1. Gene
  2. ZBTB43 - zinc finger and BTB domain containing 43 Gene

ZBTB43 - zinc finger and BTB domain containing 43 Gene

Homo sapiens

Also known as ZNF-X; ZBTB22B; ZNF297B

Gene ID: 23099 | Gene type: protein coding

About ZBTB43

Cytogenetic location: 9q33.3 Genomic coordinates (GRCh38): 9:126,804,072-126,838,210 (from NCBI)

This gene has 5 transcripts (splice variants), 161 orthologues and 4 paralogues. Broad expression in bone marrow (RPKM 18.2), testis (RPKM 10.2) and 24 other tissues.

Summary

Enables sequence-specific double-stranded DNA binding activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to be part of chromatin. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

ZBTB43 Products(2)

mRNA Protein Name
NM_001135776.2 NP_001129248.1 zinc finger and BTB domain-containing protein 43
NM_014007.4 NP_054726.1 zinc finger and BTB domain-containing protein 43
Gene Ontology
  • Molecular Function
Molecular Function GO Annotation Evidence Reference Source
enables RNA polymerase III general transcription initiation factor binding IPI
IPI: Inferred from physical interaction
16542149 GOA
enables protein binding IPI
IPI: Inferred from physical interaction
16189514 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

ZBTB43 Protein Structure

BTB

BTB: BTB/POZ domain (23 - 125)

zf-C2H2_4

zf-C2H2_4: C2H2-type zinc finger (375 - 394)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (415 - 437)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 467 a.a.
Protein Preferred Names Protein Names

zinc finger and BTB domain-containing protein 43

zinc finger and BTB domain-containing protein 22B

ZBTB43 Protein-protein interaction Information

Type
Protein Name Protein ID Interactor Interactor Species Interactor ID Detection Method Reference
Intra
ZBTB43 O43298 ZNF250 Homo sapiens P15622-3 32296183
Intra
ZBTB43 O43298 DIP2A Homo sapiens Q14689-6 25416956
Intra
ZBTB43 O43298 SYT6 Homo sapiens Q5T7P8-2 25416956
Intra
ZBTB43 O43298 SYT6 Homo sapiens Q5T7P8-2 32296183
Intra
ZBTB43 O43298 MORF4L1 Homo sapiens Q9UBU8-2 32296183
Intra
ZBTB43 O43298 CIB3 Homo sapiens Q96Q77 32296183
Intra
ZBTB43 O43298 CCDC13 Homo sapiens Q8IYE1 32296183
Intra
ZBTB43 O43298 LMO3 Homo sapiens Q8TAP4-4 32296183
Intra
ZBTB43 O43298 LMO4 Homo sapiens P61968 25416956
Intra
ZBTB43 O43298 DDX6 Homo sapiens P26196 32296183
Intra
ZBTB43 O43298 PSMD3 Homo sapiens O43242 25416956
Intra
ZBTB43 O43298 PSMD3 Homo sapiens O43242 25416956
Intra
ZBTB43 O43298 CDKL3 Homo sapiens Q8IVW4 32296183
Intra
ZBTB43 O43298 MORF4L2 Homo sapiens Q15014 25416956
Intra
ZBTB43 O43298 AP1M1 Homo sapiens Q9BXS5 25416956
Intra
ZBTB43 O43298 AP1M1 Homo sapiens Q9BXS5 32296183
Intra
ZBTB43 O43298 AP1M1 Homo sapiens Q9BXS5 25416956
Intra
ZBTB43 O43298 ZNF587 Homo sapiens Q96SQ5 32296183
Intra
ZBTB43 O43298 TCEA2 Homo sapiens Q15560 32296183
Intra
ZBTB43 O43298 ARR3 Homo sapiens P36575 25416956
Intra
ZBTB43 O43298 FAM161A Homo sapiens Q3B820 25416956
Intra
ZBTB43 O43298 FAM161A Homo sapiens Q3B820 25416956
Intra
ZBTB43 O43298 LNX1 Homo sapiens Q8TBB1 32296183
Intra
ZBTB43 O43298 LNX1 Homo sapiens Q8TBB1 29892012
Intra
ZBTB43 O43298 LNX1 Homo sapiens Q8TBB1 16189514
Intra
ZBTB43 O43298 LNX1 Homo sapiens Q8TBB1 32296183
Intra
ZBTB43 O43298 ZNF417 Homo sapiens Q8TAU3 16189514
Intra
ZBTB43 O43298 ZNF417 Homo sapiens Q8TAU3 32296183
Intra
ZBTB43 O43298 ARRB1 Homo sapiens P49407 32296183
Intra
ZBTB43 O43298 ZBTB24 Homo sapiens O43167 25416956
Intra
ZBTB43 O43298 ZBTB24 Homo sapiens O43167 25416956
Intra
ZBTB43 O43298 LMO1 Homo sapiens P25800 25416956
Intra
ZBTB43 O43298 LMO1 Homo sapiens P25800 25416956
Intra
ZBTB43 O43298 LMO1 Homo sapiens P25800 32296183
Intra
ZBTB43 O43298 LMO1 Homo sapiens P25800 25416956
Intra
ZBTB43 O43298 ATXN1 Homo sapiens P54253 32814053
Intra
ZBTB43 O43298 ATXN1 Homo sapiens P54253 32814053
Intra
ZBTB43 O43298 ATXN1 Homo sapiens P54253 32814053
Cross: Cross-species interaction Intra: Intraspecies interaction

Related Diseases

Diseases Alias
Diamond-Blackfan Anemia 4

DBA4

Rps17-Related Diamond-Blackfan Anemia

Anemia, Diamond-Blackfan, Type 4

Spastic Paraplegia 16, X-Linked

SPG16

Hereditary Spastic Paraplegia 16

X-Linked Spastic Paraplegia Type 16

Spastic Paraplegia 16, X-Linked, Complicated

X-Linked Spastic Paraplegia 16

Spastic Paraplegia 16

Spastic Paraplegia-16, X-Linked, Complicated

Spastic Paraplegia 12, Autosomal Dominant

SPG12

Hereditary Spastic Paraplegia 12

Autosomal Dominant Spastic Paraplegia Type 12

Autosomal Dominant Spastic Paraplegia 12

Spastic Paraplegia 12

Spastic Paraplegia-12

Paraplegia, Spastic, Autosomal Dominant, Type 12

Hemochromatosis Type 2

Juvenile Hemochromatosis

Juvenile Hereditary Hemochromatosis

Hfe2

Jhh

Hemochromatosis Juvenile

Iron Overload Disease Juvenile

Hemochromatosis, Juvenile

Hemochromatosis, Type 2

Hemochromatosis

Hemochromatosis, Type 1

Hereditary Spastic Paraplegia 56

Autosomal Recessive Spastic Paraplegia Type 56

Spg56

Autosomal Recessive Spastic Paraplegia 56

Masa Syndrome

L1 Syndrome

Crash Syndrome

X-Linked Hydrocephalus Syndrome

SPG1

Gareis-Mason Syndrome

Spastic Paraplegia 1, X-Linked

Corpus Callosum Hypoplasia-Retardation-Adducted Thumbs-Spasticity-Hydrocephalus Syndrome

L1cam Syndrome

Spastic Paraplegia 1

Mental Retardation, Aphasia, Shuffling Gait, And Adducted Thumbs

Clasped Thumb And Mental Retardation

Thumb, Congenital Clasped, With Mental Retardation

Adducted Thumb With Mental Retardation

Hereditary Spastic Paraplegia 1

X-Linked Complicated Hereditary Spastic Paraplegia Type 1

X-Linked Corpus Callosum Agenesis

X-Linked Spastic Paraplegia 1

L1 Disease

X-Linked Intellectual Disability - Corpus Callosum Agenesis - Spastic Quadriparesis

Adducted Thumb With Intellectual Disability

Clasped Thumb And Intellectual Disability

Intellectual Disability Aphasia Shuffling Gait Adducted Thumbs

Thumb Congenital Clasped With Intellectual Disability

X-Linked Intellectual Disability-Corpus Callosum Agenesis-Spastic Quadriparesis Syndrome

Adducted Thumbs-Mental Retardation Syndrome

Corpus Callosum Hypoplasia, Mental Retardation, Adducted Thumbs, Spastic Paraplegia, Hydrocephalus Syndrome

Mental Retardation-Clasped Thumb Syndrome

Intellectual Disability-Aphasia-Shuffling Gait-Adducted Thumbs Syndrome

Spastic Paraplegia Type 1, X-Linked

MASA

Corpus Callosum Hypoplasia-Psychomotor Retardation, Adducted Thumbs-Spastic Paraparesis-Hydrocephalus

Crash

Masa Syndrome

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 ZBTB43 VGNC VGNC:37082
Mus musculus ZBTB43 MGD MGI:1919084
Rattus norvegicus ZBTB43 RGD RGD:1310287
Felis catus ZBTB43 VGNC VGNC:67171
Macaca mulatta ZBTB43 VGNC VGNC:79101