Human ORFeome, Internal ID: 15117 | |||
BC number: N/A | Entrez Gene ID: 9949 | ||
Length: 999 | Symbol: AMMECR1 | ||
Resource Plate: GDEhISO11003 | Resource Plate Position: D03 | ||
Forward Primer: GGGGACAACTTTGTACAAAAAAGTTGGCACCATGGCGGCGGGTTGCTGCGGG | |||
Reverse Primer: GGGGACAACTTTGTACAAGAAAGTTGGCAACAGGAATAATGGTTGTATGGCGGA | |||
Description: Homo sapiens Alport syndrome mental retardation midface hypoplasia and elliptocytosis chromosomal region protein 1 isoform 2 (AMMECR1) mRNA, partial cds CHROMOSOME: X | |||
Template Information: | |||
Vendor Plate: N/A | Vendor Position: N/A | ||
Collection: | Vendor Name: N/A | ||
Vector: N/A | Catalog Number: | ||
Information Source: N/A | Library: N/A | ||
Clone ID: N/A | Genbank Accession: KU178497 | ||
GI: 957950694 | |||
MGC Coding Sequence: | |||
atggcggcgggttgctgcggggtgaagaagcagaaactgtccagttcgcccccctctggctcgggtggcggtggtggcgcctcctcctcctcccactgca gcggagagagccagtgccgagctggggagctgggactaggaggcgccggtacgcggctcaacgggctgggaggtctaaccggaggaggtagcggcagcgg ctgtaccctctctcccccccagggctgcggcggcggcggcggggggatcgccctgtcgccacctccgagctgcggagtggggaccctactttctaccccg gccgccgccacctcttcctcaccctcctcatcgtccgccgcctcgtcctcatcgccgggctcccggaagatggtggtgtcagcagagatgtgctgctttt gcttcgatgtgctctactgtcacctgtatggataccagcagccccggaccccccgattcaccaacgagccctacccactgtttgtaacatggaagattgg tcgagacaaaagattacgtggatgcataggtactttttctgccatgaatttgcattcaggactcagggagtacacacttaccagtgcccttaaagatagc cgttttcccccaatgacaagggatgagctgccacggcttttctgctcagtgtctctgctcactaactttgaagatgtctgtgattatttggactgggagg tgggtgtacatggcattagaatagaattcatcaatgaaaaaggatcaaaacgcaccgccacctacctaccggaggttgcaaaggagcaaggatgggacca tatacagaccatagactccttattgaggaaaggaggatacaaagctccgattactaatgaattcaggaaaaccataaaactgaccaggtatcgtagtgaa aagatgaccctgagctatgctgaataccttgctcatcgccagcatcatcatttccaaaatggcattgggcatccccttccgccatacaaccattattcc | |||
cDNA Sequence (including UTRs): | |||
n/a | |||