Sequence details NCBI ID: XM_004872441.1 (Coding sequence)

Details from NCBI annotation

Gene Symbol LOC101698753
Gene Name chromosome unknown open reading frame, human C19orf53, transcript variant X2
Entrez Gene ID 101698753

Database interlinks

Part of NW_004624901.1 (Scaffold)

For more information consult the page for NW_004624901.1 (Scaffold)

Genome Location

Sequence Coding sequence

Length: 294 bp    Location: 1111360..1116703   Strand: +
Raw sequence   
>XM_004872441.1
ATGGCGCAGGGTCCGCGCAAGTTCCAGCCGCGGAAGCCAAGTAAAAGCAAGTCCGCGGCAACAGCCTCAGAGCGGAACCGCGGGCCAAGGAAAGGCGGTCGGTTGATCGTCCCCAAGAAGGCACGCATCGTGCAGCAGCAGCAGATCAAGAAGGATCTAGAGATCGCGATCCGGAAGAAGATTGAGCACGACATGGTGATGAAAGCCAGCTCCAGCCTGCCCAAGAAGCTGGCACTGCTGAAGGCCCCAGTCAAGAAGAAGGGGGCCGCTGCCTCCTCTAAGACTCCTTCCTGA

Related Sequences

XP_004872498.1 Protein

LOC101698753 PREDICTED: leydig cell tumor 10 kDa protein homolog isoform X2 [Heterocephalus glaber]

Length: 97 aa      
>XP_004872498.1
MAQGPRKFQPRKPSKSKSAATASERNRGPRKGGRLIVPKKARIVQQQQIKKDLEIAIRKKIEHDMVMKASSSLPKKLALLKAPVKKKGAAASSKTPS