ZMP
si:ch211-195k18.2
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC378993 [Source:RefSeq peptide;Acc:NP_001073631]
Human Orthologue:
SATB1
Human Description:
SATB homeobox 1 [Source:HGNC Symbol;Acc:10541]
Mouse Orthologue:
Satb1
Mouse Description:
special AT-rich sequence binding protein 1 Gene [Source:MGI Symbol;Acc:MGI:105084]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa17302 | Nonsense | Available for shipment | Available now |
sa43265 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa12761 | Nonsense | Available for shipment | Available now |
sa16271 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa17302
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056205 | Nonsense | 62 | 728 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 20963009)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 20896389 |
GRCz11 | 19 | 20480712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATATAGTTCCTCTTTCTTTCAACGCAGGTAGTTTACTTCCAGTATTYTG[C/A]ATGGTGGAAMAAAGCGATGTCCCACCAWCCGAAGGGAAGCGGTCGGAGCA
Long Flanking Sequence:
GACGTTTGTATCTGAAGTGTTCATATTTTCATTTCATTTCAGCTTTATTTGTATAGCACTTTTACAATGTCGATTGTGTCAAAGCAGCTTCATATAAATTAAATTAAATAACTAAAAAATAAATGAAATAATTTTCATATACATAAATAATGTGTATGTGTGACTATAAATAATTTATACATCATTTTCTATTCTAAAGGTTGGTGAAATCCAAGATTTAAAACAGTGATGGACCATTTGGCGACCACTAGTAGCACCCAGGGGCCGGCCCTGTGTGAACCCTCTTATCCTCCCTGTAAAATGGCTCGTATGGAGAATTGTAGAGATCTGCCTGTACCTGGAGTCACACCTGTTAGCTCCAAACAGACATCACACACTAACAGGAGGAAAGGTATTCATTAATGGCCATAAATGTAGTATACCATATCAGTTCATCCCATTTTTCTGAGTAATATAGTTCCTCTTTCTTTCAACGCAGGTAGTTTACTTCCAGTATTCTG[C/A]ATGGTGGAACAAAGCGATGTCCCACCATCCGAAGGGAAGCGGTCGGAGCATGCAGAATTTGTGCTGCTGAAGAAAGACCTGCTGTTCAGCCAGATTACAGAAGCTGCATTGCAAGAGCTGGGATACACACACACCGCAGCGGCTCTGGCTACAGGTACACACACACACACACACACACACACACACACTGATGAATAATTCACACTCAATTCCAGTTGAATATTTAAGCCTAAAGGATAGGGACGGAATAGACTGCGACTATGAAAAAAACTACAACCGGCATTATATTATCTTACATTTTATGCTTTATACATAAGTTAGTATTTAGAAAATTGGTGTGGGTAAAAACTGTTTAAAAAAAAAAACAAGTGTTTTATTCTCATCAAGGTTATTCTGCTCAAACAAATATTGTGATATAGTAAGATTGTGAAAGAAGTTTCCTACTTTAATATATTTTAGGATGCAATTCGGAGCTTAAAATAGCTTTTTTAAAGGGATAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43265
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000056205 | Essential Splice Site | 156 | 728 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 20954472)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 20887852 |
GRCz11 | 19 | 20472175 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTCTTTCTT[A/T]GTGTTTCTAAATTAGAGGACTTGCCCGCTGAGCAATGGACTCATTCTACA
Long Flanking Sequence:
CAACAGTAGGAGACATGCTTCAAGACCTATACCACGTTATCACCTTAAGAATAAAGCTGCACAGGTACAACACACACACATTCACACCACACACAAACACACACACACACACACATGCTCTAAGTATCACGTTTTTCTCAAAACAATCAGAATTAAAACTCCTCTGATTTATGATTAAGGCTAATTTTCGCAGGCAATTTAGTATTAAAACTAATTTCAAAATTATTAAAAGTTATTATAGCTATTAAAGTTTTGAGGATAAACACTTAATAATGTGGCTATTTGTGAAATAATAATTATTTGTGATTAATGTCCCACAGTGTAATTAATTACTGCAGTACATTGTTTTTCTTCTTTGTTTTTGTTTTTTTTTTCTCACTGACTCACGCACATTCTCTTCTCTCTCTCTCCCTCTCTCTCTCTCTCTCTCTCTTTCTCTCTCCCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTCTTTCTCTTTCTT[A/T]GTGTTTCTAAATTAGAGGACTTGCCCGCTGAGCAATGGACTCATTCTACAGTCAGAAATGCTCTAAAGGATCTGCTTAAAGAGATGAATCAGAGCACATTGGCTAAAGAGTGTCCATTATCTCAGGTATGGCTTCTTAAAAATCTTTTTGTCTATAATAAGTCACTGTAAATAGATTTTACGGCTGGTAAAAAGTAACATTGCAATATCTAATGTCTATAGAACTTGTAGTATCACAGGATTCCTGATGAACAACAGCCTCTAAATAAATTATAGTATATAGGATCTCATATTTCCTGCGTTGAGTAGTACAAGTATCTACACAAAAGGCAGTATTATATGCCTAGTTACATTTCAAACATTCTGTACTTTATTCAGCTTAATAGCATGTACAGTTGAAGTCAAAATTATTCTGTGATTTTTATTTTTATTTTTTTAAGATATTTGTCTAATATTTTCCAATGATGTTTAACAGAGCAAGACATTTTTCACAGTATTATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12761
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 |
---|---|---|---|---|---|
ENSDART00000056205 | Nonsense | 286 | 728 | 7 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 20949792)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 20883172 |
GRCz11 | 19 | 20467495 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGCAGGCTGGGATGCCTGGTCTAGTTATGGCTCAGCTTCTCTCMCAG[C/T]AACACGCCATGTCTCAGCTCCTCACACACGCTCACACCCACTCACACATA
Long Flanking Sequence:
AATAATAATAATATATATATATATATATATATATATATATATATATATTACTAATGTTTTGCTTCTTACACTTTACATACCTGAAACTTGCCTACAGCACTTATTCATTGTTGCTTGTGTAAATTGCTTCCTTGTTCTCATTTGTAAAAAAAACATTTAATATAAAATATTTAATTTGGATATAAAACCTATACCAAACTAAAACACTGAATTTATAACAAACTGAAAAGTAATAAAAGTAATAAATTATTATTTAAAATAATCTGATTATAACTATAAGATTTTTAAAAAGGCTCCAGTGATTTTAATCCAAATACTGTAGTAATAAATGTTTCTCCCTCTTGTCAGGTGACATGAGCAGGCAGTGCACTCAGCCCTCTTCTTCCAGTCAGCCCTCGATGTTCCAGCAGCCAATGGAAGGCAGCAGTGCAGAGTCACGGGGTGTTGTCCAGATGCAGGCTGGGATGCCTGGTCTAGTTATGGCTCAGCTTCTCTCCCAG[C/T]AACACGCCATGTCTCAGCTCCTCACACACGCTCACACCCACTCACACATACCTCATCCTGCACCTCTAAAGACTCCTCCCAAATGCAATGTGTCGCCTCCAACAGTAACTCAATGTCCTTCTCCTGTCACCGACGTGTCACCTGAAATTTACCACTGGGTGCGCGAGGAGCTGAAGAGGGCAGGCGTTTCCCAAGCTGTGTTTGCACGAGTGGCCATTAACAGGACACAGGTAATATGACTTTCTCTACACACTTTATGATTATTCATCGAATGTCAATTTTTTTGTAAGGATTGGGCTGAATTATTATCATATTTAGAATTTTATTTAATATTTTTGCAATTTTTGTGACAAAGTTGCGTTTTGTCATTTTTATTTGTTTTTGTTTTTTAATATAACTGTATAGTTTTTATTATTATTATTTTATATATGCGCAATTGCGTTGATGAAGTTGTAACAAATTGTTTAAAGCTTGTTTTTTAATATATATAAATATATATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16271
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 |
---|---|---|---|---|---|
ENSDART00000056205 | Essential Splice Site | 479 | 728 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 19 (position 20944334)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 20877714 |
GRCz11 | 19 | 20462037 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAAAGTGTCACAGGCCTTGTTTGCAAAAGYCTCTGCAGCCAAGAGTCAGG[T/G]AAATAWATACAKGAGAGATCGAATACATTTAGGCWAATTAAAAACCATGA
Long Flanking Sequence:
TAATGATACAGTTTTAAATGATAGCTCATCCAAACTTTTAATTGTGTCATCATTTACTCACCATTTACTTGGTCGAGGGTGTTATTTCTTTTCTGTTGAACAATGTTGAAAAGCTGTAACCATTTCAGTATTTGTTTTTCCTACTATACAAGTAAATGGTTACAAGTTTACAACATTCTTCAGTGTATATATATTCTTATATTGTGCTCAACAAAAAAAAAAAACTAAAACTGGTAAACGGTGTGTACAGAATCATGAGAGAATTGTCATTTTTGGGTGTGCTAATCCCTTTAGGTGGCTTTTTCTGAACGCTGTTGTCATAAAAAAAAATCTGTCACCACAGGCCAAACTTTCTCCTGTTTCCAAGGATATTGTAGTGAAAGTGGAATGTGATGACACTGGAATAAACTACGGCATTTATGAAGAAATACAGCAAGAAATGAGGCGAGCAAAAGTGTCACAGGCCTTGTTTGCAAAAGTCTCTGCAGCCAAGAGTCAGG[T/G]AAATATATACATGAGAGATCGAATACATTTAGGCTAATTAAAAACCATGAAAAAAAGGTTCCACCAGCACATGTGTTAATTTATCAGATGCTTTTATCCAAAACTACTGTATATCATTTCAAATGCTGTAACAGTTAACGTCAGAATTATTAGCCCCTCTTTGAATTGTTTTTCTTTTTTTAAATATTTTACAAATGATGTTTAACAGAGCAAGGACATTTACACAGTAAGTCTGATAATATTTTTTTTCTTTTGGAGAAAGTCTTGTTTGTTGTATTTCAGCTAAAATAAAAGCAGTTTCTAGTTTTTTGAAAAACATTTTAAGGTCAAAGTTAGGCCCCTTTAAGCTCTTTTTTTTCAATAGTCTTCAGAACAAACCATCATTATACAATAACTTGCCTAATTACCCTAACCTGCCTAGTTAACCTAATTAACCTAGTTAAGCCTTTAAATGTCAACTTAAGCTGTATAGAAGTGTCTTGAAAAATATCTAGTGAAAT
Associated Phenotype:
Not determined