ZMP

zgc:101731

Ensembl ID:

ENSDARG00000040965

ZFIN ID:

ZDB-GENE-040912-57

Description:

synaptosomal-associated protein 25 [Source:RefSeq peptide;Acc:NP_001020729]

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 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa39054	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa42567	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa39054

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:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000060030	Essential Splice Site	55	209	None	8
ENSDART00000133988	Essential Splice Site	55	209	None	8

The following transcripts of ENSDARG00000040965 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 15 (position 28479853)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	29197883
GRCz11	15	29130759

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TTCCCCCTTTCGATTTCCCTGCTGCCTTCCCCCATCTCCCCCGCATGGGC[A/T]GAACAACTGGACCGCATAGAAGAGGGCTTGGATCAGATCAACAAGGACAT

Long Flanking Sequence:

CCATTTGCGTAAAGCAGATCTTCTTTTAAATAAGTGCACAAACTAAACACCATACAACAATAGCACCATCACAAACTTATATCCACAATTAATCTTTGATCAATCCAAGAAAATGGAGATGAATTGTTTCCCTCAATGCTTAATCATTTTCATTATTCTTCAACAGAGTAAAGATGCGGGCATCAGGACACTTGTTATGCTGGACGAGCAGGGAGGTAATGAGTTCCCTCTGTAGTTAAATAGAGCTAAACAATGAACTAATTACATACAAACGCCTCATTAATTATTGCATCTATAGGAAATATGTTAATGCTGCTGTATATTTACAAGATGTGGAAGTACAGACTTTGCTCTTCATTCTTATTTTCAGTACGACATATATAAATAGCTATATATGATTCTGTACATATGGAACCTTGTATGTCTTTATGTGTGCATGCTTGCATATATTTCCCCCTTTCGATTTCCCTGCTGCCTTCCCCCATCTCCCCCGCATGGGC[A/T]GAACAACTGGACCGCATAGAAGAGGGCTTGGATCAGATCAACAAGGACATGAAGGAGGCTGAGAAAAATCTGACTGACATGGCCATGTGTTGCGGTCTGTGCATCTGGCCATGTACAAAGTAGGTCTCCTCCCAGACACCTGAGCCACGGCTGGGCAGTCAATGATGTCCCCTCTCTGCCCATGCATTTGTCCCGTTGGATAAGCTGTCCTGCTTTGATGTTGCTTTATATTTGTTTGTTTTTAGCTGTTTTGTGAGCAGAGGTTGATGCAATGCCTCATGTTTTTTTTTTTTTAAATTGGAACCAATAATTTTTGGTTGGTTTTTATACATAATTGAATCCATAATTTTTACATTTATGTTGTCCATTTGGCTTGGCATTTTCAGCTAGAGCTGTTATTGATGTTCAGGGCCAGATTTACTAAATAGGCCAAATTAATGTGAGACTATAATTCCGTAAAGTGCAGGTGGGGGTGAAAAGTTTTGCAGAAATTCAAATTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa42567

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
ENSDART00000060030	Nonsense	137	209	6	8
ENSDART00000133988	Nonsense	137	209	6	8

The following transcripts of ENSDARG00000040965 do not overlap with this mutation:

Genomic Location (Zv9):

Chromosome 15 (position 28485218)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	29203248
GRCz11	15	29136124

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCTTCTCGCGTGGTGGATGAGCGAGAGAAGATGACCATGAGCGGTGGATA[T/A]ATAAGAAGGTGCCTGGACCTTTGCGCTCTTCAGCAATGTTGAATATAGTT

Long Flanking Sequence:

CCATTTCGTTTCCATGGGGCAGACGGTGTTAATACCAATGCTGCAGCCAACCACCAGGGGGAGATAAACTATTTTGGCTTTACTTTTTAAGACTGGCGCACTTCTTTAAAGCTCATGAGCCTTGACTAAAGAAGTCAGGCCAACTAAATGTTATTTACTGTGATTTTTTTTTATTTTTACTTTATATAATGTTTTGTGTGGTGAATTTGAAATCAGCTAACTGTATGCTCAGGGTCAGCACTGAACTCTGCTCGAACATTTAGGCAACTTTTGCCTAAATATCACAGATCATTTCTCAAAGTTGTGGTTGTTTGATTAGAGGTATGACTAATCTGCTACAATTTATGTCTTTCATAAATGGTTTCTCTTAGATTAAAGGACTTTGAAGCAAGTGGAGCATATAAGAAGGTGTGGGGTAATAATCAAGATGGAGTGGTGTCGAGCCAGCCATCTTCTCGCGTGGTGGATGAGCGAGAGAAGATGACCATGAGCGGTGGATA[T/A]ATAAGAAGGTGCCTGGACCTTTGCGCTCTTCAGCAATGTTGAATATAGTTTATGCTGCTTAATATTTTTGGTGGAGACCATTAATTCACCATTGGTAAATAGATGTTCACTGTTGTTTTATCGATTAAGTCAAATTAAAGGGATAGTTCAACCAAAAATGTAATTATTCATAATTTATTCTCATTTATTCATTATTTTTATGGGTTTAAACCTTTTTGTGGCATTTCTTTTTTTTGCTGAATACAAAAGAAGATTAAAAAAAAAAGTTCTTTGCTGCTGCTACCCTTTGACCTAGAGGGGTCTGGATGTAGACTTGGTGCAGTGCAATCTGAGCCGCATCCAATGCTTTTTAATAGACTCTCCTAAGCCCACCCCTAAACCTACCCCTCACAGTGACGTCATTCACACCATTTGAGTGCATTGTGTCTGACATTGCATCGCTGAGTGATGCAATCTTAGCTTGCATCATAAAGGCTGCATACAATTGCATTGACCTCCAT

Associated Phenotype:

Not determined