ZMP

LOC100330508

Ensembl ID:

ENSDARG00000078964

Human Orthologue:

ESYT2

Human Description:

extended synaptotagmin-like protein 2 [Source:HGNC Symbol;Acc:22211]

Mouse Orthologue:

Esyt2

Mouse Description:

extended synaptotagmin-like protein 2 Gene [Source:MGI Symbol;Acc:MGI:1261845]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa11660	Nonsense	Available for shipment	Available now
sa31586	Splice Site, Nonsense	Available for shipment	Available now

Mutation Details

Allele Name:

sa11660

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:

T > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110789	Nonsense	334	860	9	23

Genomic Location (Zv9):

Chromosome 7 (position 41576155)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	39912412
GRCz11	7	40183429

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

CTGAGGATTTATTTTATTGAAGCTCAGAATCTRGAAGTRAAGGACACGTA[T/A]CTTGGCGGACTAATCAAAGGCAAGTCTGACCCATATGGYATGCTGCTGGT

Long Flanking Sequence:

ATGCACCTCTTTGCATGTGAACATGCAAAATGAGTAAGGGGCTAAGGGGTAGAATTGGGAATGGGCCTTAATTTACGGTTACTCTGCAATTACAGTACATGGCAGCAAGCAATCAGCAAAGTTAAATATTTAGTCAACAGAATATATAAAGGAGAAAATCACTAATGATGCATTACCATTATTTCTTTTCCATTGGCAGTGGCTTTTCAGATCAAATGATCCAAGATATTATCAGCGCTTACATGGTGTTGCCTAACAGGATCACAGTGCCGTTGATAGGTGAGGTTGAGCTGGCACAGCTTCGCTTCCCCATGCCAAAGGTGAACACCCAAACATAACACTACCATCTCATCACTCGTTATTAAGCAAACCATGCTCACTTACTGATGTTATTATTCAGCCATCTCTTCTGCTGTCTTCTTTTATGTTTGGATCTCTCATTAGGGAGTGCTGAGGATTTATTTTATTGAAGCTCAGAATCTGGAAGTAAAGGACACGTA[T/A]CTTGGCGGACTAATCAAAGGCAAGTCTGACCCATATGGTATGCTGCTGGTCAGCAACCAACTTTTCAGAAGTAAGACAATCAAAGAGTGTCTGCACCCCAAGTGGAACGAGGTGTATGAGGTGAGTATGGAGAAACGCTATGCTTATACTGTAATACAAAGATCAAATATTACAAATCTGCATGCATGTGTTTTATCAGGCACTAGTATATGAACCTTCAGGACAACATCTGGAAATTGAGCTCTTTGATGAAGACCCAGATAAAGATGATTTCTTGGGAAGGTGCCAAATTCATTTAAATATCTAAAATGTGCAATATTGTCTATCATTTATCTTTTTAAAAGTGTGAAATGTATTGTTAATTTTTGTTCCAGTCTAATGATTGACTTGACTGAGCTTCATAAAGAACAGAAGGTTGATGAGGTATTTAAATTCTCATTCTTGTTACATTCATTTGCAATGCATGTTCTTTAACAAATGTCACCACCAGTTTTATTTTA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa31586

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 > T

Consequence:

Splice Site, Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000110789	Splice Site, Nonsense	519	860	15	23

Genomic Location (Zv9):

Chromosome 7 (position 41581014)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	7	39917271
GRCz11	7	40188288

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

ATCCAAATCCTTTTGTCAAACTGACTGTAGGACAGAAGACGTGCACAAGC[A/T]AGGTAGCATTGATTAATCAGCTTTAACATCTTAAAGTCCTGCAATGCACA

Long Flanking Sequence:

AAGAAGCATGACTTTCAAATAGCTGAGTTATGATTTATTATTTACAATAAACCAACCGGTCAGAATGTATTGCATATTTGTAATTGACTATTTAAAGGGATAGTTCTCCCCACAATTTGACTCTGTTAGTTGTCAGTTACTCACCTTTAACTTTTTTTTCTTCTAAAAAAAAAGATATTTTGAAGAATGCTGGTTGCTGAGACCAATTGACTTCCATAGGATTTTTGTTCCTACTATGGAAGTCAATGGGTGACAGTAACCAGCATTCTTCAAAACTTTTAAAGATTTAAAACCACATGAAAGAGAGTAAATAATGAGGTTATTATTTCTTTGTGTGAACTATCCCTTTGAGACTGTATCATGTTTTTTTGACTTTGTCATATCCCACCGCATACAATAATTGGGTTCTTTCTCTTTTTGTTCAACAGTCTGGTAAGAAAGTGAGCATAGATCCAAATCCTTTTGTCAAACTGACTGTAGGACAGAAGACGTGCACAAGC[A/T]AGGTAGCATTGATTAATCAGCTTTAACATCTTAAAGTCCTGCAATGCACATATACCCTGTCCTGTACTTTGCAGGTGAGGTATAAAACCAGTGAGCCACTGTGGGAAGAGACTTTCCCCTTCCTTATCAACAACCCCCAGACTCAGGAACTGGAAATTGAGGTATTCTATAAGGGATCGTCCTAAAAGCATGAATGTTTGTTAACAAATAGTCACTAAAATCATCTTAATTACTGAAATCTACTTCAATGTTTATTAATCAAAAGAAGACAGATTATTTAAAGACCAATAAAGCGTGTGTTAATTATGATTAAAAGCTCAGGATTAGTAAAAGTAAACTGACGTGTGATTTGTTTGTCTCAGGTGAAGGATAGTAAGCACAAGTGCTCTCTGGGTAGTCTACAAGTGTCTCTTGCATCTCTCCTGAATGAGGTGGACATGACTCTGAATCAGCAGTTTCCTCTGCAGAGCTCCGGCCCCAACAGCACCCTCAAACTCAAA

Associated Phenotype:

Not determined