These reference sequences exist independently of genome builds. Explain

These reference sequences are curated independently of the genome annotation cycle, so their versions may not match the RefSeq versions in the current genome build. Identify version mismatches by comparing the version of the RefSeq in this section to the one reported in Genomic regions, transcripts, and products above.

mRNA and Protein(s)

1. NM_001266760.1 → NP_001253689.1  NPC intracellular cholesterol transporter 2 precursor

   See identical proteins and their annotated locations for NP_001253689.1

   Status: PROVISIONAL

   Source sequence(s)

   JV045946

   UniProtKB/TrEMBL

   F7HRU3, I0FNJ1

   Related

   ENSMMUP00000008638.4, ENSMMUT00000009192.4

   Conserved Domains (1) summary

   cd00916
   Location:24 → 145

   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 ...

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 Mmul_10 Primary Assembly

Genomic

1. NC_041760.1 Reference Mmul_10 Primary Assembly

   Range

   136591300..136605436 complement

   Download

   GenBank, FASTA, Sequence Viewer (Graphics)

mRNA and Protein(s)

1. XM_015144113.2 → XP_014999599.1  NPC intracellular cholesterol transporter 2 isoform X2

   UniProtKB/TrEMBL

   F7HRU3, I0FNJ1

   Conserved Domains (1) summary

   cd00916
   Location:24 → 145

   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 ...

2. XM_028850263.1 → XP_028706096.1  NPC intracellular cholesterol transporter 2 isoform X1

   Conserved Domains (1) summary

   cd00916
   Location:24 → 145

   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 ...

3. XM_028850264.1 → XP_028706097.1  NPC intracellular cholesterol transporter 2 isoform X1

   Conserved Domains (1) summary

   cd00916
   Location:24 → 145

   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 ...