Difference between revisions of "EntrezGene:100049707"
From referenceTSS
(Created page with "{{GenePage |gene_id=100049707 |gene_name=spastic paraplegia 38 (autosomal dominant, Silver syndrome) |gene_symbol=SPG38 |gene_synonyms= |gene_type=unknown |hgnc_mgi_id=HGNC:33...") |
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{{GenePage | {{GenePage | ||
+ | |ensembl= | ||
+ | |gencode_transcripts= | ||
|gene_id=100049707 | |gene_id=100049707 | ||
|gene_name=spastic paraplegia 38 (autosomal dominant, Silver syndrome) | |gene_name=spastic paraplegia 38 (autosomal dominant, Silver syndrome) | ||
Line 6: | Line 8: | ||
|gene_type=unknown | |gene_type=unknown | ||
|hgnc_mgi_id=HGNC:33485 | |hgnc_mgi_id=HGNC:33485 | ||
+ | |hprd= | ||
+ | |imgt_gene-db= | ||
+ | |mim=MIM:612335 | ||
+ | |mirbase= | ||
|old_gene_ids= | |old_gene_ids= | ||
+ | |other_mrnas= | ||
+ | |refSeq_transcripts= | ||
|species=human | |species=human | ||
+ | |ucsc_genes= | ||
+ | |vega= | ||
}} | }} |
Latest revision as of 18:42, 12 June 2018
Relatad TSS IDs
"No query result."
Basic information
GeneID: | 100049707 |
---|---|
Species: | human |
Gene name: | spastic paraplegia 38 (autosomal dominant, Silver syndrome) |
Gene symbol: | SPG38 |
Gene synonyms: | |
Gene type: | unknown |
Old GeneIDs: |
Links to external databases
HGNC/MGI_ID: | HGNC:33485 |
---|---|
Ensembl: | |
Vega: | |
HPRD: | |
miRBase: | |
IMGT/GENE-DB: | |
MIM: | MIM:612335 |
Transcripts
Gencode transcripts: | |
---|---|
RefSeq transcripts: | |
UCSC genes: | |
Other_mRNAs: |