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RGD Search Result

4382 records found for search term ATP6

GENES
281 Found    View Genes for All Species
         Rattus norvegicus   34     View Rat Genes Report
         Mus musculus   33     View Mouse Genes Report
         Homo sapiens   102     View Human Genes Report
         Chinchilla lanigera   27     View Chinchilla Genes Report
         Pan paniscus   27     View Bonobo Genes Report
         Canis lupus familiaris   28     View Dog Genes Report
         Ictidomys tridecemlineatus   30     View Squirrel Genes Report

SSLPS
49 Found    View SSLPs for All Species
         Rattus norvegicus   6     View Rat SSLPs Report
         Mus musculus   32     View Mouse SSLPs Report
         Homo sapiens   11     View Human SSLPs Report

REFERENCES
37 Found    View References for All Species

CELL LINES
5 Found    View Cell Lines for All Species

VARIANTS
4010 Found    View Variants for All Species

  
Result Matrix
  Rat Mouse Hum Chin Bono Dog Squ
Genes: 34 33 102 27 27 28 30
QTLs: 0 0 0 0 0 0 0
Strains: 0 0 0 0 0 0 0
SSLPs: 6 32 11 0 0 0 0
Promoters: 0 0 0 0 0 0 0
Cell Lines: 0 0 5 0 0 0 0
Variants: 0 0 4010 0 0 0 0

Ontologies

Curators at RGD make annotations to genes, QTLs and strains using standardized vocabularies/ontologies. Your search returned annotations to the terms below.

EFO: Experimental Factor Ontology
term browser ATP6AP2-related disorder
term browser ATP6V1C1 (human)
term browser ATP6V1C2 (human)
term browser ATP6V1F (human)
term browser autosomal recessive cutis laxa type 2A
term browser immunodeficiency 47
term browser maternally-inherited spastic paraplegia
term browser V-type proton ATPase subunit C 1
term browser V-type proton ATPase subunit C 1 (human)
term browser V-type proton ATPase subunit C 1, initiator methionine removed form
term browser V-type proton ATPase subunit C 2
term browser V-type proton ATPase subunit C 2 (human)
term browser V-type proton ATPase subunit F
term browser V-type proton ATPase subunit F (human)
term browser Zimmermann-Laband syndrome 2

RDO: RGD Disease Ontology
term browser autosomal dominant congenital deafness with onychodystrophy
term browser autosomal recessive cutis laxa type IIA
term browser autosomal recessive cutis laxa type IIC
term browser autosomal recessive cutis laxa type IID
term browser autosomal recessive distal renal tubular acidosis 3 with or without sensorineural hearing loss
term browser congenital disorder of glycosylation type IIr
term browser developmental and epileptic encephalopathy 104
term browser developmental and epileptic encephalopathy 93
term browser Distal Renal Tubular Acidosis 2 with Progressive Nerve Deafness
term browser early-onset epilepsy 3
term browser immunodeficiency 47
term browser mitochondrial complex V (ATP synthase) deficiency nuclear type 3
term browser syndromic X-linked intellectual disability Hedera type
term browser wrinkly skin syndrome
term browser X-linked parkinsonism-spasticity syndrome
term browser Zimmermann-Laband Syndrome 2