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The following sections contain reference sequences that belong to a
specific genome build. Explain
This section includes genomic Reference
Sequences (RefSeqs) from all assemblies on which this gene is annotated, such as
RefSeqs for chromosomes and scaffolds (contigs) from both reference and alternate
assemblies. Model RNAs and proteins are also reported here.
Reference assembly
Genomic
-
NT_033779.5 Reference assembly
- Range
-
22015190..22017334
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_165402.3 → NP_724369.2 uncharacterized protein Dmel_CG31693, isoform A [Drosophila melanogaster]
See identical proteins and their annotated locations for NP_724369.2
Status: REVIEWED
- UniProtKB/TrEMBL
- Q7KRS1, Q8T0L2
- Conserved Domains (2) summary
-
- COG1055
Location:196 → 675
- ArsB; Na+/H+ antiporter NhaD or related arsenite permease [Inorganic ion transport and metabolism]
- cd01116
Location:205 → 674
- P_permease; Permease P (pink-eyed dilution). Mutations in the human melanosomal P gene were responsible for classic phenotype of oculocutaneous albinism type 2 (OCA2). Although the precise function of the P protein is unknown, it was predicted to regulate the ...
-
NM_001038844.2 → NP_001033933.1 uncharacterized protein Dmel_CG31693, isoform B [Drosophila melanogaster]
See identical proteins and their annotated locations for NP_001033933.1
Status: REVIEWED
- UniProtKB/TrEMBL
- Q2PDP2, Q8T0L2
- Conserved Domains (2) summary
-
- COG1055
Location:115 → 594
- ArsB; Na+/H+ antiporter NhaD or related arsenite permease [Inorganic ion transport and metabolism]
- cd01116
Location:124 → 593
- P_permease; Permease P (pink-eyed dilution). Mutations in the human melanosomal P gene were responsible for classic phenotype of oculocutaneous albinism type 2 (OCA2). Although the precise function of the P protein is unknown, it was predicted to regulate the ...