ZMP

zgc:171885

Ensembl ID:

ENSDARG00000075320

ZFIN ID:

ZDB-GENE-080220-43

Description:

hydroxyindole O-methyltransferase [Source:RefSeq peptide;Acc:NP_001108381]

Human Orthologue:

ASMT

Human Description:

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

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa30507	Nonsense	Mutation detected in F1 DNA	Not yet available
sa38232	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa30507

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 > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111787	Nonsense	106	275	3	7

Genomic Location (Zv9):

Chromosome Zv9_NA998 (position 24528)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	9	56393764
GRCz11	9	55743426

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CGAATGTGTTCCTGGTCAAGTCCAGCCCGAAGTCTCTGTATCACTCTATC[G/T]AGTACAGCTCCAGAACCATCTACCTGTGCTGGCATTACCTGAGCGACGCC

Long Flanking Sequence:

CAAATATATGCATGTAGTATATATCCACGAATTAATCAGTAAATGAATATATACTGATTTATTTGTAGATATATACTGCATGCATATATTTGAGAAAATGTTTATTTATATTTAGAAGTATAATATATATGTATATGACACAATTTATATATACATTTAGAAAACCCATGCAACAAAGTTGTATATATTTTTTTAAGTATGTGTGTATTACATATACATAATAAGCAAATATAACACACACACACACTCACGCACACACATTAATTGCAAAATTAACCCGGCTCTAATAAAAATAATCACATTTGGTGTGAATCAATCAGATCAGCCAATCAGAATCAAGCTTTCCATAGTCTCCTAATATAATGACTAGTAAATGACATGTTACACACAGAAGCCTGATGACTAATGGATGAGCTGTTTCCTCAGTTCTGTACAGTAACACAGAGATGTCGAATGTGTTCCTGGTCAAGTCCAGCCCGAAGTCTCTGTATCACTCTATC[G/T]AGTACAGCTCCAGAACCATCTACCTGTGCTGGCATTACCTGAGCGACGCCGTCCGGTGCGTAAAACAGCTACTGTGTGTTCATTCATTCATTCATTCATTCAAACAATCACTCACTCATGCATGCATTCACTCATTTATTCATTCACTCATTTATTCATTCATGCATAATTAATGTATTCATTCATTCACTCATTTATTCATGCATTCATTTGTTTACTCACTTATTCTTTAATTAAGCCATTCACCAATTCGTTCATTCATTCGTTCATTCATTCATGCATTCATTTACTCATTTATTTATTCACTCACTCATTCACTCATTCATTCATTCATTATTTCACACACACACATTCAGTCACTCACTCATGCATGCATTCACTCATTCATTTATTCACTCATTCATCCATTCATTCATTAATGCATCCATGCATTCAATCATTCATTCATTCACTCATTTATTCATGCATTCATTTGTTCACTAACTTATTTTTTAATTCAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38232

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000111787	Essential Splice Site	187	275	5	7

Genomic Location (Zv9):

Chromosome Zv9_NA998 (position 22890)

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCACAGCCTTCGACCTGACACCGTACAAGACCATCTGTGACCTCGGAGG[T/C]AAGAAGTAGATCACACACACACACACACACTCTCTCTCTCTCTCTATTTC

Long Flanking Sequence:

TCACTCAGTCATTTATTCATTAAATCCTTCATTCATCCATTCCCTCATCATTAATTGATTAATATAGGAAGACAGAGGTGTGAACAGCAGCTTTAATAATCCACATCTCTGCAGTGGAGTGGAGACTGATTATTCTATAACTCCTGTTGTTTTTCCACTGTCAGAGACGGGAAGAACCAGTATGAGAAAGCCTTTGGAGTCAACTCTAAAGACCTGTTTGAAGCCCTCTACAGGTGTGTGTGTGTGCGCGCCTGTGTGTGTGTCTGTCAGAGAGTATGTTTGTGTGAGTGAGAAAGAGTATGTGTGATGCTTTGATGTGTGTGTGTGTGTGTTTGTCTGATGCTCTGATGTGTGTGATGCTCTAATGTGTGTGTGTGTAGGTCTGATGATGAGATGGTGAAGTTTATGCACCTGATGAACTCGGTCTGGAATATCTGCGGGCGAGACGTGATCACAGCCTTCGACCTGACACCGTACAAGACCATCTGTGACCTCGGAGG[T/C]AAGAAGTAGATCACACACACACACACACACTCTCTCTCTCTCTCTATTTCTTTAGCAGTAAATCATGACAGTGTAGCTCAACACTGGTGCAGTCATGATAGTTAGAGCGCAGGATCCAGCAGATGGCGCTGTGGAGCTATTGCTGCACACACACACACACACACACACAGCTCTGACACCGTCACAGTTAAATATTGTAGAGTGTCAGCACCACAGTAAAGGATTGAGACGGGCTGTTTTGGTAAACAGATGAACAGTGAATTAGCAGCCAGTGATGCACACACACTAAAGAAAGAAAATACCTCACCGGCCACTTTATTAGGTACACCTGTCCATCTGCTCGTTAACACTAATGTCTAATCAGCCAATCACAGGGCAGCAGCTCACTGCATTTCGGCATGTAGACATGCTCAAGAGGATCTGCTGCAGTTCAGAGCGAGCATCAGAATGGAGAAGAAAGGGGATTTAAGAGACTTTGAGCGTGTATTTGAAGATATGAA

Associated Phenotype:

Not determined