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Symbol report for C19orf12

Placeholder symbol

HGNC data for C19orf12

Approved symbol
C19orf12
Approved name

chromosome 19 open reading frame 12

Locus type
gene with protein product
HGNC ID
HGNC:25443
Symbol status
Approved
Previous symbols
SPG43
Previous names
spastic paraplegia 43 (autosomal recessive)
Alias symbols
MGC10922
DKFZP762D096
NBIA4
MPAN
Alias names
neurodegeneration with brain iron accumulation 4
membrane protein-associated neurodegeneration
Chromosomal location
19q12
Gene resources for C19orf12
Ensembl
ENSG00000131943 Curated
Ensembl region in detailEnsembl gene sequence
NCBI Gene
83636 Curated
UCSC
uc031rkd.1
Alliance of Genome Resources
HGNC:25443
Nucleotide resources for C19orf12
MANE Select
NM_031448.6
ENST00000323670.14
INSDC
AK057185 Curated
ENAGenBankDDBJ
RefSeq
NM_031448 Curated
NCBI sequence viewer
Protein resources for C19orf12
UniProt/Swiss-Prot
Q9NSK7
InterProPDBeReactome
AlphaFold
AF-Q9NSK7-F1
Orthologs from selected species for C19orf12
Canis familiaris
C1H19orf12 VGNC:54839 VGNC
Equus caballus
C10H19orf12 VGNC:51001 VGNC
Macaca mulatta
C19H19orf12 VGNC:70383 VGNC
Mus musculus
1600014C10Rik MGI:1919494 Curated
Pan troglodytes
C19H19orf12 VGNC:3660 VGNC
Rattus norvegicus
C1h19orf12 RGD:1585208
Sus scrofa
C6H19orf12 VGNC:86055 VGNC
Clinical resources for C19orf12
OMIM
614297
GenCC
HGNC:25443
MedlinePlus
Search via C19orf12
DECIPHER
Search via C19orf12
ClinGen
Search via HGNC:25443
Genetic Testing Registry
Search via NCBI Gene ID 83636
ClinVar
Search via NCBI Gene ID 83636
dbVar
Search via NCBI Gene ID 83636
Orphanet
289569
Other resources for C19orf12
AmiGO
Search via Q9NSK7
QuickGO
Search via Q9NSK7
BioGPS
Search via NCBI Gene ID 83636
GeneCards
Search via HGNC:25443
Monarch
Search via HGNC:25443
WikiGenes
Search via NCBI Gene ID 83636
References for C19orf12