ZMP

AKAP9 (2 of 2)

Ensembl ID:

ENSDARG00000077668

Description:

A kinase (PRKA) anchor protein (yotiao) 9 [Source:HGNC Symbol;Acc:379]

Human Orthologue:

AKAP9

Human Description:

A kinase (PRKA) anchor protein (yotiao) 9 [Source:HGNC Symbol;Acc:379]

Mouse Orthologue:

Akap9

Mouse Description:

A kinase (PRKA) anchor protein (yotiao) 9 Gene [Source:MGI Symbol;Acc:MGI:2178217]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa30706	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa32225	Splice Site, Nonsense	Mutation detected in F1 DNA	Not yet available
sa29111	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa30706

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 > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113138	Essential Splice Site	45	467	2	10

Genomic Location (Zv9):

Chromosome 19 (position 497055)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	518047
GRCz11	19	517866

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGATTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAC[A/T]GAGAGAGCAGGAGCTGCAGCAGATGAAGGACAGAGAAGACGACACTGAGA

Long Flanking Sequence:

TAAATGAGACATATTTCAGAATAAATTCCTTATTTTAATTTTAATGAATTTTAATGAAAAATATTAATAATTGAAAAATGTAATGTAATAATGTTCATTTAAATTAATTTAATTTTAAATGAGGTGTTTTAGTTTTTTTGTTTTCGTCATTATTTTGCTTAATATAAATGACATTTTGATTTTAAAATAAATCAATTTGCTTTTTAAATTTGATATTTAAAAACTCTGATATTGATTAGATTTTAATTTTATTTTTTTATAATAAATTTTTACTGTTTTAAAAAGTTTTAATATGAGTTTTCAACATTTGTTAATGCAATATACAAGATTCCAATGCCGTCTCATGTTTGTGATGATGTTTGCTGTGCTTCAGCGGCTGGATCAGCTCTGCATGGCTTTACTGTATGGACTTCACCGCTTCACTCTTCAGTTAAAGCTTCATCTGACTCTTGATTCTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAAC[A/T]GAGAGAGCAGGAGCTGCAGCAGATGAAGGACAGAGAAGACGACACTGAGAAACAACATCTGTTTCCTCACATGCAGAGCTGCAGCACACAGACACAGCAGGTAAACAGTGTGTGAATTATACCTTGACTGAAATATTTCTTCATTAACGTTACTCTGGAATACATGTTAATATTTCATTCAATTACATCTCATTTTTTTAAGTTGAGTTATTTTTTATTTTTTTATTTAAGTTTTGAGGGGTATCGAGTGTATCGACAGTATCCTCTGATTGGCTGTTTCAGCAGTTGTCTAATTATCAAAGATGGCCTACTTTTCTTGTGAAACAACTTATCAATAAATTCATTACCATTTAAATATTGCACTTATCATTTAATTGTTTAAGTTAACTTTCAGTTTGCCAGCAGATGTCTGTAAAATGCAAACTATGTTTGATTTATCTTTGATATTTATAATCTGTTATTAACAGACAGTGATTTTGGGCTCCCCTGCACTACTTAGG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa32225

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:

C > T

Consequence:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113138	Splice Site, Nonsense	369	467	7	10

Genomic Location (Zv9):

Chromosome 19 (position 522086)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	541852
GRCz11	19	541661

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCCGACAGCGGGACGCCATGAGGGACAGCGCTGGAGGAGGACCAGAGCTG[C/T]GTATGTGCTATACACACACACACACACTCAAACACACACACACACATATG

Long Flanking Sequence:

GCATGAGAGCATGTGTGTTTTTATGTATACATGTGCATGTATCTGTATGATTGTGTGAGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATGCGCGTGTGTGCAATATTGATGTATTGTGTGTGCATTTGAGCATGAGTGGGTTTGTGTGAATGTGTGTGTGTGTGCGTGTGTGTTGTTATTGCTATATTATATTGATGTATTATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTTATATTATTCTTATGTATTGTATGTGTGTGTGTGTGTGTTCAGGGCTAATCGACGGCTACAGTGATGAGCGGCGTGCTCTGGAGCAGCAGGTGTGTGAGCGTGCGGAGCTGCAGCTGCATCTGGAGCAGGAGCTGCAGGTCACCAGCACACGGCTGCAGGAGCTGGAGCAGGAGAGATGCAGCCTGCTGGAGCACACTGAGCTGATGAGCCGACAGCGGGACGCCATGAGGGACAGCGCTGGAGGAGGACCAGAGCTG[C/T]GTATGTGCTATACACACACACACACACTCAAACACACACACACACATATGCAAGGGTGGAGAAGGAAGCTGAAGCTGTGGTCAGTGTAGTGTTGGCCAGCAGATCTGTTGGTCTGGAGCTCCGCAGGGTCAATATACATGACCCAAACCTCTGCCAAACGCCGGTTCAGTGGAGCAGCAGTGGAGATGTGGAGCTGTGGATGATGTGGAGCATGTGCTGTTCTCTGATGATCCAGCTTCACTGTCTTTCCCACATCCGGGACAGTTACGGTGTGGAGAAGCCCCAAAGAAGCGGCCCACCCAGACTGCTGATGCCCAGAGTCAAGCATGGGGGGGTCACTGATGGTTTAGACTCAATATCATGGCATTCCCTATGCCTAATACTGGTGCTAGATGGGCGCTGGGTCACTGCCAAGGACTACCCAACCATTCTGGAGGAGCAGGTGANNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa29111

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000113138	Nonsense	429	467	9	10

Genomic Location (Zv9):

Chromosome 19 (position 527075)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	19	547698
GRCz11	19	547507

KASP Assay ID:

2261-2708.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCAAGCAGCTGGAGGCGCAGCTGGAGGAGCAGCAGATGCGCTTGCAGGAG[C/T]AGCAGGAGCTCCAGCGCAGCCAGGAGGAGGACCTGCAGCAGCAGATACAG

Long Flanking Sequence:

GTGATTAATCTTTGCCCAGCACTAATTCATACATGCATTTATACAGTTTTATATTACAAAAAATTAATTAATAAATAAAAAACTACTATAGCAAAAATGACACCATGCAAAACAAAATATAGATAAATATATAATAAAAAATCATAAGTTTAGTTGTAGTGAACGGTAACAACATTGAACTTTAGCACATTGTGACTTAATAATTAATGTTCAGTTGAGATCAGACTTTAGTGAATCTGGTTGATCAGTGCATGCGAGCGAGCTGTAATAATGCCACTGACAGTGAGTTTCTGAGTGAGTGTTTCTCTGGATCTCCTCCGTCATCGTCATGTTGTGACTCTGCTGCTGTGCCGTTGTCAGACCTGCTGGAGGAGACGGAGAAGCTGCTGCAGGAGAAGGTGGAGGTGCAGCGTCAGGCGCAGAAGCAGAGCTCGGAGCTGCAGGCGCAGGTCAAGCAGCTGGAGGCGCAGCTGGAGGAGCAGCAGATGCGCTTGCAGGAG[C/T]AGCAGGAGCTCCAGCGCAGCCAGGAGGAGGACCTGCAGCAGCAGATACAGGCGCTGGAGAAGCAGACGGAGAACCACCGACGCTTCATTGACGTAAGGCGCTCACAATACAGAATGCTCTGTGAAAACACTTAACAGTTGCGAGACACTGACTTCACATCTTGCTATTCCTACAGTTTTTTGGAATTCTGAATTTGTGTCGCTATTCTGACTTTTTTGGGAAAGAAATTTCTAAATCTTTCTTGGATTTCTGAGTTTTTTCCGTTGGTATTCTGAGTTAGTCTTGCAATTTTGACAATTTTCTTGTAGTTTTGAGTTTACATTTTGTAATTCTGAGTTTTTTATTGAAATTCTGAATTTTGAGTTTTGCAATTCCAACTTTTCAGATTCCCAATTCTGAGATTTTGTTCCCTTGGATTTCTGAGTTTATGGCTTAAAAGTCTTACTTCATGGCTTGGAATTCCGAGATTTTTTTCTTGGAATTTTGAGTTTGTTTGTTTT

Associated Phenotype:

Not determined