Gene Details



SLC12A6 and homologs in 1 species are found in 240 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 385 Genes GS176836: HP:0000422 Abnormality of the nasal bridge
Expand Tier I Human 83 Genes GS172224: HP:0001770 Toe syndactyly
Expand Tier I Human GO 146 Genes GS208908: GO:0071214 cellular response to abiotic stimulus
Expand Tier I Human GO 7609 Genes GS201949: GO:0044699 single-organism process
Expand Tier I Human 1205 Genes GS176101: HP:0000924 Abnormality of the skeletal system
Expand Tier I Human GO 497 Genes GS196432: GO:0030001 metal ion transport
Expand Tier I Human CTD 382 Genes GS122940: Dimethylnitrosamine interacting genes (MeSH:D004128) in CTD
Expand Tier I Human 829 Genes GS172666: HP:0011804 Abnormality of muscle physiology
Expand Tier I Human 442 Genes GS176801: HP:0001263 Global developmental delay
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 27 Genes GS172613: HP:0003477 Peripheral axonal neuropathy
Expand Tier I Human 1562 Genes GS174500: HP:0000707 Abnormality of the nervous system
Expand Tier I Human 56 Genes GS174922: HP:0000762 Decreased nerve conduction velocity
Expand Tier I Human 535 Genes GS175107: HP:0003808 Abnormal muscle tone
Expand Tier I Human GO 8 Genes GS200987: GO:0015377 cation:chloride symporter activity
Expand Tier I Human GO 1 Genes GS204057: GO:0071477 cellular hypotonic salinity response
Expand Tier I Human 7 Genes GS172458: HP:0003448 Decreased sensory nerve conduction velocity
Expand Tier I Human 4 Genes GS174621: HP:0002111 Restrictive respiratory insufficiency
Expand Tier I Human 163 Genes GS176478: HP:0002119 Ventriculomegaly
Expand Tier I Human 107 Genes GS176899: HP:0002353 EEG abnormality
Expand Tier I Human 70 Genes GS177025: HP:0010628 Facial palsy
Expand Tier I Human 132 Genes GS171835: HP:0011329 Abnormality of cranial sutures
Expand Tier I Human 17 Genes GS176999: HP:0001290 Generalized hypotonia
Expand Tier I Human 550 Genes GS177051: HP:0001155 Abnormality of the hand
Expand Tier I Human GO 5359 Genes GS199201: GO:0031224 intrinsic to membrane
Expand Tier I Human GO 2921 Genes GS210507: GO:0006950 response to stress
Expand Tier I Human 156 Genes GS174002: HP:0000189 Narrow palate
Expand Tier I Human 1002 Genes GS174914: HP:0003011 Abnormality of the musculature
Expand Tier I Human 107 Genes GS173786: HP:0003457 EMG abnormality
Expand Tier I Human 17 Genes GS171507: HP:0002922 Increased CSF protein
Expand Tier I Human 64 Genes GS176590: HP:0001274 Agenesis of corpus callosum
Expand Tier I Human GO 490 Genes GS202261: GO:0001568 blood vessel development
Expand Tier I Human GO 4061 Genes GS207581: GO:0007275 multicellular organismal development
Expand Tier I Human 70 Genes GS171543: HP:0000276 Long face
Expand Tier I Human 146 Genes GS170968: HP:0000156 High-arched palate
Expand Tier I Human 10 Genes GS174464: HP:0002410 Aqueductal stenosis
Expand Tier I Human 489 Genes GS176385: HP:0001249 Intellectual disability
Expand Tier I Human 86 Genes GS172908: HP:0002450 Abnormality of the motor neurons
Expand Tier I Human 357 Genes GS172701: HP:0002650 Scoliosis
Expand Tier I Human 936 Genes GS174075: HP:0009121 Abnormal axial skeleton morphology
Expand Tier I Human GO 14515 Genes GS196941: GO:0008150 biological_process
Expand Tier I Human GO 844 Genes GS198212: GO:0022891 substrate-specific transmembrane transporter activity
Expand Tier I Human 1206 Genes GS176817: HP:0011446 Abnormality of higher mental function
Expand Tier I Human GO 4014 Genes GS205002: GO:0048856 anatomical structure development
Expand Tier I Human GO 128 Genes GS207410: GO:0015293 symporter activity
Expand Tier I Human GO 118 Genes GS209449: GO:0006813 potassium ion transport
Expand Tier I Human GO 14538 Genes GS199634: GO:0005623 cell
Expand Tier I Human 18 Genes GS173678: HP:0003383 Onion bulb formation
Expand Tier I Human 119 Genes GS172170: HP:0003196 Short nose
Expand Tier I Human 106 Genes GS175048: HP:0006824 Cranial nerve paralysis
Expand Tier I Human 782 Genes GS176107: HP:0000929 Abnormality of the skull
Expand Tier I Human GO 4 Genes GS198329: GO:0015379 potassium:chloride symporter activity
Expand Tier I Human 18 Genes GS175821: HP:0002091 Restrictive lung disease
Expand Tier I Human 636 Genes GS172032: HP:0000366 Abnormality of the nose
Expand Tier I Human 222 Genes GS173995: HP:0000508 Ptosis
Expand Tier I Human GO 4250 Genes GS197009: GO:0005886 plasma membrane
Expand Tier I Human 496 Genes GS175539: HP:0007256 Abnormality of pyramidal motor function
Expand Tier I Human GO 569 Genes GS209735: GO:0008324 cation transmembrane transporter activity
Expand Tier I Human 487 Genes GS173372: HP:0011297 Abnormality of the digits
Expand Tier I Human 140 Genes GS174906: HP:0000545 Myopia
Expand Tier I Human GO 433 Genes GS203054: GO:0048514 blood vessel morphogenesis
Expand Tier I Human 58 Genes GS171880: HP:0003134 Abnormality of peripheral nerve conduction
Expand Tier I Human 404 Genes GS173743: HP:0001999 Abnormal facial shape
Expand Tier I Human 1098 Genes GS176613: HP:0000271 Abnormality of the face
Expand Tier I Human GO 245 Genes GS195413: GO:0008509 anion transmembrane transporter activity
Expand Tier I Human 468 Genes GS175928: HP:0000240 Abnormality of skull size
Expand Tier I Human 1218 Genes GS170964: HP:0000152 Abnormality of head and neck
Expand Tier I Human 44 Genes GS174918: HP:0000764 Peripheral axonal degeneration
Expand Tier I Human GO 516 Genes GS194493: GO:0001944 vasculature development
Expand Tier I Human GO 761 Genes GS209613: GO:0055085 transmembrane transport
Expand Tier I Human 92 Genes GS173061: HP:0003676 Progressive disorder
Expand Tier I Human 407 Genes GS175670: HP:0007364 Aplasia/Hypoplasia of the cerebrum
Expand Tier I Human GO 4 Genes GS204058: GO:0071476 cellular hypotonic response
Expand Tier I Human 69 Genes GS170981: HP:0011361 Congenital abnormal hair pattern
Expand Tier I Human GO 57 Genes GS194296: GO:0006970 response to osmotic stress
Expand Tier I Human GO 278 Genes GS195770: GO:0015672 monovalent inorganic cation transport
Expand Tier I Human 187 Genes GS174247: HP:0000539 Abnormality of refraction
Expand Tier I Human 1055 Genes GS171274: HP:0100543 Cognitive impairment
Expand Tier I Human 46 Genes GS172570: HP:0000341 Narrow forehead
Expand Tier I Human GO 311 Genes GS209586: GO:0022804 active transmembrane transporter activity
Expand Tier I Human 697 Genes GS175981: HP:0000163 Abnormality of the oral cavity
Expand Tier I Human 140 Genes GS174860: HP:0010549 Paralysis due to lesions of the principle motor tracts
Expand Tier I Human GO 3310 Genes GS209452: GO:0006810 transport
Expand Tier I Human GO 4 Genes GS194299: GO:0006971 hypotonic response
Expand Tier I Human 525 Genes GS176100: HP:0000925 Abnormality of the vertebral column
Expand Tier I Human 837 Genes GS171848: HP:0000598 Abnormality of the ear
Expand Tier I Human 187 Genes GS171167: HP:0000235 Abnormality of the fontanelles and cranial sutures
Expand Tier I Human GO 4338 Genes GS205500: GO:0071944 cell periphery
Expand Tier I Human 78 Genes GS171959: HP:0000400 Macrotia
Expand Tier I Human 356 Genes GS173287: HP:0000315 Abnormality of the orbital region
Expand Tier I Human GO 5591 Genes GS204021: GO:0044707 single-multicellular organism process
Expand Tier I Human 394 Genes GS171394: HP:0000174 Abnormality of the palate
Expand Tier I Human 214 Genes GS172139: HP:0010993 Abnormality of the cerebral subcortex
Expand Tier I Human 43 Genes GS173055: HP:0000326 Abnormality of the maxilla
Expand Tier I Human 450 Genes GS174187: HP:0001595 Abnormality of the hair
Expand Tier I Human 63 Genes GS171802: HP:0009553 Abnormality of the hairline
Expand Tier I Human GO 6548 Genes GS209863: GO:0050896 response to stimulus
Expand Tier I Human 513 Genes GS172353: HP:0004329 Abnormality of the posterior segment of the eye
Expand Tier I Human GO 3 Genes GS204055: GO:0071472 cellular response to salt stress
Expand Tier I Human GO 978 Genes GS198214: GO:0022892 substrate-specific transporter activity
Expand Tier I Human 607 Genes GS171277: HP:0100547 Abnormality of the forebrain
Expand Tier I Human 49 Genes GS171306: HP:0003130 Abnormal peripheral myelination
Expand Tier I Human 4 Genes GS171307: HP:0003444 EMG: chronic denervation signs
Expand Tier I Human 80 Genes GS175456: HP:0100037 Abnormality of the scalp hair
Expand Tier I Human 70 Genes GS173601: HP:0010827 Abnormality of the seventh cranial nerve
Expand Tier I Human 159 Genes GS176900: HP:0000218 High palate
Expand Tier I Human GO 1 Genes GS197747: GO:0042539 hypotonic salinity response
Expand Tier I Human CTD 4391 Genes GS123768: Cyclosporine interacting genes (MeSH:D016572) in CTD
Expand Tier I Human 233 Genes GS174257: HP:0000309 Abnormality of the midface
Expand Tier I Human 23 Genes GS175301: HP:0000294 Low anterior hairline
Expand Tier I Human GO 3364 Genes GS194459: GO:0051234 establishment of localization
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 GO 12 Genes GS204056: GO:0071470 cellular response to osmotic stress
Expand Tier I Human GO 192 Genes GS207409: GO:0015291 secondary active transmembrane transporter activity
Expand Tier I Human GO 1587 Genes GS196772: GO:0048646 anatomical structure formation involved in morphogenesis
Expand Tier I Human 97 Genes GS173091: HP:0004374 Hemiplegia/hemiparesis
Expand Tier I Human 313 Genes GS176568: HP:0000486 Strabismus
Expand Tier I Human 117 Genes GS174102: HP:0011799 Abnormality of facial soft tissue
Expand Tier I Human 317 Genes GS174462: HP:0002648 Abnormality of calvarial morphology
Expand Tier I Human 395 Genes GS173137: HP:0011821 Abnormality of facial skeleton
Expand Tier I Human 397 Genes GS172134: HP:0000639 Nystagmus
Expand Tier I Human 249 Genes GS172246: HP:0001371 Flexion contracture
Expand Tier I Human GO 14537 Genes GS208012: GO:0044464 cell part
Expand Tier I Human GO 6073 Genes GS201252: GO:0044425 membrane part
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 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 386 Genes GS176202: HP:0000479 Abnormality of the retina
Expand Tier I Human 1162 Genes GS176203: HP:0000478 Abnormality of the eye
Expand Tier I Human GO 83 Genes GS195882: GO:0015108 chloride transmembrane transporter activity
Expand Tier I Human GO 804 Genes GS197478: GO:0009628 response to abiotic stimulus
Expand Tier I Human 564 Genes GS171258: HP:0011138 Abnormality of skin adnexa
Expand Tier I Human 532 Genes GS172185: HP:0002977 Aplasia/Hypoplasia involving the central nervous system
Expand Tier I Human GO 964 Genes GS209451: GO:0006811 ion transport
Expand Tier I Human 28 Genes GS172164: HP:0001182 Tapered finger
Expand Tier I Human 229 Genes GS175577: HP:0003202 Amyotrophy
Expand Tier I Human 95 Genes GS170930: HP:0001284 Areflexia
Expand Tier I Human 598 Genes GS172021: HP:0001367 Abnormal joint morphology
Expand Tier I Human 14 Genes GS173755: HP:0004691 2-3 toe syndactyly
Expand Tier I Human GO 785 Genes GS195226: GO:0015075 ion transmembrane transporter activity
Expand Tier I Human GO 4554 Genes GS196806: GO:0032502 developmental process
Expand Tier I Human 178 Genes GS176589: HP:0001273 Abnormality of the corpus callosum
Expand Tier I Human 803 Genes GS170965: HP:0000153 Abnormality of the mouth
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 401 Genes GS173449: HP:0002683 Abnormality of the calvaria
Expand Tier I Human GO 82 Genes GS207406: GO:0015294 solute:cation symporter activity
Expand Tier I Human 53 Genes GS173697: HP:0001319 Neonatal hypotonia
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 201 Genes GS175171: HP:0001315 Reduced tendon reflexes
Expand Tier I Human 46 Genes GS174921: HP:0000763 Sensory neuropathy
Expand Tier I Human GO 5623 Genes GS196808: GO:0032501 multicellular organismal process
Expand Tier I Human GO 32 Genes GS207408: GO:0015296 anion:cation symporter activity
Expand Tier I Human GO 1905 Genes GS198782: GO:0044459 plasma membrane part
Expand Tier I Human 10 Genes GS172524: HP:0001349 Facial diplegia
Expand Tier I Human 153 Genes GS175880: HP:0007370 Aplasia/Hypoplasia of the corpus callosum
Expand Tier I Human 25 Genes GS171767: HP:0003431 Decreased motor nerve conduction velocity
Expand Tier I Human 62 Genes GS171488: HP:0002921 Abnormality of the cerebrospinal fluid
Expand Tier I Human 576 Genes GS171253: HP:0002817 Abnormality of the upper limb
Expand Tier I Human GO 753 Genes GS204108: GO:0072358 cardiovascular system development
Expand Tier I Human 1488 Genes GS174131: HP:0002011 Abnormality of the central nervous system
Expand Tier I Human 121 Genes GS175588: HP:0001311 Neurophysiological abnormality
Expand Tier I Human 55 Genes GS172018: HP:0001363 Craniosynostosis
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 GO 2047 Genes GS203406: GO:0009653 anatomical structure morphogenesis
Expand Tier I Human 82 Genes GS171602: HP:0001965 Abnormality of the scalp
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 65 Genes GS175643: HP:0006989 Dysplastic corpus callosum
Expand Tier I Human GO 5243 Genes GS207615: GO:0016021 integral to membrane
Expand Tier I Human GO 357 Genes GS209923: GO:0001525 angiogenesis
Expand Tier I Human 401 Genes GS174217: HP:0005105 Abnormal nasal morphology
Expand Tier I Human 825 Genes GS175525: HP:0000004 Onset and clinical course
Expand Tier I Human 201 Genes GS171631: HP:0008051 Abnormality of the retinal pigment epithelium
Expand Tier I Human 395 Genes GS172839: HP:0010674 Abnormality of the curvature of the vertebral column
Expand Tier I Human GO 22 Genes GS202193: GO:0009651 response to salt stress
Expand Tier I Human 196 Genes GS175785: HP:0002500 Abnormality of the cerebral white matter
Expand Tier I Human 262 Genes GS176145: HP:0001780 Abnormality of toe
Expand Tier I Human 2329 Genes GS171832: HP:0000118 Phenotypic abnormality
Expand Tier I Human 444 Genes GS172928: HP:0011729 Abnormality of joint mobility
Expand Tier I Human GO 4134 Genes GS200341: GO:0051179 localization
Expand Tier I Human 185 Genes GS173065: HP:0003679 Pace of progression
Expand Tier I Human CTD 82 Genes GS121682: Phenol interacting genes (MeSH:D019800) in CTD
Expand Tier I Human GO 924 Genes GS197610: GO:0022857 transmembrane transporter activity
Expand Tier I Human 471 Genes GS173079: HP:0000496 Abnormality of eye movement
Expand Tier I Human 56 Genes GS173053: HP:0000324 Facial asymmetry
Expand Tier I Human 396 Genes GS171100: HP:0000759 Abnormality of the peripheral nervous system
Expand Tier I Human 550 Genes GS171251: HP:0003549 Abnormality of connective tissue
Expand Tier I Human 7 Genes GS172690: HP:0003378 Axonal degeneration/regeneration
Expand Tier I Human 335 Genes GS174076: HP:0009122 Aplasia/Hypoplasia affecting bones of the axial skeleton
Expand Tier I Human CTD 6287 Genes GS126584: Tetrachlorodibenzodioxin interacting genes (MeSH:D013749) in CTD
Expand Tier I Human 2 Genes GS173902: HP:0006125 Long tapered fingers
Expand Tier I Human CTD 768 Genes GS123769: 2-(1'H-indolo-3'-carbonyl)thiazole-4-carboxylic acid methyl ester interacting genes (MeSH:C548651) in CTD
Expand Tier I Human 1287 Genes GS175528: HP:0000007 Autosomal recessive inheritance
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 344 Genes GS172989: HP:0001324 Muscle weakness
Expand Tier I Human 53 Genes GS175935: HP:0000248 Brachycephaly
Expand Tier I Human 2114 Genes GS175526: HP:0000005 Mode of inheritance
Expand Tier I Human GO 128 Genes GS196999: GO:0015103 inorganic anion transmembrane transporter activity
Expand Tier I Human 51 Genes GS174123: HP:0100807 Long fingers
Expand Tier I Human 510 Genes GS174836: HP:0001098 Abnormality of the fundus
Expand Tier I Human 263 Genes GS176477: HP:0002118 Abnormality of the cerebral ventricles
Expand Tier I Human 32 Genes GS171849: HP:0000599 Abnormality of the frontal hairline
Expand Tier I Human 4 Genes GS176261: HP:0007178 Motor polyneuropathy
Expand Tier I Human GO 632 Genes GS209450: GO:0006812 cation transport
Expand Tier I Human 583 Genes GS175098: HP:0000284 Abnormality of the ocular region
Expand Tier I Human GO 7717 Genes GS207616: GO:0016020 membrane
Expand Tier I Human 776 Genes GS173787: HP:0002813 Abnormality of limb bone morphology
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 614 Genes GS176171: HP:0001250 Seizures
Expand Tier I Human GO 12778 Genes GS195214: GO:0009987 cellular process
Expand Tier I Human 231 Genes GS173288: HP:0000316 Hypertelorism
Expand Tier I Human GO 4960 Genes GS199124: GO:0051716 cellular response to stimulus
Expand Tier I Human 143 Genes GS176586: HP:0001270 Motor delay
Expand Tier I Human 532 Genes GS176170: HP:0001252 Muscular hypotonia
Expand Tier I Human GO 1193 Genes GS196168: GO:0005215 transporter activity
Expand Tier I Human 39 Genes GS172678: HP:0009117 Aplasia/Hypoplasia of the maxilla
Expand Tier I Human GO 3506 Genes GS193991: GO:0048731 system development
Expand Tier I Human 300 Genes GS176029: HP:0009116 Aplasia/Hypoplasia involving bones of the skull
Expand Tier I Human 120 Genes GS177000: HP:0001291 Abnormality of the cranial nerves
Expand Tier I Human 309 Genes GS174899: HP:0100886 Abnormality of globe location
Expand Tier I Human 79 Genes GS173516: HP:0000301 Abnormality of facial musculature
Expand Tier I Human 344 Genes GS171309: HP:0000252 Microcephaly
Expand Tier I Human 39 Genes GS173054: HP:0000327 Hypoplasia of the maxilla
Expand Tier I Human GO 753 Genes GS204107: GO:0072359 circulatory system development
Expand Tier I Human 187 Genes GS171512: HP:0007703 Abnormal retinal pigmentation
Expand Tier I Human 19 Genes GS171721: HP:0003445 EMG: neuropathic changes
Expand Tier I Human GO 1184 Genes GS197275: GO:0033554 cellular response to stress
Expand Tier I Human 2364 Genes GS175529: HP:0000001 All
Expand Tier I Human 182 Genes GS176955: HP:0000431 Wide nasal bridge
Expand Tier I Human 205 Genes GS176283: HP:0009830 Peripheral neuropathy
Expand Tier I Human GO 166 Genes GS210294: GO:0016323 basolateral plasma membrane