SLC25A46 (NM_001303250) Human Untagged Clone

CAT#: SC335359

SLC25A46 (untagged) - Human solute carrier family 25, member 46 (SLC25A46), transcript variant 3

Specifications

Product Data

• Type: Human Untagged Clone
• Tag: Tag Free
• Symbol: SLC25A46
• Synonyms: HMSN6B
• Vector: pCMV6-Entry
• E. coli Selection: Kanamycin (25 ug/mL)
• Mammalian Cell Selection: Neomycin
• Sequence Data:
  Fully Sequenced ORF

  >NCBI ORF sequence for NM_001303250, the custom clone sequence may differ by one or more nucleotides
  
  
  ATGAAAACAGAACAGCTGAATAGATTTGCTGGATTTGGTATTGGACTTGCAAGTCTCTTTACAGAAAATG
  TATTGGCACATCCTTGCATTGTTCTACGCCGCCAATGTCAGGTTAATTACCATGCTCAGCATTACCATCT
  CACTCCATTTACAGTCATCAATATTATGTACAGTTTCAACAAAACTCAGGGACCTAGAGCCCTGTGGAAA
  GGAATGGGAAGTACATTTATTGTCCAGGGAGTCACACTTGGAGCAGAAGGCATAATTAGTGAATTTACAC
  CTTTGCCAAGGGAGGTTTTACATAAATGGAGTCCTAAACAAATAGGAGAACACCTTCTACTGAAATCCCT
  AACTTACGTGGTGGCAATGCCTTTTTATTCAGCAAGTCTGATTGAAACAGTGCAGAGTGAGATAATTCGA
  GATAATACTGGCATTTTGGAGTGTGTTAAAGAAGGAATTGGAAGAGTGATAGGCATGGGAGTGCCTCATA
  GCAAACGACTTCTTCCGCTTCTTTCCTTGATCTTCCCTACGGTGCTTCATGGAGTTCTTCATTACATCAT
  CAGCTCAGTTATTCAGAAGTTTGTCCTACTAATTCTAAAGAGAAAGACTTACAATAGCCACCTAGCTGAG
  AGCACTAGCCCTGTGCAGAGTATGTTGGATGCTTATTTTCCAGAACTTATTGCTAACTTTGCTGCCAGTC
  TTTGTTCTGACGTTATACTTTACCCATTGGAAACAGTTTTGCACCGCCTTCACATTCAAGGAACACGCAC
  AATAATTGACAATACAGACCTTGGCTATGAAGTGCTTCCAATTAATACACAATATGAGGGAATGAGAGAC
  TGTATCAATACCATAAGGCAGGAGGAAGGAGTGTTTGGTTTTTATAAAGGGTTTGGTGCTGTTATAATAC
  AGTACACACTGCATGCAGCTGTTTTACAGATTACCAAAATTATTTACTCTACACTTCTTCAAAATAACAT
  TTGA
  
  
• Restriction Sites: SgfI-MluI
• ACCN: NM_001303250
• ORF Size: 984 bp
• OTI Disclaimer: Our molecular clone sequence data has been matched to the reference identifier above as a point of reference. Note that the complete sequence of our molecular clones may differ from the sequence published for this corresponding reference, e.g., by representing an alternative RNA splicing form or single nucleotide polymorphism (SNP).

Reference Data

• RefSeq: NM_001303250.1, NP_001290179.1
• RefSeq Size: 4465
• RefSeq ORF: 984
• Locus ID: 91137
• Gene Summary: This gene encodes a mitochondrial solute carrier protein family member. It functions in promoting mitochondrial fission, and prevents the formation of hyperfilamentous mitochondria. Mutation of this gene results in neuropathy and optic atrophy. [provided by RefSeq, Aug 2016]
  Transcript Variant: This variant (3) differs in the 5' UTR, lacks a portion of the 5' coding region, and initiates translation at an alternate start codon, compared to variant 1. The encoded isoform (3) has a distinct and shorter N-terminus than isoform 1. Sequence Note: This RefSeq record was created from transcript and genomic sequence data to make the sequence consistent with the reference genome assembly. The genomic coordinates used for the transcript record were based on transcript alignments.