Details from NCBI annotation

Gene Symbol Ammecr1
Gene Name Alport syndrome, mental retardation, midface hypoplasia and elliptocytosis chromosomal region gene 1, transcript variant X2
Entrez Gene ID 101715875

Database interlinks

Part of NW_004624803.1 (Scaffold)

For more information consult the page for NW_004624803.1 (Scaffold)

Genome Location

Sequence Coding sequence

Length: 891 bp    Location: 5596517..5723949   Strand: +
>XM_004861438.1
ATGGCGGCGGGTTGCTGTGGGGTAAAGAAACAGAAACTGTCCAGTTCGCCCCCCTCTGGCTCGGGTGGCGGTGGTGGCGCCTCCTCCTCCTCCCACTGCAGCGGAGAGAGCCAGTGTCGAGCTGGGGAGCTGGGACTAGGAGGCGCCGGTACGAGGCTCAACGGGCTTGGAGGTCTAACTGGAGGAGGTAGCAGCAGTGGCTGTACCCTCTCTACCCCCCAGGGTTGCGGTGGCGGCGGCGGCGGGGGGATCTCCCTCTCGCCACCTCTGAGCTGCGGAGTGGGGACCTTACTTTCTACCCCGGCCGCCGCCACCGCTTCCTCGCCCTCTTCGTCCGCCGCCTTGTCCTCATTACCGGGCTCCCGGAAGATGGTGGTTTCAGCGGAGATGTGCTGCTTTTGCTTCGATGTGCTCTACAGTCACCTGTACGGATACCAGCAGCCCCGTACCCCCCGGTTCACCAACGAGCCCTATGCCCTTAAAGATAGCCGTTTTCCCCCAATGACAAGGGATGAGCTGCCACGGCTTTTCTGCTCAGTGTCTCTGCTCACTAACTTTGAAGATGTCTGTGATTATTTGGACTGGGAGGTGGGTGTACATGGCATTAGAATAGAATTCATCAATGAAAAAGGATCAAAACGCACCGCCACCTACCTACCGGAGGTTGCAAAGGAGCAAGGATGGGACCATATTCAGACCATAGATTCCTTACTAAGGAAAGGAGGATACAAAGCTCCAATTACTAATGAATTCAGGAAAACCATAAAACTGACCAGATACCGTAGTGAAAAGATGACCCTGAGTTATGCTGAATACCTTGCTCATCGCCAACATCATCATTTTCAAAATGGCATTGGGCATCCCCTTCCGCCATACAACCATTATTCCTGA

Related Sequences

XP_004861495.1 Protein

Ammecr1 PREDICTED: AMME syndrome candidate gene 1 protein isoform X2 [Heterocephalus glaber]

Length: 296 aa     
>XP_004861495.1
MAAGCCGVKKQKLSSSPPSGSGGGGGASSSSHCSGESQCRAGELGLGGAGTRLNGLGGLTGGGSSSGCTLSTPQGCGGGGGGGISLSPPLSCGVGTLLSTPAAATASSPSSSAALSSLPGSRKMVVSAEMCCFCFDVLYSHLYGYQQPRTPRFTNEPYALKDSRFPPMTRDELPRLFCSVSLLTNFEDVCDYLDWEVGVHGIRIEFINEKGSKRTATYLPEVAKEQGWDHIQTIDSLLRKGGYKAPITNEFRKTIKLTRYRSEKMTLSYAEYLAHRQHHHFQNGIGHPLPPYNHYS