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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)
-
NM_001301347.2 → NP_001288276.1 flavin-containing monooxygenase 2 isoform b
See identical proteins and their annotated locations for NP_001288276.1
Status: REVIEWED
- Description
- Transcript Variant: This variant (3) lacks two alternate exons, and it thus differs in its 5' UTR, lacks a portion of the 5' coding region, and initiates translation at a downstream in-frame start codon, compared to variant 1. The encoded isoform (b) is shorter at the N-terminus, compared to isoform a.
- Source sequence(s)
-
AI821378, AK098145, AK304385, AL021026, AL833218, KF459607, R95468
- UniProtKB/TrEMBL
- B4E2Q9, Q5JPC7
- Conserved Domains (1) summary
-
- pfam00743
Location:1 → 312
- FMO-like; Flavin-binding monooxygenase-like
-
NM_001365900.2 → NP_001352829.1 flavin-containing monooxygenase 2 isoform c
Status: REVIEWED
- Source sequence(s)
-
AL021026, KF459607
- UniProtKB/TrEMBL
-
Q5JPC7
- Conserved Domains (1) summary
-
- cl26174
Location:1 → 467
- K_oxygenase; L-lysine 6-monooxygenase (NADPH-requiring)
-
NM_001426376.1 → NP_001413305.1 flavin-containing monooxygenase 2 isoform d
Status: REVIEWED
- Source sequence(s)
-
CP068277
-
NM_001426378.1 → NP_001413307.1 flavin-containing monooxygenase 2 isoform e
Status: REVIEWED
- Source sequence(s)
-
CP068277
-
NM_001426379.1 → NP_001413308.1 flavin-containing monooxygenase 2 isoform f
Status: REVIEWED
- Source sequence(s)
-
CP068277
- UniProtKB/TrEMBL
-
B4E2Q9
-
NM_001460.5 → NP_001451.2 flavin-containing monooxygenase 2 isoform a
Status: REVIEWED
- Description
- Transcript Variant: This variant (1), which represents the functional FMO2*1 allele, is the longer transcript and encodes the longer isoform (a)
- Source sequence(s)
-
AI821378, AK098145, AL021026, AL833218, BC005894, DB224311, KF459607, R95468
- Consensus CDS
-
CCDS1293.2
- UniProtKB/Swiss-Prot
- Q5EBX4, Q86U73, Q99518, Q9BRX1
- UniProtKB/TrEMBL
-
Q5JPC7
- Related
- ENSP00000209929.8, ENST00000209929.10
- Conserved Domains (1) summary
-
- pfam00743
Location:2 → 532
- FMO-like; Flavin-binding monooxygenase-like
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 GRCh38.p14 Primary Assembly
Genomic
-
NC_000001.11 Reference GRCh38.p14 Primary Assembly
- Range
-
171185208..171212686
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
Alternate T2T-CHM13v2.0
Genomic
-
NC_060925.1 Alternate T2T-CHM13v2.0
- Range
-
170541681..170568989
- Download
- GenBank, FASTA, Sequence Viewer (Graphics)
The following Reference Sequences have been suppressed. Explain
These RefSeqs were suppressed for the
cited reason(s). Suppressed RefSeqs do not appear in BLAST databases, related
sequence links, or BLAST links (BLink), but may still be retrieved by clicking on
their accession.version below.
-
NR_160266.1: Suppressed sequence
- Description
- NR_160266.1: This RefSeq was removed because it is not a nonsense-mediated mRNA decay (NMD) candidate but rather represents indel variation and is a protein coding transcript.