ZMP

LOC793153

Ensembl ID:

ENSDARG00000025672

Human Orthologue:

ANTXR1

Human Description:

anthrax toxin receptor 1 [Source:HGNC Symbol;Acc:21014]

Mouse Orthologue:

Antxr1

Mouse Description:

anthrax toxin receptor 1 Gene [Source:MGI Symbol;Acc:MGI:1916788]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa15102	Essential Splice Site	Available for shipment	Available now
sa38714	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa15102

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
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Mutation:

A > T

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000030064	Essential Splice Site	476	609	18	18

Genomic Location (Zv9):

Chromosome 8 (position 52745413)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	50062436
GRCz11	8	50051082

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TCATAAANTATTATTGTTTTCTCTAAATATTTCTCTCTTCTYGTTCCCTC[A/T]GGGCMGCTGTATGAAYTTCACCCGCATCAAGTCCAATCCTCCACCKCGGT

Long Flanking Sequence:

CATGATGGCAGATTTTTCAAGCTACCAGTATTTAGCTTAAAGTGACATTTTAACGGCTTAATTAGGTTTATTAAGTGAGGGTAATTAGGCAAGTCATTGTATAATGATGGGTTGTTCTGTAGACAATCGAAAAAAATATTGCTTAGGCGGCCAATAATATTGACCTTAAAATGGTTTTAAAAAATTAAAACTGCTTTTATTCTAGCCAAAATAAATCAAATAAGACTTTCTCCAGAGGAAAAAAATATTATCAGACATACTTTGAAAATTTCCTTGCTCTGGTAAACATAATTTGGGAAATATTTGAAAAATAAACTAAAACATCATCTGTATATGTGAAATACAAATATTACCTTGTATGTCATATGTGTAACTTTCATATGTTGTCGTTTATCATATTTCAATGTTAGTTGTCGCATAGCAACAAGAAACCACAACAATGCATTTTCTTCATAAAGTATTATTGTTTTCTCTAAATATTTCTCTCTTCTCGTTCCCTC[A/T]GGGCCGCTGTATGAACTTCACCCGCATCAAGTCCAATCCTCCACCGCGGTATCCATCCTACAACCATCATTCCTCCCCCATCTACACGCCCCCGCGGACCCTCAACCCACCGCCTCCACAGGGCCACCTGCCCCCTCCACCACACAGTCCACCAGCCTCCCTGTCCGGCAGCATTCCTTCAATGCCTTCATCTCCTCCACCCCACGCCATCAACCCGCCTCCACCCATTACTCCTCCTCCATCATATTCTCCGCCTCCCGTCTGGTCTCCGCCTCCTACCACCCTCTACTTTGCTCTGCCCTCCCTTCCACCTTCACCCACTTCCTCCCTGCCTCCCCCCCCTCAAGCCCCACCCCCAAGCAGAGCTCCGCCTCCAGACCGCCCACCTCCACGGCCTAGTGTGTAACTTGTAAGTGAACTACTTAAAGTCCACAGGAACTGGAAGCTGCGGACATTTTTTTTTTGTATTGTGATGCACTTCCTAGAGAAACAATATATTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38714

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
ENSDART00000030064	Nonsense	485	609	18	18

Genomic Location (Zv9):

Chromosome 8 (position 52745442)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	8	50062407
GRCz11	8	50051053

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTTCTCTCTTCTCGTTCCCTCAGGGCCGCTGTATGAACTTCACCCGCATC[A/T]AGTCCAATCCTCCACCGCGGTATCCATCCTACAACCATCATTCCTCCCCC

Long Flanking Sequence:

ATTTAGCTTAAAGTGACATTTTAACGGCTTAATTAGGTTTATTAAGTGAGGGTAATTAGGCAAGTCATTGTATAATGATGGGTTGTTCTGTAGACAATCGAAAAAAATATTGCTTAGGCGGCCAATAATATTGACCTTAAAATGGTTTTAAAAAATTAAAACTGCTTTTATTCTAGCCAAAATAAATCAAATAAGACTTTCTCCAGAGGAAAAAAATATTATCAGACATACTTTGAAAATTTCCTTGCTCTGGTAAACATAATTTGGGAAATATTTGAAAAATAAACTAAAACATCATCTGTATATGTGAAATACAAATATTACCTTGTATGTCATATGTGTAACTTTCATATGTTGTCGTTTATCATATTTCAATGTTAGTTGTCGCATAGCAACAAGAAACCACAACAATGCATTTTCTTCATAAAGTATTATTGTTTTCTCTAAATATTTCTCTCTTCTCGTTCCCTCAGGGCCGCTGTATGAACTTCACCCGCATC[A/T]AGTCCAATCCTCCACCGCGGTATCCATCCTACAACCATCATTCCTCCCCCATCTACACGCCCCCGCGGACCCTCAACCCACCGCCTCCACAGGGCCACCTGCCCCCTCCACCACACAGTCCACCAGCCTCCCTGTCCGGCAGCATTCCTTCAATGCCTTCATCTCCTCCACCCCACGCCATCAACCCGCCTCCACCCATTACTCCTCCTCCATCATATTCTCCGCCTCCCGTCTGGTCTCCGCCTCCTACCACCCTCTACTTTGCTCTGCCCTCCCTTCCACCTTCACCCACTTCCTCCCTGCCTCCCCCCCCTCAAGCCCCACCCCCAAGCAGAGCTCCGCCTCCAGACCGCCCACCTCCACGGCCTAGTGTGTAACTTGTAAGTGAACTACTTAAAGTCCACAGGAACTGGAAGCTGCGGACATTTTTTTTTTGTATTGTGATGCACTTCCTAGAGAAACAATATATTAAACAGTGGGCGTGGCTTGTTTTTCTTTAC

Associated Phenotype:

Not determined