ZMP

LOC562799

Ensembl ID:

ENSDARG00000070843

Human Orthologue:

ARID3A

Human Description:

AT rich interactive domain 3A (BRIGHT-like) [Source:HGNC Symbol;Acc:3031]

Mouse Orthologue:

Arid3a

Mouse Description:

AT rich interactive domain 3A (BRIGHT-like) Gene [Source:MGI Symbol;Acc:MGI:1328360]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa27724	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa21842	Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa27724

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000104358	Essential Splice Site	364	528	6	8

Genomic Location (Zv9):

Chromosome 11 (position 5838291)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	5806474
GRCz11	11	5803729

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTAGTTTGGTTTATTTAAATGCGTTTTCTCTTTCAATTTCTTTTTTTGTT[G/A]TAGAGGATGACGGGTTTCAGACGCGCCTGCCTGCATCTCTGGCCACACAT

Long Flanking Sequence:

ACGTTTACACATCGCTGCACAAACTGCATGTAAACACATCAACATTTCACAGTATAATATGACGTTGGTTTAAGATGTTTGCTCGATGTTGGGTTTTGGTCACTTTGTAACACAACCTAAAATCAACCATATATCAACATTATTTGACGTCGTTATTGGACATCAAAATAACATTGTCCTTAGACGCTGGTTAGACATTGACTTTTGGTCACCTGACATCACAACCTAAATCTAACCTAATATAAACATCTTATGACCTTGTGTGCCTGCTGGGCAATAACTAAATGCACTACCGAATGTTACGTTTACACACATCCACAAATTACATCAGCATCAGCTTTTCACAGCGTAATACTCACTACGCATTACTCTTGAGTACTTTTAAAAGGTCTACACACAGAAATCTCTTTGATTTGGAAAACATGTACACACGCTCTTTGATGTCCACATTTAGTTTGGTTTATTTAAATGCGTTTTCTCTTTCAATTTCTTTTTTTGTT[G/A]TAGAGGATGACGGGTTTCAGACGCGCCTGCCTGCATCTCTGGCCACACATTCAGTAGCTGCAGCACAGGCCGCGGCTGCACAAGCGGCCACCATCGCACAGGTAGCTGCTCTGGAGCAGCTGCGGGATAACCTGGAGACCGGCGAACCCCCTCGGAAAAAAATTGCACTACCACTGGAGGAACACCAGCGGTTACTGCAGAGAGCCTTGCAGCACAATCTGATGGCCATGACCGCACAAATCCCCATGAACATCCGCATCAACAATCAAGGTAGTGACACTTTAAAGGTTCAAGACACCCTGCAGTACTTTTTTAAATTTTATTTGAACAGATTTATGTGTGTTGAGCGTATTTTAAGACAACATTACCATCTGTTTGCTTTAATTGAGAGGAAAAACTGGATAATGTTGAGCTTTTGTCTGCTAATTTCATCTTTTGGGGTTAAAATAATTTTTGGGATGGGATCAAAATCTGTGACGTAGCGTGAATCTGCAAGTGCA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa21842

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
ENSDART00000104358	Nonsense	397	528	6	8

Genomic Location (Zv9):

Chromosome 11 (position 5838390)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	5806573
GRCz11	11	5803828

KASP Assay ID:

2260-3888.1 (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTCAGTAGCTGCAGCACAGGCCGCGGCTGCACAAGCGGCCACCATCGCA[C/T]AGGTAGCTGCTCTGGAGCAGCTGCGGGATAACCTGGAGACCGGCGAACCC

Long Flanking Sequence:

TCACTTTGTAACACAACCTAAAATCAACCATATATCAACATTATTTGACGTCGTTATTGGACATCAAAATAACATTGTCCTTAGACGCTGGTTAGACATTGACTTTTGGTCACCTGACATCACAACCTAAATCTAACCTAATATAAACATCTTATGACCTTGTGTGCCTGCTGGGCAATAACTAAATGCACTACCGAATGTTACGTTTACACACATCCACAAATTACATCAGCATCAGCTTTTCACAGCGTAATACTCACTACGCATTACTCTTGAGTACTTTTAAAAGGTCTACACACAGAAATCTCTTTGATTTGGAAAACATGTACACACGCTCTTTGATGTCCACATTTAGTTTGGTTTATTTAAATGCGTTTTCTCTTTCAATTTCTTTTTTTGTTGTAGAGGATGACGGGTTTCAGACGCGCCTGCCTGCATCTCTGGCCACACATTCAGTAGCTGCAGCACAGGCCGCGGCTGCACAAGCGGCCACCATCGCA[C/T]AGGTAGCTGCTCTGGAGCAGCTGCGGGATAACCTGGAGACCGGCGAACCCCCTCGGAAAAAAATTGCACTACCACTGGAGGAACACCAGCGGTTACTGCAGAGAGCCTTGCAGCACAATCTGATGGCCATGACCGCACAAATCCCCATGAACATCCGCATCAACAATCAAGGTAGTGACACTTTAAAGGTTCAAGACACCCTGCAGTACTTTTTTAAATTTTATTTGAACAGATTTATGTGTGTTGAGCGTATTTTAAGACAACATTACCATCTGTTTGCTTTAATTGAGAGGAAAAACTGGATAATGTTGAGCTTTTGTCTGCTAATTTCATCTTTTGGGGTTAAAATAATTTTTGGGATGGGATCAAAATCTGTGACGTAGCGTGAATCTGCAAGTGCAAAGGTTTCTCATTATTATTCATAGCCGAGTTTTCTTATCCTACGAGAAGAGCCTGCTTCTTAATTATTCACGAGACCACATGCTTTCTGAAGACCTGCC

Associated Phenotype:

Not determined