Human ORFeome, Internal ID: 16638 | |||
BC number: KJ901759 UCSC; | Entrez Gene ID: 6687 | ||
Length: 1284 | Symbol: SPG7 | ||
Resource Plate: Mut_GDEh1009 | Resource Plate Position: C01 | ||
Forward Primer: N/AN/A | |||
Reverse Primer: N/AN/A | |||
Description: spastic paraplegia 7 (pure and complicated autosomal recessive) CHROMOSOME: 16 | |||
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: KR710030 | ||
GI: 823670401 | |||
MGC Coding Sequence: | |||
atggccgtgctgctgctgctgctccgttccctccgccggggtccaggcccgggtcctcggccgctgtggggcccaggcccggcctggagtccagggttcc ccgccaggcccgggagggggcggccgtacatggccagcaggcctccgggggacctcgccgaggctgtaggccgagctctgcagagcttacaattgagact gctaacccctacctttgaagggatcaacggattgttgttgaaacaacatttagttcagaatccagtcagactctggcaacttttaggtggtactttctat tttaacacctcaaggttgaagcagaagaataaggagaaggataagtcgaaggggaaggcgcctgaagaggacgaagaggagaggagacgccgtgagcggg acgaccagatgtaccgagagcggctgcgcaccttgctggtcatcgcggttgtcatgagcctcctgaatgctctcagcaccagcggaggcagcatttcctg gaacgactttgtccacgagatgctggccaagggcgaggtgcagcgcgtccaggtggtgcctgagagcgacgtggtggaagtctacctgcaccctggagcc gtggtgtttgggcggcctcggctagccttgatgtaccgaatgcaggttgcaaatattgacaagtttgaagagaagcttcgagcagctgaagatgagctga atatcgaggccaaggacaggatcccagtttcctacaagcgaacaggattctttggaaatgccctgtactctgtggggatgacggcagtgggcctggccat cctgtggtatgttttccgtctggccgggatgactggaagggaaggtggattcagtgcttttaatcagcttaaaatggctcgtttcaccattgtggatggg aagatggggaaaggagtcagcttcaaagacgtggcaggaatgcacgaagccaaactggaagtccgcgagtttgtggattatctgaagagcccagaacgct tcctccagcttggcgccaaggtcccaaagggcgcactgctgctcggcccccccggctgtgggaagacgctgctggccaaggcggtggccacggaggctca ggtgcccttcctggcgatggccggcccagagttcgtggaggtcattggaggcctcggcgctgcccgtgtgcggagcctctttaaggaagcccgagcccgg gccccctgcatcgtctacatcgatgagatcgacgcggtgggcaagaagcgctccaccaccatgtccggcttctccaacacgtag | |||
cDNA Sequence (including UTRs): | |||
n/a | |||