ZMP

zgc:153372

Ensembl ID:

ENSDARG00000068967

ZFIN ID:

ZDB-GENE-060929-680

Description:

hypothetical protein LOC767695 [Source:RefSeq peptide;Acc:NP_001070101]

Human Orthologue:

AS3MT

Human Description:

arsenic (+3 oxidation state) methyltransferase [Source:HGNC Symbol;Acc:17452]

Mouse Orthologue:

As3mt

Mouse Description:

arsenic (+3 oxidation state) methyltransferase Gene [Source:MGI Symbol;Acc:MGI:1929882]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14814	Essential Splice Site	Available for shipment	Available now
sa4615	Nonsense	F2 line generated	Not yet available

Mutation Details

Allele Name:

sa14814

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099958	Essential Splice Site	244	358	7	11

Genomic Location (Zv9):

Chromosome 15 (position 29081828)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	29799858
GRCz11	15	29732734

KASP Assay ID:

2260-8653.1 (used for ordering genotyping assays)

KASP Sequence:

TGCAGGAAGTCACATTGTGGTTCACAACTCAGAACTTCAAAGAAAGATTG[G/A]TAATCYGTTTATTTGGGGTTTGGTTACAGCTTCATAGCTATTTTTGAAAG

Long Flanking Sequence:

AAAGTTACTTTTTTATTAGCTGTAAAACATAGAGCAGACAAAGCAAAAAGGGGTTTTAAGTGATATTTCACACAAAAAAAATGTCATAATTTACTCATCCTTTATTTGATCCTCCATTTGAGTTTTTTTTTTTCCTCTGTTGAACACAAATGAATATATACTAAAGAATGTTGGGGGAAAAAAGCCAATGAATTCCATAGTATTATACTATGGATGTCAATAGCTGCTTTTTTCAAAGATTCTACACAATATCTTGTTTAACAGAAGAAATACATTCATAAGTTTTAACCACTTGAGTGTAAGTAAATAAAGAGCGAAATGTAATTTTTGGGTGAACCATCCCTTTATAAAGTGTTTGATTTCATCAGGAGAGGGAATGGCTGGCGCCCTCTACTGGCGAGATCTCATCACTCTGGTGAAAGACATCGGTTTCAGCACTCCACACCTGGTTGCAGGAAGTCACATTGTGGTTCACAACTCAGAACTTCAAAGAAAGATTG[G/A]TAATCTGTTTATTTGGGGTTTGGTTACAGCTTCATAGCTATTTTTGAAAGTTATTTGTTACTTGAGGGAAGCAGATGCTTTACAGTTCAACCAGTGTTATTTTGACCTCCAATTGGTCACTGCAGGTGATGTCAAATATGCATCTGGAACTTATCGGATCTTTAAACTTCCTCAAAACTCCACCAAAAGCAAAGCTCTGGTCACATATAAAGGCAGCGTGCCTGACTGTGCCGACTGTTTTGAATTTGATTCTTCTCATTCTTTCAAGGTAAACATTTATGCATATTGACAGTTTTTACAAATTAATACGACTTATTCTGTGGTAAGTCCTGCTGATTCTTTTCCAGACAAATGTCCAAGTGCAGGTGGATGCAGAGATGGCTGCCATCCTCCAAAACACACGCTTCTCCACAGACTTTGACATTACCATTTCAGAAACTCTAGATCCAAACGAGAACGCTACTCCACAGGTAAATGAGCATCTTATTCATTATCTTATG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa4615

Status:

F2 line generated
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

T > G

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000099958	Nonsense	249	358	8	11

Genomic Location (Zv9):

Chromosome 15 (position 29081967)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	29799997
GRCz11	15	29732873

KASP Assay ID:

554-3527.1 (used for ordering genotyping assays)

KASP Sequence:

AACCAGTGTTATTTTGACCTCCAATTGGTCACTGCAGGTGATGTCAAATA[T/G]GCAWCTGGAACTTATCGGATCTTTAAACTTCCTCAAAACTCCACCAAAAG

Long Flanking Sequence:

TTGAACACAAATGAATATATACTAAAGAATGTTGGGGGAAAAAAGCCAATGAATTCCATAGTATTATACTATGGATGTCAATAGCTGCTTTTTTCAAAGATTCTACACAATATCTTGTTTAACAGAAGAAATACATTCATAAGTTTTAACCACTTGAGTGTAAGTAAATAAAGAGCGAAATGTAATTTTTGGGTGAACCATCCCTTTATAAAGTGTTTGATTTCATCAGGAGAGGGAATGGCTGGCGCCCTCTACTGGCGAGATCTCATCACTCTGGTGAAAGACATCGGTTTCAGCACTCCACACCTGGTTGCAGGAAGTCACATTGTGGTTCACAACTCAGAACTTCAAAGAAAGATTGGTAATCTGTTTATTTGGGGTTTGGTTACAGCTTCATAGCTATTTTTGAAAGTTATTTGTTACTTGAGGGAAGCAGATGCTTTACAGTTCAACCAGTGTTATTTTGACCTCCAATTGGTCACTGCAGGTGATGTCAAATA[T/G]GCATCTGGAACTTATCGGATCTTTAAACTTCCTCAAAACTCCACCAAAAGCAAAGCTCTGGTCACATATAAAGGCAGCGTGCCTGACTGTGCCGACTGTTTTGAATTTGATTCTTCTCATTCTTTCAAGGTAAACATTTATGCATATTGACAGTTTTTACAAATTAATACGACTTATTCTGTGGTAAGTCCTGCTGATTCTTTTCCAGACAAATGTCCAAGTGCAGGTGGATGCAGAGATGGCTGCCATCCTCCAAAACACACGCTTCTCCACAGACTTTGACATTACCATTTCAGAAACTCTAGATCCAAACGAGAACGCTACTCCACAGGTAAATGAGCATCTTATTCATTATCTTATGTTGCATATACAGTTGTGTCAAAATAATTAGCCCTCCTGTGAATTTTTTTCTTTTTCAAATAATTCCCAAATTATGTTTAACAGAGCAAGACGTTTTTCACAGAATGTCCTATACTATTTTTTCTTCTGGAGAAAGTCTT

Associated Phenotype:

Not determined