ZMP

gnpda1

Ensembl ID:

ENSDARG00000037307

ZFIN ID:

ZDB-GENE-050417-417

Description:

glucosamine-6-phosphate isomerase 1 [Source:RefSeq peptide;Acc:NP_001017867]

Human Orthologue:

GNPDA1

Human Description:

glucosamine-6-phosphate deaminase 1 [Source:HGNC Symbol;Acc:4417]

Mouse Orthologue:

Gnpda1

Mouse Description:

glucosamine-6-phosphate deaminase 1 Gene [Source:MGI Symbol;Acc:MGI:1347054]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22471	Nonsense	Available for shipment	Available now
sa38996	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa22471

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

Mutation:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000054266	Nonsense	65	269	3	7
ENSDART00000136909	Nonsense	65	275	2	5

The following transcripts of ENSDARG00000037307 do not overlap with this mutation:

ENSDART00000131287

Genomic Location (Zv9):

Chromosome 14 (position 24614185)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	23412709
GRCz11	14	23709954

KASP Assay ID:

2260-7520.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TACAAGAAACTGATCGAGTACCACAAGAAGGGAGAAATATCTTTTCAGTA[T/A]GTGAAAACGTTTAATATGGATGAGTATGTAGGTATGTGAGCAGACATTTA

Long Flanking Sequence:

AGCGACGCGACAAAACAGCCTTTAATAATGTGTCGCGTCGCGCTAAACAAAGTCTCCACGGTTGACTCTATAGTGTCAGTGAAGTATACCTACGGCTGCACTTCCGTCTTAATTTAACGATAATAGGGTCTAAAGTCTAAAGAAGGCAGGACTGTAACAAACACTGGGTTTCCAGGTCAATTTACCTAATCGTTTCTCTTAGACTCAGATGAAGCCATGAAGCTCATAATCCTCAATGACTACGACCAAGTCAGCGAATGGGCTGCCAAGTACATCAGGAACAGAATAAGGAAGTTTAATCCAGGTCCTGAGCGGTTCTTCACTCTGGGTCTTCCAACAGGTAGAGTCAAAACAAACTCATGCTGTGTACTATGCAAACGCATTGAACTGTGTTAAGGTATACTGTATTTGAATTGTGTTTGTATTACAGGAAGCACTCCACTTGGATGCTACAAGAAACTGATCGAGTACCACAAGAAGGGAGAAATATCTTTTCAGTA[T/A]GTGAAAACGTTTAATATGGATGAGTATGTAGGTATGTGAGCAGACATTTATGCTTGGGGATCAAGGGTTGAACTGCCTGTCATATATTTAGTTGTAACACTGAACCAAAGTGTAAGTGGTTATTGTCTTTTACAGGACTTCCCAGAGACCATCCTGAAAGTTATCATTCATTCATGTGGAATAACTTCTTCAAGCACATCGACATTCGAGCAGAAAACGCTCACATCCTGGATGGCAACGCACCCAATCTAGAGAAGGAATGTCAGGACTTTGAAGCCAAAATCAAAGCCGCAGGAGGAATTGAGCTCTTTGTTGGCGGTAAGACATAAGATTGAACTTTGTCCTTTGCATGGTATGTGAATGAACTTTGTCTTGTGCTCACATTGCAGGGATTGGACCTGATGGTCACATTGCATTCAATGAGCCTGGTTCCAGTCTTGTGTCTCGAACGCGTGTTAAGACCCTGGCTATGGACACAATTCTGGCTAATGCACGTTTCT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38996

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
ENSDART00000054266	Essential Splice Site	137	269	None	7
ENSDART00000136909	Essential Splice Site	137	275	None	5

The following transcripts of ENSDARG00000037307 do not overlap with this mutation:

ENSDART00000131287

Genomic Location (Zv9):

Chromosome 14 (position 24614573)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	23413097
GRCz11	14	23710342

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTGTCCTTTGCATGGTATGTGAATGAACTTTGTCTTGTGCTCACATTGC[A/C]GGGATTGGACCTGATGGTCACATTGCATTCAATGAGCCTGGTTCCAGTCT

Long Flanking Sequence:

TGTGTTAAGGTATACTGTATTTGAATTGTGTTTGTATTACAGGAAGCACTCCACTTGGATGCTACAAGAAACTGATCGAGTACCACAAGAAGGGAGAAATATCTTTTCAGTATGTGAAAACGTTTAATATGGATGAGTATGTAGGTATGTGAGCAGACATTTATGCTTGGGGATCAAGGGTTGAACTGCCTGTCATATATTTAGTTGTAACACTGAACCAAAGTGTAAGTGGTTATTGTCTTTTACAGGACTTCCCAGAGACCATCCTGAAAGTTATCATTCATTCATGTGGAATAACTTCTTCAAGCACATCGACATTCGAGCAGAAAACGCTCACATCCTGGATGGCAACGCACCCAATCTAGAGAAGGAATGTCAGGACTTTGAAGCCAAAATCAAAGCCGCAGGAGGAATTGAGCTCTTTGTTGGCGGTAAGACATAAGATTGAACTTTGTCCTTTGCATGGTATGTGAATGAACTTTGTCTTGTGCTCACATTGC[A/C]GGGATTGGACCTGATGGTCACATTGCATTCAATGAGCCTGGTTCCAGTCTTGTGTCTCGAACGCGTGTTAAGACCCTGGCTATGGACACAATTCTGGCTAATGCACGTTTCTTTGATGGAGATCTCTCTAAGGTGCCCACCATGGCCCTCACAGTTGGCGTTGGCACTGTGATGGATGCTAGAGAGGTATAAGTATGAATATTTCTATATGTTTGGCCACACACAGCTAAATTAGGTTGTTACATGACCTTTCCAATTAATTATCTTCTGGAACATGCTGGAGTATTGACAACTGCATTTACCAAAGCTCTGCAAGTTGTTGCTCTCATCTCTATGGACTGCAAAAAAAACATTGGTACATCTTGCAGGATCTTGCAGGGTTCCCACGCTTCTTAAAAGTACTTGCATTTCAGACATATGGATTCAAGGTCTGGAAAGTACTTAAAAACAAACATAGGTCCTTGAAAGTGCTTGAATTAAATTTAAAACTAAATTTGTTC

Associated Phenotype:

Not determined