Gene Details



SPATA7 and homologs in 1 species are found in 135 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 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 124 Genes GS175492: HP:0000512 Abnormal electroretinogram
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 64 Genes GS174379: HP:0002084 Encephalocele
Expand Tier I Human GO 7638 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 637 Genes GS207720: GO:0048609 multicellular organismal reproductive process
Expand Tier I Human 832 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 42 Genes GS174449: HP:0001123 Visual field defect
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human GO 5637 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human 384 Genes GS171708: HP:0000359 Abnormality of the inner ear
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human GO 1693 Genes GS209960: GO:0003008 system process
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 179 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human 537 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human 1228 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human GO 1597 Genes GS207991: GO:0000003 reproduction
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 188 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Human 170 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human 416 Genes GS175169: HP:0001317 Abnormality of the cerebellum
Expand Tier I Human 12 Genes GS174650: HP:0001133 Constricted visual fields
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 183 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Human 368 Genes GS170971: HP:0000407 Sensorineural hearing impairment
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 100 Genes GS176744: HP:0000987 Atypical scarring of skin
Expand Tier I Human GO 1592 Genes GS196196: GO:0022414 reproductive process
Expand Tier I Human 89 Genes GS176988: HP:0008046 Abnormality of the retinal vasculature
Expand Tier I Human 120 Genes GS171657: HP:0000613 Photophobia
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 273 Genes GS172516: HP:0001347 Hyperreflexia
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 1006 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier III Human 3178 Genes GS137407: Supplementary Table 2. Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 202 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human 64 Genes GS172899: HP:0011815 Cephalocele
Expand Tier I Human GO 5605 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 393 Genes GS205650: GO:0048232 male gamete generation
Expand Tier I Human 320 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human GO 495 Genes GS209225: GO:0007600 sensory perception
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Human GO 6585 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 78 Genes GS172553: HP:0100689 Decreased corneal thickness
Expand Tier I Human 174 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human 85 Genes GS173666: HP:0005978 Type II diabetes mellitus
Expand Tier I Human 136 Genes GS171855: HP:0000597 Ophthalmoparesis
Expand Tier I Human 201 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Human GO 637 Genes GS196811: GO:0032504 multicellular organism reproduction
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 416 Genes GS173146: HP:0011282 Abnormality of the hindbrain
Expand Tier I Human 123 Genes GS171946: HP:0002269 Abnormality of neuronal migration
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 77 Genes GS173703: HP:0000842 Hyperinsulinemia
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human 211 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human GO 579 Genes GS195583: GO:0019953 sexual reproduction
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human 157 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 103 Genes GS173741: HP:0100699 Scarring
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 392 Genes GS203862: GO:0007283 spermatogenesis
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 501 Genes GS207582: GO:0007276 gamete generation
Expand Tier I Human CTD 6285 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 498 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 699 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 1236 Genes GS202899: GO:0050877 neurological system process
Expand Tier I Human 472 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 79 Genes GS175373: HP:0011486 Abnormality of corneal thickness
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human GO 1165 Genes GS206696: GO:0044702 single organism reproductive process
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human GO 205 Genes GS209987: GO:0050953 sensory perception of light stimulus
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 66 Genes GS173753: HP:0000510 Retinitis pigmentosa
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Human 70 Genes GS221933: Mutations of 60 known causative genes in 157 families with retinitis pigmentosa (RP) based on exome sequencing
Expand Tier I Human 416 Genes GS173147: HP:0011283 Abnormality of the metencephalon
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Human 63 Genes GS221925: Capture panel of retinitis pigmentosa (RP) genes used to diagnose Irish probands
Expand Tier I Human 149 Genes GS172295: HP:0001513 Obesity
Expand Tier I Human 287 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 137 Genes GS175674: HP:0007360 Aplasia/Hypoplasia of the cerebellum
Expand Tier I Human 534 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Human 214 Genes GS222320: Genes associated with high risk of intellectual disability.
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 739 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human 95 Genes GS176989: HP:0008047 Abnormality of the vasculature of the eye
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Human 381 Genes GS175714: HP:0011389 Functional abnormality of the inner ear
Expand Tier I Human GO 204 Genes GS210485: GO:0007601 visual perception
Expand Tier I Human CTD 531 Genes GS122992: nitrosobenzylmethylamine interacting genes (MeSH:C014707) in CTD
Expand Tier I Human 96 Genes GS176616: HP:0000662 Night blindness