ZMP
si:dkey-259n11.1
Ensembl ID:
ZFIN ID:
Description:
si:dkey-259n11.1 [Source:RefSeq peptide;Acc:NP_001139087]
Human Orthologue:
ATRN
Human Description:
attractin [Source:HGNC Symbol;Acc:885]
Mouse Orthologue:
Atrn
Mouse Description:
attractin Gene [Source:MGI Symbol;Acc:MGI:1341628]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa22249 | Nonsense | Available for shipment | Available now |
sa11715 | Nonsense | Available for shipment | Available now |
sa18455 | Essential Splice Site | Available for shipment | Available now |
sa19056 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa14575 | Nonsense | Available for shipment | Available now |
sa10673 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa22249
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 |
---|---|---|---|---|---|
ENSDART00000089528 | Nonsense | 431 | 1383 | 8 | 29 |
ENSDART00000131875 | Nonsense | 431 | 1345 | 8 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 13932014)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 13940009 |
GRCz11 | 13 | 14071001 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGGTGTTCGGGCACTGCCCTCTTTATGGATACATCAGCCAAGTGCAG[C/T]AGTACAATATAGGTCAGTAACACACAGTCTTCGCAGTAGGGTTGGTTTAT
Long Flanking Sequence:
ATAGTTTATGACCAGAAACACCGTAATAAACAAAGCCAGATTGTACTGGTTTGTTTTTGTCAATTCAAAACTAATCCTTTAATCTTGAGTTTGTTAAACCACTATCATGGTACATGTTTCATGTTGTAGTTTCCGTCAGTGCATAACATATAAATAATGACTTCTTATGGAAATCCTTTGAATTCATGTTGTGTTTAACTAAGACCTGTGTGTGTAAAGCTTGTGGTTACTTATGCTGTTTGTCTTTGTGTGCAAACATTCAGGATAAAATCTACATGTACGGAGGGAAGATTGACTCCACAGGAAACGTGACGTCAGAGCTGTGGGTTTTCCACACGAGGAACCAGTCATGGGTTCTGCTCAGTCCCCGAGCTAAAGAGCAGTATGCAGTTGTGGGTCACTCAGCACACACTGTCCAACTCAATCCTGATGGATCCGAGCCTGTCATACTGGTGGTGTTCGGGCACTGCCCTCTTTATGGATACATCAGCCAAGTGCAG[C/T]AGTACAATATAGGTCAGTAACACACAGTCTTCGCAGTAGGGTTGGTTTATACATTAAAAATATGCATTATTATCACAGTTATTGCAGTTTTTGTGCTAGGCAGCAAATAATCACATCCAAAATAAGACTTTGTTTTAAATAATGAATTTGTGCAGGTTCTGTGTACATTTATATTTATATAAATGCATAAAAACCAAAATATACACATCAAATATATATAAATTGTATAATATGGTTCCGTAAACCATTATAAATAAAGAAATCCTCAAACATGTACACACATTTTTGTAGGTACATGTATAGTGCATCCGGAAAGTATTCATATAACTTTTTCACATTTTTTTTATGTTATAGCCCTATTCCAAAATTTATTAAATTAATTTATTTCCTCAAAATTCTACACACAATACACCATAATGACAATGTGAAAAAAGATTTTTCGAAATTGTTGCAAATTTATTAAAAATTAAAAACCTGAAAAATTACGTATTCACACCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa11715
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 |
---|---|---|---|---|---|
ENSDART00000089528 | Nonsense | 459 | 1383 | 9 | 29 |
ENSDART00000131875 | Nonsense | 459 | 1345 | 9 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 13939690)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 13947685 |
GRCz11 | 13 | 14078677 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAGACTCGTGGAGCACTGGTTCAAGGTGGCTATGGGCACAGCAGTGTTTA[C/A]GACCCTCAGACCCRCTCCATCTACATCCATGGAGRCTACAAAGCCTTCAC
Long Flanking Sequence:
TGACAAAGGTTTGGGCACCCCTGCTCTTGACTAATACATTTGACTGTAAAAGCACATCTAAGTGTTTCTCTAAACAGCCACAGGTCAGATTTTCATTCTTATTAGTTTAAAAACAATTCTTTTTTTTTTTTGCTTATTATTATTATTATTATTATTATTATTTGTATTATTTATTTATTTATTTTTAGCTACTTTTTCAGTGGCTTTTGTTAGTTTCGTTTAGTTTTTCATTTATTGTGATTTTTAAAATGTTATTTTAGTTAGTGACTAATAGTTTTAGTTTAAGTTTTTATTTAGTAAATAATCTTGCCACCAAATATTGAAAACTGTTTATTTAAAAATAATATTTAAAATGTAGGTGAATGAAGTGTTTAATTTTTTTGTTCACTAATTCTCATGCTGTCTTTTTCCCCTCTTCTTTTTGCAGTGAAGAACACATGGAGTGTTTTGGAGACTCGTGGAGCACTGGTTCAAGGTGGCTATGGGCACAGCAGTGTTTA[C/A]GACCCTCAGACCCGCTCCATCTACATCCATGGAGGCTACAAAGCCTTCACTGCTAATAAATACGGCTTGGCTGGTGACCTGTACCGATATGATGTGGACGAGAGAAAGTGGTGCGTTGAGCTACTTTACATGATCGAGCTGAACACTAATTGATTGTGAAATACATATTTTTACTTGATATGTTTCAGAAGGATCTATTATGTACTTTTGATTCTTATGTAAGCTCGTTCTCACCACTGAATAATAAAAAGTTGTTACTTTTTATCTCCGAACTTGGTATACAAACTTTCTGAGAGTTGTAAGATGTAAACTCGAAATTTCAAGTTAAGTCAGATTTGCGAGATATGAATTCTGACTTTATTTCATGCAATTATGACTTTATTTCTCAGAATTGCGAGGTATAAGGTCAGAATTATTCTTATCTCAGAATTCTTACTTTATATCACACAACTGCAACTTTTTTTCTCTCTGAATTCTAACTTTATATTACGCAAATCTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18455
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089528 | Essential Splice Site | 737 | 1383 | 14 | 29 |
ENSDART00000131875 | Essential Splice Site | 737 | 1345 | 14 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 13953625)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 13961620 |
GRCz11 | 13 | 14092612 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAACTGCCARTGGGAGACCAGGAATCAAGAGTGCACCACCCTGCCTGG[T/A]AACAAACGCGAWCAAACTTTYGCTGGAATKTGTGTAAATGATTGAAGCAY
Long Flanking Sequence:
ACCAGTCCCGTCTGAACAGGTGTAAATGACCTGTCGGATTCAGTTAATTACAACAGATTCAACTAAATGCCCCACTAAATGCACATTTGCCACACCACATGCATTGTTGTGTAGCTGTTAAACTGTGTGTGCCTTCCAGATGCAGATGGAGAGAAGTGTGAGCAGTATTCCGACTGCTACAGCTGTACAGCCAACACCAACAGCTGCCAGTGGTGCTCTACGCTCTGTGTGTCCAGTCACAGTAACTGCACCAGTTCTCCAGTAAGTCTGCGCTTTCATTATGCCATAACAACTTACAGATGAGTTTCTTTTCAGTTTATGAATTCATAAATAATGTAACTGTGCTCTAAATGTCTGTAGGGAGGGATAATGGAGTACGAGGCCTGTCCAAAGGATAACCCCTCCTCTGTGTGCAGTAAAAGGACCAGCTGTAAAAGTTGTGCCACAGATCAGAACTGCCAGTGGGAGACCAGGAATCAAGAGTGCACCACCCTGCCTGG[T/A]AACAAACGCGAACAAACTTTTGCTGGAATTTGTGTAAATGATTGAAGCATAGCAAAGTATAATCCTGTTTAATATCTCTGGGGCAAAATAATTATTATCGCTATTTTTATCGTTATTGTTTTTTAAAGGGATAGTTCACACAGAAATTTAAATTCTGTCTTATTTAACTCATCATGCACTAATTCAGTTCAATTCATCTTTATTTCCTTAGCGCTTTTACAATGTAGATTGTGTCAAAGCAGCTTAACATACAAGTTCTAGTAAATTAAAAATTGTATCAGTCCAGTTTTCAGAGTTGACGTTCAGTTTAGTTCAGTTTAGTGTGATGCTGAAAGTTCAAAAACTGTGGAGCAGATCCATCGATGCACAGCTCCACAAGTCCCAAACCAAGCAAGTAGGGAAGAACAAACTTAACAATTGATGAAAACGAAGGAAAACCTTGAGAGAAACCAGGCTCTGTTGGGCACGGCCATTTTTCCTCTGGGCAAATTTCTAGCACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19056
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089528 | Essential Splice Site | 933 | 1383 | 17 | 29 |
ENSDART00000131875 | Essential Splice Site | 933 | 1345 | 17 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 13959187)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 13967182 |
GRCz11 | 13 | 14098174 |
KASP Assay ID:
2260-6179.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCCCTATGGCCAGTGCATGGAGTGGTACACTATGAACAGCTGCCCACG[T/C]ACGTATGCCGGCGAAATGATTTTAAATCAAAGTATTATCTGTAATTTATT
Long Flanking Sequence:
TGCGTTTTTTGTTTTGTGATTTGTTATTGTTTTTTTATTTCTTTGTTGTTTTGTTTTGTATTTTATTTTCCACTTTCCACATCTAATATTGTATTGTACTGGAAATATATGATTAATTAATTAATATATTACTTGCTGTGATCAGATAATTATTGTAATTATAATACAATTATGATAACATATATATAGTTATTACATTAATAAATATAAAAATACTAATTTAATTAAATAAAATTCTGTATGACCTATTTCTAAAAAACATTTTTGTGTGTATTGCTCATTGAATCTCTTTAACGTTTGTGTTATTGTGCAGCGAACCACAGTGTGAAGCAGTGCCGGACCCCCTGTGCACTGCGCTCATCCTGCAGTGAATGTACCAGTGGGAGCTCTGAGTGCATGTGGTGCAGTAACATGAGGCAGTGTGTCGACTCCAACGCTTATGTGCCCTCCTTCCCCTATGGCCAGTGCATGGAGTGGTACACTATGAACAGCTGCCCACG[T/C]ACGTATGCCGGCGAAATGATTTTAAATCAAAGTATTATCTGTAATTTATTCAAATAGCAATATCAGTGACAATAATTTTTTTTTATCCACTGTGAAATAAAAAAAAAACCTCCTGTAGGGTAAATCTGTGCATGATCTAGAGATTAGAATCTGATTAAACAAATAAACACACTGTTGTGACTAGGGCTGCACAATATTTTGTTATAGCATCGATTTTGTATAGATATGCAATTTGATTTGTAAAATTATTGCAGAGTTTAACCCTAATGGAGTGAAATTGTATCATTTGCATGTTTTTTAGGCCTGGGAGAGATTTAAGTATTCATTTTACCGGTTGGAAGTTTAACAAAGGATAATTGTATTAAGTTATTTAAACAAAAACATTGCAGTGTAATTTTAACATTGAAAAAGCCTAACCTAATACCTAAGCAACCTTAATATCTATTAATAAGAACCAAATTAGAAGAAACAGAAGTCGTAGTTAATCATTGACCAATAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14575
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 |
---|---|---|---|---|---|
ENSDART00000089528 | Nonsense | 1243 | 1383 | 26 | 29 |
ENSDART00000131875 | Nonsense | 1243 | 1345 | 26 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 13998044)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 14006039 |
GRCz11 | 13 | 14137031 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTCAGATTTGTTGAGTATCTCCTGTTTTGTTTTTGTTTTGTGCAGCTG[T/A]TTCCTGTCTTTGCTTCTGGTGGCAGCAGTYGTATGGAAGATCAAGCAGAG
Long Flanking Sequence:
ATACTGTATATACTATGAAATACACACAATGCATGTAAACACACAGAACCATACAGTAGCTTCTGTGGTCGGCTGAGGTTCCTCATCATTAGTTATGTCAACTCTGCTATGATAAATTACAGCAGCTCTTCATAGCTTCAGTGTGTGTGTGTGTGTGGGTGAGTTATTCCCAAGACCAATGTTTTTCATCTCAGCACACACCTGCACTTATAAGGTATAAGCATGCACCTACACCTCCACGGTTCCCTCACATACAGCCCAGTTGTGCTATACAGGAGAGCTGCATTCATGAGCTCTGACCCTGTTTCCATGCGGATACTGATCTTTAACACTTGTGCGCTTGTGAAATGGCCTCTAATCCATTAAACATGAACAGCCCTGTGTGTGTGCTTGGGGTGTGATGTCTTTCTTTTTGTTGTTTTGTAAAGGATTATCCAGAATTCCTAATAATTGTCAGATTTGTTGAGTATCTCCTGTTTTGTTTTTGTTTTGTGCAGCTG[T/A]TTCCTGTCTTTGCTTCTGGTGGCAGCAGTCGTATGGAAGATCAAGCAGAGCTGCTGGGCGTCTCGGCGCAGAGAGGTCAGTGGTGGAGCAGCTCACTTCCTACCTGTCCCATTTGATTGATCCAGTTAGTCACGTGATGGTGTGTTTGTAGCTTTGAAGCATTTTCGAATGCTGTCAATCAAGGCAGATGCTTGTTTTTTGAACTTTGAGGGTTTCCGTATGAACATTTATTGGCCAGGGTTTCCCCGGGGAATTGGATAGCTGGAATGTCATGGTGGTTTGTATATATTTTGATTATGGAATATTAGGGATTTTTGTTTGTCGCTTTCAATTTTAGTTTCCATTTATCTCCTTCTATATACAGTTAAAGTCTGAATTATTATCCCTACTTAATTATTAGCCCCCTGAAACATTTTTCCTCAACATCTGTTTAATGGAAAGAAGTTTTTTTTTTTTCTTGTCAGTTTTTAATTTTAATTTTTAATTTTTATGAATTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10673
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 |
---|---|---|---|---|---|
ENSDART00000089528 | Nonsense | 1334 | 1383 | 28 | 29 |
ENSDART00000131875 | Nonsense | 1334 | 1345 | 28 | 29 |
Genomic Location (Zv9):
Chromosome 13 (position 14040416)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 14048411 |
GRCz11 | 13 | 14179403 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAKAAAGCAGCAGTGCTCTCCATCTTTGTTCGGTTACCCAGAGGCCCC[G/T]GAGGTATTCCTCCTCCAGGAYAGTCAGGTGGGTCTACAATCCAATGCATT
Long Flanking Sequence:
CACACGCACACACACTGAATTGTTTTAATTTAAAAAAAAATGTTTTTGTTTCCTTGAATTAATGAAAAAACTTATGCTAAAATACTGTAATCAGGCCTCATGGCATTAAGTGCTCCTCATTTGCAAGTCACTTTGGATTAAAGCTTTTTGCTAAATTAATAAATATGAATGAATTATTCTACTTATCTAAACCTACCAAAGATACACCTGCTGGGTATTTTAGTTTCATATTTATTTAAACATGCCATATCAAAACAAACAAACAAAATTATGCTGGAGAGACAAAGAACATAATCAGAAATGGCAATACAATGATTTTGCCATGTTGATAAATGTGGTATCGAATGGAGTATTTAGTACTTTGGATGTCTGATTTTAAATTTGTTTTCCTCTTCTATTATTTCCTTTTTCAGTCTGTACCAAAGCCCATAGCTCTGGAGCCCTGTTTTGGGAATAAAGCAGCAGTGCTCTCCATCTTTGTTCGGTTACCCAGAGGCCCC[G/T]GAGGTATTCCTCCTCCAGGACAGTCAGGTGGGTCTACAATCCAATGCATTTGGCCCCCACACCTAGTGTTGAACATCTTTATGCTCTTTTCTGCCAATGTTGATAGTCCCTCCCTCTCTCAATTCAAACTTTGGCATGACAAATGTTACATATATATTGCCAAAGCATTGTGATGTTTACATTAAATTGAACATGTAAAAAATTCCATAATGATAAAAAAAAAACAAATAGTAGGACTTCATCTGAAATCTGATTCTTACTGTATAGTACATTAATAGCAGTATGTGAGTTGTGTAGTATGTCCAAATTCATAGCATTTGAAAAACAGTGGGTACTTGGATGACCTTCCGGCGAGATTCTGAAGTGTGCATCCATTATCCCATAATGCCATGTGAGAGAATTCATAAATGGGAGGGAAGTGACGTGACTGCCGTGGGTAGGTCATGTGATAATGACTTATATCCTGTTAATAATATTTTAAACAGTACATTTCTTTAATC
Associated Phenotype:
Not determined