ZMP
adar
Ensembl ID:
ZFIN ID:
Description:
double-stranded RNA-specific adenosine deaminase [Source:RefSeq peptide;Acc:NP_571671]
Human Orthologue:
ADAR
Human Description:
adenosine deaminase, RNA-specific [Source:HGNC Symbol;Acc:225]
Mouse Orthologue:
Adar
Mouse Description:
adenosine deaminase, RNA-specific Gene [Source:MGI Symbol;Acc:MGI:1889575]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16847 | Nonsense | Available for shipment | Available now |
sa18476 | Nonsense | Available for shipment | Available now |
sa22832 | Nonsense | Available for shipment | Available now |
sa6428 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa817 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa16847
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 |
---|---|---|---|---|---|
ENSDART00000025629 | Nonsense | 114 | 1373 | 1 | 15 |
ENSDART00000103213 | Nonsense | 114 | 916 | 2 | 16 |
ENSDART00000130112 | Nonsense | 114 | 1380 | 2 | 17 |
ENSDART00000146708 | Nonsense | 114 | 1381 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 25775541)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23621216 |
GRCz11 | 16 | 23536248 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGTAAGCTTCCGACAAAACCAGGTGCAGTTCCTCAGGGGGCAGAGTGCA[C/T]AAGCTCCTCAGTTCAAAGCACCCCAGYCGCGAGGGTCCCAAAGCTCTAGC
Long Flanking Sequence:
TGCATTCCTTTATATATTTTTTTCTGTTATTTTCTCTCTGCAGAAAAACCTGTCTTTGATACTGTCGTGATATTGCAACCAGACAGCTGAGATTCATCCTAATACGTACACAACTTCACTAAGCCTAACGCTACACCCTCCTCAGCCCCCACCCCTGCGCTATGAGCAGAGGTAGAGGAGGGAATTACAAAGATAGCCAGCGATTTTCCCTCCCTTTCAGAAAGGGACAGCCTCAGTTTTATTCTTCTACAACCACTGGACAATCACGGGGCCCTCGTGTCCCAAGCCCCAGCTCTTTATCTGGCAGCTCTCCGCATCCTTCCTTTTACTCCTCCTACTCAAGTGGTCCTGGTGTACCTCCACGTGATCATCCTTTTCCCCCTCGTCACTCTGATCCATCCCTGTGGGCATCCCCCCAGCACGGCAGTGATCAGATCTCGGACTCAAATGGTGTAAGCTTCCGACAAAACCAGGTGCAGTTCCTCAGGGGGCAGAGTGCA[C/T]AAGCTCCTCAGTTCAAAGCACCCCAGCCGCGAGGGTCCCAAAGCTCTAGCCGAGGGGAAGAGGTCTCAACTGAGCCTATCCAGTACCAGACGGGTTATCGTGACTTTAAATCAAACAGTTACAGTTTTGGAAGAAGAAACTGTTACGGCAGAGGACAGGATAACTGGCAAGGGGAGCAGAATTTTGGACCTAAAAAAAGGTCAGGGTGGAATCACCCACACCAGAAGGGACAATATTATTCAAATCAGCACTATAAACAATTCTGGAACGCTCGGGCAAATGATTTATCCTCTGGCATCTATAATCTGAGTTTTGGTGACCGTGTAAAAAGGGTAGACACCTCTGATACCTTGTCCTGCAGTAACTCTTCTTCTAAGGTTTCCAGTTCTTCCAGCTCATTCAGAGATTCCCTGTATTTGACCCCTGAGATCCACCAACAGGTCTGTGCTTTTTTGACATCACTCAGGCCAGCTGAGACTATTCAGGCAAAGGTCTTGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18476
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025629 | Nonsense | 164 | 1373 | 1 | 15 |
ENSDART00000103213 | Nonsense | 164 | 916 | 2 | 16 |
ENSDART00000130112 | Nonsense | 164 | 1380 | 2 | 17 |
ENSDART00000146708 | Nonsense | 164 | 1381 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 25775691)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23621366 |
GRCz11 | 16 | 23536398 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGACTTTAAATCAAACAGTTACAGTTTTGGAAGAAGAAACTGTTACGGC[A/T]GAGGACAGGATAACTGGCAAGGGGAGCAGAATTTTGGACCTAAAAAAAGG
Long Flanking Sequence:
ACCCCTGCGCTATGAGCAGAGGTAGAGGAGGGAATTACAAAGATAGCCAGCGATTTTCCCTCCCTTTCAGAAAGGGACAGCCTCAGTTTTATTCTTCTACAACCACTGGACAATCACGGGGCCCTCGTGTCCCAAGCCCCAGCTCTTTATCTGGCAGCTCTCCGCATCCTTCCTTTTACTCCTCCTACTCAAGTGGTCCTGGTGTACCTCCACGTGATCATCCTTTTCCCCCTCGTCACTCTGATCCATCCCTGTGGGCATCCCCCCAGCACGGCAGTGATCAGATCTCGGACTCAAATGGTGTAAGCTTCCGACAAAACCAGGTGCAGTTCCTCAGGGGGCAGAGTGCACAAGCTCCTCAGTTCAAAGCACCCCAGCCGCGAGGGTCCCAAAGCTCTAGCCGAGGGGAAGAGGTCTCAACTGAGCCTATCCAGTACCAGACGGGTTATCGTGACTTTAAATCAAACAGTTACAGTTTTGGAAGAAGAAACTGTTACGGC[A/T]GAGGACAGGATAACTGGCAAGGGGAGCAGAATTTTGGACCTAAAAAAAGGTCAGGGTGGAATCACCCACACCAGAAGGGACAATATTATTCAAATCAGCACTATAAACAATTCTGGAACGCTCGGGCAAATGATTTATCCTCTGGCATCTATAATCTGAGTTTTGGTGACCGTGTAAAAAGGGTAGACACCTCTGATACCTTGTCCTGCAGTAACTCTTCTTCTAAGGTTTCCAGTTCTTCCAGCTCATTCAGAGATTCCCTGTATTTGACCCCTGAGATCCACCAACAGGTCTGTGCTTTTTTGACATCACTCAGGCCAGCTGAGACTATTCAGGCAAAGGTCTTGGGCAAAAAGCTTGGTCTCCCCAAGAAGATTGTTAATAAGGTTTTGTATGACCTTTTGAAGTCAAACCAAGTAGTGAAACAAGGAGAGACCCCCCCTTTGTGGAGACTCTGTGAGGAGAGCCGCGAGTCCATCAGAGAGAAAGACCAAACACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22832
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 |
---|---|---|---|---|---|
ENSDART00000025629 | Nonsense | 193 | 1373 | 1 | 15 |
ENSDART00000103213 | Nonsense | 193 | 916 | 2 | 16 |
ENSDART00000130112 | Nonsense | 193 | 1380 | 2 | 17 |
ENSDART00000146708 | Nonsense | 193 | 1381 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 25775780)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23621455 |
GRCz11 | 16 | 23536487 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCTAAAAAAAGGTCAGGGTGGAATCACCCACACCAGAAGGGACAATATTA[T/G]TCAAATCAGCACTATAAACAATTCTGGAACGCTCGGGCAAATGATTTATC
Long Flanking Sequence:
TATTCTTCTACAACCACTGGACAATCACGGGGCCCTCGTGTCCCAAGCCCCAGCTCTTTATCTGGCAGCTCTCCGCATCCTTCCTTTTACTCCTCCTACTCAAGTGGTCCTGGTGTACCTCCACGTGATCATCCTTTTCCCCCTCGTCACTCTGATCCATCCCTGTGGGCATCCCCCCAGCACGGCAGTGATCAGATCTCGGACTCAAATGGTGTAAGCTTCCGACAAAACCAGGTGCAGTTCCTCAGGGGGCAGAGTGCACAAGCTCCTCAGTTCAAAGCACCCCAGCCGCGAGGGTCCCAAAGCTCTAGCCGAGGGGAAGAGGTCTCAACTGAGCCTATCCAGTACCAGACGGGTTATCGTGACTTTAAATCAAACAGTTACAGTTTTGGAAGAAGAAACTGTTACGGCAGAGGACAGGATAACTGGCAAGGGGAGCAGAATTTTGGACCTAAAAAAAGGTCAGGGTGGAATCACCCACACCAGAAGGGACAATATTA[T/G]TCAAATCAGCACTATAAACAATTCTGGAACGCTCGGGCAAATGATTTATCCTCTGGCATCTATAATCTGAGTTTTGGTGACCGTGTAAAAAGGGTAGACACCTCTGATACCTTGTCCTGCAGTAACTCTTCTTCTAAGGTTTCCAGTTCTTCCAGCTCATTCAGAGATTCCCTGTATTTGACCCCTGAGATCCACCAACAGGTCTGTGCTTTTTTGACATCACTCAGGCCAGCTGAGACTATTCAGGCAAAGGTCTTGGGCAAAAAGCTTGGTCTCCCCAAGAAGATTGTTAATAAGGTTTTGTATGACCTTTTGAAGTCAAACCAAGTAGTGAAACAAGGAGAGACCCCCCCTTTGTGGAGACTCTGTGAGGAGAGCCGCGAGTCCATCAGAGAGAAAGACCAAACACAGTCTTCAAAAGATTTGGAAAAAGAGCCAGGTCAGAGTCCATATATAAACCAGAAAGTTGGTGGAGATTTCACTACCACCAGTACTCCCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6428
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025629 | Nonsense | 545 | 1373 | 1 | 15 |
ENSDART00000103213 | Nonsense | 545 | 916 | 2 | 16 |
ENSDART00000130112 | Nonsense | 545 | 1380 | 2 | 17 |
ENSDART00000146708 | Nonsense | 545 | 1381 | 2 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 25776835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23622510 |
GRCz11 | 16 | 23537542 |
KASP Assay ID:
554-5388.1 (used for ordering genotyping assays)
KASP Sequence:
GTTAGACAATGACAATGTTTTTGGTAACACAGAAATTGACATTCCTGGCT[T/G]AGAACCGGTATCCAAAGCAAGTGACCTTTCCTCCTCAACCCATCGGAACT
Long Flanking Sequence:
CTCTGAAGGTGACGATAGCTGTGAAAAGTTGCTTGCAGATCAGGATAAAAAGACTCTTTCACCTACAGTGCAGTCTGTAACATTGTCAACAATGGCTGATTCTAAAGATAGCAAAGAGAAGATCCTACAGTACCTCTATGAAGCAGGTACGGGAAATGCACTTGTGATTGCCAAAAATCTTGGCCTGCGAAGTGCCAAGCAGGTCAATCCCACACTTTATGCCTTGGAGAAACAAGGTGATGTAAACCGCAACACTGAAGTTAATCCACCTACCTGGGAGCTAAGTGCACACAGACAGGAAAAGATGGACCGCCAACGAAAAGCTGCTGCAACTGCAAACCAGGATGTAAACAGTGCTGCAACTCTAAGTTTGGAAGATGACGAGATTGCAAATGTAGCTTTGGTCAACTTTGAGCCAATGGAAGGAGGTGGAAAACCATTGGTTGAGATGTTAGACAATGACAATGTTTTTGGTAACACAGAAATTGACATTCCTGGCT[T/G]AGAACCGGTATCCAAAGCAAGTGACCTTTCCTCCTCAACCCATCGGAACTTTCAGCCCAATCAGTTTCCCTACTATCAGGAGACTCCCAGTAACGGAGGAGAACAGTCACAGTGGGCATCTGATGATATTCCAGAGTTCCTGAACACAATTCGTTCTGAGGTTGCAGTTTCCTTGGCTGCACCCCCTCCCCCGACCCAAAGCATGGAGTCAAACAGATTGCAGAAACTAAAAGAGGCCCGTAGTAAGAACCCAGTTAGCGGGCTGATGGAGTTTGCACAGCATCTTGGATACACTTGTGAATTCCTACTTTTAGAACAGTCTGGACCCTCACATGACCCCAGGTTAGTTGATGGAAAAGGTTTTTTTATACATGCAGAGCAATAGTTTGTTTGTTTTAAAATTATGTTTTAGACAGGCTTTTTTAAAAGTGAGTGTTAACAAGGAAGATACGCACCTGTGAATAGTTTAGGACTTTGTCAAATGTCTCATGAAATTAAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa817
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000025629 | Nonsense | 992 | 1373 | 8 | 15 |
ENSDART00000103213 | None | None | 916 | 9 | 16 |
ENSDART00000130112 | Nonsense | 999 | 1380 | 10 | 17 |
ENSDART00000146708 | Nonsense | 1000 | 1381 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 16 (position 25787935)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 23633610 |
GRCz11 | 16 | 23548642 |
KASP Assay ID:
554-0721.1 (used for ordering genotyping assays)
KASP Sequence:
GTAGAAAAATTCTTGCAACTATTGTGATGCGCAATGGAACGGACAGTCTT[G/T]GAAAAGTTGTCAGCCTCGGGACAGGTACAAATACACACACAGACTCGGTT
Long Flanking Sequence:
GCAGCCTTTAGTAAATCATTCAAAAAAAGTGCCTCTCAAAGCAAAAAGCGTGTTCGGTGTGATCGGCCCCTTAGGCAGCACAATGCGTTACTGTAATGTTGTTGTTGTAGTAGTAGTAGTAGTAGAAGTAATTATAGTAAAAGTAAAAATCAGTATATTATGTGATGTTACATAATAAATAATTGAACTGTTGAATTAATAAATTGGAATTATTAAAAAAAATGGTGCCATTACACCTCAAGTGTGCATGGTTTTCTAATAATTAACTTTTAAGATGGATAATAAATAAACAGTCAATTATTTAGTTTATGCTATAGTAATAATAATCAAATATTCTTGTAAATTTTTTTTAGTTGCCAGTATCAGGGAGTACAATTCATGATCAGATCGCCATGCTAAGCCATCAGCGCTTCAATGCCCTCACTGCACGCATCCAGCACAGCCTTCTGGGTAGAAAAATTCTTGCAACTATTGTGATGCGCAATGGAACGGACAGTCTT[G/T]GAAAAGTTGTCAGCCTCGGGACAGGTACAAATACACACACAGACTCGGTTACAGCAAACATGATGCGTGCACTGTAATTAAAGAAGTGCTGTAATTGTTCTTGTCTGATGTCTCTAGGAAACCGCTGTGTTAAAGGAGAGGAGCTCAGTCTTCGTGGGGACACTGTAAATGACTGCCATGCAGAAATCATCTCCAGAAGAGGCTTTATCCGGTATCAGCTTGCAGAAGATTTTTCTTTCTCTCTCACTGTCAATCCCATAATTCTTTTTCTTCTCCTTCTGCTACTTTTCCCATCTTGTTCTTCAAGATAGCGTCTTATTTCACAGCAGCTCATAAATATATTGAATTTATATTTGGTTTTCTGCAGAATATTAGAATGTCTGCTTGTATGCCTAATATATTCTTTAAATCTCTGGCTGTCAAAGATTAAGGTATATTTGTTTTATAAAACACAAAATATAAAGTGTATAAATTTTAGCTTATATTACTATATAATATAT
Associated Phenotype:
Not determined