ZMP
si:dkey-48m5.3
Ensembl ID:
ZFIN ID:
Human Orthologue:
EHBP1L1
Human Description:
EH domain binding protein 1-like 1 [Source:HGNC Symbol;Acc:30682]
Mouse Orthologue:
Ehbp1l1
Mouse Description:
EH domain binding protein 1-like 1 Gene [Source:MGI Symbol;Acc:MGI:3612340]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10687 | Essential Splice Site | Available for shipment | Available now |
sa41675 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45408 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44726 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa27622 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10687
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089205 | Essential Splice Site | 86 | 2382 | 3 | 30 |
ENSDART00000137657 | None | None | 568 | None | 12 |
ENSDART00000139226 | Essential Splice Site | 86 | 195 | 3 | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 27521612)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26924406 |
GRCz11 | 10 | 26886119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGTTTGGCCCGTTCCCGAGAATGTGGACATTACAGTCACACTCTACAGGG[T/C]AGGACATATTAATATAATGCATTAATCCATGCCATATGCAACATGTTAAA
Long Flanking Sequence:
TATATACAGGTCATAATAAGTGTGATGTTTAATTTTTACATGAATATATTGGTGGTTATTTTTATTATTATGTAACATTTTATCTCATATTTTGCATTTTGTTTTCATAAAAGCTATTTAAAACTTTAAAGTAGACATTTGACTTGCCCTTAAGATTTTTCAGTGTATTTCAAATCATAGTTATGTTCAATATGTTATAAACACATGCCATTTTTGTATATCTGTGTGTGCATAGCAAGTTAGTATATATTTGGTTAGATTATTTCTAGACTTTCTTCCCAAGCTTTCAGATGTAATAGTTTTCTGACATTTTGAATTATTATTATTATAACCATGTCTTTGTTTGCAGTGATTTGCAGGTGCTTACAGTAATCATTATAAATGTCTTTTCTTTCCTTGTAAGCTTCATTCATGGCAGCCAGGCATCAAAAATCCTTACAGGGGAATGGTGGTTTGGCCCGTTCCCGAGAATGTGGACATTACAGTCACACTCTACAGGG[T/C]AGGACATATTAATATAATGCATTAATCCATGCCATATGCAACATGTTAAAGATACTGCCACATAGATGCTAAACAGTATTATAATTTTAGATTTTTTTTTCACAGGATCCACATGCAGATGAGTTTGAAGACAAAGAGTGGACATTTTTTATTGAGAATGTAAGTGCCCTCGTAAATGATTATTTAAATTTAGTTGTTTTTTTTAAACAAAGGGACTAAGCCAAAGGAAAATGAATGAATGAATTTTTTTTAACAATATATTTTTTATTTGCGTTAATTATTATTATTATTATTATTATTATTATTATTATTATATTGTTATCATTATTATTATCATCATCAATTTTATTATTTATTTTATTAATAATCATACTATTTAATAATGATAATAATGATAATAGTAATTATAATTATTATTTTTAATATTATTATTATGTTGTTATTATAATTATAATTATTATATTGTTGTTGTTGTTGTTATTATTTTTATTTTTATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41675
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 |
---|---|---|---|---|---|
ENSDART00000089205 | Nonsense | 990 | 2382 | 16 | 30 |
ENSDART00000137657 | None | None | 568 | None | 12 |
ENSDART00000139226 | None | None | 195 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 27537477)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26940271 |
GRCz11 | 10 | 26901984 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTTTAAGTGAACCAGTGTCCCAGCAGCCACTACCCTCCATTGTCCTT[A/T]AACCACAGCCATCTGAGTCTGTTAAGGAAAAGAAAATAGAAGCTGTTAAA
Long Flanking Sequence:
TACAAGAACAAGAGAATACATTGAGAGATGAGGAGATACATGAGCACAAAACACCTCAGAAAATGCCAAAGTTAGAAACTAAATCCTCAAAAAAGTCTGTAGAATCAGGGTAAGAGATATTTTGATAGTCTCTAATGATGGACCATGATTAAATTCTTGCATGTTTTGCATGAGTTTTGCCACACATCATTTTAAGTGTGTTTTGGGGTGTTTGTATACTCTCAACTATTAACAGGAGAGTGGGATTTGGCAAGCCATACAAACTGAAGATTTGGATATAAGCTTCTGATACTGGCTTCATATTTGCATTAGTGTTATAATAGGCAAATATGTGTGAATAGAGACTCGTTATTGCATGCTTTGGTCAAAACAAGGTAGGTAAAGAGTGACATAAACCCTATTCCTTACCTCACAGAGATGAAAAAGCAGTTTCTGAGGATGCTGAGAATTGTATTTTAAGTGAACCAGTGTCCCAGCAGCCACTACCCTCCATTGTCCTT[A/T]AACCACAGCCATCTGAGTCTGTTAAGGAAAAGAAAATAGAAGCTGTTAAAGTCAGTATACCGGTCCGTATGAAGCCTGCGCTTCCTGTGATCTCCCCTGCTGCTTCTGTAAAGGGAAAGGACAACAGGACATCGCTACATCTGGAGGAACTTTGCCCTATGACGCCCAACCAGTCTCTGGATACAGAGTCCTACGGAAATAGTTTAAGGAAAAAGGTCACGTTTGAAGCAGAAAGTGTGTTGTGGGCCACAGTAGAGGAGAAAACAAAAGAAAACAGTGATGAGGGTGTAAGCTTGGGCGAGTTGAAACTGGAGAAGGAGGTTCTGGATAAGGGGTAAGTTAACCCCCGAGGCATGGAGTTTTGTGGAGACTATTGGGGATTGCATGCTTTGCAAGAACTACTGTTTAAACGTTAAGGCTGATTTATACTTCTGCGTCAAATGCCGGTGTATGCTACGGCGCTGACGCATAGCCCTTCGCCGTGGCCGTCGCGTCGCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45408
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 |
---|---|---|---|---|---|
ENSDART00000089205 | Nonsense | 1061 | 2382 | 16 | 30 |
ENSDART00000137657 | None | None | 568 | None | 12 |
ENSDART00000139226 | None | None | 195 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 27537690)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26940484 |
GRCz11 | 10 | 26902197 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCCAACCAGTCTCTGGATACAGAGTCCTACGGAAATAGTTTAAGGAAA[A/T]AGGTCACGTTTGAAGCAGAAAGTGTGTTGTGGGCCACAGTAGAGGAGAAA
Long Flanking Sequence:
GTATACTCTCAACTATTAACAGGAGAGTGGGATTTGGCAAGCCATACAAACTGAAGATTTGGATATAAGCTTCTGATACTGGCTTCATATTTGCATTAGTGTTATAATAGGCAAATATGTGTGAATAGAGACTCGTTATTGCATGCTTTGGTCAAAACAAGGTAGGTAAAGAGTGACATAAACCCTATTCCTTACCTCACAGAGATGAAAAAGCAGTTTCTGAGGATGCTGAGAATTGTATTTTAAGTGAACCAGTGTCCCAGCAGCCACTACCCTCCATTGTCCTTAAACCACAGCCATCTGAGTCTGTTAAGGAAAAGAAAATAGAAGCTGTTAAAGTCAGTATACCGGTCCGTATGAAGCCTGCGCTTCCTGTGATCTCCCCTGCTGCTTCTGTAAAGGGAAAGGACAACAGGACATCGCTACATCTGGAGGAACTTTGCCCTATGACGCCCAACCAGTCTCTGGATACAGAGTCCTACGGAAATAGTTTAAGGAAA[A/T]AGGTCACGTTTGAAGCAGAAAGTGTGTTGTGGGCCACAGTAGAGGAGAAAACAAAAGAAAACAGTGATGAGGGTGTAAGCTTGGGCGAGTTGAAACTGGAGAAGGAGGTTCTGGATAAGGGGTAAGTTAACCCCCGAGGCATGGAGTTTTGTGGAGACTATTGGGGATTGCATGCTTTGCAAGAACTACTGTTTAAACGTTAAGGCTGATTTATACTTCTGCGTCAAATGCCGGTGTATGCTACGGCGCTGACGCATAGCCCTTCGCCGTGGCCGTCGCGTCGCTGACGTGCACCTCTCAAAAATGTAACTACACGTCACAACGACACGTAGCGCAAGCTCTGTGATTGGTAGGCTTGGTAGCGCTGATGAGTTTGGGCGGGACTGAGAGCCGTGTGAATGGTGCGAGCCTGATGGAGCGATTGTTTACAAGTGTGGAGTCCCGTGAAGGAGCTCCGGATGGAAAGTTTTGTTTTGAGTTTACCTCATAGTTAAAGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44726
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089205 | Nonsense | 1070 | 2382 | 16 | 30 |
ENSDART00000137657 | None | None | 568 | None | 12 |
ENSDART00000139226 | None | None | 195 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 27537718)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26940512 |
GRCz11 | 10 | 26902225 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTACGGAAATAGTTTAAGGAAAAAGGTCACGTTTGAAGCAGAAAGTGTGT[T/A]GTGGGCCACAGTAGAGGAGAAAACAAAAGAAAACAGTGATGAGGGTGTAA
Long Flanking Sequence:
GGGATTTGGCAAGCCATACAAACTGAAGATTTGGATATAAGCTTCTGATACTGGCTTCATATTTGCATTAGTGTTATAATAGGCAAATATGTGTGAATAGAGACTCGTTATTGCATGCTTTGGTCAAAACAAGGTAGGTAAAGAGTGACATAAACCCTATTCCTTACCTCACAGAGATGAAAAAGCAGTTTCTGAGGATGCTGAGAATTGTATTTTAAGTGAACCAGTGTCCCAGCAGCCACTACCCTCCATTGTCCTTAAACCACAGCCATCTGAGTCTGTTAAGGAAAAGAAAATAGAAGCTGTTAAAGTCAGTATACCGGTCCGTATGAAGCCTGCGCTTCCTGTGATCTCCCCTGCTGCTTCTGTAAAGGGAAAGGACAACAGGACATCGCTACATCTGGAGGAACTTTGCCCTATGACGCCCAACCAGTCTCTGGATACAGAGTCCTACGGAAATAGTTTAAGGAAAAAGGTCACGTTTGAAGCAGAAAGTGTGT[T/A]GTGGGCCACAGTAGAGGAGAAAACAAAAGAAAACAGTGATGAGGGTGTAAGCTTGGGCGAGTTGAAACTGGAGAAGGAGGTTCTGGATAAGGGGTAAGTTAACCCCCGAGGCATGGAGTTTTGTGGAGACTATTGGGGATTGCATGCTTTGCAAGAACTACTGTTTAAACGTTAAGGCTGATTTATACTTCTGCGTCAAATGCCGGTGTATGCTACGGCGCTGACGCATAGCCCTTCGCCGTGGCCGTCGCGTCGCTGACGTGCACCTCTCAAAAATGTAACTACACGTCACAACGACACGTAGCGCAAGCTCTGTGATTGGTAGGCTTGGTAGCGCTGATGAGTTTGGGCGGGACTGAGAGCCGTGTGAATGGTGCGAGCCTGATGGAGCGATTGTTTACAAGTGTGGAGTCCCGTGAAGGAGCTCCGGATGGAAAGTTTTGTTTTGAGTTTACCTCATAGTTAAAGTTGTTGCACGTCCGCCGGTTCCTGCCTCAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27622
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089205 | Nonsense | 1172 | 2382 | 17 | 30 |
ENSDART00000137657 | None | None | 568 | None | 12 |
ENSDART00000139226 | None | None | 195 | None | 6 |
Genomic Location (Zv9):
Chromosome 10 (position 27538909)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 10 | 26941703 |
GRCz11 | 10 | 26903416 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCACAACTCAAGATGAACTTGAAGATGACCTGAAGTCTGTAGATGTGTG[T/A]TCAGAGACCCAACTCAGCCATGACCTGGATGTGAAAACTGACAAGTACCT
Long Flanking Sequence:
GGGTTACGCCGGGTATACGCAGAAGTATAAACCCAGGCTTTAGGGGTCAGTGGAAGTTTTTTGCTTATTTGTAAAAAACGAACATGTTCCAGACCCCAAACGTTTTTAACAGTTGTGTATGTTGATATTTTTAATCATTTCAGCATCACATCATCAATCTATCAGTTCATTATGCCTGAGCTTCTAATGCATCTCTTGAAATAAGCATTTGTTTTACTTGCTGGGAGGGGGAGAATTTTGATGATTAAAGGTTATTCTTGTCACTTAAACCTTTTGGTTCATGGCAGCCAACTTGGTCAGAAAAAATCAGAAATCAAGTCTAAGGAGCAAGATGATTCCTTCATTTCCACTCATAAAAACACTAACCAAGAATGCCAGGAAATAGAAAAGACAATAGACAAGGATGATTCAGATGATAAGCAGATGGTGAAAACCGACAGTGAGACTATTTGCACAACTCAAGATGAACTTGAAGATGACCTGAAGTCTGTAGATGTGTG[T/A]TCAGAGACCCAACTCAGCCATGACCTGGATGTGAAAACTGACAAGTACCTGGACTCAAGCAAACAGGAGCATGACTCTGATCAAGAGGATGTATCTGTAGGCTTCATACGGGGGATTTTTGGTGTCCTTTATAAAGGGTAAGTGGGATGGATGTGAGATTTGTGGAGTTTCCTTTGACTTGGCATCTGCATGGCTGTATTTTGAAACATAAATGTTGTCATTGTGACCATGCATTTGCAAGAAAGCTTTTGCATCTAGTGTTAGGGTGTCCTATAGTAGAGAGAAGCATAGCCTGCTTGTTTGATGAATTAGTAACTAGTGCTGGCTTTTTGTGAACGGAAACTATTGGTTCAATGTAATTATGTCATCTAAATGTCCTCATCCTTTAGTTATGAGACTGTGACGTCTATACTACAGCAGCCAAGCGAAGCAGAAACAGATGTTCAAGATGACCCAATCTTGGACAACCAAGATGGACCCGTGGTTGAAATTCTTCCTCC
Associated Phenotype:
Not determined