ZMP

ankle2

Ensembl ID:

ENSDARG00000035607

ZFIN ID:

ZDB-GENE-030131-6090

Description:

ankyrin repeat and LEM domain-containing protein 2 [Source:RefSeq peptide;Acc:NP_001119867]

Human Orthologue:

ANKLE2

Human Description:

ankyrin repeat and LEM domain containing 2 [Source:HGNC Symbol;Acc:29101]

Mouse Orthologue:

Ankle2

Mouse Description:

ankyrin repeat and LEM domain containing 2 Gene [Source:MGI Symbol;Acc:MGI:1261856]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa26430	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa40384	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa26430

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000090521	Essential Splice Site	400	961	7	13
ENSDART00000142531	None	None	206	None	3
ENSDART00000145210	Essential Splice Site	400	961	7	13

Genomic Location (Zv9):

Chromosome 5 (position 20732307)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	18444766
GRCz11	5	18948558

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAGGGTAAAGTTCAAGAAGTCAAACAGAAAATAAATGAATATTTAGAAG[G/A]TAAGCTGATGATATTACTTGTTGTATTTAATTTAACATGTTGATCAAGTG

Long Flanking Sequence:

AGATTTAAATCTTTGCAATGCTTTGTTGGGTTGCGTTTTATGAGGAGAATGCATTCAGAGACATTACCATATAAGCCAGGATTATTTTGATGCCAATGTTTGACATCTTTTGTGTCTGAAACATGCTGTTGAGTTCTAAAATCATATTTAGGCAGATGTCCTATTAAGATTTGTAACCGATTCAAAACAATAATTTATCCTTTGTGTTTCATAGGGGTTTGAGACACCTCTTCACTTCGCATGCAAGTTTGGCTGCCCAGAGGTTGTAAACATACTCTGTTCTCATCCAGACATTGACAAGAACTGCAAGAACAAGTATAACCAGAAACCCTGTGAGGTAATGCAACCATGACGCATTAAATTTCAATATGAGGATTTCATAATTTATTAAAGCTTATTTACTACTCATTGTATTGCCCTTATTTAGGTTATTTGTGAAAGAATGAAAGAAAAGGGTAAAGTTCAAGAAGTCAAACAGAAAATAAATGAATATTTAGAAG[G/A]TAAGCTGATGATATTACTTGTTGTATTTAATTTAACATGTTGATCAAGTGCATTCCATGGACTAATGCTGAATTCTGATTGGCCACAGAGCGATTGTACATCCCTTTGCTGCGAGCCACTGATAACTCCTCCCAGGCTGTGATTGGTGCTCCTTGGTCTCCTGAGCCAATGGAATCCCTTTCGCCATGGTTACCCAGAAGTCCAAAGGATCCAGTTATGGCAGTCAGGGCCTTTGCTGGACCTTTAAGTCCATCCAAAGTAAGTTTAATGTAGAATTTATAAGTATATTATTTATGTAATGGGACATAAAGACAATTCTGTGTCTGTGAGTGATCAAAATGTGGGCTTCTAGGCGGATGAGTTCAGACGAGCGTGGAAAACTCCTCCCAGAGAGCGGGCAGACCATTTTCACAACATCCTGAAGTCTGACCCGGACCGTGGAGCAGAAAGAGTTGGCAGGTTTGTTCTAAGATATGATTAAAGAATCCGAACATTACTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa40384

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
ENSDART00000090521	Nonsense	776	961	11	13
ENSDART00000142531	None	None	206	None	3
ENSDART00000145210	Nonsense	776	961	11	13

Genomic Location (Zv9):

Chromosome 5 (position 20730560)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	18443019
GRCz11	5	18946811

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GTTCAGATGAGTACTTTCTGGCCAGTGAGCGGCTGGAACCTATAAACCAA[C/T]AGACTATAGATACTTCAGGGTGCGAGCGCATGATCTGCGCCAGGTCAAAG

Long Flanking Sequence:

GACTGGAGTTTCACATCCTCCCAGTGTCCCACAGCGCTGACCTCATAGAAGCGGCGGCAGAGCAGGACCTGCTGCTCTCAGAGAAATCCATGATCTCCAGCAGTAAAAATGGCCTTTGCGAACAGGGCTCCGGTGATAGGACTCCAAACGGGGACAAAGTATCGCCTCGTATCTGCGGTTCCTCCAATTCCTGCATGCTGTCACCAATCTCAAACTTAATGGCAGAGTTTGAGAGGATGTCTTTGCTGGATGAGCCTGATAGGACAAACAGAGAGAGGAGGAGGAGCGGAGGGAAACGTCAGACCACAGAGCTCACCTCTGGACTGGGACGCCTTTCGCTGTCTTCTGAAGACGACTCTGTGTTTGAGAAAGACAGGACGTCTGCTTTGCGGGCAGCAGAGAATGATGGAACAGAGAGGAGAAATGAGGTGGACGTGAGGTCCAGTGCGAGTTCAGATGAGTACTTTCTGGCCAGTGAGCGGCTGGAACCTATAAACCAA[C/T]AGACTATAGATACTTCAGGGTGCGAGCGCATGATCTGCGCCAGGTCAAAGTCCTGGGATCATGGGGGAAGAGACCTCAGCTCCTCGGGGTCTTCCAGCTCCTACAGATCACTCGACAGCTCTCAGGACTTCATACTGCGGACTCCTCCAAGAGTGACCAAAGGCCTCTTCATTGAAGGGTGAGAAGAGCTTGTCTGTGGTTATTATAATGTGTTTCAGTATGAAGTCTTTACTAGGGGTGTGGGAAATTACTATCTAACAGAGTATTTGTTGTTTTATTTAGAGCGGTGGTTCTGAGGTTTTAAAAATGTATTGCTATTCTCTCTTTTGAATAGATTCTGGGCTTAATTTTTAACAGCAGATGGCGCTGTATTATTTTACAACAGGGGTGTCATAACCTCAGTCCTGGAGGGCCAGTGTCCTACATATTTTAGTTACAGCCCCCACTAATAATAGTATACTAGAAGCTTCCAGGCACGTGTGTTGAAGGAAGTTGAAGCT

Associated Phenotype:

Not determined