OR7D2 olfactory receptor family 7 subfamily D member 2
Information
- Symbol
- OR7D2
- Type
- protein-coding
- Description
- olfactory receptor family 7 subfamily D member 2
- Entrez Gene ID
- 162998
- Genome
- hg19
- Position
- chr19:9,289,655-9,299,494
- Genome
- hg38
- Position
- chr19:9,178,979-9,188,818
- HGNC
- HGNC:8378 HGNC
- Ensembl
- ENSG00000188000 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 4 |
Uncertain significance | 0 | 44 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
48 |
![]() |
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 | HTPCRH03 |
SYNONYM | OR19-10 |
SYNONYM | OR19-4 |
HGNC | HGNC:8378 HGNC |
Ensembl | ENSG00000188000 Ensembl |
AllianceGenome | HGNC:8378 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000641288.2 | hg38 | chr19 | 9,178,979 | 9,188,818 | 9,840 |
ENST00000344248.4 | hg38 | chr19 | 9,185,594 | 9,188,818 | 3,225 |
ENST00000642043.1 | hg38 | chr19 | 9,178,979 | 9,188,780 | 9,802 |
ENST00000642043.1 | hg19 | chr19 | 9,289,655 | 9,299,456 | 9,802 |
ENST00000641288.2 | hg19 | chr19 | 9,289,655 | 9,299,494 | 9,840 |
ENST00000344248.4 | hg19 | chr19 | 9,296,270 | 9,299,494 | 3,225 |
Genome browser