ZMP
si:ch211-234b19.1
Ensembl ID:
ZFIN IDs:
Description:
Zgc:171602 protein [Source:UniProtKB/TrEMBL;Acc:A8WFU5]
Human Orthologue:
EPHB1
Human Description:
EPH receptor B1 [Source:HGNC Symbol;Acc:3392]
Mouse Orthologue:
Ephb1
Mouse Description:
Eph receptor B1 Gene [Source:MGI Symbol;Acc:MGI:1096337]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33018 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa19866 | Essential Splice Site | Available for shipment | Available now |
sa10531 | Nonsense | Available for shipment | Available now |
sa16453 | Nonsense | Available for shipment | Available now |
sa17732 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa33018
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 |
---|---|---|---|---|---|
ENSDART00000111635 | Nonsense | 142 | 229 | 1 | 2 |
ENSDART00000128457 | Nonsense | 161 | 985 | 2 | 15 |
ENSDART00000145347 | None | None | 657 | None | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 46545110)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 46618746 |
GRCz11 | 2 | 46471350 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCACTTTCGAAAAATGGCTTTTATCTGGCATTTCAGGACTATGGGGCATG[C/A]ATGTCCCTGCTTTCAGTACGTGTGTTTTATAAGAAATGCCCCAGTGTGGT
Long Flanking Sequence:
GAATAATGTCATTTTATGTCTATGATCACATGCGTGCTAAACCTCCTATTGTTTCTTTTTTTTTTTTTTTTCCAGTGGGAGGAAGTAAGCGGCTATGATGAAAACCTCAACACCATCCGAACATACCAGGTGTGCAATGTCTTCGAGTCCAACCAGAACAACTGGCTGCTCACCACATTCATCGCTCGTCGTGGCGCTCAGCGGATCTATGTGGAAATGCGTTTCACTGTCCGAGACTGCAGCAGTATTCCGCGAGTGCCTGGATCCTGTAAGGAGACCTTTAACTTGTACTACTATGAAACGGACTCTGTTATCGCCACCAAGGGTACGGCGTTCTGGATGGAGGCCCCGTATTTAAAAGTGGACACTATTGCTGCGGACGAAAGCTTCTCGCAGGTGGATTTTGGTGGTCGGTTGATGAAAGTGAACACGGAGGTGCGGAGCTTCGGTCCACTTTCGAAAAATGGCTTTTATCTGGCATTTCAGGACTATGGGGCATG[C/A]ATGTCCCTGCTTTCAGTACGTGTGTTTTATAAGAAATGCCCCAGTGTGGTGCAGAACTTTGCAATCTTTCCAGAGACTATGACTGGAGCAGAGAGCACCTCCCTGGTGATTGCTCGTGGGATGTGCATCCCAAATTCAGAGGAAGTGGATGTACCAATTAAGTTGTACTGTAATGGCGATGGGGACTGGATGGTTCCGATTGGGAGCTGCACATGCAAGGCAGGATTCGAGCCGGACAATGGGAACATCTGTCGAGGTAAGAGTTTGGTGTTGATCTTTGTTCGCTGCAATATATTTATTGGGTGTTTTGAATATAATTTTTTTAGATAATGGGAAATCGTGGATCATTTCTGAGGTATTGATTAGCATTTCTCATAGAAAAAAAAGTCCAAGTTGTTTCCAATGGAGTTTATGTTGAGTTACAGTTGGTCTACCTCATAGTACAGCAGTGGTTCTCAATTCCTGCCCACAAGGATCAGTTCATGGATCTCTTTCCGTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19866
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111635 | None | None | 229 | None | 2 |
ENSDART00000128457 | Essential Splice Site | 452 | 985 | 5 | 15 |
ENSDART00000145347 | Essential Splice Site | 153 | 657 | 2 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 46699653)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 46769166 |
GRCz11 | 2 | 46621770 |
KASP Assay ID:
2259-2615.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCCCAATGGCATTATTCTCGATTATGAGCTGCGCTACTATGAGAAG[G/A]TAAGAGCGTGTGTTTGTGTGTGTGTTGCACTTGAGAGAAAACTGCTCTCT
Long Flanking Sequence:
CTACAATAATGCATTAAGCTATGTAGTGGTAACAGACCTCTTGAGTTATTTTGTAGAGTGTGATTTTGTAATTTGCTCAAAATATGATTAATTATCATATTTAACGGGGTCTTTTGACATTCACAGTTTGCCACAGGTTTATTGTGAGAGTCGAGTATAGGTGTAGGTTTGGATAGAACGATGTAATAAGCAGTTTTTACTGTAAAAACCACATTGTATCAATGGTGAGTCCTTATAAAACACCAAAACCAAAGTGTGTGTGAGTGCTTCATTTCTGAAAGTGGCAGATCAATTCACTAGCTAAGTACACGCAGCAGGGATGACGGCTGTTTGAAATGATTTTTCCTCACTTGCTTTTTCTTCTCTCTTTTGCAGCTCCGTCTATTGTTCCCATAATGCATCAGGTCAGCTCTACCATGAAGAGCATCACGTTATCATGGCCACAGCCTGAGCAGCCCAATGGCATTATTCTCGATTATGAGCTGCGCTACTATGAGAAG[G/A]TAAGAGCGTGTGTTTGTGTGTGTGTTGCACTTGAGAGAAAACTGCTCTCTTGTCTCGTTTCTTCCTAGAGGTTTATGGATGTTTTTCACATTTCGAGTTTCGTTTGAACACTTTAACGCACGACTGCAATTGGGTCAAATGGAAGAGAAAAGGTGATTCAGTCGTCTGCTTCGTTGTGAATTGACTCTTTGACTTGTTTAAATGGTGGCTGTGAAGCTGTCAGCTGTTATTTGTTGGCTCTGGAACAGTATTTCTGTTTAATAAGCTGCGCTGAAAGAACTTCAGACTCTTAACTATGACAGTTTACATTTATGAATTTTCCTTTTATCCAAAGCCACTGAGCATTAGAAAGCATGATTCATGCCTCAAAATCAGAGCGAAGTGAATGGTCGTAATCTCTGTAAACCCACTAAAATTACAGTTTGATTGGTTACTACTTTATACAGGGTGTCCACTGGATCCTAAAAAGTCTTTAAGGGTGCTTTCACACCTGTGAATCG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10531
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111635 | None | None | 229 | None | 2 |
ENSDART00000128457 | Nonsense | 611 | 985 | 9 | 15 |
ENSDART00000145347 | Nonsense | 291 | 657 | 6 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 46772335)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 46841848 |
GRCz11 | 2 | 46694452 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGACCCCTTCAYCTATGAAGACCCCAATGAAGYGGTCAGAGAATTTGCC[A/T]AAGAGATCGACGTCTCSACGGTCAAGATYGAGGARGTCATTGGGGCAGGT
Long Flanking Sequence:
GACTTTATTTACATCAATTCCCAACCCTCTTTACTTTCTACATGTTCATAAGAATCTATTGTTATCATCAGCATCAAGCAGTATTCACTGTAATAGTTTTCATATTTCAGAGACATTTGCTCCACTTTAGATTGCCACTCGTTTAGCCACTCACAATGCATTTGTTTATTTACTTCTCGGATAAATGCATTAAAACAGAAATGCTCTATAATAATGTGCTTAGACTTGACCTCGTTTCGTTTCGATCATAAAATAGATTTGCCGTAATGCTGTTTTATAGCCACACTGAAATGAAAACTGTTAATAACAGGGTGTAAAATCATTTCGGAGAATAAATTGTGTTGAATTGTGCTGTTTTTTTAGAGCTCACTCTTAGGCCAGATCTGTCGAACTGCCACACGCCCATGGGCTGCCCGACACTGCCAGGCTCTCCGGGCATGAAGATCTACATCGACCCCTTCACCTATGAAGACCCCAATGAAGCGGTCAGAGAATTTGCC[A/T]AAGAGATCGACGTCTCGACGGTCAAGATCGAGGAAGTCATTGGGGCAGGTGCGTGGTGTGTTTTTCTCTATGTGTATATATAGTTGAAGTCAAAATTATTAGCCCTCCTTTTCAAATATTTCCTAAATTTTTGCAGTATTTCCTATAATATATATTTTTTTCTTCTGGAAAAAGTCTTATTTGTTTTATTTTGGCTAGAATAAAAGCAGTTTCAGGATCTACTTATGTTAATCCAGGATCGTACTCGGCAAAATCACAAAGTGCATGTAGTAAAGTAGGGATTTCATTCGGAAAGATTGGGGAAATGCACATTTGAAGATGAGACCTGGGGAAAAATTGCTGGGAATTTAAAATTAACGTTGAGACATTAGAACATGTCTTATACAGTTCATATTTTTCATAGATTTTACTGGACTCATAAGAGACTGTTCAAAGCAGGTTTCACAAATGATCCAGAATGCTGGTGATAACAAGAAGTAACAGGTGACCTATTTCATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16453
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 |
---|---|---|---|---|---|
ENSDART00000111635 | None | None | 229 | None | 2 |
ENSDART00000128457 | Nonsense | 643 | 985 | 10 | 15 |
ENSDART00000145347 | Nonsense | 323 | 657 | 7 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 46773837)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 46843350 |
GRCz11 | 2 | 46695954 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGGTGAGTTTGGGGAGGTTTATAAAGGTCGACTGAAACTCCCTGGAAAA[C/T]GAGAGCTCTACGTTGCCATCAAAACAYTGAAGGCGGGATATTCGGAGAAG
Long Flanking Sequence:
TTGTTCTGCTTTCATGTTAATGCTCTGTATTTGATATTCATCTGCATCATTTGAAGTAGAAAAAATCAATAAAAAGTTCAAATCATAAAAAAAAGAAATATTGGTGAAAGAGTTTTGGGAGAGTTCTTATAACTTAACCGACACCTCCTCCTCGCTATTTCTGTTTGTTGTCAAAACTGACAAATGGAGGTATGTTAGCCATGCCTAATGCCTCAGACAGAGCTAACCTGAGAATTTAACTGGAAACAAACAAGAAACCATTATATTTTTCTTAATGACATGCACCAATGCTAATATAACCATATCGGTAGTTTTGATTTCATTTGCACTTTTAAAATGTTTAACCTACTGCCACAATGCAATAACTAAAGTGATTCAAATTCTTTCAGCAATAGTAGCTTTATTGTGTGTCTAATGGTGTTAATTATATCTCATTTATTCTGTGTGCCTCAGGTGAGTTTGGGGAGGTTTATAAAGGTCGACTGAAACTCCCTGGAAAA[C/T]GAGAGCTCTACGTTGCCATCAAAACACTGAAGGCGGGATATTCGGAGAAGCAGAGGCGTGACTTTCTGTCCGAGGCATCGATCATGGGTCAGTTTGACCATCCTAACATCATCCGTCTGGAGGGGGTGGTGACCAAAAGCCGTCCAGTGATGATCGTCACCGAGTTCATGGAGAACGGCGCTCTCGACTCCTTCCTCAGGGTAAATGCAACATCCAAAACAAGTGTTTCTGTCTGTCTGCTTCTCTCTCTCTCTCTCTCTCTGCTTCATTCTTTCCCTGTGGCACGGAGAAGTATGCTGTTTAATCGATGTTCAGCCTATTTTTTTCAATCTCATGGATTGGTTCTTGCTAGCTTTGATCTGGTGCCGCAATAAAGGGATGCTTTGAAGTTGGCTTAGAAATCCAGCACATCCGAGTAGCATCAGCATCGATCCGCACCCCCCACTCTGTTTGTTATCGTGCGTTCGATTCAAAGCTTTCTCTTGTGCAACATGGCGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17732
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 |
---|---|---|---|---|---|
ENSDART00000111635 | None | None | 229 | None | 2 |
ENSDART00000128457 | Nonsense | 767 | 985 | 11 | 15 |
ENSDART00000145347 | Nonsense | 447 | 657 | 8 | 12 |
Genomic Location (Zv9):
Chromosome 2 (position 46775396)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 46844909 |
GRCz11 | 2 | 46697513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTCAACAGCAACCTTGTGTGCAAGGTGTCGGACTTCGGCCTGTCCCGTTA[T/A]CTGCAGGAAGACACMTCTGAYCCCACCTATACYAGCTCACTGGTAAGRCC
Long Flanking Sequence:
GATCCCATAATGCAATCATTGATCAATAAATTATAAATAAATATAATCAGAAAATATATAGGAAGAGACATAGGAAAGGAAAGAAAACAAAGACACCACAAAGATGCAAAAAACTATTGGTCAAAATATAATATTGAAAATGAGGACTTTATATTTCTGCTGGAGTATTACACGTCATCCACCATTGTCTTGTCTTTGGTCTTTTTTTTTTCTAGTCTTCAGAATAAAGATGTATTTACAGTTTAAACGATCTCCATTGCTTGAGGTCAAGCTTTGAGATATTAGTGAATTTAATGTGATGTCTGCGTTTACTCTGTTGTATGGCAGCAAAACGATGGTCAGTTCACAGTGATCCAGCTGGTGGGGATGTTGAGAGGAATAGCTGCAGGGATGAAGTACCTGTCGGAGATGAATTACGTCCACCGGGACCTGGCCGCCCGCAACATCCTGGTCAACAGCAACCTTGTGTGCAAGGTGTCGGACTTCGGCCTGTCCCGTTA[T/A]CTGCAGGAAGACACATCTGACCCCACCTATACTAGCTCACTGGTAAGACCTTTTCAGACTTGCAACTTTATTTTTAACAGAAGCTAATAGACGACAGCCTGGTGAATAGGGGAGGCTCTTTTTTCTTAAAAAAGTGGACCTTTTTGCAGCTATTTCTTTTATTTTGTATTTATTAATGGGGTTTATATATTATTTTTTGTTACATTAAAGCACATTTTAGCTTGATATTGCTGGTATCACAATGTTCTCCATAAAGACATTTTGTAATTTTCTCACTGTGAAACATATAAACTTAATTTTTGATTTTTAATATTATGATTTTTAATCCTCAAATTCCCGATTATCAAGTAGCATCTCAGCCAATCATTGTCTTGTAATAGCAAAATTTACATCAAAGGAAAAATTATTTATTCTGATTTTAAAGACAAAAATGGACCCTTATTATAGATTTTGTGATCCAACTATGTGTTAAACTGTAAGTTTTATGTGATATTTTTTAT
Associated Phenotype:
Not determined