ZMP

zgc:162232

Ensembl ID:

ENSDARG00000070874

ZFIN ID:

ZDB-GENE-070410-45

Description:

acetylserotonin O-methyltransferase [Source:RefSeq peptide;Acc:NP_001103947]

Human Orthologue:

ASMT

Human Description:

acetylserotonin O-methyltransferase [Source:HGNC Symbol;Acc:750]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa36427	Nonsense	Mutation detected in F1 DNA	Not yet available
sa11754	Essential Splice Site	Available for shipment	Available now
sa485	Essential Splice Site	Confirmed mutation in F2 line	Not yet available

Mutation Details

Allele Name:

sa36427

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
ENSDART00000086885	Nonsense	12	348	2	9

Genomic Location (Zv9):

Chromosome 17 (position 26657484)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	26797403
GRCz11	17	26815794

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGGACATTCTTCATCATGGCTGAGCATTTGTCCCAGAGTGAACTGGACTA[T/A]CCTTTCAAGCTTTTGGAATATTTCAATGGATTCAGGATCTCTAAGGTTTG

Long Flanking Sequence:

CTGTGGTCAGGGCATAATAATCGAGATCGTGGTCTCGTGAGCAGCTCGCTTGAAAGATTTTGTGGTTACACAATAATAACGGTACATTGTTTCACAGTGACCGGCTTTGTGAAAGTGTGTAAACCACAGATTCTGATAAACCTACACTATGAGTGCATTTAGACTGCAAATAATCTATATTTTCATAACATTGTCTTATCTGGACATGAGCATCGTATCTTTGCATTATCTAGTCGATCTTCAGAACAGAAAATATCATGGCCAGGCAGGGAACCTAGTTGACACAGGATAAAATCATTTATCTTTTTTGGAATGATGCTCTAAAAGCAGCTTCTAGTGTGTACTTTCATGTTTTATCTTCACTTGTCAAGAACTGTTAAGATTTGATCAATAATATAACTGGAAGTCTCTTTAATTGTGACACTGATTCTGTCATTGACTATAGCAGAAAGGACATTCTTCATCATGGCTGAGCATTTGTCCCAGAGTGAACTGGACTA[T/A]CCTTTCAAGCTTTTGGAATATTTCAATGGATTCAGGATCTCTAAGGTTTGTGTTTCATGTTTTGTCTTTGTAAACACACATTGCTTTAATCGGTCATGCTTGCTTTGACGTGGATCAACCTCAAGAATCATTAGCAGTTCATAACAATAACTATTTACCATGACATTTATAAGTGGATTTATGAGTAAATGTTTTATGTGAGAGCATCTATTATTTGTGTCAGTCCACTGTTGTGTCCCATGTAGCGCTCAGGACTGCTTTCGCCTCCAGCAGGACCAGCCTATGACTTATTAAAAGCCCCAGTCAAACACTAAAATGACTCAGGAGTCTGTTGTCCCATGAGACTTTAAGTAAGGTCCTTTAGTGCTTAAAAGGATTATGAAGTAACGGAAGTTTGTAAAAAAAATAAAAAATAAAATTCAGTTTTTGTACTCTGAGGCAACTTAAAGTGATCTAGATAAAGGTAAATGGAGTCTTGTAAATTGTGAATAGAAATTAAA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa11754

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
ENSDART00000086885	Essential Splice Site	27	348	2	9

Genomic Location (Zv9):

Chromosome 17 (position 26657530)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	26797449
GRCz11	17	26815840

KASP Assay ID:

2261-1128.1 (used for ordering genotyping assays)

KASP Sequence:

ACTATCCTTTCAAGCTTTTGGAATATTTCAATGGATTCAGGATCTCTAAG[G/A]TTTGTGTTTCATGTTTTGTCTTTGTAAACACACATTGCTTTAATCGGTCA

Long Flanking Sequence:

CGCTTGAAAGATTTTGTGGTTACACAATAATAACGGTACATTGTTTCACAGTGACCGGCTTTGTGAAAGTGTGTAAACCACAGATTCTGATAAACCTACACTATGAGTGCATTTAGACTGCAAATAATCTATATTTTCATAACATTGTCTTATCTGGACATGAGCATCGTATCTTTGCATTATCTAGTCGATCTTCAGAACAGAAAATATCATGGCCAGGCAGGGAACCTAGTTGACACAGGATAAAATCATTTATCTTTTTTGGAATGATGCTCTAAAAGCAGCTTCTAGTGTGTACTTTCATGTTTTATCTTCACTTGTCAAGAACTGTTAAGATTTGATCAATAATATAACTGGAAGTCTCTTTAATTGTGACACTGATTCTGTCATTGACTATAGCAGAAAGGACATTCTTCATCATGGCTGAGCATTTGTCCCAGAGTGAACTGGACTATCCTTTCAAGCTTTTGGAATATTTCAATGGATTCAGGATCTCTAAG[G/A]TTTGTGTTTCATGTTTTGTCTTTGTAAACACACATTGCTTTAATCGGTCATGCTTGCTTTGACGTGGATCAACCTCAAGAATCATTAGCAGTTCATAACAATAACTATTTACCATGACATTTATAAGTGGATTTATGAGTAAATGTTTTATGTGAGAGCATCTATTATTTGTGTCAGTCCACTGTTGTGTCCCATGTAGCGCTCAGGACTGCTTTCGCCTCCAGCAGGACCAGCCTATGACTTATTAAAAGCCCCAGTCAAACACTAAAATGACTCAGGAGTCTGTTGTCCCATGAGACTTTAAGTAAGGTCCTTTAGTGCTTAAAAGGATTATGAAGTAACGGAAGTTTGTAAAAAAAATAAAAAATAAAATTCAGTTTTTGTACTCTGAGGCAACTTAAAGTGATCTAGATAAAGGTAAATGGAGTCTTGTAAATTGTGAATAGAAATTAAATCGGAGCTAGTCATAACACAATATAAAAATAATAAATATGAAATAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa485

Status:

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

Availability:

Not yet available

Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086885	Essential Splice Site	86	348	3	9

Genomic Location (Zv9):

Chromosome 17 (position 26660188)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	26800107
GRCz11	17	26818498

KASP Assay ID:

554-0336.1 (used for ordering genotyping assays)

KASP Sequence:

CTGATGGTTGCCATTGAGATTGTGGATGTGGAAGTGGTGCAGGGAAACGG[T/G]AAGCTGCTTAACAATCTCATCATTCCACCACAATTGGCTGGAAATAACCT

Long Flanking Sequence:

CCAATTTTTTACTATGGAAATCAATGGGTTACATCAACCAGCATTTTTAATGTATATATATATTTTTTGTGTGTGTTCATCAGAAGAAGAAGACTCAATAAGGTTTGTTTTAAAACACAAGGGAGAATAAATAGGCATGAAATAATTTTTTGGCTCTAAACAATCTTTTTAATGAGAGACACCAGTGTGTCAATTTTCTCAACAAATTAAGTTCTACAAACTTTTGAAAAATTTGATTGTTTACTCAAATGTTTTGAGGCAATATATTTGCACAAATATTTTATCCAATCTGGAATGATTACCTAAATTTCTCCTCTCCTCCAGGCGATATTTTCAGCTTGTGAGTTAGGGGTGTTCGACCTGCTCCTCCAGTCCCAAAAGCCTCTGAGTGCAGCTGAAGTGGCAGAGCAGCTTGGCACCAGTCAAGATGGCATTGAGCGTCTGCTGGATCTGATGGTTGCCATTGAGATTGTGGATGTGGAAGTGGTGCAGGGAAACGG[T/G]AAGCTGCTTAACAATCTCATCATTCCACCACAATTGGCTGGAAATAACCTAGATTCTTCTAAAACAAAGACATTTTATGTGTTTGTTCACACATCATGCTTTCATTGTGTCTAGTATATCAGAAAAAAACTTTAAAAAAAAGCTTTACCTCTCTAAAGCTTTACCTCTGTCTTCTCTCAAAGCTCTTTATAGCAGTACAGATGTTGCTAATCTCTACCTGGCCAAAAGCAGCCCCAAATCTCTGCATGATTTGATCATTTATTCCTCTCAGACCATCTACCCGCTCTGGAACAATCTGGTAGACGCTGTTAGGTAGGTTCATCCATCCCAGTTTTGAGACACTTAATTTTTATTCTGAAATTTGTTCCAACATTTGGAGATCTAAATATAATGAACACTTTTCCTTCATTTCCACATTATTCCCAGTTGTCATGGATTTAGTTGGTTAAATACGCTTAAAATCTTGGATTTTTTATAATATTTAGTTTATTTTTTGGAAA

Associated Phenotype:

Not determined