22697

• Gene Symbol: AMMECR1
• Gene Name: Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1
• Gene Aliases: AMMERC1
• Chromosome Location: Chr.X: 110194186 - 110440233 on Build GRCh38
• UniGene ID: Hs.656243
• Species: Human
• Species Specific ID (Flybase ID): -

siRNA Details

Gene Symbol: AMMECR1
Interrogated Sequence		Translated Protein	Targeted Exon(s)	siRNA Location	IMAGE Clone ID
RefSeq	NM_001171689.1	NP_001165160.1	4	842
	NM_015365.2	NP_056180.1	2	655
GenBank mRNA	AJ007014.1	-	2	742
	AK001703.1	-	2	178
	AK091430.1	-	4	842
	AK314596.1	-	2	586
	KU178497.1	-	2	574

More Information

Additional Information:

This siRNA no longer meets our design criteria. We suggest you choose a different siRNA for this gene or contact Tech Support for more information.

Gene Ontology Categories:

Process(es)

biological_process

Function(s)

molecular_function
protein binding