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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_033777.3 Reference assembly
- Range
-
30745479..30746290 complement
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
mRNA and Protein(s)
-
NM_170521.3 → NP_733400.1 Niemann-Pick type C-2h, isoform B [Drosophila melanogaster]
See identical proteins and their annotated locations for NP_733400.1
Status: REVIEWED
- UniProtKB/TrEMBL
-
Q8IMH5
- Related
-
FBpp0085083
- Conserved Domains (1) summary
-
- cl00274
Location:26 → 126
- ML; The ML (MD-2-related lipid-recognition) domain is present in MD-1, MD-2, GM2 activator protein, Niemann-Pick type C2 (Npc2) protein, phosphatidylinositol/phosphatidylglycerol transfer protein (PG/PI-TP), mite allergen Der p 2 and several proteins of ...
-
NM_143567.4 → NP_651824.1 Niemann-Pick type C-2h, isoform A [Drosophila melanogaster]
See identical proteins and their annotated locations for NP_651824.1
Status: REVIEWED
- UniProtKB/TrEMBL
-
Q9VA41
- Related
-
FBpp0085084
- Conserved Domains (1) summary
-
- cd00916
Location:26 → 153
- Npc2_like; Niemann-Pick type C2 (Npc2) is a lysosomal protein in which a mutation in the gene causes a rare form of Niemann-Pick type C disease, an autosomal recessive lipid storage disorder characterized by accumulation of low-density lipoprotein-derived ...
-
NM_001260447.2 → NP_001247376.1 Niemann-Pick type C-2h, isoform C [Drosophila melanogaster]
See identical proteins and their annotated locations for NP_001247376.1
Status: REVIEWED
- UniProtKB/TrEMBL
-
Q9VA41
- Conserved Domains (1) summary
-
- cd00916
Location:26 → 153
- Npc2_like; Niemann-Pick type C2 (Npc2) is a lysosomal protein in which a mutation in the gene causes a rare form of Niemann-Pick type C disease, an autosomal recessive lipid storage disorder characterized by accumulation of low-density lipoprotein-derived ...