Hypercalciuria, Absorptive, 2; Hca2

Table of contents:

Description
Related genes
Clinical Features
Incidence and onset information
Alternative Names
Researches and researchers
Gene Panels
Sources and references

Genes related to Hypercalciuria, Absorptive, 2; Hca2

ADCY10

View recommended genes panels

Clinical Features

Phenotypes and symptoms related to Hypercalciuria, Absorptive, 2; Hca2

Nephrolithiasis
Hypercalciuria
Rickets
Hypophosphatemic rickets
Calcium oxalate nephrolithiasis

Incidence and onset information

— Currently we don't have prevalence information about this disease (Not enough data available about incidence and published cases.)
— No data available about the known clinical features onset.

Alternative names

Hypercalciuria, Absorptive, 2; Hca2 Is also known as hypercalciuria, familial idiopathic.

Researches and researchers

Currently, we don't have any information about doctors, researches or researchers related to this disease. Please contact us if you would like to appear here.

Hypercalciuria, Absorptive, 2; Hca2 Recommended genes panels

Panel Name, Specifity and genes Tested/covered
Hypercalciuria via ADCY10 Gene Sequencing with CNV Detection. By PreventionGenetics PreventionGenetics (United States). ADCY10 Specificity 100 % Genes 100 %
Nephrolithiasis and Nephrocalcinosis Sequencing Panel with CNV Detection. By PreventionGenetics PreventionGenetics (United States). SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, VDR, XDH, SLC2A9, CA2, CASR, SLC22A12, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A, HOGA1, CYP24A1 , (...) View the complete list with 9 more genes Panel complete gene list SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, VDR, XDH, SLC2A9, CA2, CASR, SLC22A12, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A, HOGA1, CYP24A1, AGXT, GRHPR, HNF4A, HPRT1, KCNJ1, APRT, OCRL, ATP6V1B1, ATP6V0A4 Specificity 4 % Genes 100 %
Nephrolithiasis and related disorders NGS panel. By Connective Tissue Gene Tests (United States). SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, XDH, SLC2A9, CA2, CASR, SLC22A12, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A, HOGA1, CYP24A1, AGXT , (...) View the complete list with 10 more genes Panel complete gene list SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, XDH, SLC2A9, CA2, CASR, SLC22A12, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A, HOGA1, CYP24A1, AGXT, GNA11, GRHPR, HNF4A, HPRT1, AP2S1, KCNJ1, APRT, OCRL, ATP6V1B1, ATP6V0A4 Specificity 4 % Genes 100 %
Nephrolithiasis and related disorders Comprehensive panel. By Connective Tissue Gene Tests (United States). SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, XDH, SLC2A9, CA2, CASR, SLC22A12, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A, HOGA1, CYP24A1, AGXT , (...) View the complete list with 10 more genes Panel complete gene list SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, XDH, SLC2A9, CA2, CASR, SLC22A12, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A, HOGA1, CYP24A1, AGXT, GNA11, GRHPR, HNF4A, HPRT1, AP2S1, KCNJ1, APRT, OCRL, ATP6V1B1, ATP6V0A4 Specificity 4 % Genes 100 %
Nephrolithiasis and related disorders Deletion / Duplication panel. By Connective Tissue Gene Tests (United States). SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, XDH, SLC2A9, CA2, CASR, SLC22A12, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A, HOGA1, CYP24A1, AGXT , (...) View the complete list with 10 more genes Panel complete gene list SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, XDH, SLC2A9, CA2, CASR, SLC22A12, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A, HOGA1, CYP24A1, AGXT, GNA11, GRHPR, HNF4A, HPRT1, AP2S1, KCNJ1, APRT, OCRL, ATP6V1B1, ATP6V0A4 Specificity 4 % Genes 100 %
ADCY10. By Fulgent Genetics Fulgent Genetics (United States). ADCY10 Specificity 100 % Genes 100 %
KidneySeq - 264 Genes. By Iowa Institute of Human Genetics University of Iowa (United States). ROBO2, CNNM2, SALL1, ATXN10, SCNN1A, SCNN1B, SCNN1G, SDCCAG8, BMP4, SEMA3E, SGPL1, SIX1, SIX2, SIX5, SLC12A1, SLC17A5, SLC2A2, SLC34A1, SLC3A1, SLC4A4 , (...) View the complete list with 230 more genes Panel complete gene list ROBO2, CNNM2, SALL1, ATXN10, SCNN1A, SCNN1B, SCNN1G, SDCCAG8, BMP4, SEMA3E, SGPL1, SIX1, SIX2, SIX5, SLC12A1, SLC17A5, SLC2A2, SLC34A1, SLC3A1, SLC4A4, SLC5A1, SLC5A2, SLC7A9, SLC9A3R1, SLIT2, SMARCAL1, TBX18, HNF1B, TNFRSF1A, TNXB, TRPC6, TSC1, TSC2, CEP41, TTR, UMOD, UPK3A, VDR, VHL, VPS33B, WNT4, WT1, XDH, ZMPSTE24, ARL6, NEK8, NPHS2, SLC2A9, IFT122, CA2, CACNA1D, CACNA1H, ANLN, CD2AP, TMEM237, WNK1, WNK4, CASR, SALL4, TRAP1, CD151, MAGED2, TRIM32, NLRP3, BSND, ACTN4, SCARB2, ZNF423, PLCE1, SRGAP1, XPO5, SARS2, INVS, CEP83, SLC22A12, TRPM6, SOX17, KCTD1, ALG1, WDR19, IFT27, NUP205, CRB2, GRIP1, BBS7, COQ8B, NPHP4, CHD1L, KIF14, SLC41A1, GREM1, TTC8, CLCN5, COQ6, CLCNKA, CLCNKB, SLC34A3, VIPAS39, CLDN16, CLDN19, CHD7, ADCY10, IFT74, INPP5E, KIF12, AHI1, COL4A1, COL4A3, COL4A4, COL4A5, COL4A6, PDSS2, FREM1, CREBBP, DHTKD1, INF2, B9D1, TCTN3, C2CD3, TMEM216, HOGA1, CTNS, COQ2, ARHGAP24, FREM2, ARL13B, CUBN, CUL3, TTC21B, OFD1, TCTN2, CPLANE1, CYP11B1, WDR73, CYP24A1, TCTN1, CSPP1, BBS10, DACH1, BBS12, ANKS6, TMEM138, C8orf37, WDPCP, XPNPEP3, BBIP1, TMEM107, TMEM67, DGKE, DHCR7, B9D2, IQCB1, NUP93, DLC1, DLG1, CEP290, DSTYK, IFT140, RPGRIP1L, FAN1, CEP164, WDR35, CC2D2A, IFT80, DMP1, GLIS2, DYNC2H1, IFT43, NUP107, BBS9, IFT172, KIF7, E2F3, EGF, EHHADH, EMP2, ENPP1, AGTR1, AGXT, EYA1, FAH, FAT1, FGA, FGF20, FGF23, FGFR1, FN1, FOXP1, FXYD2, GATA3, GDNF, ALMS1, GLA, GLI3, GPC3, GRHPR, GSN, HNF4A, HPRT1, HSD11B2, CFI, APOE, ITGA3, ITGA8, ITGB4, APOL1, JAG1, ANOS1, KCNJ1, KCNJ10, APRT, KCNJ5, AQP2, KLHL3, LAMB2, LMNA, LMX1B, LYZ, LZTFL1, ARHGDIA, MEFV, MKKS, MKS1, MYH9, MYO1E, NEK1, NOTCH2, NPHP1, NPHP3, NPHS1, NR3C2, OCRL, ATP6V1B1, PAX2, PBX1, ATP6V0A4, ATP7B, PHEX, AVPR2, PKD1, PKD2, PKHD1, PMM2, B2M, BBS1, BBS2, PTPRO, BBS4, BBS5, RET Specificity 1 % Genes 100 %
Nephrolithiasis Panel. By Blueprint Genetics (Finland). SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, VDR, XDH, SLC2A9, CA2, CASR, GPHN, SLC22A12, MOCOS, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A , (...) View the complete list with 14 more genes Panel complete gene list SLC12A1, SLC26A1, SLC34A1, SLC3A1, SLC7A9, SLC9A3R1, VDR, XDH, SLC2A9, CA2, CASR, GPHN, SLC22A12, MOCOS, CLCN5, SLC34A3, CLDN16, CLDN19, ADCY10, FAM20A, HOGA1, CYP24A1, AGXT, GNA11, ALPL, GRHPR, HNF4A, HPRT1, KCNJ1, APRT, MOCS1, OCRL, ATP6V1B1, ATP6V0A4 Specificity 3 % Genes 100 %

You can get up to 0 more panels with our dedicated tool

Learn more

Sources and references

You can check the following sources for additional information.

OMIM MESH Rare Disease Search Engine

If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like TIETZ ALBINISM-DEAFNESS SYNDROME; TADS RENAL GLUCOSURIA; GLYS OPTIC ATROPHY 2; OPA2 HEREDITARY MOTOR AND SENSORY NEUROPATHY V AUTOSOMAL DOMINANT HYPERINSULINISM DUE TO KIR6.2 DEFICIENCY 2Q23.1 MICRODELETION SYNDROME OSTEOPETROSIS AND INFANTILE NEUROAXONAL DYSTROPHY