ZMP

LOC100333576

Ensembl ID:

ENSDARG00000074326

Human Orthologue:

MCM8

Human Description:

minichromosome maintenance complex component 8 [Source:HGNC Symbol;Acc:16147]

Mouse Orthologue:

Mcm8

Mouse Description:

minichromosome maintenance deficient 8 (S. cerevisiae) Gene [Source:MGI Symbol;Acc:MGI:1913884]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa10066	Nonsense	Available for shipment	Available now
sa36290	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa10066

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
ENSDART00000114691	Nonsense	113	852	3	18

Genomic Location (Zv9):

Chromosome 17 (position 4098953)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	4173786
GRCz11	17	4331911

KASP Assay ID:

2261-0509.1 (used for ordering genotyping assays)

KASP Sequence:

CAGGTTTTGTTGAAAGTTCACCTTATGTTGAGAAAATAAAGGTGTTTGAG[C/T]AGTACTTCACATCACAGATCGATCTTTATGATAAGGTATTTAAAAGGCTT

Long Flanking Sequence:

GATGCTGGGCAGCCAGCAAACAGCGCGTTACAGTAATCCAGCCTAGAAGTCATAAAAGCATAGACTAGCATAAAAGCATTACATCGCTTTGTAAACATTTATTATTACTATTTGTTGAGTCTCCCCATACAGTTTTATAGAGCGCTTGAACCCGGAAACCGATTCGTGTGACGTCACACTTAACAAGCAGATAGCGCATGTGTTTGGACTGTTGGGGAAACCGGAGCAACCGGAGGAAACCCACGCCAACACGGGGAGAACATGCAAACTCCACACAGAAATGCCAACTGACCCAGCCGGGACTCAAACCAGTGACTTTTTTGCAGCGAGGCCACAGTGATAACCACTGAGCCACCAAGCCACCTTTCATTTTCATCGAGTTAAAAATATATATTCTTAACCTGGCATATGTGACTTAATTTTTTGTGTGACTTGCATCTGCTCCTTTTCCAGGTTTTGTTGAAAGTTCACCTTATGTTGAGAAAATAAAGGTGTTTGAG[C/T]AGTACTTCACATCACAGATCGATCTTTATGATAAGGTATTTAAAAGGCTTTTCTGTATATTTCTAGGATTCTTCATTTAGCATCAACATATACATTTTTCTTGTTGCTTATTCTCTTAGGATGAGATTGAAAGGAAAGGCAGCATTCTGGTGGACTACAAAGACCTTCTGTCCAACAAACAGGTTTCACACTCCCTACCGGATCTGGCCAGAGATCTTAAGGAAATGCCAGAGAAAATTCTAGACTGCTTGGGTGTAGCAATTCATCAGGTGGGTTTTGGGTTGTGTTTTGCAAGGTTGTTTTAGTAAACGAAGACTAAAACTATTGGCCAAAAAACAAATTATTGGTAAATAAATAAAAATAAATAAAATAAAAAGTCGCAATAAATATGGATATAACTGGGCGGCACGGTGGCCCAGTGGTTAGCACTGTCACCTCACAGCAGGAAGTTAGCTGGTTCGAGTCCCTGCTGGGTCAGTTGGCATTTCTGTGTGAAGTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36290

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000114691	Nonsense	447	852	11	18

Genomic Location (Zv9):

Chromosome 17 (position 4113354)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	4188189
GRCz11	17	4346314

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CTTGTTAAAGCTGGGTTGGCTCTGGCTCTGTTTGGAGGATGTCAGAAGTA[T/A]GTTGATGATAAAAACCGTATCCCGATAAGAGGAGACCCGCATATGCTCAT

Long Flanking Sequence:

TCCATATAACTCCAAAGCCAGAAACTAAGCTTTTTTTTTTTTTTTGCAAAGCAACTGATGATCAACAACAAAAAATGTACCTCTTCCTAACAAGGAAAACCACTAACAACAAAGAATACATAATAATATGGCGTATTAGCTTTGGAATTAAAAAATATGGTTATAATAGAAGTCAATAGGGCAAAAACAGCCCCCAACATAATAAAGGGGTAGTCAGTTTGTTTATTTATTTTTTTAATTTGCGAAGCATTTTCCCAAAATTTATGTCATAATAAGATTTGTCAGCAAAAATCATTCCATTTGTTGAAATGCAGAGAAAGTTGTGGCCAAATTAAGCCTCAAAATCCGCCAGAGTCGAGGACAGCATGCCTAACAGCACGCAAGGGTTAATAAATGAATGGTAAAGCTATAAAATGGTTGGACTTATTTGGGTTTGTTTGTTTTTCTCAGCTTGTTAAAGCTGGGTTGGCTCTGGCTCTGTTTGGAGGATGTCAGAAGTA[T/A]GTTGATGATAAAAACCGTATCCCGATAAGAGGAGACCCGCATATGCTCATCGTTGGAGACCCTGGACTTGGCAAAAGTCAGATGTTACAGGTACATGACCTTGTAAACCTCCTCTATTGCATGCATTACCTTGATGATTGTGTGTGTGTTTTTTAAATCTTTAATGCTGTTGTATTTGTGTTAATCCAGGCTGTGTGTAACGTGGCCCCACGGGGTGTTTACGTATGTGGAAACACAACCACCACCTCAGGACTGACTGTTTCTCTATCCCGGGACAGCGGATCCGGAGACTACGCTCTTGAGGCTGGAGCATTGGTGCTGGGAGATCAAGGTATTTAAAACAAAGTCCATTTTTTGGGTATTAAAGGTTCTGAATTATGGGGTCCATATCTGTTGGTAAATTATCCGCTGTCGAGGGAAACTTTCCTCAATGTCTAGACCTAAAATCTGCTTATCTTAAGGCCAGTATACACCAAGCTGACACCAAACAATTGGTGCTG

Associated Phenotype:

Not determined