ZMP

zgc:101017

Ensembl ID:

ENSDARG00000074451

ZFIN ID:

ZDB-GENE-040801-116

Description:

Meiotic nuclear division protein 1 homolog [Source:UniProtKB/Swiss-Prot;Acc:Q6DC61]

Human Orthologue:

MND1

Human Description:

meiotic nuclear divisions 1 homolog (S. cerevisiae) [Source:HGNC Symbol;Acc:24839]

Mouse Orthologue:

Mnd1

Mouse Description:

meiotic nuclear divisions 1 homolog (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1924165]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11730	Nonsense	Available for shipment	Available now
sa39614	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa11730

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
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000054265	Nonsense	145	220	6	8
ENSDART00000141648	Nonsense	145	205	6	8

Genomic Location (Zv9):

Chromosome 1 (position 24044923)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	24496694
GRCz11	1	25187523

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CAGCATTGAAAGGTCAGCGAGATCAGATGAAGGTCGAAAWAGAGAAGTAC[C/T]AAGAATGTGATCCAGCGGTGGTGGAGGAAATTCGTGAGTAAACTTTTCAY

Long Flanking Sequence:

GATTCAGCATAAATTGCACTATAAAATAAGTAAATTACCATAAAAATACTTTCTAAACTTTCACAAATAATGTTAAATGACAATATAATGTTAAATATATATTTCATTGATAAATCTACCATTTACTGGTGATTTGTTTCTATGAAAAAAAAAGCTTCGTAATACCATCGATCAAACAGATATTTGTTTAAAAAATAACGTGTACATTTTATTGCAGAAGTGTAATGTTTTTTTGTTTTGTTTGTGTAGCTTGAGGATGGCAGTCAGCGTAAAAAAGCCCTTCAGCAAGCAGTTGACAAAGCCAAAGTGGGACGTGAAGTCAATGTACATGTTCATCTGTCTTTCTCTCTGAGCTACATGATTATACATCTCTTATGTTTGTGGGCCTTGTGTGACTCTTGATTTTGTTGCATGTTTAGGAGGAGAGAGAGGATCTCTTAAAGGAGCTCACAGCATTGAAAGGTCAGCGAGATCAGATGAAGGTCGAAATAGAGAAGTAC[C/T]AAGAATGTGATCCAGCGGTGGTGGAGGAAATTCGTGAGTAAACTTTTCATTTGAATGTCATGGATGAATGACACTCTAAGAAATAATTTGTGTTTTTATCTGAAAACACACACACACACACACACACACACACACACACACACACACACACACACCACACACACACACACACACATTTATATATATATATATATATATATATATATATATATATATATATATATATTTTGCATTTTAACTGATTTGAATTTAAAATAAAAATGATACGTACACTTTAAAAAATCTTACGTGCTATTTACAAAAAAAATAGTGGTAACACTATTGCACGTATTATTTTTAAGTAAATTATTAACTTGATTTTTTTAAGCAAAAACCACTTGAATGAATCATGTGAAAATTACAAAAAATTTTGAGTGATAGATGCAGATTTTAATATTATTAGCGGAATGTGCTTTTATAATTTAAGCAAATCCACCACCATTTACTCATATCTATTTTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39614

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000054265	Essential Splice Site	171	220	8	8
ENSDART00000141648	None	None	205	None	8

Genomic Location (Zv9):

Chromosome 1 (position 24071268)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	1	24523039
GRCz11	1	25213868

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTTCGAAAATTCCCTCCATTCACCCCATCTCCCCTTTTCTTCCTTTACC[A/G]GGGGGAACTTTTGGGAACTACCTGATCTCATACCTCCTTACATGCTCATT

Long Flanking Sequence:

CCTATTTAGCATATAAGTAGAGAAACAGAAACTAACCAGACAGTAATGTGTCAATTGTGAACCCGGGCAAAATCACAAAAATATCGATATTGTTAAGTGAGTGTACATTGTTTTGCTTTTTTTATTCTTGCCATAATAATAAAAAAAAGTTTGTAGAGAAACCCATGTTGCCTTGTCATTAAAATTTTAATAAAGCTTAATAGGTAAAACTGTCCGAGATATGAACAAAAGCAAGTAATGCATCTAAGTTTAAAATAAATCTTGAATGGTTATAAAAATCTTTATAATCATTCAAATAATTTAAAAGTGAAATTTCACAAACTGATTTTGAGAGAAGCATGTGATATGATTGATTGTGGCTGGTCTCTCATCTATAATCATTAGTAAGCCAATCGGATCATTCCAAACTCATTATAAATAGCCTGACTAACATAACTCTCTCATCTTCTTTTTTCGAAAATTCCCTCCATTCACCCCATCTCCCCTTTTCTTCCTTTACC[A/G]GGGGGAACTTTTGGGAACTACCTGATCTCATACCTCCTTACATGCTCATTGACCAGGCAGGAGCCCTGGGCTCATCATTTATCTCCAAGCTCAGGGTTCTCTCCTGGGACAGCATGCCAAACCTGCTATTATTATCAGCAAGCAATATCCTAGTCTAAACTCAATATACTAATTAAAATAATTAGTTAAGAAATCTTCAATAATATTAATGATATGACGTAGTTCTGGAAACTTTCTACTTTTCTGGTTATCCGTCTTATTTAACGGTCAGTTTCTTTTGACCGCCCCCTGTAATTTTAAAGTATATTACAACGGCAAACGTGTCAAGTCTAAAAGCCTTGTCTGCTGTGTGGCAACAGGCGAAAGTATAAATCATCCTTGATTGGCTCTTAGATCAACATTAAGTAAAAATATCCAGAGCTTATCATAGTCATCGACATGAATTTTATTATGATTTGATATGATATCGTTTATCGGCCCAACACTAGTCTTATATTATG

Associated Phenotype:

Not determined