ZMP
si:dkey-189g17.2
Ensembl ID:
ZFIN ID:
Description:
si:dkey-189g17.2 [Source:RefSeq peptide;Acc:NP_001122014]
Human Orthologue:
RBM44
Human Description:
RNA binding motif protein 44 [Source:HGNC Symbol;Acc:24756]
Mouse Orthologue:
Rbm44
Mouse Description:
RNA binding motif protein 44 Gene [Source:MGI Symbol;Acc:MGI:2685663]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa21473 | Nonsense | Available for shipment | Available now |
sa9695 | Nonsense | Available for shipment | Available now |
sa1407 | Nonsense | Available for shipment | Available now |
sa21474 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa21473
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 |
---|---|---|---|---|---|
ENSDART00000101765 | Nonsense | 282 | 956 | 7 | 18 |
ENSDART00000136249 | None | None | 167 | None | 7 |
ENSDART00000139270 | None | None | 93 | None | 4 |
The following transcripts of ENSDARG00000069758 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 23696458)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 22852244 |
GRCz11 | 9 | 22663113 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAAGTAGAAAGCAGGGAAGATGCCAAACATTTTAAGGACACATCAGCC[C/T]AAGCGAGCTTCTGCCTCGATATGGAGCTTGATGTGCAGAGTCAGGTTCAG
Long Flanking Sequence:
ATTCACACAGAGAGAGAGATGTTTATATCTATTTAAGTTCCAGGTACCCAACATTTTATGGTTCATCTGGGTGTCAAAACTGTGGGACTAGTTGTCCATTTGGTACCAAGAAGTGCACCCGTTGTGGTGTTCACATTGTGATTTCACAGGACAAAATCAGTGTGTCAGGTAAGACGACATGACTTTAATTAATTCTCAAGCTGCTGCAGTACTGATTATTACTTTCTTGTTCAGAGAATGAAAAACAACTTCAGCTGCTCCCAAACAGCCTAAAAGAAGAGCTAAATGTTTTCCAAACTTCCCAAAGTAATGTTGAAATGCAAAATATCCATTTAGGTTGCACGCAAAGCACCCTAAACACTAGGAGCAAACAGAGAAGCCCTGAAGCGCATCCTCATTTCTACAGTAAAGGAATGTGTTCTCATGCCCAGTGCCTCTCTCAGCTGTGGCAGGAAGTAGAAAGCAGGGAAGATGCCAAACATTTTAAGGACACATCAGCC[C/T]AAGCGAGCTTCTGCCTCGATATGGAGCTTGATGTGCAGAGTCAGGTTCAGAGAAATGACAACACCCAAAATAACCAAAATCAATCATATAATCCCACTGAAGAAAATGACCACAATGTGGACCAGGAAACCATGCCAGAATACTACAGTTTTAGTAGCATCAGCTTAGACCACACTGCATGGAGCAATGGCAGCCAGAGTGCAGAGACAGGGTTCAATGATTCAATCACTGCTACCAAAGGCAGTACAGAACTCTCAGATGAACTATCAGAGGCTGCCAACAGCACTGCTGCAAACTCTACCGATTGTTTCTCTTGTGTCAGCAATTCATTTGAGCTGGCTGAAGAGTCAGGAGACTGTCTTGACTCAAGATATGAGCAACAGATAAACAAGAGCAATGTGGGTTCCTCACCAAAATCCAAATCTAGCGCTTCTGTCTATGTGGACCAAATGATAGATGCCTGTGGTGATTTCAGAGCTTTTTTTACATCTACTTGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9695
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101765 | Nonsense | 311 | 956 | 7 | 18 |
ENSDART00000136249 | None | None | 167 | None | 7 |
ENSDART00000139270 | None | None | 93 | None | 4 |
The following transcripts of ENSDARG00000069758 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 23696547)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 22852333 |
GRCz11 | 9 | 22663202 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTCAGGTTCAGAGAAATGACAACACCCAAAATAACCAAAAYCAATCATA[T/G]AATCCCACWGAAGAAAATGACYACAATGTGGACCAGGAAACCATGCCAGA
Long Flanking Sequence:
AGTTGTCCATTTGGTACCAAGAAGTGCACCCGTTGTGGTGTTCACATTGTGATTTCACAGGACAAAATCAGTGTGTCAGGTAAGACGACATGACTTTAATTAATTCTCAAGCTGCTGCAGTACTGATTATTACTTTCTTGTTCAGAGAATGAAAAACAACTTCAGCTGCTCCCAAACAGCCTAAAAGAAGAGCTAAATGTTTTCCAAACTTCCCAAAGTAATGTTGAAATGCAAAATATCCATTTAGGTTGCACGCAAAGCACCCTAAACACTAGGAGCAAACAGAGAAGCCCTGAAGCGCATCCTCATTTCTACAGTAAAGGAATGTGTTCTCATGCCCAGTGCCTCTCTCAGCTGTGGCAGGAAGTAGAAAGCAGGGAAGATGCCAAACATTTTAAGGACACATCAGCCCAAGCGAGCTTCTGCCTCGATATGGAGCTTGATGTGCAGAGTCAGGTTCAGAGAAATGACAACACCCAAAATAACCAAAATCAATCATA[T/G]AATCCCACTGAAGAAAATGACCACAATGTGGACCAGGAAACCATGCCAGAATACTACAGTTTTAGTAGCATCAGCTTAGACCACACTGCATGGAGCAATGGCAGCCAGAGTGCAGAGACAGGGTTCAATGATTCAATCACTGCTACCAAAGGCAGTACAGAACTCTCAGATGAACTATCAGAGGCTGCCAACAGCACTGCTGCAAACTCTACCGATTGTTTCTCTTGTGTCAGCAATTCATTTGAGCTGGCTGAAGAGTCAGGAGACTGTCTTGACTCAAGATATGAGCAACAGATAAACAAGAGCAATGTGGGTTCCTCACCAAAATCCAAATCTAGCGCTTCTGTCTATGTGGACCAAATGATAGATGCCTGTGGTGATTTCAGAGCTTTTTTTACATCTACTTGTGCAACAAAGACTGATCAGACCTTCCAGGTGAAAAATGTCGCTACTGACACAGACTTGCCTGCTGTCAGCCATGAAAAAGATACTCAGACCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1407
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 |
---|---|---|---|---|---|
ENSDART00000101765 | Nonsense | 886 | 956 | 18 | 18 |
ENSDART00000136249 | None | None | 167 | None | 7 |
ENSDART00000139270 | None | None | 93 | None | 4 |
The following transcripts of ENSDARG00000069758 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 23705533)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 22861319 |
GRCz11 | 9 | 22672188 |
KASP Assay ID:
554-1328.1 (used for ordering genotyping assays)
KASP Sequence:
CTGGAAAGGTTGACCAACGTGTGCAACTCGCCCACAGCCTCTGGAACATG[T/A]GTGCCACAGCACTACGCCACCATGGGAAGCTTCGACACAATCATGGCCCG
Long Flanking Sequence:
GATTTGTTCTGTAAAATGATCTGAACTCTCCATCACTAATGTTAATAGCAGTTTATTTTCTAATACACTATGTATTTGACAAGTCAAACCCTGTCTGAGCCAAATGACTAATCCAAGCAGAGCAGGTTCATGTAAAGAAAAGTCTCTTTAAATTGCTCATTTGAGACTGAGATAATGGACATGATTTTTGACTTCGGGTTTATGTAGATTTGTTGTGCAATATCCTGCCTAAAATTCATGTTTATACGGTTATAAACACTTTGTTTTGTTTGGTGCCACAGCCAGTAACTTGTCAAATGTGACATTTGTGCTTGTTCAATTTTAACACTGATAAATAAATTTTCTCTTTTTTATTTTATTTTATTTATTTTTTTATTTTACATTTTTAATTTTTATATTCCAAAGCCTTAATGTCATGTGTATGTTTTAAATCAGGGGCCGCGCTGCAGTCTGGAAAGGTTGACCAACGTGTGCAACTCGCCCACAGCCTCTGGAACATG[T/A]GTGCCACAGCACTACGCCACCATGGGAAGCTTCGACACAATCATGGCCCGGCTGTCAGAGCGCCACCCAAACGTTGCCCGGCAGAGGATCGTAGATGCCCTGCTGGAATTGCGGGCCAAGCATCAGGGCTTCCTCAGTGGTCTTCCGTTGAGATCTATTGTAGATATGACCTCTGAGCTTCTCACACAGACCTCCAGTTCCGCTCGTGTTTGAGTTTGTGGTATTTTAAGCAAGTTAAAGGGATAGTTCACCCAAAAATTTACATTTTGTTTTTAATTGTTTCTAAATTGAGGTATTTTGAAGAATTCTGGAAACCAGTAGCCAATGATTGGGTAGGAAAAATATTATGGAAGTTGATGGCTACTGGTTTCCAACATTCTTCCTTTGTTTGTTCCTTTGGCCTTGTAAATAGTTCCCTCGCCAGTTATATTTTTGCAGGTAACTTTAGTGCTACGTTCAACCATTTCGTTGTAGTTCTTGTTCATGACACTTCCTTCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21474
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 |
---|---|---|---|---|---|
ENSDART00000101765 | Nonsense | 889 | 956 | 18 | 18 |
ENSDART00000136249 | None | None | 167 | None | 7 |
ENSDART00000139270 | None | None | 93 | None | 4 |
The following transcripts of ENSDARG00000069758 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 9 (position 23705540)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 9 | 22861326 |
GRCz11 | 9 | 22672195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTTGACCAACGTGTGCAACTCGCCCACAGCCTCTGGAACATGTGTGCCA[C/T]AGCACTACGCCACCATGGGAAGCTTCGACACAATCATGGCCCGGCTGTCA
Long Flanking Sequence:
TCTGTAAAATGATCTGAACTCTCCATCACTAATGTTAATAGCAGTTTATTTTCTAATACACTATGTATTTGACAAGTCAAACCCTGTCTGAGCCAAATGACTAATCCAAGCAGAGCAGGTTCATGTAAAGAAAAGTCTCTTTAAATTGCTCATTTGAGACTGAGATAATGGACATGATTTTTGACTTCGGGTTTATGTAGATTTGTTGTGCAATATCCTGCCTAAAATTCATGTTTATACGGTTATAAACACTTTGTTTTGTTTGGTGCCACAGCCAGTAACTTGTCAAATGTGACATTTGTGCTTGTTCAATTTTAACACTGATAAATAAATTTTCTCTTTTTTATTTTATTTTATTTATTTTTTTATTTTACATTTTTAATTTTTATATTCCAAAGCCTTAATGTCATGTGTATGTTTTAAATCAGGGGCCGCGCTGCAGTCTGGAAAGGTTGACCAACGTGTGCAACTCGCCCACAGCCTCTGGAACATGTGTGCCA[C/T]AGCACTACGCCACCATGGGAAGCTTCGACACAATCATGGCCCGGCTGTCAGAGCGCCACCCAAACGTTGCCCGGCAGAGGATCGTAGATGCCCTGCTGGAATTGCGGGCCAAGCATCAGGGCTTCCTCAGTGGTCTTCCGTTGAGATCTATTGTAGATATGACCTCTGAGCTTCTCACACAGACCTCCAGTTCCGCTCGTGTTTGAGTTTGTGGTATTTTAAGCAAGTTAAAGGGATAGTTCACCCAAAAATTTACATTTTGTTTTTAATTGTTTCTAAATTGAGGTATTTTGAAGAATTCTGGAAACCAGTAGCCAATGATTGGGTAGGAAAAATATTATGGAAGTTGATGGCTACTGGTTTCCAACATTCTTCCTTTGTTTGTTCCTTTGGCCTTGTAAATAGTTCCCTCGCCAGTTATATTTTTGCAGGTAACTTTAGTGCTACGTTCAACCATTTCGTTGTAGTTCTTGTTCATGACACTTCCTTCACAGAGTGAA
Associated Phenotype:
Not determined