ZMP
ENSDARG00000036420
Ensembl ID:
Human Orthologues:
ABR, BCR
Human Descriptions:
active BCR-related gene [Source:HGNC Symbol;Acc:81]
breakpoint cluster region [Source:HGNC Symbol;Acc:1014]
breakpoint cluster region [Source:HGNC Symbol;Acc:1014]
Mouse Orthologues:
Abr, Bcr
Mouse Descriptions:
active BCR-related gene Gene [Source:MGI Symbol;Acc:MGI:107771]
breakpoint cluster region Gene [Source:MGI Symbol;Acc:MGI:88141]
breakpoint cluster region Gene [Source:MGI Symbol;Acc:MGI:88141]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10997 | Nonsense | Available for shipment | Available now |
sa15342 | Nonsense | Available for shipment | Available now |
sa34040 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa25359 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa20906 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10997
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 |
---|---|---|---|---|---|
ENSDART00000052906 | Nonsense | 14 | 828 | 1 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 21551065)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 20141501 |
GRCz11 | 7 | 20393469 |
KASP Assay ID:
2259-8666.1 (used for ordering genotyping assays)
KASP Sequence:
CTGCTGCTGATGGAGCTCTTTTCTGAGRCTGTGGAATATCTGAAGRCYTA[T/A]GGCATCTCACCTGGTACCACTGTTTTGTTTRATAGTAACTACACMAATAA
Long Flanking Sequence:
AAAAGGGCGGTCAAGGCATTAGGGTCTAGATTTATGTTAATAGCTTCATTAAGTGTTTCAAGAACACTGGACCAGAAATGTGTCAATTTAGGGCAACTCCAGAACATATGGAGATGGTTAGCAGGAGACTGCTCACAGCACTGACTGGCATCACTTCTATCAGAACTTTGATTTGCTAGTTTGGCATTGGTTGAATGAGCTCTATGGAACTCCTGAGTACTTGACATTTTAATCAGATAAATGCAGCATTGGTGAGATCCACGGCATATTTTTAAAGTAGGTAAGCAGTAGCTTCCTGTCCTAAGTAACGTGACTTGTTTTCTTTTTTTTAATGAACGTGACACTTTCCCCGCCTATGTCTTAGAAGCAGGAAGAACGTGAGCTTGTCAACCTCAAACTGTCAGAGTGTGATAGCGAGAGGATTCACATCACGAGCTGAAGAGCTGCTCTCTGCTGCTGATGGAGCTCTTTTCTGAGGCTGTGGAATATCTGAAGGCTTA[T/A]GGCATCTCACCTGGTACCACTGTTTTGTTTAATAGTAACTACACCAATAATAATCAATGATTGTTTCTGAACTGTCATCCGATAATCTGGTGTGTTTTTATATTTTAATAGTGACTGAGGATGAAATGATGGATTCTGACCTACTACATGATGTGTTCCCTGAGGAGTCAGACTGGGGGTCTCATGGCTCTATGCAAACTGAACCATGTTTGCCATCCACACCAGTAAGAAATGACAGAAGTATCTTATTAGTGAGGTCCTGTTTGTATGTTGATTCATTTTACCGTCACCAGTGTATATCAATAGCTCTATTCAAGTGTATAGTCTTTGTCATAGATTCTCAGTGCTGACCCAGCAAATAGTTTTGTGTTTATTAGACGTCTAAACATAGACACATTGGCTATAACGAGGCTAAACTTGGGCTGTCAGTGAAAATCTAATAGACATCTGAGAATAGCCCAAAACCCGACTAGTCGTCAGATAGACAGATTAGACAGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15342
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 |
---|---|---|---|---|---|
ENSDART00000052906 | Nonsense | 297 | 828 | 9 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 21560531)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 20150967 |
GRCz11 | 7 | 20402935 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
WCTTTAAAAYGAATCATCATATATGCAWGTGTGCATGTCTGCAGAGACGT[C/T]AACTGATGCGTGATGGGTTTGTGGTTGATGTGTGTGAAAGTGGGCACAAC
Long Flanking Sequence:
TTAAAAATGTTTTTAAAATTTCTTTATGAAACCTAAAAGGGAAAAATACTGATACAACTAAACGTAGTGGGCAAAAACCAACACACTTTCTTTGTTCATTTAACTTCACAGCTCTCCTGTACAAGCCGTTAGACAGAGTGATGAAAACCACCCTCGTCTTGCACGTGAGACACTGCTCAATATCTCCCATTTATTTATAAATATTCACTCATACCTATGGATTTATGACCTTGTTCTGCTTCATCCTCAGGACTTGTGGAAGCACACGCCCCCCGAACACCCTGACAGCATCACACTGCAGGAAGCGCTCCGTCTTTCGAGCAGCTTTATGTCTGGGGTGAATGAAAGGTCGCAGTGCAAACAGCCAGTCATGCTGTGCAGAGGAGAGGTACTGCAACGCTTCACATGATGCGTGTCACATGTGTTCCTTGTATGCTGATTATTTGTTAAACTTTAAAATGAATCATCATATATGCATGTGTGCATGTCTGCAGAGACGT[C/T]AACTGATGCGTGATGGGTTTGTGGTTGATGTGTGTGAAAGTGGGCACAACCTGAGACACCTCTTCCTGTACACAGACATGCTGCTGTGTGCTAAACTGACAAACGCAGGGTGAGTTTCCTCCAACCAGAGCTCACTGAGCATGTGGCATCATGCTTCATTCATCAGAGGCCTGTTGCACAAAACAAAGTGAACAAATTCTGGGTGGCAGTTTCAGGTAGACAAAACAAATCCAACTTGGTTTAGATCTGGTTAAGTGGTTGCACAATGCTTGATTTAAATTGTCTTGGAATATTATCAGAAATATAATGAATTTAAACACATTTACGAAACAGAAATATAAAACAGAACGTTTAAGAAGGCAACTTAATGAAAATGTTATTTTATCAGTGCAAATGAATCAACTCATTTTAATAATGTAGGATCACCAACAGCTCAGAAGTCAGTTGTTTTAAAATCCTTATTTATTAAGGAACAATTTAGATGTAAATATTTAAAAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34040
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:
A > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052906 | Essential Splice Site | 509 | 828 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 21570019)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 20160455 |
GRCz11 | 7 | 20412423 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACATGCATTAAAAAACATCTTCCATTAATTCATGTCACTTGCCCTTTC[A/T]GGTGCGTATGTTTGTGTGGAAGTAGACGGCTTTGAGTGTTACGACAGGCG
Long Flanking Sequence:
GTGCAGTCTATTTCAGTTCTTCAAACTAGCAACGCACCAACAATGCGGGTTAACACACTTCTATTTTAGACTGAAACAACCATGATTTCACAAAGTGGCACAAATGGATTTGCTATTTAAACAACATTGCAAAAAAGTGAAAATTAGGGTTGTGCTAGTCTTGAAAATAGCAGCAAATCGCGCCAAATACGTCTTGCGCCTTATTGTGCCGGGTGTATGATAAGACCCTAAATATTTACAGTTTTACACCTTTTTTTGTCTGAAATACAATTAATTACAAAAAAAGTTTACTGTAATAATTAAAAAATATATATGTAATAATAAATCATAGGTAATAAAAATAGCATTTTCTAGGGAAATAAAGTATATCGTTATCACAATTCTCAACAACAATATTGCATATTTTTTCAGTATAGTGTAGCCCTAATAAATACCTAAAAAAATTTCAGTCAACATGCATTAAAAAACATCTTCCATTAATTCATGTCACTTGCCCTTTC[A/T]GGTGCGTATGTTTGTGTGGAAGTAGACGGCTTTGAGTGTTACGACAGGCGAAAACAAACCAGCCTTTCGGCCTTCTGTGTTACACCACAATGGGATGAGGTTAGTCGTGGGAGGCAGTTGTGAATGTTTAAGAACCGGTTTATGCAATGTATGATCTACAATGTATGCAATTTACTCAATTGATCTTAATTAGCACTATGTGTGGTAATATGGTGTACAGGAGCTTGTGTTTATAGTGGACGGAGCTAAGCAGCTGTTCCTGGTTTTCGTGTGTCAGTACGAGAATGACACACAGAACGACATCGTGGGCAGAACAGTCTTAAATGTGAGTATATGAACTCTAGCCCTAAATTTGTAAAGTCAAGAAAAAGATTTTATTTGAGCTTTTTGTCTAATTGATGTATTTGTTTGTTTAAAATAGATTAAAAGGATGCTGTAAGTGCAGCCTGATCTCTTGAGGAACCTAACTATTTTACGTTTTGTCAGTTTAGTGGCTAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25359
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 |
---|---|---|---|---|---|
ENSDART00000052906 | Essential Splice Site | 576 | 828 | 16 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 21570346)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 20160782 |
GRCz11 | 7 | 20412750 |
KASP Assay ID:
554-7849.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACGAGAATGACACACAGAACGACATCGTGGGCAGAACAGTCTTAAATG[T/C]GAGTATATGAACTCTAGCCCTAAATTTGTAAAGTCAAGAAAAAGATTTTA
Long Flanking Sequence:
ATAGGTAATAAAAATAGCATTTTCTAGGGAAATAAAGTATATCGTTATCACAATTCTCAACAACAATATTGCATATTTTTTCAGTATAGTGTAGCCCTAATAAATACCTAAAAAAATTTCAGTCAACATGCATTAAAAAACATCTTCCATTAATTCATGTCACTTGCCCTTTCAGGTGCGTATGTTTGTGTGGAAGTAGACGGCTTTGAGTGTTACGACAGGCGAAAACAAACCAGCCTTTCGGCCTTCTGTGTTACACCACAATGGGATGAGGTTAGTCGTGGGAGGCAGTTGTGAATGTTTAAGAACCGGTTTATGCAATGTATGATCTACAATGTATGCAATTTACTCAATTGATCTTAATTAGCACTATGTGTGGTAATATGGTGTACAGGAGCTTGTGTTTATAGTGGACGGAGCTAAGCAGCTGTTCCTGGTTTTCGTGTGTCAGTACGAGAATGACACACAGAACGACATCGTGGGCAGAACAGTCTTAAATG[T/C]GAGTATATGAACTCTAGCCCTAAATTTGTAAAGTCAAGAAAAAGATTTTATTTGAGCTTTTTGTCTAATTGATGTATTTGTTTGTTTAAAATAGATTAAAAGGATGCTGTAAGTGCAGCCTGATCTCTTGAGGAACCTAACTATTTTACGTTTTGTCAGTTTAGTGGCTAATTCGTACGAATTCAGTTGCACAAAAATTTATTTTTAAAAGGAGACATGGAACCCAACCCCACCCCTAAACCCAACTGTCACTGGGAGACGAGCAAATCATACTATATAACATAATTGTATAAATCAATCATTCTGACCCAAACAGTGTATTTTCTGGCCGTTTGATTTTCATTTTATGCTTAAAATCATTAGGATATTAGACAAGTTATAAATCTTCATTGTCCACACATGTGGAAAATCGTTCTTGGACTCTCAAATACAAAACACACACACAGCACAAACACAAAGCTGCCTACACCACAGATTACCAACACACAACCCTGGCTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20906
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000052906 | Essential Splice Site | 759 | 828 | 21 | 22 |
Genomic Location (Zv9):
Chromosome 7 (position 21577431)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 20167867 |
GRCz11 | 7 | 20419835 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTTACTCTAGCCTGACCTCATCTCACATCTGACCTTTTTGCATTCTTC[A/T]GAGTTGCAGAGAGGAAGGAAGAGAATAAAATGTCCTTGAGTAATTTGGCC
Long Flanking Sequence:
TTTTTTTTTTACCTTGCATACATATTAGCCCGTTGTTGGGGACTCCCCAAACTAAATATAATTTTTTTATAATCCATAATAAGGGCACTTTAAAAGAATTTTTCTTGCTTTACAATGAAGCATTACCATAGAAAAATACAATAACAATATAACAAACGATGCTAAATCAAGTAAAAAGAATCCCTAAATGATTTTAATAGAGATTTAAAAGACCTCACTGAATTGATTTACAAAGTGATGATGAATAAGCATTTGAAAAAACCATCTCTCTGTTTGTCTGTCTATCTGGCTGTGTCAGACATCGCTGATCCATTTGTCAGAGCAGACAGCTTGCTGAGTCTGCTGCAGTCTCTACCAGATGTGAACCGCAACACTCTGCTCTTCCTCTTACACCACCTGAGACGGTACACAACATCCTTTTCAATACGTAACTCTCAAAACACTGATTTAGCTTTACTCTAGCCTGACCTCATCTCACATCTGACCTTTTTGCATTCTTC[A/T]GAGTTGCAGAGAGGAAGGAAGAGAATAAAATGTCCTTGAGTAATTTGGCCACAGTGTTCGGCCCCAGTCTCTTGCGCCCCCCAGTGTCTCGTGTTGACATATCCCAAGAAGTGGAAGTTCAGGTGGGTTATTTCTGTACAATATCTTCTGTAGCAGATTATTAACTGGTGTGTTGTGCAGTAGAGTTGTATATACGGTAAAAAGTCTAGTAAAAGCAATTATTTTCTTTGAAGACTGTGAGATGTCTGTTTCTCATTTTCTGAAGTTTATTTCAGGAGATGTAAAACAATAGATTTATACCTCTGGAGACTAGCGCATGTTCCTTATAATTGCATGCACTTCTATAATGAAGATCAAATATGGGTGAAATAATGTTGAACTCATTTTTTCATCATCTACTGGTAAGATTCAGAAGGTCATGATTCACGCTGCTTAAATAATTACTTTATATAGCTTTATTTTATATTCTCAGGAGATACAAAACAGATGTTTTGGCACAA
Associated Phenotype:
Not determined