Gene Details



FRMD7 and homologs in 1 species are found in 76 GeneSets:


- Entrez   - GeneNetwork   - Allen Brain Atlas   - Comparative Toxicogenomics Database  

Select gene sets below using the check boxes, and then add them to a project using the pull down below. You can also create a project using the pull down. To view a set, click on the GeneSetID:GeneSet Description shown in green below.
Expand Tier I Human GO 4567 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human GO 1434 Genes GS206618: GO:0050793 regulation of developmental process
Expand Tier I Human 10 Genes GS172863: HP:0000666 Horizontal nystagmus
Expand Tier I Human GO 3409 Genes GS195113: GO:0071841 cellular component organization or biogenesis at cellular level
Expand Tier I Human GO 331 Genes GS206569: GO:0045664 regulation of neuron differentiation
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human GO 1213 Genes GS204438: GO:0051128 regulation of cellular component organization
Expand Tier I Human GO 1724 Genes GS198004: GO:0007399 nervous system development
Expand Tier I Human GO 2824 Genes GS209411: GO:0048869 cellular developmental process
Expand Tier I Human GO 4213 Genes GS195112: GO:0071840 cellular component organization or biogenesis
Expand Tier I Human GO 3125 Genes GS197892: GO:0043228 non-membrane-bounded organelle
Expand Tier I Human GO 1456 Genes GS205144: GO:0048468 cell development
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human GO 1789 Genes GS208893: GO:0005856 cytoskeleton
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 1096 Genes GS208716: GO:2000026 regulation of multicellular organismal development
Expand Tier I Human GO 3307 Genes GS195110: GO:0071842 cellular component organization at cellular level
Expand Tier I Human GO 3513 Genes GS193991: GO:0048731 system development
Expand Tier I Human 538 Genes GS175390: HP:0011007 Age of onset
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 700 Genes GS205439: GO:0031175 neuron projection development
Expand Tier I Human 129 Genes GS174657: HP:0001425 Heterogeneous
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human GO 649 Genes GS207805: GO:0043005 neuron projection
Expand Tier I Human GO 930 Genes GS200809: GO:0030030 cell projection organization
Expand Tier I Human GO 397 Genes GS209887: GO:0050767 regulation of neurogenesis
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 4 Genes GS174356: HP:0012043 Pendular nystagmus
Expand Tier I Human GO 291 Genes GS199165: GO:0043025 neuronal cell body
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 44 Genes GS174662: HP:0001423 X-linked dominant inheritance
Expand Tier I Human GO 1010 Genes GS196988: GO:0045595 regulation of cell differentiation
Expand Tier I Human GO 986 Genes GS204095: GO:0030182 neuron differentiation
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human GO 312 Genes GS206305: GO:0044297 cell body
Expand Tier I Human 570 Genes GS171453: HP:0003674 Onset
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human GO 3125 Genes GS199272: GO:0043232 intracellular non-membrane-bounded organelle
Expand Tier I Human GO 8137 Genes GS202316: GO:0050789 regulation of biological process
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human GO 1224 Genes GS208482: GO:0042995 cell projection
Expand Tier I Human 166 Genes GS171901: HP:0010985 Gonosomal inheritance
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 794 Genes GS209568: GO:0048666 neuron development
Expand Tier I Human GO 1770 Genes GS194455: GO:0051239 regulation of multicellular organismal process
Expand Tier I Human GO 1067 Genes GS196002: GO:0048699 generation of neurons
Expand Tier I Human GO 7689 Genes GS206623: GO:0050794 regulation of cellular process
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 8622 Genes GS196930: GO:0065007 biological regulation
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 493 Genes GS200286: GO:0060284 regulation of cell development
Expand Tier I Human GO 637 Genes GS201839: GO:0044463 cell projection part
Expand Tier I Human GO 440 Genes GS209602: GO:0051960 regulation of nervous system development
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 827 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human GO 93 Genes GS202123: GO:0030426 growth cone
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 255 Genes GS176610: HP:0003593 Infantile onset
Expand Tier I Human GO 95 Genes GS202122: GO:0030427 site of polarized growth
Expand Tier I Human GO 1136 Genes GS205691: GO:0022008 neurogenesis
Expand Tier I Human 2 Genes GS176749: HP:0006934 Congenital nystagmus
Expand Tier I Human GO 213 Genes GS197927: GO:0010975 regulation of neuron projection development
Expand Tier I Human GO 256 Genes GS195002: GO:0031344 regulation of cell projection organization
Expand Tier I Human GO 4097 Genes GS194307: GO:0016043 cellular component organization
Expand Tier I Human GO 2661 Genes GS207797: GO:0030154 cell differentiation
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4070 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 2 Genes GS173202: HP:0007739 Mildly reduced visual acuity
Expand Tier I Human 82 Genes GS175765: HP:0001419 X-linked recessive inheritance
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 160 Genes GS175806: HP:0001417 X-linked inheritance
Expand Tier I Human GO 4024 Genes GS205002: GO:0048856 anatomical structure development