ZMP
si:dkeyp-20g2.6
Ensembl ID:
ZFIN ID:
Description:
stromal antigen 2 [Source:RefSeq peptide;Acc:NP_001093498]
Human Orthologue:
STAG2
Human Description:
stromal antigen 2 [Source:HGNC Symbol;Acc:11355]
Mouse Orthologue:
Stag2
Mouse Description:
stromal antigen 2 Gene [Source:MGI Symbol;Acc:MGI:1098583]
Alleles
There are 5 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa11496 | Essential Splice Site | Available for shipment | Available now |
| sa9551 | Essential Splice Site | Available for shipment | Available now |
| sa20396 | Nonsense | Available for shipment | Available now |
| sa13330 | Nonsense | Available for shipment | Available now |
| sa33585 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11496
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045782 | Essential Splice Site | 160 | 1201 | 4 | 31 |
| ENSDART00000137655 | Essential Splice Site | 209 | 1246 | 7 | 34 |
| ENSDART00000045782 | Essential Splice Site | 160 | 1201 | 4 | 31 |
| ENSDART00000137655 | Essential Splice Site | 209 | 1246 | 7 | 34 |
Genomic Location (Zv9):
Chromosome 5 (position 25181070)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23008335 |
| GRCz11 | 5 | 23512135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGTCAGACTCACAGGTCAGAGCGTTCAGACACACCAGCACTCTGGCAG[G/A]TTGGTGAACTCRGGCTGGATMTCATTYAGTTTTAAGCATATTACCAMAGW
Long Flanking Sequence:
CATTATAGCAAATCTTAGTGTAAACGTCAGTTTCTAAACTGTTTCCCAGATACTAATATTGTGACCATATATAAAAGATGAATCACTACCTCACCGTTTGAGATTAGGTGTGGGTATAAACATTGCCCATCATACTTTTCAGTTGTATCACTGCACACTGTGTGCATATATTATCGGTGGGTTTGATAATTGCTAAGTAGGATGTGATCCTGGATTAACATCTATGTTATTTCTGTTCTGTTCATACTAACCAAGCCGATGGATGTGTGTATAAAGTTTGTTTTTGTGTGTTTAGGACAGTGGCGATTATCCGCTGGCGATGGCAGGTCCAGCGTGGAAGAAGTTTAAAACAAACTTGTGTGAGTTCATCGCGACCCTGGTCCGACAGTGCCAGTACAGCATCATCTATGATGAGTACATGATGGACACGCTCATCTCTCTGCTCACCGGCCTGTCAGACTCACAGGTCAGAGCGTTCAGACACACCAGCACTCTGGCAG[G/A]TTGGTGAACTCGGGCTGGATATCATTCAGTTTTAAGCATATTACCACAGTACACCAGCAATACACTTGAATGCTAATAATTTTCATGAAAAATGCAAGGTTAGGAGATGATTTTATATTTAGAAGAATAAATTTTTTCTTCTTATTAATAGGTTTTGCAAGGTCTTAAAACCCTTAAATTTCAAAAACTTCAAAAGTTTTAGGTCTTAAAAAGTTGTAAATTCGCTGAAATATTGTATTCAAGGTTTTTAAACACTTTAAAGAGCCCATATTATGGGTTTTTGAAAATTCCCCTCCATGTAGTGTGTAACACAGCTCTAAGTGAAGTGGAGTATCCAGCTAAGGCTTAAATCTGTTAGTGTACAGTGTTAAAAACGGTTGATTCATCTAAAAAAGAGTCGACTCATAGTGCTTCAAACGAGTCGCCTTGATACGGATTCATTAGGTGTTTCGCCATGACGTACGAACGAAACCAAGTTATTCACGTGCACGCGCAAACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9551
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045782 | Essential Splice Site | 160 | 1201 | 4 | 31 |
| ENSDART00000137655 | Essential Splice Site | 209 | 1246 | 7 | 34 |
| ENSDART00000045782 | Essential Splice Site | 160 | 1201 | 4 | 31 |
| ENSDART00000137655 | Essential Splice Site | 209 | 1246 | 7 | 34 |
Genomic Location (Zv9):
Chromosome 5 (position 25181070)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23008335 |
| GRCz11 | 5 | 23512135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTGTCAGACTCACAGGTCAGAGCGTTCAGACACACCAGCACTCTGGCAG[G/A]TTGGTGAACTCRGGCTGGATMTCATTYAGTTTTAAGCATATTACCAMAGW
Long Flanking Sequence:
CATTATAGCAAATCTTAGTGTAAACGTCAGTTTCTAAACTGTTTCCCAGATACTAATATTGTGACCATATATAAAAGATGAATCACTACCTCACCGTTTGAGATTAGGTGTGGGTATAAACATTGCCCATCATACTTTTCAGTTGTATCACTGCACACTGTGTGCATATATTATCGGTGGGTTTGATAATTGCTAAGTAGGATGTGATCCTGGATTAACATCTATGTTATTTCTGTTCTGTTCATACTAACCAAGCCGATGGATGTGTGTATAAAGTTTGTTTTTGTGTGTTTAGGACAGTGGCGATTATCCGCTGGCGATGGCAGGTCCAGCGTGGAAGAAGTTTAAAACAAACTTGTGTGAGTTCATCGCGACCCTGGTCCGACAGTGCCAGTACAGCATCATCTATGATGAGTACATGATGGACACGCTCATCTCTCTGCTCACCGGCCTGTCAGACTCACAGGTCAGAGCGTTCAGACACACCAGCACTCTGGCAG[G/A]TTGGTGAACTCGGGCTGGATATCATTCAGTTTTAAGCATATTACCACAGTACACCAGCAATACACTTGAATGCTAATAATTTTCATGAAAAATGCAAGGTTAGGAGATGATTTTATATTTAGAAGAATAAATTTTTTCTTCTTATTAATAGGTTTTGCAAGGTCTTAAAACCCTTAAATTTCAAAAACTTCAAAAGTTTTAGGTCTTAAAAAGTTGTAAATTCGCTGAAATATTGTATTCAAGGTTTTTAAACACTTTAAAGAGCCCATATTATGGGTTTTTGAAAATTCCCCTCCATGTAGTGTGTAACACAGCTCTAAGTGAAGTGGAGTATCCAGCTAAGGCTTAAATCTGTTAGTGTACAGTGTTAAAAACGGTTGATTCATCTAAAAAAGAGTCGACTCATAGTGCTTCAAACGAGTCGCCTTGATACGGATTCATTAGGTGTTTCGCCATGACGTACGAACGAAACCAAGTTATTCACGTGCACGCGCAAACCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20396
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:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000045782 | Nonsense | 268 | 1201 | 7 | 31 |
| ENSDART00000137655 | Nonsense | 317 | 1246 | 10 | 34 |
Genomic Location (Zv9):
Chromosome 5 (position 25177760)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23005025 |
| GRCz11 | 5 | 23508825 |
KASP Assay ID:
2259-5724.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATGTGGATGAAGATGTACAGTGAGGCGTTTCTTAATGACAGTTACCTG[A/T]AGTACGTGGGCTGGACCATGTATGATAAGGTATCAAACGCATGCACACAG
Long Flanking Sequence:
CTGAACGCAACAAGAGCATCGGCAAACGAGCCAATGAACGTTTGGAACTATTGCTGCAGAAGCGCAAAGAGGTGAGGCACATACCCACACGCACATGTAATCTATTGCCAGACAAAACATTTTGTATACAAAATATTAGGTTCACCAGTTACTGTGAAGGTTCGACTTTTTGTCTTAATTTGGTGCAAAATGAGGCAACAAATCTGATTCAAGCATGTTTTTTCTACAATATTTAGCTCCAGGAAAACCAGGATGAGATTGAGAATATGATGAATGCCATTTTTAAAGGTGTATTCATCCACAGATACAGGTGTGCAGATTTCTAAAAATTTGATTGAGTGAATTACTAATATTTTGAAAAAATAACATTTTATAAGAGCTGATTTATTATTTAATGTATGTGCAGGGATGTGATTGCTGAGATCCGAGTCGTATGCATTGAGGAGATTGGCATGTGGATGAAGATGTACAGTGAGGCGTTTCTTAATGACAGTTACCTG[A/T]AGTACGTGGGCTGGACCATGTATGATAAGGTATCAAACGCATGCACACAGATTGATTGTTATGCAGTTTAGATCAAAACCAGAGAACAATATATCAGTACAATGTTTCCTCCAAAAAATAATGTATAATTTATTATTCAACATTTGAAAGAATTAGTGTGCCATACCATGCTAGAAGAACGATGTTTGACCTAAAATCAAAGGCACTTGATTTTGTAGAAATCAAAATGCAAACAACTGTAGCACAAAGAAAGATTACAACTAAAGAAAAGAGTGGGAAGATAAAAGAACTTTCAGTACTGTGTTTGACCGATTGTATTTTGTCAGCCAGTGTTTTTTGGAAGACTTAAATGAGTTAGTAACAGAAAAGATGTAGCGTGCTACATCTGTGAAAACTGTCAATTTACAGTTGATAGACAGTGGTGGAAAGAGTACTTAAAAATCATACTTGTGTATAAGTTGCATTACCTGCCCAAAATGTAGTGCAAGCAGCGTAAAAGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13330
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 |
|---|---|---|---|---|---|
| ENSDART00000045782 | Nonsense | 478 | 1201 | 13 | 31 |
| ENSDART00000137655 | Nonsense | 527 | 1246 | 16 | 34 |
Genomic Location (Zv9):
Chromosome 5 (position 25173113)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23000378 |
| GRCz11 | 5 | 23504178 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCATGWTCTGTGCTGTCAGACAGACTTGTGAGTGTCACCCACCCATCGGT[C/T]GAGGCACTGGGAAAAGGGTAAGACACACAAAACATTTWGATTTTGCTATT
Long Flanking Sequence:
GTCTATATCTATCTACCCATCTATCTGTCTATCTACCTGTCTGTTTATATATCTACCTACCCATCCATCTATCTATCTTTCTTTCTGTACATTCAAACAATAATTGAAATCCATCCTCCCTTCTAGATTAACTGAACAAATTTCAAGAAATATATTTTTAAATGATCGTTCGTATGTTTTAGCTGCATGAGCATGGTGCCTACCTTGTGGACAGTTTGTGGGACTGTGCATCAGAGCTGCTGAAGGACTGGGAGAGTATGATCAGCCTGCTGCTGGATGAACCCTTTCCTGGAGAAGAGGGTAATATGGCCATCAAATGCACACACTTGCATCTGTTACGAGTTCATTGTGTCTGGAGCACAATTAGTCTAGAAATCTTACTTCAAGCGATCAACACTTCGTTGTCTGTTTCAGCTCTCAGTGATGCTCAGGAAGTTGCTCTGATTGAGATCATGTTCTGTGCTGTCAGACAGACTTGTGAGTGTCACCCACCCATCGGT[C/T]GAGGCACTGGGAAAAGGGTAAGACACACAAAACATTTTGATTTTGCTATTTTAGTAAGGATATCCCATGAAAAACAGTGCTTATTTTCTAAACCCCCAAATTGTCCAAAGAAGTATTGTATTTGAAAGCAGGCATACAATATAAATTCACCTTAAGTATGTTAATTACCTTATTGGGACTTCTTGGGTGTTTAATTTTAAACCATAAAAATCATAACTTCATGTTTTTTTATTTATTTACTGTACTTTTGATTTCAGCAGATTCACATATATTCTATAAAAAAAACCCATAAATAAGTAAATGCTGTCATTTTAATTTCCTCTTTTCGTGTCTCTTCAAACATTAATGCTGATTTTTATTCTCCCACAGGTTCTCACAGCTAAAGAAAAGAAAACCCAGTTGGATGATCGAACAAAGATCACAGAAACATTTGCTGTGGCTCTTCCTCTGTTACTGGCTAAAGTACGTGGTTCTCTGCCTGCCAAAAAGTGCATAATGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33585
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 |
|---|---|---|---|---|---|
| ENSDART00000045782 | Essential Splice Site | 483 | 1201 | 13 | 31 |
| ENSDART00000137655 | Essential Splice Site | 532 | 1246 | 16 | 34 |
Genomic Location (Zv9):
Chromosome 5 (position 25173094)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 23000359 |
| GRCz11 | 5 | 23504159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAGACTTGTGAGTGTCACCCACCCATCGGTCGAGGCACTGGGAAAAGGG[T/C]AAGACACACAAAACATTTTGATTTTGCTATTTTAGTAAGGATATCCCATG
Long Flanking Sequence:
TCTATCTGTCTATCTACCTGTCTGTTTATATATCTACCTACCCATCCATCTATCTATCTTTCTTTCTGTACATTCAAACAATAATTGAAATCCATCCTCCCTTCTAGATTAACTGAACAAATTTCAAGAAATATATTTTTAAATGATCGTTCGTATGTTTTAGCTGCATGAGCATGGTGCCTACCTTGTGGACAGTTTGTGGGACTGTGCATCAGAGCTGCTGAAGGACTGGGAGAGTATGATCAGCCTGCTGCTGGATGAACCCTTTCCTGGAGAAGAGGGTAATATGGCCATCAAATGCACACACTTGCATCTGTTACGAGTTCATTGTGTCTGGAGCACAATTAGTCTAGAAATCTTACTTCAAGCGATCAACACTTCGTTGTCTGTTTCAGCTCTCAGTGATGCTCAGGAAGTTGCTCTGATTGAGATCATGTTCTGTGCTGTCAGACAGACTTGTGAGTGTCACCCACCCATCGGTCGAGGCACTGGGAAAAGGG[T/C]AAGACACACAAAACATTTTGATTTTGCTATTTTAGTAAGGATATCCCATGAAAAACAGTGCTTATTTTCTAAACCCCCAAATTGTCCAAAGAAGTATTGTATTTGAAAGCAGGCATACAATATAAATTCACCTTAAGTATGTTAATTACCTTATTGGGACTTCTTGGGTGTTTAATTTTAAACCATAAAAATCATAACTTCATGTTTTTTTATTTATTTACTGTACTTTTGATTTCAGCAGATTCACATATATTCTATAAAAAAAACCCATAAATAAGTAAATGCTGTCATTTTAATTTCCTCTTTTCGTGTCTCTTCAAACATTAATGCTGATTTTTATTCTCCCACAGGTTCTCACAGCTAAAGAAAAGAAAACCCAGTTGGATGATCGAACAAAGATCACAGAAACATTTGCTGTGGCTCTTCCTCTGTTACTGGCTAAAGTACGTGGTTCTCTGCCTGCCAAAAAGTGCATAATGCTTCAGTGATATAATGAACAA
Associated Phenotype:
Not determined