ZMP

si:dkey-123f20.1

Ensembl ID:

ENSDARG00000059425

ZFIN ID:

ZDB-GENE-060526-196

Description:

gamma-2-syntrophin [Source:RefSeq peptide;Acc:NP_001119899]

Human Orthologue:

SNTG2

Human Description:

syntrophin, gamma 2 [Source:HGNC Symbol;Acc:13741]

Mouse Orthologue:

Sntg2

Mouse Description:

syntrophin, gamma 2 Gene [Source:MGI Symbol;Acc:MGI:1919541]

Alleles

There are 2 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa6456	Essential Splice Site	Mutation detected in F1 DNA	Not yet available
sa16222	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa6456

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 > G

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082586	Essential Splice Site	136	543	6	17
ENSDART00000141083	Essential Splice Site	136	540	6	17

Genomic Location (Zv9):

Chromosome 17 (position 3203844)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	3415866
GRCz11	17	3456885

KASP Assay ID:

554-5295.1 (used for ordering genotyping assays)

KASP Sequence:

KCTGCAGGTCAACGGCATTAACGTGGAGAAATGCACACATGAGGAAGTGG[T/G]GAGTACTGGACGGCTCTTTCATCTGTGGTCTTGAAATGACATTGATGCAG

Long Flanking Sequence:

AGATAGATAGATAGACAGACGGACGGACGGACGGACGGACGGACGGACGGACGGACGGACGGACGGACAGATAGATAGATAGACAGATGGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATAGATACTGTTACGTAGTGAATATAGTTAAATTTATTTATAATAAATTATGAAATGTATAAATTACTATTATTTTTTATTTTGATAATAAATTGACTGGTTGTGTTACAGACAATATAATTAAAATGTAATATATATATATATATTAAGTTATGACTTGTGTAAATTGTTATTTTGTTTTTATTCTAATTATAAATTGCCTGGTTTTGTTACAGTACATAAAATCTAAGTGTAATATAATCACCATATTAAATGTGGTTGTTTGTGATGGGAATAATGTGCGCTTATATAAGCCTGTCGCTCTTGTCTTTCTCTGCAGGTCAACGGCATTAACGTGGAGAAATGCACACATGAGGAAGTGG[T/G]GAGTACTGGACGGCTCTTTCATCTGTGGTCTTGAAATGACATTGATGCAGAATTAATCCCCAGTTTCATCAGACGCCGCTGGAGCGAACAAGCCCTTCATATCAGCGGCCAGAGTTTGCTTCTCGCTGTAAAGTCTATAAATGATCGATCGCTGGGAGATTCAGCACAAACACTCGCAGCTTTACCCTGTCAATCCACACAGACTGATGCTTTTCCATCAGGACGCCGCTGTTCACTCATTTTATTTGTATCTGAAAATACTAATAGCCAGAGTTGGGCCAAAATAAGTGAAATGTATTTTTAAAAAACATATCATGATTTTAAAAGTCAACATGAAATCAAGATCAATAATTTAGGGTGGAGCTATCAGTCCTTTTGGGTGGAGCTATCAGTCCTTTTGTGTGGAGCTTTCAGTACTTTAGGGTGGGGCTATTGGTCATTTAGTGTGGAGCTATTGGTCTTTTGGGGTGGAGCTATTAGTCATTTAGGGTGGAGCTATC

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa16222

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
Order Allele From EZRC

Mutation:

T > C

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000082586	Essential Splice Site	239	543	9	17
ENSDART00000141083	Essential Splice Site	239	540	9	17

Genomic Location (Zv9):

Chromosome 17 (position 3237418)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	17	3449440
GRCz11	17	3490459

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

TGTTCATGGCTCGAAKCTCTCGACGCAAAGCTGGAACCGACAAATTAAGG[T/C]ACGGTARTCCGCCGTGATGCTGTARGGTTTTGCCACGCGCCGCTCCCAAT

Long Flanking Sequence:

AGTTTTTGCTGTGTTTTCCAGAAGAGCTTGTAGACTAAATATAGTAAGCAGCTGCTTTACACTTTCATCATATTTTTCCTGTGTGTGCGCACATGTGCAAATGTATATGTGTTTGCTTGTGTTTGTGTGTGTGTGAATATGCATAGAAAATGTCATGCATTTATGTAAGGCCACTGTAATCCTCATTCATTTGTAAAATACTGCAGGATCGCGTTGAGCCGCAGTTATTATCTGTCAGCCGATGCTTTTGAATCTGGCGACACGGTTGTTATGAGGCCGCTGGCAGCGCGATCAAAGGGCAGCGGATGGCACTAAAACGAGCTGTTTCTGCCCCGTCCTCTCACTCTCTCCCTCTCATTTATTCCATCTAGGCCCCGTCGTCGCCCTCCTCACCTTCGGCTAATGAACCAAAGTATGAGAAACGCTGGCTGGATGCCGTCACCCTCCCTCTGTTCATGGCTCGAATCTCTCGACGCAAAGCTGGAACCGACAAATTAAGG[T/C]ACGGTAATCCGCCGTGATGCTGTAGGGTTTTGCCACGCGCCGCTCCCAATGTTGGTTTTGCAAGCATTTTTCATTTAGGTGAGAGGATGTTAAATCCAATATCTATGCAGCGGCATGCCGTGTCTGGAAAGGTCAGCGATGCAGCAAGAGGAGCAAGAGGAAAACCTCTAAACTTCCATCCCATATGGAAAAAATAAAATAAAATGATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATCTCCCCTGTTTACTTTTCCCCAAATTTCTGTTTAACGGACAGATTTCTTCAACACATTTCTAAACATAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTGACTAGATATTCTTCAAGACACTTCTATACAGCTTAAAGAGACTTTTAAAGGCTCAACTAGGTTGATTAAGTTAACTAGGCAGG

Associated Phenotype:

Not determined