ZMP

EPHA5

Ensembl ID:

ENSDARG00000058284

Description:

EPH receptor A5 [Source:HGNC Symbol;Acc:3389]

Human Orthologue:

EPHA5

Human Description:

EPH receptor A5 [Source:HGNC Symbol;Acc:3389]

Mouse Orthologue:

Epha5

Mouse Description:

Eph receptor A5 Gene [Source:MGI Symbol;Acc:MGI:99654]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa41602	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa38783	Nonsense	Mutation detected in F1 DNA	Not yet available
sa34860	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa41602

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081140	Essential Splice Site	51	983	3	17

Genomic Location (Zv9):

Chromosome 10 (position 12478449)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	12597783
GRCz11	10	12555912

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAAATCTTTTTTTTTTTATGAAAAACTCTGTTTTTCTTGTTTTTTTTTTC[A/T]GTGGGAAGAAATCGGAGAGGTGGATGAGAACTATGCACCAATTCACACAT

Long Flanking Sequence:

TTTAGGGGTACACATGAGCAAAATTACGCATTTACAACCACATCTACGTCAAAAACAGTATACCATCACTTAATCTTTTTGAGATTCTTTTTTCCTCAAACAAAGAATAGAAAAATACATTTATTTAAATCATTGCCCTATCTGTGTCCTTTAGGCCTGTTGTCCTGCATATTTCAATTCCAATCCCAATTAGACACACCTGAACCAACTAATGAAGCTCTTTCTGGGTACACTAGAAACCTCCAGACAGGTGTGTTGAATGAAGTTGTAGCTAAACTATTCAGGACACTGGCCCTCCATGACCAATTTTAGCATTCCTGAATTAAGGCCTTAAGTGATATAGGACTACATTTATTGCTTCCTGATTTGGTATTGACCAAAATAACCAAGAGGACTGATCTACAACTGTGAAAATACCTTTAGTTTCTAAAACTCTTTTTTTTTTGATCAAAAATCTTTTTTTTTTTATGAAAAACTCTGTTTTTCTTGTTTTTTTTTTC[A/T]GTGGGAAGAAATCGGAGAGGTGGATGAGAACTATGCACCAATTCACACATACCAAGTGTGCAAAGTGATGGAGCACAACCAGAACAACTGGTTGCAGACCAACTGGATATTAACCCAAGGTGCCCAGCGAGTGTTCCTGGAGCTCAAGTTCACCCTACGGGACTGCAACAGTCTCCCCGGAGGTCTGGGGACGTGCAAGGAGACTTTCAACGTGTACTATTACGAAACCAATGATGAGGAGAGAAGGAATATTCGGGAAAGCCAGTACTCAAAGATTGACACCATTGCCGCCGACGAGAGCTTTACGGAGCTTGATCTCGGAGACAGAGTCATGAAGCTAAACACGGAAGTTAGGGATCTGGGTCCACTGACCAAAAAAGGCTTCTACTTGGCTTTCCAAGACCTGGGCGCGTGTATCGCCCTCGTGTCCGTCCGTGTCTTCTACAAAAAGTGTCCTTTTGTTGTCAGGAATTTGGCCCTTTTCCCGGATACTATAACTG

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa38783

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:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081140	Nonsense	80	983	3	17

Genomic Location (Zv9):

Chromosome 10 (position 12478540)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	12597874
GRCz11	10	12556003

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATTCACACATACCAAGTGTGCAAAGTGATGGAGCACAACCAGAACAACTG[G/A]TTGCAGACCAACTGGATATTAACCCAAGGTGCCCAGCGAGTGTTCCTGGA

Long Flanking Sequence:

TTCCTCAAACAAAGAATAGAAAAATACATTTATTTAAATCATTGCCCTATCTGTGTCCTTTAGGCCTGTTGTCCTGCATATTTCAATTCCAATCCCAATTAGACACACCTGAACCAACTAATGAAGCTCTTTCTGGGTACACTAGAAACCTCCAGACAGGTGTGTTGAATGAAGTTGTAGCTAAACTATTCAGGACACTGGCCCTCCATGACCAATTTTAGCATTCCTGAATTAAGGCCTTAAGTGATATAGGACTACATTTATTGCTTCCTGATTTGGTATTGACCAAAATAACCAAGAGGACTGATCTACAACTGTGAAAATACCTTTAGTTTCTAAAACTCTTTTTTTTTTGATCAAAAATCTTTTTTTTTTTATGAAAAACTCTGTTTTTCTTGTTTTTTTTTTCAGTGGGAAGAAATCGGAGAGGTGGATGAGAACTATGCACCAATTCACACATACCAAGTGTGCAAAGTGATGGAGCACAACCAGAACAACTG[G/A]TTGCAGACCAACTGGATATTAACCCAAGGTGCCCAGCGAGTGTTCCTGGAGCTCAAGTTCACCCTACGGGACTGCAACAGTCTCCCCGGAGGTCTGGGGACGTGCAAGGAGACTTTCAACGTGTACTATTACGAAACCAATGATGAGGAGAGAAGGAATATTCGGGAAAGCCAGTACTCAAAGATTGACACCATTGCCGCCGACGAGAGCTTTACGGAGCTTGATCTCGGAGACAGAGTCATGAAGCTAAACACGGAAGTTAGGGATCTGGGTCCACTGACCAAAAAAGGCTTCTACTTGGCTTTCCAAGACCTGGGCGCGTGTATCGCCCTCGTGTCCGTCCGTGTCTTCTACAAAAAGTGTCCTTTTGTTGTCAGGAATTTGGCCCTTTTCCCGGATACTATAACTGGGGCTGATTCCTCGCAGCTTCTGGAGGTGTCAGGGACCTGCGTCAACAACTCGGTGGCCGATGAACTTCCCAGGATGCATTGCAGTGCTGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa34860

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000081140	Essential Splice Site	324	983	5	17

Genomic Location (Zv9):

Chromosome 10 (position 12539230)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	10	12658012
GRCz11	10	12616141

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TATAACTTTATACATTTTGTAGTTAGGTTATAATACTCTTATCATATTTC[A/T]GGGCCTCCTTCTGCTCCACGTAATGCTATCTCCAACGTAAATGAAACCAG

Long Flanking Sequence:

AGACCTCGAGCTCAGAGGCTGTATAACTGTATAAAAGGATAAAACATGAAATAATAATAATAATAATAATATAAAAAAACATAAATTATTTGTGCCCAGCTTTGACATAATTAAAGTTATCTTAGAGAAAGAGGGAGAGAGGGTAAGCAGAGAGTAAGAACTAAAGCGAGAATGAGATAGCAGCAAAGAGCAGAGCGGGAAAAGAGAAAGAGCAAAGTTTACTGCCTATTTTGTATCTTTCTTGACCATGTAAACAAAGCATAAATACTGAGACATACAAACTGACCAATCAACATGCAAAACACCTAAGGAACACACACATCTTACCCAGGCCCTGATTTTATCAGAATCTGTATGGTTTTGTTTTTTTGTTTTTTTGATGGAAATGACTTGTTTTGTTATAAAAGCAAATGCATATGATAATTTACATTCGTACAACTCTATATAACCTATAACTTTATACATTTTGTAGTTAGGTTATAATACTCTTATCATATTTC[A/T]GGGCCTCCTTCTGCTCCACGTAATGCTATCTCCAACGTAAATGAAACCAGTGTGTTTTTGGAGTGGACTGCGCCTGAAGACACCGGTGGCCGGAAAGACGTGAGATACAACATCCTCTGCAGTAAAATCAGCACCGACTCGGGTCACTACGAGCCATGTGGAAGCCATGTGCGGTTTCTGCCTCAGCGTACGGGCTTGAGAAACACCTCGGTTATGGTCGTGGATCTCCTAGCTCACACCAACTACACGTTTGAAGTGGAGGCTATGAACGGTGTGTCAGATCTAACTGGCCCTCCGCGTCAGTATGTCTCGCTCAATGTCACCACCAACCAAGCAGGTGAGCAGATTTGTCCCCCTGGAATTGTTTCCATTACATGCTAAGCTTAACATGTCAAAGTTTGAGTCTTACAGACAAGCTTGAACAGGCTTTGGAGTGTAAGAGTTATGTGGCATAAAAAAAAAAAAAAAAACTATAAAGGTGTCAGGAGAATGTGAAGAAA

Associated Phenotype:

Not determined