ZMP
st14b
Ensembl ID:
ZFIN ID:
Description:
suppression of tumorigenicity 14 (colon carcinoma) b [Source:RefSeq peptide;Acc:NP_001071205]
Human Orthologue:
ST14
Human Description:
suppression of tumorigenicity 14 (colon carcinoma) [Source:HGNC Symbol;Acc:11344]
Mouse Orthologue:
St14
Mouse Description:
suppression of tumorigenicity 14 (colon carcinoma) Gene [Source:MGI Symbol;Acc:MGI:1338881]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa43648 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa32350 | Essential Splice Site | Available for shipment | Available now |
sa23942 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa43648
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:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000087910 | Nonsense | 162 | 753 | 5 | 17 |
ENSDART00000101153 | Nonsense | 144 | 848 | 5 | 19 |
ENSDART00000147860 | Nonsense | 162 | 864 | 5 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 24568924)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25254598 |
GRCz11 | 21 | 25291203 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCTTCTTCTTTTGTAGTGAAGGCAATAATAATGGTATTATTGCATATTA[C/A]TTGTCTGAGTTTAATGTGCGGGAATCCAAAGTATCTGCTTTGGAAGAGGC
Long Flanking Sequence:
TTAATAATTGCAATAATGGCTGAATTAGTCTGCTAAGTATGGCACAAACCTCCATTAATTGCTCAAAAAATCTATTATCAAGAGGTTTGGGATGTGATTTGTCAAATTACTCTTGCATAAAAACCTTACAATTGTCTTGAAAATTGAAATACAATTAGTTGAGGTGTGGTATTTGTAGTCTTTTATTGTAAAGTAAAAGCGCGCCCAACCTGCTGTTAGTAATTTTAATATAATATTCCAGCAGCCCGCTGTCACTTATGTCAGGACTAACTGATGAAAGTAAATAGTATAAAGCTTATATTTTCATAGGAATGTCTTAAGATTCGATTACCAGTACATGAGGATAACTAAACATTCTGGAAACAAAACCTTCAGTGTTTTACAACATCACAAATTATAATGACTCATTTAATTCGATGAATTGAATTTTTGTTTACCGAGTTTCTGTTTTTCTTCTTCTTTTGTAGTGAAGGCAATAATAATGGTATTATTGCATATTA[C/A]TTGTCTGAGTTTAATGTGCGGGAATCCAAAGTATCTGCTTTGGAAGAGGCTATTGCATCCATGGATGACACAGAAAATACCAGGAAAAGCCGAAGAGGGTTCAGTCGCATGACTGACAGCCTCATCATTGATGGCATTACTTCAGGAGGTAAATCTACTACCAAACAGTTTCATGTTACTTGTTTAGGCCTGTCACTTCTTTTAATCCAGCCAGGAACTTCTTAGGGACAAGAAACAAACAATGAACAAAGGAATAGGGGAATCGTTTTAATCAGTGTTGACTTGTATAAACTTAATTGATTTAATTATCAACATCTATAAGAGCAAAGACAATAAGAGACTTGTTTCAAATTTGTATTTTTCCATCCAATCCACCAAGGAACACCTAACAAATGGCATCACACTAAAATGAAAGGTAGAATCCAACCTAGTTATCTCAGAGGAAGATTGGTTGAGTATGTGCTCTGTACAGCCCAACTTCTTCCAGCTCTGGTACTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32350
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 |
---|---|---|---|---|---|
ENSDART00000087910 | Essential Splice Site | 422 | 753 | 11 | 17 |
ENSDART00000101153 | Essential Splice Site | 517 | 848 | 13 | 19 |
ENSDART00000147860 | Essential Splice Site | 533 | 864 | 13 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 24562481)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25248155 |
GRCz11 | 21 | 25284760 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTGATGGGGTGAATGACTGTGGAGATAACACTGATGAGGAAAACTGTG[G/A]TAGGGATAAAAGGAGCTCTCAAATCAGGAAATACAGCGCAAGTGTAATGG
Long Flanking Sequence:
CAGTCAAATCAAACCAATTAACAGTAAAATTCAATTCTGACCGTTCCTATGTGAGTGAAGGATTTTCTGCAGAGTTTGAGGCCTTTGAACCCACCAATCGTGAGTAGAATCATGTTTTTTTTAAAGGGGTTGTTTATGTTCTAAGCCAGTCCACATGCTAAAAAATTACTCTGTCACCTTTCCACAGCCTGTCCTGGAAGATTTGAGTGTGACAATGATCTGTGTATTTCATCTGACCAGCATTGTGATGGGTACAATGACTGTGGTGATATGAGTGATGAGAGAGGCTGCAGTAAGTTTATATCATCATTTCTTGAACACATGGACGTTTTAGTTAAGGTACTGAGCATATTAATGATGTTGCTTTTTTTTTTCTTTACCCATGCATCCAGTGTGTAATGAGACTCAAATCCAATGCAAGAATGGCTTCTGTAAGCCCAGCTTCTGGGGCTGTGATGGGGTGAATGACTGTGGAGATAACACTGATGAGGAAAACTGTG[G/A]TAGGGATAAAAGGAGCTCTCAAATCAGGAAATACAGCGCAAGTGTAATGGAGACAGCTTCAGGTTGTTCATTCGATCTTTTCTGCAGGGAATTGCAAAACTTGGGAGTTCAGGTGTCGAAGTGGCCGCTGCATCTCAGCACAGAAGCAGTGCAATGGCTACAACGACTGTGGCGATGGTTCTGATGAATCTCGGTGTGCGAAATGTAAGGAAAAAAATTATTGAATCAAAGGTATTTTGCTGTTAGCTGCATTACCTGGGGCCTCATGTACAAAGACTTGCGTTGAATCTATACTAAAACATTGCGTTTGTGCAAAGCTGTAAATGTGCGTACGCAGTAAAAAATTCAGATGTATAAAACACTGTTTAAGCGGAATCACATGCATATTCTCTTTGTACATCTGAATTAATGTGAAACTGAGCGCACGTGCACGAATGCAAAACCCCTCCCTGCCTCCTCCCCCTAATAAATATGGTAATGACTCTACTTTAACAGAACCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23942
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 |
---|---|---|---|---|---|
ENSDART00000087910 | Nonsense | 603 | 753 | 15 | 17 |
ENSDART00000101153 | Nonsense | 698 | 848 | 17 | 19 |
ENSDART00000147860 | Nonsense | 714 | 864 | 17 | 19 |
Genomic Location (Zv9):
Chromosome 21 (position 24557418)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 25243092 |
GRCz11 | 21 | 25279697 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACACAAAGAAGTGTGTTGCGCATCATTCCTCACCCTCAGTATGATCACT[C/A]GAGCTACGACAATGACATCGCTCTAATGGAGCTGGACAGTCCTGTGACTC
Long Flanking Sequence:
GTCTCAGTATTCAGTATACATGAGATCTCATGAATTTCAAGAAACATGTATTTTTGGTCAACATTACAAAGTTAAGACTTCTGTATTTCTGATGTGGTTCATGATGTTTATGTTATTTTGTAGAATGTGGGAAGAAGCCTCACAAGTCCAGTCGTATTGTCGGTGGAAAAGACTCAGATGAGGGAGAATGGCCCTGGCAGGTCAGCCTCCACATGAAGACGCAAGGTCATGTGTGTGGTGCGTCTGTTATCAGTAACAGCTGGCTGGTCACTGCTGCTCACTGCGTGCAAGATAATGATCAATTCAGGTGAGTTCTAATCTGCTTTGGCTTTCTCCTTCCCTCCTGAGCTGATTCTGAATGGCTTTTTGTTTTTTTTTTGCTAGATATTCACAGGCTGACCAGTGGGAGGTCTATCTAGGCCTACACAACCAGGGCGAGACTAGTAAATCTACACAAAGAAGTGTGTTGCGCATCATTCCTCACCCTCAGTATGATCACT[C/A]GAGCTACGACAATGACATCGCTCTAATGGAGCTGGACAGTCCTGTGACTCTGAATCAGAACATCTGGCCCATCTGCTTACCTGATCCCACACATTACTTCCCAGCCGGAAAATCTGTATGGATCACTGGCTGGGGCAAGTTAAGAGAGGGAAGCGGTAAGTTGTGTAACATAAACCTTCATTACCATTTCAGTTTGAAGTTGATAAGGTTCTTTTATGTATTTGGAAGAAGTTTGACTTATTTGATACAGCATAAGTAGCCATTCAGAGTTTTTATTATTCATTTTTAATGAGATTTTTTATGTATTTTTATTTACTGATATGGTACTCATTAGCTACTGACAATATCGATAAGCTGAGACGTTCCTTTTCTAATTCAGTTTATTCTGCATTGTCAGTAGCTTATGCTATGGGTGTCATATAAAATTGCCATTTTGAAACAAACACATTAAAATGCCATGTTGCAACAACCACAAGGCTAATAAGTGAAGGAAAAATTTC
Associated Phenotype:
Not determined