ZMP

zgc:114142

Ensembl ID:

ENSDARG00000035652

ZFIN ID:

ZDB-GENE-050913-41

Description:

diamine N-acetyltransferase 1 [Source:RefSeq peptide;Acc:NP_001025370]

Human Orthologue:

SAT1

Human Description:

spermidine/spermine N1-acetyltransferase 1 [Source:HGNC Symbol;Acc:10540]

Mouse Orthologue:

Sat1

Mouse Description:

spermidine/spermine N1-acetyl transferase 1 Gene [Source:MGI Symbol;Acc:MGI:98233]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa20335	Nonsense	Available for shipment	Available now
sa33523	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa20335

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000051699	Nonsense	95	171	4	6
ENSDART00000147691	None	None	88	5	7

The following transcripts of ENSDARG00000035652 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 5 (position 4346425)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	4006094
GRCz11	5	4339129

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCACCTATGACCCCTGGATTGGGAAACTGCTCTACCTGGAAGATTTCTA[C/A]GTCATGAAGGAGTATCGGGGTATGAATGTGAGCTCGTCATTTTTAGATGA

Long Flanking Sequence:

TTTGCACAAAAAAAACACCATTCTTAGTGTAAAAATAATGATTTATTAATGATTCACTGAACTGAGCTGAACTAAACTTAAACTCTAAAAAACTGAACTACACTGTTCCAATTTACTATGACCTTTTATGTGAAGCTGCTTTGACACAATCTTCATTGTAAAAGCGCTATACAAATAAAGCTAAATTGAAAAAATGAAATTCGCAGTGTGATATAAATGCTCAAATCAACACAACAAAAGTGAAAGAAAAAGGCTTAAATGAAGATTTGACACCTGAATGACGTGACTGTGGTGTATGCGAGGGTTGGTGTAAACCACAGCCAATTGTAAACAAGCTGTGAATATCATCTCGATGTAAATGTTCATAATGTGAAAGTGAAAACAGCAGCAGTGGAGTGATATTGAGCTGTTTTTCCAGGTCATGTGATCGTTGGCTTTGCCATGTATTATTTCACCTATGACCCCTGGATTGGGAAACTGCTCTACCTGGAAGATTTCTA[C/A]GTCATGAAGGAGTATCGGGGTATGAATGTGAGCTCGTCATTTTTAGATGATCAGATTAGTGAGACACTGTAATGTAACACTTTTCTCTCAACACAAATTAGGTTTCGGGATTGGGTCTGAAATCCTGAAGAAACTCAGTCAGGTGAGTCTAACCTTGACATCTGTTTCAGTGGGCAATGAGTGAGCTGTTCCTCTGTTAATCAAACCACATTCAAAACAAATGCACTTCTTATATATTTGCAAAAATAAATAAGTAAATAAAAAGAAGAGCTTCAGTGGGGAAAAGTGCAAAAGTATGTGTCACAACTAAAAAAACAAGACGTGGAACCCAAATGCAAGTAAAAAGTCTTTATTGCTTAACTTATGTTGAGAAATGCAAAAGCAATCGTTCGTTAATTGAGAAAAAGAAGTGCGTGTAAAAGAAGTGCACAAACCGTACATGCATTTAAGAGTGAAGAAGAACGATTACAGTAAATGTGGAAAAAGTTCACAAGTGAACG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa33523

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000051699	Essential Splice Site	102	171	None	6
ENSDART00000147691	Essential Splice Site	None	88	None	7

The following transcripts of ENSDARG00000035652 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 5 (position 4346525)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	5	4006194
GRCz11	5	4339229

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCAGATTAGTGAGACACTGTAATGTAACACTTTTCTCTCAACACAAATT[A/C]GGTTTCGGGATTGGGTCTGAAATCCTGAAGAAACTCAGTCAGGTGAGTCT

Long Flanking Sequence:

CACTGTTCCAATTTACTATGACCTTTTATGTGAAGCTGCTTTGACACAATCTTCATTGTAAAAGCGCTATACAAATAAAGCTAAATTGAAAAAATGAAATTCGCAGTGTGATATAAATGCTCAAATCAACACAACAAAAGTGAAAGAAAAAGGCTTAAATGAAGATTTGACACCTGAATGACGTGACTGTGGTGTATGCGAGGGTTGGTGTAAACCACAGCCAATTGTAAACAAGCTGTGAATATCATCTCGATGTAAATGTTCATAATGTGAAAGTGAAAACAGCAGCAGTGGAGTGATATTGAGCTGTTTTTCCAGGTCATGTGATCGTTGGCTTTGCCATGTATTATTTCACCTATGACCCCTGGATTGGGAAACTGCTCTACCTGGAAGATTTCTACGTCATGAAGGAGTATCGGGGTATGAATGTGAGCTCGTCATTTTTAGATGATCAGATTAGTGAGACACTGTAATGTAACACTTTTCTCTCAACACAAATT[A/C]GGTTTCGGGATTGGGTCTGAAATCCTGAAGAAACTCAGTCAGGTGAGTCTAACCTTGACATCTGTTTCAGTGGGCAATGAGTGAGCTGTTCCTCTGTTAATCAAACCACATTCAAAACAAATGCACTTCTTATATATTTGCAAAAATAAATAAGTAAATAAAAAGAAGAGCTTCAGTGGGGAAAAGTGCAAAAGTATGTGTCACAACTAAAAAAACAAGACGTGGAACCCAAATGCAAGTAAAAAGTCTTTATTGCTTAACTTATGTTGAGAAATGCAAAAGCAATCGTTCGTTAATTGAGAAAAAGAAGTGCGTGTAAAAGAAGTGCACAAACCGTACATGCATTTAAGAGTGAAGAAGAACGATTACAGTAAATGTGGAAAAAGTTCACAAGTGAACGTAATAATAAAAAATATAAGTTGGAATTTTTTTAATTTACATGCATTATTTTTTCACAATTACATGCACAATTATATGCACTTATTTTTTGACCATTAAGT

Associated Phenotype:

Not determined