ZMP

ST18

Ensembl ID:

ENSDARG00000091410

Description:

suppression of tumorigenicity 18 (breast carcinoma) (zinc finger protein) [Source:HGNC Symbol;Acc:18

Human Orthologue:

ST18

Human Description:

suppression of tumorigenicity 18 (breast carcinoma) (zinc finger protein) [Source:HGNC Symbol;Acc:18

Mouse Orthologue:

St18

Mouse Description:

suppression of tumorigenicity 18 Gene [Source:MGI Symbol;Acc:MGI:2446700]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa14218	Nonsense	Available for shipment	Available now
sa37935	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa14218

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
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Mutation:

C > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000127491	Nonsense	10	766	1	23

Genomic Location (Zv9):

Chromosome 24 (position 36615729)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	35234644
GRCz11	24	35120909

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

GGGGAGGCGTTTGGGGTCCYGGGCTGGTGGCCAGGCGTCTGGAGCTGGAC[C/T]GAGCTCGGCTGAACCTCAGTCTTCTAGAGCAGGCCATGGTGCTGCAGTCT

Long Flanking Sequence:

TCTCAGATAAAGACCTTCTGGAAGACTCCATCTATCACAACACGAAGCCTCACCACTTGTTGTCCTGGTCGGATCAAGCCAGCGAAGGTTCGCCAGATCTAGACACTCACATCTCCGAACACCAGAACCAGCGAGACGAGGAGAACAACCAGGACTTTGAAGCCAAAAACCAAGAGGACATCAGAGCTGGCTTTCACCTGTCTCCAGATAGAGAAGAAGACGAGGAAGAATGGAGCGCTCCGGCATCTCTAACACCAGTCAACGGGATCAATCACAGCCCCAGCCCGCCTGCAGACGACGCTCTAATGAAAAGGCTCCGGATGGGACAGCAACTCCATGAAGACGCTTTCTCCATGTTCATGAACAGAAACAGCGGAGGAGCTTTGATGGAGGAGTACGGATCTGCTAGAGAGTTCAGCGACAGCGAGGAGGAGCTCAGGATGGAGGAGCGGGGAGGCGTTTGGGGTCCCGGGCTGGTGGCCAGGCGTCTGGAGCTGGAC[C/T]GAGCTCGGCTGAACCTCAGTCTTCTAGAGCAGGCCATGGTGCTGCAGTCTGAGCACAGACAGGTTCTCCACAGTGCCTATAAAGATATGGACCGCTTCTTCTTGGAGCAGATGAATCACGAACGAAGGCAGCAGAGGATGATGGAGATGGATGCTCGCAGCTTGTACCATAGCAACAAAGGTCAGACTTTTACTAATGTCTTTGTTTTTATTTGTTGGTTGCTGAAAGGGTAGAAGAACTAAGAATATTGAAATAATTTTAAATAAAATAGACATGGGGTGTCTCAGTGGTCAGCACTATCGCCTCACAGCAAGAAGGTCGCTGGTTCGAATCCAAACTGGGCCATTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTTGTGTGGGTTTCCTCCGGGTACTCCGGTTTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa37935

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000127491	Nonsense	44	766	1	23

Genomic Location (Zv9):

Chromosome 24 (position 36615832)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	24	35234747
GRCz11	24	35121012

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GCACAGACAGGTTCTCCACAGTGCCTATAAAGATATGGACCGCTTCTTCT[T/A]GGAGCAGATGAATCACGAACGAAGGCAGCAGAGGATGATGGAGATGGATG

Long Flanking Sequence:

CACTCACATCTCCGAACACCAGAACCAGCGAGACGAGGAGAACAACCAGGACTTTGAAGCCAAAAACCAAGAGGACATCAGAGCTGGCTTTCACCTGTCTCCAGATAGAGAAGAAGACGAGGAAGAATGGAGCGCTCCGGCATCTCTAACACCAGTCAACGGGATCAATCACAGCCCCAGCCCGCCTGCAGACGACGCTCTAATGAAAAGGCTCCGGATGGGACAGCAACTCCATGAAGACGCTTTCTCCATGTTCATGAACAGAAACAGCGGAGGAGCTTTGATGGAGGAGTACGGATCTGCTAGAGAGTTCAGCGACAGCGAGGAGGAGCTCAGGATGGAGGAGCGGGGAGGCGTTTGGGGTCCCGGGCTGGTGGCCAGGCGTCTGGAGCTGGACCGAGCTCGGCTGAACCTCAGTCTTCTAGAGCAGGCCATGGTGCTGCAGTCTGAGCACAGACAGGTTCTCCACAGTGCCTATAAAGATATGGACCGCTTCTTCT[T/A]GGAGCAGATGAATCACGAACGAAGGCAGCAGAGGATGATGGAGATGGATGCTCGCAGCTTGTACCATAGCAACAAAGGTCAGACTTTTACTAATGTCTTTGTTTTTATTTGTTGGTTGCTGAAAGGGTAGAAGAACTAAGAATATTGAAATAATTTTAAATAAAATAGACATGGGGTGTCTCAGTGGTCAGCACTATCGCCTCACAGCAAGAAGGTCGCTGGTTCGAATCCAAACTGGGCCATTTCTGTGTGGAGTTTGCATGTTCTCCCTGTGTTTGTGTGGGTTTCCTCCGGGTACTCCGGTTTCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNCCACAGTCTAAAGACATGTGGTATAGATGATTTGAATAGACTAAACTGGCCGTAGTGTATGTGTGTGAATGTGATTGTGTATATGGATGTTTC

Associated Phenotype:

Not determined