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  2. MYPOP - Myb related transcription factor, partner of profilin Gene

MYPOP - Myb related transcription factor, partner of profilin Gene

Homo sapiens

Also known as P42pop

Gene ID: 339344 | Gene type: protein coding

About MYPOP

Cytogenetic location: 19q13.32 Genomic coordinates (GRCh38): 19:45,890,023-45,902,613 (from NCBI)

This gene has 1 transcript (splice variant) and 93 orthologues. Ubiquitous expression in brain (RPKM 2.5), spleen (RPKM 2.4) and 25 other tissues.

Summary

Predicted to enable DNA-binding transcription repressor activity, RNA polymerase II-specific and RNA polymerase II cis-regulatory region sequence-specific DNA binding activity. Predicted to be involved in negative regulation of transcription by RNA polymerase II. Predicted to be active in nucleus. [provided by Alliance of Genome Resources, Apr 2022]

MYPOP Products(1)

mRNA Protein Name
NM_001012643.4 NP_001012661.1 myb-related transcription factor, partner of profilin

MYPOP Protein Structure

Myb_DNA-bind_5

Myb_DNA-bind_5: Myb/SANT-like DNA-binding domain (16 - 92)

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  • 399 a.a.
Protein Preferred Names Protein Names

myb-related transcription factor, partner of profilin

myb-related protein p42POP

Related Diseases

Diseases Alias
Myopathy, Centronuclear, 1

Autosomal Dominant Centronuclear Myopathy

CNM1

Centronuclear Myopathy 1

Ad-Cnm

Myopathy, Centronuclear, Autosomal Dominant

Myotubular Myopathy, Autosomal Dominant

Centronuclear Myopathy, Autosomal, Modifier Of

Autosomal Dominant Myotubular Myopathy

Dnm2-Related Centronuclear Myopathy

Centronuclear Myopathy Autosomal Dominant

Myopathies, Structural, Congenital

Myopathy, Centronuclear, Type 1

Neuronopathy, Distal Hereditary Motor, Type Iia

HMN2A

Hmn Iia

Neuropathy, Distal Hereditary Motor, Type Iia

Dhmn2a

Distal Hereditary Motor Neuronopathy Type 2a

Distal Hereditary Motor Neuropathy Type Iia

Neuronopathy, Distal Hereditary Motor, Type 2a

Spinal Muscular Atrophy, Distal, Adult, Autosomal Dominant, Iia

Charcot-Marie-Tooth Disease, Spinal, Iia

Autosomal Dominant Adult Spinal Muscular Atrophy Iia

Spinal Charcot-Marie-Tooth Disease Iia

Neuronopathy, Distal Hereditary Motor, 2a

Charcot-Marie-Tooth Disease Spinal Iia

Spinal Muscular Atrophy Distal Adult Autosomal Dominant Iia

Neuropathy, Motor, Distal, Hereditary, Type 2a

Nemaline Myopathy 11, Autosomal Recessive

NEM11

Nemaline Myopathy 11

Nemaline Myopathy 10

NEM10

Myopathy, Nemaline, Type 10

Carey-Fineman-Ziter Syndrome 1

Carey-Fineman-Ziter Syndrome

CFZS

Congenital Nonprogressive Myopathy With Moebius And Robin Sequences

Myopathy, Congenital Nonprogressive, With Moebius Sequence And Robin Sequence

Cfz Syndrome

Carey Fineman Ziter Syndrome

Myopathy, Congenital Nonprogressive With Moebius And Robin Sequences

Myopathy-Moebius-Robin Syndrome

CFZS1

Moebius Sequence, Robin Complex, And Hypotonia

Congenital Non-Progressive Myopathy With Moebius And Robin Sequences

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
Mus musculus MYPOP MGD MGI:2446472
Canis familiaris MYPOP VGNC VGNC:43587
Bos taurus MYPOP VGNC VGNC:58393
Rattus norvegicus MYPOP RGD RGD:1565160