ZMP
si:ch211-89p1.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein (LOC558111) [Source:UniProtKB/TrEMBL;Acc:A2BFD1]
Human Orthologue:
DDX31
Human Description:
DEAD (Asp-Glu-Ala-Asp) box polypeptide 31 [Source:HGNC Symbol;Acc:16715]
Mouse Orthologue:
Ddx31
Mouse Description:
DEAD/H (Asp-Glu-Ala-Asp/His) box polypeptide 31 Gene [Source:MGI Symbol;Acc:MGI:2682639]
Alleles
There are 6 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa26493 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa40456 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa13609 | Nonsense | Available for shipment | Available now |
| sa20446 | Nonsense | Available for shipment | Available now |
| sa40457 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa26493
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 |
|---|---|---|---|---|---|
| ENSDART00000051473 | Nonsense | 155 | 673 | 5 | 19 |
| ENSDART00000143183 | None | None | 218 | None | 5 |
| ENSDART00000148314 | Nonsense | 221 | 739 | 6 | 20 |
Genomic Location (Zv9):
Chromosome 5 (position 31354790)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29116147 |
| GRCz11 | 5 | 29716300 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGAAAACATTGGCATATGGGATTCCAATGGTTCAGTTTTTACAAGCGATT[C/T]AACCGAAAGTCAAGGCAAGTCAAGTCTTGAACAACTCAATTTAAAAAAAA
Long Flanking Sequence:
TTCATATGCATTTCTGCTCTCAACTATTTGACAGGTGGCCACGCTCCATAAGGTGTTGAACGTTAGCAGTATGACGAGGTACTGCAAGTTCATCTTACACTTTGTTTTGTCCCCTAGCTTTGTTTTGTTTTGTAATTGACATTGTCTCTCTTTTAGTGTCCAGAAACAGACCATACCAGTGCTGATGTCTGGTAAAGATGCTGTAGTGCGCTCCCAGACTGGATCAGGTGGGGTTTTTGATGTAAATAAATTTTATTAAATTAAAATATAAAAATATAAGATGTATAACCGAATTACTAGAGTAACAAAATGTTGAGTGTCATATTAAACATTAAATTGAATTTTATATTGAATGTGTGGTTTGAAAACTATAAAAATAGAAGTCATGAAAGTGTTTGTTAGAGAAAGAATGTGCTGTATGTAAGGTTTGTTTATTTATGTGTTGTACAGGGAAAACATTGGCATATGGGATTCCAATGGTTCAGTTTTTACAAGCGATT[C/T]AACCGAAAGTCAAGGCAAGTCAAGTCTTGAACAACTCAATTTAAAAAAAATAATTTTAACAGTAAAGTTACTACAGTGAAAAAATGGTTATCAGTATGAATACCCATACTTTACCAGAATCCGGTAAATAACCATAAATTGACATTACCAGAATTCCCTACGTGGCACTTCACATTTGATGTGTTATTGTTGAAATAACTCTTTTTCTATTTTTTTATTTAACTTGTTAGTTATATACATATTTTATCCGTTTAATTTAAAACCAGAAAAAATGTTGCTACTGTGTTTGTTATAATGTGTTTCTGACAGCCAATGCTGCCTTTGACATTTTGCTTTTCTTTTTCGTTTAAAAAAAAAAAAAAATTAACAGTGAAATTTGACCAATGTACTATTTTCAGCTCATGCTTTGTTCGGTTGTAGTTTACGTTCTGAAATATATATAAATATATATTGTAATTGTAATTGTGAAACCACTTGGACAAACCAATCAACCCTTGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40456
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 > A
Consequence:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051473 | Essential Splice Site | 188 | 673 | 7 | 19 |
| ENSDART00000143183 | None | None | 218 | None | 5 |
| ENSDART00000148314 | Essential Splice Site | 254 | 739 | 8 | 20 |
Genomic Location (Zv9):
Chromosome 5 (position 31355927)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29117284 |
| GRCz11 | 5 | 29717437 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCTCAGCTTGCCTTGCAGAGCTTTCAGATGTTTCAGAAGCTTCTTAGAG[T/A]GAGAATTTACCTCTTTTTCTATATTTCTGAAGTCATTGAAATTTCACAAA
Long Flanking Sequence:
GCACCTCAGTGCTGAACATTTACACAGAGTTTAACCTATGGCTGCAATGAATGCAAAACAGGGCAGTTTGTATAAGTCTACATTATAGTCAACGTTTAAATCCCTGCTCACGGACCTTTCTTCTTGTCTAATTGCTGTCCTATCATCCAGTTACTGTTCTACTGTGCCAAAAGAAGCCTGCAAAAAATAAATCTTTTAATAAAATTTCTACTACATTTTGTACTTTGTCAAAAAATTTGCTAAGGATCTGTTTTTACAGTTATAAACATCAACTTTCGGTATTATAAAGGAACATTTTTTTTAATTTTTCAGAGATCGGATGGGCCTTTAGCTGTTGTGATTGTTCCAACCAGAGAGGTACTTTATTGTAGTTATTCTAAATAATGTCATTTTAAATTTCTCTTTATGTACTTATTGTGTTTCTGTCTAAAATGCCTCTCTGATTTCTGTCCCTCAGCTTGCCTTGCAGAGCTTTCAGATGTTTCAGAAGCTTCTTAGAG[T/A]GAGAATTTACCTCTTTTTCTATATTTCTGAAGTCATTGAAATTTCACAAAAATGCTGGTCTTTAAAAAAAAAAAAAAACTTAATATATGCATGTATTTGTTTTAGCCTTTCACCTGGATTGTTCCAGGAGTTTTAATGGGAGGAGAGAAAAAGAAAGCAGAAAAAGCCAGGTAAACAATATATAATTTTTGATTAATAATAATAATAATAATTCCTTACATTTATATAGCGCTTTTCTGGGCACTCAAAGCGCTTTACACAGTGGGGGGAATCTCCTCATCCACCACCAGTGTGCAGCATCCACCTGGATGACACGACGGCAGCCATTTTGCGCCAGACCGCACACCACACACCAGCTGATTGGTGGAGAGGAGACAGTGATGCAGCCAATTGAATATGGGGATGGTTAGGAGGCCATGATGGACAAAGGCCAGTGGGCAGATTTGGCCAGGATGCCGGGGTTAAACCCCTACTATTTTTCGAAGAACATCCTGGGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13609
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051473 | Nonsense | 347 | 673 | 11 | 19 |
| ENSDART00000143183 | None | None | 218 | None | 5 |
| ENSDART00000148314 | Nonsense | 413 | 739 | 12 | 20 |
Genomic Location (Zv9):
Chromosome 5 (position 31357893)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29119250 |
| GRCz11 | 5 | 29719403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGACTRCAGCAGCACGTGGTGGTGGTGCCCAGCAAGCTCCACCTGGTCTG[T/A]TTGGCTGCCKTTATTCTGGCCAAATGCAAGGTAGAGAGGACCGTTTGTTA
Long Flanking Sequence:
GTAAAGCTGTTCACTAATGCTTTCACACAATGAGGTAAAGTTTGAGTGAATGTAAAGTTGAGACAGTTAATGCTCACTATATACAGTAGGAACTACATCATTGACTTTATTCTAACAGAAGCAGCTTGGAATAATCTGACAGGCCCTTTATCTCTGTGAATAGCAAAAGTTTTCAAGGACCTTTCCAGTTTAAGCAGCTCTACTTCGTCACAATAACGTCTTACTCTTCCAACATTTTCGATCACAAAAGCATTTTGGGTGACAATCTACATATGTACGCGAGCGCTTAAGCTGATCGTGTTCTCTGCACTTGCAGGACTGTCCCGATTAGCCAGTATCAGTATGAAGGATCCTGTGAGTGTCCATGTGTCAGAGGGGAGTGAGGAGACAGTTGAAGCGTGTCCCCAGGCGGCCCCTCAGGCTCTGTCAGACAGCTACGCAGTGCCTGAGAGACTACAGCAGCACGTGGTGGTGGTGCCCAGCAAGCTCCACCTGGTCTG[T/A]TTGGCTGCCTTTATTCTGGCCAAATGCAAGGTAGAGAGGACCGTTTGTTAATCCCCACTTATTAATGTGCAGTGTTATGCTGCAGATCAACTCTTGTTATTTCTGTTTGTATATAGTTTTTTTTTTTTTTTTTTTTTTAAAGAAAATGCTTAATCTCACTAAGGCATATGCAGATATTCTACATTATATTGTAATAATGAGATGGCACAATTTTGATGTCATGGATACTTCAAAATATTGTGAATAATTATTTAAGCTTTAAGAGTGCTTTTGGAGAATATTCACGTTGTATTTGCAGAGGTGTCCATAACAGCGGCAAATATTTGGAGACTTAATTGCATTGCTTAATAGTTCAAACATTTTCACATGAATCTTCCCTACTATATGCTAAAATGTTGATTGAAAATTGTGTAAATATTTATAAGGCTATTGTATGTTAATACTGTGAAATACAGCTTTAATAGTTCACATTGGTTAATTTAACTAAATTAAAATGAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20446
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 > A
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051473 | Nonsense | 439 | 673 | 14 | 19 |
| ENSDART00000143183 | Nonsense | 7 | 218 | 1 | 5 |
| ENSDART00000148314 | Nonsense | 505 | 739 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 5 (position 31364937)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29126294 |
| GRCz11 | 5 | 29726447 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAATAGTTTTTTGTTTATTTTTCCCTCAGGATGTAGCTGCACGTGGTT[T/A]GGATTTGCCTCAGGTTACTTGGATTGTTCAGGTTTGATTTCTTCATGTTC
Long Flanking Sequence:
TGACATATTTTTTTGCATACGGCATCTTAATAGCAATACTTTTGTTTACTGCAGCAAAGTTGACATGACAACTGTTTTAAACCATTGCTGAGCGCTGCGTTTGGTGTTTTTAGGTGCAAATAGGCTTATGCGTGAATGCCTCCTAATTCCGCACATGGTAAACATTTTGCTGTGAAAACCGGTCGCATGACCACAATTTTATGCACTCACACAAATGCTCTCAAATATATTTTGACCAAACGGTTGCAATTTCAAGCCCTGTTCAATGTAAAATCTCATTTCAACATCATTTTACTAAAGATTTTAATAGTTTATTACAATAAACTTTTATATTAATATTATTAATAGTTTATTACCATAATAATAATGATAGCAGTGTTTCCACATTTCTCTAAAACATCTGATGTGCTTATTTTGTTTCAAGTTCATAGTTTAAATGCTGGTTAAATATTTAATAGTTTTTTGTTTATTTTTCCCTCAGGATGTAGCTGCACGTGGTT[T/A]GGATTTGCCTCAGGTTACTTGGATTGTTCAGGTTTGATTTCTTCATGTTCAAGATTTTATCATTTGCATAATTGCCAGTGTGCAACATATAAACAAATTTATTCAATTTCTTCACAAAACTTCTAAATATTCTGTATATTTTTAAATGAGTGTCATGTTTCTGTTTTAGTACAATCCTCCAGTTTCTGCAGCAGAATATGTTCATCGTGTGGGCCGCACAGCTCGAATCGGAGCTCAGGGTAGCAGCCTGCTCTTTCTCACCCCCTCCGAGACCGCTTTTGTGGATGTGCTGGCCAATCACAACATCAGGTGTGTGACAGGCCTCTCTCTTATCTATCAGGTACTTCTCATTTCAGTGAACTCCTGTGGGACCAGTCCTCTGTGATGGTGGATGAGCTCCAGTCCCTGACAATGTGATTAAAGATGGTCAAACTGCTCTTGTCTCTGTTCCAAAGCCCACAATACAGCAGTCGAGAGCTGGACTGATGAGTCTGTGCTGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40457
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000051473 | Nonsense | 663 | 673 | 19 | 19 |
| ENSDART00000143183 | None | None | 218 | None | 5 |
| ENSDART00000148314 | Nonsense | 729 | 739 | 20 | 20 |
Genomic Location (Zv9):
Chromosome 5 (position 31383715)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 29145072 |
| GRCz11 | 5 | 29745225 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGACAGTGGCATGGATGGACAATCTAAGGCTAAGAAGAAAAGGAAAAAT[A/T]AGAAGGGTCAAGCAGAGGAATCTACCGATGCATAAAGTGGCCAATACAGG
Long Flanking Sequence:
TCAGCCAGTCTCAAGCCGGCCACACACTGTCTGCGTCTGCTTTTTGCAGGTTTAAGATTTCAGATCTGCACTTCATGATGCTGAGAGCCATTTAATTTCAGATATATACAGAAAATGAGTTTAATACAAAAAGGTTCTGTTAGTTAATGAATTTACTAGCATGAGCAGATCTTGTATTTATTCACCTTTGGTAATGTTAGTCAATGAAAATAAAGTTGTTCTTGTTAACTCAGAGCAGTAATGTTAACAAGCACAAGTTGAGATTTTAATAATGCATTAGTAAATGTTGAACTATGATTAATAAATGCTGTACAAGTATTGTTCATGTTACTAAATACGTGAGTTAATGGGACTTTGTTGTAAAGTGTGATCTGTTTGTTTAAATGTTTTTCAGCCCTCCCAAGAAACTCACAGCAAAGCAGCGGGTGTCAAACCTCATGCGTTCAGAGTATGACAGTGGCATGGATGGACAATCTAAGGCTAAGAAGAAAAGGAAAAAT[A/T]AGAAGGGTCAAGCAGAGGAATCTACCGATGCATAAAGTGGCCAATACAGGAGAGATCAGAGATGCTCTTTTCGTTTGGGAAGTGCTGAGGTTAGAGTTGTCGTGACCAGGTGGATTCTCAGGGTTGAACACACAGGTGTTTTTCCACAGAGTAACATTTTTTTAGATGTGAAAAAGCACAACCGGTCAGCAGAACAATCTGGGAATTTGCTCAATGCAAAAGCTTAGTTGCAGATGGGAAAATGAGCATGCATGGATTTCTTGCAGTGGGTTTATGAATTTATTTTTATAAATATTCTGCCTTATTTAAGCAATATTTTATTAAAAAAATGCTGAATTTGACTTTTTTAGGATGATTGTATTTAATATCTGTCTAATTAAATCTGACAAAGCACTGCATCCAAACGTGTTTCACAATCAGCAGCGACCAAACATCACATGGCTTTCATACAGGAGCTTCTGAGAACTCTGTTAAACTGTTTGCTGAAAGCGTTTAGCTCG
Associated Phenotype:
Not determined