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Results 1 - 10 of 15 for Accessory
  1. MRAP gene 
    ... for making a protein called melanocortin-2 receptor accessory protein (MRAP). This protein transports another protein, called ... specific low MW protein GCCD2 melanocortin-2 receptor accessory protein MRAP_HUMAN Tests of MRAP PubMed MELANOCORTIN ...
    https://medlineplus.gov/genetics/gene/mrap - Genetics
  2. ATP6V0A4 gene 
    ... H+ transporting, lysosomal (vacuolar proton pump) non-catalytic accessory protein 1B ATPase, H+ transporting, lysosomal V0 subunit a4 H(+)-transporting two-sector ATPase, noncatalytic accessory protein 1B RdRTA2 RTA1C RTADR STV1 V-ATPase ...
    https://medlineplus.gov/genetics/gene/atp6v0a4 - Genetics
  3. BSND gene 
    ... deafness (Barttin) barttin barttin CLCNK-type chloride channel accessory beta subunit BSND_HUMAN deafness, autosomal recessive 73 DFNB73 Tests of BSND PubMed BARTTIN CLCNK-TYPE ACCESSORY SUBUNIT BETA; BSND NCBI Gene ClinVar Birkenhager R, ...
    https://medlineplus.gov/genetics/gene/bsnd - Genetics
  4. HCFC1 gene 
    ... protein phosphatase 1, regulatory subunit 89 VCAF VP16-accessory protein Tests of HCFC1 PubMed HOST CELL FACTOR ...
    https://medlineplus.gov/genetics/gene/hcfc1 - Genetics
  5. CTC1 gene 
    ... About This Health Condition AAF-132 AAF132 alpha accessory factor 132 C17orf68 conserved telomere capping protein 1 ...
    https://medlineplus.gov/genetics/gene/ctc1 - Genetics
  6. REEP1 gene 
    The REEP1 gene provides instructions for making a protein called receptor expression-enhancing protein 1 (REEP1), which is found in nerve cells (neurons) in ...
    https://medlineplus.gov/genetics/gene/reep1 - Genetics
  7. Wolff-Parkinson-White syndrome 
    ... an extra connection in the heart, called an accessory pathway, that allows electrical signals to bypass the ... atria to the ventricles faster than usual. The accessory pathway may also transmit electrical impulses abnormally from ...
    https://medlineplus.gov/.../condition/wolff-parkinson-white-syndrome - Genetics
  8. Ataxia neuropathy spectrum 
    ... POLG) compromises catalytic efficiency and interaction with the accessory subunit. J Biol Chem. 2005 Sep 9;280( ...
    https://medlineplus.gov/.../condition/ataxia-neuropathy-spectrum - Genetics
  9. Familial glucocorticoid deficiency 
    ... LA. Missense mutations in the melanocortin 2 receptor accessory protein that lead to late onset familial glucocorticoid ...
    https://medlineplus.gov/.../familial-glucocorticoid-deficiency - Genetics
  10. RNASEH2C gene 
    ... Crouch RJ, Cerritelli SM. Contributions of the two accessory subunits, RNASEH2B and RNASEH2C, to the activity and ...
    https://medlineplus.gov/genetics/gene/rnaseh2c - Genetics
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