Human cDNA
Basic Informations | Advanced Informations |
Clone information |
Clone ID | hMU000562 |
Korean Unigene Clone | IRAT-06-G10 | |
Original Clone | IRAK-13-K22 | |
Vector | pCMV-SPORT6 | |
Gene | SLC25A4 | |
Gene Description | solute carrier family 25 member 4 | |
Clone sequence size | 1319 (bp) | |
Fullness | F | |
Mutation | - | |
Amino acid - mutation | - | |
Price | \77,000 (부가세 포함가) |
Clone information |
5' end sequenced Length | 1319 |
Sequence | GCGTCGCGCAGGGTCGGGGACTGCGCGGCGGTGCCAGGCCGGGCG TGGGCGAGAGCACGAACGGGCTGCCTGCGGGCTGAGAGCGTCGAG CTGTCACCATGGGTGATCACGCTTGGAGCTTCCTAAAGGACTTCC TGGCCGGGGGCGTCGCCGCTGCCGTCTCCAAGACCGCGGTCGCCC CCATCGAGAGGGTCAAACTGCTGCTGCAGGTCCAGCATGCCAGCA AACAGATCAGTGCTGAGAAGCAGTACAAAGGGATCATTGATTGTG TGGTGAGAATCCCTAAGGAGCAGGGCTTCCTCTCCTTCTGGAGGG GTAACCTGGCCAACGTGATCCGTTACTTCCCCACCCAAGCTCTCA ACTTCGCCTTCAAGGACAAGTACAAGCAGCTCTTCTTAGGGGGTG TGGATCGGCATAAGCAGTTCTGGCGCTACTTTGCTGGTAACCTGG CGTCCGGTGGGGCCGCTGGGGCCACCTCCCTTTGCTTTGTCTACC CGCTGGACTTTGCTAGGACCAGGTTGGCTGCTGATGTGGGCAAGG GCGCCGCCCAGCGTGAGTTCCATGGTCTGGGCGACTGTATCATCA AGATCTTCAAGTCTGATGGCCTGAGGGGGCTCTACCAGGGTTTCA ACGTCTCTGTCCAAGGCATCATTATCTATAGAGCTGCCTACTTCG GAGTCTATGATACTGCCAAGGGGATGCTGCCTGACCCCAAGAACG TGCACATTTTTGTGAGCTGGATGATTGCCCAGAGTGTGACGGCAG TCGCAGGGCTGGTGTCCTACCCCTTTGACACTGTTCGTCGTAGAA TGATGATGCAGTCCGGCCGGAAAGGGGCCGATATTATGTACACGG GGACAGTTGACTGCTGGAGGAAGATTGCAAAAGACGAAGGAGCCA AGGCCTTCTTCAAAGGTGCCTGGTCCAATGTGCTGAGAGGCATGG GCGGTGCTTTTGTATTGGTGTTGTATGATGAGATCAAAAAATATG TCTAATGTAATTAAAACACAAGTTCACAGATTTACAGTGAACTTG ATCTACAAGTTCACAGATCCATTGTGTGGTTTAATAGACTATTCC TAGGGGAAGTAAAAAGATCTGGGATAAAACCAGACTGAAAGGAAT ACCTCAGAAGAGATGCTTCATTGAGTGTTCATTAAACCACACATG TATTTTGTATTTATTTTACATTTAAATTCCCACAGCAAATAGAAA ATAATTTATCATACTTGTACAATTAACTGAAGAATTGATAATAAC TGAATGTGAAACATCAATAAAGACCACTTAATGCACGCTTTCTAA AAAAAAAAAAAAAA |
vector name | |
vector source | |
enzyme site(DNA insert) | |
sequencing primer | |
vector sequence | |
Gene Location | Chromosome | 4 | |||||||||||
Location | 4q35 | ||||||||||||
Strand |
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Database links | RefSeq | NM_001151 | |||||||||||
KEGG Genes | 291 | ||||||||||||
GeneCard | SLC25A4 |
sequence | sequence of CDS | ATGGGTGATCACGCTTGGAGCTTCCTAAAGGACTTCCTGGCCGGGGGCGTCGCCGCTGCCGTCTCCAAGACCGCGGTCGCCCCCATCGAGAGGGTCAAACTGCTGCTGCAGGTCCAGCATGCCAGCAAACAGATCAGTGCTGAGAAGCAGTACAAAGGGATCATTGATTGTGTGGTGAGAATCCCTAAGGAGCAGGGCTTCCTCTCCTTCTGGAGGGGTAACCTGGCCAACGTGATCCGTTACTTCCCCACCCAAGCTCTCAACTTCGCCTTCAAGGACAAGTACAAGCAGCTCTTCTTAGGGGGTGTGGATCGGCATAAGCAGTTCTGGCGCTACTTTGCTGGTAACCTGGCGTCCGGTGGGGCCGCTGGGGCCACCTCCCTTTGCTTTGTCTACCCGCTGGACTTTGCTAGGACCAGGTTGGCTGCTGATGTGGGCAAGGGCGCCGCCCAGCGTGAGTTCCATGGTCTGGGCGACTGTATCATCAAGATCTTCAAGTCTGATGGCCTGAGGGGGCTCTACCAGGGTTTCAACGTCTCTGTCCAAGGCATCATTATCTATAGAGCTGCCTACTTCGGAGTCTATGATACTGCCAAGGGGATGCTGCCTGACCCCAAGAACGTGCACATTTTTGTGAGCTGGATGATTGCCCAGAGTGTGACGGCAGTCGCAGGGCTGGTGTCCTACCCCTTTGACACTGTTCGTCGTAGAATGATGATGCAGTCCGGCCGGAAAGGGGCCGATATTATGTACACGGGGACAGTTGACTGCTGGAGGAAGATTGCAAAAGACGAAGGAGCCAAGGCCTTCTTCAAAGGTGCCTGGTCCAATGTGCTGAGAGGCATGGGCGGTGCTTTTGTATTGGTGTTGTATGATGAGATCAAAAAATATGTCTAA |
sequence of protein | MGDHAWSFLKDFLAGGVAAAVSKTAVAPIERVKLLLQVQHASKQISAEKQYKGIIDCVVRIPKEQGFLSFWRGNLANVIRYFPTQALNFAFKDKYKQLFLGGVDRHKQFWRYFAGNLASGGAAGATSLCFVYPLDFARTRLAADVGKGAAQREFHGLGDCIIKIFKSDGLRGLYQGFNVSVQGIIIYRAAYFGVYDTAKGMLPDPKNVHIFVSWMIAQSVTAVAGLVSYPFDTVRRRMMMQSGRKGADIMYTGTVDCWRKIAKDEGAKAFFKGAWSNVLRGMGGAFVLVLYDEIKKYV | |
Database link | RefSeq | NM_001151 |
UniProt | ||
CCDS |
Gene Ontology Provided by GOA (www.ebi.ac.uk/GOA)
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Disease | Summary |
This gene is a member of the mitochondrial carrier subfamily of solute carrier protein genes. The product of this gene functions as a gated pore that translocates ADP from the cytoplasm into the mitochondrial matrix and ATP from the mitochondrial matrix into the cytoplasm. The protein forms a homodimer embedded in the inner mitochondria membrane. Mutations in this gene have been shown to result in autosomal dominant progressive external opthalmoplegia and familial hypertrophic cardiomyopathy. [provided by RefSeq, Jun 2013] |
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