ZMP
wu:fc17g12
Ensembl ID:
ZFIN ID:
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 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa35700 | Nonsense | Available for shipment | Available now |
sa39003 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35701 | Nonsense | Available for shipment | Available now |
sa44808 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa35700
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 |
---|---|---|---|---|---|
ENSDART00000088094 | Nonsense | 179 | 1269 | 6 | 33 |
Genomic Location (Zv9):
Chromosome 14 (position 29517555)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 28191475 |
GRCz11 | 14 | 28497433 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGTTCAAGTCTAGTTTCTGTGAGTTTATTGGCGTGTTGGTGCGGCAGTG[T/A]CAGTACAGCATCATCTATGATGAGTACATGATGGACACAGTCATCTCATT
Long Flanking Sequence:
ACTAAATTTTGTGCAGAAATAGGAAAAAATGTCTGCAGATTCTGTCTGGCCCTACCTATAAGGTTTTAAATAGGGATGCACAGTATTGGAAAAATCTGACATTGCAATATTTTGTTGTGCTGCAATATATTTCAGCTTTAAAAACACTGTTTTACACAGTTTTAAAAACACTGTGCTCCTTGATATGAATAATTCTTAAAATGATGTGACTCTTGCAGGTGTTGTGTCTGGTGAGATGTTTCGCAACATGCAAAACTCAGAGATTATCAGGAAGATGACGGAAGAGTTTGATGAGGTAAAAATTTACTTTCAAACACAAGAGCCAATATCCCCACTCACTTACTGCTGAATTACTTTTATGAATTACTGTGTGCGCACACAAGTAAAGAGTTGATCTTATTACAGGACAGCGGCGACTACCCACTCACCATGACAGGGCCACAGTGGAAGAAGTTCAAGTCTAGTTTCTGTGAGTTTATTGGCGTGTTGGTGCGGCAGTG[T/A]CAGTACAGCATCATCTATGATGAGTACATGATGGACACAGTCATCTCATTGCTCACCGGACTTTCTGATTCGCAAGTCCGAGCCTTTAGACACACCAGCACACTGGCAGGTCAGTGTCTCTGCTCTTATGTTTATATATATGTGAACTTTTTTTTTGCTTGATTTGAATATATGCGTCACAATGCTATGTTTTGATTTGTTTTTCCCCTATAGCTATGAAGCTGATGACAGCTCTCGTGAATGTAGCGCTGAACCTCAGCATCAACATGGACAACACTCAGCGGCAGTATGAAGCAGAGAGAAACAAGATGATTGGCAAGAGGGCCAACGACAGACTAGAGCTCCTGCTTCAGAAACGAAAGGAGGTGAGTTTCCTTTAAAGCTCCCATGAAATTTAAATAAAGTGTTTTAGACGTTAGTGACAGTATTGTTAGTTCATAGGATATCTATAAGCTAGTGTCCACCAAAACAGGAACACAATTTGCATTTAGTAGATATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39003
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 |
---|---|---|---|---|---|
ENSDART00000088094 | Nonsense | 495 | 1269 | 14 | 33 |
Genomic Location (Zv9):
Chromosome 14 (position 29524700)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 28198620 |
GRCz11 | 14 | 28504578 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGACTGTGCAGCAGAGCTCCTGAAGGACTGGGAATGCATGATCAGCTTGT[T/A]ACTGGATGAGCCACTGCCTGGAGAGGAAGGTCTGACCCTGTGACCCATCA
Long Flanking Sequence:
AACGCTTCTGATGTTCTTGAGGTAGGATACGTGAGGGTTAAGGACAGGTTTGGTGGTATGGGTTGGTTTAAGAAAAGGTCAACAGTGTAGTTACAGAAAGTAATAACAGATGCGATTACATGCAGGTATTTCATCAATCATAAGTACAATGTAAAACATATGTATTCACAATAAGTACATTGTAACAAATTAATAATATGACTGTAAGTACATATTAGTTAGGGTAACAGGCTAATATAAAGTTGGACCCGACAGGGGGCTTAAATGCCACCAGTAATTTAACTAAATTTTTCACCTATTTGTTATAAATTCACAAAAACTGAAAACTGAATGTGTCTCCATTGTTTCAGCTAGCTATAAAATGTCCCTCTATTATCTGATATGTTTTAACATGTTATGTTTTGGTCCTTAGCTTCACGAGCATGCGGCCTATCTAGTGGACAGCATGTGGGACTGTGCAGCAGAGCTCCTGAAGGACTGGGAATGCATGATCAGCTTGT[T/A]ACTGGATGAGCCACTGCCTGGAGAGGAAGGTCTGACCCTGTGACCCATCACCAGATCATACAGCATTGACTTTGACTTGTTCCAAAGGGAGCGAGATATTAATTACCTCTGCATGTGTCTTCCAGCTCTGACGGACAGACAGGAGACGGCTCTGATCGAGATCTTGCTGTGCACCATCCGTCAGGCTGCAGAGTGCCATCCTCCTGTGGGCAGAGGCACGGGCAAAAGGGTAAGGCTCAATGCCACACGTATCGACCAGCCCTTGATGACGAATCCCTGCTTTCACGTGTTACCTGTTACACGCTGTTCTCAATTCTCACTTGATCTCGTTTCAGGTTCTGACAGCGAAGGAGAAGAAGACTCAGCTTGACGACCGGACGAGAATGACGGAGCTCTTTGCTATAGCACTGCCAGCTTTACTTGCAAAGGTTAAAAGTCCTTTAAAAGTCAAAACTAAAACAAAGTTGGTGTTTACTGAGCATTGAACGTGAAAGAATAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35701
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 |
---|---|---|---|---|---|
ENSDART00000088094 | Nonsense | 598 | 1269 | 17 | 33 |
Genomic Location (Zv9):
Chromosome 14 (position 29527692)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 28201612 |
GRCz11 | 14 | 28507570 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTGCAACTGCCTCAGTTTTTTGATCTGGAGATCTACACCACAGGGCGTT[T/A]AGAAAAGGTTTGAGCAAAGAACAAATACACTGAATGATTTTTCTTATTGG
Long Flanking Sequence:
GCCTCAAAACGACACTTGCGCCAAGCTTAAACTACCAAAAGACTACTGCGTCACGCCTTGCGCCACACTGCGCCGGGTGTATGATAGGGCCCTATAACATGTGCACAAATTCTTTTAGCAAAAAAAATCATCACCAAAATTTTCTTCATGTAAAAACTCTTCGGCATTAAACATTTTATTAGACTGTAATAGTTCTAGTCTTATTGAGGAACTTTTGAATTATAAAAACTTGAAAAAATGCTTTTAATGTGGTTCTTTCAAATTTATTTTGTTTTAGATAAAAATACTTTAACCAGCATAGATTTAATTTTGGAAAAACTAAACTTGATTATCACCATGTATGTAGCCAAAATAGATGGCATACTGAAAAGAAAGAATGGAAAAAGAAAGTGATAGATGTATTTTTTTCTTCATGCAGTACTCTGTGGATGCAGAGAAAGTGACAAATCTGCTGCAACTGCCTCAGTTTTTTGATCTGGAGATCTACACCACAGGGCGTT[T/A]AGAAAAGGTTTGAGCAAAGAACAAATACACTGAATGATTTTTCTTATTGGACATATTGTATAGAACGTTAATAAAAGCCTTCTTCTCTATTGACTTGCAGCATCTAGATTCATTGTTAAGACAAATCAGAGAGATTGTGGAGAAGCACACGGACACAGACGTACTTGAAGCTTGCTCCAAAACCTACCACTCCCTGTGCAACGAGGAGTTCACCATCTTTAACCGGGTGGATATCGCTCGCAGCCAGCTCTTGGATGAGCAAGTGGACAAGTTCAACAAACTTTTGGAGGACTTTCTGCAGGAGGTCAGGACAGCGTTTGTTCTATTATTATAACAGAGCAAAATTTGAGAGAATATTTAAGTTTTTCTATTGCAAAAGGGAATGTCTTTTTTAATTTTGAGGTTTCCATCTTCAACTGATTGAAGTTTATTTGGTCTACATTTTATATGAATGTTTGTTAGCAGTCATTCTCTAAAGCTCTAAATAATATTTTTGCTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44808
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 |
---|---|---|---|---|---|
ENSDART00000088094 | Nonsense | 851 | 1269 | 24 | 33 |
Genomic Location (Zv9):
Chromosome 14 (position 29533266)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 28207186 |
GRCz11 | 14 | 28513144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTTGAAACAGATGGACAGCAGGATGATGAAGCTGGAAAAATCGAAGCTT[T/A]GCACAAGAGGCGAAATCTGCTGGCCGCATACTGCAAACTGATTATTTACA
Long Flanking Sequence:
GAGGAAGAGAAGCTCTCGAACCTTTAGTATACACACCTGAAGCATCCCTGCAGTCCGAGCTTCTAAATTTCATCCTGGACCACGTCTTCATTGACCAGGATGAAGACAGCAACAGCACAGGTCTATCACTGCTAATGGCATAATGACTTTCAGTTAAAGCTAACAGGCTTTTTGCAATGGATTTGGCACTCCTGGCTGTTTAATGTTGAATGCTAACACTAAGACAACACAAAGAAAATTGGCTTTAGAAGCGTTTAATTGATTGATTAGAGCTGCTAGCAACACTTAATCCTGTTGTGCACTGAGCTTGAGGTCAAGTAAACTGACTAGTTTAAAACATCAACTTGAGTTTCAGGTAGATGTGTTTGAAGGGTGACCACTAGAGGGCAGCTGTTTTCCAGTTTGGGCTTGTTGAAGTCAGGTGCAGCATTTGAACGTGTTTCGCTTTATCTTTGAAACAGATGGACAGCAGGATGATGAAGCTGGAAAAATCGAAGCTT[T/A]GCACAAGAGGCGAAATCTGCTGGCCGCATACTGCAAACTGATTATTTACAATGTAGTTGAGATGAGCACTGGTGCAGATATTTTCAAGCAATACATGAGGGTGAGTCCACTTCTTTTTCAAATCTGTTTTACAGTGTTTTTTGCAAAATAAGATAATGATGAATTGTATTAAGAAAAGAAAACAAACACATACATTTAATTTCATATAGAAATAATATTAATAAAATGAATGGGTAACACTTAAAAAATGGTCCATTGGTAGTGTTAGTTAATGGATTTATTAACATTAAATGTTAGTATTGCATTTATTATGGCAATTATTCACGTTAGTTAATGTTATTTAGGTTAAATAATGTTAGTTCAGGTTAACTCTCTTTGCATTAACCAATGTTAACAAGCACAGCTTTTGGCATCAGTTAATATTGAACTATGATTATTAAATGCTATGATTAATAATAAAGTTTACTGATTGACCATTATTCTCAAGTTATACCAACTAA
Associated Phenotype:
Not determined