Genomic Map
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Target Gene Details
Entrez Gene ID: | 7587 |
Gene Name: | zinc finger protein 37A |
Gene Aliases: |
KOX21, ZNF37 |
Location: |
Chr.10:38094327-38150293 on Build GRCh38 |
Assay Gene Location: | Within Exon 10 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| ZNF37A | NM_001007094.2 | 8 | 3506 | NP_001007095.1 |
| NM_001178101.1 | 7 | 3028 | NP_001171572.1 | |
| NM_001324245.1 | 7 | 2957 | NP_001311174.1 | |
| NM_001324246.1 | 8 | 3502 | NP_001311175.1 | |
| NM_001324247.1 | 8 | 3247 | NP_001311176.1 | |
| NM_001324248.1 | 7 | 3212 | NP_001311177.1 | |
| NM_001324249.1 | 7 | 3208 | NP_001311178.1 | |
| NM_001324250.1 | 8 | 3322 | NP_001311179.1 | |
| NM_001324251.1 | 8 | 3326 | NP_001311180.1 | |
| NM_001324256.1 | NP_001311185.1 | |||
| NM_001324257.1 | NP_001311186.1 | |||
| NM_001324258.1 | NP_001311187.1 | |||
| NM_001324259.1 | 8 | 3556 | NP_001311188.1 | |
| NM_001324260.1 | 7 | 3078 | NP_001311189.1 | |
| NM_003421.2 | 7 | 3032 | NP_003412.1 | |
| XM_005252586.3 | 2 | 2633 | XP_005252643.1 | |
| XM_011519656.2 | 8 | 3414 | XP_011517958.1 | |
| XM_011519657.2 | 8 | 3236 | XP_011517959.1 | |
| XM_011519658.2 | 7 | 2954 | XP_011517960.1 | |
| XM_017016618.1 | 8 | 3551 | XP_016872107.1 | |
| XM_017016619.1 | 7 | 3087 | XP_016872108.1 | |
| XM_017016620.1 | 8 | 3555 | XP_016872109.1 | |
| XM_017016621.1 | XP_016872110.1 | |||
| XM_017016622.1 | 8 | 3551 | XP_016872111.1 | |
| AJ492195.1 | 7 | 2996 | CAD37331.1 | |
| BX647089.1 | 8 | 3491 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv6465 | Chr.10:38088734 - 38133197 on Build GRCh38 | Deletion |
 ZNF37A
|
| nsv1040704 | Chr.10:37651096 - 38162989 on Build GRCh38 | Gain |
ZNF33BP1
ZNF25
ZNF37A
ZNF33A
ZNF248
|
| esv3576438 | Chr.10:38002320 - 38607542 on Build GRCh38 | Gain |
SEPT7P9
LINC00999
ZNF37A
LOC100129055
ZNF33A
HSD17B7P2
|
| nsv550419 | Chr.10:38022849 - 38212726 on Build GRCh38 | Gain |
ZNF37A
LOC100129055
ZNF33A
|
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Additional Information:
For this assay, SNP(s) [rs79524569] 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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