Gene Details



SNRPN and homologs in 1 species are found in 318 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 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human GO 844 Genes GS203097: GO:0003723 RNA binding
Expand Tier I Human 17 Genes GS173032: HP:0007513 Generalized hypopigmentation
Expand Tier I Human 17 Genes GS176433: HP:0000044 Hypogonadotrophic hypogonadism
Expand Tier I Human 877 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 4 Genes GS171930: HP:0007010 Poor fine motor coordination
Expand Tier I Human 231 Genes GS176771: HP:0001000 Abnormality of skin pigmentation
Expand Tier I Human GO 5184 Genes GS208954: GO:0006139 nucleobase-containing compound metabolic process
Expand Tier I Human 39 Genes GS174330: HP:0002714 Downturned corners of mouth
Expand Tier I Human 173 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human 41 Genes GS171926: HP:0007018 Attention deficit hyperactivity disorder
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 274 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
Expand Tier I Human 82 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Human 541 Genes GS174385: HP:0002088 Abnormality of the lung
Expand Tier I Human 1176 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human 1222 Genes GS171998: HP:0001939 Abnormality of metabolism/homeostasis
Expand Tier I Human 55 Genes GS173418: HP:0000144 Decreased fertility
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human 99 Genes GS175130: HP:0000750 Delayed speech and language development
Expand Tier I Human 20 Genes GS175316: HP:0000565 Esotropia
Expand Tier I Human 201 Genes GS175802: HP:0003272 Abnormality of the hip bone
Expand Tier I Human 17 Genes GS176999: HP:0001290 Generalized hypotonia
Expand Tier I Human 60 Genes GS175897: HP:0000939 Osteoporosis
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human 407 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 122 Genes GS173384: HP:0002750 Delayed skeletal maturation
Expand Tier I Human 152 Genes GS174979: HP:0011061 Abnormality of dental structure
Expand Tier I Human 182 Genes GS174612: HP:0001600 Abnormality of the larynx
Expand Tier I Human 641 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 49 Genes GS173815: HP:0000736 Short attention span
Expand Tier I Human 318 Genes GS173392: HP:0003330 Abnormal bone structure
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human GO 3853 Genes GS197016: GO:0032991 macromolecular complex
Expand Tier I Human 288 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human GO 12482 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 161 Genes GS171633: HP:0008373 Puberty and gonadal disorders
Expand Tier I Human 486 Genes GS171461: HP:0011121 Abnormality of skin morphology
Expand Tier I Human GO 5348 Genes GS194039: GO:1901363 heterocyclic compound binding
Expand Tier I Human 283 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Human 72 Genes GS171187: HP:0000140 Abnormality of the menstrual cycle
Expand Tier I Human 38 Genes GS171381: HP:0001558 Decreased fetal movement
Expand Tier I Human 375 Genes GS176038: HP:0002795 Functional respiratory abnormality
Expand Tier III Human 728 Genes GS1229: Differential gene expression among Heroin Abusers
Expand Tier I Human 375 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human GO 9412 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Human 6 Genes GS175963: HP:0000060 Clitoral hypoplasia
Expand Tier I Human 69 Genes GS176657: HP:0000054 Micropenis
Expand Tier I Human 120 Genes GS172358: HP:0003117 Abnormality of circulating hormone level
Expand Tier I Human 209 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 66 Genes GS176153: HP:0100820 Glomerulopathy
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 156 Genes GS172363: HP:0004324 Increased body weight
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human 598 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human 147 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 58 Genes GS171388: HP:0001557 Prenatal movement abnormality
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 36 Genes GS172711: HP:0000219 Thin upper lip vermilion
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 174 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 80 Genes GS172726: HP:0000268 Dolichocephaly
Expand Tier I Human GO 6347 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 210 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human 80 Genes GS172801: HP:0000752 Hyperactivity
Expand Tier I Human 140 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human 423 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 36 Genes GS173707: HP:0000846 Adrenal insufficiency
Expand Tier I Human 148 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human GO 7308 Genes GS201431: GO:0005515 protein binding
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human GO 8948 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human CTD 2014 Genes GS126646: Carbon Tetrachloride interacting genes (MeSH:D002251) in CTD
Expand Tier I Human 50 Genes GS177055: HP:0005599 Hypopigmentation of hair
Expand Tier I Human 43 Genes GS171083: HP:0001328 Specific learning disability
Expand Tier I Human 146 Genes GS176098: HP:0000927 Abnormality of skeletal maturation
Expand Tier I Human 157 Genes GS171718: HP:0002808 Kyphosis
Expand Tier I Human 112 Genes GS174412: HP:0007477 Abnormal dermatoglyphics
Expand Tier I Human 472 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human 284 Genes GS175594: HP:0011014 Abnormal glucose homeostasis
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 88 Genes GS174101: HP:0001018 Abnormal palmar dermatoglyphics
Expand Tier I Human 407 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 950 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Human 736 Genes GS173290: HP:0011354 Generalized abnormality of skin
Expand Tier I Human 17 Genes GS174402: HP:0001611 Nasal speech
Expand Tier I Human 69 Genes GS170981: HP:0011361 Congenital abnormal hair pattern
Expand Tier I Human GO 12162 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human 282 Genes GS172060: HP:0001508 Failure to thrive
Expand Tier I Human 29 Genes GS172941: HP:0000786 Primary amenorrhea
Expand Tier I Human 16 Genes GS175957: HP:0000066 Labial hypoplasia
Expand Tier I Human GO 3891 Genes GS203908: GO:0016070 RNA metabolic process
Expand Tier I Human GO 9515 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 46 Genes GS172542: HP:0000830 Anterior hypopituitarism
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 48 Genes GS176364: HP:0008034 Abnormal iris pigmentation
Expand Tier I Human 46 Genes GS172570: HP:0000341 Narrow forehead
Expand Tier I Human 484 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 4 Genes GS175959: HP:0000064 Hypoplastic labia minora
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 90 Genes GS172611: HP:0003474 Sensory impairment
Expand Tier I Human 389 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 28 Genes GS172285: HP:0000826 Precocious puberty
Expand Tier I Human 273 Genes GS174338: HP:0002719 Recurrent infections
Expand Tier I Human 72 Genes GS175158: HP:0011747 Abnormality of the anterior pituitary
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 442 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human 181 Genes GS175907: HP:0004349 Reduced bone mineral density
Expand Tier I Human 5 Genes GS172793: HP:0001531 Failure to thrive in infancy
Expand Tier I Human 113 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human 250 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 132 Genes GS174606: HP:0001608 Abnormality of the voice
Expand Tier I Human 200 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 72 Genes GS172350: HP:0000135 Hypogonadism
Expand Tier I Human 222 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 8 Genes GS175819: HP:0002591 Polyphagia
Expand Tier I Human 122 Genes GS176258: HP:0004370 Abnormality of temperature regulation
Expand Tier I Human GO 5928 Genes GS205047: GO:0006807 nitrogen compound metabolic process
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human GO 7259 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human 393 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 236 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human 316 Genes GS175597: HP:0011013 Abnormality of carbohydrate metabolism/homeostasis
Expand Tier I Human 108 Genes GS175595: HP:0011017 Abnormality of cell physiology
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 200 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 86 Genes GS172871: HP:0010490 Abnormality of the palmar creases
Expand Tier I Human 733 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 35 Genes GS176655: HP:0000056 Abnormality of the clitoris
Expand Tier I Human 148 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 454 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 198 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human 62 Genes GS173993: HP:0000506 Telecanthus
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 86 Genes GS172544: HP:0000834 Abnormality of the adrenal glands
Expand Tier I Human 270 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Human 33 Genes GS174504: HP:0000709 Psychosis
Expand Tier I Human 199 Genes GS176660: HP:0000050 Hypoplastic genitalia
Expand Tier I Human 1046 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Human 10 Genes GS171554: HP:0001385 Hip dysplasia
Expand Tier I Human 51 Genes GS172933: HP:0003745 Sporadic
Expand Tier I Human 381 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 242 Genes GS175909: HP:0004348 Abnormality of bone mineral density
Expand Tier I Human 203 Genes GS171621: HP:0100851 Abnormal emotion/affect behavior
Expand Tier I Human 77 Genes GS173703: HP:0000842 Hyperinsulinemia
Expand Tier I Human 917 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human 604 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier I Human 88 Genes GS173329: HP:0000682 Abnormality of dental enamel
Expand Tier I Human 207 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 186 Genes GS173355: HP:0002205 Recurrent respiratory infections
Expand Tier I Human 12 Genes GS174026: HP:0002033 Poor suck
Expand Tier I Human 3 Genes GS173017: HP:0007015 Poor gross motor coordination
Expand Tier I Human 72 Genes GS176656: HP:0000055 Abnormality of female external genitalia
Expand Tier I Human GO 8645 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 985 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human 22 Genes GS176435: HP:0000046 Scrotal hypoplasia
Expand Tier III Human 2273 Genes GS137413: Supplementary Table 2. CNA Overall results of WGCNA combined with differential expression between alcoholics and controls
Expand Tier I Human GO 143 Genes GS207056: GO:0005681 spliceosomal complex
Expand Tier I Human 17 Genes GS176514: HP:0007328 Impaired pain sensation
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 469 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human 39 Genes GS174016: HP:0000717 Autism
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 20 Genes GS173655: HP:0000823 Delayed puberty
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 9 Genes GS174398: HP:0001614 Hypernasal speech
Expand Tier I Human 430 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Human GO 16864 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 170 Genes GS173476: HP:0002311 Incoordination
Expand Tier I Human 16 Genes GS172805: HP:0000789 Infertility
Expand Tier I Human 514 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 11 Genes GS175898: HP:0010535 Sleep apnea
Expand Tier I Human GO 5337 Genes GS201239: GO:0046483 heterocycle metabolic process
Expand Tier I Human 737 Genes GS175601: HP:0002086 Abnormality of the respiratory system
Expand Tier I Human 487 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 4 Genes GS174390: HP:0007874 Almond-shaped palpebral fissure
Expand Tier I Human 54 Genes GS175220: HP:0009887 Abnormality of hair pigmentation
Expand Tier I Human 4 Genes GS175965: HP:0200005 Abnormal shape of the palpebral fissure
Expand Tier I Human 5 Genes GS173152: HP:0002236 Frontal upsweep of hair
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 511 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human 286 Genes GS173167: HP:0100491 Abnormality of the joints of the lower limbs
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 256 Genes GS175602: HP:0002087 Abnormality of the upper respiratory tract
Expand Tier I Human 7 Genes GS173484: HP:0000876 Oligomenorrhea
Expand Tier I Human 26 Genes GS176003: HP:0100651 Type I diabetes mellitus
Expand Tier I Human 208 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 76 Genes GS174649: HP:0000954 Single transverse palmar crease
Expand Tier I Human 489 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 435 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human GO 10576 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 33 Genes GS195490: GO:0030532 small nuclear ribonucleoprotein complex
Expand Tier I Human 7 Genes GS173822: HP:0100720 Hypoplasia of the ear cartilage
Expand Tier I Human 72 Genes GS176488: HP:0010720 Abnormal hair pattern
Expand Tier I Human 529 Genes GS172667: HP:0011805 Abnormality of muscle morphology
Expand Tier I Human GO 4682 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human 94 Genes GS174879: HP:0002104 Apnea
Expand Tier I Human 532 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 196 Genes GS174756: HP:0011947 Respiratory tract infection
Expand Tier I Human 177 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human 153 Genes GS175067: HP:0001159 Syndactyly
Expand Tier I Human 1203 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 46 Genes GS175481: HP:0000992 Cutaneous photosensitivity
Expand Tier I Human 554 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human DRG 868 Genes provisional GS86977: Table S1: All transcripts significantly different in abundance between the majority of heroin subjects and their matched controls [DRG]
Expand Tier I Human 234 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human 155 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Human 676 Genes GS174331: HP:0002715 Abnormality of the immune system
Expand Tier I Human 177 Genes GS171047: HP:0008736 Hypoplasia of penis
Expand Tier I Human GO 9526 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 9155 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 184 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Human GO 6256 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human 121 Genes GS176672: HP:0000980 Pallor
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human GO 15151 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 596 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 50 Genes GS171995: HP:0001764 Small feet
Expand Tier I Human 248 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human 322 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human CTD 1069 Genes GS121343: Flavonoids interacting genes (MeSH:D005419) in CTD
Expand Tier I Human 12 Genes GS174326: HP:0003199 Decreased muscle mass
Expand Tier I Human GO 10561 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human GO 5400 Genes GS194111: GO:0097159 organic cyclic compound binding
Expand Tier I Human 11 Genes GS174057: HP:0100738 Abnormal eating behavior
Expand Tier I Human 23 Genes GS176653: HP:0000058 Abnormality of the labia
Expand Tier I Human 262 Genes GS171645: HP:0011843 Abnormality of skeletal physiology
Expand Tier I Human 341 Genes GS176245: HP:0011443 Abnormality of coordination
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 171 Genes GS173019: HP:0000819 Diabetes mellitus
Expand Tier I Human 5 Genes GS171673: HP:0004283 Narrow palm
Expand Tier I Human 39 Genes GS174048: HP:0000729 Autism spectrum disorder
Expand Tier I Human 257 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 54 Genes GS175896: HP:0000938 Osteopenia
Expand Tier I Human GO 5908 Genes GS195199: GO:0005634 nucleus
Expand Tier I Human 42 Genes GS173404: HP:0000141 Amenorrhea
Expand Tier I Human 85 Genes GS173666: HP:0005978 Type II diabetes mellitus
Expand Tier I Human 14 Genes GS173223: HP:0007730 Iris hypopigmentation
Expand Tier I Human CTD 148 Genes GS127114: Methylnitronitrosoguanidine interacting genes (MeSH:D008769) in CTD
Expand Tier I Human 45 Genes GS171463: HP:0004279 Short palm
Expand Tier I Human 7 Genes GS176526: HP:0010721 Abnormal hair whorl
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human GO 4415 Genes GS203072: GO:0090304 nucleic acid metabolic process
Expand Tier I Human CTD 23 Genes GS125190: Atenolol interacting genes (MeSH:D001262) in CTD
Expand Tier I Human GO 549 Genes GS207972: GO:0030529 ribonucleoprotein complex
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 147 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human 18 Genes GS176941: HP:0002791 Hypoventilation
Expand Tier I Human 261 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 1068 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 423 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Human 695 Genes GS177031: HP:0011442 Abnormality of central motor function
Expand Tier I Human 401 Genes GS170791: HP:0010978 Abnormality of immune system physiology
Expand Tier I Human 541 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 19 Genes GS173827: HP:0002916 Abnormality of chromosome segregation
Expand Tier I Human 6 Genes GS172175: HP:0002275 Poor motor coordination
Expand Tier I Human 469 Genes GS174505: HP:0000708 Behavioural/Psychiatric Abnormality
Expand Tier I Human 17 Genes GS173375: HP:0010832 Abnormality of pain sensation
Expand Tier I Human 94 Genes GS176560: HP:0001010 Hypopigmentation of the skin
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 20 Genes GS172286: HP:0000824 Growth hormone deficiency
Expand Tier I Human 41 Genes GS176434: HP:0000045 Abnormality of the scrotum
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 98 Genes GS170997: HP:0000080 Abnormality of genital physiology
Expand Tier I Human 77 Genes GS171254: HP:0002360 Sleep disturbance
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human GO 652 Genes GS197734: GO:0006396 RNA processing
Expand Tier I Human 780 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 433 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 78 Genes GS173104: HP:0000670 Carious teeth
Expand Tier I Human 75 Genes GS171608: HP:0011338 Abnormality of mouth shape
Expand Tier I Human 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human CTD 480 Genes GS123538: testosterone enanthate interacting genes (MeSH:C004648) in CTD
Expand Tier I Human 148 Genes GS172295: HP:0001513 Obesity
Expand Tier I Human GO 6605 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 542 Genes GS175673: HP:0100022 Abnormality of movement
Expand Tier I Human 138 Genes GS173081: HP:0000494 Downslanted palpebral fissures
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 326 Genes GS202209: GO:0008380 RNA splicing
Expand Tier I Human GO 2479 Genes GS201249: GO:0044428 nuclear part
Expand Tier I Human GO 8545 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human GO 5347 Genes GS203642: GO:0006725 cellular aromatic compound metabolic process
Expand Tier I Human GO 5567 Genes GS207923: GO:0034641 cellular nitrogen compound metabolic process
Expand Tier I Human 3 Genes GS173436: HP:0005968 Temperature instability
Expand Tier I Human 61 Genes GS175742: HP:0011733 Abnormality of adrenal physiology
Expand Tier I Human 40 Genes GS176115: HP:0000540 Hypermetropia
Expand Tier I Human 15 Genes GS176408: HP:0000446 Narrow nasal bridge
Expand Tier I Human GO 11869 Genes GS198263: GO:0005488 binding
Expand Tier I Human 344 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 238 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human GO 5526 Genes GS194040: GO:1901360 organic cyclic compound metabolic process
Expand Tier I Human GO 3277 Genes GS194088: GO:0003676 nucleic acid binding