Genomic Map
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Target Gene Details
Entrez Gene ID: | 51199 |
Gene Name: | ninein |
Gene Aliases: |
SCKL7 |
Location: |
Chr.14:50719763-50831121 on Build GRCh38 |
Assay Gene Location: | Overlaps Intron 32 - Exon 33 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| NIN | NM_016350.4 | NP_057434.4 | ||
| NM_020921.3 | NP_065972.3 | |||
| NM_182946.1 | NP_891991.1 | |||
| XM_011536817.1 | XP_011535119.1 | |||
| XM_011536822.1 | XP_011535124.1 | |||
| XM_011536823.2 | XP_011535125.1 | |||
| AB046785.2 | BAB13391.2 | |||
| AF186776.1 | AAG17027.1 | |||
| AF212162.2 | AAF23015.2 | |||
| AF223938.1 | AAK00629.1 | |||
| AF223939.1 | AAK00630.1 | |||
| AF302773.2 | AAG33512.2 | |||
| AK025652.1 | ||||
| AK026083.1 | ||||
| AK027054.1 | BAB15640.1 | |||
| AY027794.1 | AAK27375.1 | |||
| AY027795.1 | AAK27376.1 | |||
| AY027796.1 | AAK27377.1 | |||
| AY736182.1 | AAU86898.1 | |||
| BC090932.1 | AAH90932.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv564840 | Chr.14:50704161 - 50733474 on Build GRCh38 | Gain |
 NIN
|
| nsv1040775 | Chr.14:50676760 - 50853094 on Build GRCh38 | Gain |
NIN
LOC105370489
|
Back To TopMore Information
Set Membership: |
Intragenic
Non-exonic
DGV Variation
|
Gene Ontology Categories:
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