U.S. flag

An official website of the United States government

Format

Send to:

Mus musculus nuclear factor I/B (Nfib), transcript variant 2, mRNA

NCBI Reference Sequence: NM_001113210.3

FASTA Graphics 

Feature
Display: FASTA GenBank Help
Details

Supplemental Content

Change region shown

Customize view

Reference sequence information

Recent activity

  • Mus musculus nuclear factor I/B (Nfib), transcript variant 2, mRNA
    Mus musculus nuclear factor I/B (Nfib), transcript variant 2, mRNA
    gi|2719984711|ref|NM_001113210.3|
    Nucleotide
  • Hepatolenticular Degeneration
    Hepatolenticular Degeneration
    A rare autosomal recessive disease characterized by the deposition of copper in the BRAIN; LIVER; CORNEA; and other organs. It is caused by defects in the ATP7B gene encoding ...<br/>Year introduced: 1964(1963)
    MeSH
  • Homocystinuria
    Homocystinuria
    Autosomal recessive inborn error of methionine metabolism usually caused by a deficiency of CYSTATHIONINE BETA-SYNTHASE and associated with elevations of homocysteine in plasm...<br/>Year introduced: 1969(1967)
    MeSH

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

See more...