ZMP

st14a

Ensembl ID:

ENSDARG00000061173

ZFIN ID:

ZDB-GENE-030131-6496

Description:

matriptase [Source:RefSeq peptide;Acc:NP_001035441]

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
sa39215	Nonsense	Mutation detected in F1 DNA	Not yet available
sa23372	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa39215

Status:

Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.

Availability:

Not yet available

Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086952	Nonsense	514	834	15	20
ENSDART00000098558	Nonsense	507	827	15	20
ENSDART00000121994	None	None	233	None	7
ENSDART00000135386	None	None	191	None	6
ENSDART00000140672	None	None	77	None	3

Genomic Location (Zv9):

Chromosome 18 (position 42974128)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	44564019
GRCz11	18	44557473

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CAGCTTGTTTGACATAGTTGTTCTCTTTTCTGGCAGGATGTAGAGCTGAT[C/T]AATTTAAGTGCAAGAACGATAAATGCATCTCAGAGAAGCAGAAGTGTGAT

Long Flanking Sequence:

AAGAACCAAAGTGAGGCTGCGGTGGGAAGAAACCTGGAAGTGTAGGACCTGGACTGTAAACATTGCAGTAACATGCTGTGCACTACAAACCTCCAGCTGTTGCCGACATTTCAAAATGCAGAAAACATCACTTTAAAATCATTTAGTTAAGTTTAATTTAAACAATTAAAAGCAATTTAGCATCAAACAACATCACAATCTTTGTAAGAGTAATATGCTCAAGTGTCCTCCTAGGCTTCAGTTAATGGCACCAGTTAAACACCGTGGGGACGCTTTCCTGCTTCAGCCTATGTAAGCCTATGAACACCAGAACCTAAAATCTCTTTAATTGTTAAAGTTATTTATCAAATTATTTTCAGTCATTTTATCTTGAAATCTGATGCTCAGCAGGTCCCCAGGGACCGTCGTCTCTTTCTTTCTTCCTCATTCTCTGTGACCAAAATGCATTCACAGCTTGTTTGACATAGTTGTTCTCTTTTCTGGCAGGATGTAGAGCTGAT[C/T]AATTTAAGTGCAAGAACGATAAATGCATCTCAGAGAAGCAGAAGTGTGATGGCAAAGATGACTGTAATGATGGCTCGGATGAAGAGGGCTGTGCAAGAACTGGTATGTCGGATAATAAACGTGTATAATATATATAGGGAGAGCATTTTGATTAGATGGGTTTTCCTTTTTGGAAAAGCACTTAAAACTTTGTTTAAGGCAGTTTTAAAAACTCACCTGCTCTTGGTTATCACAGAGTAAAATTAGCTATATACACCAAAATCTGTGTTGTACAAGGCTGTAAACAATTTATTATGTTGCTGTAAAGTTGGTCATTTTAACATTGGAGTCAATGGAAATGTGCTCTGTGTTGGAGCCAGTCCTAGTGGCCTTTTAGTGAATTGCAGTTTCAGATACATCTGATCGGTTTCACGAGGGAAAGCGGGAGGTTGTCGCTTGTTTTTATATTATATATTATTATTCTTTCTGATGTATTTTTATTGTTGTCAATCTATGTATTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa23372

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
Order Allele From EZRC

Mutation:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000086952	Essential Splice Site	737	834	18	20
ENSDART00000098558	Essential Splice Site	730	827	18	20
ENSDART00000121994	Essential Splice Site	136	233	5	7
ENSDART00000135386	None	None	191	None	6
ENSDART00000140672	None	None	77	None	3

Genomic Location (Zv9):

Chromosome 18 (position 42977096)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	18	44566987
GRCz11	18	44560441

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCAGGGACATCTGTCTTTATCAGTGGCTGGGGCGCCACTAGAGAAGGAGG[T/G]CAGCAAAAAAGCTTAGAACTCATAACTTTGTCCTGGTGTGTGATTTCATT

Long Flanking Sequence:

CAGTTGGTTATAAATTATACAAAGTATTTTATATCGAAGTGTATATTTGAGGGTTTTATTTCATAGTTTTTAATATTGTTTTATTAAAAGCATATTGATTATTTTTTTTAAAGTAGTGTTGACTTCAAGTGAGAATCTAATGGGACTCAAGACTATTATAATCCATTATATTTACCATATTTTACACATTTACACTGAAAGAGAAACATGCATATCTTGTGAATTCTCAGGTATTCTCAGCCAGGCACGTGGGAAGTATTTTTGGGTCTTCATTCACAAAAAGATAAATTGACGGCAACAAAGAGATTGCTCAAGCAAGTCATTCCTCATCCATATTACAACGCCTACACCTATGACAACGACATCGCCCTGATGGAGATGGAATCGCCCGTGACCTTCAGCGACACCATTCGACCTGTTTGTTTGCCCACTGCCACGGACACTTTCCCTGCAGGGACATCTGTCTTTATCAGTGGCTGGGGCGCCACTAGAGAAGGAGG[T/G]CAGCAAAAAAGCTTAGAACTCATAACTTTGTCCTGGTGTGTGATTTCATTAGTAATGGGTGTGTTCATGTTTATTAAAGGCTCCGGAGCGACGGTGCTGCAGAAAGCAGAGGTTCGCATCATCAACAGCACCGTGTGTAATCAGCTGATGGGGGGTCAGATTACATCCCGCATGACGTGTGCTGGCGTTCTCTCAGGAGGAGTGGATGCCTGTCAGGTGGGTTATAACTGAGTCTTTTAGTACTTCACCATAGATCAGTGGTCAGTGATGGCTCGTTTCCACTGACTGGTACATTACGGTACAGTTCGGGTTGGTACGGGTCACCTTTATCAGGCTTGCGATTCCCCTACCAAGGGTATCCTTTTGGTGGGTGTGGTGTACGACAAAGTTTCAGTCGACGTCATTCTCGCTCAAGAAATTGTCTACAGTAAAGCTGTATAGGTTGCTTATCATATGAGAAGCAGTTCTCAAAAAACAGATGCTTTATACACACAAATACT

Associated Phenotype:

Not determined