ZBTB24 - zinc finger and BTB domain containing 24 Gene

Also Known as BIF1; ICF2; PATZ2; ZNF450

Species: Homo sapiens

Gene Type: protein coding
Gene ID: 9841

About ZBTB24

Cytogenetic location: 6q21 Genomic coordinates (GRCh38): 6:109,462,594-109,483,219 (from NCBI)

This gene has 10 transcripts (splice variants), 186 orthologues, 36 paralogues and is associated with 2 phenotypes. Ubiquitous expression in lymph node (RPKM 6.3), testis (RPKM 4.0) and 25 other tissues.

Summary

This gene encodes a protein similar to a protein in rodents which is induced by bone morphogenic protein 2 in vitro. [provided by RefSeq, Aug 2011]

ZBTB24 Products (2)

mRNA Protein Name
NM_001164313.2 NP_001157785.1 zinc finger and BTB domain-containing protein 24 isoform 2
NM_014797.3 NP_055612.2 zinc finger and BTB domain-containing protein 24 isoform 1
Molecular Function GO Annotation Evidence References Source
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 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

ZBTB24 Protein Structure

BTB

BTB: BTB/POZ domain (27 - 132)

zf-C2H2_6

zf-C2H2_6: C2H2-type zinc finger (295 - 304)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (310 - 332)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (336 - 358)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (364 - 388)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (421 - 444)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (448 - 472)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (478 - 500)

  • 0
  • 200
  • 400
  • 600
  • 697 a.a.
Protein Preferred Names Protein Names

zinc finger and BTB domain-containing protein 24

  • POZ (BTB) and AT hook containing zinc finger 2

ZBTB24 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method References
Intra
ZBTB24 O43167 KRT40 Homo sapiens Q6A162 25416956
Intra
ZBTB24 O43167 KRT40 Homo sapiens Q6A162 25416956
Intra
ZBTB24 O43167 KRTAP10-8 Homo sapiens P60410 25416956
Intra
ZBTB24 O43167 KRTAP10-8 Homo sapiens P60410 32296183
Intra
ZBTB24 O43167 KRTAP10-8 Homo sapiens P60410 32296183
Intra
ZBTB24 O43167 KRTAP10-8 Homo sapiens P60410 32296183
Intra
ZBTB24 O43167 KRTAP10-9 Homo sapiens P60411 25416956
Intra
ZBTB24 O43167 KRTAP10-9 Homo sapiens P60411 25416956
Intra
ZBTB24 O43167 KRTAP10-5 Homo sapiens P60370 25416956
Intra
ZBTB24 O43167 KRTAP10-5 Homo sapiens P60370 25416956
Intra
ZBTB24 O43167 KRTAP10-7 Homo sapiens P60409 25416956
Intra
ZBTB24 O43167 KRTAP10-7 Homo sapiens P60409 25416956
Intra
ZBTB24 O43167 KRTAP4-2 Homo sapiens Q9BYR5 25416956
Intra
ZBTB24 O43167 KRTAP4-2 Homo sapiens Q9BYR5 25416956
Intra
ZBTB24 O43167 MID2 Homo sapiens Q9UJV3-2 25416956
Intra
ZBTB24 O43167 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
ZBTB24 O43167 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
ZBTB24 O43167 MID2 Homo sapiens Q9UJV3-2 25416956
Intra
ZBTB24 O43167 MID2 Homo sapiens Q9UJV3-2 32296183
Intra
ZBTB24 O43167 BCL11A Homo sapiens Q9H165-2 25416956
Intra
ZBTB24 O43167 BCL11A Homo sapiens Q9H165-2 25416956
Intra
ZBTB24 O43167 ZNF79 Homo sapiens Q15937 32296183
Intra
ZBTB24 O43167 ZNF79 Homo sapiens Q15937 32296183
Intra
ZBTB24 O43167 ZNF79 Homo sapiens Q15937 32296183
Intra
ZBTB24 O43167 ZNF792 Homo sapiens Q3KQV3 32296183
Intra
ZBTB24 O43167 ZNF792 Homo sapiens Q3KQV3 32296183
Intra
ZBTB24 O43167 ZNF792 Homo sapiens Q3KQV3 32296183
Intra
ZBTB24 O43167 ZNF526 Homo sapiens Q8TF50 32296183
Intra
ZBTB24 O43167 ZNF526 Homo sapiens Q8TF50 32296183
Intra
ZBTB24 O43167 ZNF526 Homo sapiens Q8TF50 32296183
Intra
ZBTB24 O43167 DDHD1 Homo sapiens Q8NEL9-2 32296183
Intra
ZBTB24 O43167 DDHD1 Homo sapiens Q8NEL9-2 32296183
Intra
ZBTB24 O43167 DDHD1 Homo sapiens Q8NEL9-2 32296183
Intra
ZBTB24 O43167 TLE5 Homo sapiens Q08117-2 32296183
Intra
ZBTB24 O43167 TLE5 Homo sapiens Q08117-2 32296183
Intra
ZBTB24 O43167 TLE5 Homo sapiens Q08117-2 32296183
Intra
ZBTB24 O43167 ZNF837 Homo sapiens Q96EG3 32296183
Intra
ZBTB24 O43167 ZNF837 Homo sapiens Q96EG3 32296183
Intra
ZBTB24 O43167 ZNF837 Homo sapiens Q96EG3 32296183
Intra
ZBTB24 O43167 FCHO1 Homo sapiens A0A0C3SFZ9 32296183
Intra
ZBTB24 O43167 FCHO1 Homo sapiens A0A0C3SFZ9 32296183
Intra
ZBTB24 O43167 KRTAP10-6 Homo sapiens P60371 32296183
Intra
ZBTB24 O43167 KRTAP10-6 Homo sapiens P60371 32296183
Intra
ZBTB24 O43167 KRTAP10-6 Homo sapiens P60371 32296183
Intra
ZBTB24 O43167 SPMIP2 Homo sapiens Q96LM5 32296183
Intra
ZBTB24 O43167 SPMIP2 Homo sapiens Q96LM5 32296183
Intra
ZBTB24 O43167 SPMIP2 Homo sapiens Q96LM5 32296183
Intra
ZBTB24 O43167 POU6F2 Homo sapiens P78424 32296183
Intra
ZBTB24 O43167 POU6F2 Homo sapiens P78424 32296183
Intra
ZBTB24 O43167 POU6F2 Homo sapiens P78424 32296183
Intra
ZBTB24 O43167 TMEM121 Homo sapiens Q9BTD3 32296183
Intra
ZBTB24 O43167 TMEM121 Homo sapiens Q9BTD3 32296183
Intra
ZBTB24 O43167 TMEM121 Homo sapiens Q9BTD3 32296183
Intra
ZBTB24 O43167 ZMYM6 Homo sapiens O95789-4 32296183
Intra
ZBTB24 O43167 ZMYM6 Homo sapiens O95789-4 32296183
Intra
ZBTB24 O43167 ZMYM6 Homo sapiens O95789-4 32296183
Intra
ZBTB24 O43167 POGZ Homo sapiens Q7Z3K3 32296183
Intra
ZBTB24 O43167 POGZ Homo sapiens Q7Z3K3 25416956
Intra
ZBTB24 O43167 POGZ Homo sapiens Q7Z3K3 25416956
Intra
ZBTB24 O43167 POGZ Homo sapiens Q7Z3K3 32296183
Intra
ZBTB24 O43167 KRTAP2-4 Homo sapiens Q9BYR9 32296183
Intra
ZBTB24 O43167 KRTAP2-4 Homo sapiens Q9BYR9 32296183
Intra
ZBTB24 O43167 KRTAP2-4 Homo sapiens Q9BYR9 32296183
Intra
ZBTB24 O43167 BACH2 Homo sapiens Q9BYV9 32296183
Intra
ZBTB24 O43167 BACH2 Homo sapiens Q9BYV9 32296183
Intra
ZBTB24 O43167 BACH2 Homo sapiens Q9BYV9 32296183
Intra
ZBTB24 O43167 BACH2 Homo sapiens Q9BYV9 33961781
Intra
ZBTB24 O43167 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
ZBTB24 O43167 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
ZBTB24 O43167 SSX2IP Homo sapiens Q9Y2D8 25416956
Intra
ZBTB24 O43167 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
ZBTB24 O43167 BLZF1 Homo sapiens Q9H2G9 31515488
Intra
ZBTB24 O43167 BLZF1 Homo sapiens Q9H2G9 25416956
Intra
ZBTB24 O43167 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
ZBTB24 O43167 BLZF1 Homo sapiens Q9H2G9 25416956
Intra
ZBTB24 O43167 BLZF1 Homo sapiens Q9H2G9 32296183
Intra
ZBTB24 O43167 BLZF1 Homo sapiens Q9H2G9 25416956
Intra
ZBTB24 O43167 GMCL1 Homo sapiens Q96IK5 32296183
Intra
ZBTB24 O43167 GMCL1 Homo sapiens Q96IK5 32296183
Intra
ZBTB24 O43167 GMCL1 Homo sapiens Q96IK5 32296183
Intra
ZBTB24 O43167 HMBOX1 Homo sapiens Q6NT76 25416956
Intra
ZBTB24 O43167 KLF15 Homo sapiens Q9UIH9 29892012
Intra
ZBTB24 O43167 KLF15 Homo sapiens Q9UIH9 31515488
Intra
ZBTB24 O43167 KLF15 Homo sapiens Q9UIH9 32296183
Intra
ZBTB24 O43167 KLF15 Homo sapiens Q9UIH9 32296183
Intra
ZBTB24 O43167 KLF15 Homo sapiens Q9UIH9 32296183
Intra
ZBTB24 O43167 TRAF2 Homo sapiens Q12933 32296183
Intra
ZBTB24 O43167 TRAF2 Homo sapiens Q12933 32296183
Intra
ZBTB24 O43167 TRAF2 Homo sapiens Q12933 32296183
Intra
ZBTB24 O43167 MCIDAS Homo sapiens D6RGH6 32296183
Intra
ZBTB24 O43167 MCIDAS Homo sapiens D6RGH6 32296183
Intra
ZBTB24 O43167 ZBTB9 Homo sapiens Q96C00 32296183
Intra
ZBTB24 O43167 ZBTB9 Homo sapiens Q96C00 32296183
Intra
ZBTB24 O43167 ZBTB9 Homo sapiens Q96C00 32296183
Intra
ZBTB24 O43167 KRTAP5-9 Homo sapiens P26371 25416956
Intra
ZBTB24 O43167 ZRANB1 Homo sapiens Q9UGI0 32296183
Intra
ZBTB24 O43167 ZRANB1 Homo sapiens Q9UGI0 32296183
Intra
ZBTB24 O43167 ZRANB1 Homo sapiens Q9UGI0 32296183
Intra
ZBTB24 O43167 GOLGA6L9 Homo sapiens A6NEM1 32296183
Intra
ZBTB24 O43167 GOLGA6L9 Homo sapiens A6NEM1 32296183
Intra
ZBTB24 O43167 PHC2 Homo sapiens Q8IXK0 25416956
Intra
ZBTB24 O43167 ZNF71 Homo sapiens Q9NQZ8 32296183
Intra
ZBTB24 O43167 ZNF71 Homo sapiens Q9NQZ8 32296183
Intra
ZBTB24 O43167 ZNF71 Homo sapiens Q9NQZ8 32296183
Intra
ZBTB24 O43167 MDFI Homo sapiens Q99750 32296183
Intra
ZBTB24 O43167 MDFI Homo sapiens Q99750 32296183
Intra
ZBTB24 O43167 MDFI Homo sapiens Q99750 25416956
Intra
ZBTB24 O43167 MDFI Homo sapiens Q99750 32296183
Intra
ZBTB24 O43167 MDFI Homo sapiens Q99750 19060904
Intra
ZBTB24 O43167 MDFI Homo sapiens Q99750 19060904
Intra
ZBTB24 O43167 MDFI Homo sapiens Q99750 25416956
Intra
ZBTB24 O43167 TRIM41 Homo sapiens Q8WV44 32296183
Intra
ZBTB24 O43167 TRIM41 Homo sapiens Q8WV44 25416956
Intra
ZBTB24 O43167 TRIM41 Homo sapiens Q8WV44 32296183
Intra
ZBTB24 O43167 TRIM41 Homo sapiens Q8WV44 25416956
Intra
ZBTB24 O43167 TRIM41 Homo sapiens Q8WV44 32296183
Intra
ZBTB24 O43167 TSC22D4 Homo sapiens Q9Y3Q8 25416956
Intra
ZBTB24 O43167 TSC22D4 Homo sapiens Q9Y3Q8 25416956
Intra
ZBTB24 O43167 TSC22D4 Homo sapiens Q9Y3Q8 32296183
Intra
ZBTB24 O43167 TSC22D4 Homo sapiens Q9Y3Q8 32296183
Intra
ZBTB24 O43167 TSC22D4 Homo sapiens Q9Y3Q8 32296183
Intra
ZBTB24 O43167 CEP70 Homo sapiens Q8NHQ1 25416956
Intra
ZBTB24 O43167 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
ZBTB24 O43167 CEP70 Homo sapiens Q8NHQ1 25416956
Intra
ZBTB24 O43167 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
ZBTB24 O43167 CEP70 Homo sapiens Q8NHQ1 32296183
Intra
ZBTB24 O43167 DVL3 Homo sapiens Q92997 32296183
Intra
ZBTB24 O43167 DVL3 Homo sapiens Q92997 32296183
Intra
ZBTB24 O43167 DVL3 Homo sapiens Q92997 32296183
Intra
ZBTB24 O43167 LNX1 Homo sapiens Q8TBB1 32296183
Intra
ZBTB24 O43167 LNX1 Homo sapiens Q8TBB1 32296183
Intra
ZBTB24 O43167 LNX1 Homo sapiens Q8TBB1 32296183
Intra
ZBTB24 O43167 ZBTB43 Homo sapiens O43298 25416956
Intra
ZBTB24 O43167 LDOC1 Homo sapiens O95751 25416956
Intra
ZBTB24 O43167 LDOC1 Homo sapiens O95751 32296183
Intra
ZBTB24 O43167 LDOC1 Homo sapiens O95751 31515488
Intra
ZBTB24 O43167 LDOC1 Homo sapiens O95751 25416956
Intra
ZBTB24 O43167 LDOC1 Homo sapiens O95751 32296183
Intra
ZBTB24 O43167 TRIM37 Homo sapiens O94972 32296183
Intra
ZBTB24 O43167 TRIM37 Homo sapiens O94972 32296183
Intra
ZBTB24 O43167 TRIM37 Homo sapiens O94972 32296183
Intra
ZBTB24 O43167 ZBTB8A Homo sapiens Q96BR9 25416956
Intra
ZBTB24 O43167 ZBTB8A Homo sapiens Q96BR9 32296183
Intra
ZBTB24 O43167 ZBTB8A Homo sapiens Q96BR9 32296183
Intra
ZBTB24 O43167 ZBTB8A Homo sapiens Q96BR9 32296183
Intra
ZBTB24 O43167 CEP76 Homo sapiens Q8TAP6 32296183
Intra
ZBTB24 O43167 CEP76 Homo sapiens Q8TAP6 32296183
Intra
ZBTB24 O43167 CEP76 Homo sapiens Q8TAP6 32296183
Intra
ZBTB24 O43167 TSGA10 Homo sapiens Q9BZW7 25416956
Intra
ZBTB24 O43167 TSGA10 Homo sapiens Q9BZW7 25416956
Intra
ZBTB24 O43167 CCNDBP1 Homo sapiens O95273 25416956
Intra
ZBTB24 O43167 CCNDBP1 Homo sapiens O95273 25416956
Intra
ZBTB24 O43167 LRRC18 Homo sapiens Q8N456 32296183
Intra
ZBTB24 O43167 LRRC18 Homo sapiens Q8N456 32296183
Intra
ZBTB24 O43167 LRRC18 Homo sapiens Q8N456 32296183
Intra
ZBTB24 O43167 PICK1 Homo sapiens Q9NRD5 32296183
Intra
ZBTB24 O43167 PICK1 Homo sapiens Q9NRD5 32296183
Intra
ZBTB24 O43167 PICK1 Homo sapiens Q9NRD5 32296183
Intra
ZBTB24 O43167 LHX8 Homo sapiens Q68G74 32296183
Intra
ZBTB24 O43167 LHX8 Homo sapiens Q68G74 32296183
Intra
ZBTB24 O43167 LHX8 Homo sapiens Q68G74 32296183
Intra
ZBTB24 O43167 CDA Homo sapiens P32320 32296183
Intra
ZBTB24 O43167 CDA Homo sapiens P32320 32296183
Intra
ZBTB24 O43167 CDA Homo sapiens P32320 32296183
Intra
ZBTB24 O43167 TSPYL2 Homo sapiens Q9H2G4 32296183
Intra
ZBTB24 O43167 TSPYL2 Homo sapiens Q9H2G4 32296183
Intra
ZBTB24 O43167 TSPYL2 Homo sapiens Q9H2G4 32296183
Intra
ZBTB24 O43167 ZNF639 Homo sapiens Q9UID6 32296183
Intra
ZBTB24 O43167 ZNF639 Homo sapiens Q9UID6 32296183
Intra
ZBTB24 O43167 ZNF639 Homo sapiens Q9UID6 32296183
Intra
ZBTB24 O43167 RALY Homo sapiens Q53GL6 32296183
Intra
ZBTB24 O43167 RALY Homo sapiens Q53GL6 32296183
Intra
ZBTB24 O43167 RALY Homo sapiens Q53GL6 32296183
Intra
ZBTB24 O43167 PDE4DIP Homo sapiens Q5VU43-2 32296183
Intra
ZBTB24 O43167 PDE4DIP Homo sapiens Q5VU43-2 32296183
Intra
ZBTB24 O43167 PDE4DIP Homo sapiens Q5VU43-2 32296183
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome 2
  • ICF2

  • Icf Syndrome 2

  • Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome, Type 2

Immunodeficiency-Centromeric Instability-Facial Anomalies Syndrome
  • Icf Syndrome

  • Immunodeficiency Syndrome, Variable

  • Ciid

  • Centromeric Instability, Immunodeficiency Syndrome

  • Immune Deficiency, Variable, With Centromeric Instability Of Chromosomes 1, 9, And 16

  • Icf

Syndromic X-Linked Intellectual Disability Nascimento Type
  • Mental Retardation, X-Linked Syndromic, Nascimento-Type

  • X-Linked Intellectual Disability-Nail Dystrophy-Seizures Syndrome

Non-Syndromic X-Linked Intellectual Disability 93
  • Mrx93

  • X-Linked Mental Retardation With Macrocephaly

Non-Syndromic X-Linked Intellectual Disability 97
  • Mrx65

  • Mrx97

  • Mrxz

  • X-Linked Mental Retardation 65

  • X-Linked Mental Retardation 97

Intellectual Developmental Disorder, Autosomal Dominant 23
  • MRD23

  • Intellectual Disability-Facial Dysmorphism Syndrome Due To Setd5 Haploinsufficiency

  • Mental Retardation, Autosomal Dominant 23

  • Autosomal Dominant Non-Syndromic Intellectual Disability 23

  • Autosomal Dominant Intellectual Developmental Disorder 23

  • Autosomal Dominant Mental Retardation 23

  • Mental Retardation, Autosomal Dominant, Type 23

Helsmoortel-Van Der Aa Syndrome
  • HVDAS

  • Mrd28

  • Adnp Syndrome

  • Adnp-Related Syndromic Intellectual Disability-Autism Spectrum Disorder

  • Mental Retardation, Autosomal Dominant 28

  • Adnp-Related Multiple Congenital Anomalies - Intellectual Disability - Autism Spectrum Disorder

  • Mental Retardation, Autosomal Dominant 28, Formerly

  • Mrd28, Formerly

  • Autosomal Dominant Mental Retardation 28

  • Adnp-Related Intellectual Disability And Autism Spectrum Disorder

  • Adnp-Related Multiple Congenital Anomalies-Intellectual Disability-Autism Spectrum Disorder

Hepatic Venoocclusive Disease With Immunodeficiency
  • VODI

  • Hepatic Veno-Occlusive Disease-Immunodeficiency Syndrome

  • Hepatic Veno-Occlusive Disease With Immunodeficiency

  • Familial Veno-Occlusive Disease With Immunodeficiency

  • Veno-Occlusive Disease And Immunodeficiency Syndrome

  • Vodi Syndrome

  • Vodi - [Veno-Occlusive Disease Immunodeficiency] Syndrome

Syndromic X-Linked Intellectual Disability Claes-Jensen Type
  • Mental Retardation, X-Linked, Syndromic, Claes-Jensen Type

  • Mrxscj

  • Mrxsj

  • Syndromic X-Linked Intellectual Disability Due To Jarid1c Mutation

  • Syndromic X-Linked Mental Retardation Jarid1c-Related

Granulomatous Hepatitis
Cogan-Reese Syndrome
Retinitis Pigmentosa 40
  • RP40

  • Retinitis Pigmentosa-40

  • Retinitis Pigmentosa, Type 40

Ohdo Syndrome, Sbbys Variant
  • Say-Barber-Biesecker-Young-Simpson Syndrome

  • SBBYSS

  • Young-Simpson Syndrome

  • Blepharophimosis-Intellectual Disability Syndrome, Sbbys Type

  • Yss

  • Sbbys Variant Of Ohdo Syndrome

  • Blepharophimosis - Intellectual Disability Syndrome, Sbbys Type

  • Young Simpson Syndrome

  • Sbbyss Syndrome

  • Ohdo Syndrome, Say-Barber-Biesecker-Young-Simpson Variant

  • Blepharophimosis And Mental Retardation Syndrome, Say-Barber/Biesecker/Young-Simpson Type

  • Blepharophimosis-Intellectual Deficit Syndrome, Say-Barber/Biesecker/Young-Simpson Type

  • Bmrs Sbbys

  • Ohdo Syndrome, Say-Barber-Biesecker Variant

  • Say-Barber-Biesecker-Young-Simpson Variant Of Ohdo Syndrome

  • Hypothyroidism-Dysmorphism-Postaxial Polydactyly-Intellectual Disability Syndrome

  • Say-Barber-Biesecker Variant Of Ohdo Syndrome

Tatton-Brown-Rahman Syndrome
  • TBRS

  • Dnmt3a Overgrowth Syndrome

  • Tatton-Brown-Rahman Overgrowth Syndrome

  • Dos

  • Dnmt3a-Related Overgrowth Syndrome

  • Doid:0112339

  • Dose

Cerebellar Ataxia, Deafness, And Narcolepsy, Autosomal Dominant
  • Autosomal Dominant Cerebellar Ataxia, Deafness And Narcolepsy

  • ADCADN

  • Autosomal Dominant Cerebellar Ataxia, Deafness, And Narcolepsy

  • Adca-Dn Syndrome

  • Autosomal Dominant Cerebellar Ataxia-Deafness-Narcolepsy Syndrome

  • Adca-Dn

  • Autosomal Dominant Cerebellar Ataxia-Hearing Loss-Narcolepsy Syndrome

  • Ataxia, Cerebellar, Deafness, And Narcolepsy, Autosomal Dominant

Ohdo Syndrome
  • Young Simpson Syndrome

  • Ohdo Blepharophimosis Syndrome

  • Blepharophimosis Syndrome Ohdo Type

  • Blepharophimosis Intellectual Disability Syndromes

  • Bmrs

  • Blepharophimosis-Intellectual Disability Syndrome

  • Mental Retardation, Congenital Heart Disease, Blepharophimosis, Blepharoptosis, And Hypoplastic Teeth

  • Sbbys Syndrome

  • Say Barber Biesecker Young-Simpson Syndrome

  • Blepharophimosis-Intellectual Disability Syndrome, Ohdo Type

  • Bmrs, Ohdo Type

  • Blepharophimosis Syndrome, Ohdo Type

  • Ohdo-Madokoro-Sonoda Syndrome

  • Blepharophimosis - Intellectual Disability Syndrome, Ohdo Type

  • Blepharophimosis - Intellectual Disability Syndrome

Yunis-Varon Syndrome
  • Cleidocranial Dysplasia With Micrognathia, Absent Thumbs, And Distal Aphalangia

  • Yunis Varon Syndrome

  • YVS

  • Cleidocranial Dysplasia-Micrognathia-Absent Thumbs Syndrome

  • Cleidocranial Dysplasia, Micrognathia, Absent Thumbs, & Distal Aphalangia

  • Yunis-Varón Syndrome

Kabuki Syndrome 1
  • Kabuki Syndrome

  • Niikawa-Kuroki Syndrome

  • Kabuki Make-Up Syndrome

  • Kms

  • KABUK1

  • Kabuki Make Up Syndrome

  • Nks

  • Kabuki Makeup Syndrome

  • Kabuki Syndrome, Type 1

Non-Syndromic X-Linked Intellectual Disability
  • X-Linked Non-Syndromic Intellectual Disability

  • Non-Specific X-Linked Mental Retardation

  • X-Linked Non-Specific Intellectual Disability

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
Bos taurus ZBTB24 VGNC VGNC:37068
Felis catus ZBTB24 VGNC VGNC:102551
Mus musculus ZBTB24 MGD MGI:3039618
Rattus norvegicus ZBTB24 RGD RGD:1306951
Canis familiaris ZBTB24 VGNC VGNC:48528
Macaca mulatta ZBTB24 VGNC VGNC:79310
Others ZBTB24 NCBI