PROP1 - PROP paired-like homeobox 1 Gene

Also Known as CPHD2; PROP-1

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 5626

About PROP1

Cytogenetic location: 5q35.3 Genomic coordinates (GRCh38): 5:177,992,235-177,996,242 (from NCBI)

This gene has 1 transcript (splice variant), 1 gene allele, 109 orthologues, 50 paralogues and is associated with 5 phenotypes. Low expression observed in reference dataset.

Summary

This gene encodes a paired-like homeodomain transcription factor in the developing pituitary gland. Expression occurs prior to and is required for expression of pou domain transcription factor 1, which is responsible for pituitary development and hormone expression. Mutations in this gene have been associated with combined pituitary hormone deficiency-2 as well as deficiencies in luteinizing hormone, follicle-stimulating hormone, growth hormone, Prolactin, and thyroid-stimulating hormone. [provided by RefSeq, Sep 2011]

PROP1 Products (1)

mRNA Protein Name
NM_006261.5 NP_006252.4 homeobox protein prophet of Pit-1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
23732115 GOA
enables sequence-specific double-stranded DNA binding IDA
IDA: Inferred from direct assay
28473536 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

PROP1 Protein Structure

Homeobox

Homeobox: Homeobox domain (70 - 126)

  • 0
  • 100
  • 200
  • 226 a.a.
Protein Preferred Names Protein Names

homeobox protein prophet of Pit-1

  • pituitary-specific homeodomain factor

PROP1 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
PROP1 O75360 METTL15 Homo sapiens A6NJ78-4 32296183
Intra
PROP1 O75360 METTL15 Homo sapiens A6NJ78-4 32296183
Intra
PROP1 O75360 UBE2I Homo sapiens Q7KZS0 32296183
Intra
PROP1 O75360 UBE2I Homo sapiens Q7KZS0 32296183
Intra
PROP1 O75360 UBE2I Homo sapiens Q7KZS0 32296183
Intra
PROP1 O75360 P4HA3 Homo sapiens Q7Z4N8 32296183
Intra
PROP1 O75360 P4HA3 Homo sapiens Q7Z4N8 32296183
Intra
PROP1 O75360 P4HA3 Homo sapiens Q7Z4N8 32296183
Intra
PROP1 O75360 OLIG3 Homo sapiens Q7RTU3 32296183
Intra
PROP1 O75360 TEKT5 Homo sapiens Q96M29 32296183
Intra
PROP1 O75360 KRTAP19-7 Homo sapiens Q3SYF9 32296183
Intra
PROP1 O75360 KRTAP19-7 Homo sapiens Q3SYF9 32296183
Intra
PROP1 O75360 KRTAP19-7 Homo sapiens Q3SYF9 32296183
Intra
PROP1 O75360 NR1D2 Homo sapiens Q6NSM0 32296183
Intra
PROP1 O75360 NR1D2 Homo sapiens Q6NSM0 32296183
Intra
PROP1 O75360 NR1D2 Homo sapiens Q6NSM0 32296183
Intra
PROP1 O75360 KRTAP8-1 Homo sapiens Q8IUC2 32296183
Intra
PROP1 O75360 KRTAP8-1 Homo sapiens Q8IUC2 32296183
Intra
PROP1 O75360 KRTAP8-1 Homo sapiens Q8IUC2 32296183
Intra
PROP1 O75360 SPMIP6 Homo sapiens Q8NCR6 32296183
Intra
PROP1 O75360 SPMIP6 Homo sapiens Q8NCR6 32296183
Intra
PROP1 O75360 SPMIP6 Homo sapiens Q8NCR6 32296183
Intra
PROP1 O75360 COX6B2 Homo sapiens Q6YFQ2 32296183
Intra
PROP1 O75360 COX6B2 Homo sapiens Q6YFQ2 32296183
Intra
PROP1 O75360 COX6B2 Homo sapiens Q6YFQ2 32296183
Intra
PROP1 O75360 TLE5 Homo sapiens Q08117-2 32296183
Intra
PROP1 O75360 TLE5 Homo sapiens Q08117-2 32296183
Intra
PROP1 O75360 TLE5 Homo sapiens Q08117-2 32296183
Intra
PROP1 O75360 ACTMAP Homo sapiens Q5BKX5-3 32296183
Intra
PROP1 O75360 ACTMAP Homo sapiens Q5BKX5-3 32296183
Intra
PROP1 O75360 ACTMAP Homo sapiens Q5BKX5-3 32296183
Intra
PROP1 O75360 FAM168A Homo sapiens Q92567-2 32296183
Intra
PROP1 O75360 FAM168A Homo sapiens Q92567-2 32296183
Intra
PROP1 O75360 FAM168A Homo sapiens Q92567-2 32296183
Intra
PROP1 O75360 C6orf15 Homo sapiens Q6UXA7 32296183
Intra
PROP1 O75360 C6orf15 Homo sapiens Q6UXA7 32296183
Intra
PROP1 O75360 C6orf15 Homo sapiens Q6UXA7 32296183
Intra
PROP1 O75360 POU6F2 Homo sapiens P78424 32296183
Intra
PROP1 O75360 POU6F2 Homo sapiens P78424 32296183
Intra
PROP1 O75360 POU6F2 Homo sapiens P78424 32296183
Intra
PROP1 O75360 TMEM42 Homo sapiens Q69YG0 32296183
Intra
PROP1 O75360 TMEM42 Homo sapiens Q69YG0 32296183
Intra
PROP1 O75360 TMEM42 Homo sapiens Q69YG0 32296183
Intra
PROP1 O75360 UFSP1 Homo sapiens Q6NVU6 32296183
Intra
PROP1 O75360 UFSP1 Homo sapiens Q6NVU6 32296183
Intra
PROP1 O75360 UFSP1 Homo sapiens Q6NVU6 32296183
Intra
PROP1 O75360 SMUG1 Homo sapiens Q53HV7-2 32296183
Intra
PROP1 O75360 SMUG1 Homo sapiens Q53HV7-2 32296183
Intra
PROP1 O75360 SMUG1 Homo sapiens Q53HV7-2 32296183
Intra
PROP1 O75360 ABHD11 Homo sapiens Q8NFV4-4 32296183
Intra
PROP1 O75360 ABHD11 Homo sapiens Q8NFV4-4 32296183
Intra
PROP1 O75360 ABHD11 Homo sapiens Q8NFV4-4 32296183
Intra
PROP1 O75360 KRTAP19-6 Homo sapiens Q3LI70 32296183
Intra
PROP1 O75360 KRTAP19-6 Homo sapiens Q3LI70 32296183
Intra
PROP1 O75360 KRTAP19-6 Homo sapiens Q3LI70 32296183
Intra
PROP1 O75360 CIMIP2A Homo sapiens Q6J272 32296183
Intra
PROP1 O75360 CIMIP2A Homo sapiens Q6J272 32296183
Intra
PROP1 O75360 CIMIP2A Homo sapiens Q6J272 32296183
Intra
PROP1 O75360 KRTAP19-1 Homo sapiens Q8IUB9 32296183
Intra
PROP1 O75360 KRTAP19-1 Homo sapiens Q8IUB9 32296183
Intra
PROP1 O75360 KRTAP19-1 Homo sapiens Q8IUB9 32296183
Intra
PROP1 O75360 OXER1 Homo sapiens Q8TDS5 32296183
Intra
PROP1 O75360 OXER1 Homo sapiens Q8TDS5 32296183
Intra
PROP1 O75360 OXER1 Homo sapiens Q8TDS5 32296183
Intra
PROP1 O75360 PSMB11 Homo sapiens A5LHX3 32296183
Intra
PROP1 O75360 PSMB11 Homo sapiens A5LHX3 32296183
Intra
PROP1 O75360 ARSA Homo sapiens P15289 32296183
Intra
PROP1 O75360 ARSA Homo sapiens P15289 32296183
Intra
PROP1 O75360 ARSA Homo sapiens P15289 32296183
Intra
PROP1 O75360 KRTAP6-3 Homo sapiens Q3LI67 32296183
Intra
PROP1 O75360 KRTAP6-3 Homo sapiens Q3LI67 32296183
Intra
PROP1 O75360 RNF4 Homo sapiens P78317 32296183
Intra
PROP1 O75360 RNF4 Homo sapiens P78317 32296183
Intra
PROP1 O75360 RNF4 Homo sapiens P78317 32296183
Intra
PROP1 O75360 HNRNPF Homo sapiens P52597 32296183
Intra
PROP1 O75360 PLEKHB2 Homo sapiens Q96CS7 32296183
Intra
PROP1 O75360 PLEKHB2 Homo sapiens Q96CS7 32296183
Intra
PROP1 O75360 PLEKHB2 Homo sapiens Q96CS7 32296183
Intra
PROP1 O75360 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
PROP1 O75360 CYSRT1 Homo sapiens A8MQ03 32296183
Intra
PROP1 O75360 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
PROP1 O75360 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
PROP1 O75360 TRIM42 Homo sapiens Q8IWZ5 32296183
Intra
PROP1 O75360 PSMB4 Homo sapiens P28070 32296183
Intra
PROP1 O75360 PSMB4 Homo sapiens P28070 32296183
Intra
PROP1 O75360 PSMB4 Homo sapiens P28070 32296183
Intra
PROP1 O75360 TBX22 Homo sapiens Q9Y458 32296183
Intra
PROP1 O75360 TBX22 Homo sapiens Q9Y458 32296183
Intra
PROP1 O75360 TBX22 Homo sapiens Q9Y458 32296183
Intra
PROP1 O75360 CRYBA1 Homo sapiens P05813 32296183
Intra
PROP1 O75360 CRYBA1 Homo sapiens P05813 32296183
Intra
PROP1 O75360 CRYBA1 Homo sapiens P05813 32296183
Intra
PROP1 O75360 TINAGL1 Homo sapiens Q9GZM7 32296183
Intra
PROP1 O75360 TINAGL1 Homo sapiens Q9GZM7 32296183
Intra
PROP1 O75360 TINAGL1 Homo sapiens Q9GZM7 32296183
Intra
PROP1 O75360 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
PROP1 O75360 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
PROP1 O75360 MAGED1 Homo sapiens Q9Y5V3 32296183
Intra
PROP1 O75360 TLE5 Homo sapiens Q08117
Y2H
23732115
Intra
PROP1 O75360 CFAP68 Homo sapiens Q9H5F2 32296183
Intra
PROP1 O75360 CFAP68 Homo sapiens Q9H5F2 32296183
Intra
PROP1 O75360 CFAP68 Homo sapiens Q9H5F2 32296183
Intra
PROP1 O75360 DAZAP2 Homo sapiens Q15038 32296183
Intra
PROP1 O75360 DAZAP2 Homo sapiens Q15038 32296183
Intra
PROP1 O75360 DAZAP2 Homo sapiens Q15038 32296183
Intra
PROP1 O75360 HOXA1 Homo sapiens P49639 32296183
Intra
PROP1 O75360 BATF2 Homo sapiens Q8N1L9 32296183
Intra
PROP1 O75360 BATF2 Homo sapiens Q8N1L9 32296183
Intra
PROP1 O75360 BATF2 Homo sapiens Q8N1L9 32296183
Intra
PROP1 O75360 EFEMP2 Homo sapiens O95967 32296183
Intra
PROP1 O75360 EFEMP2 Homo sapiens O95967 32296183
Intra
PROP1 O75360 EFEMP2 Homo sapiens O95967 32296183
Intra
PROP1 O75360 HDHD3 Homo sapiens Q9BSH5 32296183
Intra
PROP1 O75360 HDHD3 Homo sapiens Q9BSH5 32296183
Intra
PROP1 O75360 HDHD3 Homo sapiens Q9BSH5 32296183
Intra
PROP1 O75360 INTS11 Homo sapiens Q5TA45 32296183
Intra
PROP1 O75360 INTS11 Homo sapiens Q5TA45 32296183
Intra
PROP1 O75360 INTS11 Homo sapiens Q5TA45 32296183
Intra
PROP1 O75360 TEKT4 Homo sapiens Q8WW24 32296183
Intra
PROP1 O75360 TENT5B Homo sapiens Q96A09 32296183
Intra
PROP1 O75360 SUMO1 Homo sapiens P63165 32296183
Intra
PROP1 O75360 SUMO1 Homo sapiens P63165 32296183
Intra
PROP1 O75360 SUMO1 Homo sapiens P63165 32296183
Intra
PROP1 O75360 METTL27 Homo sapiens Q8N6F8 32296183
Intra
PROP1 O75360 METTL27 Homo sapiens Q8N6F8 32296183
Intra
PROP1 O75360 METTL27 Homo sapiens Q8N6F8 32296183
Intra
PROP1 O75360 ZNF503 Homo sapiens Q96F45 32296183
Intra
PROP1 O75360 ZNF503 Homo sapiens Q96F45 32296183
Intra
PROP1 O75360 ZNF503 Homo sapiens Q96F45 32296183
Intra
PROP1 O75360 C1orf94 Homo sapiens Q6P1W5 32296183
Intra
PROP1 O75360 C1orf94 Homo sapiens Q6P1W5 32296183
Intra
PROP1 O75360 C1orf94 Homo sapiens Q6P1W5 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Pituitary Hormone Deficiency, Combined, 2
  • Panhypopituitarism

  • Combined Pituitary Hormone Deficiency

  • CPHD2

  • Ateliotic Dwarfism With Hypogonadism

  • Pituitary Dwarfism Iii

  • Hanhart Dwarfism

  • Simmond'S Disease

  • Simmonds' Disease

  • Cphd

  • Pituitary Hormone Deficiency, Combined

  • Hormone Deficiency, Pituitary, Combined, Type 2

  • Pituitary Dwarfism Type 3

  • Sheehan Syndrome

Combined Pituitary Hormone Deficiencies, Genetic Forms
  • Congenital Hypopituitarism

  • Pituitary Hormone Deficiency, Combined 1

  • Congenital Combined Pituitary Hormone Deficiency

  • Non-Acquired Combined Pituitary Hormone Deficiency

  • Cphd1

  • Familial Congenital Hypopituitarism

  • Multiple Pituitary Hormone Deficiencies, Genetic Forms

  • Combined Pituitary Hormone Deficiencies, Genetic Form

  • Hormone Deficiency, Pituitary, Combined, Type 1

Non-Acquired Panhypopituitarism
  • Genetic Panhypopituitarism

46,Xy Partial Gonadal Dysgenesis
  • 46,Xy Pgd

  • 46,Xy Partial Testicular Dysgenesis

Hypothyroidism Due To Deficient Transcription Factors Involved In Pituitary Development Or Function
Hypopituitarism
  • Pituitary Hypofunction

  • Pituitary Insufficiency

  • Pituitary Hormone Deficiency

  • Subpituitarism

  • Hypophyseal Dystrophy

  • Hypohypophysism

  • Anterior Pituitary Insufficiency

  • Deficient Secretion Of One Or More Pituitary Hormones

  • Hypopituitarism Syndrome

  • Pituitary Deficiency

  • Pituitary Failure

  • Pituitary Insufficiency Nos

  • Anterior Pituitary Hypofunction

  • Deficient Secretion Of All Pituitary Hormones

  • Hypopituitary Dwarfism

  • Hyposomatotropic Dwarfism

  • Hypophyseal Dwarfism

  • Hypopituitary Cachexia

  • Hypophyseal Short Stature

  • Panhypopituitarism Syndrome

  • Pituitary Cachexia

  • Juvenile Hypopituitarism

  • Pituitary Dwarfism

  • Pituitary Gland Hypofunction

  • Primary Hypopituitarism

  • Secondary Hypogonadism

  • Prepubertal Panhypopituitarism

  • Prepubertal Dwarfism

  • Postpartum Panhypopituitary Syndrome

  • Postpartum Hypopituitarism

  • Pituitary Short Stature

  • Pituitary Infantilism

  • Pituitary Hypogonadism

  • Pituitary Hypoadrenocorticism

Pituitary Tumors
  • Pituitary Tumor

  • Pituitary Neoplasms

Hypothyroidism, Congenital, Nongoitrous, 4
  • Tsh Deficiency

  • CHNG4

  • Thyrotropin Deficiency, Isolated

  • Pituitary Cretinism

  • Congenital Nongoitrous Hypothyroidism 4

  • Isolated Thyrotropin Deficiency

  • Thyroid-Stimulating Hormone Deficiency

  • Hypothyroidism, Congenital, Nongoitrous 4

  • Thyroid-Stimulating Hormone, Deficiency Of

  • Isolated Thyroid-Stimulating Hormone Deficiency

  • Isolated Tsh Deficiency

  • Hypothyroidism, Congenital, Nongoitrous, Type 4

  • Secondary Hypothyroidism

  • Tsh - [Thyroid Stimulating Hormone] Deficiency

Hypogonadism
Pituitary Gland Disease
  • Pituitary Diseases

  • Pituitary Dysfunction

  • Pituitary Disease

  • Pituitary Deficiency

  • Pituitary Disorders

Septooptic Dysplasia
  • Septo-Optic Dysplasia

  • De Morsier Syndrome

  • Growth Hormone Deficiency With Pituitary Anomalies

  • SOD

  • Pituitary Hormone Deficiency, Combined, 5

  • Septo-Optic Dysplasia Spectrum

  • Septo-Optic Dysplasia With Growth Hormone Deficiency

  • Pituitary Hormone Deficiency, Combined 5

  • Hypopituitarism And Septooptic 'Dysplasia'

  • GHDPA

  • CPHD5

  • Dysplasia, Septo-Optic

  • Kallmann Syndrome

Hypogonadotropic Hypogonadism
  • Klinefelter Syndrome

  • Klinefelter'S Syndrome

  • Xxy Syndrome

  • Xxy Trisomy

  • Hypogonadotropism

  • 47, Xxy

  • Congenital Idiopathic Hypogonadotropic Hypogonadism

  • Isolated Congenital Gonadotropin Deficiency

  • 47,Xxy Syndrome

  • 47, Xxy Syndrome

  • Klinefelters Syndrome

  • Hypogonadism

  • Klinefelter Syndrome In Males

  • Klinefelter Syndrome, Unspecified

  • Klinefelter Syndrome Karyotype 47, Xxy

Empty Sella Syndrome
  • Empty Sella Turcica

  • Empty Sella

Hypothyroidism
  • Thyroid Diseases

  • Thyroid Disease

  • Thyroid Deficiency

  • Thyroid Insufficiency

  • Dysfunction Thyroid

  • Thyroid Dysfunction

Craniopharyngioma
  • Neoplasm Of Rathke'S Pouch

  • Adamantinomatous Tumor

  • Craniopharyngeal Duct Tumor

  • Dysodontogenic Epithelial Tumor

  • Rathke'S Pouch Tumor

Sheehan Syndrome
  • Postpartum Hypopituitarism

  • Sheehan'S Syndrome

  • Postpartum Panhypopituitarism

  • Postpartum Panhypopituitary Syndrome

  • Postpartum Pituitary Necrosis

  • Simmond'S Disease

Kallmann Syndrome
  • Hypogonadism With Anosmia

  • Kallman'S Syndrome

  • Anosmic Hypogonadism

  • Anosmic Idiopathic Hypogonadotropic Hypogonadism

  • Hypogonadotropic Hypogonadism And Anosmia

  • Hypogonadotropic Hypogonadism-Anosmia Syndrome

  • Olfacto-Genital Pathological Sequence

  • Familial Hypogonadism With Anosmia

  • Kallman Syndrome

  • Dysplasia Olfactogenitalis Of De Morsier

  • Kallmann'S Syndrome

  • Congenital Hypogonadotropic Hypogonadism With Anosmia

Pituitary Hypoplasia
  • Hypoplasia Of The Pituitary Gland

Tungiasis
  • Tunga Penetrans Infestation

  • Chigger Flea

  • S Penetrans

  • Sarcopsylla Penetrans

  • T Penetrans

  • Tunga Penetrans

  • Sand-Flea Infestation

  • Jiggers Infestation

  • Chigoe Infestation

  • Jigger Disease

Complement Component 2 Deficiency
  • C2D

  • C2 Deficiency

  • Complement 2 Deficiency

  • Complement Component-2

Isolated Growth Hormone Deficiency, Type Ia
  • Ighd Ia

  • Primordial Dwarfism

  • Isolated Growth Hormone Deficiency Type Ia

  • Sexual Ateleiotic Dwarfism

  • Pituitary Dwarfism I

  • IGHD1A

  • Illig-Type Growth Hormone Deficiency

  • Growth Hormone Deficiency, Isolated, Type Ia

  • Congenital Ighd Type Ia

  • Congenital Isolated Gh Deficiency Type Ia

  • Congenital Isolated Growth Hormone Deficiency Type Ia

  • Pituitary Dwarfism 1

  • Growth Hormone Deficiency, Isolated, Autosomal Recessive

  • Autosomal Recessive Isolated Growth Hormone Deficiency

  • Isolated Growth Hormone Deficiency Type 1a

  • Congenital Ighd

  • Congenital Isolated Gh Deficiency

  • Congenital Isolated Growth Hormone Deficiency

  • Growth Hormone Deficiency, Isolated Autosomal Recessive

  • Illig Type Growth Hormone Deficiency

  • Non-Acquired Isolated Growth Hormone Deficiency

  • Growth Hormone Deficiency, Isolated, 1a

  • Growth Hormone Deficiency Isolated Autosomal Recessive

  • Dwarfism, Primordial

  • Dwarfism

Seckel Syndrome 5
  • SCKL5

  • Seckel Syndrome, Type 5

Microcephaly 1, Primary, Autosomal Recessive
  • MCPH1

  • Premature Chromosome Condensation Syndrome

  • Pcc Syndrome

  • Primary Autosomal Recessive Microcephaly 1

  • Microcephaly, Primary Autosomal Recessive, 1

  • Premature Chromosome Condensation With Microcephaly And Mental Retardation

  • Microcephaly Vera

  • True Microcephaly

  • Microcephaly, Type 1, Primary, Autosomal Recessive

  • Autosomal Recessive Primary Microcephaly

Acth Deficiency, Isolated
  • Adrenocorticotropic Hormone Deficiency

  • IAD

  • Congenital Isolated Acth Deficiency

  • Isolated Acth Deficiency

  • Isolated Adrenocorticotropic Hormone Deficiency

  • Adrenocorticotropic Hormone Deficiency

  • Adrenocorticotropic Hormone [Acth] Deficiency

  • Secondary Adrenocortical Insufficiency

Isolated Growth Hormone Deficiency, Type Ii
  • Ighd Ii

  • Isolated Growth Hormone Deficiency Type Ii

  • IGHD2

  • Growth Hormone Deficiency, Isolated, Type Ii

  • Congenital Ighd Type Ii

  • Congenital Isolated Gh Deficiency Type Ii

  • Congenital Isolated Growth Hormone Deficiency Type Ii

  • Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency Autosomal Dominant

  • Growth Hormone Deficiency, Isolated, Autosomal Dominant

  • Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency, Autosomal Dominant

  • Autosomal Dominant Isolated Growth Hormone Deficiency

  • Autosomal Dominant Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency

  • Isolated Growth Hormone Deficiency Type 2

  • Growth Hormone Deficiency, Isolated Autosomal Dominant

  • Growth Hormone Deficiency, Isolated, 2

  • Growth Hormone Deficiency Isolated Autosomal Dominant

Hypothyroidism, Central, With Testicular Enlargement
  • X-Linked Central Congenital Hypothyroidism With Late-Onset Testicular Enlargement

  • CHTE

  • Hypothyroidism, Central, And Testicular Enlargement

  • Igsf1 Deficiency Syndrome

  • X-Linked Central Congenital Hypothyroidism With Late-Onset Macroorchidism

  • Central Hypothyroidism And Testicular Enlargement

  • Hypothyroidism, Central, Testicular Enlargement

Isolated Growth Hormone Deficiency
  • Congenital Ighd

  • Congenital Isolated Gh Deficiency

  • Congenital Isolated Growth Hormone Deficiency

  • Non-Acquired Isolated Growth Hormone Deficiency

  • Pituitary Dwarfism

  • Dwarfism, Pituitary

  • Isolated Somatotropin Deficiency

  • Isolated Congenital Growth Hormone Deficiency

  • Familial Isolated Growth Hormone Deficiency

  • Ighd

  • Dwarfism, Growth Hormone Deficiency

  • Growth Hormone Deficiency Dwarfism

  • Isolated Gh Deficiency

  • Isolated Hgh Deficiency

  • Isolated Human Growth Hormone Deficiency

  • Isolated Somatotropin Deficiency Disorder

  • Dwarfism Pituitary

Situs Inversus
  • Situs Inversus Viscerum

  • Laterality Sequence

  • Complete Transposition

  • Siv

Adamantinous Craniopharyngioma
  • Adamantinous Rathke'S Pouch Tumor

  • Craniopharyngioma, Adamantinomatous

  • Adamantinomatous Craniopharyngioma

Congenital Hypothyroidism
  • Cretinism

  • Neonatal Hypothyroidism

  • Ch

  • Cht

  • Congenital Myxedema

  • Myxedema, Congenital

  • Endemic Cretinism

  • Congenital Iodine-Deficiency Syndrome

  • Fetal Iodine Deficiency Syndrome

  • Congenital Iodine-Deficiency Hypothyroidism Nos

Cryptorchidism, Unilateral Or Bilateral
  • Cryptorchidism

  • Undescended Testicle

  • Undescended Testis

  • Cryptorchism

  • Undescended Testicles

  • CRYPTO

  • Impaired Testicular Descent

  • Cryptosporidiosis

  • Retained Testis

  • Unilateral Cryptorchidism

  • Unilateral Undescended Testis

  • Nondescent Unilateral Testicle

  • Unilateral Cryptorchism

  • Ectopic Testis, Unilateral

  • Bilateral Cryptorchidism

  • Bilateral Cryptorchism

  • Bilateral Nondescent Testicle

  • Bilateral Undescended Testes

  • Bilateral Ectopic Testes

Holoprosencephaly
  • Holoprosencephaly Sequence

  • Hpe

  • Hpe - [Holoprosencephaly]

46,Xy Sex Reversal
  • Swyer Syndrome

  • Pure Gonadal Dysgenesis 46,Xy

  • Gonadal Dysgenesis, Xy Female Type

  • Gonadal Dysgenesis, 46,Xy

  • 46,Xy Cgd

  • 46,Xy Complete Gonadal Dysgenesis

  • 46,Xy Pure Gonadal Dysgenesis

  • 46 Xy Gonadal Dysgenesis

  • 46, Xy Cgd

  • 46, Xy Complete Gonadal Dysgenesis

  • 46, Xy Pure Gonadal Dysgenesis

  • Xy Pure Gonadal Dysgenesis

  • Female With 46,Xy Karyotype

  • Xy Females

Congenital Nervous System Abnormality
  • Congenital Neurologic Anomaly

  • Congenital Nervous System Disorder

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
Rattus norvegicus PROP1 RGD RGD:628759
Mus musculus PROP1 MGD MGI:109330
Macaca mulatta PROP1 VGNC VGNC:110442
Canis familiaris PROP1 VGNC VGNC:45014
Bos taurus PROP1 VGNC VGNC:33366
Others PROP1 NCBI