ZMP
atp7b
Ensembl ID:
Human Orthologue:
ATP7B
Human Description:
ATPase, Cu++ transporting, beta polypeptide [Source:HGNC Symbol;Acc:870]
Mouse Orthologue:
Atp7b
Mouse Description:
ATPase, Cu++ transporting, beta polypeptide Gene [Source:MGI Symbol;Acc:MGI:103297]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33814 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40636 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20647 | Nonsense | Available for shipment | Available now |
sa33815 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17744 | Nonsense | Available for shipment | Available now |
sa9976 | Essential Splice Site | Available for shipment | Available now |
sa40637 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33814
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030246 | Nonsense | 39 | 1364 | 1 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 10004831)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9858638 |
GRCz11 | 6 | 10094177 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCGGCGGAGAGCAGCTCTGCATGAAGGACTGCAAACCCCTGTGCCACTG[C/A]GACCCGGAGCTCTGCGTTTGCTCTTTACCACAGAATAGTAAAGATGGACC
Long Flanking Sequence:
TCCCACAGCATTATTTTCTTCTTATTTTCAGTGTTCATACTTCAATACTGTCAGCTTTGCTGTGGAGAGCTATTCGGTTTGTTCAGAACTGATTTACAACCTTTATTTGTGTTAGTTTTGCACTCGATGACATAAATCAGTTTAATCATTGACAGAAAATGTACGAGCAAAAGTTTGCCCGGCGGTGACGTGTGCAAACTCAACCGGGGCAGATGATCGTGAAGACACGCGGAGCGCAAAACCTGCGGGGATTTAAACGCGCGCGCACCATCACGCCACAGGACGGCACAGACATGTCACACACCTGAGACTCCTGCTTTGCAATTGTTTGTTAACGAAAGGTAATCTAAACTCCGGTCTTAGGTCTTCTGGGACACCGGCACAATGAATAAACTCAGTCCTTTCAGTAATCTTGCCAAGTTTATCTCCAAGTCGCCTGATAATGGGCCAGTCGGCGGAGAGCAGCTCTGCATGAAGGACTGCAAACCCCTGTGCCACTG[C/A]GACCCGGAGCTCTGCGTTTGCTCTTTACCACAGAATAGTAAAGATGGACCCACGGAATATAAGGTCAGTTTCTATTATTACAGTTAGGATAGCAAACACGTTTAAAATGAGGGAAAACTGCGTTTAAAAATTTCCAGAATGATACCTAAATATTTTCTACAAAAGTTGTAGACCTATCTGAAGCCTAATTGTAAAATAACAGTACACAGTGGTACACTCAGAAAAGAAGGTTTAAGGTACAAAATCTGTCAGTGGGCTGGCTTTTCAAAAGATACACGTTATCTAAAGAGACCTACAATTACATTTTAGTAAGGAAATTCTAGATTTTCACAACGTTACTCTAATTTTTCACAGTAAATTACATTAGTATCACTTTACAGCATTTAACAAATATTCAAAGTAATGTTTTGTATTCAGATTTTTACATGATTACTGTAAAAAGGGCTTTATCTTTTACATGTTAGTTAAAGGAAATTAAACAGTTTTTATTTCATTCAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40636
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030246 | Nonsense | 134 | 1364 | 2 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 10007192)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9860999 |
GRCz11 | 6 | 10096538 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGAACAAATTGGTCGTCTTGAAGGTGTCATTGGAGTCCAGGTGTCTT[T/A]GAGCGATAAAGAAGCCATTTTGAGGTTTAACCCTGCAAAGGTAACACCAG
Long Flanking Sequence:
GTCATCAAAACTCAATTGTAACAGTGCAAATGTCTTAAGAGCAGGAGAAAATGCATGTCTTGTGATTGTTCAGTTGGACAACCTTTACTAATCTGCTCTCTTTGATGCTGTGAGATGGAAAAATGTTATGCTAATCCTTCTGCTTGGTTAACGGGTGCTTTGTAGTTCCTTTTAAATGCAGTAAGAAGGAGCTTGTCAGATACACAAAGTGAAACAACATAATATGCCAATAAACTGTTAAGCAATATCTTTAAGCTAATCATTTAAACCATTTGTTTAGGAGAATGGAAGTCAACAGGAGGGTTGGATCCCTACAAAACATGCTTTTGATAATTTTGGTTATGAACCAGATGGACTGAAGCACAACTTAGTCCACCAGTTGCCCTCCGAGGAGGGCATGGTGAAGATCCAGGTGGAGGGAATGACCTGTCAGTCATGTGTCCGGTCTATTGAAGAACAAATTGGTCGTCTTGAAGGTGTCATTGGAGTCCAGGTGTCTT[T/A]GAGCGATAAAGAAGCCATTTTGAGGTTTAACCCTGCAAAGGTAACACCAGAGGATATGAGAAAGCGTATTGAAGACATGGGGTTTGATGCTTTAATTCTGGCTTTGCAAGGTCAAATACAGCCTTTGTCGACTGATTGGTCTGAGGTGACGTTAGGAGTTGAAGGGATGCATTGCGGGTCATGTGTGAAGAACATAACCGAGACCTTGTCGGGAATGTTGGGTGTCAACTCTGTATTTGTCTCATTGGAAAAAGGAAGTGTGGACCTTAGGTTTGACCCATCCCTGCTGACACTAGAGACGGTTAAAGGGTTCCTGGAGGAGATTCCGCCAGGCAATTTTAGGGTTTCCATTCCTGGTTGGAGCTCTAGATTAAATTCTGCCAGTACTCCGACCCAGAGTGTCACCATTGGAATAGAAGGAATGACATGCAACTCTTGTGTTCAAGCCATTGAGGGGATGATGTCCCAGAGAGCTGGGGTATGCTCCATAAAAGTTTACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20647
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 |
---|---|---|---|---|---|
ENSDART00000030246 | Nonsense | 141 | 1364 | 2 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 10007213)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9861020 |
GRCz11 | 6 | 10096559 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGGTGTCATTGGAGTCCAGGTGTCTTTGAGCGATAAAGAAGCCATTT[T/A]GAGGTTTAACCCTGCAAAGGTAACACCAGAGGATATGAGAAAGCGTATTG
Long Flanking Sequence:
CAGTGCAAATGTCTTAAGAGCAGGAGAAAATGCATGTCTTGTGATTGTTCAGTTGGACAACCTTTACTAATCTGCTCTCTTTGATGCTGTGAGATGGAAAAATGTTATGCTAATCCTTCTGCTTGGTTAACGGGTGCTTTGTAGTTCCTTTTAAATGCAGTAAGAAGGAGCTTGTCAGATACACAAAGTGAAACAACATAATATGCCAATAAACTGTTAAGCAATATCTTTAAGCTAATCATTTAAACCATTTGTTTAGGAGAATGGAAGTCAACAGGAGGGTTGGATCCCTACAAAACATGCTTTTGATAATTTTGGTTATGAACCAGATGGACTGAAGCACAACTTAGTCCACCAGTTGCCCTCCGAGGAGGGCATGGTGAAGATCCAGGTGGAGGGAATGACCTGTCAGTCATGTGTCCGGTCTATTGAAGAACAAATTGGTCGTCTTGAAGGTGTCATTGGAGTCCAGGTGTCTTTGAGCGATAAAGAAGCCATTT[T/A]GAGGTTTAACCCTGCAAAGGTAACACCAGAGGATATGAGAAAGCGTATTGAAGACATGGGGTTTGATGCTTTAATTCTGGCTTTGCAAGGTCAAATACAGCCTTTGTCGACTGATTGGTCTGAGGTGACGTTAGGAGTTGAAGGGATGCATTGCGGGTCATGTGTGAAGAACATAACCGAGACCTTGTCGGGAATGTTGGGTGTCAACTCTGTATTTGTCTCATTGGAAAAAGGAAGTGTGGACCTTAGGTTTGACCCATCCCTGCTGACACTAGAGACGGTTAAAGGGTTCCTGGAGGAGATTCCGCCAGGCAATTTTAGGGTTTCCATTCCTGGTTGGAGCTCTAGATTAAATTCTGCCAGTACTCCGACCCAGAGTGTCACCATTGGAATAGAAGGAATGACATGCAACTCTTGTGTTCAAGCCATTGAGGGGATGATGTCCCAGAGAGCTGGGGTATGCTCCATAAAAGTTTACTTACAGGAAAAGAAGGGAATTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33815
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 |
---|---|---|---|---|---|
ENSDART00000030246 | Nonsense | 282 | 1364 | 2 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 10007635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9861442 |
GRCz11 | 6 | 10096981 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAGAGTGTCACCATTGGAATAGAAGGAATGACATGCAACTCTTGTGTT[C/T]AAGCCATTGAGGGGATGATGTCCCAGAGAGCTGGGGTATGCTCCATAAAA
Long Flanking Sequence:
GGTCTATTGAAGAACAAATTGGTCGTCTTGAAGGTGTCATTGGAGTCCAGGTGTCTTTGAGCGATAAAGAAGCCATTTTGAGGTTTAACCCTGCAAAGGTAACACCAGAGGATATGAGAAAGCGTATTGAAGACATGGGGTTTGATGCTTTAATTCTGGCTTTGCAAGGTCAAATACAGCCTTTGTCGACTGATTGGTCTGAGGTGACGTTAGGAGTTGAAGGGATGCATTGCGGGTCATGTGTGAAGAACATAACCGAGACCTTGTCGGGAATGTTGGGTGTCAACTCTGTATTTGTCTCATTGGAAAAAGGAAGTGTGGACCTTAGGTTTGACCCATCCCTGCTGACACTAGAGACGGTTAAAGGGTTCCTGGAGGAGATTCCGCCAGGCAATTTTAGGGTTTCCATTCCTGGTTGGAGCTCTAGATTAAATTCTGCCAGTACTCCGACCCAGAGTGTCACCATTGGAATAGAAGGAATGACATGCAACTCTTGTGTT[C/T]AAGCCATTGAGGGGATGATGTCCCAGAGAGCTGGGGTATGCTCCATAAAAGTTTACTTACAGGAAAAGAAGGGAATTGTAACATTTGACTCCACTGTGACCTGTCCGGAAGAACTGCGGGCAGAGATTGAAGACATGGGATTTGAAGCGTGGCTGAATCAAGGTAGGTATTTGCTAATACATAATAAATATAGCTGATTGTAGTGTCACAACTTATTATGAAATATAATGGGTGTGTCTAAAATCACTTACTACTTCAATAGTACTACATTTAAATTTACAACATGACTGTCAGAAAAGTATATTCTATGTAGTATGATTGGAATTCTGATGTACTACGCCATTATCACATGACCTACCCGTGTCAGTTGCGCTGCTTCACTTCCATTCATGACTTCTGTCGCGTGGCATTGTAGTGTAGTCCCTTGGATGCACACTTTAGAATCTAGTATTACAGTTGAAGTCAGGATTATTAGCCCCCCTTTGAAGTTTTTTTTCTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17744
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 |
---|---|---|---|---|---|
ENSDART00000030246 | Nonsense | 572 | 1364 | 7 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 10018473)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9872280 |
GRCz11 | 6 | 10107819 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTKGGATCCCAGTGATKGGYCTGATGATCTACATGATGGTGATGGACAGT[C/T]AGCACAAGGAACATGGAGGCTCCATGCCTGCGGACCAGAACATCCTCCCT
Long Flanking Sequence:
TCTGTAGTGTATGAGTGTATGTGTGCGTGTATGTTTCCCAGAGAAGGGTTGCGGGTGGAAGGGCAACCGCTGCATAAAAATGTGCTGGATAGGTTGGTGGTTTATTCCGCTGTGGCAACCCCAGATTAATAAAGAGGACTAAGCCGACAAGAAAATGAATGAATTAATAAAATAAACAGTGTCCCTTATTGTAAATTGTTACTATTATTTTTACTTACGCATTTCCATTTTTCCCCCCCTGTTCTTTAGGGTTTGGGTTTTGGTGTGTCTTTAATAAAAAACGAGGGATTGAACAACACGCTGGATCACCAAGAGGAAATTCGGCAGCAAGTATCTTTTTTAACCTCATTTATTTTGCATGTGTGTGTTTATCTGAGAGAGTGTGAGTGTAATAGTGTAAACTGCTGTGCACCTGCAGATGGAAGCATTCGTTTCTGTTCAGCCTTGTGTTTGGGATCCCAGTGATGGGTCTGATGATCTACATGATGGTGATGGACAGT[C/T]AGCACAAGGAACATGGAGGCTCCATGCCTGCGGACCAGAACATCCTCCCTGGTCTTTCCATTATTAACCTGGCCTTTTTCCTGCTCTGCACTCCTGTTCAGGTACAGAAACTTCTCCATCAGAGATGAGACCTTTTATTAACAATTATATTTTAAACAAATGGCAAGAGGAGTGGGATACTCAGGAAAACAATAAATTACACGAAATCCAGCCTGAAATTACACACAGAGGTTTAAGACATTTTAAGAAACGAGCTGATTAGGTCATTTTTACCAGATGTCGTATTGGACATACAAGATTAACACATAAATTTTTACTCAAAGATGAAGACCCTATCCAATGTTTGCACTGTAAAGCCCCAATGGACTGCAAAACACATTTTACTGGACTGCCCTGCTTTTAATGACTCCAGAAAGACTTTTTATGATGAGAACTCTCTTAAGGACATTTGTAACAAAGTGATACCAGAAAAAGTATTCGAATTTTGAACATGTATTAAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9976
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030246 | Essential Splice Site | 757 | 1364 | 11 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 10024616)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9878423 |
GRCz11 | 6 | 10113962 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTCAGTGGTTCAACTGTAAACATACAAAATCTKACATTATTTGTMATTTC[A/C]GGAGAGCCGATGCCGGTGATWAAGAAAGCAGGCAGTTGTGTGATCGCAGG
Long Flanking Sequence:
TCATGTGTCAGAGAGGAGCAGGTGTCTGTGGATCTGGTGCAGAGGGGTGATGTGGTGAAGGTGGCACCCGGGGGAAAGTTCCCTGTCGACGGGAAGGTCATTGAAGGCACGTCTATGGCAGACGAGTCTCTGATCACAGGTAAGACTTTAACTCTTGAGTTTGAGTGTTTTTGGATGCTAAATTTGTTATGGTACATAGTAGATTTTCTCAGTGATTTACCTTAAAAAGGAGCAAAAAGTAAATCCCAAATGACATTAATTTAAAGAGGTAATTGAAAATTGAAATGATAATTGAAAAACTCTTGTCATTCTAATTCCCTGAGACCTGCGGTCTTCTTCACAACACAAATTAAGATATTTTAGATGAAATCCAAGAGCTCCCTCATCCTCCATAGACAGCTCAAAGTTCAGAAAAGGAGCCAAAAACATTGTCAGAACATTCTATGTGTCTTCAGTGGTTCAACTGTAAACATACAAAATCTTACATTATTTGTCATTTC[A/C]GGAGAGCCGATGCCGGTGATTAAGAAAGCAGGCAGTTGTGTGATCGCAGGCTCGATTAATGCTCATGGAGCTCTGCTGGTGGAAGCCACACATGTCGGATCAGAGACCACACTCAGCCAGATCGTCAAACTAGTGGAAGAGGCCCAGACATCAAAGGTAATGCATAACACACACACACACACACACACACACAAACACACACACACACACACACACACACACAAACACACACACACACACACACACACACACATATAGCCGCAGGAATGCAGACCTCTACACTATACCTTTAATAGGTTCTGTGGGACCAGCCAGTTTTTAAAATAAATTTCCGAATAAAACACGGTAGCAGTCGGGAACTCTGGTGTAATTTGAACGGGAGTGGGCAGCCTATCTATAGTAGTCCCGAGAGAAAGATTGAGCGCTCCCAAGAAAGAGAGAGAGCGCATCCGCTGTCAGGTCGGGTAGAAAACAGGGCGGATCGGACAGCAGGTGAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40637
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000030246 | Nonsense | 855 | 1364 | 13 | 21 |
Genomic Location (Zv9):
Chromosome 6 (position 10027027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 9880834 |
GRCz11 | 6 | 10116373 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTGTGTGTTAAAAATGCTTCTTATCTGTGTGTGATTTCTACAGGGTTA[C/A]AACCAAAACATCTCGCGAACAGAGGTGATCGTTCGCTTTGCCTTCCAGGC
Long Flanking Sequence:
GCATAGAAGAAACTGCACATTTTAAAGCATGTCACGGGACCTTTAGGATCATATATAATTGTTTATAGAGGTATAGTGTAGAATCTGTTGCTCATGTAAATAGATTTTTTATTTATGTCTATATCATCATTGGCAATCATTTAAGTTGAACATGTCATTTTCATGTTTAAAAGTGTGTGCGGCGGTTAGGATTTCTCTTTTTAGGTGAACTAACCCTTTAATGTTTCTGATTTGCCATCCCCAGTCATTAATTGTCCTCTTCTATTGATAGGCACCCATTCAACAGTTAGCAGACAAACTGAGTGGCTACTTTGTTCCCTTCATAGTGGTGATCTCTATCCTAACAGTGACAGCATGGCTCATCATTGGCTTTCTGGACTTTGACGTTGTGTCAAAAAATTTCCCTGTGAGTTACGGCAACTTATTGTGTCTAAATATTCTTCATTTCACTGGTGTGTGTTAAAAATGCTTCTTATCTGTGTGTGATTTCTACAGGGTTA[C/A]AACCAAAACATCTCGCGAACAGAGGTGATCGTTCGCTTTGCCTTCCAGGCCTCCATCACCGTTTTGTCCATTGCCTGCCCCTGTTCACTGGGTCTGGCCACCCCGACTGCTGTGATGGTGGGCACAGGGGTGGGGGCACAGAACGGCATCCTCATAAAGGGAGGAGAACCCCTGGAAATGGCCCACAAGGCAATGCTCATTGAATTCCTTCTGAGTCTGTTTATTAAAGGGGTAGTTCACCCAAAATTGCCAGTTTACTCTAAACTTATAAATGTTTCTACTTCTGTTGAACACAAAGGAAGATATTTTGAAGAATGTTGAGAAATAAGCATCAATAGTAGGAACAAAATAAACTAATAAAGTCAATGGCTGTTTTTTTCCCCAAACATTTTTTGTAATTTTGTGTTCAATAGAAGAAACTCAAATGTGTTTGGAACAAGTGAAGGACGAGTAAATGATGACAGAATTTTCATTTTAGGGTGAACTATTTGTAATATGGA
Associated Phenotype:
Not determined