NFYC nuclear transcription factor Y subunit gamma
Information
- Symbol
- NFYC
- Type
- protein-coding
- Description
- nuclear transcription factor Y subunit gamma
- Entrez Gene ID
- 4802
- Genome
- hg19
- Position
- chr1:41,204,510-41,237,275
- Genome
- hg38
- Position
- chr1:40,738,838-40,771,603
- MIM
- 605344 OMIM
- HGNC
- HGNC:7806 HGNC
- Ensembl
- ENSG00000066136 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 10 |
Ranking
| ClinVar | |
|---|---|
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0 |
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0 |
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0 |
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10 |
![]() |
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 |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | CBF-C |
| SYNONYM | CBFC |
| SYNONYM | H1TF2A |
| SYNONYM | HAP5 |
| SYNONYM | HSM |
| SYNONYM | NF-YC |
| MIM | 605344 OMIM |
| HGNC | HGNC:7806 HGNC |
| Ensembl | ENSG00000066136 Ensembl |
| AllianceGenome | HGNC:7806 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000425457.6 | hg38 | chr1 | 40,691,716 | 40,771,139 | 79,424 |
| ENST00000427410.6 | hg38 | chr1 | 40,691,689 | 40,771,126 | 79,438 |
| ENST00000447388.8 | hg38 | chr1 | 40,691,704 | 40,771,603 | 79,900 |
| ENST00000308733.9 | hg38 | chr1 | 40,738,838 | 40,771,603 | 32,766 |
| ENST00000456393.6 | hg38 | chr1 | 40,691,743 | 40,771,601 | 79,859 |
| ENST00000440226.7 | hg38 | chr1 | 40,735,315 | 40,771,093 | 35,779 |
| ENST00000372652.5 | hg38 | chr1 | 40,709,357 | 40,771,603 | 62,247 |
| ENST00000372651.5 | hg38 | chr1 | 40,709,543 | 40,770,940 | 61,398 |
| ENST00000372654.5 | hg38 | chr1 | 40,691,838 | 40,771,102 | 79,265 |
| ENST00000372653.5 | hg38 | chr1 | 40,692,013 | 40,771,106 | 79,094 |
| ENST00000308733.9 | hg19 | chr1 | 41,204,510 | 41,237,275 | 32,766 |
| ENST00000372651.5 | hg19 | chr1 | 41,175,215 | 41,236,612 | 61,398 |
| ENST00000372652.5 | hg19 | chr1 | 41,175,029 | 41,237,275 | 62,247 |
| ENST00000372653.5 | hg19 | chr1 | 41,157,685 | 41,236,778 | 79,094 |
| ENST00000372654.5 | hg19 | chr1 | 41,157,510 | 41,236,774 | 79,265 |
| ENST00000425457.6 | hg19 | chr1 | 41,157,388 | 41,236,811 | 79,424 |
| ENST00000427410.6 | hg19 | chr1 | 41,157,361 | 41,236,798 | 79,438 |
| ENST00000456393.6 | hg19 | chr1 | 41,157,415 | 41,237,273 | 79,859 |
| ENST00000440226.7 | hg19 | chr1 | 41,200,987 | 41,236,765 | 35,779 |
| ENST00000447388.8 | hg19 | chr1 | 41,157,376 | 41,237,275 | 79,900 |
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