ZMP
satb2
Ensembl ID:
ZFIN ID:
Description:
DNA-binding protein SATB2 [Source:RefSeq peptide;Acc:NP_001122004]
Human Orthologue:
SATB2
Human Description:
SATB homeobox 2 [Source:HGNC Symbol;Acc:21637]
Mouse Orthologue:
Satb2
Mouse Description:
special AT-rich sequence binding protein 2 Gene [Source:MGI Symbol;Acc:MGI:2679336]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31727 | Nonsense | Available for shipment | Available now |
sa11148 | Essential Splice Site | Available for shipment | Available now |
sa7194 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa31727
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 |
---|---|---|---|---|---|
ENSDART00000088791 | Nonsense | 69 | 737 | 2 | 10 |
ENSDART00000088876 | Nonsense | 69 | 834 | 2 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 33629003)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32784949 |
GRCz11 | 9 | 32595695 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCGTGCTCTCTTGCAGGTTTGATGATTCCTGTCTTCTGCGTGGTGGAG[C/T]AGATGGATGGAGGGATGATTTCCGATGGAGAGAGCCGAGAGGAACATGCT
Long Flanking Sequence:
TGGACGGTTCGTCCATGTTGACTATTTGCATGGGCTGTGAAACCTGGGACAAACCATTGACCCTGGCCAGCTTATTCACATGCAAATGATGATCCTATTAATCATTAATGAGTTCTAATGAACAGGCTTTTCTGGTGAACAGCACGTGGCAGCTTATACAAATAATGCTACGCTTGATTTAGAAATCAGCTGTGAGAGAGATTTTTAGGTTTTTTTCTATAATTTTTGTACTGAATATATATTAATGGAGTGACTGGGGATATTTCATCAGGAGTAAGTCAATCTGCCCACTGGGAGTAAATGAACAAATCTAGGAAAGTAAAATTTACTTTTAGGTGAATTACATCAATGACTTTTTCTAAAATATTTGTGTATTGTGTACATACTGTATATCTTTTCCAGCAGATATTAATACATTTTTGGTCTTCTCTGTTAGCTAATGATTTCCATCTTCGTGCTCTCTTGCAGGTTTGATGATTCCTGTCTTCTGCGTGGTGGAG[C/T]AGATGGATGGAGGGATGATTTCCGATGGAGAGAGCCGAGAGGAACATGCTGAGTTTGTGCTGGTCAGGAAGGACATCCTCTTCACTCAACTGGTGGAGACTGCTCTCCTCGCCCTCGGCTACTCTCACAGTTCTGCAGCCCAGGCTCATGGTGAGTTCAACACTGCCCTCACATTTACTCACACCTGCATTTTCAGGTTAAAAAAACATGCAACTTCACATTACATTTACACCGTGATGATTCAGAAGTTTTATGAGGAACTTTTAAATTGTATTTTGATTTAATTTTAAATCTGTCTGCACATTCCTAAAGCAAAAAAAACATGATATAATATGGTTATAGTTGTATAAATGATTTAAAAATGATAATATTTAATAATGTCTTCATCTTCAATATTTAATAAATAATATAATCCTGCGATGTGACTATTGTGGATACACACATTGTGATATCGATGCTCAAACAATAAATTGTGCAGTCCTAATTAGAATGATTCATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11148
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 > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088791 | None | None | 737 | None | 10 |
ENSDART00000088876 | Essential Splice Site | 250 | 834 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 33612703)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32768649 |
GRCz11 | 9 | 32579395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGTTTTAGGYGATTATTTGTGGCAAGGACGGGAGGGCTCAGAAATCAAGG[G/T]TAAGCTCTAAAGTATCTTTGGGTAAAGGACTGACTTTGATTTCTTAGCTT
Long Flanking Sequence:
AGCGGCAGGTCCTATCCTACAGCTCTGCTGTTTAAGCCTCTTAGCATCCAAATGCCTGTGACAATTTTCCTCCTCTCATTGCCCCTTCAAAAAGTGAAATAATTACACAGCAGGACAGATCAAAGTAGGGACTAAACCCCAAGTGCAGAGAGAGAGAGCGCCAACAAAGAATAAAGCGATCCTCGGTATGCTGACAGAGTAAGTGGTGTTGAGTTACACCGAGCCCCCTCCATTAGTTCTGCTGTTTGCCTCCCAGAGCTAAACACTCAGCCCGCATTGCCAGATGTGTGTGCCAGTACGGAGGGACTCCATTGGGTGACTCACGTGTCAGTCATACAGTTGTAAGCCAGAGTTGTAAAACTGTCTATTCATGAAAGAACATTATTGTTTCATCATGAGCATGATTGAGTTAATGAATGCTTTTGTCACTTACCATGAGTTTCTCATGTCTGTTTTAGGCGATTATTTGTGGCAAGGACGGGAGGGCTCAGAAATCAAGG[G/T]TAAGCTCTAAAGTATCTTTGGGTAAAGGACTGACTTTGATTTCTTAGCTTGAACAGTAGAGAGTTTGTTCTGGTGCCTCATACACATCTTTATCCCTCTATAGTTGAACGGGACAATATCGCAGACTTCTGTGTATTAGCCCAGCGTCCACCTCCTCACCTCACTGCACTGGGACAACTCGGCCCATTGAACAGCGCTGGCTCCCTGGTAAAAGGCAACTCAGGAGAACCTCAGAATTCAGCTCAGTCTCAGCCTCCACCTCAAGGGCAGCCACAACCCCCATCATCTCTTGGGCAGCTCCATCACAGTCCTCCACTAAGGGCACAGGTGCCTCCTCCACCTCCTCCTGCCGCCCTGCAGCCTCTTTTGGCACCTGGAGGACTTCTCTCACCCCAGCTCAGTCCACAGCTGGTCCGGCAGCAGTTGGCCATGGCTCATCTTATCAACCAGCAGCTGGCCGTCAGCCGCCTCCTGCATCAGCACCCACAGGCTCTTAACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa7194
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 |
---|---|---|---|---|---|
ENSDART00000088791 | Nonsense | 716 | 737 | 10 | 10 |
ENSDART00000088876 | Nonsense | 730 | 834 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 9 (position 33594022)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 32749968 |
GRCz11 | 9 | 32560714 |
KASP Assay ID:
554-5043.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGATCTGCCCAAACATACCATTGTTAAGTTCTTTCAGAACCAACGTWA[T/A]CATGTGAAGCATCATGGACGACTGAAGGAGCTCGGATCGGAGGGCGGCGG
Long Flanking Sequence:
GTCTGGTTGGATTTTTACCAGAGTTGATCCCATACTCAAGTGCACTGAGGACATTAACTCCAAAAGACATTCATTGAAATGGCACTTTGAACTTTTAAGCAGTGTTTCAATTATTCTATACTGCTGACACAAGTTTAGGTAACTAAACTTAAAAAAAAAAGATTAAAAAAACTCTCAATTTTCTTTTCTCATCAGGCACTTCACAGACAGCCCATGCAGCCACTGAAGGACCACTCTCCTATTCGAGAAGACCCTATTCCCAGTTCTGGAGCTGAAGAGAACCCTCAGGCCAACACAGGTTCTGGAAACAATGGACCGGTTGTCAGTGTCACCAAAAAACCTCGCTCTCGCACCAAGATCTCTCTGGAAGCTCTTGGCATCTTACAGAGCTTTATCCAGGATGTGGGTCTATACCCTGACCAGGAAGCCATACACACTCTGTCAGCCCAACTGGATCTGCCCAAACATACCATTGTTAAGTTCTTTCAGAACCAACGTTA[T/A]CATGTGAAGCATCATGGACGACTGAAGGAGCTCGGATCGGAGGGCGGCGGTGTAGACGTGGCTGAGTATCGAGACGAGGAGCTGCTTTCCAGTTCAGAGGATGCAGAGTCCAGTGAAGATGGTCACGAGGAGATCTACAGTGGGCATGAGAGTGCCCCGGCTGGAGCAGCCAACTCTGTCTCAACTCCAGCTCTTTCTTCTGTCCAAGATGAAAATAAAGACAAATGCTTGCCTCTGGGAACAGTCAGACCCAACTCTCTGCCCCCATGCAGTTCATCCTCAAGTCCCAGAGATCAAGCAGACTATCAGAGATAAACCAGCCTCAGCAAAGACTATACTGTAGGTAGGGAAAGGCAAAGAGTGAGCACTTACATCAGTTATGCAGTGGAGAAGAGAGTGTTGTGGACAGCTTAGAAACTTACTGGCAAAGACGCAGTGTCTTTTTAAGACCTGCTAAAGGCAAACAGAACCAGACAAGATTTGCATTTTGATTAAGGGGA
Associated Phenotype:
Not determined