ZMP

snap25b

Ensembl ID:

ENSDARG00000058117

ZFIN ID:

ZDB-GENE-980526-392

Description:

Synaptosomal-associated protein 25-B [Source:UniProtKB/Swiss-Prot;Acc:Q6PC54]

Human Orthologue:

SNAP25

Human Description:

synaptosomal-associated protein, 25kDa [Source:HGNC Symbol;Acc:11132]

Mouse Orthologue:

Snap25

Mouse Description:

synaptosomal-associated protein 25 Gene [Source:MGI Symbol;Acc:MGI:98331]

Alleles

There are 3 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa32130	Essential Splice Site	Available for shipment	Available now
sa7432	Missense	Mutation detected in F1 DNA	Not yet available
sa36346	Essential Splice Site	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa32130

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:

A > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080927	Essential Splice Site	None	203	2	8

Genomic Location (Zv9):

Chromosome 17 (position 12200459)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	12182981
GRCz11	17	12337047

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

GGTCTGCCACACTCTAACCCAAAGCATTTTCCCTCTCTTTTATTTTCTCT[A/G]GCTTTCAAGTAAGAGCTACACTTTCCGTTTGAGTTGAGCAGCTCATCCCT

Long Flanking Sequence:

GTAGGTTTGTATTATCTATTATTTTAATTAATGATGTTATTAGTTAAGATACAGATCTGGGAAAACTATTTTTAACCTAATTTATTAATTAGGGGGGTAAATCCCCCCCAAACCTCCCTGTAATTCGCACCCTGCTTAAACCACATGTTTTTGGACTGTGGGGAAAACTGTAGCACCCAGAGGAAACCCACATGAACACTGCGAAAAATTCATAAACCAATTCTTCATTGTAAAATCTTTATATTTTTTGTGAGTTTTTTTGAGTCCTTAAACTGATGAGTTTCTGTGAATGAACCTGAATATTTCCACAATACTTGCACTCGTCTTCAAAGAACAATACTTTGACAATCATGTGACTTTCTTCTCTGTATGAGTTGCTTTTAAATTCTGTTTGCTCATTGAACTTTTTTAATGCAATGCTGAACCAGATCTGTCTAAAGGACTCACTTTGGTCTGCCACACTCTAACCCAAAGCATTTTCCCTCTCTTTTATTTTCTCT[A/G]GCTTTCAAGTAAGAGCTACACTTTCCGTTTGAGTTGAGCAGCTCATCCCTCCATCCACCATGGCAGACGAGTCCGACATGCGCAACGAGCTGAATGACATGCAGGCCAGAGCCGATCAGCTGGGCGATGAAGTAAGTACACCTTCAACCTCCAGGTCTATAAATAACCCCTAAATACGACAACAAGTGTGTATAAATAGACCCGTCCCAGTGTGAAGGAGAATGAACACACCATGACTTCCAGACACTCGGATTCACATAGGAGTATCATGCATGGAAATAGATGCCAATTACATATATGACATGCGAGTTCATATTTGGATTTCACATATACAGTTAAAGTCCGAACTATGTATATTTGTTCCCCAATTTCTGTTCAACAGAAAGATTTTTTTCACCACATATCTAAACATAATAGTTTTATTAATTAATTTCTAATAACTGATTTATTTTATATTTGCCATGATGACAATACATAACTGGGTATTTAACAAGATGCTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa7432

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:

A > T

Consequence:

Missense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080927	Missense	60	203	5	8

Genomic Location (Zv9):

Chromosome 17 (position 12180062)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	12162584
GRCz11	17	12316650

KASP Assay ID:

554-4033.1 (used for ordering genotyping assays)

KASP Sequence:

TTTTCGGGGGCTGTAATTGACTAATGTTTAAATCAGAGCAACTGGAGCGC[A/T]TCGAAGAGGGAATGGATCAGATCAATAAGGACATGAAAGAAGCAGAAAAG

Long Flanking Sequence:

TAGACCAAGTTCTTGGCATGATCTAGCCTAACCACTCATCACATCGTTAAAGTTCTGCGTAGATGTGTTTCTGGACAGCTTAGATGTCATTTGTCATCACCGTTTGTCTGCCAGGATGCAAAGTCTCATTTCATTGCTGTCACCCCTTTGTCCTGACCAGAACAACTCGAGCGTGTTGAAGATGGCATGAACCATATCAACAAAGACATGATGGAAGCTGAGAAAAGTTTAAAAGATGTAGGCAAATGCTGTGGACTAGTATGTCCCTGCGACAAGTAGGTACTGGTGAAGCGTCCAAGGCTCTCACCTGTCTGCTGCTGTCTGACTGTCTCTTGTCACTGTGAATGTTTAAGCCTCTCTCTTTCTTTTTGTCCCTCTCTTTTCCTCCTTGCCTTTCCCTTCTCTTTCTCTCTTTGTCCCCCTTTTCCATACTCTTTATTTCTTTTCTTTTTTTCGGGGGCTGTAATTGACTAATGTTTAAATCAGAGCAACTGGAGCGC[A/T]TCGAAGAGGGAATGGATCAGATCAATAAGGACATGAAAGAAGCAGAAAAGAATTTGACGGATCTAGGAAATCTCTGTGGTCTATGTCCGTGTCCATGTAACAAGTAGGTGATGCCTGTCGCCTGCCTGCCTGCTTGCCTGAACCCGACAAATAGGAAAAAAAAAAAAAGATAAAGCACGTGGCCAGTTTGCACGCTCGCTCTTGCTCGCTCCGTAGCTGCGAATTTCCCCCTTTGCTCTGCCTGGACTACTTCTCTGTGCATGGGGATGCTGGTAGAGCTAAGTCCGTCTGCGGCGCCACTGGTTAACCCATAGTTGTAGCTGTAGGCCCTGCTCTCTGCCGGCTGAATGCGCAAATTTGCTGGGCTCCATGCTTCACTGATCCTTTGGTCAAGGACTGTTGTTCGTAAATGTTAAGTGCCTGCTTGATATGCATGTGCTACTTTTGGAAATGCAAGCATTACACACTTTTTAAATGAACCGCAGATTAAATATTCACAT

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa36346

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 > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000080927	Essential Splice Site	94	203	5	8

Genomic Location (Zv9):

Chromosome 17 (position 12179957)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	12162479
GRCz11	17	12316545

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TGACGGATCTAGGAAATCTCTGTGGTCTATGTCCGTGTCCATGTAACAAG[T/C]AGGTGATGCCTGTCGCCTGCCTGCCTGCTTGCCTGAACCCGACAAATAGG

Long Flanking Sequence:

GTCTGCCAGGATGCAAAGTCTCATTTCATTGCTGTCACCCCTTTGTCCTGACCAGAACAACTCGAGCGTGTTGAAGATGGCATGAACCATATCAACAAAGACATGATGGAAGCTGAGAAAAGTTTAAAAGATGTAGGCAAATGCTGTGGACTAGTATGTCCCTGCGACAAGTAGGTACTGGTGAAGCGTCCAAGGCTCTCACCTGTCTGCTGCTGTCTGACTGTCTCTTGTCACTGTGAATGTTTAAGCCTCTCTCTTTCTTTTTGTCCCTCTCTTTTCCTCCTTGCCTTTCCCTTCTCTTTCTCTCTTTGTCCCCCTTTTCCATACTCTTTATTTCTTTTCTTTTTTTCGGGGGCTGTAATTGACTAATGTTTAAATCAGAGCAACTGGAGCGCATCGAAGAGGGAATGGATCAGATCAATAAGGACATGAAAGAAGCAGAAAAGAATTTGACGGATCTAGGAAATCTCTGTGGTCTATGTCCGTGTCCATGTAACAAG[T/C]AGGTGATGCCTGTCGCCTGCCTGCCTGCTTGCCTGAACCCGACAAATAGGAAAAAAAAAAAAAGATAAAGCACGTGGCCAGTTTGCACGCTCGCTCTTGCTCGCTCCGTAGCTGCGAATTTCCCCCTTTGCTCTGCCTGGACTACTTCTCTGTGCATGGGGATGCTGGTAGAGCTAAGTCCGTCTGCGGCGCCACTGGTTAACCCATAGTTGTAGCTGTAGGCCCTGCTCTCTGCCGGCTGAATGCGCAAATTTGCTGGGCTCCATGCTTCACTGATCCTTTGGTCAAGGACTGTTGTTCGTAAATGTTAAGTGCCTGCTTGATATGCATGTGCTACTTTTGGAAATGCAAGCATTACACACTTTTTAAATGAACCGCAGATTAAATATTCACATGTTGTTTACTGGAGGCTGGCAGAGCTGGCTTTTTGTATGGGTTCTCTAAAGGCGAAGCATGTCAATGCATGTGGGTGAGATGGTGGGATAAGTTATCCTGGCGAT

Associated Phenotype:

Not determined