Busch Lab

ZMP

ENSDARG00000060754

Ensembl ID:
ENSDARG00000060754
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
sa24739 Nonsense Available for shipment Available now
sa32549 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa24739
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085942 Nonsense 235 841 7 20
Genomic Location (Zv9):
Chromosome Zv9_scaffold3455 (position 307978)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 37155254
GRCz11 15 37056868
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAAGAGTTCTCGTCTCCAGGAAACCCTAAGTCATACCCAGCTTACTCC[C/T]GATGCCAGTGGCAGATCCGCGCCAATAAAGGCTCCGCCATCATTGTCAAG
Long Flanking Sequence:
ATATCGCCTAGCTCTAGTATGAGCTGAATTTTACGTAAATCTTTTGCTATTTGAAAATTTAATAAAAACATGCAAATTTTTTTTTAGAAATGAAATGAAATTAATTAAACATTATTAAAATAATGTGTATTTTAGGGTCTTAAAACATATTCAAAGTTCTATTCCATTACTAAAAACTGAGTTTAAACATTTTTTCGATCAAAGCAGATCCACATGTGAGGGTTAAAATGCAAAGTATTTAAATTTTTATTAAAGATTGTGCATTTTTTAACCTGTTGTGTGCTGCTCATTCAGGCAAATGCAAACACACAAGTTCTCGTTTGCTGAATACCTCAGCTAGTTTAAATTAACAAGCATGAAACCAATACACTGTAAGATTCTGCATTTCTAATTTTTTTTTCTTTCTGTTGTCAGAAAACTGCTTTTTCTCTCTCACCGCTGACCCCACCACCAAAGAGTTCTCGTCTCCAGGAAACCCTAAGTCATACCCAGCTTACTCC[C/T]GATGCCAGTGGCAGATCCGCGCCAATAAAGGCTCCGCCATCATTGTCAAGTTCAAGACCTTCAACATCGAGGATGACTGTTACAATGACTTTGTGGCGATTTATGACTCTCTAAGTCCTGACCGCTCTCGTGCCATCACAAAGTGAGATGATCCTTTCACACACTACTTCTAGATCAGTGGTTCTCAAACTTTTTTCACCAGTACCACCTTAGAAAAAAATTGTCTCTCCAAGTACCACCTTACGACCCTATTTTTTAACCAGTATTAAAAAATAGCGTCGTAGGCCTAATTAAGCAGCTACAGGTGTGCACAGTTTAAAAATGATGCAAATTAATTCCTATTATTAAGAATATGTATTATTGTCAATCACTTTAAACATTTTTAATAGTCTGAACATTAACTGTGCTTGCAGATTAAAAAAAAAAAGTTTTAGTTAAAATGTGCTTTTAAAAGTTCATTAAAAATTACCTGTTCTTAAAAAGTAAAAAGAAAACTGCTG
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa32549
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Order Allele From ZIRC
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000085942 Nonsense 444 841 12 20
Genomic Location (Zv9):
Chromosome Zv9_scaffold3455 (position 315431)
Other Location(s):
Assembly Chromosome Position
GRCz10 15 37147801
GRCz11 15 37049415
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCCTTACTGTTTTCCTGTTTTCACCCTCACTGATGTTATCTCCAGCTTG[C/A]CCTGGTCAGTTTGCTTGCAGTTCAGGCTATTGTATCAGAAAAGAGCAGCT
Long Flanking Sequence:
TAATCATTGTCGTGGCTGCTCTGCTTAGCTCCTCATTCTACCGCTGTTGTGCTTGGTCCCTTAATTGCTGCTTGCAGTTCTATTTCTAGTATAGTTGTGCTATTATTTTTTGCTGTAGGATTACTTTAGCTTTTGTTGTACCAGCAATTCTTTATTTTCTCCATTTTAAAGGTATTGTGGGGAGAAGAGTAGACTTGTTATCTCTAGCAAGTCTAATGTCTTGGAAGTAAAGTTTCATTCGGATGAATCCTACACTGATAAGGGGTTCAAGCTCACTTACACCGCATTTGACCCTGTAAACCGTAAGTAAGCTTTGTGATTCAGTATTACCATCTACCATGTTGTAATGAATATAAGTCACTATTAAATAATCTGAAATTTGCTGCAACATAAATCCCAATTTTTATACTTATCTATTATTAACATTATTAACAATATATTTTGCATTGAATCCTTACTGTTTTCCTGTTTTCACCCTCACTGATGTTATCTCCAGCTTG[C/A]CCTGGTCAGTTTGCTTGCAGTTCAGGCTATTGTATCAGAAAAGAGCAGCTCTGCGACGGCTGGAACGACTGCCAAGACATGAGCGATGAGAAAAATTGCAGTAAGTCTCATCCCTGGCAGCATTTTTGCTCAGACTAAATTAAACCTTTCAATTTATGAATCTGAATTTTGATTAGCCCCATCAAACAGGATATTGATTTGGAATGACAGGAAGACGAATTTACAAACTTGCAATCAAAACACGAGAGGGATCTCATCAGGCAAAGTGAATAATTAGATTTTAATAATTTTTTGTTGATTTTTATTCCTTGATCTAAAAACAGGCTCTTGAAATCCTTGAAAGTGTCAATGTTTAATTCCTCCTGAGGACTTGAAACCTACAATTAATTTGTATATAAACGAAACATTGCAAAGAAAATGGGACAACTGCATATATAATAAATTACATGAAATTATTCATTCATTTTCTTGTCGGCTTAGTCCTTTTATTAATCTGAGGT
Associated Phenotype:
Not determined