RXFP4 relaxin family peptide/INSL5 receptor 4
Information
- Symbol
- RXFP4
- Type
- protein-coding
- Description
- relaxin family peptide/INSL5 receptor 4
- Entrez Gene ID
- 339403
- Genome
- hg19
- Position
- chr1:155,911,429-155,912,878
- Genome
- hg38
- Position
- chr1:155,941,638-155,943,087
- MIM
- 609043 OMIM
- HGNC
- HGNC:14666 HGNC
- Ensembl
- ENSG00000173080 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
Uncertain significance | 0 | 52 |
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
54 |
![]() |
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 | GPCR142 |
SYNONYM | GPR100 |
SYNONYM | RLN3R2 |
SYNONYM | RXFPR4 |
MIM | 609043 OMIM |
HGNC | HGNC:14666 HGNC |
Ensembl | ENSG00000173080 Ensembl |
AllianceGenome | HGNC:14666 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000368318.5 | hg38 | chr1 | 155,941,638 | 155,943,087 | 1,450 |
ENST00000368318.5 | hg19 | chr1 | 155,911,429 | 155,912,878 | 1,450 |
Genome browser