ZMP

mark2

Ensembl ID:

ENSDARG00000032458

ZFIN ID:

ZDB-GENE-080215-4

Human Orthologue:

MARK2

Human Description:

MAP/microtubule affinity-regulating kinase 2 [Source:HGNC Symbol;Acc:3332]

Mouse Orthologue:

Mark2

Mouse Description:

MAP/microtubule affinity-regulating kinase 2 Gene [Source:MGI Symbol;Acc:MGI:99638]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa9740	Nonsense	Available for shipment	Available now
sa34062	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa9740

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
Order Allele From EZRC

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000005329	Nonsense	164	788	7	19

Genomic Location (Zv9):

Chromosome 7 (position 26104507)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	24666259
GRCz11	7	24937416

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ACCTTCTCTYTTTATCTCTCCAGATTGTCTCAGCTGTGCAGTATTGCCAT[C/T]AGAAGTGTATTGTACACCGAGATCTCAAGGTGAGAATTTGTTTCTGTGTG

Long Flanking Sequence:

ATGCATTGAGTTGCTGCCATTTGATTGGTTTAGAAATTTGCGTTAAGGAGCAGTTGGACAGGTGTACCTAATAAAGTGGCTGGTGAGTGTATATGTATATATAAATTACTTTGGTTTTTAACATAACTCAAGTTAAATACATTCTAAATATAAAATTCAAAAGAAGGATCACATGAACCTGAAAAACTGAGACATGTCAATTTTATATTTTAGATATTTTTGTAATGTATTAAATGCTAAACTTTTTTAAGCATATACAATTTGGAACAGTATTTGTGTGTGACAGGTGGTGTTCAGTTGTTCTTTGCAATTAGGAGTGTGTCTCTAACTCTGCTGAGTGAACATGTGTGTGTATGATGGCTTAATTACTGATAGAACAGCTCAATTAAAGAGGCACAACTCCCATGAGCTGCCGAAATTACTTCACCTACTCCTCTGATTACTCACCACACCTTCTCTCTTTATCTCTCCAGATTGTCTCAGCTGTGCAGTATTGCCAT[C/T]AGAAGTGTATTGTACACCGAGATCTCAAGGTGAGAATTTGTTTCTGTGTGTGTGTTTGTGAGGCTCTATTCAGCTATACAGTCACCTTTCAGATGGTCTTTAGTAGCCCTTCTGTGTCTGTCATCAATGTCCATTACAGATGTCCAGGTGAAGGAATGAGTCCTCTGTTCAAACAAACACACACACACACACATGCTATCCTGAGCTCTGAACTCTGAAACTGCTGACCTCAGATCCTGTCCATGTTCAGATGAAAGGAAGTGTCTTTCTGGATGAACTGTTCCCTTCATAACTGAAGTTGCTTATTGGTCTAAACCATCATCACAGTGAGCCTTGAACCTTGTAGTCAGTCATTCAGAACATTTGCATGGACAACAGCATTCTGATATTATCACATTTAAGCCAATACTCTGATTACGAATCAGCCGTGTAAACAGGCTACTCTAAGTGTAAACAAAGAAATATTGATATTTTAGGGTGTTTTCACACCTGTAGTTCGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34062

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
ENSDART00000005329	Essential Splice Site	174	788	8	19

Genomic Location (Zv9):

Chromosome 7 (position 26111114)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	24672866
GRCz11	7	24944023

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCTCTTTTTTTGGCAGCGCATGTCTTCATTTTGTCCTCTTTTCCCCCTT[A/G]GGCTGAAAATCTTTTATTGGATGCTGACATGAACATAAAGATCGCTGACT

Long Flanking Sequence:

CATATTTCAATCAGCCACTGAGTGAACATACAAATTAGCTATATTAAGAACAACAAAGCTAAATTGAAGAGTTTAAAGTAGAAGGACAATATAATTGCAGCTTAACGAGGCATGTATGTTGCCCCCATGCCTTATTCATCCCTTTCTTTGTTGCTGTGTGTTTGCGTGTTGTAAAAGTTTGGCTTTATTGGCAGAGTAATATTTAACTCAGCAAAACGAGCCCAGTTAGCACCCGCTTCTGTTGCTAGGAAACACGGCCTCCCTGTGCGGCTAAAGTTAGTGTGTAGATGTTGAGTGGCAGCACAGAGGGCAAGTGTCTACACACACGCATAATAGCATGAGTGAACTAGTTAGGAAGATTTGGACAAACACATTGAAGGAAGAGAAACAACATTTCTAGCTGTTGCTGACTGAAATATGAACCTGTAGCTGCTTTTCATGTCAGATGCAATCTCTTTTTTTGGCAGCGCATGTCTTCATTTTGTCCTCTTTTCCCCCTT[A/G]GGCTGAAAATCTTTTATTGGATGCTGACATGAACATAAAGATCGCTGACTTTGGCTTCAGTAATGAGTTTACGGTGGGCAATAAATTGGACACGTTTTGCGGTAGCCCACCGTATGCAGCCCCTGAGCTCTTCCAGGGCAAGAAGTATGACGGGCCAGAGGTGGATGTGTGGAGTCTGGGTGTCATTCTCTACACACTGGTCAGTGGCTCGCTGCCATTTGACGGGCAGAACCTGAAGGTGAAGGATACCAAATGTCTTAAAGGAATAGTTCACCCAATAATGAAAATCATCATTTATTCACTCTTTATTTTTTCCAAACCTGTTTGAGTTTCTTTTTTCTGTTTAATACAAAAAAGATATTCTGAAGAATGTTGGAATGGAAACTGTTAGCCATTGACTTCCATAATATACATTTTTTTCTATGGAATTTAGTAGCTATCAGTTTCCAACGGAACAGGAAAAGTAACTTATTAAGGTTTGGAGCCTTCATTTTAGAATG

Associated Phenotype:

Not determined