ZMP

dmc1

Ensembl ID:

ENSDARG00000055883

ZFIN ID:

ZDB-GENE-060331-93

Description:

meiotic recombination protein DMC1/LIM15 homolog [Source:RefSeq peptide;Acc:NP_001018618]

Human Orthologue:

DMC1

Human Description:

DMC1 dosage suppressor of mck1 homolog, meiosis-specific homologous recombination (yeast) [Source:HG

Mouse Orthologue:

Dmc1

Mouse Description:

DMC1 dosage suppressor of mck1 homolog, meiosis-specific homologous recombination (yeast) Gene [Sour

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35266	Essential Splice Site	Available for shipment	Available now
sa35265	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa35266

Status:

Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Order Allele From ZIRC

Mutation:

G > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078284	Essential Splice Site	128	342	6	14
ENSDART00000078284	Essential Splice Site	128	342	6	14

Genomic Location (Zv9):

Chromosome 12 (position 20454796)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	19236640
GRCz11	12	19358514

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACTCCTTGGAGGAGGTGTGGAGAGTATGGCCATCACCGAGGCTTTTGGTG[G/A]TAGGGTGATGTTTTGATTTGAAACCATAATGATATGTTACGCATTTTCCG

Long Flanking Sequence:

TCGATCAAGGAGGTTGTAAATGTAATATGTTCTGTTCATTCATGCAGACATGCGGATTCCAGACAGCATCTGAATACTGCATCAAGAGAAAGCAAGTGTTTCACATCACAACTGGCAGTTTGGAGTTTGAGTAAGAAGCTTTATATGTCTTACATTTTTAGACACCAAATTTTATTTGTGGCTAGAATTTGTTTTTGTGTGGTGAACTGAACAATTTAAGTATAATCTACAAAACTGGCAAGGTAAATAAACTGAAATATGCAAGTTTTGGAGGACTCATTTACTCCAATAAATTGAGGCAAAGAGTTTACTTTATTCATTTAGTTCAGTCAACTTATTAAGGTTTTCAGTGTACAAGCAGTAACATGTTGTTTTATATATGTTTTCCGATGAAAGTCTTACATTGTTGACATGAAAGGAGAAACGGTTTATTCATATTTACTTTAGCAAACTCCTTGGAGGAGGTGTGGAGAGTATGGCCATCACCGAGGCTTTTGGTG[G/T]TAGGGTGATGTTTTGATTTGAAACCATAATGATATGTTACGCATTTTCCGTACATCACTTCTGCCAAAATGATATGTTTTTGTCTTTGTGAATTGTTTCCCATGCCTCATTTAGAATTCAGAACTGGAAAGACTCAGCTCTCACATACTCTGTGTGGTAAGAATGAATCTTGTGTAAATGTTAAATGCGGAATTTAATTCTCATTTTTAGACCATTCACATCATTTTGTTTTCTTTTTTTCCTTCAGTTACTGCTCAGCTTCCTGGGGAATATGGGTACACAGGAGGAAAGGTCATCTTCATTGATACCGAAAACACCTTGTATCATTTATGCATTTGCTTGCTGTGTGTGAGTGATTCATTTTACTAAATCCATTTCATATGGAGAAGTCATTCTGAACTTTTTACCTTAATAATTGTGAACATCAGTCGGCCTGAGAGGCTGAAGGACATCGCTGACAGATTCAATGTGGATCATGACGCTGTTCTGGACAATGTGCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35265

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 > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000078284	Essential Splice Site	128	342	6	14
ENSDART00000078284	Essential Splice Site	128	342	6	14

Genomic Location (Zv9):

Chromosome 12 (position 20454796)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	12	19236640
GRCz11	12	19358514

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACTCCTTGGAGGAGGTGTGGAGAGTATGGCCATCACCGAGGCTTTTGGTG[G/A]TAGGGTGATGTTTTGATTTGAAACCATAATGATATGTTACGCATTTTCCG

Long Flanking Sequence:

TCGATCAAGGAGGTTGTAAATGTAATATGTTCTGTTCATTCATGCAGACATGCGGATTCCAGACAGCATCTGAATACTGCATCAAGAGAAAGCAAGTGTTTCACATCACAACTGGCAGTTTGGAGTTTGAGTAAGAAGCTTTATATGTCTTACATTTTTAGACACCAAATTTTATTTGTGGCTAGAATTTGTTTTTGTGTGGTGAACTGAACAATTTAAGTATAATCTACAAAACTGGCAAGGTAAATAAACTGAAATATGCAAGTTTTGGAGGACTCATTTACTCCAATAAATTGAGGCAAAGAGTTTACTTTATTCATTTAGTTCAGTCAACTTATTAAGGTTTTCAGTGTACAAGCAGTAACATGTTGTTTTATATATGTTTTCCGATGAAAGTCTTACATTGTTGACATGAAAGGAGAAACGGTTTATTCATATTTACTTTAGCAAACTCCTTGGAGGAGGTGTGGAGAGTATGGCCATCACCGAGGCTTTTGGTG[G/A]TAGGGTGATGTTTTGATTTGAAACCATAATGATATGTTACGCATTTTCCGTACATCACTTCTGCCAAAATGATATGTTTTTGTCTTTGTGAATTGTTTCCCATGCCTCATTTAGAATTCAGAACTGGAAAGACTCAGCTCTCACATACTCTGTGTGGTAAGAATGAATCTTGTGTAAATGTTAAATGCGGAATTTAATTCTCATTTTTAGACCATTCACATCATTTTGTTTTCTTTTTTTCCTTCAGTTACTGCTCAGCTTCCTGGGGAATATGGGTACACAGGAGGAAAGGTCATCTTCATTGATACCGAAAACACCTTGTATCATTTATGCATTTGCTTGCTGTGTGTGAGTGATTCATTTTACTAAATCCATTTCATATGGAGAAGTCATTCTGAACTTTTTACCTTAATAATTGTGAACATCAGTCGGCCTGAGAGGCTGAAGGACATCGCTGACAGATTCAATGTGGATCATGACGCTGTTCTGGACAATGTGCT

Associated Phenotype:

Not determined