ZMP

zgc:123296

Ensembl ID:

ENSDARG00000040387

ZFIN ID:

ZDB-GENE-051120-39

Description:

monocyte to macrophage differentiation protein [Source:RefSeq peptide;Acc:NP_001032496]

Human Orthologue:

MMD

Human Description:

monocyte to macrophage differentiation-associated [Source:HGNC Symbol;Acc:7153]

Mouse Orthologue:

Mmd

Mouse Description:

monocyte to macrophage differentiation-associated Gene [Source:MGI Symbol;Acc:MGI:1914718]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6879	Nonsense	Mutation detected in F1 DNA	Not yet available
sa40005	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa6879

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000059117	Nonsense	133	239	5	7

Genomic Location (Zv9):

Chromosome 3 (position 11816309)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	11598007
GRCz11	3	11564550

KASP Assay ID:

554-4861.1 (used for ordering genotyping assays)

KASP Sequence:

AATCTCCGGGAACTCGGGCCRCTYGCCGCTCACATGCGCTGGTTTGTGTG[G/A]TTGATGGCGGCTGCCGGAACAATCTATGTGTTTAATTACCAYGAAAAGTA

Long Flanking Sequence:

TTTCATGAGTTTCGAGTGACTGAAGCGGCCGCAGCTTTTGGTCACTTTCCTATGAGAGCGTGAATAATTCAGTGTTCTTGAGCGCTTCGCTAGAGAACTGAAGTGGGATTTAACTCCAGTTACTGAGCATCTTTATTTATCAGCGGTCACTTAACAGACCATCCATTATACATTAGATTTAAGATTATTAAGAAATACAAACACCAATTCAAATTATGAACAGAACTCGAACAACAGAAAACAATAGCACAAAATCCTAGTTTGTTTGTACTAGTTAGGCTTTTGCCATTTGTTTTCTGTTGTTCAAGTCTTGTTTATATATTAAATCTGTAATTGAATTGGTTTATTACAAAGGGACTAGCATAGTAAACTAGTCTTTGGGCTAATTTATGTGACATCTTTCTCTGTGACTCTCACTACGTTTTTTTGTGTGTGTTTGTGTGCAGGTTGAATCTCCGGGAACTCGGGCCGCTTGCCGCTCACATGCGCTGGTTTGTGTG[G/A]TTGATGGCGGCTGCCGGAACAATCTATGTGTTTAATTACCACGAAAAGTATGTTGGACATCACCTAAATATCTAATTCAGACATCATATTTTAATTATTGGCCAGGATTGATGATGGACAGCAGGGAAATAGGGTATTGAATATGTCCCAATTTTTCTCAGGAAACATATTTATAAACATGCCGTTGACTTGGAGTTTAGATCAGATGTTGATAACAACCAAAGCAATCCGTACATGCAAAGAAAATAAATCTAATTAGTATTAAAGTTATGCTTGATAAAAATGAAATGGCTCTGGGAAAAAGTGTTGAACATATGAAGAAAGGGAGGTATAGAAAGCAGTGAAAGCCCAGACAGCAGCTGAAACCTCTCAGTAGTTCTTCAGGAACCCTCTGCCCTTCCTCCTTGTAAATGAAAATGAATATCAGCTGCTTCTGTCCAACATCAACATTCTCAGGATGATGAAGATGAAACTAGAGTGGACATTTCAGCAAGACAATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40005

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000059117	Essential Splice Site	149	239	5	7

Genomic Location (Zv9):

Chromosome 3 (position 11816358)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	3	11598056
GRCz11	3	11564599

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGTTGATGGCGGCTGCCGGAACAATCTATGTGTTTAATTACCACGAAAAG[T/G]ATGTTGGACATCACCTAAATATCTAATTCAGACATCATATTTTAATTATT

Long Flanking Sequence:

CTATGAGAGCGTGAATAATTCAGTGTTCTTGAGCGCTTCGCTAGAGAACTGAAGTGGGATTTAACTCCAGTTACTGAGCATCTTTATTTATCAGCGGTCACTTAACAGACCATCCATTATACATTAGATTTAAGATTATTAAGAAATACAAACACCAATTCAAATTATGAACAGAACTCGAACAACAGAAAACAATAGCACAAAATCCTAGTTTGTTTGTACTAGTTAGGCTTTTGCCATTTGTTTTCTGTTGTTCAAGTCTTGTTTATATATTAAATCTGTAATTGAATTGGTTTATTACAAAGGGACTAGCATAGTAAACTAGTCTTTGGGCTAATTTATGTGACATCTTTCTCTGTGACTCTCACTACGTTTTTTTGTGTGTGTTTGTGTGCAGGTTGAATCTCCGGGAACTCGGGCCGCTTGCCGCTCACATGCGCTGGTTTGTGTGGTTGATGGCGGCTGCCGGAACAATCTATGTGTTTAATTACCACGAAAAG[T/G]ATGTTGGACATCACCTAAATATCTAATTCAGACATCATATTTTAATTATTGGCCAGGATTGATGATGGACAGCAGGGAAATAGGGTATTGAATATGTCCCAATTTTTCTCAGGAAACATATTTATAAACATGCCGTTGACTTGGAGTTTAGATCAGATGTTGATAACAACCAAAGCAATCCGTACATGCAAAGAAAATAAATCTAATTAGTATTAAAGTTATGCTTGATAAAAATGAAATGGCTCTGGGAAAAAGTGTTGAACATATGAAGAAAGGGAGGTATAGAAAGCAGTGAAAGCCCAGACAGCAGCTGAAACCTCTCAGTAGTTCTTCAGGAACCCTCTGCCCTTCCTCCTTGTAAATGAAAATGAATATCAGCTGCTTCTGTCCAACATCAACATTCTCAGGATGATGAAGATGAAACTAGAGTGGACATTTCAGCAAGACAATGATTTAAAGCACAGCCAAGGAAACATTTAGGCACTAGGTTAGGAAAAGTG

Associated Phenotype:

Not determined