ZMP
sec23ip
Ensembl ID:
ZFIN ID:
Description:
SEC23-interacting protein [Source:RefSeq peptide;Acc:NP_001070847]
Human Orthologue:
SEC23IP
Human Description:
SEC23 interacting protein [Source:HGNC Symbol;Acc:17018]
Mouse Orthologue:
Sec23ip
Mouse Description:
Sec23 interacting protein Gene [Source:MGI Symbol;Acc:MGI:2450915]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa15118 | Essential Splice Site | Available for shipment | Available now |
sa13215 | Essential Splice Site | Available for shipment | Available now |
sa42209 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22306 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa15118
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087553 | Essential Splice Site | 45 | 977 | 2 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 25775602)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25421262 |
GRCz11 | 13 | 25551712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATCATGTATTGATATTAAAAATGATGCTAGATTTTTGTTTTTCTCTGTGC[A/T]GAAGATGCCRGTGAAGTYGGAGAAGAAGACAGCTTTCTTGGTCWGACAAC
Long Flanking Sequence:
CCAGACACTAGGTCCAATCATACAAAAGACAGACGAAACAGTACAAACCACACAATACACATTAAAAAGACAGTTAGAAAGCCTATATTTTTTATCAAAGGTGACTGATAACGCACCTCAGTAAGCCTAGGGTTATCAACAACATTAAAATGCTAGAGAATGCTTTGAGAATTAGATCAAACTTCTCATCAAAGCAAAAAACCTTACAGAATAATTCTCTTGCAATGTATTTTACAGTATTTAATAATCCTTGTTAACATCAGTAATAAAATATATTTTCATGTAAGTTCACAAGATGGCAGTAGAACTAAACATTTCAGTAACATGTGATTATGTTCTTCACATACCCTATTTTACTTTTTGTTTATTTCCAATTGAAAAGAAAAAAATTAAGGAACTCCATGTTGAATTATTCTTAACGCTCTTCTGACACCATTCCTGCACCACTCTATCATGTATTGATATTAAAAATGATGCTAGATTTTTGTTTTTCTCTGTGC[A/T]GAAGATGCCAGTGAAGTTGGAGAAGAAGACAGCTTTCTTGGTCAGACAACATCTACAGCTCCTCAGACCTCCACGTTCAATTATTTCTCAAACACTGCCAACAGTAGTGACCCGTTTGCTTCTATAGGGCAGCAGTCATGCCCACCTCCAGCTGCCAATTTTATTCCATCAACAACAGGCCCGTTACCGGCATCCATCGCAGCTAGTCTGCCTCTAAACCCACCTGTATCCCACATGAACCCAGTTCAGCAGTATGGCAGTGTTGCTAATCAAGCCCCTATGCGCACATACACACCCCCACCTAATGCACCCACTCCTCCTCCTCCCCAGAGCTCCCAGCAGTCCTATAACCCATATCGTCACACAGCGGTCAGTAGCAAAGCTAATCCTTACCTCATGGCTCCTGAATTACAGCAGCAGCCCCCCAGTCAAACACCTCAGCATCTGAACCCCTACTCTCAGCCCACACCTACTCCATCCTTCCAGACTCCACCCACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13215
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 |
---|---|---|---|---|---|
ENSDART00000087553 | Essential Splice Site | 378 | 977 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 25778475)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25424135 |
GRCz11 | 13 | 25554585 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGACTGGAGTTYCCATCKGGTGAGACCATCGTGATGCACAATCCAAAGG[T/C]ACAACACTATCAGATTGATGGKAAACTATGGAAGCTTAGTTCASTCACAT
Long Flanking Sequence:
TCACATCATCTTTGTCATGTAATTTATAGGAAATGAACTCCTTTAAAAGTGTTTTTCTGCATGCCAAGAGCATGTGGACACTCTTAGTCTGTTTCACCACATAGTCACGTTGCAATCTGTTGCTTCAGTTCAGCCAGATCCAGAGAGTGTGATTGTATGTACGGATGGAGGACGCTATGATGTTCAACTGTACGACCGCACACGGACCTCTGTGTACTGGGAAGAGGACCCCACAGAGGTCCGCCGCTGTACTTGGTTCTACAAAGGAGATACAGACAGTCGCTTTATCCCCTATTCAGAAGACTTCAGTGAAAAGCTGGAGGTTTGTGCTTTTCTGTAAAACTATATTCTGAATGCTGGCTCTTCAGGACGTCATTTAATTTTTCAATGTTGTGTGTGTTGTAAACAGGCGGAATATAAGAAAGCAGTCACTACTAATCAGTGGCACCGCAGACTGGAGTTTCCATCTGGTGAGACCATCGTGATGCACAATCCAAAGG[T/C]ACAACACTATCAGATTGATGGGAAACTATGGAAGCTTAGTTCAGTCACATTAAAAAAATATACAAAATTACCTCAAAATTTTGTATTTTTTTGAAATTGCTTGTGAATATCTCACAGTTTAAGGCAAAAAAAAAGATTTGATAAAAGAAAAAAAAATGAATTGTAAGATAAAATACGCAGAATAGCAAGAAATAAAAAAAATAAATAAACAATGTTGAGAAATAATCAGTTGTGAGATGGAACAAATAAGCTGCAAGTTATATGAAATCAACTCAGAACTGGATTAAGTAATCTTTGGATTGCAAGAAATAATATCTGAAATGTCAGAATTAATGTCAGAATTGCAAGAAATGAGGTTAGAATTTTTATTTTTTAGGAATTATACAAAACAGAAAAAGGAAAATAGTCAGAACTGTGTGGAGAGATCAAGTCAGAATTGTCATTGAAAGTCACAATTACCTTATGTTCATTTGTGGCTGAAATGTGCTTCCATAGTTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42209
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 |
---|---|---|---|---|---|
ENSDART00000087553 | Essential Splice Site | 449 | 977 | 7 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 25779412)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25425072 |
GRCz11 | 13 | 25555522 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCATTGGTCCTGTCTGTGATCTGCGGTTTAGGAGTATGGTGGAGTGCGG[T/C]ATGTTACACTAAGTTACTCTCCAGATCAAATACAGTTTTTAAGACATTCA
Long Flanking Sequence:
TTGTCATTGAAAGTCACAATTACCTTATGTTCATTTGTGGCTGAAATGTGCTTCCATAGTTAACATTGTTTCTTTTAGCTTAACTGTGCTTTGTTCCTCCTCAGGTGATTGTGCAGTTTCAGCCATCTGCTGTTGCTGATGAATGGGGTACAACACAGGATGGCCAGACTCGACCTCGCGTTGTCAAGAGGGGTGTAGACGATGATCATGATGAAGTCCCTGATGGTAAATAACTTCTGACGTTAGAATTCTCATTTTCTTACTTAATCCAGACAGAAATTTGTGATAAAAAAAAAAATTCTCATCTTAAAATTCCCTTAAATTTCAGAATATGATATGTCAAACAATATTTAAATGTAAATGCTTGGCATAGAGGAATGACTGAAGATTATTGCAATTTCCTGTCTAGGTGAGATGCCTCAGGTTGATCATCTGGTTTTTATGGTGCACGGCATTGGTCCTGTCTGTGATCTGCGGTTTAGGAGTATGGTGGAGTGCGG[T/C]ATGTTACACTAAGTTACTCTCCAGATCAAATACAGTTTTTAAGACATTCAATAGGTTAAAGTTATGGGGATAGTTCACCCAAAGCTGAACATTTTGCCATTGTTTATTCACCCTTTGCTTGTTTCAAATCTACAGTATTCAAACATTCAACAATGTTTTTTAAATTGTCCCAAGACAAGAATGGGTGTTGTTCAGTAGTTTTAGGACAACTTTGATAAAGGTATTGAACCACTTTAAATGTTAACTACTGTATTTCTTTTGAATACATGAGATAATATTTTGAAGAAAGCTGGAAACCTGCAACCATTGACTTTCACCGTATTTTTTTTTCCAGCAATGGATGTTAATGGTTAGCGATTTTTCAGCTTCCCTAAAAATATAATCTTTGTGGTCAATGGAAGAAAGTTGTAAAGGTCTGAAACCAAAAACATTTTCTATTTTGGGGGGAACTTTCGCTTTAATAATTTAGTCCATTTAACATATCCTACTTCAAGTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22306
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087553 | Essential Splice Site | 834 | 977 | 15 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 25787397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 25433057 |
GRCz11 | 13 | 25563507 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGCCGGTTTTGGTCCCTCATCATAAAGGGAGGAAAAGGCTTCATCTCGG[T/G]AATGTATTAGACCATTTCTGTGCATTTTTTGAATGATCTTTCTCATTTAT
Long Flanking Sequence:
AAAAGATAAGACTAGTAATAGTGATTGCAGTTACTAGCCACTACATGTGGAGTGTAATTTTTTTTTGTGTGTGTGTGAATGTTCTCGTGCAGGTGTCAGTGATCTATCATGCTCTGGACTTTGAACCGGTGAGTTTCTTCGCTCTGGGTTCTCCCATCGGGATGTTTCTAACTGTTCGTGGAGTGGAGAAAATTGAAGAGTCTTACCAGCTTCCCACCTGCAAAGGGTTCTTCAACATCTACCATCCTGTGAGTGCTGTGTCTTAGCTTGTCTACTGCTTATCTACAACTTTTGGAAACAAAAACATCTTAGAACCAAACTGTCTGTGTAAATCGAGAGTAATGGACAAGTTAAATTGTGCAGATACAATAATGAGCCTCTTCTTTGTGCTTTTAGCTGGATCCAGTTGCTTATAGAATTGAACCCATGATCTTACCAGACATTGACCTGGAGCCGGTTTTGGTCCCTCATCATAAAGGGAGGAAAAGGCTTCATCTCGG[T/G]AATGTATTAGACCATTTCTGTGCATTTTTTGAATGATCTTTCTCATTTATTTTGAATTTAAAAATGAAAAACAATGTTTATGATAGTTATTGATTAAATCATAAGTACTTTAAATATTAATACATTTTAACTATAATATGTATATATCATATCATTGGGGCGGCACAGTGGCTCATTGGTTAGCACTGTCACCTCACAGCAAGCAGGTCGCTAGTTCGAGTCCCAGCTTGGTCAGTTGGCGATTCTGTGTGGAGTTTGCATGTTTTCCCAGAGTTCTTGTGGATTTCCTCCGGGTGCTCCAGTTTCGCCCACAAGTCCAAAGACATGCACTATAGGTGTAATTAAATAAACTAAATTGGCCTTAGTGTATGTGTGTGAATGAATGTGTATGGGTGTTTCCCAATACTGGGTTGCAGCTGAAAGGGCATCCACTGTGATAAACATTTGCTGGAATAGTTGGAATAGTTCATTTCACTGTGGTGACCCTAGAAATAGAGACT
Associated Phenotype:
Not determined