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Gene Info
| Gene Information For: | Hs. FANCF, Fanconi anemia, complementation group F | | Sequence ID: | NM_022725
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- This gene is found in these
cDNA libraries
from the following tissue types:
b-cell, bone, bone marrow, brain, cerebellum, cerebrum, cervix, colon, embryonic tissue, endocrine, esophagus, eye, fetus, gastrointestinal tract, heart, kidney, liver, lung, lymph node, lymphoreticular, mammary gland, muscle, nervous, pancreas, pancreatic islet, pooled tissue, prostate, salivary gland, skin, spleen, stem cell, stomach, synovium, testis, thymus, thyroid, uncharacterized tissue, uterus, vascular
- SAGE Anatomic Viewer
- SAGE Digital Northern
- Monochromatic SAGE/cDNA Virtual Northern
- Two-dimensional array displays (similar expression pattern in NCI60 microarray data or SAGE data)
| Cytogenetic Location (from UniGene) |
| Chromosomal Position (from UCSC) |
| Chromosomal Position: | 11: 22602659 - 22603936 |
| Full-Length MGC Clones for This Gene |
| IMAGE Id | Status | Accession |
GenBank Def Line |
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| 5239725 | Full Length | BC063038 | Fanconi anemia, complementation group F |
| 5538578 | Full Length | BC047028 | Fanconi anemia, complementation group F |
| 7939712 | Full Length | BC093867 | Fanconi anemia, complementation group F |
| 8069313 | Full Length | BC101807 | Fanconi anemia, complementation group F |
RefSeq
Related Sequences
| Homologs (from HomoloGene) |
Note: Both orthologs and
paralogs are included.
Gene classification by the European Bioinformatics Institute, as recorded in GOA (GO Annotation@EBI)
| NCI-Nature Pathway Interaction Database |
Pathway information courtesy of BioCarta
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