Genomic Map
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Target Gene Details
Entrez Gene ID: | 5744 |
Gene Name: | parathyroid hormone like hormone |
Gene Aliases: |
BDE2, HHM, PLP, PTHR, PTHRP |
Location: |
Chr.12:27958084-27974187 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 4 - Exon 4 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| PTHLH | NM_002820.2 | NP_002811.1 | ||
| NM_198964.1 | NP_945315.1 | |||
| NM_198965.1 | NP_945316.1 | |||
| NM_198966.1 | NP_945317.1 | |||
| XM_011520774.2 | XP_011519076.1 | |||
| XM_011520775.2 | XP_011519077.1 | |||
| XM_017019674.1 | XP_016875163.1 | |||
| XM_017019675.1 | XP_016875164.1 | |||
| AK313476.1 | ||||
| BC005961.1 | AAH05961.1 | |||
| BG676028.1 | ||||
| BG679319.1 | ||||
| BG680355.1 | ||||
| BI752853.1 | ||||
| J03580.1 | AAA60216.1 | |||
| J03802.1 | AAA60218.1 | |||
| M26958.1 | AAO49791.1 | |||
| M26959.1 | AAO49793.1 | |||
| M26960.1 | AAN76483.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| esv3628956 | Chr.12:27969159 - 27972559 on Build GRCh38 | Loss |
 PTHLH
|
| nsv557864 | Chr.12:27899261 - 28277169 on Build GRCh38 | Gain |
PTHLH
LOC729291
CCDC91
|
| nsv557876 | Chr.12:27961883 - 28572171 on Build GRCh38 | Gain |
LOC101928705
PTHLH
LOC729291
CCDC91
|
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Additional Information:
For this assay, SNP(s) [rs148094002] 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
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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