ZMP

syt14b

Ensembl ID:

ENSDARG00000001891

ZFIN ID:

ZDB-GENE-041014-36

Description:

Novel protein similar to vertebrate synaptotagmins [Source:UniProtKB/TrEMBL;Acc:Q5RGA2]

Human Orthologue:

SYT14

Human Description:

synaptotagmin XIV [Source:HGNC Symbol;Acc:23143]

Mouse Orthologue:

Syt14

Mouse Description:

synaptotagmin XIV Gene [Source:MGI Symbol;Acc:MGI:2444490]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa43388	Nonsense	Mutation detected in F1 DNA	Not yet available
sa43387	Nonsense	Mutation detected in F1 DNA	Not yet available

Mutation Details

Allele Name:

sa43388

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
ENSDART00000045840	Nonsense	433	535	11	11
ENSDART00000136079	Nonsense	296	398	4	4

Genomic Location (Zv9):

Chromosome 20 (position 9420615)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	9254884
GRCz11	20	9242623

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ACCAGGTGGTGCTAACTCACTTTTTCCTCTCGCCTTCCATCAGACACTTA[T/A]GTGAAGCTTACAATGCTGGACTCCAAAGGGAAGGAGATGTCTAAATGTAA

Long Flanking Sequence:

AGCTTCATCTAATATAGAAGTTATCATTAAAAAAATGTAAAATTTGCAGAGATATATAAAAATAAAGTGTTGCACATTGATACATTAAATACAGGGTATTTCCTACCCTGTTAAATCATTGTTGATAATATTTGTAAAAATCATTAACATGATCATTCGTCTAATATCATTAATTATTACCAAAAACATGAAGTATATTTAAAAGTAAATTGAGCAAATTTGTTATTTGAGAAGTGTAATCGGTATCCAAGAAGTAGCTCTCAGTTTCATAAAGGTTGGTGACCCCTGTTATAGAGTTTATAGTGTGGGGATAGAATATAGCACACTAAAATAATCATATAATCCTGCAACTTTAAAAATATCATGTAGTAAAAGTTATGTAGCTAGTATTACATTTCTTGTATTAGCTTGTAACACATGCATTTGGTAGTGCATGAGATCATCTTCACCACCAGGTGGTGCTAACTCACTTTTTCCTCTCGCCTTCCATCAGACACTTA[T/A]GTGAAGCTTACAATGCTGGACTCCAAAGGGAAGGAGATGTCTAAATGTAAGACCTCTGTCTGCCGTGGCCAGCCCAACCCAACCTACAAAGAGACATTTGTCTTCCAGGTGGCACTTTTTCAGCTATCTGAGGTCACCCTCCAGGTATCTGTGTACAGTCGCCGGAGTAGCATGAAGAGGAGAGAGCGGGTAGGTTGGGTCGCTCTGGGCCTCAACAGCACCACAGAGGAGCAAGAGGAGCACTGGACTCAAATGAAGGAGTCAGAGGGTCAGCAAGTCTGCCATTGGCACACACTCATCGATTCCTAGGGGAAGCAGTTTAAAAATGTGGTTTTACAAATTTGAGTAAGAGTTACTGCTAAGTTTCAAGGTGTGTCCTAATTTACTGACTCATGTCACTCCAGAGTCATTTGAAATTTAGAGTGGCATGAGGGTGAGTAAATGGCTATTGGCTATTCTAAAACTGGGTTTAAAGTTAGTCTCTGTACTGAAATTTGGGC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa43387

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
ENSDART00000045840	Nonsense	481	535	11	11
ENSDART00000136079	Nonsense	344	398	4	4

Genomic Location (Zv9):

Chromosome 20 (position 9420473)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	20	9254742
GRCz11	20	9242481

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

AGACATTTGTCTTCCAGGTGGCACTTTTTCAGCTATCTGAGGTCACCCTC[C/T]AGGTATCTGTGTACAGTCGCCGGAGTAGCATGAAGAGGAGAGAGCGGGTA

Long Flanking Sequence:

ATTAACATGATCATTCGTCTAATATCATTAATTATTACCAAAAACATGAAGTATATTTAAAAGTAAATTGAGCAAATTTGTTATTTGAGAAGTGTAATCGGTATCCAAGAAGTAGCTCTCAGTTTCATAAAGGTTGGTGACCCCTGTTATAGAGTTTATAGTGTGGGGATAGAATATAGCACACTAAAATAATCATATAATCCTGCAACTTTAAAAATATCATGTAGTAAAAGTTATGTAGCTAGTATTACATTTCTTGTATTAGCTTGTAACACATGCATTTGGTAGTGCATGAGATCATCTTCACCACCAGGTGGTGCTAACTCACTTTTTCCTCTCGCCTTCCATCAGACACTTATGTGAAGCTTACAATGCTGGACTCCAAAGGGAAGGAGATGTCTAAATGTAAGACCTCTGTCTGCCGTGGCCAGCCCAACCCAACCTACAAAGAGACATTTGTCTTCCAGGTGGCACTTTTTCAGCTATCTGAGGTCACCCTC[C/T]AGGTATCTGTGTACAGTCGCCGGAGTAGCATGAAGAGGAGAGAGCGGGTAGGTTGGGTCGCTCTGGGCCTCAACAGCACCACAGAGGAGCAAGAGGAGCACTGGACTCAAATGAAGGAGTCAGAGGGTCAGCAAGTCTGCCATTGGCACACACTCATCGATTCCTAGGGGAAGCAGTTTAAAAATGTGGTTTTACAAATTTGAGTAAGAGTTACTGCTAAGTTTCAAGGTGTGTCCTAATTTACTGACTCATGTCACTCCAGAGTCATTTGAAATTTAGAGTGGCATGAGGGTGAGTAAATGGCTATTGGCTATTCTAAAACTGGGTTTAAAGTTAGTCTCTGTACTGAAATTTGGGCAGGTAAGGGCAAAACAAATCCCTTGTTCACTCTCAATACTGCGGCCATAAATTTGCTTAGCACTTTTAAAACAATAAGGATTGTAGTATATAATTAAATATGGGTGTTGAAATGTTGACAAACTAAAATCTTACATCTAATT

Associated Phenotype:

Not determined