Human ORFeome, Internal ID: 18381
BC number:  KJ892435 UCSC; Entrez Gene ID:  7809
Length: 963Symbol:  BSND
Resource Plate: Mut_GDEh1016Resource Plate Position:  F05
Forward Primer:  N/AN/A
Reverse Primer:  N/AN/A
Description:  Bartter syndrome, infantile, with sensorineural deafness (Barttin) CHROMOSOME: 1
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: KR711769
GI:  823673879
MGC Coding Sequence: 
atggctgacgagaagaccttccggatcggcttcattgtgctggggcttttcctgctggccctcggtacgttcctcatgagccatgatcggccccaggtct
acggcaccttctatgccatgggcagcgtcatggtgatcaggggcatcatctggagcatgtgccagtgctaccccaagatcaccttcgtccctgctgactc
tgactttcaaggcatcctctccccaaaggccatgggcctgctggagaatgggcttgctgccgagatgaagagccccagtccccagccgccctatgtaagg
ctgtgggaggaagccgcctatgaccagagcctgcctgacttcagccacatccagatgaaagtcatgagctacagtgaggaccaccgctccttgctggccc
ctgagatggggcagccgaagctgggaaccagtgatggaggagaaggtggccctggcgacgttcaggcctggatggaggctgccgtggtcatccacaaggg
ctcagacgagagtgaaggggaaagacgcctaactcagagctggcccggccccctggcctgtccccagggccctgcccccttggcttccttccaagatgac
ctggacatggactccagtgaaggcagcagccccaatgcatctccacatgacagggaggaagcttgttccccacaacaggaacctcagggctgcaggtgcc
cgctggaccgcttccaagactttgccctgattgatgccccaacgttggaggatgagccccaagaggggcagcagtgggaaatagccctgcccaacaactg
gcagcggtacccaaggacaaaggtggaggagaaggaggcttcggacacaggtggggaggaacctgagaaggaagaggaagacctgtactatgggctgcca
gatggagccggggacctcctcccggacaaggagctgggttttgagcctgacacccaaggctga
cDNA Sequence (including UTRs): 
n/a