- DDX3ILA1 [Search on AGR]
Homo sapiens ASSOCIATED WITH Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB
- FPASL [Search on AGR]
Homo sapiens ASSOCIATED WITH Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB
- LINC03009 [Search on AGR]
Homo sapiens ASSOCIATED WITH Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB; INTERACTS WITH 2-palmitoylglycerol
- Krtap13-1 [Search on AGR]
Homo sapiens Hair keratins and hair keratin-associated proteins (KAPs), such as KRTAP13-1, are the main structural proteins of hair fibers (Rogers et al., 2002 [PubMed 12359730]).[supplied by OMIM, Mar 2008]
- Aptr [Search on AGR]
Homo sapiens ASSOCIATED WITH Chromosome 7q11.23 Deletion Syndrome, Distal, 1.2-MB; INTERACTS WITH acrylamide; aristolochic acid A; benzo[a]pyrene
- Slc2a12 [Search on AGR]
Homo sapiens SLC2A12 belongs to a family of transporters that catalyze the uptake of sugars through facilitated diffusion (Rogers et al., 2002). This family of transporters show conservation of 12 transmembrane helices as well as functionally significant amino acid residues (Joost and Thorens, 2001 [PubMed 11780753]).[supplied by OMIM, Mar 2008]
- Dnaaf9 [Search on AGR]
Homo sapiens This gene encodes an uncharacterized protein with a C-terminal coiled-coil region. The gene is located on chromosome 20p13 in a 1.8 Mb region linked to a spinocerebellar ataxia phenotype, but this gene does not appear to be a disease candidate. [provided by RefSeq, Dec 2011]
- Pacrg [Search on AGR]
Mus musculus PHENOTYPE: Along with altered levele of the Qki transcript, both Pacrg and Park2 are inactivated as a result of a 1.85 Mb deletion in the in the quaking mouse. The quaking mouse is a spontaneous dysmyelinating mutant that demonstrates abnormal locomotion, tremor, tonic-clonic seizures, and reduced male fertility. [provided by MGI curators]
- mb [Search on AGR]
Rattus norvegicus Enables oxygen binding activity. Involved in several processes, including cellular response to nitric oxide; cold acclimation; and oxygen transport. Located in cytosol and mitochondrion. Used to study acute kidney failure. Biomarker of acute kidney failure; hyperthyroidism; hypothyroidism; iron deficiency anemia; and pulmonary hypertension. Orthologous to human MB (myoglobin); INTERACTS WITH (R,R,R)-alpha-tocopherol; 17beta-estradiol; 2,3,7,8-tetrachlorodibenzodioxine.