1. Gene
  2. ZBTB11 - zinc finger and BTB domain containing 11 Gene

ZBTB11 - zinc finger and BTB domain containing 11 Gene

Homo sapiens

Also known as MRT69; ZNF913; ZNF-U69274

Gene ID: 27107 | Gene type: protein coding

About ZBTB11

Cytogenetic location: 3q12.3 Genomic coordinates (GRCh38): 3:101,648,889-101,677,132 (from NCBI)

This gene has 15 transcripts (splice variants), 213 orthologues, 38 paralogues and is associated with 1 phenotype. Ubiquitous expression in bone marrow (RPKM 8.1), testis (RPKM 5.9) and 25 other tissues.

Summary

Predicted to enable DNA-binding transcription factor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in regulation of transcription, DNA-templated. Located in nucleoplasm. Implicated in autosomal recessive non-syndromic intellectual disability. [provided by Alliance of Genome Resources, Apr 2022]

ZBTB11 Products(1)

mRNA Protein Name
NM_014415.4 NP_055230.2 zinc finger and BTB domain-containing protein 11

ZBTB11 Protein Structure

BTB

BTB: BTB/POZ domain (204 - 306)

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (569 - 591)

zf-C2H2_4

zf-C2H2_4: C2H2-type zinc finger (597 - 619)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (665 - 688)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (721 - 745)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (780 - 803)

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (822 - 846)

zf-C2H2

zf-C2H2: Zinc finger, C2H2 type (859 - 880)

zf-H2C2_2

zf-H2C2_2: Zinc-finger double domain (900 - 923)

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  • 1053 a.a.
Protein Preferred Names Protein Names

zinc finger and BTB domain-containing protein 11

Related Diseases

Diseases Alias
Intellectual Developmental Disorder, Autosomal Recessive 69

MRT69

Mental Retardation, Autosomal Recessive 69

Autosomal Recessive Intellectual Developmental Disorder 69

Chromosome 3q13.31 Deletion Syndrome

3q13 Microdeletion Syndrome

Monosomy 3q13

Chromosome 3, Monosomy 3q13

Del(3)(Q13)

Syndromic Intellectual Disability
Galactosemia Iii

Galactose Epimerase Deficiency

Gale Deficiency

Udp-Galactose-4-Epimerase Deficiency

Epimerase Deficiency Galactosemia

Galactosemia Type 3

Gale-D

Uridine Diphosphate Galactose-4-Epimerase Deficiency

GALAC3

Galactosemia 3

Generalized Uridine Diphosphate Galactose-4-Epimerase Deficiency

Erythrocyte Uridine Diphosphate Galactose-4-Epimerase Deficiency

Galactosemia Type Iii

Udp-Galactose-4'-Epimerase Deficiency

Generalized Galactose Epimerase Deficiency

Generalized Gale Deficiency

Generalized Gale-D

Generalized Udp-Galactose-4-Epimerase Deficiency

Generalized Epimerase Deficiency Galactosemia

Erythrocyte Galactose Epimerase Deficiency

Erythrocyte Gale Deficiency

Erythrocyte Gale-D

Erythrocyte Udp-Galactose-4-Epimerase Deficiency

Erythrocyte Epimerase Deficiency Galactosemia

Galactosemias

Classical Galactosemia

Udpglucose 4-Epimerase Deficiency Disease

Combined Malonic And Methylmalonic Aciduria

CMAMMA

Combined Malonic And Methylmalonic Acidemia

Aciduria, Combined Malonic And Methylmalonic

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 ZBTB11 RGD RGD:1308275
Mus musculus ZBTB11 MGD MGI:2443876
Felis catus ZBTB11 VGNC VGNC:102871
Bos taurus ZBTB11 VGNC VGNC:37059
Macaca mulatta ZBTB11 VGNC VGNC:82563
Canis familiaris ZBTB11 VGNC VGNC:48521