SUCO SUN domain containing ossification factor
Information
- Symbol
- SUCO
- Type
- protein-coding
- Description
- SUN domain containing ossification factor
- Entrez Gene ID
- 51430
- Genome
- hg19
- Position
- chr1:172,501,489-172,580,973
- Genome
- hg38
- Position
- chr1:172,532,349-172,611,833
- MIM
- 619434 OMIM
- HGNC
- HGNC:1240 HGNC
- Ensembl
- ENSG00000094975 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 46 |
Likely benign | 0 | 260 |
Conflicting classifications of pathogenicity | 0 | 6 |
Uncertain significance | 0 | 418 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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64 |
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654 |
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2 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | C1orf9 |
SYNONYM | CH1 |
SYNONYM | OPT |
SYNONYM | SLP1 |
MIM | 619434 OMIM |
HGNC | HGNC:1240 HGNC |
Ensembl | ENSG00000094975 Ensembl |
AllianceGenome | HGNC:1240 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000616058.4 | hg38 | chr1 | 172,533,118 | 172,611,831 | 78,714 |
ENST00000263688.4 | hg38 | chr1 | 172,533,150 | 172,611,833 | 78,684 |
ENST00000367723.8 | hg38 | chr1 | 172,532,349 | 172,611,833 | 79,485 |
ENST00000610051.5 | hg38 | chr1 | 172,533,183 | 172,610,279 | 77,097 |
ENST00000367723.8 | hg19 | chr1 | 172,501,489 | 172,580,973 | 79,485 |
ENST00000616058.4 | hg19 | chr1 | 172,502,258 | 172,580,971 | 78,714 |
ENST00000263688.4 | hg19 | chr1 | 172,502,290 | 172,580,973 | 78,684 |
ENST00000610051.5 | hg19 | chr1 | 172,502,323 | 172,579,419 | 77,097 |
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