Gene Details



B3GALTL and homologs in 5 species are found in 476 GeneSets:


- Entrez   - Ensembl   - GeneNetwork   - STRING   - 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 83 Genes GS172224: HP:0001770 Toe syndactyly
Expand Tier I Human 99 Genes GS172242: HP:0004930 Abnormality of the pulmonary vasculature
Expand Tier I Human 19 Genes GS171191: HP:0000412 Prominent ears
Expand Tier I Human 4 Genes GS172627: HP:0000659 Peters anomaly
Expand Tier I Human 1181 Genes GS171644: HP:0011842 Abnormality of skeletal morphology
Expand Tier I Human GO 590 Genes GS205780: GO:0044723 single-organism carbohydrate metabolic process
Expand Tier I Human 269 Genes GS172261: HP:0000357 Abnormal location of ears
Expand Tier I Human 645 Genes GS172294: HP:0001510 Growth delay
Expand Tier I Human 845 Genes GS174134: HP:0002012 Abnormality of the abdominal organs
Expand Tier I Human 379 Genes GS171596: HP:0000164 Abnormality of the teeth
Expand Tier I Human 47 Genes GS173284: HP:0000311 Round face
Expand Tier I Human 178 Genes GS176151: HP:0000256 Macrocephaly
Expand Tier I Mouse 693 Genes GS136854: Theiler's murine encephalomyelitis virus induced demyelinating disease susceptibility 7 (Tmevd7, Published QTL Chr 5)
Expand Tier I Human 491 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 360 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 150 Genes GS175411: HP:0100871 Abnormality of the palm
Expand Tier I Human 786 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human 177 Genes GS172293: HP:0001511 Intrauterine growth retardation
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human 141 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human 426 Genes GS175332: HP:0000032 Abnormality of male external genitalia
Expand Tier I Human 31 Genes GS176849: HP:0010743 Short metatarsal bone
Expand Tier I Human 324 Genes GS172843: HP:0000481 Abnormality of the cornea
Expand Tier I Human 81 Genes GS172821: HP:0000213 Thin lips
Expand Tier I Human 53 Genes GS171286: HP:0002996 Limited elbow movement
Expand Tier I Human 121 Genes GS172789: HP:0001537 Umbilical hernia
Expand Tier I Human 954 Genes GS172054: HP:0001507 Growth abnormality
Expand Tier I Mouse GO 8406 Genes GS177404: GO:0005737 cytoplasm
Expand Tier I Human GO 4169 Genes GS207925: GO:0034645 cellular macromolecule biosynthetic process
Expand Tier I Human GO 12234 Genes GS201251: GO:0044424 intracellular part
Expand Tier I Human GO 772 Genes GS196729: GO:0005789 endoplasmic reticulum membrane
Expand Tier I Human 117 Genes GS172063: HP:0000107 Renal cysts
Expand Tier I Human 392 Genes GS171126: HP:0000022 Abnormality of male internal genitalia
Expand Tier I Human 202 Genes GS176242: HP:0004207 Abnormality of the 5th finger
Expand Tier I Mouse 446 Genes GS136345: nitrous oxide antinociception 2 (Noan2, Published QTL Chr 5)
Expand Tier I Human 17 Genes GS174162: HP:0000960 Sacral dimple
Expand Tier I Human 456 Genes GS171436: HP:0000077 Abnormality of the kidney
Expand Tier I Human 210 Genes GS174857: HP:0200006 Slanting of the palpebral fissure
Expand Tier I Human 348 Genes GS176615: HP:0000277 Abnormality of the mandible
Expand Tier I Human 47 Genes GS171564: HP:0000383 Abnormality of periauricular region
Expand Tier I Mouse 446 Genes GS135655: cocaine induced activation 7 (Cocia7, Published QTL Chr 5)
Expand Tier I Human 1169 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human 535 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human 492 Genes GS171226: HP:0000812 Abnormal internal genitalia
Expand Tier I Human 179 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 403 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human 179 Genes GS174214: HP:0009466 Radial deviation of finger
Expand Tier I Human GO 3885 Genes GS201367: GO:0019538 protein metabolic process
Expand Tier I Human 157 Genes GS176639: HP:0011356 Regional abnormality of skin
Expand Tier I Mouse GO 9740 Genes GS186744: GO:0043226 organelle
Expand Tier I Mouse GO 11364 Genes GS182835: GO:0005622 intracellular
Expand Tier I Mouse 499 Genes GS136101: lupus NZB x NZW 3 (Lbw3, Published QTL Chr 5)
Expand Tier I Human 186 Genes GS173740: HP:0009485 Radial deviation of the hand or of fingers of the hand
Expand Tier I Human 170 Genes GS173988: HP:0000501 Glaucoma
Expand Tier I Human 23 Genes GS176653: HP:0000058 Abnormality of the labia
Expand Tier I Mouse GO 6473 Genes GS184448: GO:0044425 membrane part
Expand Tier I Human 446 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human 358 Genes GS175500: HP:0000517 Abnormality of the lens
Expand Tier I Human 164 Genes GS174994: HP:0002059 Cerebral atrophy
Expand Tier I Human 121 Genes GS170890: HP:0006483 Abnormal number of teeth
Expand Tier I Human 46 Genes GS173611: HP:0002219 Facial hypertrichosis
Expand Tier I Human 364 Genes GS173991: HP:0000505 Visual impairment
Expand Tier I Human 14 Genes GS176681: HP:0100277 Periauricular skin pits
Expand Tier I Human GO 259 Genes GS194337: GO:0043413 macromolecule glycosylation
Expand Tier I Human 1289 Genes GS175528: HP:0000007 Autosomal recessive inheritance
Expand Tier I Human 1073 Genes GS171815: HP:0001574 Abnormality of the integument
Expand Tier I Human 68 Genes GS170896: HP:0004404 Abnormality of the nipple
Expand Tier I Human 544 Genes GS172354: HP:0004328 Abnormality of the anterior segment of the eye
Expand Tier I Human 90 Genes GS171587: HP:0001561 Polyhydramnios
Expand Tier I Human 19 Genes GS172450: HP:0006610 Wide intermamillary distance
Expand Tier I Human 2121 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human 512 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 32 Genes GS172593: HP:0010609 Skin tags
Expand Tier I Mouse GO 5103 Genes GS192512: GO:0003824 catalytic activity
Expand Tier I Human 56 Genes GS176473: HP:0003498 Disproportionate short stature
Expand Tier I Human GO 7808 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 784 Genes GS171647: HP:0011844 Abnormal appendicular skeleton morphology
Expand Tier I Human 10 Genes GS174981: HP:0011063 Abnormality of incisor morphology
Expand Tier I Human 435 Genes GS175979: HP:0009115 Aplasia/Hypoplasia involving the skeleton
Expand Tier I Human 232 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human 6 Genes GS174977: HP:0011065 Conical incisor
Expand Tier I Human 56 Genes GS171030: HP:0010946 Dilatation of the renal pelvis
Expand Tier I Human 84 Genes GS172316: HP:0003026 Short long bones
Expand Tier I Human 7 Genes GS173777: HP:0000190 Abnormality of oral frenula
Expand Tier I Mouse 671 Genes GS135738: dextran sodium sulfate induced colitis QTL1 (Dssc1, Published QTL Chr 5)
Expand Tier I Human GO 8595 Genes GS197244: GO:0044237 cellular metabolic process
Expand Tier I Human 72 Genes GS171658: HP:0000612 Iris coloboma
Expand Tier I Human 53 Genes GS173835: HP:0003422 Vertebral segmentation defect
Expand Tier I Human 19 Genes GS172292: HP:0010781 Skin dimples
Expand Tier I Human 302 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier II Mouse 329 Genes GS35276: Striatum Gene expression correlates of Maximum startle response to 85 db in Males BXD
Expand Tier I Human 6 Genes GS171947: HP:0002263 Exaggerated cupid's bow
Expand Tier I Human 20 Genes GS173098: HP:0000676 Abnormality of the incisor
Expand Tier I Human 311 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 57 Genes GS171029: HP:0010944 Abnormality of the renal pelvis
Expand Tier I Human 55 Genes GS171548: HP:0001388 Joint laxity
Expand Tier I Human 123 Genes GS176695: HP:0009811 Abnormality of the elbow
Expand Tier I Human 240 Genes GS172433: HP:0002644 Abnormality of pelvic girdle bone morphology
Expand Tier I Human 33 Genes GS175790: HP:0008771 Aplasia/Hypoplasia of the ear
Expand Tier I Human 40 Genes GS171166: HP:0000236 Abnormality of the anterior fontanelle
Expand Tier I Human 73 Genes GS175158: HP:0011747 Abnormality of the anterior pituitary
Expand Tier I Human 2374 Genes GS175529: HP:0000001 All
Expand Tier I Human 253 Genes GS171634: HP:0008050 Abnormality of the palpebral fissures
Expand Tier I Human 224 Genes GS175459: HP:0009484 Deviation of the hand or of fingers of the hand
Expand Tier I Human 112 Genes GS176480: HP:0009826 Hypoplasia involving bones of the extremities
Expand Tier I Mouse 3267 Genes GS127938: Striatum - Allen Mouse Brain Atlas
Expand Tier I Human 188 Genes GS171167: HP:0000235 Abnormality of the fontanelles and cranial sutures
Expand Tier I Human 5 Genes GS176211: HP:0000475 Broad neck
Expand Tier I Mouse GO 11124 Genes GS184447: GO:0044424 intracellular part
Expand Tier I Human 397 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 384 Genes GS173810: HP:0002597 Abnormality of the vasculature
Expand Tier I Mouse GO 9717 Genes GS186740: GO:0043229 intracellular organelle
Expand Tier I Human 86 Genes GS174858: HP:0200007 Abnormal size of the palpebral fissures
Expand Tier I Human 384 Genes GS175333: HP:0000035 Abnormality of the testis
Expand Tier I Human 137 Genes GS171202: HP:0100627 Displacement of the external urethral meatus
Expand Tier I Human 607 Genes GS175191: HP:0002060 Abnormality of the cerebrum
Expand Tier I Human 94 Genes GS171105: HP:0006494 Aplasia/Hypoplasia involving bones of the feet
Expand Tier I Human 61 Genes GS171609: HP:0011339 Abnormality of upper lip vermillion
Expand Tier I Human GO 2373 Genes GS195036: GO:0031090 organelle membrane
Expand Tier I Human 221 Genes GS172288: HP:0000358 Posteriorly rotated ears
Expand Tier I Human 7 Genes GS170966: HP:0000402 Stenosis of the external auditory canal
Expand Tier I Human 474 Genes GS171448: HP:0000606 Abnormality of the periorbital region
Expand Tier I Human GO 14644 Genes GS208012: GO:0044464 cell part
Expand Tier I Human 1 Genes GS175140: HP:0008569 Microtia, second degree
Expand Tier I Human GO 6151 Genes GS201252: GO:0044425 membrane part
Expand Tier I Human GO 835 Genes GS210330: GO:0006412 translation
Expand Tier I Human GO 17054 Genes GS210212: GO:0005575 cellular_component
Expand Tier I Human 518 Genes GS174081: HP:0004322 Short stature
Expand Tier I Human 21 Genes GS176680: HP:0100276 Skin pits
Expand Tier I Mouse 591 Genes GS136094: long bones 4 (Lbn4, Published QTL Chr 5)
Expand Tier I Human 388 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Mouse GO 7644 Genes GS188399: GO:0044238 primary metabolic process
Expand Tier I Human 514 Genes GS173020: HP:0000818 Abnormality of the endocrine system
Expand Tier I Human 76 Genes GS172219: HP:0010301 Spinal dysraphism
Expand Tier I Human 211 Genes GS175164: HP:0011927 Short digit
Expand Tier I Human 168 Genes GS170980: HP:0011362 Abnormal hair quantity
Expand Tier I Human 12 Genes GS176182: HP:0000073 Ureteral duplication
Expand Tier I Human 123 Genes GS175583: HP:0010438 Abnormality of the ventricular septum
Expand Tier I Human 64 Genes GS175226: HP:0008713 Genitourinary tract malformation
Expand Tier I Human 13 Genes GS173446: HP:0008684 Aplasia/hypoplasia of the uterus
Expand Tier I Human 140 Genes GS175471: HP:0001172 Abnormality of the thumb
Expand Tier I Human 40 Genes GS175995: HP:0000465 Webbed neck
Expand Tier I Human 1210 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human 101 Genes GS176684: HP:0008678 Renal hypoplasia/aplasia
Expand Tier I Human 262 Genes GS172033: HP:0000369 Low-set ears
Expand Tier I Human 175 Genes GS174377: HP:0005927 Aplasia/Hypoplasia involving bones of the hand
Expand Tier I Human 220 Genes GS171791: HP:0000370 Abnormality of the middle ear
Expand Tier I Human 414 Genes GS172195: HP:0000504 Abnormality of vision
Expand Tier I Human 83 Genes GS172098: HP:0000582 Upslanted palpebral fissure
Expand Tier I Human GO 261 Genes GS196254: GO:0016757 transferase activity, transferring glycosyl groups
Expand Tier I Human 1569 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 56 Genes GS175733: HP:0010049 Short metacarpal
Expand Tier I Human 77 Genes GS172300: HP:0001991 Aplasia/Hypoplasia of the toes
Expand Tier I Human GO 323 Genes GS202501: GO:0009101 glycoprotein biosynthetic process
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Mouse GO 13187 Genes GS182834: GO:0005623 cell
Expand Tier I Human 132 Genes GS171835: HP:0011329 Abnormality of cranial sutures
Expand Tier I Human 553 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5436 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Mouse 716 Genes GS136308: nurturing ability QTL 1 (Naq1, Published QTL Chr 5)
Expand Tier I Human 411 Genes GS173083: HP:0000492 Abnormality of the eyelid
Expand Tier I Human 90 Genes GS170889: HP:0006482 Abnormality of dental morphology
Expand Tier I Human 189 Genes GS176745: HP:0010866 Abdominal wall defect
Expand Tier I Human 10 Genes GS174976: HP:0011064 Abnormal number of incisors
Expand Tier I Human 291 Genes GS175335: HP:0000036 Abnormality of the penis
Expand Tier II Mouse 459 Genes GS83975: cocaine induced activation 7 (Cocia7, Published QTL, Chr 5)
Expand Tier I Human 46 Genes GS173617: HP:0011220 Prominent forehead
Expand Tier I Human GO 12561 Genes GS199635: GO:0005622 intracellular
Expand Tier I Human 145 Genes GS171586: HP:0001560 Abnormality of the amniotic fluid
Expand Tier I Human 112 Genes GS172569: HP:0000343 Long philtrum
Expand Tier I Human 285 Genes GS175125: HP:0000028 Cryptorchidism
Expand Tier I Mouse 496 Genes GS136451: postnatal body weight growth 13 (Pbwg13, Published QTL Chr 5)
Expand Tier I Human 65 Genes GS176590: HP:0001274 Agenesis of corpus callosum
Expand Tier I Human 105 Genes GS175571: HP:0011492 Abnormality of corneal stroma
Expand Tier I Human 43 Genes GS176332: HP:0008873 Disproportionate short-limb short stature
Expand Tier I Human GO 9471 Genes GS196943: GO:0008152 metabolic process
Expand Tier I Human 139 Genes GS171397: HP:0000177 Abnormality of upper lip
Expand Tier I Human 211 Genes GS173206: HP:0003241 Genital hypoplasia
Expand Tier I Human 25 Genes GS175426: HP:0010767 Sacrococcygeal pilonidal abnormality
Expand Tier I Human 157 Genes GS171968: HP:0000405 Conductive hearing impairment
Expand Tier I Human 55 Genes GS173685: HP:0001641 Abnormality of the pulmonary valve
Expand Tier I Human 941 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14623 Genes GS196941: GO:0008150 biological_process
Expand Tier I Mouse 671 Genes GS136956: weight 4 (Wght4, Published QTL Chr 5)
Expand Tier I Human 93 Genes GS176289: HP:0002120 Cerebral cortical atrophy
Expand Tier I Human GO 14645 Genes GS199634: GO:0005623 cell
Expand Tier I Human 158 Genes GS171900: HP:0011452 Functional abnormality of the middle ear
Expand Tier I Human 36 Genes GS172711: HP:0000219 Thin upper lip vermilion
Expand Tier I Human 189 Genes GS176449: HP:0001671 Abnormality of the cardiac septa
Expand Tier I Human 9 Genes GS174193: HP:0001592 Selective tooth agenesis
Expand Tier I Human 245 Genes GS176694: HP:0009810 Abnormality of the joints of the upper limbs
Expand Tier II Mouse 39 Genes GS34254: Whole Brain Gene expression correlates of Activity in altered context during presentation of cue in Males BXD
Expand Tier I Human 111 Genes GS176907: HP:0009804 Reduced number of teeth
Expand Tier I Human GO 6369 Genes GS201256: GO:0044422 organelle part
Expand Tier I Human 212 Genes GS171106: HP:0006496 Aplasia/Hypoplasia involving bones of the upper limbs
Expand Tier I Human 525 Genes GS175814: HP:0011024 Abnormality of the gastrointestinal tract
Expand Tier I Human 150 Genes GS176233: HP:0004209 Clinodactyly of the 5th finger
Expand Tier I Human 405 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1103 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human 60 Genes GS170970: HP:0000154 Wide mouth
Expand Tier I Human GO 259 Genes GS207026: GO:0006486 protein glycosylation
Expand Tier I Human 470 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 64 Genes GS176161: HP:0100589 Urogenital fistula
Expand Tier I Human 90 Genes GS174101: HP:0001018 Abnormal palmar dermatoglyphics
Expand Tier I Human 889 Genes GS175016: HP:0001626 Abnormality of the cardiovascular system
Expand Tier I Human 409 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human 210 Genes GS175990: HP:0000463 Anteverted nares
Expand Tier I Human GO 9574 Genes GS209564: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Human 189 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 47 Genes GS172542: HP:0000830 Anterior hypopituitarism
Expand Tier I Human 1060 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 189 Genes GS172253: HP:0001376 Limitation of joint mobility
Expand Tier I Human 180 Genes GS175902: HP:0003468 Abnormality of the vertebrae
Expand Tier I Human 702 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 114 Genes GS173262: HP:0000864 Abnormality of the hypothalamus-pituitary axis
Expand Tier I Human 529 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 842 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 237 Genes GS171395: HP:0000175 Cleft palate
Expand Tier I Human 545 Genes GS175015: HP:0001627 Abnormality of the heart
Expand Tier I Human 215 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human 2 Genes GS173348: HP:0000233 Thin vermilion border
Expand Tier I Human 88 Genes GS172871: HP:0010490 Abnormality of the palmar creases
Expand Tier I Human 737 Genes GS176186: HP:0000079 Abnormality of the urinary system
Expand Tier I Human 150 Genes GS175149: HP:0009179 Deviation of the 5th finger
Expand Tier I Human 3 Genes GS173936: HP:0008726 Hypoplasia of the vagina
Expand Tier I Mouse 713 Genes GS136027: hypercholesterolemia (Hypch, Published QTL Chr 5)
Expand Tier I Human 89 Genes GS176824: HP:0000204 Cleft upper lip
Expand Tier I Human 10 Genes GS175747: HP:0000013 Hypoplasia of the uterus
Expand Tier I Human 148 Genes GS171552: HP:0001382 Joint hypermobility
Expand Tier I Human 72 Genes GS176656: HP:0000055 Abnormality of female external genitalia
Expand Tier I Mouse GO 202 Genes GS185104: GO:0019318 hexose metabolic process
Expand Tier I Human 319 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 8 Genes GS171513: HP:0007700 Anterior segment dysgenesis
Expand Tier I Human 27 Genes GS173688: HP:0001642 Pulmonic stenosis
Expand Tier I Human 212 Genes GS176185: HP:0100790 Hernia
Expand Tier I Human 487 Genes GS171789: HP:0001392 Abnormality of the liver
Expand Tier I Human 1 Genes GS176827: HP:0000200 Short lingual frenulum
Expand Tier I Human 578 Genes GS172030: HP:0000365 Hearing impairment
Expand Tier I Human 78 Genes GS175969: HP:0000069 Abnormality of the ureter
Expand Tier I Human 20 Genes GS171084: HP:0009603 Deviation/Displacement of the thumb
Expand Tier I Human 601 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 438 Genes GS173024: HP:0000811 Abnormal external genitalia
Expand Tier I Human 174 Genes GS173901: HP:0002007 Frontal bossing
Expand Tier I Human 3 Genes GS170895: HP:0006485 Agenesis of incisor
Expand Tier I Mouse 3375 Genes GS127927: Hypothalamus - Allen Mouse Brain Atlas
Expand Tier I Human 808 Genes GS170965: HP:0000153 Abnormality of the mouth
Expand Tier I Human 281 Genes GS171204: HP:0011314 Abnormality of long bone morphology
Expand Tier I Human GO 10639 Genes GS203594: GO:0043226 organelle
Expand Tier I Human GO 4713 Genes GS205364: GO:0010467 gene expression
Expand Tier I Human GO 1736 Genes GS208734: GO:0016740 transferase activity
Expand Tier I Human 153 Genes GS175067: HP:0001159 Syndactyly
Expand Tier I Human GO 6769 Genes GS210002: GO:0044444 cytoplasmic part
Expand Tier I Human 1208 Genes GS171168: HP:0000234 Abnormality of the head
Expand Tier I Human 229 Genes GS171908: HP:0004298 Abnormality of the abdominal wall
Expand Tier I Human 8 Genes GS172759: HP:0100819 Intestinal fistula
Expand Tier I Human 558 Genes GS175530: HP:0000002 Abnormality of body height
Expand Tier I Human GO 5152 Genes GS209009: GO:1901576 organic substance biosynthetic process
Expand Tier I Human 67 Genes GS172844: HP:0000482 Microcornea
Expand Tier I Human 274 Genes GS172372: HP:0000648 Optic atrophy
Expand Tier I Human 168 Genes GS175668: HP:0007369 Atrophy/Degeneration affecting the cerebrum
Expand Tier I Human GO 9585 Genes GS203593: GO:0043227 membrane-bounded organelle
Expand Tier I Human GO 250 Genes GS201922: GO:0019318 hexose metabolic process
Expand Tier I Human 124 Genes GS171102: HP:0006493 Aplasia/Hypoplasia involving bones of the lower limbs
Expand Tier I Human GO 1205 Genes GS194505: GO:1901135 carbohydrate derivative metabolic process
Expand Tier I Human 142 Genes GS171178: HP:0000238 Hydrocephalus
Expand Tier I Human 114 Genes GS174643: HP:0005120 Abnormality of cardiac atrium
Expand Tier I Mouse GO 5859 Genes GS182404: GO:0031224 intrinsic to membrane
Expand Tier I Human 5 Genes GS175816: HP:0011026 Aplasia/Hypoplasia of the vagina
Expand Tier I Human GO 6278 Genes GS210000: GO:0044446 intracellular organelle part
Expand Tier I Mouse 693 Genes GS135889: free running period 2 (Frp2, Published QTL Chr 5)
Expand Tier I Human 1495 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 55 Genes GS172018: HP:0001363 Craniosynostosis
Expand Tier I Human 112 Genes GS173465: HP:0001654 Abnormality of the heart valves
Expand Tier I Human GO 15286 Genes GS194087: GO:0003674 molecular_function
Expand Tier I Human 599 Genes GS171424: HP:0002814 Abnormality of the lower limb
Expand Tier I Human 50 Genes GS171995: HP:0001764 Small feet
Expand Tier I Human 251 Genes GS171793: HP:0000377 Abnormality of the pinna
Expand Tier I Human 324 Genes GS175304: HP:0000290 Abnormality of the forehead
Expand Tier I Human 67 Genes GS172588: HP:0001831 Short toe
Expand Tier I Mouse GO 23365 Genes GS177356: GO:0003674 molecular_function
Expand Tier I Human GO 5320 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Mouse GO 440 Genes GS188916: GO:0044723 single-organism carbohydrate metabolic process
Expand Tier I Human GO 10624 Genes GS203590: GO:0043229 intracellular organelle
Expand Tier I Human 12 Genes GS173568: HP:0000698 Conical teeth
Expand Tier I Human 75 Genes GS174446: HP:0001120 Abnormality of corneal size
Expand Tier I Human GO 2464 Genes GS199032: GO:0036211 protein modification process
Expand Tier I Human 398 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human 80 Genes GS171836: HP:0011328 Abnormality of fontanelles
Expand Tier I Human 196 Genes GS172034: HP:0000368 Low-set, posteriorly rotated ears
Expand Tier I Human 197 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Human 258 Genes GS172272: HP:0001197 Abnormality of prenatal development or birth
Expand Tier I Human 263 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human GO 2558 Genes GS194336: GO:0043412 macromolecule modification
Expand Tier I Mouse GO 9049 Genes GS180166: GO:0008152 metabolic process
Expand Tier I Human 46 Genes GS171463: HP:0004279 Short palm
Expand Tier I Human 2339 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 14 Genes GS172339: HP:0004467 Preauricular pit
Expand Tier I Mouse GO 1149 Genes GS179957: GO:0005783 endoplasmic reticulum
Expand Tier I Human 66 Genes GS174788: HP:0000239 Large fontanelles
Expand Tier I Mouse GO 555 Genes GS183122: GO:0005975 carbohydrate metabolic process
Expand Tier I Human 551 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 150 Genes GS175074: HP:0001156 Brachydactyly syndrome
Expand Tier I Human 337 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Mouse 2944 Genes GS127937: Striatum-like amygdalar nuclei - Allen Mouse Brain Atlas
Expand Tier I Human GO 280 Genes GS207949: GO:0005996 monosaccharide metabolic process
Expand Tier I Human 263 Genes GS176692: HP:0009815 Aplasia/Hypoplasia of the extremities
Expand Tier I Human 33 Genes GS174510: HP:0008551 Microtia
Expand Tier I Human 69 Genes GS172585: HP:0001832 Abnormality of the metatarsal bones
Expand Tier I Human 426 Genes GS175268: HP:0001167 Abnormality of finger
Expand Tier I Mouse 2962 Genes GS127936: Striatum ventral region - Allen Mouse Brain Atlas
Expand Tier I Human 75 Genes GS172096: HP:0000581 Blepharophimosis
Expand Tier I Human 34 Genes GS171601: HP:0001964 Aplasia/Hypoplasia of metatarsal bones
Expand Tier I Human 186 Genes GS171144: HP:0005280 Depressed nasal bridge
Expand Tier I Mouse GO 8145 Genes GS190714: GO:0016020 membrane
Expand Tier I Human 130 Genes GS171905: HP:0004297 Abnormality of the biliary system
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 51 Genes GS172345: HP:0000130 Abnormality of the uterus
Expand Tier I Human 162 Genes GS175958: HP:0000795 Abnormality of the urethra
Expand Tier I Human 221 Genes GS171139: HP:0005288 Abnormality of the nares
Expand Tier I Human 588 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human 780 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
Expand Tier I Human 616 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12850 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 68 Genes GS172110: HP:0002983 Micromelia
Expand Tier I Human 49 Genes GS171726: HP:0005107 Abnormality of the sacrum
Expand Tier I Human GO 6651 Genes GS200648: GO:0044260 cellular macromolecule metabolic process
Expand Tier I Human 123 Genes GS171384: HP:0001551 Abnormality of the umbilicus
Expand Tier I Human 29 Genes GS171563: HP:0000384 Preauricular skin tag
Expand Tier I Human 174 Genes GS171148: HP:0011218 Abnormal shape of the frontal region
Expand Tier I Human 107 Genes GS172094: HP:0000589 Coloboma
Expand Tier I Human 11 Genes GS171174: HP:0001540 Diastasis recti
Expand Tier I Human 421 Genes GS174917: HP:0000765 Abnormality of the thorax
Expand Tier I Human 48 Genes GS172742: HP:0006887 Intellectual disability, progressive
Expand Tier I Human 120 Genes GS171607: HP:0011337 Abnormality of mouth size
Expand Tier I Human 121 Genes GS175023: HP:0001629 Ventricular septal defect
Expand Tier I Human 62 Genes GS174139: HP:0005914 Aplasia/Hypoplasia involving the metacarpal bones
Expand Tier I Human 111 Genes GS174806: HP:0001631 Defect in the atrial septum
Expand Tier I Human 346 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Mouse 562 Genes GS135798: elevated maze behavior 2 (Elmaz2, Published QTL Chr 5)
Expand Tier I Human 56 Genes GS171290: HP:0000126 Hydronephrosis
Expand Tier I Human 17 Genes GS173373: HP:0002937 Hemivertebrae
Expand Tier I Human GO 919 Genes GS197025: GO:0044432 endoplasmic reticulum part
Expand Tier I Human 445 Genes GS175423: HP:0010461 Abnormality of the male genitalia
Expand Tier I Human 118 Genes GS172076: HP:0001163 Abnormality of the metacarpal bones
Expand Tier I Human GO 789 Genes GS204928: GO:0042175 nuclear outer membrane-endoplasmic reticulum membrane network
Expand Tier I Human 129 Genes GS174925: HP:0000769 Abnormality of the breast
Expand Tier I Human 358 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human 308 Genes GS172100: HP:0000587 Abnormality of the optic nerve
Expand Tier I Human GO 7311 Genes GS194267: GO:0043170 macromolecule metabolic process
Expand Tier I Human GO 5047 Genes GS210357: GO:0044249 cellular biosynthetic process
Expand Tier I Human 394 Genes GS172362: HP:0004325 Decreased body weight
Expand Tier I Mouse 3315 Genes GS127939: Thalamus - Allen Mouse Brain Atlas
Expand Tier I Mouse 568 Genes GS135468: blood pressure QTL 4 (Bpq4, Published QTL Chr 5)
Expand Tier I Human 203 Genes GS174706: HP:0000553 Abnormality of the uvea
Expand Tier I Human 515 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human 202 Genes GS171413: HP:0004097 Deviation of finger
Expand Tier I Human 199 Genes GS171637: HP:0008872 Feeding difficulties in infancy
Expand Tier I Human 271 Genes GS172637: HP:0010460 Abnormality of the female genitalia
Expand Tier I Mouse GO 242 Genes GS179489: GO:0016757 transferase activity, transferring glycosyl groups
Expand Tier II Mouse 699 Genes GS84175: METH responses for climbing (Published QTL, Chr 5)
Expand Tier I Human 1051 Genes GS174453: HP:0001438 Abnormality of the abdomen
Expand Tier I Mouse GO 23855 Genes GS180164: GO:0008150 biological_process
Expand Tier I Human 922 Genes GS176333: HP:0007319 Morphological abnormality of the central nervous system
Expand Tier I Human GO 8702 Genes GS205255: GO:0044238 primary metabolic process
Expand Tier I Human 990 Genes GS171833: HP:0000119 Abnormality of the genitourinary system
Expand Tier I Human GO 4276 Genes GS207858: GO:0009059 macromolecule biosynthetic process
Expand Tier I Human 433 Genes GS172260: HP:0000356 Abnormality of the outer ear
Expand Tier I Mouse 3343 Genes GS127930: Midbrain - Allen Mouse Brain Atlas
Expand Tier I Human GO 551 Genes GS194503: GO:1901137 carbohydrate derivative biosynthetic process
Expand Tier I Human 74 Genes GS171850: HP:0002414 Spina bifida
Expand Tier I Human 220 Genes GS175994: HP:0000464 Abnormality of the neck
Expand Tier I Human GO 790 Genes GS199922: GO:0005975 carbohydrate metabolic process
Expand Tier I Human 567 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human GO 5321 Genes GS209455: GO:0003824 catalytic activity
Expand Tier I Mouse GO 8072 Genes GS184218: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 3254 Genes GS200602: GO:0044267 cellular protein metabolic process
Expand Tier I Human 10 Genes GS171129: HP:0000059 Hypoplastic labia majora
Expand Tier I Human 187 Genes GS171907: HP:0004299 Hernia of the abdominal wall
Expand Tier I Human 387 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 271 Genes GS176826: HP:0000202 Oral cleft
Expand Tier I Human 72 Genes GS176436: HP:0000047 Hypospadias
Expand Tier I Human 882 Genes GS174646: HP:0000951 Abnormality of the skin
Expand Tier I Human 7 Genes GS175395: HP:0003561 Birth length <3rd percentile
Expand Tier I Human 275 Genes GS170962: HP:0000159 Abnormality of the lip
Expand Tier I Human 282 Genes GS175900: HP:0009118 Aplasia/Hypoplasia of the mandible
Expand Tier I Mouse GO 5588 Genes GS193061: GO:0044444 cytoplasmic part
Expand Tier II Mouse 510 Genes GS84176: METH responses for climbing (Published QTL, Chr 5)
Expand Tier I Mouse GO 8630 Genes GS192624: GO:0043231 intracellular membrane-bounded organelle
Expand Tier I Mouse GO 8650 Genes GS186743: GO:0043227 membrane-bounded organelle
Expand Tier I Human 170 Genes GS174488: HP:0000525 Abnormality of the iris
Expand Tier I Human 84 Genes GS175531: HP:0000003 Multicystic kidney dysplasia
Expand Tier I Human 129 Genes GS173247: HP:0007957 Reduction of corneal clarity
Expand Tier I Mouse GO 224 Genes GS191043: GO:0005996 monosaccharide metabolic process
Expand Tier I Human 176 Genes GS175103: HP:0000288 Abnormality of the philtrum
Expand Tier I Human 189 Genes GS176004: HP:0100656 Thoracoabdominal wall defects
Expand Tier I Mouse GO 23784 Genes GS193268: GO:0005575 cellular_component
Expand Tier I Human 117 Genes GS173868: HP:0002143 Abnormality of the spinal cord
Expand Tier I Human 6 Genes GS175963: HP:0000060 Clitoral hypoplasia
Expand Tier I Human 602 Genes GS176718: HP:0000078 Abnormality of the genital system
Expand Tier I Human 1213 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human 119 Genes GS172170: HP:0003196 Short nose
Expand Tier I Human 533 Genes GS174494: HP:0002564 Malformation of the heart and great vessels
Expand Tier I Human 264 Genes GS173014: HP:0010936 Abnormality of the lower urinary tract
Expand Tier I Mouse GO 5734 Genes GS190713: GO:0016021 integral to membrane
Expand Tier I Human 56 Genes GS171189: HP:0000142 Abnormality of the vagina
Expand Tier I Human 639 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 89 Genes GS174323: HP:0004414 Abnormality of the pulmonary artery
Expand Tier I Human 490 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human GO 5223 Genes GS207857: GO:0009058 biosynthetic process
Expand Tier I Human 19 Genes GS171506: HP:0009623 Proximal placement of thumb
Expand Tier I Human 61 Genes GS172737: HP:0010991 Abnormality of the abdominal musculature
Expand Tier I Human GO 9005 Genes GS201023: GO:0071704 organic substance metabolic process
Expand Tier I Human GO 2464 Genes GS196595: GO:0006464 cellular protein modification process
Expand Tier I Human 114 Genes GS174412: HP:0007477 Abnormal dermatoglyphics
Expand Tier I Human 473 Genes GS171893: HP:0011458 Abdominal symptom
Expand Tier I Human 1223 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 136 Genes GS173751: HP:0000998 Hypertrichosis
Expand Tier I Mouse GO 13186 Genes GS191106: GO:0044464 cell part
Expand Tier I Mouse 671 Genes GS135661: correlation in cytokine production 1 (Cora1, Published QTL Chr 5)
Expand Tier I Human GO 384 Genes GS202500: GO:0009100 glycoprotein metabolic process
Expand Tier I Human 16 Genes GS175957: HP:0000066 Labial hypoplasia
Expand Tier I Human 592 Genes GS172031: HP:0000364 Hearing abnormality
Expand Tier I Mouse GO 6 Genes GS177759: GO:0006004 fucose metabolic process
Expand Tier I Human 303 Genes GS172416: HP:0002242 Abnormality of the intestine
Expand Tier I Human 486 Genes GS176241: HP:0010935 Abnormality of the upper urinary tract
Expand Tier I Human 104 Genes GS175835: HP:0007759 Opacification of the corneal stroma
Expand Tier I Human 344 Genes GS174378: HP:0000518 Cataract
Expand Tier I Human 23 Genes GS173237: HP:0008905 Rhizomelic short stature
Expand Tier I Human 453 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 237 Genes GS174292: HP:0011968 Feeding difficulties
Expand Tier I Human 239 Genes GS174066: HP:0100737 Abnormality of the hard palate
Expand Tier I Human 35 Genes GS176655: HP:0000056 Abnormality of the clitoris
Expand Tier I Human 610 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 111 Genes GS173580: HP:0011994 Abnormality of the atrial septum
Expand Tier I Mouse GO 8414 Genes GS185585: GO:0044710 single-organism metabolic process
Expand Tier I Mouse 715 Genes GS135510: body weight females and males day 10 (Bwefm, Published QTL Chr 5)
Expand Tier I Human GO 1281 Genes GS196726: GO:0005783 endoplasmic reticulum
Expand Tier I Human 397 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 398 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 489 Genes GS171999: HP:0001760 Abnormality of the foot
Expand Tier I Human 36 Genes GS172842: HP:0000480 Retinal coloboma
Expand Tier I Human 34 Genes GS170804: HP:0003298 Spina bifida occulta
Expand Tier I Human 78 Genes GS174649: HP:0000954 Single transverse palmar crease
Expand Tier I Human 26 Genes GS176368: HP:0000260 Wide anterior fontanel
Expand Tier I Human GO 1771 Genes GS196284: GO:0012505 endomembrane system
Expand Tier I Human 534 Genes GS172360: HP:0004323 Abnormality of body weight
Expand Tier I Human 151 Genes GS174920: HP:0000766 Abnormality of the sternum
Expand Tier I Human 235 Genes GS175523: HP:0000008 Abnormality of female internal genitalia
Expand Tier I Human 129 Genes GS172916: HP:0003312 Abnormal form of the vertebral bodies
Expand Tier I Human 33 Genes GS171455: HP:0008772 Aplasia/Hypoplasia of the external ear
Expand Tier I Human 154 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Human GO 9213 Genes GS202415: GO:0044710 single-organism metabolic process
Expand Tier I Human 97 Genes GS174919: HP:0000767 Pectus excavatum
Expand Tier I Human 249 Genes GS176844: HP:0000429 Abnormality of the nasal alae
Expand Tier I Mouse 3289 Genes GS127932: Pallidum - Allen Mouse Brain Atlas
Expand Tier I Human 579 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 9128 Genes GS194133: GO:0005737 cytoplasm
Expand Tier I Human 281 Genes GS176231: HP:0010938 Abnormality of the external nose
Expand Tier I Human 51 Genes GS171296: HP:0008897 Postnatal growth retardation
Expand Tier I Human 66 Genes GS175643: HP:0006989 Dysplastic corpus callosum
Expand Tier I Mouse 591 Genes GS135404: body growth late QTL 14 (Bglq14, Published QTL Chr 5)
Expand Tier I Human 403 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 313 Genes GS176642: HP:0011355 Localized skin lesion
Expand Tier I Human 18 Genes GS171852: HP:0000593 Abnormality of the anterior chamber
Expand Tier I Human GO 16 Genes GS194498: GO:0006004 fucose metabolic process
Expand Tier I Human 56 Genes GS175055: HP:0001080 Biliary tract abnormality
Expand Tier I Human 202 Genes GS174764: HP:0007367 Atrophy/Degeneration affecting the central nervous system
Expand Tier I Human 82 Genes GS172000: HP:0001761 Pes cavus
Expand Tier I Human 169 Genes GS171752: HP:0001713 Abnormality of cardiac ventricle
Expand Tier I Mouse GO 1686 Genes GS191796: GO:0016740 transferase activity
Expand Tier I Human GO 262 Genes GS208698: GO:0070085 glycosylation
Expand Tier I Human 282 Genes GS172572: HP:0000347 Micrognathia
Expand Tier I Human 36 Genes GS171790: HP:0000372 Abnormality of the auditory canal
Expand Tier I Human 472 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 2 Genes GS175433: HP:0007833 Anterior chamber synechiae
Expand Tier I Human 2 Genes GS173562: HP:0000690 Agenesis of maxillary lateral incisor