Human ORFeome, Internal ID: 18380 | |||
BC number: KJ892435 UCSC; | Entrez Gene ID: 7809 | ||
Length: 963 | Symbol: BSND | ||
Resource Plate: Mut_GDEh1016 | Resource Plate Position: E05 | ||
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/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: KR711768 | ||
GI: 823673877 | |||
MGC Coding Sequence: | |||
atggctgacgagaagaccttccggatcggcttcattgtgctggggcttttcctgctggccctcggtacgttcctcatgagccatgatcggccccaggtct acggcaccttctatgccatgggcagcatcatggtgatcgggggcatcatctggagcatgtgccagtgctaccccaagatcaccttcgtccctgctgactc tgactttcaaggcatcctctccccaaaggccatgggcctgctggagaatgggcttgctgccgagatgaagagccccagtccccagccgccctatgtaagg ctgtgggaggaagccgcctatgaccagagcctgcctgacttcagccacatccagatgaaagtcatgagctacagtgaggaccaccgctccttgctggccc ctgagatggggcagccgaagctgggaaccagtgatggaggagaaggtggccctggcgacgttcaggcctggatggaggctgccgtggtcatccacaaggg ctcagacgagagtgaaggggaaagacgcctaactcagagctggcccggccccctggcctgtccccagggccctgcccccttggcttccttccaagatgac ctggacatggactccagtgaaggcagcagccccaatgcatctccacatgacagggaggaagcttgttccccacaacaggaacctcagggctgcaggtgcc cgctggaccgcttccaagactttgccctgattgatgccccaacgttggaggatgagccccaagaggggcagcagtgggaaatagccctgcccaacaactg gcagcggtacccaaggacaaaggtggaggagaaggaggcttcggacacaggtggggaggaacctgagaaggaagaggaagacctgtactatgggctgcca gatggagccggggacctcctcccggacaaggagctgggttttgagcctgacacccaaggctga | |||
cDNA Sequence (including UTRs): | |||
n/a | |||