ZMP
syncripl
Ensembl ID:
ZFIN ID:
Description:
synaptotagmin binding, cytoplasmic RNA interacting protein, like [Source:RefSeq peptide;Acc:NP_9559
Human Orthologue:
SYNCRIP
Human Description:
synaptotagmin binding, cytoplasmic RNA interacting protein [Source:HGNC Symbol;Acc:16918]
Mouse Orthologue:
Syncrip
Mouse Description:
synaptotagmin binding, cytoplasmic RNA interacting protein Gene [Source:MGI Symbol;Acc:MGI:1891690]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa23192 | Essential Splice Site | Available for shipment | Available now |
sa15108 | Nonsense | Available for shipment | Available now |
sa23193 | Essential Splice Site | Available for shipment | Available now |
sa32175 | Nonsense | Available for shipment | Available now |
sa44878 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa23192
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037450 | Essential Splice Site | 126 | 558 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 50802902)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50193719 |
GRCz11 | 17 | 50272788 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCAAAGTGTCAGACTCTACTAAAGGACCAGACGAGGCCAAAATCAAAG[T/G]CAGTCTGCTTCACTTCTCTACTGTCTGTTCTGTCCAGCCGCTGTTGGTTC
Long Flanking Sequence:
GCTATAATAAAATCCTTTTCATAGAAAGGTTAGTTATGAACATTTATACACAAGTATTAAGATAAAGATGACCCAAACCATACCCTACTGTACCGTACCGATTTTGTTTTTAGTGCGATCAGTTTGGTAAATTGTATTGAATTATGAATTTAAATCGATTTAAACATCAAAGGCAAATCAGTGTTCGTAACAATGACAACAAAATTAAACAAATGACAAGCATGGTTTCCTTTAAGCTTAATTATCGGTCTTATATGTTAAGTGTGATTTAAGCGTGATTTAGTTGAGAAGGAGAACTCAATGGTTCTGATGCGGTCTCAGTTTCTCTTTTTATTCCTGTCCACTTGCTGGCACACACACGCACCTCATGCTCACTTCATGTTTTGCACAGAATAAAAGTGCCTTCCTCTGTGGAGTGATGAAGACGTACAGGCAGAGGGAGAAGCAGGGGACCAAAGTGTCAGACTCTACTAAAGGACCAGACGAGGCCAAAATCAAAG[T/G]CAGTCTGCTTCACTTCTCTACTGTCTGTTCTGTCCAGCCGCTGTTGGTTCTCGTTCGTTCTTTTACTATTGATCCAGTTACAAGTGCTTTTCTGTGTGCCGCTTCGCCAGGCTCTGCTGGAGAGAACTGGCTATACGCTTGACGTGACGACAGGCCAGCGCAAATATGGTGGTCCGCCTCCAGGATCGACCCATGCCGGAGTGCAGCCCACCATCGGCACAGAGGTCAGTCTTGGAGTCTAATAGATTCACATCAGCACACCGTTATTCTGATCTGATTCGTTTGGTTGTGTTTTTTAACACTAGAACCGCAAGGGGTCATTGTATGCCTAAAACCACCAGTGTGGTCTAAAATAAAAACACCACTGTGTTCTCAAAGAAGATGAAAAAATTATACTATATTTTTAATGTGTTTTAGTTTGAGGGGTTTTTATGCAGGCTACAATCACTTTCAGAACAAGAATTAGAAGTAAATACTAGTGTTGTCAAAAGTATTGAGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15108
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037450 | Nonsense | 158 | 558 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 50803106)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50193923 |
GRCz11 | 17 | 50272992 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCAGCGCAAATATGGTGGWCCGCCTCCAGGATCGACCCATGCCGGAGTR[C/T]AGCCCACCATCGGCACAGAGGTCAGTCTYGGAGTCTAATAGATTSWCAWC
Long Flanking Sequence:
TTAAACAAATGACAAGCATGGTTTCCTTTAAGCTTAATTATCGGTCTTATATGTTAAGTGTGATTTAAGCGTGATTTAGTTGAGAAGGAGAACTCAATGGTTCTGATGCGGTCTCAGTTTCTCTTTTTATTCCTGTCCACTTGCTGGCACACACACGCACCTCATGCTCACTTCATGTTTTGCACAGAATAAAAGTGCCTTCCTCTGTGGAGTGATGAAGACGTACAGGCAGAGGGAGAAGCAGGGGACCAAAGTGTCAGACTCTACTAAAGGACCAGACGAGGCCAAAATCAAAGTCAGTCTGCTTCACTTCTCTACTGTCTGTTCTGTCCAGCCGCTGTTGGTTCTCGTTCGTTCTTTTACTATTGATCCAGTTACAAGTGCTTTTCTGTGTGCCGCTTCGCCAGGCTCTGCTGGAGAGAACTGGCTATACGCTTGACGTGACGACAGGCCAGCGCAAATATGGTGGTCCGCCTCCAGGATCGACCCATGCCGGAGTG[C/T]AGCCCACCATCGGCACAGAGGTCAGTCTTGGAGTCTAATAGATTCACATCAGCACACCGTTATTCTGATCTGATTCGTTTGGTTGTGTTTTTTAACACTAGAACCGCAAGGGGTCATTGTATGCCTAAAACCACCAGTGTGGTCTAAAATAAAAACACCACTGTGTTCTCAAAGAAGATGAAAAAATTATACTATATTTTTAATGTGTTTTAGTTTGAGGGGTTTTTATGCAGGCTACAATCACTTTCAGAACAAGAATTAGAAGTAAATACTAGTGTTGTCAAAAGTATTGAGTTCAGTATTAATCGATACTGAAATTTTAAAAACATCCATTACTTGCTAACATTTCAGTGCTGTTGAGCGCGTTCTTAAACAGCGCTGATTGGTCGTAGTGTTCACCGGGGGTCCGTTCTTCGTACGTGGATAACTCAGTTAGCTGGATTTGGATATTGACGGTTTGACACAATCCAGGATCGTTTCGTTCTTCAAAGCTGATCCGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23193
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
G > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037450 | Essential Splice Site | 223 | 558 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 50805206)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50196023 |
GRCz11 | 17 | 50275092 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTTCGTCACCTTCTGCACTAAAGAGGCTGCTCAAAAAGCGGTCAAGCTG[G/A]TAAGTGCTGATCTGTTAGTCCTCGCGCAGCTTGCTGGAGTCAGGGCAGTG
Long Flanking Sequence:
TTCAGCACGTGAACACGATGGCCAATCAGTGGTGTTAAAGACAAAAAAATACAAACTCCCACGGACCGTAACAGATAGTAAGAGGCAAGAAACATTCAACAGCTTTAATCATGAAGTCAATAAATATTTGGAGCTACTCCACAGGCCTCAACACTTGTTAAACACCCCGGCCTCTCCCATGGCGCTCAGCATTTTAACTTGGTGTTAAATTCTTTCCCAATTAAAGGACGTTTATTCCAAAGGTTTGGTTCAACTTGCAAAAGAAGGATCACGATCTTTAGCTGTGTTCGATCTCTGATTGTTATGACCGTTGTTGTTGGCAGATTTTTGTGGGAAAGATCCCGAGAGATCTGTTTGAGGACGAGCTGGTCCCTCTGTTTGAGAAAGCCGGACCCATCTGGGATCTGCGTCTGATGATGGACCCTCTCAGTGGGCTGAACAGAGGATATGCCTTCGTCACCTTCTGCACTAAAGAGGCTGCTCAAAAAGCGGTCAAGCTG[G/A]TAAGTGCTGATCTGTTAGTCCTCGCGCAGCTTGCTGGAGTCAGGGCAGTGTGTGGATTGTGATTCTGATCTCCTCTGCAGTGTAACAACAATGAAATACGGCCCGGTAAACACATCGGCGTCTGCATCTCTGTTGCCAACAATCGTCTGTTTGTGGGCTCCATCCCCAAGAGCAAAACTAAGGATCAGATCGTGGAGGAGTTTGCCAAAGTTACTGGTTCGTGATGATGATCGTTTTTGTTTACAGTTTAAGATGGCATTTGTTTCACTGATGTATGTCATATGGACAGAATAAAAAGTCTCTCATTTCATATAATTAATCTAATTGAGCCCTTAAATAGCTTTTTAGGCTGAATATATCTACGCTGTAATACAGGGATGTCAAACTCAATTCTTGGAGGGACACAGTTTATGTCCAACCCTAATTAAACACACCTGATCAAACTAATTGAGTCCTTCAGGCTTGTTTGAAACCTACAAGTAAGTGTGTTGGAGCAGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32175
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037450 | Nonsense | 417 | 558 | 10 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 50808449)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50199266 |
GRCz11 | 17 | 50278335 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCAATTGAAATCGTCTTCGCAAAGCCGCCCGATCAGAAGAGGAAAGAG[C/T]GAAAGGCCCAGAGACAAGCTGCTAAAACTCAAATGTAAGAGCATTTATAG
Long Flanking Sequence:
GTTTCTGAAATTAAAATACAGAACTGAACAAATATATTTACACACTTTTGCTTAAGTAAATAAATGGATTGAATGATGCGCTCAACCTGCAGATTTCTGCACACACAGATTTTGTGTGGGCCTAAAAAGAGGTGAATTGTCAAATTATACTGACCTTTACTGTCATTTTTACATGTGTTATTCAGGTCAAAGTCCTCTTTGTAAGAAACCTGGCGAGCACAGTAACAGAAGAGCTCCTGGAGAAGACGTTCTGTCAGTTCGGCAAACTGGAAAGGGTTAAAAAGCTGAAAGACTACGCCTTCATCCACTTCGAGGAGAGAGATGGGGCCGTCAAGGTGATCGTCTCTTTAGTCGTCTTGAGTTCAGAGGTAGTCAGTGACGTTTGTGCAGATTTTAACCAGTCTTTTCCACAGGCTCTCGCGGAATTGCATGGGAAGGACTTAGAAGGGGAACCAATTGAAATCGTCTTCGCAAAGCCGCCCGATCAGAAGAGGAAAGAG[C/T]GAAAGGCCCAGAGACAAGCTGCTAAAACTCAAATGTAAGAGCATTTATAGAGCTTTGCAGTGGCAGTCCTCATTCACTTCTATTTTACTTGCTTCCACGTGCTTCAGAGGATCATAGAGCCCTATATATTAAAGGCTGTTATCGCCCACATCTGTTAAACTGGTCGATTCTAAACCGCATGCGTTTGTTGCAGGTATGATGAGTATTATTACTACGGCCCACCGCACGTGCATCAGCCGACAAGAGCGAGGGGACGAGGTGCTAGAGGTTATTCGTATCCGCATGACTATTACAGCTATGAGGATTATTACAACTACTATGGCTACGACTATCACAACTACCGAGGCGGCTACGACGACCCCTACTACGGCTACGACGACTTCCAGGCTCACGTGCGAGGAAGAGGAAACAGAGGAGTGCGAGTGCCCACACTGTCCCGAGGACGTGGCTCCAGCGTCAGCAGAGGACGAGCCGCTTTCTGCCAGCGCGGGGCTCCAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44878
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000037450 | Missense | 460 | 558 | 12 | 13 |
Genomic Location (Zv9):
Chromosome 17 (position 50808739)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 17 | 50199556 |
GRCz11 | 17 | 50278625 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAGAGCGAGGGGACGAGGTGCTAGAGGTTATTCGTATCCGCATGACTA[T/G]TACAGCTATGAGGATTATTACAACTACTATGGCTACGACTATCACAACTA
Long Flanking Sequence:
GACTACGCCTTCATCCACTTCGAGGAGAGAGATGGGGCCGTCAAGGTGATCGTCTCTTTAGTCGTCTTGAGTTCAGAGGTAGTCAGTGACGTTTGTGCAGATTTTAACCAGTCTTTTCCACAGGCTCTCGCGGAATTGCATGGGAAGGACTTAGAAGGGGAACCAATTGAAATCGTCTTCGCAAAGCCGCCCGATCAGAAGAGGAAAGAGCGAAAGGCCCAGAGACAAGCTGCTAAAACTCAAATGTAAGAGCATTTATAGAGCTTTGCAGTGGCAGTCCTCATTCACTTCTATTTTACTTGCTTCCACGTGCTTCAGAGGATCATAGAGCCCTATATATTAAAGGCTGTTATCGCCCACATCTGTTAAACTGGTCGATTCTAAACCGCATGCGTTTGTTGCAGGTATGATGAGTATTATTACTACGGCCCACCGCACGTGCATCAGCCGACAAGAGCGAGGGGACGAGGTGCTAGAGGTTATTCGTATCCGCATGACTA[T/G]TACAGCTATGAGGATTATTACAACTACTATGGCTACGACTATCACAACTACCGAGGCGGCTACGACGACCCCTACTACGGCTACGACGACTTCCAGGCTCACGTGCGAGGAAGAGGAAACAGAGGAGTGCGAGTGCCCACACTGTCCCGAGGACGTGGCTCCAGCGTCAGCAGAGGACGAGCCGCTTTCTGCCAGCGCGGGGCTCCAGGATCCAGCCGCGGGGGCCGGGGCTCCAGAGGAGGCCTCCAGCAGAGATGCCGAGTGGTACGTGATGTGACAAATATATCACGGTAGAAGTCATCTCATATTCTGATAGCGATATAGATCACAATATAACACATTTTCTGTACATTCAGTTCATATTGATCACAGAGTTGAGGCCTTTATACAATGAAGTCTGAAATATTACTTGTTATACGTATTCAAATCTGAAAAATTCATCACACACACACACACACACACACGCAGGAAATATTGGGTCCACCCATCCTTAGATTGCG
Associated Phenotype:
Not determined