FOXRED2 FAD dependent oxidoreductase domain containing 2
Information
- Symbol
- FOXRED2
- Type
- protein-coding
- Description
- FAD dependent oxidoreductase domain containing 2
- Entrez Gene ID
- 80020
- Genome
- hg19
- Position
- chr22:36,883,269-36,903,268
- Genome
- hg38
- Position
- chr22:36,487,222-36,507,221
- MIM
- 613777 OMIM
- HGNC
- HGNC:26264 HGNC
- Ensembl
- ENSG00000100350 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 6 |
Uncertain significance | 0 | 98 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
104 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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
|
Category | : |
|
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 | ERFAD |
MIM | 613777 OMIM |
HGNC | HGNC:26264 HGNC |
Ensembl | ENSG00000100350 Ensembl |
AllianceGenome | HGNC:26264 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000684868.1 | hg38 | chr22 | 36,487,222 | 36,507,221 | 20,000 |
ENST00000688825.1 | hg38 | chr22 | 36,488,272 | 36,507,077 | 18,806 |
ENST00000689211.1 | hg38 | chr22 | 36,488,505 | 36,507,040 | 18,536 |
ENST00000692693.1 | hg38 | chr22 | 36,488,277 | 36,507,055 | 18,779 |
ENST00000397224.9 | hg38 | chr22 | 36,487,190 | 36,507,040 | 19,851 |
ENST00000397223.4 | hg38 | chr22 | 36,489,987 | 36,506,530 | 16,544 |
ENST00000691242.1 | hg38 | chr22 | 36,488,272 | 36,506,830 | 18,559 |
ENST00000685224.1 | hg38 | chr22 | 36,488,272 | 36,507,040 | 18,769 |
ENST00000687273.1 | hg38 | chr22 | 36,488,505 | 36,507,062 | 18,558 |
ENST00000685612.1 | hg38 | chr22 | 36,488,272 | 36,507,051 | 18,780 |
ENST00000688870.1 | hg38 | chr22 | 36,488,272 | 36,506,800 | 18,529 |
ENST00000216187.10 | hg38 | chr22 | 36,488,242 | 36,507,022 | 18,781 |
ENST00000686024.1 | hg38 | chr22 | 36,488,269 | 36,507,040 | 18,772 |
ENST00000397224.9 | hg19 | chr22 | 36,883,237 | 36,903,087 | 19,851 |
ENST00000684868.1 | hg19 | chr22 | 36,883,269 | 36,903,268 | 20,000 |
ENST00000216187.10 | hg19 | chr22 | 36,884,289 | 36,903,069 | 18,781 |
ENST00000397223.4 | hg19 | chr22 | 36,886,034 | 36,902,577 | 16,544 |
ENST00000691242.1 | hg19 | chr22 | 36,884,319 | 36,902,877 | 18,559 |
ENST00000685224.1 | hg19 | chr22 | 36,884,319 | 36,903,087 | 18,769 |
ENST00000685612.1 | hg19 | chr22 | 36,884,319 | 36,903,098 | 18,780 |
ENST00000686024.1 | hg19 | chr22 | 36,884,316 | 36,903,087 | 18,772 |
ENST00000688825.1 | hg19 | chr22 | 36,884,319 | 36,903,124 | 18,806 |
ENST00000692693.1 | hg19 | chr22 | 36,884,324 | 36,903,102 | 18,779 |
ENST00000689211.1 | hg19 | chr22 | 36,884,552 | 36,903,087 | 18,536 |
ENST00000687273.1 | hg19 | chr22 | 36,884,552 | 36,903,109 | 18,558 |
ENST00000688870.1 | hg19 | chr22 | 36,884,319 | 36,902,847 | 18,529 |
Genome browser