ZMP
add3a
Ensembl ID:
ZFIN ID:
Description:
gamma-adducin [Source:RefSeq peptide;Acc:NP_955957]
Human Orthologue:
ADD3
Human Description:
adducin 3 (gamma) [Source:HGNC Symbol;Acc:245]
Mouse Orthologue:
Add3
Mouse Description:
adducin 3 (gamma) Gene [Source:MGI Symbol;Acc:MGI:1351615]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37548 | Nonsense | Available for shipment | Available now |
sa819 | Nonsense | Available for shipment | Available now |
sa11284 | Nonsense | Available for shipment | Available now |
sa11322 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa37548
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 |
---|---|---|---|---|---|
ENSDART00000027803 | Nonsense | 291 | 644 | 7 | 15 |
ENSDART00000040538 | Nonsense | 291 | 672 | 11 | 18 |
ENSDART00000049075 | Nonsense | 291 | 645 | 8 | 14 |
ENSDART00000140015 | None | None | 239 | None | 7 |
ENSDART00000141247 | None | None | 64 | None | 5 |
ENSDART00000142857 | None | None | 103 | None | 5 |
The following transcripts of ENSDARG00000040874 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 32930870)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 30292000 |
GRCz11 | 22 | 30241195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGTGAAAGATATTTGTTTGTGTGTGTGCGTGCATTGCAGGTATTGGTTT[T/A]AAGGAATCATGGCATTGTAGCTCTCGGAGAGACCATTGAAGAGGCCTTTC
Long Flanking Sequence:
TTCTTGAATTAAGATTTTTTTGATATTTGGAGTAAGAAAAGCATTTTTTGCAGTGAATAGCTTTAGGAGAGGAGTTTCTTTCAGATATTTTAGTCTTAAAAAAACTATATTTTGACGTTTAAATGGGATAAAAGTACTTTTCCTTCCTTAAGCCAGTATAATTACTACTCCACTTTGACGTGCGCTGATCTCTTCTATCATATGTCAGGTGTCGTCTATGAAGTGCGGCCTTTTGCCCATCTCCCAGGAGGCTCTGATCCTGGGTGACATTGCCTACTACAACTACCAGGGCAGTCTGGATGAACAGGAGGAGCGTGTAGAGCTCCAGAAGGCTCTCGGCCCCACGGCGAAGGTAAACAACTCCTCTCTTGCAGCAAAAAATACCACTCTCTTGCATATATCCTTCAGATGTGGTTAAGTGTGACCACAAAAAATGCAGTTGGTATGTAAATGTGAAAGATATTTGTTTGTGTGTGTGCGTGCATTGCAGGTATTGGTTT[T/A]AAGGAATCATGGCATTGTAGCTCTCGGAGAGACCATTGAAGAGGCCTTTCACTACATTTACGGCGCTCAGTATGCCTGTGAAATTCAGGTAAAAAGTTCATGATGCTTATCAGGTTGGATACATCAACCTCATACACTCAGTACACTCATAAATATGACCTTAAGACTTGTAGATGTTAAGCCTTGTGTTTTTGTAGACATGCTTGTCCTTTTCGTTTTAATTTTTGTGATCATTTTGGCTGTGTTAAATCAAACTGCTGTTTTTTTTTACTCAAAGTATATATATTTTAGCCTCATTTCCTTTCATACGTTTTCATACATTACACTAGAGACCAAAATTGGTGAGCTTGTCACGATAAGTCATTTATGTTGTGCAATATATTGTCATTGAAACTATTGCGATAAGTGTTATTATTGTCGTTTAAAACCAGTTTATGTCTTTTTATACACTCACTGGCCACTCTATTAGGTACATGTTATTCATACAGGATTGGGCCCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa819
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 |
---|---|---|---|---|---|
ENSDART00000027803 | Nonsense | 336 | 644 | 8 | 15 |
ENSDART00000040538 | Nonsense | 336 | 672 | 12 | 18 |
ENSDART00000049075 | Nonsense | 336 | 645 | 9 | 14 |
ENSDART00000140015 | None | None | 239 | None | 7 |
ENSDART00000141247 | None | None | 64 | None | 5 |
ENSDART00000142857 | None | None | 103 | None | 5 |
The following transcripts of ENSDARG00000040874 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 32932974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 30294104 |
GRCz11 | 22 | 30243299 |
KASP Assay ID:
554-0723.1 (used for ordering genotyping assays)
KASP Sequence:
CTAGGTGAATGCRTTCTCCTGTGCTGGAGGAATGGAGAACCTGATCGTGT[T/A]GGATCTGGAGAAGTTTAAAGCTCGTACRCAGGGAGTGGCACAAGTTGGAR
Long Flanking Sequence:
TTCACCTTAAAGGGTTAAACAAATAAAGCACAGCACTACTACAGTTACAGAAAAGTTTGCGCTGTTAAAATTCAATTAACTTTTAATACGTTTTGGTGCGATTATCACCCGCTATAAAAATAAAAAAACATGAATGAATGTTTTGAGTGAAAAGCTGTAATGTAGCCATGGCGGGATCAATTTTGGCATGGCACCCCTCCATGGAAGAAGTAATGTAGCGGAAACCATGCATAATAAACAGAGTAAAAGCCATAATACACTTAAAAAAACAGCCATAAAAAACTGAAACAAAGTATATAATGTTTTAAATTCTGGTACATTCCAGGAATTCAAATTGGTAGGAGAGTTGTGTAGTTCTAGTAAATTGAGTTCTGTTCAGTTTAGTATTCAGTTAAGTATAAAACTTTAAACAAAGTATAATTTGTCTAAAAATGTCCTTGTTTTTTTTTTCTAGGTGAATGCGTTCTCCTGTGCTGGAGGAATGGAGAACCTGATCGTGT[T/A]GGATCTGGAGAAGTTTAAAGCTCGTACACAGGGAGTGGCACAAGTTGGAGTCAACATGGGCTCTCAGCAGAAGTGGAGGTTGGGAGAGCTGGAGTTTGAGTCACTCATGAGGATGCTGGACAACCTGGTATGTATTGACTTAAGATCAAGTAGTCTATTCATGATCCTGACTATGAGTTCCATATCTAGTAATCTATAATGACAGACAACGGAGTAGTGAAGACATAAAACAAACAGTTACTCACATTTGTGAGGTGCAGAACTACTGTTTGATTCAATAGAGTCAGCACAACGCATTTACTTCTGAAAGTACACCATCAAACTGAGCCTTGTTTGAAAACACCTGTAAAATTAATTGGAAAAAGGACTAAGTTCTCACTGCCAGTCTTTTTGCAACATCCTGTTGTCTACATAGGTCTGCATTTGACTTTTTTTGTGTTTTAATTACTACAATGTAAATCAGTGAGCGGAACTAAACAGGCAATGATGTACAAGTAGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11284
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027803 | Nonsense | 380 | 644 | 9 | 15 |
ENSDART00000040538 | Nonsense | 380 | 672 | 13 | 18 |
ENSDART00000049075 | Nonsense | 380 | 645 | 10 | 14 |
ENSDART00000140015 | None | None | 239 | None | 7 |
ENSDART00000141247 | None | None | 64 | None | 5 |
ENSDART00000142857 | None | None | 103 | None | 5 |
ENSDART00000027803 | Nonsense | 380 | 644 | 9 | 15 |
ENSDART00000040538 | Nonsense | 380 | 672 | 13 | 18 |
ENSDART00000049075 | Nonsense | 380 | 645 | 10 | 14 |
ENSDART00000140015 | None | None | 239 | None | 7 |
ENSDART00000141247 | None | None | 64 | None | 5 |
ENSDART00000142857 | None | None | 103 | None | 5 |
ENSDART00000027803 | Nonsense | 380 | 644 | 9 | 15 |
ENSDART00000040538 | Nonsense | 380 | 672 | 13 | 18 |
ENSDART00000049075 | Nonsense | 380 | 645 | 10 | 14 |
ENSDART00000140015 | None | None | 239 | None | 7 |
ENSDART00000141247 | None | None | 64 | None | 5 |
ENSDART00000142857 | None | None | 103 | None | 5 |
The following transcripts of ENSDARG00000040874 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 32938787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 30299917 |
GRCz11 | 22 | 30249112 |
KASP Assay ID:
554-6166.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTGTGTYTTATAGACGTSTGTGNTTTTTTTTCCYGTCTTCCAGGGATA[C/A]AGGACTGGCTACACATACCGGCACCCCATCGTGCGGGAGAAACCCCGACA
Long Flanking Sequence:
TTTGTATTTATAGAATTTAATACTTATTTTAACAATATAAATAGTAAGAGTAGGTGTTGTTATAGGACCTTGACCTTATTATTCACGGATGAGCAGGCGCAGACATTGGAACCTTTTTGTGTCAAGACTTCCGATCTTATTCACTTCCATTGATTTTTAGACTTTAAAAATGGCTCGTTATGCTGCTTGATGTTGCAAACTGATGCTATCCTATTATATCATTCTACTTTTTATGTGTACTCATGAACACACTTCTTTGTCACTCATTCATTGATGAGTGAACCAGAAGTTCAAAAACAAGTGCACTTCCGCATTGCAGAATTAAGTCAATAGGACAGTAGCTTGACAGGAATCAAAGTTGGAAAGAGAGAGGTGGGGGACGGATCAAGGAAATTTCATAAGCCAGGTCTTGAATGCGGGAACCAAAAGTGCAATGCTGCTATATGTTAATCTTGTGTTTTATAGACGTGTGTGTTTTTTTTTCCCGTCTTCCAGGGATA[C/A]AGGACTGGCTACACATACCGGCACCCCATCGTGCGGGAGAAACCCCGACACAAGAGCGAAGTGGAGATTCCTGCAACAGTGACGGCCTTCATGTTCGATGAGGATGACGCTCCACGCTTCCCTCTAAAGCTCCTGCAGCAGCGGCAGCAGAGAGAGAAAACACGCTGGCTCAACTCTCCAAACTGCTACATGAAGGTGAACGTGGCGGACGGCGCCAGCGAAGAGAACCGACGCACCAAGACCACGGTGAGACTGAGACTAAAATGATGTTTTCGTGAATCTAGTTTTTACAAGCCTGCATGTTACATTGGCATTGGTGATATCTTGAACCACACAGAATCTGAGACTATTATTGAGGCTGTTTATTTACATGTGTAAATATATATTTATTCAGTATTTATATTCATTTCAGTAATATTATTGAATAGTAGGTAAATGTTTATATGATTTATTTACTGTAGAGTATGTAAAGAAATATCATATATTAACTTGTTATATGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11322
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000027803 | Nonsense | 380 | 644 | 9 | 15 |
ENSDART00000040538 | Nonsense | 380 | 672 | 13 | 18 |
ENSDART00000049075 | Nonsense | 380 | 645 | 10 | 14 |
ENSDART00000140015 | None | None | 239 | None | 7 |
ENSDART00000141247 | None | None | 64 | None | 5 |
ENSDART00000142857 | None | None | 103 | None | 5 |
ENSDART00000027803 | Nonsense | 380 | 644 | 9 | 15 |
ENSDART00000040538 | Nonsense | 380 | 672 | 13 | 18 |
ENSDART00000049075 | Nonsense | 380 | 645 | 10 | 14 |
ENSDART00000140015 | None | None | 239 | None | 7 |
ENSDART00000141247 | None | None | 64 | None | 5 |
ENSDART00000142857 | None | None | 103 | None | 5 |
ENSDART00000027803 | Nonsense | 380 | 644 | 9 | 15 |
ENSDART00000040538 | Nonsense | 380 | 672 | 13 | 18 |
ENSDART00000049075 | Nonsense | 380 | 645 | 10 | 14 |
ENSDART00000140015 | None | None | 239 | None | 7 |
ENSDART00000141247 | None | None | 64 | None | 5 |
ENSDART00000142857 | None | None | 103 | None | 5 |
The following transcripts of ENSDARG00000040874 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 32938787)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 30299917 |
GRCz11 | 22 | 30249112 |
KASP Assay ID:
554-6166.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTGTGTYTTATAGACGTSTGTGNTTTTTTTTCCYGTCTTCCAGGGATA[C/A]AGGACTGGCTACACATACCGGCACCCCATCGTGCGGGAGAAACCCCGACA
Long Flanking Sequence:
TTTGTATTTATAGAATTTAATACTTATTTTAACAATATAAATAGTAAGAGTAGGTGTTGTTATAGGACCTTGACCTTATTATTCACGGATGAGCAGGCGCAGACATTGGAACCTTTTTGTGTCAAGACTTCCGATCTTATTCACTTCCATTGATTTTTAGACTTTAAAAATGGCTCGTTATGCTGCTTGATGTTGCAAACTGATGCTATCCTATTATATCATTCTACTTTTTATGTGTACTCATGAACACACTTCTTTGTCACTCATTCATTGATGAGTGAACCAGAAGTTCAAAAACAAGTGCACTTCCGCATTGCAGAATTAAGTCAATAGGACAGTAGCTTGACAGGAATCAAAGTTGGAAAGAGAGAGGTGGGGGACGGATCAAGGAAATTTCATAAGCCAGGTCTTGAATGCGGGAACCAAAAGTGCAATGCTGCTATATGTTAATCTTGTGTTTTATAGACGTGTGTGTTTTTTTTTCCCGTCTTCCAGGGATA[C/A]AGGACTGGCTACACATACCGGCACCCCATCGTGCGGGAGAAACCCCGACACAAGAGCGAAGTGGAGATTCCTGCAACAGTGACGGCCTTCATGTTCGATGAGGATGACGCTCCACGCTTCCCTCTAAAGCTCCTGCAGCAGCGGCAGCAGAGAGAGAAAACACGCTGGCTCAACTCTCCAAACTGCTACATGAAGGTGAACGTGGCGGACGGCGCCAGCGAAGAGAACCGACGCACCAAGACCACGGTGAGACTGAGACTAAAATGATGTTTTCGTGAATCTAGTTTTTACAAGCCTGCATGTTACATTGGCATTGGTGATATCTTGAACCACACAGAATCTGAGACTATTATTGAGGCTGTTTATTTACATGTGTAAATATATATTTATTCAGTATTTATATTCATTTCAGTAATATTATTGAATAGTAGGTAAATGTTTATATGATTTATTTACTGTAGAGTATGTAAAGAAATATCATATATTAACTTGTTATATGA
Associated Phenotype:
Not determined