CDC73 - cell division cycle 73 Gene

Also Known as HYX; FIHP; HPTJT; HRPT1; HRPT2; C1orf28

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 79577

About CDC73

Cytogenetic location: 1q31.2 Genomic coordinates (GRCh38): 1:193,122,031-193,254,815 (from NCBI)

This gene has 13 transcripts (splice variants), 215 orthologues and is associated with 92 phenotypes. Ubiquitous expression in thyroid (RPKM 11.2), prostate (RPKM 9.6) and 25 other tissues.

Summary

This gene encodes a tumor suppressor that is involved in transcriptional and post-transcriptional control pathways. The protein is a component of the the PAF protein complex, which associates with the RNA polymerase II subunit POLR2A and with a Histone Methyltransferase complex. This protein appears to facilitate the association of 3' mRNA processing factors with actively-transcribed chromatin. Mutations in this gene have been linked to hyperparathyroidism-jaw tumor syndrome, familial isolated hyperparathyroidism, and parathyroid carcinoma. [provided by RefSeq, Jul 2009]

CDC73 Products (1)

mRNA Protein Name
NM_024529.5 NP_078805.3 parafibromin
Molecular Function GO Annotation Evidence References Source
enables RNA polymerase II complex binding IDA
IDA: Inferred from direct assay
15923622 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
15923622 GOA
Biological Process GO Annotation Evidence References Source
involved in mRNA 3'-end processing IMP
IMP: Inferred from mutant phenotype
21329879 GOA
involved in negative regulation of G1/S transition of mitotic cell cycle IDA
IDA: Inferred from direct assay
16989776 GOA
involved in negative regulation of cell population proliferation IDA
IDA: Inferred from direct assay
16989776 GOA
involved in negative regulation of epithelial cell proliferation IMP
IMP: Inferred from mutant phenotype
18987311 GOA
involved in negative regulation of fibroblast proliferation IMP
IMP: Inferred from mutant phenotype
18987311 GOA
involved in negative regulation of myeloid cell differentiation IDA
IDA: Inferred from direct assay
20541477 GOA
involved in negative regulation of transcription by RNA polymerase II IMP
IMP: Inferred from mutant phenotype
18987311 GOA
involved in positive regulation of Wnt signaling pathway IDA
IDA: Inferred from direct assay
16630820 GOA
involved in positive regulation of cell cycle G1/S phase transition IMP
IMP: Inferred from mutant phenotype
15923622 GOA
involved in positive regulation of mRNA 3'-end processing IMP
IMP: Inferred from mutant phenotype
19136632 GOA
involved in positive regulation of transcription by RNA polymerase II IDA
IDA: Inferred from direct assay
16307923 GOA
involved in protein destabilization IMP
IMP: Inferred from mutant phenotype
18987311 GOA
involved in transcription elongation by RNA polymerase II IDA
IDA: Inferred from direct assay
20178742 GOA
Cellular Component GO Annotation Evidence References Source
part of Cdc73/Paf1 complex IDA
IDA: Inferred from direct assay
16307923 GOA
located in nucleus IDA
IDA: Inferred from direct assay
15923622 GOA
EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

CDC73 Protein Structure

CDC73_C

CDC73_C: RNA pol II accessory factor, Cdc73 family, C-terminal (233 - 525)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 500
  • 531 a.a.
Protein Preferred Names Protein Names

parafibromin

  • Familial isolated hyperparathyroidism

CDC73 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62 15923622
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62
GMS
15923622
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62 33961781
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62
GMS
16024656
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62
GMS
20178742
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62 28514442
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62 20178742
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62 29774127
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62 19136632
Intra
CDC73 Q6P1J9 CTR9 Homo sapiens Q6PD62 26496610
Intra
CDC73 Q6P1J9 RTF1 Homo sapiens Q92541
GMS
20178742
Intra
CDC73 Q6P1J9 RTF1 Homo sapiens Q92541 20178742
Intra
CDC73 Q6P1J9 RTF1 Homo sapiens Q92541
GMS
15923622
Intra
CDC73 Q6P1J9 MTUS2 Homo sapiens Q5JR59-3 25910212
Intra
CDC73 Q6P1J9 MTUS2 Homo sapiens Q5JR59-3 25910212
Intra
CDC73 Q6P1J9 MTUS2 Homo sapiens Q5JR59-3 25910212
Intra
CDC73 Q6P1J9 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
CDC73 Q6P1J9 MTUS2 Homo sapiens Q5JR59-3 32296183
Intra
CDC73 Q6P1J9 PTPN11 Homo sapiens Q06124-2 26742426
Intra
CDC73 Q6P1J9 RNF20 Homo sapiens Q5VTR2 32296183
Intra
CDC73 Q6P1J9 RNF20 Homo sapiens Q5VTR2 32296183
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5 15923622
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5
TAP
24981860
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5
GMS
20178742
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5 26496610
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5 19136632
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5 33961781
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5
GMS
15923622
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5
GMS
16024656
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5 28514442
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5 29774127
Intra
CDC73 Q6P1J9 PAF1 Homo sapiens Q8N7H5 20178742
Intra
CDC73 Q6P1J9 POLR2A Homo sapiens P24928 15923622
Intra
CDC73 Q6P1J9 POLR2A Homo sapiens P24928 26659056
Intra
CDC73 Q6P1J9 ALAS1 Homo sapiens P13196 25910212
Intra
CDC73 Q6P1J9 ALAS1 Homo sapiens P13196 25910212
Intra
CDC73 Q6P1J9 ALAS1 Homo sapiens P13196 25910212
Intra
CDC73 Q6P1J9 ALAS1 Homo sapiens P13196 25416956
Intra
CDC73 Q6P1J9 VPS37B Homo sapiens Q9H9H4 25416956
Intra
CDC73 Q6P1J9 VPS37B Homo sapiens Q9H9H4 25416956
Intra
CDC73 Q6P1J9 RABEP1 Homo sapiens Q15276 32296183
Intra
CDC73 Q6P1J9 RABEP1 Homo sapiens Q15276 32296183
Intra
CDC73 Q6P1J9 CTNNB1 Homo sapiens P35222 16630820
Intra
CDC73 Q6P1J9 CTNNB1 Homo sapiens P35222
Y2H
16630820
Intra
CDC73 Q6P1J9 CTNNB1 Homo sapiens P35222 16630820
Intra
CDC73 Q6P1J9 CTNNB1 Homo sapiens P35222 29774127
Intra
CDC73 Q6P1J9 BCL9 Homo sapiens O00512 17113272
Intra
CDC73 Q6P1J9 BCL9 Homo sapiens O00512 16630820
Intra
CDC73 Q6P1J9 FSD2 Homo sapiens A1L4K1 25416956
Intra
CDC73 Q6P1J9 FSD2 Homo sapiens A1L4K1 25910212
Intra
CDC73 Q6P1J9 FSD2 Homo sapiens A1L4K1 25910212
Intra
CDC73 Q6P1J9 FSD2 Homo sapiens A1L4K1 25910212
Intra
CDC73 Q6P1J9 FSD2 Homo sapiens A1L4K1 25416956
Intra
CDC73 Q6P1J9 FSD2 Homo sapiens A1L4K1 25416956
Intra
CDC73 Q6P1J9 KMT2A Homo sapiens Q03164 20541477
Intra
CDC73 Q6P1J9 GOLGA6L9 Homo sapiens A6NEM1 32296183
Intra
CDC73 Q6P1J9 GOLGA6L9 Homo sapiens A6NEM1 32296183
Intra
CDC73 Q6P1J9 GOLGA2 Homo sapiens Q08379 32296183
Intra
CDC73 Q6P1J9 GOLGA2 Homo sapiens Q08379 25910212
Intra
CDC73 Q6P1J9 GOLGA2 Homo sapiens Q08379 25910212
Intra
CDC73 Q6P1J9 GOLGA2 Homo sapiens Q08379 25910212
Intra
CDC73 Q6P1J9 GOLGA2 Homo sapiens Q08379 25416956
Intra
CDC73 Q6P1J9 GOLGA2 Homo sapiens Q08379 32296183
Intra
CDC73 Q6P1J9 CSTF2 Homo sapiens P33240 19136632
Intra
CDC73 Q6P1J9 CSTF2 Homo sapiens P33240 19136632
Intra
CDC73 Q6P1J9 HSF2BP Homo sapiens O75031 32296183
Intra
CDC73 Q6P1J9 HSF2BP Homo sapiens O75031 32296183
Intra
CDC73 Q6P1J9 TFCP2 Homo sapiens Q12800 25416956
Intra
CDC73 Q6P1J9 TFCP2 Homo sapiens Q12800 25910212
Intra
CDC73 Q6P1J9 TFCP2 Homo sapiens Q12800 25910212
Intra
CDC73 Q6P1J9 TFCP2 Homo sapiens Q12800 25910212
Intra
CDC73 Q6P1J9 CPSF4 Homo sapiens O95639 19136632
Intra
CDC73 Q6P1J9 CEP70 Homo sapiens Q8NHQ1 25910212
Intra
CDC73 Q6P1J9 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
CDC73 Q6P1J9 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
CDC73 Q6P1J9 CEP70 Homo sapiens Q8NHQ1 25910212
Intra
CDC73 Q6P1J9 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
CDC73 Q6P1J9 CEP70 Homo sapiens Q8NHQ1
Y2H
21900206
Intra
CDC73 Q6P1J9 CEP70 Homo sapiens Q8NHQ1 25910212
Intra
CDC73 Q6P1J9 TRIM23 Homo sapiens P36406 32296183
Intra
CDC73 Q6P1J9 TRIM23 Homo sapiens P36406 32296183
Intra
CDC73 Q6P1J9 MTUS2 Homo sapiens Q5JR59 25416956
Intra
CDC73 Q6P1J9 MTUS2 Homo sapiens Q5JR59 25416956
Intra
CDC73 Q6P1J9 EHMT2 Homo sapiens Q96KQ7 29774127
Intra
CDC73 Q6P1J9 EHMT2 Homo sapiens Q96KQ7 29774127
Intra
CDC73 Q6P1J9 TSGA10 Homo sapiens Q9BZW7 25416956
Intra
CDC73 Q6P1J9 TSGA10 Homo sapiens Q9BZW7 25910212
Intra
CDC73 Q6P1J9 TSGA10 Homo sapiens Q9BZW7 25910212
Intra
CDC73 Q6P1J9 TSGA10 Homo sapiens Q9BZW7 25910212
Intra
CDC73 Q6P1J9 TSGA10 Homo sapiens Q9BZW7 25416956
Intra
CDC73 Q6P1J9 KASH5 Homo sapiens Q8N6L0 25910212
Intra
CDC73 Q6P1J9 KASH5 Homo sapiens Q8N6L0 25910212
Intra
CDC73 Q6P1J9 KASH5 Homo sapiens Q8N6L0 25910212
Intra
CDC73 Q6P1J9 KASH5 Homo sapiens Q8N6L0 25416956
Intra
CDC73 Q6P1J9 KASH5 Homo sapiens Q8N6L0 25416956
Intra
CDC73 Q6P1J9 PICK1 Homo sapiens Q9NRD5 32296183
Intra
CDC73 Q6P1J9 PICK1 Homo sapiens Q9NRD5 32296183
Intra
CDC73 Q6P1J9 PICK1 Homo sapiens Q9NRD5 32296183
Intra
CDC73 Q6P1J9 SETDB1 Homo sapiens Q15047 29774127
Intra
CDC73 Q6P1J9 SETDB1 Homo sapiens Q15047 29774127
Intra
CDC73 Q6P1J9 LEO1 Homo sapiens Q8WVC0 33961781
Intra
CDC73 Q6P1J9 LEO1 Homo sapiens Q8WVC0
GMS
15923622
Intra
CDC73 Q6P1J9 LEO1 Homo sapiens Q8WVC0
GMS
16024656
Intra
CDC73 Q6P1J9 LEO1 Homo sapiens Q8WVC0
GMS
20178742
Intra
CDC73 Q6P1J9 LEO1 Homo sapiens Q8WVC0 29774127
Intra
CDC73 Q6P1J9 LEO1 Homo sapiens Q8WVC0 15923622
Intra
CDC73 Q6P1J9 LEO1 Homo sapiens Q8WVC0
TAP
24981860
Intra
CDC73 Q6P1J9 LEO1 Homo sapiens Q8WVC0 26496610
Intra
CDC73 Q6P1J9 LEO1 Homo sapiens Q8WVC0 19136632
Cross: Cross-species interaction Intra: Intraspecies interaction

CDC73 Antibodies

Cat. No. Product Name Application Reactivity
HY-P81455 HRPT2/Parafibromin Antibody (YA1200) IHC-P Human
HY-P81455A HRPT2/Parafibromin Antibody (YA1200)(PBS only) IHC-P Human

Related Diseases

Diseases Alias
Hyperparathyroidism 2 With Jaw Tumors
  • Hyperparathyroidism-Jaw Tumor Syndrome

  • Hpt-Jt

  • HRPT2

  • Familial Primary Hyperparathyroidism With Multiple Ossifying Jaw Fibromas

  • Parathyroid Adenoma With Cystic Changes

  • Hereditary Hyperparathyroidism-Jaw Tumor Syndrome

  • Hyperparathyroidism 2

  • Hyperparathyroidism, Familial Primary, With Multiple Ossifying Jaw Fibromas

  • Hyperparathyroidism-Jaw Tumor Syndrome, Hereditary

  • Familial Cystic Parathyroid Adenomatosis

  • Hyperparathyroidism-Jaw Tumor Syndrome, Type 2

  • Parathyroid Adenomatosis, Familial Cystic

Hyperparathyroidism 1
  • Familial Isolated Hyperparathyroidism

  • Fihp

  • HRPT1

  • Hyperparathyroidism, Familial Isolated Primary

  • Hyperparathyroidism, Familial Primary

  • Familial Primary Hyperparathyroidism

  • Fihpt

  • Hyperparathyroidism, Familial, Isolated, Primary

  • Hyperparathyroidism 3

  • Parathyroid Adenoma, Familial

Parathyroid Carcinoma
  • Parathyroid Cancer

  • Parathyroid Neoplasms

  • Malignant Tumor Of Parathyroid Gland

  • PRTC

  • Carcinoma Of Parathyroid Gland

  • Malignant Neoplasm Of Parathyroid Gland

  • Parathyroid Gland Adenocarcinoma

  • Parathyroid Gland Cancer

  • Parathyroid Neoplasm

  • Parathyroid Gland Carcinoma

  • Malignant Neoplasm Of The Parathyroid

  • Neoplasm Of Parathyroid Gland

  • Parathyroid Gland Neoplasm

  • Cancer Of The Parathyroid

  • Cancer Of The Parathyroid Gland

  • Malignant Neoplasm Of Parathyroid

  • Malignant Parathyroid Gland Neoplasm

  • Malignant Parathyroid Gland Tumor

  • Malignant Parathyroid Neoplasm

  • Malignant Parathyroid Tumor

  • Malignant Tumor Of Parathyroid

  • Parathyroid Adenocarcinoma

  • Neoplasm Of The Parathyroid Gland

  • Carcinoma, Parathyroid

Parathyroid Adenoma
  • Adenoma Of Parathyroid

  • Adenoma Of The Parathyroid Gland

  • Parathyroid Gland Adenoma

Breast Cancer
  • Breast Carcinoma

  • Male Breast Cancer

  • Breast Cancer, Familial

  • Malignant Neoplasm Of Breast

  • Breast Cancer, Susceptibility To

  • Breast Cancer, Early-Onset

  • Malignant Tumor Of Breast

  • Carcinoma Of Male Breast

  • Breast Cancer, Invasive Ductal

  • Breast Cancer, Protection Against

  • Breast Cancer, Somatic

  • Breast Cancer, Male

  • Breast Cancer, Lobular, Somatic

  • Breast Tumor

  • Mammary Cancer

  • Mammary Tumor

  • Malignant Neoplasm Of Male Breast

  • Mammary Carcinoma

  • Male Breast Carcinoma

  • Familial Cancer Of Breast

  • Invasive Ductal Breast Carcinoma

  • Breast Cancer Susceptibility

  • Breast Cancer, Male, Susceptibility To

  • Breast Cancer, Early-Onset, Susceptibility To

  • Malignant Tumor Of The Breast

  • Mammary Neoplasm

  • Primary Breast Cancer

  • Neoplasm Of Male Breast

  • Carcinoma Of Breast

  • Breast Cancer In Men

  • Familial Breast Cancer

  • Cancer Of Breast

  • BC

  • Breast Cancer Familial

  • Breast Cancer Familial Male

  • Breast Cancer, Familial Male

  • Breast Male Carcinoma

  • Breast Neoplasms

  • Breast Neoplasms, Male

  • Mammary Tumors

  • Mammary Carcinomas

  • Cancer, Breast

  • Cancer, Breast, Susceptibility

  • Invasive Breast Ductal Carcinoma

  • Breast Neoplasm

  • Susceptibility To Breast Cancer

  • Mammary Neoplasms

  • Animal Mammary Neoplasms

  • Primary Malignant Neoplasm Of Breast

  • Infiltrating Ductal Carcinoma Of Breast

  • Infiltrating Duct Carcinoma Of Unspecified Site

  • Infiltrating Ductular Carcinoma Of Unspecified Site

  • Invasive Breast Carcinoma Of No Special Type

  • Microinvasive Carcinoma Of Breast

  • Carcinoma With Apocrine Differentiation

Bap1 Tumor Predisposition Syndrome
  • Bap1-Related Tumor Predisposition Syndrome

  • Common Syndrome

  • Bap1 Cancer Syndrome

  • Bap1-Tpds

  • Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, And Other Internal Neoplasms

  • Tumor Predisposition Syndrome

  • Tumor Susceptibility Linked To Germline Bap1 Mutations

  • Cutaneous/Ocular Melanoma, Atypical Melanocytic Proliferations, Other Internal Neoplasms

  • Tumor Predisposition

Inherited Cancer-Predisposing Syndrome
  • Hereditary Cancer-Predisposing Syndrome

Hyperparathyroidism
  • Hyperparathyroidism And Other Disorders Of Parathyroid Gland

  • Parathyroid Hyperfunction

  • Hpth - [Hyperparathyroidism]

  • Parathyroid Gland Hyperfunction

  • Parathyroid Glandular Hyperfunction

Ossifying Fibroma
  • Peripheral Ossifying Fibroma

  • Fibro-Osteoma

  • Fibroma Ossifying

  • Fibroma, Ossifying

Fibroma
Primary Hyperparathyroidism
  • Familial Primary Hyperparathyroidism

  • Hyperparathyroidism, Primary

  • Hyperparathyroidism Primary

  • Hypocalciuric Hypercalcemia, Familial, Type 1

  • Familial Benign Hypercalcemia

  • Familial Hyperparathyroidism

  • Parathyroid Enlargement

Parathyroid Gland Disease
  • Parathyroid Diseases

  • Disease Of Parathyroid Glands

  • Parathyroid Disease

Cdc73-Related Disorders
Multiple Endocrine Neoplasia
  • Men

  • Multiple Endocrine Adenomatosis

  • Multiple Endocrine Neoplasia Syndrome

  • Adenomatosis, Familial Endocrine

  • Endocrine Neoplasia, Multiple

  • Familial Endocrine Adenomatosis

  • Mea

  • Multiple Endocrine Neoplasms

  • Multiple Endocrine Neoplasia Type 1

Parathyroid Oncocytic Adenoma
  • Parathyroid Gland Oncocytic Adenoma

Multiple Endocrine Neoplasia, Type Iia
  • Multiple Endocrine Neoplasia Type 2a

  • Sipple Syndrome

  • Multiple Endocrine Neoplasia Type 2

  • MEN2A

  • Men2

  • Ptc Syndrome

  • Multiple Endocrine Neoplasia, Type 2

  • Multiple Endocrine Neoplasia Iia

  • Men 2a

  • Pheochromocytoma And Amyloid Producing Medullary Thyroid Carcinoma

  • Multiple Endocrine Neoplasia, Type 2a

  • Pheochromocytoma And Amyloid-Producing Medullary Thyroid Carcinoma

  • Multiple Endocrine Neoplasia Ii

  • Men2 Syndrome

  • Men-2a Syndrome

  • Multiple Neoplasia 2a

  • Multiple Neoplasia Type 2

Multiple Endocrine Neoplasia, Type I
  • Multiple Endocrine Neoplasia Type 1

  • MEN1

  • Wermer Syndrome

  • Multiple Endocrine Neoplasia 1

  • Multiple Endocrine Neoplasia, Type 1

  • Men I

  • Endocrine Adenomatosis, Multiple

  • Mea I

  • Men Type I

  • Wermer'S Syndrome

  • Men1 Syndrome

  • Multiple Endocrine Adenomatosis

  • Endocrine Adenomatosis Multiple

  • Men 1

  • Familial Multiple Endocrine Neoplasia Type I

  • Neoplasia, Endocrine, Multiple, Type 1

  • Multiple Endocrine Neoplasia

Adenoma
  • Acinar Cell Adenoma

  • Adenomas

  • Acinic Cell Adenoma

Fibrous Dysplasia
  • Fibrous Dysplasia Of Bone

Clear Cell Adenoma
Hereditary Wilms' Tumor
  • Hereditary Wilms Tumor

  • Hereditary Wilms Tumour

  • Hereditary Wilms' Tumour

  • Wt1

Familial Hypocalciuric Hypercalcemia
  • Familial Benign Hypercalcemia

  • Fbh

  • Fbhh

  • Fhh

  • Familial Benign Hypocalciuric Hypercalcemia

  • Hypocalciuric Hypercalcemia, Familial, Type 1

Water-Clear Cell Adenoma
Bone Benign Neoplasm
Malignant Fibrous Histiocytoma Of Bone
  • Malignant Fibrous Histiocytoma Of The Bone

Hypocalciuric Hypercalcemia, Familial, Type I
  • HHC1

  • Familial Hypocalciuric Hypercalcemia 1

  • Fhh1

  • Familial Benign Hypercalcemia 1

  • Fbh1

  • Hypocalciuric Hypercalcemia, Type I

  • Fhh Type 1

  • Hhc

  • Fhh

  • Hypercalcemia, Familial Benign

  • Hypocalciuric Hypercalcemia Type I

  • Familial Hypocalciuric Hypercalcemia Type 1

  • Hypocalciuric Hypercalcemia, Familial, Type 1

  • Familial Hypocalciuric Hypercalcemia Type I

  • Familial Benign Hypercalcemia Type 1

  • Hypercalcemia, Familial Benign Type 1

  • Hypocalciuric Hypercalcemia, Familial 1

  • Familial Benign Hypocalciuric Hypercalcemia 1

  • Fbhh1

Hypocalciuric Hypercalcemia, Familial, Type Ii
  • HHC2

  • Familial Hypocalciuric Hypercalcemia 2

  • Fbh2

  • Familial Hypocalciuric Hypercalcemia Type 2

  • Hypocalciuric Hypercalcemia, Type Ii

  • Fhh Type 2

  • Familial Benign Hypercalcemia, Type Ii

  • Hypercalcemia, Familial Benign, Type Ii

  • Hypocalciuric Hypercalcemia Type Ii

  • Familial Benign Hypercalcemia, Type 2

  • Hypercalcemia, Familial Benign Type 2

  • Hypocalciuric Hypercalcemia, Familial, Type 2

  • Hypocalciuric Hypercalcemia, Familial 2

  • Familial Benign Hypercalcemia Type Ii

  • Hypocalciuric Hypercalcemia-2

Osteitis Fibrosa
  • Osteitis Fibrosa Cystica

  • Hyperparathyroid Bone Disease

  • Osteitis Fibrosa Cystica Generalisata

  • Von Recklinghausen'S Bone Disease

  • Osteitis Fibrosa Disseminata

Thyroid Gland Hurthle Cell Carcinoma
  • Oncocytic Carcinoma Of The Thyroid

  • Thyroid Cancer, Hurthle Cell

Multiple Endocrine Neoplasia, Type Iv
  • Multiple Endocrine Neoplasia Type 4

  • MEN4

  • Multiple Endocrine Neoplasia 4

  • Neoplasia, Endocrine, Multiple, Type Iv

Connective Tissue Benign Neoplasm
  • Soft Tissue Neoplasms

  • Mesenchymal Tissue Neoplasm

  • Neoplasm Of Soft Tissue

  • Neoplasm Of Soft Tissues

  • Soft Tissue Benign Neoplasm

  • Tumor Of The Soft Tissue

  • Soft Tissue Neoplasm

Lipoadenoma
Hypocalciuric Hypercalcemia, Familial, Type Iii
  • HHC3

  • Familial Hypocalciuric Hypercalcemia 3

  • Fbh3

  • Familial Hypocalciuric Hypercalcemia Type 3

  • Hypercalcemia, Familial Benign, Oklahoma Type

  • Hypocalciuric Hypercalcemia, Type Iii

  • Fhh Type 3

  • Hypocalciuric Hypercalcemia Type Iii

  • Familial Benign Hypercalcemia, Type Iii

  • Hypercalcemia, Familial Benign, Type Iii

  • Fbhok

  • Familial Benign Hypercalcemia, Oklahoma Variant

  • Familial Benign Hypercalcemia, Type 3

  • Hypercalcemia, Familial Benign, Type 3

  • Hypocalciuric Hypercalcemia, Familial, Type 3

  • Hypocalciuric Hypercalcemia, Familial 3

  • Familial Benign Hypercalcemia 3

  • Familial Benign Hypercalcemia Oklahoma Type

  • Familial Benign Hypocalciuric Hypercalcemia 3

  • Fbhh3

  • Fhh3

Epulis
  • Epulides

  • Gingival Polyp

  • Polyp Of Gum

Endocrine Organ Benign Neoplasm
Mineral Metabolism Disease
  • Mineral Metabolism Disorder

  • Disorder Of Mineral Metabolism

Wilms Tumor 1
  • Nephroblastoma

  • Wilms Tumor

  • WT1

  • Wilms' Tumor

  • Bilateral Wilms Tumor

  • Wilms Tumor, Type 1

  • Wilms Tumor, Somatic

  • Adult Nephroblastoma

  • Wt1 Disorder

  • Renal Embryonic Tumor

  • Adult Kidney Wilms Tumor

  • Childhood Kidney Wilms Tumor

  • Nonanaplastic Kidney Wilms Tumor

Diseases Alias
Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Waldenstroem'S Macroglobulinemia

Waldenstroem'S Macroglobulinemia

Macroglobulinemia Of Waldenstrom

Lymphoplasmacytic Lymphoma With Igm Gammopathy

Lymphoplasmacytic Lymphoma

Orthologs Information

Species Symbol Source ID
Felis catus CDC73 VGNC VGNC:60665
Rattus norvegicus CDC73 RGD RGD:1311766
Bos taurus CDC73 VGNC VGNC:27083
Mus musculus CDC73 MGD MGI:2384876
Macaca mulatta CDC73 VGNC VGNC:70766
Canis familiaris CDC73 VGNC VGNC:39011
Others CDC73 NCBI