ZMP

agxt2

Ensembl ID:

ENSDARG00000087194

ZFIN ID:

ZDB-GENE-050913-100

Description:

alanine--glyoxylate aminotransferase 2, mitochondrial [Source:RefSeq peptide;Acc:NP_001028922]

Human Orthologue:

AGXT2

Human Description:

alanine--glyoxylate aminotransferase 2 [Source:HGNC Symbol;Acc:14412]

Mouse Orthologue:

Agxt2

Mouse Description:

alanine-glyoxylate aminotransferase 2 Gene [Source:MGI Symbol;Acc:MGI:2146052]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa31054	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa23861	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa31054

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
ENSDART00000122370	Essential Splice Site	30	484	1	17

Genomic Location (Zv9):

Chromosome 21 (position 9082095)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	11052216
GRCz11	21	11144844

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGTCCTGCCCCAGATTCCCCCATGTGACTTTAAACCTGAGCCCTATCAGG[T/C]AAGAGGCTTATATCTGAGGACAGTGATAATAATCACACTGATATCATATC

Long Flanking Sequence:

TAAATGAGTGGATAGACAGACGAACAGACAAATCAATAGAGAGATGAATGTATGAAAATACAAACAGACATGTAGATAGATTAGAAAGATGATAGAATATAGATGATGCAAACAGATGAAAGGAGTAACAGAGAGAAAAAGTAGATCGATGAATTGTTGAATGAATAGATAGATAAAAGATAGATGTATGAATGTATGAACAGACACAGACAGATGCATAGACAGATGAATAGATGGAGTAATAAAAAGATAGACATAGAGAGAGACAGACAGATGAGCACATACTGTTACACATGAAAGCTGATGCCCTGTGACTTATAATAGGATAAAAAAAGGATAAAAATAGGATAAAAAGGGCTGGAAACATTGTGACACATCACTGGCACTAAATGTACTGTACCTCCGCTCAGGTGTGCTGTGCCAGAAAACAGCAGTCAAACATCCATCAGCGGTCCTGCCCCAGATTCCCCCATGTGACTTTAAACCTGAGCCCTATCAGG[T/C]AAGAGGCTTATATCTGAGGACAGTGATAATAATCACACTGATATCATATCATCTCACTTTAAGCTTGAATGACTCTTCTTACAGGGCATGTCTAAAGAGCGTTTACTAGATATTCGGAAACACAACTGTAACCCTATGACCATGAAGGTAACCTACTACAAGAAGCCGGTCTTCATAAACCAGGGCCACATGCAGTGGTTGTGGGACGTGGACGGAAGGCGATATCTGGACTTGTTCGCAGGGGTGGCCACCGTCAGTGTTGGACACTGCAACCCGTATGATTCAGTTTATTTCCATGCCACATTTATAGTTTCATTTTTTTATTTGATGATAGGGCTGACCGATATTGGAAAAAAATCTAACATTGCGATATACCGTGTTATTCTGAGATATTAATTAGGGCTGCACAATATATCGTTTCAGCATCGATATCGCAATGTGTGCATCCGTTACATTGCAGGGTCTTAAATGTCAAGTATGGGTTATTGTTGACCAGGAGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23861

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:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000122370	Nonsense	67	484	2	17

Genomic Location (Zv9):

Chromosome 21 (position 9082288)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	21	11052409
GRCz11	21	11145037

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGAAGGTAACCTACTACAAGAAGCCGGTCTTCATAAACCAGGGCCACATG[C/T]AGTGGTTGTGGGACGTGGACGGAAGGCGATATCTGGACTTGTTCGCAGGG

Long Flanking Sequence:

GTATGAACAGACACAGACAGATGCATAGACAGATGAATAGATGGAGTAATAAAAAGATAGACATAGAGAGAGACAGACAGATGAGCACATACTGTTACACATGAAAGCTGATGCCCTGTGACTTATAATAGGATAAAAAAAGGATAAAAATAGGATAAAAAGGGCTGGAAACATTGTGACACATCACTGGCACTAAATGTACTGTACCTCCGCTCAGGTGTGCTGTGCCAGAAAACAGCAGTCAAACATCCATCAGCGGTCCTGCCCCAGATTCCCCCATGTGACTTTAAACCTGAGCCCTATCAGGTAAGAGGCTTATATCTGAGGACAGTGATAATAATCACACTGATATCATATCATCTCACTTTAAGCTTGAATGACTCTTCTTACAGGGCATGTCTAAAGAGCGTTTACTAGATATTCGGAAACACAACTGTAACCCTATGACCATGAAGGTAACCTACTACAAGAAGCCGGTCTTCATAAACCAGGGCCACATG[C/T]AGTGGTTGTGGGACGTGGACGGAAGGCGATATCTGGACTTGTTCGCAGGGGTGGCCACCGTCAGTGTTGGACACTGCAACCCGTATGATTCAGTTTATTTCCATGCCACATTTATAGTTTCATTTTTTTATTTGATGATAGGGCTGACCGATATTGGAAAAAAATCTAACATTGCGATATACCGTGTTATTCTGAGATATTAATTAGGGCTGCACAATATATCGTTTCAGCATCGATATCGCAATGTGTGCATCCGTTACATTGCAGGGTCTTAAATGTCAAGTATGGGTTATTGTTGACCAGGAGCTTGTAGATTAATGTCAAACTATAACGATTTAAATTTTTTTAATTTCATTTGTTTGTTTTTTCTGTTAAACATATCAAGTTCGTTTAAAACATCAGGCACAAGAAACAATAGCATTTCTAGCTTAACAAAGATTAATTAAATCACATTGTTATAGTAAAGTGTCATTTTACATATTTATGTCCAACTGCCATTT

Associated Phenotype:

Not determined