ZMP

SYNRG

Ensembl ID:

ENSDARG00000073926

Description:

synergin, gamma [Source:HGNC Symbol;Acc:557]

Human Orthologue:

SYNRG

Human Description:

synergin, gamma [Source:HGNC Symbol;Acc:557]

Mouse Orthologue:

Synrg

Mouse Description:

synergin, gamma Gene [Source:MGI Symbol;Acc:MGI:1354742]

Alleles

There are 4 alleles of this gene:

Allele Name	Consequence	Status	Availability
sa22603	Nonsense	Available for shipment	Available now
sa1618	Essential Splice Site	Available for shipment	Available now

Mutation Details

Allele Name:

sa22603

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:

C > A

Consequence:

Nonsense

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115129	Nonsense	1197	1409	17	24

Genomic Location (Zv9):

Chromosome 15 (position 14935132)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	15980095
GRCz11	15	15916117

KASP Assay ID:

None (used for ordering genotyping assays)

KASP Sequence:

None

Flanking Sequence:

TCCAACACCCTAAATGAAAAACCAGCGCTGCCGATCATCCGCGACAAGTA[C/A]AAGGACCTTACAGGAGAGGTTGAGGTCAGTTAGTCAGTCACTCTTTCTAT

Long Flanking Sequence:

TTGTTAAATAACTGTCTAATTATAATTTCCTTATAATAGTTATTATGGATACTATTTGGGTATTTGTAAAAAGTAATCATTTTAACCTTTAATAATACGTTAAACACAGTAAATATGTTCACTCACATGTATTCTCAATGTAAAGAAACTTGTTTACTTCAACTTTTACTTGGTAGTTTTATTGTAATGGTATTTATGAACATTAATTTTCAAATTGTTAAAAAAGAAAAAAAAGTTTAAGCCTAAAAATTTCCTGCATTAAAATAAAGGCAATGTTTCTAAGAACTTGGCATGCATGCAGACTCATTTTCTTTATCATGGACACTCTCATTTGTCATTGACCCGTTTATTTTTGGCAAAGGTTCCCATAAGCGCAGCCACAGTCTGGGAGAAAAGGAAATCGTACGCTCCATCCCCTCTCCTGCCCCTGAGCAGCCCTTCAGAGACCGATCCAACACCCTAAATGAAAAACCAGCGCTGCCGATCATCCGCGACAAGTA[C/A]AAGGACCTTACAGGAGAGGTTGAGGTCAGTTAGTCAGTCACTCTTTCTATTCTTTTCCTCCTCATCTCTTCAAGCACACAGACAGCTTCTCCTTGTTGAATACAGCCTGAGGTTTCTCAATGAACAAAGCTCTCATTCTGTTTCATCTGTTTCTCCCACTGTCTCTGCTCTAAACTGGCAGGAGAGTGAGCGATACGCGTATGAATGGCAGAGGTGTTTGGAGAGCGCTCTACAGGTAATGTATACCCCCACATACATTCCCATATAGAGTTTTGCTCTTGCTTATATAACCATATCATTCTTTAGATAGTCTTGTCATATTCACTTAATAAATCACTGCTTCCACCAAATCACTGGTTTTTTATTCAGCAGACATAAACTCTTTTCACAAGTATTAACCATAGCCATCAGAGGAGGTCATTTACATGCACTACTAGGGCTCTATTTTGACGGTCCATGCGCAAAACGCAGGGCGCAAATGCTTTCAGGGCGTGTCAGGA

Associated Phenotype:

Not determined

Mutation Details

Allele Name:

sa1618

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:

G > A

Consequence:

Essential Splice Site

Transcripts:

Transcript ID	Consequence	Amino Acid Affected	Amino Acid Total	Exon Affected	Exon Total
ENSDART00000115129	Essential Splice Site	1342	1409	21	24

Genomic Location (Zv9):

Chromosome 15 (position 14925711)

Other Location(s):

Assembly	Chromosome	Position
GRCz10	15	15970674
GRCz11	15	15906696

KASP Assay ID:

554-1559.1 (used for ordering genotyping assays)

KASP Sequence:

AAGAGCTGGCGTGTGGAGTGTGCCTGCTYAATGTGGACTCACGCAGCAAG[G/A]TCTGTACACAYAAACATCTGCATATTACCATTAGTAACACACACAAAACA

Long Flanking Sequence:

AGTGCAATAGCATAGAACAGATTGCCGAACAGTGCTTTGTCATGCAGTTCTCTCATGGGAGAATATCAATGCCAGCAGATAATATTAGAGCTGTGCGGTCAGATAATATCAGCTCGGGAGGATACGAGTCGCAGCACAGCGCTGAAAAACCACAAACGCTCAGAAGTATAATAAAAATAACCATGGTTTGGAGGGGTTGGAGGCTTTTCCTGCTGTTTTGGGCAGATTTGAGCTGATGTATTGATCTGCAGGGCCAATCAACCGCTGTGAGGCTGATGGGCTGCTTCACTGGCCTCTGCCATCTGATGTTTGACAGACAGGCAGGGATTTGTGGACAATTGCTTTTTAAGAACTGTATTCATTGAGTGTGTGCGTGTGTTTTTCTGTAGCCTGATGAGAGCTCGCTGGACTTCTCCTCCTGTATACTGAGGCACGGCATTAAGAATGCCAAAGAGCTGGCGTGTGGAGTGTGCCTGCTCAATGTGGACTCACGCAGCAAG[G/A]TCTGTACACATAAACATCTGCATATTACCATTAGTAACACACACAAAACACTCATTAAAAAGAAGTTGTTTGGATTTAAGTAAGCAAATATCAAGATACTAGGGTTGGACTTTTACCACAGAGATTTCTTTAGCACAGCTATGGACTTTTTTTGTGTGGATTTAATTTATTTCTTAGCTACACGGTTGAGTAAAATCTAAATATTTGTTTTCCCTGCTAAAAAATCCAGCTTAAACCAGCCTAGGCTGGTTGGCTGGTTTTAGCTGGTTGACCAGCCTGGTTTTAGAGAGGTTTTGGCCATTTCCAGCCTGGTCTTAGCTGGTCAGGCTGGGAGATGACCAGCTAAAACCAGCTTGACCAGCCTAGCCAGGCTGGGAGCCCAGCCGAAACCAGTTATGTCCAGCTTAAACCAGGCTGGTCAAGCTGGTTTTAGCTGGATTTAGCTGGTTATTTTCCAGCCTGACCAGCTAAGACCAGCCTGGAAATTGCTGGAAACCAGC

Associated Phenotype:

Not determined