ZMP

zgc:101853

Ensembl ID:

ENSDARG00000036894

ZFIN IDs:

ZDB-GENE-041212-13, ZDB-GENE-041212-13

Description:

hypothetical protein LOC494049 [Source:RefSeq peptide;Acc:NP_001008592]

Human Orthologue:

AIMP1

Human Description:

aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 [Source:HGNC Symbol;Acc:1064

Mouse Orthologue:

Aimp1

Mouse Description:

aminoacyl tRNA synthetase complex-interacting multifunctional protein 1 Gene [Source:MGI Symbol;Acc:

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa30008	Nonsense	Mutation detected in F1 DNA	Not yet available
sa37799	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa30008

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000053569	Nonsense	33	282	3	7
ENSDART00000129872	Nonsense	33	282	4	8

Genomic Location (Zv9):

Chromosome 23 (position 44869210)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	45643738
GRCz11	23	45405010

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGCTGCAGGCGTCAGTGAGGGAGGAGAAGAAACTGCTGGTAGAAAACGCC[A/T]AACTGAAGAAAGACATCGACGACCTGAAGAACCTGCTGCAGGACACACAG

Long Flanking Sequence:

CATACACACACTAATGCATACATTCACACATACTCACACACAGATATGCATACACGCTTGTCACAGTTACACGCACACATGAATACCCATGTATACACAGACACACACACACCTTGGCATCGACTCTCGATTGTTAAAGCCTCAGAACCAAGGAATCGATTCTTTCCGATTGATGCCTCTGAGTAAATGAATCAGTTATGTTTTGGAAGCGATTCTTAATGAATCAAAATAAACGAACTGATTCTTTGCTGGAATCGACTCTGGAGTCTGGCGTTCTGTGTGATCATTGGGCTGATTTCTGCTGCTGCTGTTTGGATGATGTCGCAGTGCTTCACCTGATGGTTGTGTGTTTGTGTTTTGTTGGTTGTTTTCTAGCATTCTGCTGTTCATCGTGTTGTTTTGGATGATGTTGATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACAGTGCTGCAGGCGTCAGTGAGGGAGGAGAAGAAACTGCTGGTAGAAAACGCC[A/T]AACTGAAGAAAGACATCGACGACCTGAAGAACCTGCTGCAGGACACACAGAAGAGGAAAGCAGGTACTACACACACACACACACACACACACACACACACACACACACACACACACACACAAACACACATGGGGATTCCTACTAGCTGTGTTTCCATCTAAAGATTTAGATTTATGTGCAAATCTGGAATATTGCATCAAAGATGTTCAAATGAATCAGCGTTTCCAGCCAATGACATATAAAAGAGCACAAACCCATCACTTCCTGCAGAACTGGAGCTAATATCAGTCGGAGAGGTGCAGTTTAGTGCAGTCGATTCTGTTTAGGAATCAACTATCGATTGTTACTGCTTCAGAATCAAGGAGATGATTCTTTTTTGCAATCGACTCTGGAGTGTTAACACCTCAGAATCAACCAATTGATTCTTTTTAGGAATCAACTTGATTCTTATTTATTACTCTTTTATCCATTCTTAACACCTCTGAATAAATGAATCAGTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37799

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
ENSDART00000053569	Essential Splice Site	54	282	3	7
ENSDART00000129872	Essential Splice Site	54	282	4	8

Genomic Location (Zv9):

Chromosome 23 (position 44869275)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	23	45643673
GRCz11	23	45404945

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCGACGACCTGAAGAACCTGCTGCAGGACACACAGAAGAGGAAAGCAGG[T/C]ACTACACACACACACACACACACACACACACACACACACACACACACACA

Long Flanking Sequence:

GTTACACGCACACATGAATACCCATGTATACACAGACACACACACACCTTGGCATCGACTCTCGATTGTTAAAGCCTCAGAACCAAGGAATCGATTCTTTCCGATTGATGCCTCTGAGTAAATGAATCAGTTATGTTTTGGAAGCGATTCTTAATGAATCAAAATAAACGAACTGATTCTTTGCTGGAATCGACTCTGGAGTCTGGCGTTCTGTGTGATCATTGGGCTGATTTCTGCTGCTGCTGTTTGGATGATGTCGCAGTGCTTCACCTGATGGTTGTGTGTTTGTGTTTTGTTGGTTGTTTTCTAGCATTCTGCTGTTCATCGTGTTGTTTTGGATGATGTTGATTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGACAGTGCTGCAGGCGTCAGTGAGGGAGGAGAAGAAACTGCTGGTAGAAAACGCCAAACTGAAGAAAGACATCGACGACCTGAAGAACCTGCTGCAGGACACACAGAAGAGGAAAGCAGG[T/C]ACTACACACACACACACACACACACACACACACACACACACACACACACACACACAAACACACATGGGGATTCCTACTAGCTGTGTTTCCATCTAAAGATTTAGATTTATGTGCAAATCTGGAATATTGCATCAAAGATGTTCAAATGAATCAGCGTTTCCAGCCAATGACATATAAAAGAGCACAAACCCATCACTTCCTGCAGAACTGGAGCTAATATCAGTCGGAGAGGTGCAGTTTAGTGCAGTCGATTCTGTTTAGGAATCAACTATCGATTGTTACTGCTTCAGAATCAAGGAGATGATTCTTTTTTGCAATCGACTCTGGAGTGTTAACACCTCAGAATCAACCAATTGATTCTTTTTAGGAATCAACTTGATTCTTATTTATTACTCTTTTATCCATTCTTAACACCTCTGAATAAATGAATCAGTTGTATTTTGCAATCAACTCTCGATTCTCTGGAATCAAGGAATCGATTCCCTCTTGGAATCGACTCT

Associated Phenotype:

Not determined