ZMP

LOC555957

Ensembl ID:

ENSDARG00000033589

Human Orthologue:

EPHB3

Human Description:

EPH receptor B3 [Source:HGNC Symbol;Acc:3394]

Mouse Orthologue:

Ephb3

Mouse Description:

Eph receptor B3 Gene [Source:MGI Symbol;Acc:MGI:104770]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa37568	Nonsense	Mutation detected in F1 DNA	Not yet available
sa3165	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa37568

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
ENSDART00000050395	Nonsense	97	974	2	15

Genomic Location (Zv9):

Chromosome 22 (position 38839141)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	35985955
GRCz11	22	35972517

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGTTTACTGTAAGAGACTGCAATAGCATTCCCAACATTCCAGGATCATGT[A/T]AAGAGACCTTCAATCTGTTCTACTACGAGTCCGACTCGGATTCAGCCACC

Long Flanking Sequence:

CGGTTATATTGTTTCTTAGCCACGGTGCGTAGGGCTTTAGCTCAGAAAGAGCAATTTACTGCCTGCAGTACCTTTGCAGCGTAACACCTCAGGTTTCTAAAGCCCTGGATAACATCACAATGAGAATGCTTCATTTATAATACTGACAATATTGCGTATTGTGCAACACTTTAGATAAAACATCTGCTATTGCTATCGTTCTCTAGAATAATCCTTGCATGCAGTGTATATGAAGGACATTGTCAAGGTGAACTTGTGTGTTGTTTCATATCTGCGACTCACAATGCTCTCTTTTTTTAATGCAGTGGGAGGAAGTTAGCGGTTACGATGATGCCATGAACCCCATCCGAACGTACCAAGTGTGCAACGTTCGCGAACTCAACCAGAACAACTGGCTACGCAGTGACTTCATCCCGCGGAAGGACGTTCTCCGCGTTTACGTGGAGATGAAGTTTACTGTAAGAGACTGCAATAGCATTCCCAACATTCCAGGATCATGT[A/T]AAGAGACCTTCAATCTGTTCTACTACGAGTCCGACTCGGATTCAGCCACCGCCACCAGTCCTTTTTGGATGGAGAACCCTTACGTTAAGGTGGACACCATTGCTCCGGATGAGAGCTTCTCCATGTTGGAATCCGGTCGGGTCAACACTAAGATTCGCAGCTTTGGTCCACTTTCCAAGGCTGGTTTTTATTTGGCTTTCCAAGACTTGGGTGCCTGCATGTCTTTAATCTCCGTCCGGGCTTTCTACAAGAAGTGTTCCACAACCATTGCCAATTTTGCCGTCTTCCCAGAAACAGCCACTGGCGCTGAGGCCACGTCACTAGTCATTGCCCCTGGGACTTGCGTACCAAACGCTCTGGAGGTTTCTGTCCCTCTTAAACTCTACTGCAATGGAGACGGAGAATGGATGGTTCCTGTGGGTTCCTGCACTTGCATGGCTGGGTTTGAGCCTGCAGTTAAGGAGACGCAGTGTCAAGGTGAGTGCTGATATATATATTTT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa3165

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000050395	Essential Splice Site	557	974	7	15

Genomic Location (Zv9):

Chromosome 22 (position 38856618)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	22	36003432
GRCz11	22	35932085

KASP Assay ID:

554-2736.1 (used for ordering genotyping assays)

KASP Sequence:

GGACTGGTCTTCATCAYTGTTGTTGTGGTTATTGCCATTGTCTGCCTGAG[G/A]TAAACAACACTTTTGCTGCATTTATAACTACTGTATATGCAACTAGATGNT

Long Flanking Sequence:

CAACCCTAATCAAACACACCTGAACAAGCTAATCAAGCTCTTACTAGGTATACTTGAAGCATTCAGGCAGGTGTGTTGAGGCAAGTTGGAGCTAAACCCTGCAGGGACACCGGCCCTCCAGGACCAAGATTGGTGACCCCTGCTTGTAAACATTCACTCCATCGGACTCTTGACTCTCAGCACCGCCCATGTTCGGCAGAGCCACCAAGCCAACCAATCAAAGAGCTAGAGCTACACGTCATTGCGATGACGCTGGTTACTCGACCAAGTGAAGGCTGCACCGGACCATGCACGTGCGCTTGATGCAGAAGTATAAATCAGCCTATAGTAGTCCAAGAAATGCTATATGAAAATAGATATGAGGAATATATGTTGTGTTTCCATCACACAGCTGATGCAGACAAGGCACTACAGGAGCAGTTACCCCTCATTGTGGGCTCTCTGACCGCAGGACTGGTCTTCATCATTGTTGTTGTGGTTATTGCCATTGTCTGCCTGAG[G/A]TAAACAACACTTTTGCTGCATTTATAACTACTGTATATGCAACTAGATGTTAATAGGTACTAGGTATACCTATAAAACAACAAATATCTCTAAATGAGTGTGTAATTTAGGTCACCCATAATGCCAATGTCAATTAATAGATGTAGTATCGGGCACTATGAGAAGCAGTTTCATTCCGGGTTGTCAGTAATTTTGGATCTTGTAAACTGCAGCCAGTGGTCTCAAATGTACATGTGCCCTATATTGGAATTCCACAGCGTGCTGGTGATTGTTGGCAAAGTCACTTTCCATCCTGTGGCCATCTTCCCATCACTCCAGTTGAGGGGCAAGCCATCTGTGTGTTTAAAGCCTTATCATGCTAAAACTCTCAATTTGCACTCTCTTTCTTTCCAATCACACAGTGTGTTTCAGTATCTTAACTTGTAGGCCTTGGCATATTCCGGAACTGAATTTGAATTGGAAATGAGATACAAATCACCAGCGGGTATTATTGGCCCGGT

Associated Phenotype:

Not determined