ZMP
LOC100329589
Ensembl ID:
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 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44398 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44399 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa44400 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa39506 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44398
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064388 | Nonsense | 63 | 355 | 1 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_NA135 (position 1163)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN149753.1 | 1163 |
GRCz11 | KN149753.1 | 1163 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAGGACAGTTCGATCATGCCAACATCCTGCGTCTGGAGGGGGTCATCACC[A/T]GAGGTCAGAGCACACACAAACACTATGCATTGCATAGGTTTACATTGTTT
Long Flanking Sequence:
TGTCTCTGTTATATTGTGTGAGGAAAGAATTCTGCAGGCATGCGCCGGTTTAAGTCCAGCTGTATGATTCCTGCATCCAGTATGATTCCTCCTATCCCAGCTTCTGTTTCTACAAGTGTCTCAATAATGAAGACTGTTTGAACTTTGTTTTTTGTTCTACAGCGAGCTTGATCAGCCTACCTATATATAGATTTGATTGAATGATTGATTTGGAAATGGATCCATTCAGTAAGGAAAGATCTCAGTGTTGCTCTGGGATGCACAGTTGTCTCAATAGAATACTCATTAGTGTGTGTGCGTGTGTGTGTGTGTGTGCAGGAGATTTTGGTGAGGTATGCCGCGGCTGCCTGAAGCTGCCCAGTAAGCGTGATCTGCCGGTGGCCATAAAGACTCTGAGAGCCGGATGTTCAGAGAAGCAGCGGCGCTCCTTTCTCAGCGAAGCGGGAATTCTAGGACAGTTCGATCATGCCAACATCCTGCGTCTGGAGGGGGTCATCACC[A/T]GAGGTCAGAGCACACACAAACACTATGCATTGCATAGGTTTACATTGTTTCTCCATTTCCAGTTACCTTAATATTGGTGAAAGCATAACAAAAGCAATGAGTATGACTTAACATATAGGAAAGAACAAACTTGAAGGGACAATATGATGGATAAAGAAAGGAATGACCTTGTTAAAAGTGTTACAGGCATGACAGGGGTCCATCTCTGTAGGAAAATAAGTCACAATGCTCATGTTATTTGCTCCATTTCATACAGCTCTCACACTTTAAATCTGAGCATTGTGATTGCAGATCAGCATTTAAGCATTTGTTAGTGCGATGTTCCAAAATGTGCATGTAATAGGTGGGAGGAAGTGATCTGACTCCTGCAGATGTGCACATGGGGATACTGATGCTGAAGCTATATATTGTGGCGAATCACTAAAGAGCGTCCTTCAGTAGAAAACAAAAGGCTTTGAGTGTGAATGAGAGGACAGATGGAGTGGAGGAGAGCATGATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44399
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:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064388 | Essential Splice Site | 64 | 355 | 1 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_NA135 (position 1168)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN149753.1 | 1168 |
GRCz11 | KN149753.1 | 1168 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGTTCGATCATGCCAACATCCTGCGTCTGGAGGGGGTCATCACCAGAGG[T/C]CAGAGCACACACAAACACTATGCATTGCATAGGTTTACATTGTTTCTCCA
Long Flanking Sequence:
CTGTTATATTGTGTGAGGAAAGAATTCTGCAGGCATGCGCCGGTTTAAGTCCAGCTGTATGATTCCTGCATCCAGTATGATTCCTCCTATCCCAGCTTCTGTTTCTACAAGTGTCTCAATAATGAAGACTGTTTGAACTTTGTTTTTTGTTCTACAGCGAGCTTGATCAGCCTACCTATATATAGATTTGATTGAATGATTGATTTGGAAATGGATCCATTCAGTAAGGAAAGATCTCAGTGTTGCTCTGGGATGCACAGTTGTCTCAATAGAATACTCATTAGTGTGTGTGCGTGTGTGTGTGTGTGTGCAGGAGATTTTGGTGAGGTATGCCGCGGCTGCCTGAAGCTGCCCAGTAAGCGTGATCTGCCGGTGGCCATAAAGACTCTGAGAGCCGGATGTTCAGAGAAGCAGCGGCGCTCCTTTCTCAGCGAAGCGGGAATTCTAGGACAGTTCGATCATGCCAACATCCTGCGTCTGGAGGGGGTCATCACCAGAGG[T/C]CAGAGCACACACAAACACTATGCATTGCATAGGTTTACATTGTTTCTCCATTTCCAGTTACCTTAATATTGGTGAAAGCATAACAAAAGCAATGAGTATGACTTAACATATAGGAAAGAACAAACTTGAAGGGACAATATGATGGATAAAGAAAGGAATGACCTTGTTAAAAGTGTTACAGGCATGACAGGGGTCCATCTCTGTAGGAAAATAAGTCACAATGCTCATGTTATTTGCTCCATTTCATACAGCTCTCACACTTTAAATCTGAGCATTGTGATTGCAGATCAGCATTTAAGCATTTGTTAGTGCGATGTTCCAAAATGTGCATGTAATAGGTGGGAGGAAGTGATCTGACTCCTGCAGATGTGCACATGGGGATACTGATGCTGAAGCTATATATTGTGGCGAATCACTAAAGAGCGTCCTTCAGTAGAAAACAAAAGGCTTTGAGTGTGAATGAGAGGACAGATGGAGTGGAGGAGAGCATGATAAGCCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44400
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 |
---|---|---|---|---|---|
ENSDART00000064388 | Nonsense | 84 | 355 | 3 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_NA135 (position 2900)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN149753.1 | 2900 |
GRCz11 | KN149753.1 | 2900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACACTATGATGATCGTGGTGGAGAGCATGGTGAACGGAGCGCTGGACT[C/A]GTTCCTGCGGGTGAGAGAATCTGTGTGGTTTTTCTGACTCAGCGGACGGG
Long Flanking Sequence:
CTGTATCCTCCGCTCAGTGAATCCTCCAGATTGTTGGTGTCGATGGACATGACTGAGGGATTGTCTTTTCATCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTCTCTGCATCCATCCGTCCATCCTCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTATCTAGATAGATAGATAGTGTAGTTCTGCTGCTCTGTTGTTCTCTCTGACTGTATATAATCTCTTACGTAACTCTCTTTTATAAAAGTATGTTTGTGTGGATGTCGGTGAAGCCCAGCGTGTCCTCTTCATGTCCTCTGAAGCAGTAAACACACTGATGATAATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTCATGCTGCAGGCAACACTATGATGATCGTGGTGGAGAGCATGGTGAACGGAGCGCTGGACT[C/A]GTTCCTGCGGGTGAGAGAATCTGTGTGGTTTTTCTGACTCAGCGGACGGGAAATCTTCAGACGTGCATCAGATATTTAGGAGTGCTGGGCTAAGATTAATCACAATAATCACATCCAGAATAAAGTTTGTTTTGACTAAATATATGTGTATCAGCTATATTAATTAGGCATATGTGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNTGTATATATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTATCACCACAGCAGAATGAACTGCCAACTAGTCCAGCATATGTTTTACACAGTGGATGCCCTTCCAGCAGCAATCCAGTAGTGGAAAACACCCATACACACTCATTCACACACACACTCATACACTAGTGCCAGTGTAGTTGATCAGTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39506
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000064388 | Nonsense | 136 | 355 | 4 | 8 |
Genomic Location (Zv9):
Chromosome Zv9_NA135 (position 5097)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | KN149753.1 | 5097 |
GRCz11 | KN149753.1 | 5097 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGGCGGCTGGCGGCTCATAAAGTGCTGGTCAACAGCAGTCTGGTCTGC[A/T]AAGTGTCCGGCTTCAGACCGCTGCAGGACGACAAGATCGAGGCCGTTTAC
Long Flanking Sequence:
AATGCACCAAAGCCACTGAGAACAACTGTAATTGAGCATTGTCTAACATTTTCTGCCAAATCTCCATTCCTTCATATTTATTTCCCTGTCTTTGTCCTGTATCCTTTTCTTCTGTTTCTCTTGTGCATTTTCTCTATTATTATTCCCTTTTTCTTTTCTTCTGCATCTTTTCTTCACATTTCTTTCCCTTAGCTTTGCTTTTACCTTTAATTTTAAATTTACTTTGCGTTTTCTAAAATTTTCTGCCAAATTTCTCTATTCCTTTCCCTTTATTTTCCTGTAATCTTTTTCTTTTCTCTTGTGCATCTTCTCGATTGTTTCCTCCTCTGATTCTCCATGTGTTTTTTTTCTGTCAGAAACACGAGGGTCAGCTGACGGTGCTGCAGCTGGCGGATCTGCTGAGCGGAGTTGCGTCTGGGATGAAATATCTGACAGAGATGGGTTTCCTCCATCGGCGGCTGGCGGCTCATAAAGTGCTGGTCAACAGCAGTCTGGTCTGC[A/T]AAGTGTCCGGCTTCAGACCGCTGCAGGACGACAAGATCGAGGCCGTTTACAGCACGCTCGTGAGTCTTTCTCCATCGCTTCACAGTCAGCATATTGGTAGTTTTCAGTCATGTGACCTATGACAAAACAATGAGCCATAATGGCGGCTACACTGGGAACTCCATACACTGCGAAAATGCTTGTCTTACGTAGAGGTTTTTGTCTTGATTCTATCCCAAATATCTAAAGATTTTTTTAAATCAAATGCATTTTTAGACAAGCAATAAATACAGTTTCAGAAATAATGAGTCAAAATTAAAAGAGTTTTACCTTAATATAAGCTAAATAATCTGCCAATGGGGTAGAAAATAATCTAGTTTCCACGTTGTAAGATTATACACACATGTGGGCATATTGCTCGTAGACTTATTAATCATACAGAATGTGTTTGTTCATAATGTGGAAAAGCCCACCGTCTCCTGTAATGGTAGGCTTTGCTGTAGGGTGATTGTCAGTTGTCC
Associated Phenotype:
Not determined