ZMP

si:ch211-192p3.2

Ensembl ID:

ENSDARG00000020395

ZFIN ID:

ZDB-GENE-061207-15

Description:

Novel protein similar to human microtubule associated monoxygenase, calponin and LIM domain containi

Human Orthologue:

MICAL2

Human Description:

microtubule associated monoxygenase, calponin and LIM domain containing 2 [Source:HGNC Symbol;Acc:24

Mouse Orthologue:

Mical2

Mouse Description:

microtubule associated monoxygenase, calponin and LIM domain containing 2 Gene [Source:MGI Symbol;Ac

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa24630	Splice Site, Nonsense	Available for shipment	Available now
sa31109	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa24630

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

Mutation:

C > T

Consequence:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000109672	Splice Site, Nonsense	198	298	5	8
ENSDART00000139013	Splice Site, Nonsense	198	628	5	13

Genomic Location (Zv9):

Chromosome 25 (position 16587993)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	16134537
GRCz11	25	16230937

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TAAAAGGAGTTCAGTGTTTTTCAGTTTGACCCTGTGTTTGCATTTCAGGG[C/T]AGGGATGGAGGGCTGAGATCCGGCCGGCCGATAATCCTGTCTCCGACTAT

Long Flanking Sequence:

TGGCTGTAACTTCCTAATAAAAAAATCCTCATAGATTAATGGAAGCAAAAGCAGGGCCAAAGCAGATCATGAAAACTGACACCTTCCCACTATGTACCCTTGACAACACATATACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACACAGACTCACATACACACACTACTGATACCAAGAAAGTTTGTGCCGCCTTTCTGCGTCAGTGGCACTCAGCAGTCTGCATTGTGTGAATGATAAACTCTCAGTAGTGTGCTATATATAAAGTCAGGGGTCGTTTAGGTCTGTAACACCTCTTCTGCTATGTATTGCATCATTGGCCTGATGTCAAAAAAAGGATAGAACCGGGACAAATGCTAGTAAGCTTTTTTTTTCCTGGCAGCTTCACACACTTACTGTATTTTGAAATCTGCAATAAACATAAAAGGAGTTCAGTGTTTTTCAGTTTGACCCTGTGTTTGCATTTCAGGG[C/T]AGGGATGGAGGGCTGAGATCCGGCCGGCCGATAATCCTGTCTCCGACTATGAGTTTGATGTGATAATCGGGGCAGATGGAAGGAGAAGCACTCTTGATGGTGATTAATTGTTTAGATTTGATTCTGCACAGTAGTTTTGATATTATGATGTTTTCAGGTGAAGGAGTATTGTCGGTAATAAAAAATCATTAATAGTATAATTTCCAAATTATGTTTAATATGTTAACAAAAGGATTTTTCACAGTGTTTCCCATACTTTTTTTTCTTCAGGATAAAGTATTATTTTCTTTATTTCGGCTAGAATAAAAGCAGTTTTTAATTGTTTGAAAAACATTTTAAGTTCAATATTGTTAGCCCCCTTAAGAAATGTGTTTTTTCGATTGTCTACAGAAAAAACCTTCATTATAAAATGATTTTCCTCATGCATCTACTACATTATCTACTGTGTCTACTAACTATCGATTATTAAATTAATGTACAGTGAGTGACAGTTCAAAATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa31109

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
ENSDART00000109672	Essential Splice Site	231	298	6	8
ENSDART00000139013	Essential Splice Site	231	628	6	13

Genomic Location (Zv9):

Chromosome 25 (position 16590338)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	25	16136882
GRCz11	25	16233282

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTAAGTTTGAGCCAAATCAAGCAAACGTAGCCTAATGTTGTTTCTGCTCC[A/T]GGCTTCAGGAGAAAGGAGTTCAGAGGTAAACTAGCCATCGCCATCACTGC

Long Flanking Sequence:

AAGTAACTTGAAATCTTCAAGTTTTATGCTATTATGCTTCTAGCACTTTTAACATTTTACTGTTAATAATTTTCATGTTAAAAATGTTGCAAGGGTTAACATGTTTATTGTTTTACATGTGGCTAATATGTTTTAGCGTGTTGCTAGCAGGTTTAGCACTTATATTAGCATGTTTTTAACAGTTTTGCTATAGGGCTACCACATTGTTAACCTGTTCTTAGCACAGTTTAACATACTGTTAGGGAAAATTAGCATTTATAGCATGTTGCTAGCATATTTAGTATTTAGTAATCATTGATTGGCATGATATTAACATGTTTCTTGCATGGTAAGCTTATTATTAACATGTAATAGCATGTTGCTAGCACATCTTACCTCATGTTTACCAACTTGTTAGCAATTTGCAATCATGCTTCTAGTGTGAATGAGCATGTCTGCTCATCACCAATGTTAAGTTTGAGCCAAATCAAGCAAACGTAGCCTAATGTTGTTTCTGCTCC[A/T]GGCTTCAGGAGAAAGGAGTTCAGAGGTAAACTAGCCATCGCCATCACTGCCAACTTCGTCAATCGCAACACCACTGCCGAGGCCAAAGTGGAGGAGATCAGCGGAGTGGCCTTCATCTTCAACCAGAAGTTCTTCCTGGAACTCAAGGAGGAGACGGGTGAGATTATACTCCTTATTATGACCTGCTTCACATGATAATAAGTACCTCAAATACCTTTTTATTGATTAGTGGTGAACAAAGTACATATCTTCCTCAAATTTTTAAAAATTTTACTCAATTTAAAGTGCAAAATTATAAATATTTTATGTACTTGTGTAGTAAAAGTTTATTGTTGAATGTTTATTTTGGAAGAGACTCTTCATGTACTGTACTGTAGTTCTTAGGATTTCCAGTATTTGACTAATTTTGAATCCGTTTGTAAATAAACTGAATCATTAAACTAGTGACTCATTCTGAGCTGATCATTTGAATCAATGAATCATTAGCTGCAGATGCTCTT

Associated Phenotype:

Not determined