ZMP
ephb3a
Ensembl ID:
ZFIN ID:
Description:
Ephrin type-B receptor 3 [Source:UniProtKB/Swiss-Prot;Acc:O13147]
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18039 | Nonsense | Available for shipment | Available now |
sa39770 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19673 | Nonsense | Available for shipment | Available now |
sa19672 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa18039
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040209 | Nonsense | 117 | 925 | 3 | 16 |
ENSDART00000048840 | None | None | 499 | None | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 7779713)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 8197367 |
GRCz11 | 2 | 7995372 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTCCCAACATCCCCGGTTCCTGTAAAGAGAMCTTTAATCTGTTCTACTA[T/A]GAATCAGACGGAGACATGGCCACGGCAAGCAGCCCACCGTGGAGGGAGAA
Long Flanking Sequence:
TTATTACATTCCACCTGCTTACACCATGTCACATTCAATTGAAACTATACACAAGAAAGATTTCTATAAACTAAATGTGATGAAGGTCACATGTTTTACTTGGCTTCACTTGTGCTAGTTTTATCTGAAAGAAGTGCTGCGGTAGAACCTTATGATAAACCACACTCTCGTTACACCATTCCAGAGGTCTAATAGAATCTGCTGCCATTTTTCAATTGGACATTTAATTCCAGGAAAGTTGATCGCGCAATCAGTGACAGTATTTTATGTCCTTCTCAGTGGGAGGAAGTGAGCGGATATGATGACCACTTGAGCCCCATCAGGACTTACCAGGTCTGTAACGTGCTGGAGCCCAATCAGAACAACTGGCTCCGTACAGACTTCATTCCCCGTCGAGGAGTCCTCCGAGTCTACGTGGAGCTCAAGTTCTCTGTGCGGGACTGTGGCAGTATTCCCAACATCCCCGGTTCCTGTAAAGAGACCTTTAATCTGTTCTACTA[T/A]GAATCAGACGGAGACATGGCCACGGCAAGCAGCCCACCGTGGAGGGAGAATCCTTATGTAAAGGTCAGCCACAATAATCACTTGTTTTAGTTTAAGACTTTGCATAATGATACATTTTTACAACGTTTTGCTGAATGGAGGTTTAATTTTAAAGAGAGAAGGAAAATTCTGTCATACTCTTTTGTTGTCACAAACATATCTCTTTGGATAACGATACAATTTTAAAATGCTTTGCTAAGTGGAGGCATTTTTTAAAGGGAAAATTAAAATTATGTCATCTTTTAGACTACTTACTCTTATGTTACTTTTTTATACTCTTATGAAACTTATATCACTTTGCGTAATGGCATAATTTTACAATATTTTGCTTAATGGCTGTATGGTTTTAAAGAAAGAAGTCCTGTCATCATTTACTTCAGGGAGAAGGGGGGGGGGATCCCTGGTCAGTACTACCAAGGTCATAGATATATACACTAGATGTCGCCTGGCCTATTGTTGTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39770
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040209 | Nonsense | 401 | 925 | 6 | 16 |
ENSDART00000048840 | None | None | 499 | None | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 7764069)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 8181723 |
GRCz11 | 2 | 7979728 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGGCAGAGAGGCAGGCGGCAGTGAGGAATCTGCAGGCACACACACATTA[C/A]AGCTTTGAGATTCAGGCTGTGAACGGCGTGTCCCCCAAGAGCCCGTCCAG
Long Flanking Sequence:
TTTATTTTTTATTTATTTATTTATTTATTATTTATTTTAGAAATCAGGGATTTTAAATTAAATGTGTATGTGATTTATTCAATCATACTTCCAAACAGTAAAAAAATGTTAATATGTGTTTAATTACTTTAAAGAGTAACATCTACCTAATTTATCCCATAAAATGACAGAAGTAATATTTTGAACTGGAACAGAGCCATTTAATTTAGCTCACCATTTTTTTTTTTCACTGCCTAAAAATCCATTTTCTCCTTAGCTGTTCCCTCAGCTCCATTAAACGTGATCTCCAGCGTCAACGAGACTTCGGTGTCCCTCGAGTGGTCCGAGCCTCGGGATTCGGGCGGTCGAGGGGACGTGGTGTATAACGTGGTGTGTAAAAAGTGTCTTCACGATGGTGGCTCTTGTGCGCGCTGCGATGACAATGTGGAGGTCTCGCCGCGTCGCCTGGGTCTGGCAGAGAGGCAGGCGGCAGTGAGGAATCTGCAGGCACACACACATTA[C/A]AGCTTTGAGATTCAGGCTGTGAACGGCGTGTCCCCCAAGAGCCCGTCCAGCCCACAGTACACCACTGTCAATATCACCACCAATCAAGCAGGTGAGAGACTCATTTTCAATCATCTAAGGAACTACACCGTACGACAAATCTGTTCATTAACGCTTCTGTATTTGTGTGTCTTTCCTTTATTCACAATTGTAAATTGCATTATGGGGTCTTGATCTCTGCTCTGTCGACTTTTGATGTTGAAAATTCAACTCTACAGTTTAACAAAGTGACTTTTATTGACTTTTATTTTAGTAGCTTTGAGATAATATAATATTTAATAAATAATTTATAGAGAAATAAGTCTTTAAAATAACAGAAAATGTACTGGCAGTTTATTACAAGATTTTGTAGCATATTATACAACACCAACCCAGACAATATATATAACTTAAAACTATTAAAAATGTTAATAAACATCACATTTTTTCGAACTTTCGATGGTTAAAAGTTGTTGGAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19673
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040209 | Nonsense | 504 | 925 | 8 | 16 |
ENSDART00000048840 | Nonsense | 42 | 499 | 3 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 7759413)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 8177067 |
GRCz11 | 2 | 7975072 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGCCAAAGTGGAGGGTTTGAAGGCTGGCACGGTGTACTCTGTGCAGGTT[C/T]GAGCTCGGACGGTAGCTGGGTATGGACGGTATAGCAACCCGGTGGATTTC
Long Flanking Sequence:
TGATCCTGGATTATGAGATCAAGTACCAGGAGAGGGTGAGGAACTGCTGTGCATCTAAATCACCCCCTGACTGAAGAACTCTTGAACCCGAGCCAGATGACATTACACCAGGCGCCCAGCATGGGTTTAACTGGCGTGAGCTCAAAGTAACCCTGGCTCGACTTAAAGTGGAGAACAATGGAACAACAGATGGCTACCGGTCAAACCCCAATGGCTAATGCTAAAAAGAGTGGCGCTTAATTCGCCTGTAGGATTTACTTGGGTGTTTGGGTGTTGCTTTTGTCTTTTCGGATACTTTTGATCCGCTAATTGCAGTGGAAACTTGTTAGCTTAACATTCACTTTAAGCACTGAATGACTTGAGAGTGTTGTTTTGGCTAAAGGAACTATATGTGTGTGTGTTTTCCTCAGGGAGAGTCCTTCTCTCATACGGTCACAGCTCAGCACACTTCTGCCAAAGTGGAGGGTTTGAAGGCTGGCACGGTGTACTCTGTGCAGGTT[C/T]GAGCTCGGACGGTAGCTGGGTATGGACGGTATAGCAACCCGGTGGATTTCAGTACAAGTCTTTATGGTGAGGATGTTGATGTTTTCTTTTTTGGCATCTGGTACTGTGTGCAACGTTTTTAATAGGCCAAACCATGTAAGGCTACTTATAGGAAAGGGAAGTCTTCAGATCTTAACCCTTGTGTGCTGTTGGGGATGTTTTAATGATTTTGAGTCTCATCATTGAGACTCAACAATGCTCTCTTGGCAAATTTACTGCCCTTTCGTTTTGTTAGTGGTGGTTTTTGCCCCATTGACTTCCATTATAATGACATGTTTTGATTGCAAGCCATAAAGCTAACACAGGCTCATTCTGAAAACGTAGTCCCGCGAACGTTTCTGGAGATTGCGAATTATGTAGCCTGAGGTACGTATGGCTGCATTTAATTTTTTAAGTGAACGTTGAGGGGCGGTATGATGCCATTCCTTTTGGCACTTACTGGCTGACCGCTTACCTCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19672
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000040209 | Nonsense | 808 | 925 | 14 | 16 |
ENSDART00000048840 | Nonsense | 382 | 499 | 10 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 7721495)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 8139149 |
GRCz11 | 2 | 7937154 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGTTCACCTCTGCCAGCGACGTGTGGAGCTATGGCATTGTGATGTG[G/A]GAAGTAATGTCATTCGGAGAGCGGCCGTACTGGGACATGAGTAATCAAGA
Long Flanking Sequence:
ATTAGACCATGCGCCCCACGCATAGCGTATTTTCCCATCCTTAAAATAGCAGAAGTGTATTCGGACACGCCCTTAATGCTTTTGCGCCATGCGTTTTACTCTTTGCACCTAGATCGTTAAAAGAGAACCCTAAATGTGTGATGTAGGAAAGAGTGTTGGTTGGTATATGATGGTCAGCAGGTCATATCTGTGTGTGTTTTGCAAACTGCTTTTCATCTCAGATTAATGAGCTGGAGCTGGGTCTTCTCTCTAATTAGGCATCCACAGACTCCTGTGGTGTTAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGCGTGTTTTAGATGTAACCGTTTTCTTCATGTGTTGTATTGTAGGGTGGGAAGATCCCGATTCGCTGGACGGCTCCCGAAGCTATCGCCTTCAGGAAGTTCACCTCTGCCAGCGACGTGTGGAGCTATGGCATTGTGATGTG[G/A]GAAGTAATGTCATTCGGAGAGCGGCCGTACTGGGACATGAGTAATCAAGACGTACGTCAGCTTCTTATGCTTTCGTCAAATCGAAATCAAGTTTGCGTCACATTTCAGTTCTAAATGATAAGAAAGAAATATTGGTAACACTTTACAATAAGGTTCATTAGTTAATGCATTTACTAACATGAACTAATCATGAACAACACATGTACAGCATTTATTAATCATAATTGAACATTTACTAATGCATTATTGACATCCAAGTCCATGCTTGTTAACATTAGTTAATGCACCATGAGTTAACATGAACTAACAATGAACTACTGTATATTCATTAACTAACGTTAACTAACATGAACAAATACAGTAGTAAATGTATTGTTCATTGTTTGTTCATGTTAGTAAATGCATTAATTAACATAAACTAATTAACCTTATTGTAAAGTGTGACCGAAATATTAAAGCAAAAGATGATTCTGTATAGGCCTGCATTGACATAAAATGTG
Associated Phenotype:
Not determined