ZMP
stag1
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate stromal antigen 1 (STAG1) [Source:UniProtKB/TrEMBL;Acc:B0V0X2]
Human Orthologue:
STAG1
Human Description:
stromal antigen 1 [Source:HGNC Symbol;Acc:11354]
Mouse Orthologue:
Stag1
Mouse Description:
stromal antigen 1 Gene [Source:MGI Symbol;Acc:MGI:1098658]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa13423 | Nonsense | Available for shipment | Available now |
sa25109 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa17076 | Nonsense | Available for shipment | Available now |
sa19759 | Essential Splice Site | Available for shipment | Available now |
sa12166 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa13423
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088110 | Nonsense | 369 | 1278 | 11 | 34 |
ENSDART00000142601 | Nonsense | 350 | 1251 | 11 | 33 |
Genomic Location (Zv9):
Chromosome 2 (position 24853283)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25428060 |
GRCz11 | 2 | 25083694 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TAATGTCAGAACTTTCTTGTTTTCCAGCAAGGTGAAGTGCGCTTGAAGTG[T/A]TTGAAAGCCTTACAAAACCTTTACACAAACCGTGAACTGTTTCCAAAACT
Long Flanking Sequence:
TGGAGTTGGAAAAAGTGCCTGAGCATCAGGTGCATTGATGCAGTGTGGTTGCCCAGGATCATAAAAAATAGAAGAGTCTTTTCTAAAGTCAACAAAAAAAAATGCATTGCAAGACACCTCAAGATTTTAGAAGTAAAATCGTGTTCCACATCCAACATCAAAACTTTCATTACCATTAAAGTTCTTATTCTTTTGTTTTAGTGCCATAATTATCTCTTTCTTAATTCTTCATTTCACCAAACACTCCAAAGTCACTAACAGAAAAACAAGTTTAAGAACAACAAACTAACTTTTTGAGTGCATTGGATTTTGTTTGAATGTTTAAGAAACTCATTTTGTTGTGAATTAGGCAGAACGTTTTCGTCGGAAGTTCAAATGTGCGTATAAATACAAAAAAAATATAGGCAGTTATTAGTGAATGAGATCCAGTGTTTTCCCATTGTCTCTTCTTAATGTCAGAACTTTCTTGTTTTCCAGCAAGGTGAAGTGCGCTTGAAGTG[T/A]TTGAAAGCCTTACAAAACCTTTACACAAACCGTGAACTGTTTCCAAAACTTGAGCTCTTCACAAACCGCTTCAAGGTAAGAGTGCTGTTCAGTGACAGAATTAAGAGTTCTCTGAATGTCTGCTCCATATTAACCCTGCTGAATTGTCCTGACAGGACCGTATCGTGTCCATGACGCTGGATAAAGAGTATGATGTTGCTGTGGAGGCCATCAGACTGGTCACGCTCATCCTGCAGTGAGTGAAGCTCAGATGCTGATTGTGACTGGAGACTGGATGCTTTCCTTCATCAAATGTTGTTGATTTGTTCAGGGGTAGTGAGGATGCTCTGTCTAATGAAGACTGTGAGAATGTGTATCATCTGGTGTATTCAGCTCACAGGCCTGTAGCAGTGGCTGCTGGGGAGTTTCTACATCGGAAGTGAGCCAGCTAAACATCTTTGACTATAATTTTCTTTTTTATTATTTCATTTTTTCTTAATTACATTTAACACTTACAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25109
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 |
---|---|---|---|---|---|
ENSDART00000088110 | Essential Splice Site | 570 | 1278 | 17 | 34 |
ENSDART00000142601 | Essential Splice Site | 551 | 1251 | 17 | 33 |
Genomic Location (Zv9):
Chromosome 2 (position 24856595)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25431372 |
GRCz11 | 2 | 25087006 |
KASP Assay ID:
554-7826.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTATGTTTCTTTAAAACCCAAAAGGTATTCAGTTTAGTCTATTATTATGC[A/T]GGTCTTGACTGCGAAAGAAAGGAAGATGCAGATTGATGACAAAAACAAAT
Long Flanking Sequence:
TAATTTAATGCTTTTTAAAATATTTCCTAGGAGCTGTATAAAGGGTTGATAATTTTTTTTCAGCACATTTTACATATAAGTTTATAATAATAACTAATTACTTATGACCAATTTCTTTTGTCTTTGCAATGATAGAACATGCTATTTTACTAGTTATTTTGCAAGATACTAGTATTCATCTTAAGTTTAATTTAAAGACTCAACTAGGTTAATTAGTTTAACTATACAAGTCACCCTCATTGTCTTCTAAATATATTCATGTCTTTCTGTGTCTCTGTGTTTGTGTTCAGTGTTGGCAGACAGACAGGAGAGTTCTCTGATTGAACTGACTGTATGTACCATTCGTCAGGCTGCAGAGGCCCATCCGCCAGTGGGGAGAGGAACTGGAAAAAGGGTAAAAGACCTTTACCTCGCGAGCTACTTTATATGGCTAATAACACCTGCTTCAGTTTATGTTTCTTTAAAACCCAAAAGGTATTCAGTTTAGTCTATTATTATGC[A/T]GGTCTTGACTGCGAAAGAAAGGAAGATGCAGATTGATGACAAAAACAAATTAACAGAGCATTTCATCATGGCTCTCCCCATGCTGCTCTCAAAAGTAGGACAAAGAGCCTTCTGTTTTTATGCTTCCATACATCAAAACTTTTCATTTATGTATTAATAAAGCTGTTTTTCACTTACAGTACCAGACAGATTCAGAGAAAGTAGCCAATCTTCTGCAGATCCCACAGTACTTTGACCTGGACGTGTACAGCGCTGGGAGAATGGAGAAGGTGAGATGTTTCTTCATCTATATCTGCTTTGTCTACACCCCATGACACTTTGCATGAATTATGGGAGTAACTTTTATTAAATTTGATGCAATTATGAAGTGTTTTTTTTTTTTTGGGGAAAATGGGTACAAGAGGTGCTATTTTTATCCTCACAGATCTTCCATTAACAAACTTCCATTAAAAACCTTTTTGCAGCAATATTATGGACGTATATTGAATATTACTGTACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17076
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 |
---|---|---|---|---|---|
ENSDART00000088110 | Nonsense | 616 | 1278 | 18 | 34 |
ENSDART00000142601 | Nonsense | 597 | 1251 | 18 | 33 |
Genomic Location (Zv9):
Chromosome 2 (position 24856820)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25431597 |
GRCz11 | 2 | 25087231 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TACAGTACCAGACAGAWTCAGAGAAAGTAGCCAATCTTCWKCAGATCCCA[C/T]AGTACTTTGACCTGGACGTGTACAGCGCTGGGAGAATGGAGAAGGTGAGA
Long Flanking Sequence:
ACAAGTCACCCTCATTGTCTTCTAAATATATTCATGTCTTTCTGTGTCTCTGTGTTTGTGTTCAGTGTTGGCAGACAGACAGGAGAGTTCTCTGATTGAACTGACTGTATGTACCATTCGTCAGGCTGCAGAGGCCCATCCGCCAGTGGGGAGAGGAACTGGAAAAAGGGTAAAAGACCTTTACCTCGCGAGCTACTTTATATGGCTAATAACACCTGCTTCAGTTTATGTTTCTTTAAAACCCAAAAGGTATTCAGTTTAGTCTATTATTATGCAGGTCTTGACTGCGAAAGAAAGGAAGATGCAGATTGATGACAAAAACAAATTAACAGAGCATTTCATCATGGCTCTCCCCATGCTGCTCTCAAAAGTAGGACAAAGAGCCTTCTGTTTTTATGCTTCCATACATCAAAACTTTTCATTTATGTATTAATAAAGCTGTTTTTCACTTACAGTACCAGACAGATTCAGAGAAAGTAGCCAATCTTCTGCAGATCCCA[C/T]AGTACTTTGACCTGGACGTGTACAGCGCTGGGAGAATGGAGAAGGTGAGATGTTTCTTCATCTATATCTGCTTTGTCTACACCCCATGACACTTTGCATGAATTATGGGAGTAACTTTTATTAAATTTGATGCAATTATGAAGTGTTTTTTTTTTTTTGGGGAAAATGGGTACAAGAGGTGCTATTTTTATCCTCACAGATCTTCCATTAACAAACTTCCATTAAAAACCTTTTTGCAGCAATATTATGGACGTATATTGAATATTACTGTACAGCATAAAATAATCTGGAGGAACAAAAGACAGTGAAGGGTTTTGTCAGATCAGTTTTATTGAAGTTTTGTTTTGTCCACATATTATAACAAAGTACAAAGGCATTAAAATTAAAGAAAGAAATAACGGCAGAAAATGTAAAAAAACAACATCACAAACTAGCCATTAACAACGTTAGCTCACTCTGAAAACGTAGCCCTGTATACAGTTCGTTTCTGGAGATCGCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19759
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000088110 | Essential Splice Site | 630 | 1278 | 18 | 34 |
ENSDART00000142601 | Essential Splice Site | 611 | 1251 | 18 | 33 |
Genomic Location (Zv9):
Chromosome 2 (position 24856866)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25431643 |
GRCz11 | 2 | 25087277 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCACAGTACTTTGACCTGGACGTGTACAGCGCTGGGAGAATGGAGAAGG[T/A]GAGATGTTTCTTCATCTATATCTGCTTTGTCTACACCCCATGACACTTTG
Long Flanking Sequence:
TCTCTGTGTTTGTGTTCAGTGTTGGCAGACAGACAGGAGAGTTCTCTGATTGAACTGACTGTATGTACCATTCGTCAGGCTGCAGAGGCCCATCCGCCAGTGGGGAGAGGAACTGGAAAAAGGGTAAAAGACCTTTACCTCGCGAGCTACTTTATATGGCTAATAACACCTGCTTCAGTTTATGTTTCTTTAAAACCCAAAAGGTATTCAGTTTAGTCTATTATTATGCAGGTCTTGACTGCGAAAGAAAGGAAGATGCAGATTGATGACAAAAACAAATTAACAGAGCATTTCATCATGGCTCTCCCCATGCTGCTCTCAAAAGTAGGACAAAGAGCCTTCTGTTTTTATGCTTCCATACATCAAAACTTTTCATTTATGTATTAATAAAGCTGTTTTTCACTTACAGTACCAGACAGATTCAGAGAAAGTAGCCAATCTTCTGCAGATCCCACAGTACTTTGACCTGGACGTGTACAGCGCTGGGAGAATGGAGAAGG[T/A]GAGATGTTTCTTCATCTATATCTGCTTTGTCTACACCCCATGACACTTTGCATGAATTATGGGAGTAACTTTTATTAAATTTGATGCAATTATGAAGTGTTTTTTTTTTTTTGGGGAAAATGGGTACAAGAGGTGCTATTTTTATCCTCACAGATCTTCCATTAACAAACTTCCATTAAAAACCTTTTTGCAGCAATATTATGGACGTATATTGAATATTACTGTACAGCATAAAATAATCTGGAGGAACAAAAGACAGTGAAGGGTTTTGTCAGATCAGTTTTATTGAAGTTTTGTTTTGTCCACATATTATAACAAAGTACAAAGGCATTAAAATTAAAGAAAGAAATAACGGCAGAAAATGTAAAAAAACAACATCACAAACTAGCCATTAACAACGTTAGCTCACTCTGAAAACGTAGCCCTGTATACAGTTCGTTTCTGGAGATCGCGAATTATGTAGCCAGAAGTACGTATAGCTGCATTCCATTTTAAAATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12166
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 |
---|---|---|---|---|---|
ENSDART00000088110 | Essential Splice Site | 1110 | 1278 | 29 | 34 |
ENSDART00000142601 | Essential Splice Site | 1090 | 1251 | 29 | 33 |
Genomic Location (Zv9):
Chromosome 2 (position 24869718)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 25444495 |
GRCz11 | 2 | 25100129 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATACGCAGCAAGAAGGGCCGACCGCCRCYGCACAAGAAACGCATTGAGG[G/T]TTAGCACGACACCACMCATACTCMTRCTGACATRCACAGGTGTAAAAYAT
Long Flanking Sequence:
ATTGCTCAATAATTAATGAGAAAATGTAGTATGAAGTGATGTGTAAAAAATCGGTAATCTGTTTGGGCTGAAGTGACAAACTGAAAGCTTTGGATGTTTGTATCAGTTTTCTATCTTCTAAACACGAATTTTGTCATAGTATTGAAGCACACTAGCTAATAGATATCTTTTAAACTAACAAACTGAAACTCACATCTAATTTTTTTCTTTTAATTTCACAAGACCTTTAAAAAACTTTTTCACTTGCTGGACAAAGTGAGGCATAGACATTTATGTTTGTGTTTGGCTCTGCAGACATGCATATCTGGAGAAGTTCATGACGGAGCAGATGATGGAGCGGCGGGAGGACATCTGGCTTCCACTCATCTCCTACAGGAACTCTCTGCTGACGGGTGGAGATGAAGATCGCATGTCCATCACCAGCGGCAGCAGCAGTAGCAAAGCTGGATCCATACGCAGCAAGAAGGGCCGACCGCCACTGCACAAGAAACGCATTGAGG[G/T]TTAGCACGACACCACCCATACTCATGCTGACATACACAGGTGTAAAATATTTGAGTCATTTTATTTGATTACTATGCTATTTGGAGGAAGAAATGGTACACTTCAGTTGCAAATTTTTTTCATGTGCCATATGGTGAAAATCTGGGTATACCTAGGTATATATAGCTGAATAGAGTTCAGTGCATTGAAATGACATACTGTTTGCCTCAAACACCATTGTTTCTTTGTTCTCATGTCAATGCAATGAGTGTGTTAAATCTCAGTGAAAATCAGGCCAATCGGAACAAAACAAAGACTGTTACATTGCACACACAGGATCAATAATATGCATGCCCCAGGCTGCATTTGATTGGACATTATATTGTTTTCTATTCGTTGCGTAATGACGTGGAGGAATGCTGAATGGGGATGCTGGTGGGTGTAAAGTAAAAGACTATAGAACACACTTTAGTACAGTACACTCATAGAAAACAATGTTTAGTTGGCACAGCATGAAACTT
Associated Phenotype:
Not determined