ZMP

ENSDARG00000086626

Ensembl ID:

ENSDARG00000086626

Human Orthologue:

ZFAT

Human Description:

zinc finger and AT hook domain containing [Source:HGNC Symbol;Acc:19899]

Mouse Orthologue:

Zfat

Mouse Description:

zinc finger and AT hook domain containing Gene [Source:MGI Symbol;Acc:MGI:2681865]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36129	Nonsense	Mutation detected in F1 DNA	Not yet available
sa11133	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa36129

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
ENSDART00000125838	Nonsense	688	1266	1	1

Genomic Location (Zv9):

Chromosome 16 (position 27309920)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	25155607
GRCz11	16	25070639

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GAGTCTTCTGAGGAAATGGAAATTGATTCGGAATCTCTTAGTGAAGGCTA[T/A]CAAGTGTTCATTACTAACAAAGGCGTGAAGCGGTATGTTTGCATCGAGTG

Long Flanking Sequence:

GCTCCTCTGAAATCCGCATCTCCTACGGTTAACAGAGTTGAACTCAAGCCCCACACCTTAGACAGCAGCACTACAGCGATGCAAATCTCGAAAAACAATCAAATGTCATCACACCACGTGAATATTGGTGTAGGCACAGAGCCGATAAAGGTTGAGGAGCATCACACAGAATTTCCTATTGACAAGAAAAATCAGATTCATCCACCAAAACCTCCTGAGCACAGCTCTAAACCAACTGAGTCAACCATTAACTCAGTTAAACTACCAGAAAACATGGCTAGTATGAAAGAAGAAGAAGAAAAGGAGAAATTGGATGAAAAGCAGTGGACCATGCCACTGGATGATGCTGAAATTGATACACTAGTAGATGGGGAGCAAAAGGATTCAGATGAGGATGATTTGGCTGACATGGATGAAGACGACTGTTATGAAGAGGATGATGTCAATGTAGAGTCTTCTGAGGAAATGGAAATTGATTCGGAATCTCTTAGTGAAGGCTA[T/A]CAAGTGTTCATTACTAACAAAGGCGTGAAGCGGTATGTTTGCATCGAGTGCCAAAGAAGCTATTCTCGGCAGTTTACTCTAAAAGAGCACCTGAAGGTTTGTGAGGCGAGGATTTTAAAGGAGCAAACTATTGAGAATAAGATAGCTGATTTGCCTGGGCCAATTAAAAAATTTCCATGTCCTCAATGTGGCAAATTTTTCAGCCGTAAAGATAATATGAATATGCATCAAAAAAAGTGCCACGGAAAAACTGCTGTACCTGCAGTAGTAAGCACCAGAACAGAGCCTAAAACTCCTGTAGCCCAAGAAAACCTGTTTGTCCTGTCACCATCCACAGAAAACAAAGCAGTACAACAGGAAACTCCTCAAAATACTAGCAGTAGCAGAAACTGGGGGATTATGTCACTTCCATCTGTTCTCCCAAGAAAAGTGACATGTGAATGCGGAGCCTCATTCACTTGTCCTCGACTACTCTTCGAACATCTGCAGCAGCATGCCCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11133

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:

A > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000125838	Nonsense	744	1266	1	1

Genomic Location (Zv9):

Chromosome 16 (position 27310086)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	16	25155773
GRCz11	16	25070805

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TAAAGGAGCAAACTAYTGAGAATAAGATAGCTGATTTGCCTGGGCCAATT[A/T]AAAAATTTCCATGTCCTCAATGTGGCAAATTTTTCAGCCGTAAAGATAAT

Long Flanking Sequence:

CAGAATTTCCTATTGACAAGAAAAATCAGATTCATCCACCAAAACCTCCTGAGCACAGCTCTAAACCAACTGAGTCAACCATTAACTCAGTTAAACTACCAGAAAACATGGCTAGTATGAAAGAAGAAGAAGAAAAGGAGAAATTGGATGAAAAGCAGTGGACCATGCCACTGGATGATGCTGAAATTGATACACTAGTAGATGGGGAGCAAAAGGATTCAGATGAGGATGATTTGGCTGACATGGATGAAGACGACTGTTATGAAGAGGATGATGTCAATGTAGAGTCTTCTGAGGAAATGGAAATTGATTCGGAATCTCTTAGTGAAGGCTATCAAGTGTTCATTACTAACAAAGGCGTGAAGCGGTATGTTTGCATCGAGTGCCAAAGAAGCTATTCTCGGCAGTTTACTCTAAAAGAGCACCTGAAGGTTTGTGAGGCGAGGATTTTAAAGGAGCAAACTATTGAGAATAAGATAGCTGATTTGCCTGGGCCAATT[A/T]AAAAATTTCCATGTCCTCAATGTGGCAAATTTTTCAGCCGTAAAGATAATATGAATATGCATCAAAAAAAGTGCCACGGAAAAACTGCTGTACCTGCAGTAGTAAGCACCAGAACAGAGCCTAAAACTCCTGTAGCCCAAGAAAACCTGTTTGTCCTGTCACCATCCACAGAAAACAAAGCAGTACAACAGGAAACTCCTCAAAATACTAGCAGTAGCAGAAACTGGGGGATTATGTCACTTCCATCTGTTCTCCCAAGAAAAGTGACATGTGAATGCGGAGCCTCATTCACTTGTCCTCGACTACTCTTCGAACATCTGCAGCAGCATGCCCAGGAGTCCTACATTTGTCCACACTGTGGTGAGAGCTTGCAGTCGTGGATGGATTTTGAAGCCCATCAGCAATTGCACAAACAATCTCAAAGTTCAAATGAGCAAAGAGGTCCCCAACAGCGTCCTCATACGTTTTCCCAAGCGCTGCCATTACATGCTCCAACACGA

Associated Phenotype:

Not determined