Genomic Map
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Target Gene Details
Entrez Gene ID: | 23493 |
Gene Name: | hes related family bHLH transcription factor with YRPW motif 2 |
Gene Aliases: |
CHF1, GRIDLOCK, GRL, HERP1, HESR2, HRT2, bHLHb32 |
Location: |
Chr.6:125747592-125762243 on Build GRCh38 |
Assay Gene Location: | Overlaps Exon 5 - Intron 5 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HEY2 | NM_012259.2 | NP_036391.1 | ||
| XM_017010627.1 | XP_016866116.1 | |||
| XM_017010628.1 | XP_016866117.1 | |||
| XM_017010629.1 | XP_016866118.1 | |||
| AB044755.1 | BAA96781.1 | |||
| AF173901.1 | AAF20173.1 | |||
| AF232238.1 | AAF37296.1 | |||
| AF237949.1 | AAF44781.1 | |||
| AF311884.1 | AAG31157.1 | |||
| AJ249545.1 | CAB56839.1 | |||
| AK289943.1 | ||||
| AK303890.1 | ||||
| BC007707.2 | AAH07707.1 | |||
| BI549391.1 | ||||
| BT020067.1 | AAV38870.1 | |||
| BT020068.1 | AAV38871.1 |
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Additional Information:
For this assay, SNP(s) [rs112235907,rs112677723] 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
Non-exonic
non-DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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