ZMP

dmtf1

Ensembl ID:

ENSDARG00000025824

ZFIN ID:

ZDB-GENE-040718-413

Description:

Cyclin-D-binding Myb-like transcription factor 1 [Source:UniProtKB/Swiss-Prot;Acc:Q6DG03]

Human Orthologue:

DMTF1

Human Description:

cyclin D binding myb-like transcription factor 1 [Source:HGNC Symbol;Acc:14603]

Mouse Orthologues:

4932411N23Rik, Dmtf1

Mouse Descriptions:

RIKEN cDNA 4932411N23 gene Gene [Source:MGI Symbol;Acc:MGI:3045322]
cyclin D binding myb-like transcription factor 1 Gene [Source:MGI Symbol;Acc:MGI:1344415]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa33393	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa40225	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa33393

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000029084	Essential Splice Site	220	645	7	17
ENSDART00000133214	Essential Splice Site	220	590	7	16

Genomic Location (Zv9):

Chromosome 4 (position 8723617)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	9660465
GRCz11	4	9661381

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATACAGACGTGTGTTGCGAATGTACGATAACCGCAACCACGTAGGCAAG[T/C]AAGGACGTAGCTGCTTTTGTTTGTTAGTTCAACAGATTTACACCCCATTT

Long Flanking Sequence:

ACTGGTCAATAAGGGTGAGTATTAAATAATCAGCATATTAAATTATATTCAGAAAATATTCAATATTCAGTATTTAATACACAACTCTCATTGCCCTAATATATGATAATGGCACAATCTGATAAAACCCAATATATTAAATTTACATCAGATAGTCAGGATATCTGTCATATATATACTCAGGTCACAAATGGAAACAGGGTATGTGGTCAAAAGAAGAGATTGATCTCCTGATGACCAACATAGAGCTTTATCTAAAGGTGAGCATGCTTTATCACATTGCAGCGTCTTTCAGTGTCTTGCATTCCTCATTCTTCATCTGTCTGTTCATTTGAACTCAGAACCGAGGGATTCAAGACCCTGCGGAGATCATCTTCGAGATGTCCAAAGAGGAGAGAAAGGATTTTTACCGCAGTATAGCCTGTGGTTTGAACAGGCCGCTGTTTGCTGTATACAGACGTGTGTTGCGAATGTACGATAACCGCAACCACGTAGGCAAG[T/C]AAGGACGTAGCTGCTTTTGTTTGTTAGTTCAACAGATTTACACCCCATTTGGAAGTGTTTATGTTGCAAAAACTAAATCGTGTTGTGTTGCTTTTTTGTCGTTTAGATACACTGATGAGGAGATCAATAAACTGAAAGAGTAAGTTTAGTTTTAGTTCTGAATGGCGTTGAAATGTGATCTGAATTTGTGTGAGTCTGCATTGACTAAACTTGTGTGTGTTATTAGACTAAGGCAGAAACATGGAAATGACTGGGCCACCATTGGGTCAGCTCTTGGCCGCAGCGCATCGTCTGTAAAGGATCGCTGCAGACTCATGAAAGACACATGCAACACCGGTCAGCTTTGCTACTCTTTTGATTTATTATCATTTTATTACACTTGTGTACAGTAGTCAACATTTGAAGTGGATCAAAGATTTATTTTCCGAATCATTCTAAGACAGAATGGGTGTTGTTTACTAGTTTTAGGACAGCTTAGAAACACTTTTGATGACACTGAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40225

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000029084	Essential Splice Site	445	645	12	17
ENSDART00000133214	None	None	590	None	16

Genomic Location (Zv9):

Chromosome 4 (position 8720909)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	4	9657757
GRCz11	4	9658673

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CACCGCTCTGCAGATCCCGGTCCAGATCCCAGTGCAGATCACACACGTCT[G/T]TGAGTGTATATATATATATAAAAGGAGCTTTTGTGACTGTTGTTTCAGTG

Long Flanking Sequence:

CAATGCCTGTATTTAAATTTACATTTTAAGCAATTATCGGCCGATTTTTGCGGGTACTTTACAGCTTTATAACTGTAACTGATTAATTTTGATTTATTAATCATAACTGTATATGATCAGGATAGCAGAGCTGGAAGTGGAGGATGAAAATGAGATCAACTGGGATATTCTGGCTAGTGGATGGAGCAGCGTTCGCTCGCCCCAGTGGCTGCGGAGCAAATGGTGGACCATCAAAAGACAAGTGGCCAATCACAAGGAACTTCCCTTTCCTGGTGAGACCTCATAGGTGAGCATGCGTTCAGTGTGCTGTGAGTGCAGATGCTGAAGTAAGTTTTCTGTGTGTTTAGTGTTGCTGAAAGGGCTGCAGGATGTTGTGGAGGCACCGCCGTCTACCATGAACAAGGTGGTGGTGGTCGGTTCAAGATCTGCTAATGCTTCGCCCAGTCCTGTCACCGCTCTGCAGATCCCGGTCCAGATCCCAGTGCAGATCACACACGTCT[G/T]TGAGTGTATATATATATATAAAAGGAGCTTTTGTGACTGTTGTTTCAGTGGATAGCTTCAATAATCTTGAAGTTTTATCAATTTAATTGTAATAAATTTATCCAATAAGCAAACAGTTATTTTAAAGTGGAATTTAGTGGAATATGAAAATAAATATTTAATTAAATGATTTATTTTACCAATTCTAGTTTTTTTTTTTGTAAATAAAATGTTAAATGAGCAACTTTTTCGATATAATATTAATTATATTATGTAAAATAGTGTAAATCTTTAGAGTTGTCATACAGAAATCTGACATATGGCCATATATGAGCATTAAATTTCTGAATGGGTAGAAAGATCAGTGCTAGATGATTTATGATGGTTATGTAAGTTTAATAGATGCAGTTTGTCTCTTTAATTGCACTTTTCCTCTTTCTACAGCTTCTTCAGATGGTTCGAGTGGTACTTCAGACAGTGAAACGATCACATTGAACTCCGGAGCTTTACAGACCTTTGAA

Associated Phenotype:

Not determined