ZMP

epha4b

Ensembl ID:

ENSDARG00000011600

ZFIN ID:

ZDB-GENE-030826-6

Description:

eph receptor A4b [Source:RefSeq peptide;Acc:NP_705944]

Human Orthologue:

EPHA4

Human Description:

EPH receptor A4 [Source:HGNC Symbol;Acc:3388]

Mouse Orthologue:

Epha4

Mouse Description:

Eph receptor A4 Gene [Source:MGI Symbol;Acc:MGI:98277]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa13595	Splice Site, Nonsense	Available for shipment	Available now
sa39899	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa13595

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:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000007709	Splice Site, Nonsense	661	923	11	15
ENSDART00000037292	Splice Site, Nonsense	714	976	15	19

Genomic Location (Zv9):

Chromosome 2 (position 40252987)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	40646177
GRCz11	2	40500411

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

ATAATATAATTAGTATTGCTCACACATTTGTCTTGTCTTTTCTCTTGCAG[A/T]AGCATGATGGGCAGTTCACAGTYATTCAGCTGGTGGGCATGATGCGTGGC

Long Flanking Sequence:

TATAGTTTGAAATGTATGCTCTTCTTCTCCCCTAAGGGCTTATTATCTGTTGCCATCTTGTGGTGGAACGTCAACCATCTTTGTTCTGCTTAATGGCAGGCTGATGGCTGCTGATGCGCTGAATGTCTGAAATTAAACATATTTTAAATATGCACTATTTTATAAATAAACTGCATAAATGCAATCTAAACAACTATATTCTCACAAATGTCTCAAAAGTACATTATGTTGTCCAATAGCTGCAATATTTGTCAAACTGTAGTGAGTTTATTGATCTGATGTCACTCTATGTGGGCGGAGTAATACACAATAGTGAAGAGGGTGTATGAGTGCTGTTATAGCACGGCTATCAGCCAATCAAATTCAAGAACCAGAAAGAACTACTGTCATATAATAAAATAAATTATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATATAATTAGTATTGCTCACACATTTGTCTTGTCTTTTCTCTTGCAG[A/T]AGCATGATGGGCAGTTCACAGTCATTCAGCTGGTGGGCATGATGCGTGGCATCGCTTCAGGAATGAAATATCTGTCTGATATGAGCTACGTCCACCGTGATCTGGCAGCTCGCAACATCTTGGTCAACAGTAACCTGGTGTGCAAAGTGTCTGACTTTGGCCTGTCCAGAGTGCTGGAGGATGATCCTGAAGCTGCGTATACAACACGGGTAAAGCATCTTTTCTTTATTAATGTTGTAGATTTAGCATCTATTTTTACAGCTTGGATCGAAGGTTGCATATGTAACCATCGTTCCCTGAAGGAGAGAATAGAGACATTAAGTCAGGAATTCAATTAAATTTAAGCTTATTGGTATTGTATTTTGCTTTTCACTTTAATTATTGTTCCAAAAGCATCTTTGCAAAAAGTGCATGTTAGTACATCACCGTCAAATCAGAAAGTTAAGGTCATGTATATAGGGTGGAAAGTATATTAACAGTGCTCAGCATTTATGTGTACA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa39899

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
ENSDART00000007709	Nonsense	813	923	13	15
ENSDART00000037292	Nonsense	866	976	17	19

Genomic Location (Zv9):

Chromosome 2 (position 40259640)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	2	40652830
GRCz11	2	40507064

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACTGCCCCGTGGTCCTTCATCAGCTCATGCTGGACTGCTGGGAGAAAAGC[A/T]GAAGTGAACGGCCCAAATTCGGGCAGATCGTCAACACTCTTGACAAACTT

Long Flanking Sequence:

TATTAAAACTATTATGTTTAGAAATGTGTTAAAAAAAATCCTCTCTCTGTTAAACAGAAATTGGGGAAAAAACCAGGGGGGCTAATAATTCTGACTTTATATGTATATGAAACTGTATATGAAAATAAATATTTATGTAAAGTTAAATATTAAATGGAAAGTCAACTAATTAAATTTTGCTGTCATTTAGTCACCAACATTATCCCAAACCTCTATGACTTTCTTTATTATGCAGAACACAAAAGATATTTTGAAAAATGTTGGTAATTGTTTTAAATCCCCTTGATTAGTTGGCAGTAAATGGAAATCAATAGAAACCCAAACTGTAGAAAGTAAGAAACACGTACCAACATGAATGAAGCTTTTGTTCTTTGCATGTTTTGACTCCTGTGTCTTTGTTGTAGGTGATTAAAGCTATAGATGAGGGTTACAGGCTTCCCGCCCCAATGGACTGCCCCGTGGTCCTTCATCAGCTCATGCTGGACTGCTGGGAGAAAAGC[A/T]GAAGTGAACGGCCCAAATTCGGGCAGATCGTCAACACTCTTGACAAACTTATCCGCAACCCCAACAGTCTGAAGGAGCTCGCTAACAGCTCAGTTTGGTGAGAAACTTAATTTCATTTAAATCCAGCTGATGTTTAAGCACAGCTAAAGGCATTGGACAATATGCTTATAACTGTGTTTATGGCGTTTTTTGGCCCTAGGTTAAGTCAGTTGGAGTCTGGTTGAAGTCAAAATTGACAATAAATGTTCTTTGTCACCTCACAATGTTTTTCTTGTGGTGAACAGTTAATCTGTGCCCAATTAATGTTTCTGTTGACATCCGTGTAATAACAGACAGAATGTATATGAAAAACTATGATTTCTGTTTCAAATTAAGGCTTCATATCCAAAATGCATAACAGTTTCCACAAAACAAAGTGACATGTCAGAGTAATTTTAACTTAGATAGTAAAAAAAAAAATACTGACCATTGTTTGATTTTTCTTTATTGTTTTCCCTTAT

Associated Phenotype:

Not determined