NFYA nuclear transcription factor Y subunit alpha
Information
- Symbol
- NFYA
- Type
- protein-coding
- Description
- nuclear transcription factor Y subunit alpha
- Entrez Gene ID
- 4800
- Genome
- hg19
- Position
- chr6:41,040,713-41,070,142
- Genome
- hg38
- Position
- chr6:41,072,974-41,102,403
- MIM
- 189903 OMIM
- HGNC
- HGNC:7804 HGNC
- Ensembl
- ENSG00000001167 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 18 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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18 |
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0 |
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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
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Entry | Origin | Type | Annotation |
Type | ID |
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SYNONYM | CBF-A |
SYNONYM | CBF-B |
SYNONYM | HAP2 |
SYNONYM | NF-YA |
MIM | 189903 OMIM |
HGNC | HGNC:7804 HGNC |
Ensembl | ENSG00000001167 Ensembl |
AllianceGenome | HGNC:7804 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000353205.5 | hg38 | chr6 | 41,072,983 | 41,097,950 | 24,968 |
ENST00000341376.11 | hg38 | chr6 | 41,072,974 | 41,102,403 | 29,430 |
ENST00000341376.11 | hg19 | chr6 | 41,040,713 | 41,070,142 | 29,430 |
ENST00000353205.5 | hg19 | chr6 | 41,040,722 | 41,065,689 | 24,968 |
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