfamily C, member 1 NM_001145124.1 NP_001138596.1 4


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