Human ORFeome, Internal ID: 16672 | |||
BC number: KJ891117 UCSC; | Entrez Gene ID: 2055 | ||
Length: 861 | Symbol: CLN8 | ||
Resource Plate: Mut_GDEh1015 | Resource Plate Position: A01 | ||
Forward Primer: N/AN/A | |||
Reverse Primer: N/AN/A | |||
Description: ceroid-lipofuscinosis, neuronal 8 (epilepsy, progressive with mental retardation) CHROMOSOME: 8 | |||
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: KR710064 | ||
GI: 823670469 | |||
MGC Coding Sequence: | |||
atgaatcctgcgagcgatgggggcacatcagagagcatttttgacctggactatgcatcctgggggatcggctccacgctgatggtcgctggctttgtct tctacttgggcgtctttgtggtctgccaccagctgtcctcttccctgaatgccacttaccgttctttggtggccagagagaaggtcttctgggacctggc ggccacgcgtgcagtctttggtgttcagagcacagccgcaggcctgtgggctctgctgggggaccctgtgctgcatgccgacaaggcgcgtggccagcag aactggtgctggtttcacatcacgacagcaacgggattcttttgctttgaaaatgttgcagtccacctgtccaacttgatcttccggacatttgacttgt ttctggttatccaccatctctttgcctttcttgggtttcttggctgcttggtcaatctccaagctggccactatctagctatgaccacgttgctcctgga gatgagcacgccctttacctgcgtttcctggatgctcttaaaggcgggctggtccgagtctctgttttggaagctcaaccagtggctgatgattcacatg tttcactgccgcatggttctaacctaccacatgtggtgggtgtgtttctggcactgggacggcctggtcagcagcctgtatctgcctcatttgacactgt tccttgtcggactggctctgcttacgctaatcattaatccatattggacccataagaagactcagcagcttctcaatccggtggactggaacttcgcaca gccagaagccaagagcaggccagaaggcaacgggcagctgctgcggaagaagaggccatag | |||
cDNA Sequence (including UTRs): | |||
n/a | |||