ZMP

arg2

Ensembl ID:

ENSDARG00000039269

ZFIN ID:

ZDB-GENE-030131-1334

Description:

arginase-2, mitochondrial [Source:RefSeq peptide;Acc:NP_955905]

Human Orthologue:

ARG2

Human Description:

arginase, type II [Source:HGNC Symbol;Acc:664]

Mouse Orthologue:

Arg2

Mouse Description:

arginase type II Gene [Source:MGI Symbol;Acc:MGI:1330806]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6316	Nonsense	Mutation detected in F1 DNA	Not yet available
sa28149	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa6316

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
ENSDART00000057377	Nonsense	74	347	3	8

Genomic Location (Zv9):

Chromosome 13 (position 33252343)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	32898291
GRCz11	13	33028741

KASP Assay ID:

554-4573.1 (used for ordering genotyping assays)

KASP Sequence:

CCTAATGTATTGTAGACTACCCTGTTCATGATTTCGGAGACCTGACCTTC[A/T]AGCATCTGGAAAAAGATGAGCACTTCATGCACGTGCCGTTCCCACGCACA

Long Flanking Sequence:

CAATCTGTCTCTTAGCTTATGACAATCAACTCCTGAGTTCCTTCATATTTAGCTTGTTTTTTTATTCAGAAAGCACATCTAGTGTTTTAAACATGCCTACTTGGGCTGTAGTTTTTACATCTATTCCTGTTAAGAGGCCACTGGCTTGTACATGTGCCTATCGATGGTCATTTAAAATCTGATGAGTAATTCAACACGGTCTGGTTTGGTTCTGTCAGCTGTTTGAACCTTCCTCCGTTTCTCCTATAGTTTCTACCTACATTTGCATGTTTGGAATTGAGTGACAGAGCTGTCAACAACCAGCTTTACCTTTTTTTTTTTTCATCTTGCCAGCATGTAATGAATAAAATAGTTTGGGAAAGGAGTGAGCATTTGTGAAAGTGTTAATATGTTCATGTTAATGTCATTATAATGGTCACGTGAAGAAAACTATGTGATTAATTTGTTCAACCTAATGTATTGTAGACTACCCTGTTCATGATTTCGGAGACCTGACCTTC[A/T]AGCATCTGGAAAAAGATGAGCACTTCATGCACGTGCCGTTCCCACGCACAGTTGGACGTGCCAATCAGTTGCTCTCTGGAGCTGTGAGTGGGGCGGTGGGAGCAGGACACACTTGCATCATGCTGGGGGGAGATCACAGGTACACACAGTTCACAATGTTTTTTCCAATACACTTTGTATGAACTAATCAGGAAAAATCTGACTTGTTTACTATGATTTTTATTGTCTTATGCCAATTTTTAGGTTACAATATCTGCAAAATATTTTGGTATGTAGTAGAGTTGCACGATTTCTTGATAAACAGAGTTGGAGATCATCATTTCTCTTCAGTTCTTAACAAAACACATGTAAATGATGCAGTCCATTTTATAAAATGTTTACAAATGATCTTTAATAATAGATATTGGGAGAAAAGGCTTCACTTATAAATCAGGATTAATAATATGATCTTCATTTGAAGTACTGAGTTCTTTTAAAAGGTGATTTGCTTCTGTTTATAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa28149

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 > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000057377	Nonsense	140	347	4	8

Genomic Location (Zv9):

Chromosome 13 (position 33253181)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	13	32899129
GRCz11	13	33029579

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGCTCAGTGGAAGGCCATTCTCAGCAGTGTCCTGACCTGTGTCTGATATG[G/A]GTGGACGCACATGCGGATATCAACACGCCTCTGACTTCACCTTCGGGAAA

Long Flanking Sequence:

CAAAACACATGTAAATGATGCAGTCCATTTTATAAAATGTTTACAAATGATCTTTAATAATAGATATTGGGAGAAAAGGCTTCACTTATAAATCAGGATTAATAATATGATCTTCATTTGAAGTACTGAGTTCTTTTAAAAGGTGATTTGCTTCTGTTTATATCTGTTGTGTTTTAATCAGTTTGTCGGAATGGAAAATGTGTTCATAATAAGTTACCTATTTTACTAGTCTTTCCATTCATGTCTTCCTGGCAGAGGAAGTGTTATGGTACTCTAAACTGAGCTTAGTGTTATCGCTTCACTTGTTATCAATTTGTACTTATAGTTTGTATTTCCATGTAGCTGATTACAACGTTTCAGAACACCGATTACTAATAAGAAATGATGTCATCCAGTCTGTTTTGAATTCAGCTTAGTTCTCGATGTTTTTATCCACACAGCTTAGCGATTGGCTCAGTGGAAGGCCATTCTCAGCAGTGTCCTGACCTGTGTCTGATATG[G/A]GTGGACGCACATGCGGATATCAACACGCCTCTGACTTCACCTTCGGGAAACCTCCACGGCCAGTCTGTAGCTTTCTTACTAAAGGACCTGCAGAACAAGGTGATTAGTGTTTGTGCAAACAATTACGTCTGTGATCCAAAGACATGCTGATGCAGTCTCTGGCATGACTACAATTCACTATTCACAATGAAAAATCATTAGTCTCAGAAGAAGTAACACTTTGTAATGACTTAATCTTTTAGAAATATCCTTAGTATTGTCCTTTTGAACAGCTGAAGCCTTTATCTTCTAATTTGTAACTTGCAGATGCCCAAAGTTCCCGGATTTTCCTGGATGAAGCCGTTCCTGTCTGCCAGAGATCTGGTGTACATTGGTCTTAGAGATGTGGATCCAGGCGAGCAGTAAGTACACCGCGTTTCGTCCCAAAATGACATCCAGGATTTGGCACCTGTTGCTTGTTCTCTAAAGCCAAATTGGCTATTGTGTCATGTCACAGACTA

Associated Phenotype:

Not determined