RAB18 (NM_001256415) Human Untagged Clone
CAT#: SC330423
RAB18 (untagged) - Homo sapiens RAB18, member RAS oncogene family (RAB18), transcript variant 4
"NM_001256415" in other vectors (2)
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Specifications
Product Data | |
Type | Human Untagged Clone |
Tag | Tag Free |
Symbol | RAB18 |
Synonyms | RAB18LI1; WARBM3 |
Vector | pCMV6 series |
Sequence Data |
>NCBI ORF sequence for NM_001256415, the custom clone sequence may differ by one or more nucleotides
ATGGACGAGGACGTGCTAACCACCCTGAAGATCCTCATCATCGGCGAGAGTGGGGTGGGCAAGTCCAGCC TGCTCTTGAGGTTCACAGATGATACGTTTGATCCAGAACTTGCAGATACTGCTGGTCAAGAGAGGTTTAG AACATTAACTCCCAGCTATTATAGAGGTGCACAGGGTGTTATATTAGTTTATGATGTCACAAGAAGAGAT ACATTTGTTAAACTGGATAATTGGTTAAATGAATTGGAAACATACTGTACAAGAAATGACATAGTAAACA TGCTAGTTGGAAATAAAATCGATAAGGAAAATCGTGAAGTCGATAGAAATGAAGGCCTGAAATTTGCACG AAAGCATTCCATGTTATTTATAGAGGCAAGTGCAAAAACCTGTGATGGTGTACAATGTGCCTTTGAAGAA CTTGTTGAAAAGATCATTCAGACCCCTGGACTGTGGGAAAGTGAGAACCAGAATAAAGGAGTCAAACTGT CACACAGGGAAGAAGGCCAAGGAGGAGGAGCCTGTGGTGGTTATTGCTCTGTGTTATAA |
Restriction Sites | SgfI-MluI |
ACCN | NM_001256415 |
ORF Size | 549 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_001256415.1, NP_001243344.1 |
RefSeq Size | 4931 |
RefSeq ORF | 549 |
Locus ID | 22931 |
Protein Families | Druggable Genome |
Gene Summary | The protein encoded by this gene is a member of a family of Ras-related small GTPases that regulate membrane trafficking in organelles and transport vesicles. Knockdown studies is zebrafish suggest that this protein may have a role in eye and brain development. Mutations in this gene are associated with Warburg micro syndrome type 3. Alternatively spliced transcript variants have been found for this gene. [provided by RefSeq, Jan 2012] Transcript Variant: This variant (4) uses an alternate donor splice site at an internal exon, and lacks another coding exon compared to variant 1. However, it maintains the reading frame, and encodes a shorter isoform (4) missing an internal protein segment compared to 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. |
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