Genomic Map
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Target Gene Details
Entrez Gene ID: | 399 |
Gene Name: | ras homolog family member H |
Gene Aliases: |
ARHH, TTF |
Location: |
Chr.4:40191011-40244764 on Build GRCh38 |
Assay Gene Location: | Within Exon 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| RHOH | NM_001278359.1 | 1 | 251 | NP_001265288.1 |
| NM_001278360.1 | 1 | 251 | NP_001265289.1 | |
| NM_001278361.1 | 1 | 251 | NP_001265290.1 | |
| NM_001278362.1 | 1 | 251 | NP_001265291.1 | |
| NM_001278363.1 | 1 | 251 | NP_001265292.1 | |
| NM_001278364.1 | NP_001265293.1 | |||
| NM_001278365.1 | NP_001265294.1 | |||
| NM_001278366.1 | NP_001265295.1 | |||
| NM_001278367.1 | NP_001265296.1 | |||
| NM_001278368.1 | NP_001265297.1 | |||
| NM_001278369.1 | NP_001265298.1 | |||
| NM_004310.4 | 1 | 251 | NP_004301.1 | |
| XM_011513692.1 | 1 | 169 | XP_011511994.1 | |
| AK313744.1 | ||||
| AW402442.1 | ||||
| BC014261.2 | AAH14261.1 | |||
| BG025818.1 | 1 | 222 | ||
| BI818548.1 | ||||
| BI908453.1 | 1 | 109 | ||
| BM457874.1 | ||||
| BU934664.1 | ||||
| CD703012.1 | 1 | 204 | ||
| DA383563.1 | 1 | 163 | ||
| DA815617.1 | 1 | 93 | ||
| DA906265.1 | 1 | 252 | ||
| DA950405.1 | 1 | 124 | ||
| DA951252.1 | ||||
| DB115332.1 | ||||
| DB119883.1 | 1 | 101 | ||
| Z35227.1 | 1 | 106 | CAA84538.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv950578 | Chr.4:40196981 - 40206280 on Build GRCh38 | Duplication |
 RHOH
|
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Additional Information:
For this assay, SNP(s) [rs114246246] are located under a primer or probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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