ZMP

epha8

Ensembl ID:

ENSDARG00000023609

ZFIN ID:

ZDB-GENE-041014-269

Description:

Novel protein similar to vertebrate Eph family of receptors [Source:UniProtKB/TrEMBL;Acc:Q5SPQ0]

Human Orthologue:

EPHA8

Human Description:

EPH receptor A8 [Source:HGNC Symbol;Acc:3391]

Mouse Orthologue:

Epha8

Mouse Description:

Eph receptor A8 Gene [Source:MGI Symbol;Acc:MGI:109378]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa21965	Nonsense	Available for shipment	Available now
sa35149	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa21965

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
ENSDART00000041800	Nonsense	764	1027	13	17
ENSDART00000136107	Nonsense	466	729	12	16

Genomic Location (Zv9):

Chromosome 11 (position 40099557)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	38600967
GRCz11	11	38867863

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTTTCTCTCCTCCTGCAAACAGAGACACGACGGTCAGTTCACCATTATT[C/T]AGCTGGTTGGGATTCTGCGTGGCATCGCGGCTGGCATGACTTACTTGGCT

Long Flanking Sequence:

AGTAAGTAGTCTTGTATTATATATATATATATATATATATATAATCTGCACTGTAAACCCTATTGTGTTGAAATATAAAACCCCTTCAGCTTCCTGATCACCCTGTCTAGGTTTATCTCTTAATAATGACCGGCTGAATGTACACTGGTCCTCAAGTAAATCAATAATTCACCCACAGCAGAGTAAAAAGTGAAGAAAACAAAAAAACTCCAATTTCTCTTGCATCATCTCTCCAATCTCCTGACATCTTCTTCTCCGTCTTTTTTTCTTCTCTGTGTTTTCTGCGTTCTCCACCAAGGCAAACCGGTAATGATCATCACAGAGTACATGGAGAACGGCTCCTTGGACTCTTTCTTGAGGGTCTGTAAACACGTTTCCGTTTGTTCTCTTATATCTCTGCAGTTCAGCTTCGCCTCAGCGAATCTCCCTGTGAAGCCCAGTTCAATCTTTTCTTTCTCTCCTCCTGCAAACAGAGACACGACGGTCAGTTCACCATTATT[C/T]AGCTGGTTGGGATTCTGCGTGGCATCGCGGCTGGCATGACTTACTTGGCTGATCTGGGTTACGTCCACCGGGATTTGGCCGCCAGAAACGTTCTGGTCAACAGTAATCTGGTGTGCAAGATCTCAGACTTCGGGCTTTCACGAGTGCTGGAGGACGATCCTGATGCAGCGTATACCACCAGCGTGAGTTTAACACACTGTTTACTGTTGTAAAGCATATGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGAGCCCTTATTAATAAAAAGATTAGGCCGAAAAGAAAATGAATGAATGAATGAATAAAATATAAAACTAAATTTAATGAATAAAATAAAATTAGATTAACACTGCACAACACGGGTAAGATGTCTGATACCGCTTTAATTATTATTGTGAAAAGGCTATATTTTATGTAAACACATGCGCTATTAGTAAATTGCATGTAGTGTATAAGTGCATGTGTAAATGGTGTATGTGTAACGGAGGCCAGCTAG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa35149

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000041800	Essential Splice Site	875	1027	15	17
ENSDART00000136107	Essential Splice Site	577	729	14	16

Genomic Location (Zv9):

Chromosome 11 (position 40101993)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	11	38603403
GRCz11	11	38870299

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AATGCAATATCTCACATATAAATTCTTTCTTTTTTTTTTTTTTTTACCTC[A/G]GGTGATCAAGTCCGTAGAGGAGGGTTACCGTCTCCCAGCCCCCATGGGCT

Long Flanking Sequence:

GCCTTTAAACCAAAATAATTTTAAAACGTTTTATTAATAAAAGTATTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTATTAATGATATTGTTGTTGTTTTTTGTTGTTGTTATTGATAATAAGCCTTAAAACCAAAATAACATTACAAAACACAAGATAACTAACTATTATTATTATTATTATTATTATTATTATTATTATTATTCTAACAATATCAAGAAGAAGAATAATGACAAAAAAAAAGTAATTTTAACAATCATTTTAATTGTTTCCACAGCTATTAAGGTAGTATTTTTTTATTTTAATTAAAATGAATTATAATATTCTTAACACCTTTGGCTAAATTTATTTTGGCATTAAATTGCAGTAAACTAGAACAAAAATGAACCTGTCTTCATAGAAATGCTACTTTTTTGACAAACTGAAAAGTTAATGCAATATCTCACATATAAATTCTTTCTTTTTTTTTTTTTTTTACCTC[A/G]GGTGATCAAGTCCGTAGAGGAGGGTTACCGTCTCCCAGCCCCCATGGGCTGCCCCGGGGCCCTCCACACCCTCATGCTGGACTGCTGGCAGAAAGACCGCAACGAAAGACCCAAATTCTGCCAGATCGTCACAGTCCTGGACAAACTGATCCGCACTCCTGAAACACTCAAATCAGTGGAAACATTGTGCAGGTGAGCTCCTGTAATTAATACAATCCTAATGGATAATAAAAGCAATGTGTCATTCAATAAAATTATAAATAAGTATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATTTATATATCACTTTAATAATGCACACATCTAACATTATAATGAAAAGCATTCGACTGCTTTCTTAACTTTTTATGCTCATTTAAGACAAAATTAGCTGTTTTGAAAAAAAAAACACCAAGATTGAGATATTTATTATTATTATTATTATTATTATTATTATTATTATTATTATTAT

Associated Phenotype:

Not determined