Human ORFeome, Internal ID: 15117
BC number:  N/AEntrez Gene ID:  9949
Length: 999Symbol:  AMMECR1
Resource Plate: GDEhISO11003Resource 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/AVendor Position:  N/A
Collection:  Vendor Name: N/A
Vector: N/ACatalog 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