Assay Details
Target Gene Details
| Entrez Gene ID: | 56912 | 
| Gene Name: | intraflagellar transport 46 | 
| Gene Aliases: | C11orf2, C11orf60, CFAP32 | 
| Location: | Chr.11:118544528-118575624 on Build GRCh38 | 
| Assay Gene Location: | Within Exon 14 | 
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID | 
|---|---|---|---|---|
| IFT46 | NM_001168618.1 | 12 | 1627 | NP_001162089.1 | 
| NM_020153.3 | 13 | 1780 | NP_064538.3 | |
| XM_011542905.2 | 13 | 4522 | XP_011541207.1 | |
| XM_011542906.2 | 12 | 4364 | XP_011541208.1 | |
| XM_017018017.1 | 12 | 1519 | XP_016873506.1 | |
| XM_017018018.1 | 11 | 1490 | XP_016873507.1 | |
| AJ249980.1 | 12 | 1554 | CAB96537.1 | |
| AK025480.1 | 13 | 1739 | BAB15146.1 | |
| AK289521.1 | 12 | 1478 | ||
| AL136934.1 | 12 | 1462 | CAB66868.1 | |
| BC011647.2 | 12 | 1465 | AAH11647.1 | |
| BC012802.2 | 12 | 1558 | AAH12802.1 | |
| BC022856.1 | 12 | 1588 | AAH22856.1 | 
Target Gene Details
| Entrez Gene ID: | 84866 | 
| Gene Name: | transmembrane protein 25 | 
| Gene Aliases: | - | 
| Location: | Chr.11:118531088-118546670 on Build GRCh38 | 
| Assay Gene Location: | Within Intron 9 | 
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID | 
|---|---|---|---|---|
| TMEM25 | NM_001144037.1 | NP_001137509.1 | ||
| NM_001144038.1 | NP_001137510.1 | |||
| XM_017018431.1 | XP_016873920.1 | |||
| AK027305.1 | BAB55029.1 | |||
| AK075437.1 | BAC11620.1 | 
Target Copy Number Variation Details
| DGV Version: | Release date: 2016-05-15, GRCh GRCh38 | 
| Target Variation | Location | CNV Subtype | Genes | 
|---|---|---|---|
| nsv1044281 | Chr.11:118503814 - 118554704 on Build GRCh38 | Gain |  LOC101929089  TMEM25  TTC36  KMT2A  IFT46 | 
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Additional Information:
				    	 
					    	
					        	
					            	For this assay, SNP(s) [rs112051935] 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  Intronic  Non-exonic  DGV Variation | 
Gene Ontology Categories:
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 Genomic Map
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