ZMP
si:dkey-91m11.5
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC560226 [Source:RefSeq peptide;Acc:NP_001116725]
Human Orthologue:
BCR
Human Description:
breakpoint cluster region [Source:HGNC Symbol;Acc:1014]
Mouse Orthologue:
Bcr
Mouse Description:
breakpoint cluster region Gene [Source:MGI Symbol;Acc:MGI:88141]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa31660 | Essential Splice Site | Available for shipment | Available now |
sa21327 | Nonsense | Available for shipment | Available now |
sa16588 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa31660
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062073 | Essential Splice Site | 771 | 1291 | 9 | 23 |
ENSDART00000137009 | Essential Splice Site | 770 | 1290 | 9 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31418326)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 30561052 |
GRCz11 | 8 | 30570284 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTACCGACATTCTGCTCTGCGCTAAATTGAAGAAACAAACTGGAGGG[T/C]AAGACATGATTTATTTTTCATTCCTATAGAATCATTGTTGTTTGTCTTTT
Long Flanking Sequence:
TGTCTTGTCTTGAGTCACAGGGTTTCACTAGAGACAAATTGCTGGACATTTGGACGCATACACCACCTAATCTACCCGCTATACACTTTTTATACACATATACACACTTATTTAACATACTTTACGTGCCAATTTGCACATAACAGTTGCACAAATAACGTTGTATATAGTAATATATCTGCACATACACTTGTAAGTTTGTATATTTGCATTCACTACTTACTTATATTTTTAAATATATTTATTATCTGTTTTTTTGTCCTGTCTCTGTAATTCTGTTGCACTTTAGGAGCTCTGTCATGTAAACAAATTCCTTGTATGTGTGAACATACCTAACAATAATGCTCTTTCTTTCTTTCTTATTCTTGTCTTTGAAGAATCGACAGCTTCTTCGAGACCAGTTTATGGTGGAGTTAGTAGAAGGTGCACGAAAACTGCGACACGTCTTCCTCTTTACCGACATTCTGCTCTGCGCTAAATTGAAGAAACAAACTGGAGGG[T/C]AAGACATGATTTATTTTTCATTCCTATAGAATCATTGTTGTTTGTCTTTTTTGCCATCTGCTGTTGATTGTCATGTATGTGAGCGCTGGTTTGGATGTCTATGTATGTGTGTGTGTGTGTGTTCAGGAAGGGGCAGCAGTATGACTGTAAGTGGTATATCCCGCTAGCGGACGTCACCTTCCAGACCATCGATGAGTCTGAGTCCTCGCCTGTTCCACAGATACCAGAAGAGGAGATTGATGCTTTGAAGGTCAAGATCTCTCAGATCAAAAACGAGATCCAGCGGGAAAAGGTGGATGAGATCATCAGAAATGCTCTTCTACTGCCAAAAAAATCAGCTTTTTGTTGACTGTTTTCAATCTGGTCTCTCTGTGTGTTCAGAGAGTGTGTAAAGGAGGAAAAGTGCTGGATCGCCTCAGGAAGAAACTGTGCGAACAGGAATCGCTGCTTCTCCTTATGTCTCCCTGCATGGCCTTCAGAGTCAGTAACAGGAACGGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21327
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062073 | Nonsense | 881 | 1291 | 12 | 23 |
ENSDART00000137009 | Nonsense | 880 | 1290 | 12 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31419930)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 30562656 |
GRCz11 | 8 | 30571888 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTCAGGGTTATACATTCCTGATTTCATCTGACTATGAACGAGAAGAATG[G/A]AGAGAAGTCATTCGGGAGCAGCAGAAAAAATGTAAGCACTTACAAGATGT
Long Flanking Sequence:
AGTAGATTTTAAATTAAATTATGTAGTTTCTTATGGCCTGTTAGGAGAAATTAGCTTGTTTTAATCATGAACTAGCTTAATGCTATAAATAATTTATAAATAATATAGAGGAGGCACAGCATTCTGCAAACCTTATTCAAAGCTTAAGCGTTTTTTGGGGGTAAAATTATTTAAAAAGTCATGAGAACAAAGTACAAAGATGTTTTTTTTCTTCAAACTTTTAATGTGTTGCTAATACAATGTTTAAAAAACATATTAGGTGTTTGTGTTACCTTTAAATTATTTATTAAATCATTAATTGGTATTAAATGCTTAGGTTATCCTTCATAAGTCCTGGGAAAAGCTCAGTACATTGTCAAAAGATGCAAATGTAACATGAATTTAGATATGTAAGTAAGCTGTTTTCAAAAGTTCTTATCTCTTGTGCCCTTCTTGTGTTTTATTTCTTTATTTCAGGGTTATACATTCCTGATTTCATCTGACTATGAACGAGAAGAATG[G/A]AGAGAAGTCATTCGGGAGCAGCAGAAAAAATGTAAGCACTTACAAGATGTTCCTCACAAAATCTTCCTAACTTCTTTACAGTCTCTTATTTCCAGTTAAAAGCAGATACAGCTGGCTCCAATGACTAAGTCGCTTGTGTTTGTTTCAGGTTTCAAGAGTTTTTCTTTGACTTCTCTGGAGTTGCAGATGCTTACAAACTCTTGCGTGAAGCTACAGACAGTTCACAGCATTCCTCTGACAGTCAATAAAGATGGTGCGTGTTTAATTTTTTTGTTTTGCTTTGCTTTGTTTTGCCCTCTGACAGTTAATAAAGATGGTGAGTGTTTGTTTGTTTTTTTTTGTTTTTTTTTTTGTTTTGATTTGTGTTTTGTTCTCTGAAAGTCAATAAAGATGGTGAGTTTTTTGTTTTGTTTTGTTTCCTGACAGTCAATAAACATGGTGAGTTTAGTTTTTTTTTTTTTTTTTAAGTTTCATTTTGTTTTGTTTAGTTTTGCTTTGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16588
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000062073 | Essential Splice Site | 1024 | 1291 | 16 | 23 |
ENSDART00000137009 | Essential Splice Site | 1023 | 1290 | 16 | 23 |
Genomic Location (Zv9):
Chromosome 8 (position 31424264)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 30566990 |
GRCz11 | 8 | 30576222 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGATGATGGCGAAAACATKGATCGCGTCATGGCCAAGGGGCAGATTCAGG[T/C]ACGGCTTTTTCAGTTTGGACYKTATCAGAATTACTTTMACTCTACGTTTT
Long Flanking Sequence:
TAGAAAAAGTGTTTAGTGTAATATTTGTACAAAATTTAACATGTAACCACAATGTTGTCTGTTCTCTCCCTGACCTCAGATCTGTACTGTACATTGGAGGTGGACTCGTTCGGCTACTTTGTGAACAAGGCAAAGACTCGTGTTTACAGAGACACTACAGAGCCAAACTGGAACGAGGTCAGAAATATAAACCGCCCACAACCACACAGTTGTCTACAATGAATGTTAATAAAAACACACACAGTAATGTTTATCTCAGTATGGTGCAGTTCCACTTTGTGCCACGAATTGACACTAGAAATGCAGCTGTAAATATGCAAACGGATGTAATGCTGGTTGAATGCTGTGATTGAATGAAGGTTGAATTTTGTGTTGACAGGAGTTTGAGATCGAGCTGGAGGGCTCACAGACCCTCAGACTGCTGTGTTATAGTAAAATCAAACAGTGCAGGGATGATGGCGAAAACATTGATCGCGTCATGGCCAAGGGGCAGATTCAGG[T/C]ACGGCTTTTTCAGTTTGGACTTTATCAGAATTACTTTCACTCTACGTTTTTAGTGCTTGAGTAGAGCTGCACATTTATTAAAAAACAAATTGTAACAAAATGTAATTAATTACTATTAATTATTTAACTTTATTAATAACTGACAAGTTAAATTTTAACTGACATATTAAATATTAATATTAACTTACATAAACTCACTTCTCTCTAGATTAATCTATTGCATGCTATTAATAAGGAAATTTTTACATTCATTTTTGTTTTGAATGTTTTTTATTAAGTTGAATGAATTTTATTAAGTCAGACCGTACATCCCAGGGTAAAAAACTAAAAATAAATAATAATAAAAAAAACTTCATAGTGTTTTGTTTATATTTTAACACAGAAAGATTCAATTAAATTAAATAATTCAATAATTCAATTCAATTAAAATGTTATAATATTTTTTTTTATTTAGTATTTTTAAAGTATTAAAGTTAAAAGTTAATTAATTAAAAACTGTG
Associated Phenotype:
Not determined