ZMP
syncrip
Ensembl ID:
ZFIN ID:
Description:
heterogeneous nuclear ribonucleoprotein Q [Source:RefSeq peptide;Acc:NP_999861]
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 2 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa36944 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa25128 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa36944
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:
G > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058779 | Nonsense | 4 | 630 | 2 | 11 |
| ENSDART00000129870 | Nonsense | 68 | 694 | 2 | 12 |
| ENSDART00000132186 | None | None | 238 | None | 7 |
The following transcripts of ENSDARG00000040184 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 2762591)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 2716685 |
| GRCz11 | 20 | 2733424 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAATAATTTGGCTCATTGCATTTGAACAGATTTCTGGAGACATGGCCACT[G/T]AACATATTAATGGGAATGGTACAGAAGACGCAATGGACACGGCTGCTGCA
Long Flanking Sequence:
TTTAAAGCGTTACCTTTCTGTGTATGTGGAGGCTGTACTTGTATTGTGTGTGGCAGTGATGTTTAACATCCCTTTAGCTTGTGCTCTAGTTTAGTCTTTTTCTGGAGTTTAACGGTGGCGTCACTCGTTCTTCGCTTTGTTATAAAGATATAGATGGCTGAAATGAGGAACAGAAGCACCACAACCTTCATTTGAGCTCCTGAACTGCTTTCAGCATTTAGTCATGTTTTAATATAGTAAATTGGGTTTTTGGTGGGAGAGATATCCATTGCCTGCCTGTAGTTAATTTATTTTTTGGGGAAGGTTTGCAAAGATGCTTTACACATTTATGGAGCTGTATTGGACAAAGTGAAACCTCATTGCATGCAGGTTTAAGCTACCAAACGAAAGCAAATGCTACACATGAAATTGAATGCCCACTTAATTTGTGTAACTGTCTACCAAAACCTGCAATAATTTGGCTCATTGCATTTGAACAGATTTCTGGAGACATGGCCACT[G/T]AACATATTAATGGGAATGGTACAGAAGACGCAATGGACACGGCTGCTGCAGTTACCCATTCTGACCACTTCAACACTTTATTAGAAGCTGGTTTACCACAAAAAGTTGCTGAAAAGCTAGATGAAATTTACCTAGCAGGTAAGCCAAAACTTGAACCCTCTAAATTGACTCATCCATCTTGTCACATTCAGTGCATGTTGAACTGTACGTGTATGTTTTCTTGCATAGGGAATTGGCAGGTAATTGGCAACTTTGTGTGGTTTCATTGCAAAATGGGTACTGCAGCGTTAAAGTGACGCTGAATTGTAATGGCACACCGGGCCGCAGGAAATAAAGGCTGGATTGAGCGTGTCTGCTGCGATCCTGAGAGCAGCCTTTCTGGGGATTAGCTCTCCGTTGTTAAAAGGGTGTGGGGAGGGGTCTGTCCCGGGGGTAGGACGCGGGCCAGCTGGGCATATGCCGGGACAATAGAGGCAGCTGTCTGGAGCGGAGACAGGTGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25128
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:
C > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000058779 | Nonsense | 217 | 630 | 6 | 11 |
| ENSDART00000129870 | Nonsense | 281 | 694 | 6 | 12 |
| ENSDART00000132186 | Nonsense | 119 | 238 | 5 | 7 |
The following transcripts of ENSDARG00000040184 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 20 (position 2766709)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 20 | 2720803 |
| GRCz11 | 20 | 2737542 |
KASP Assay ID:
554-7888.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTAAACAGGGGCTACGCTTTTCTCACTTTCTGCACTAAAGAGGCTGCA[C/T]AGGAGGCTGTCAAGCTGGTAATTCAATCCGAGTTTATTGCTTTACAATAA
Long Flanking Sequence:
AGCCTATTTGTGGCTGATGTAAAAGCCCATAGAAGTTAAAATGTGGAATAGTTGGATATGTGTTAAAGTGTCTTCTGCATTTAAAAATATAAACAACATTACATTAAAACTACTCAATTATGAAATGAAAAGCAAACTGTAAGAAATAATAGGATGCAACTATTTACATCCAGGGTGAGAAAATGCATGTCTGCTAGGGCAGTTTCTTCCAGAATAATCTGAAGTAGTTTCCATTTTTTCCATTTATGTTTGACTGTTATTACTTGAGTTTAGATAGTTGCATCAGCCCCAGTCTGTCTTTTAAGGCTCACTTACCACTCCATTCCCCCTCCGTCCTGCAGATCTTTGTTGGGAAGATCCCGAGGGACCTGTTTGAAGATGAGCTCGTGCCTCAGTTTGAAAAGGCAGGGCCGATCTGGGACCTGCGTCTGATGATGGATCCCCTGAGTGGCCTAAACAGGGGCTACGCTTTTCTCACTTTCTGCACTAAAGAGGCTGCA[C/T]AGGAGGCTGTCAAGCTGGTAATTCAATCCGAGTTTATTGCTTTACAATAATTGTTTTAAAGCAGCTTCTCACATTATTGCAGTAAAATCTAAGTTAATGTACATTAAGTGATATTTTAGGAGGAAATTCAGAGTTATTGATCTAATTGCAGGATCTTTTGACTTTATTAGTGTTTGTTTTGAATCATACATGAATATTAAACGATTGTGATTGTCAATTTTATATTAAATACTTTGTAAATGTTGCCATGAATATAGCCAATGTTGCTGATGTGGCATTAAAGCATGCATGCATACAAACAAACAAATACATAAATGTATAAATTAATTTGTTTTTATCATTATATTTGTACAAATAAAGGGATAGATCACCAAAAAGGCCCAATCACCCTTAAGTGGGACCAAACTTTTAAGTTTTTTTTCTTCTGTTGAACACAAGGTATTTTGATGAAAGCTGGAAACCTCTTACTGACCTCCGTAGTAGGAAAAGCAAATACTATG
Associated Phenotype:
Not determined