ZMP

STX18

Ensembl ID:

ENSDARG00000035763

Description:

syntaxin 18 [Source:HGNC Symbol;Acc:15942]

Human Orthologue:

STX18

Human Description:

syntaxin 18 [Source:HGNC Symbol;Acc:15942]

Mouse Orthologue:

Stx18

Mouse Description:

syntaxin 18 Gene [Source:MGI Symbol;Acc:MGI:1918366]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa35612	Nonsense	Mutation detected in F1 DNA	Not yet available
sa22396	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa35612

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:

G > T

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000051893	Nonsense	32	315	1	11

Genomic Location (Zv9):

Chromosome 14 (position 161001)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	233897
GRCz11	14	20469

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

CCGTCAAAACGCGGAATAAAGCGCTCGGGCTGATGGAGACTACCGGGAGA[G/T]AAGAACCGGGAGCCCAGAAGAGACCCAGACCGAGACAGAGGGACAGTTTT

Long Flanking Sequence:

TTGATTCCCTCATCCTCCACTCACACTGCAGTGCTGATAAACACATCTGAAGACAACTAGATAGAGGAGAATGCTGGAAAAAACAGCACAGTAGGAACATCATCATCATCATCATCATCATCATCATCATGTGTGGAAGTCAGCGTCTGTTTTCCAGCATTCTTCAAAATATCTGCCGCTGTGTTCGACAGATGAACTCAAACAAGCGGAGGATGAGGAGATGATGACACAGTTCAGTTTATAAACACTTTCAATAACCCCTTAATAGTACACTATTCCTTAAACTGCAGGAGGAGTGTGTACCCTGTAGTGTGCACTGTGTAGGGTGCAGTCTAGTGTAGGGCACTGCTGATGACAGGCGGTAGTTTCGTCGCCGGTGAATGACGTCAGAGCGCGACGTGTCAGTCATGGCGGCCGATATTACACTGCTGTTCAAAGCGAGCGTGAAAACCGTCAAAACGCGGAATAAAGCGCTCGGGCTGATGGAGACTACCGGGAGA[G/T]AAGAACCGGGAGCCCAGAAGAGACCCAGACCGAGACAGAGGGACAGTTTTAGCTGCAAAGCCCGAGAAGTGGTGAGATAAACACACACACACACACACACACACACACACAGGGGGGAAGTTGGGTTTATTTGAGCACATTTGCACTTTCTCCTTAATTCTATAAGTTCGGCTAGTAACGTTAGTTAGCATTGTTTGCTAATGTAAACAAGACAGTGACGTCAGCAGCAGCAGGCTGAGTGTTGAACAGAGCTCAGTCAGACAGTGCTGAGGAGGATCAGAGGTCTGTGTACATCTGATCTCAGACACAATACTCAGAGTCATGATAAACAATACAGTCATAAAGCTGCCACTGCTCAAAAATGAAGCTGAATGCGAATATAAAACCAACATTACCTCTAACACAAACACACACACACACACTCTTCAAATGACGATAATATCACACTTGCAGACATTTATCAGCCAGTCATACAGCCGAGCAGAAGCTGATGATGATGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa22396

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:

T > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000051893	Essential Splice Site	147	315	5	11

Genomic Location (Zv9):

Chromosome 14 (position 157860)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	14	230759
GRCz11	14	23607

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AAATCTGTGTGTGTGTGTGATCAGTCCTCTTGATCAGTGATGTGCAGAGA[T/G]GAACAGTCCTTCACAATCTTCTGTTTACTGAAATCAAATGAGGATATCTA

Long Flanking Sequence:

GTGTGTGTGTGTGTGTGTGTGTGTGTGCAGTGTGATGAGCTCTGAAGTGTCCCGCATGACGGACAGCGAGCGTGATCAGATCGATCAGGATGCGCAGATCTTCATGAGGACGTGTGCAGAGGCCATCAGCCAGCTGCGCTCCGAGAGTACGACACACTCACACACACACACACACAAACACACACACACACACACACTCCATTGCAGCTTGACTGTAAATAATAGTAAATACTCAATGAATGTCAGTCATGTGGGCTGTGTGTGTAATAACTCTGTGTGTGTGTCTGTCTGTGTGTGTGTGTGTGTGTCTGTCTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTGTCGTTCAGTGGACAAAAAGCAGGTCTCCATGCAGGTGAAGGACCATCGAGCAGCAGTGTTGGACCTGATAGACTCATATCTGAAAGGTACACATACACACTTGTGTAAATCTGTGTGTGTGTGTGATCAGTCCTCTTGATCAGTGATGTGCAGAGA[T/G]GAACAGTCCTTCACAATCTTCTGTTTACTGAAATCAAATGAGGATATCTACATGTGGACACTGGGCAGAAGTATTGGCACCTCTATATAGCTCTTGTGTGTGTGTGTGTGTGTTTGTGTGTGTGTGTNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNACACACATACATTTGCATATACATACAAACACACACACACATTTACACATGCTTTAACACACACACACACACAGACACACACACACACACACAGTAGAGCAGTGGTTCTCATTGTTCGCTTGAGTCTCAAAAGAAATCATGCCCACCGCCAGCCGAAATCATGTCGCTGCTGTAGAGATATTCCAGTGTATCATGCGCTGTGTGTGTGTGTGTGTGTTGCAGATAAACCAGTCTCAGATGGAAATGTTGATTTGTGGGAGGAAAACAGAGTCG

Associated Phenotype:

Not determined