ZMP
si:dkeyp-122a9.3
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate low density lipoprotein-related protein 1B (Deleted in tumors) (
Human Orthologue:
LRP1B
Human Description:
low density lipoprotein receptor-related protein 1B [Source:HGNC Symbol;Acc:6693]
Mouse Orthologue:
Lrp1b
Mouse Description:
low density lipoprotein-related protein 1B (deleted in tumors) Gene [Source:MGI Symbol;Acc:MGI:21511
Alleles
There are 12 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa753 | Essential Splice Site | Available for shipment | Available now |
sa1481 | Nonsense | Available for shipment | Available now |
sa13305 | Nonsense | Available for shipment | Available now |
sa10588 | Nonsense | Available for shipment | Available now |
sa17465 | Essential Splice Site | Available for shipment | Available now |
sa12543 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa753
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 |
---|---|---|---|---|---|
ENSDART00000135768 | Essential Splice Site | 259 | 1629 | 5 | 35 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 14604112)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14435019 |
GRCz11 | 22 | 14459594 |
KASP Assay ID:
554-0660.1 (used for ordering genotyping assays)
KASP Sequence:
GAGAACCATATCTTATTTGCAAATATAGACGGTACCAAAAGACACAAAGG[T/C]AAGTGCTTTCTTATCTCAAATCTAAGTCTTGATTAAAATTGACATTAACA
Long Flanking Sequence:
TCATCTGAACACCAAGGCAAATATATGTAGTTTTTCTCCTCAATTTTGACTAAAGGTGAGTGTTTCAAAAATAAAGTTGAAATAATGCAGCTGAAGGCTTCAATAGAAGCACTTTACATTGATCACTGCAACAACCTCAGAGCTCACAGTAGGTGTGTGTTTAAAGATTGATCAGATATGGTGAAAAATCAACTCCCCTGTGGAGAAAATGAATGTAGTATGTGGGTTTACCTCCGGAACATGACTGTTGCACTCTATTGCATCGTTTAAAGCTACATCAAATCCCATTGGTGCCTTAGGTATGTGTTCTGGATCGACTGTTGTGAACAGCCCCAAATTGGACGGATCGGGATGGACGGCAGCAAGCCACGCGTCATAATTGATACAGAAATACGCTCTCCTTCAGCTTTGACCATTGACCACGTCAACAAAAGGATTTACTGGGCTGACGAGAACCATATCTTATTTGCAAATATAGACGGTACCAAAAGACACAAAGG[T/C]AAGTGCTTTCTTATCTCAAATCTAAGTCTTGATTAAAATTGACATTAACAAATTTTTGCTCCAACTTCCAGTCCCTATACAAGACATAGGTGGAGTAACGGGTCTCACATTGTTTGAGGACTTCATTTACTGGAGTGACCAGAAGTCCAAAACCCTCAGTCGCTCTCACAAGACGTCGGGCGGTAAACAAACCGAGCTCCTCAGCTCATGGCAAACCATTCGAGACATTCAAGTCTACCATCCGCTCCGACAGCCTGACGGTATTACAGCGGGAAGCTTCTTGGATAAGTCTACAGTTGACTGTTTGGGTTAGAGTCAAGACTCCCATGTTGATCCAGGATTGTTTTTGATTTGTTTGTTGTTTGTCCTCAGTGCCTAAACATCAGTGCCAGGTGACTAATGGAGGGTGCAGCCACCTCTGCCTGCTTTCGCCTGGAGGGGGATACAAGTGTGCTTGCCCTACGCACTTCTACCTGGCAAATGACAACAAAACCTGTCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1481
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000135768 | Nonsense | 460 | 1629 | 10 | 35 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 14598984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14429891 |
GRCz11 | 22 | 14454466 |
KASP Assay ID:
554-1406.1 (used for ordering genotyping assays)
KASP Sequence:
TGATATATAGTGCAGTGATGTCCTTGTTTGCATTTGCTTTCAGACTCATA[T/G]ATCTGCCTGTCGGGTCAGTTTAAGTGCACACACCGGCAGAAGTGCATCCC
Long Flanking Sequence:
TCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCTTTCATTTCATTCATTTTTCTTTTTCATTTTCATAAATTTTTTGGGTTTCTTTGTCTTTTCTGTTTCTATTCACTTGTTTTTTTTTCTGTAGTTTTTTTCCTCCTGTATAACCCTTGTGCTTTCATTCGTTCATTTATTTTAATAATTTCTCTGTTCTTCTGTTCCTCCAGCGGAGTTTAAATGTCAGCCCGGCAGGTTTCAATGCGGGACAGGTCTGTGTGCTCTTCCTCCCTTCATCTGCGATGGAGAGAACGACTGCGGAGACAACTCGGATGAAGCCAACTGTGGTAATTACAGATTGATGGATGCATAAATGGAGCCTGCATAATAACACGTGATATATAGTGCAGTGATGTCCTTGTTTGCATTTGCTTTCAGACTCATA[T/G]ATCTGCCTGTCGGGTCAGTTTAAGTGCACACACCGGCAGAAGTGCATCCCTATAAACCTGCGCTGTAATGGACAAGACGACTGCGGTGACGGGGAAGATGAAACCGACTGCCGTAAGATACTTTTTTTATGTGTTTTTAAGTCAATGGTAACGAATGGCAAAGTTTTTTGAATTCTGTATACAATGGATTCAAGGAAGCTGACAAGTTTAGAAAGAATGTTGAGAGTTGAAAAATAGATTAAATCTGGTTCTTTATCTCCTTATAATGTGTTTACTGGCTCATAAAACATTCAACAAAATGTGTGAGAAGGTTCAACCAGAATATAATAAAATCAACATTGACGGTTTTCTTTTTCCTTTCTTTTCTTTTAACTTGCTTCTTCACTTTTTGTTTAGTTGTTAATTCTGTTTTTCAACCTTTCTGTCGACCTTTCATTTTTTATTGTTCTTTCCTTTTTTATTTTGTTTGTTTTGTGCATTCTGGTTGTTCTTTTCATATT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa13305
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 |
---|---|---|---|---|---|
ENSDART00000135768 | Nonsense | 692 | 1629 | 15 | 35 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 14566981)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14397888 |
GRCz11 | 22 | 14422463 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAGGAGGCTGTGTTTTGGCTGCTCAGCGCTGCGATGGACAGAACGACTG[C/A]GCAGATGGGTCAGATGAGGTCAGTTYAGTTCATAMACACTGAAWAATACM
Long Flanking Sequence:
TTCTCTATTCTTTTTCTTCTTTTTTTTTTAAGTGAAGGTCTCTCTCCTGTCTTTTTTCAGTCTGGCTCTTGAATTTTTCATCTTGGTTTGCTGTGGCCAGATTACCCGAGTATATCCACGGCTGCGACCGCTGACTGAAATATTCTGACCGTAAGAAGCGCTGCAGATGCATTCAGAAAGCTCACACTTTTTTTTCCCCCTGTCGACTCGAGGAAAGTCAGGGGAATTTTACCCTGTGATTAATATTAATGCGTCTGAAAACACTTGAGAAAGTGCAGGCCAGGTCTCTCAGACTCTACAGCAGAGAAGAGTCACGCGGAGCTTTCCAGGAACACACGCATCTTTTATTGTTGATGAATGTTTCAAAGGAGTGTGAGTTTGATGTTGTGTTGATGTTGTGTTTGTGCAGCTCGGCCGACGGCTTGCGGTCTGAACGAGTATGTGTGTGTTGGAGGAGGCTGTGTTTTGGCTGCTCAGCGCTGCGATGGACAGAACGACTG[C/A]GCAGATGGGTCAGATGAGGTCAGTTTAGTTCATACACACTGAATAATACATTATTATGTGTTTTTTGTTTCTGTGTGTGTGAGAAAGAGAGTTATGGATCATATTGTTATTGTTGTTACAAGTCATTTTGGTCATTTATTTCTAAATGTAATTATTTAGTGATTACATACTGCAGTCTGCAGTATTACCAGTGTAGATTATTATTATTATTATTATTATTATTATTATTATTATTACTAATATTATTATTATTATTAATAATAATAACAATAATAATAATAATAATAATAATAATAATAATAATAATAATTAACATAATTGGCAATGTATTTTGTTAATAATAATAGTTCACTCACATAATTAATTTAATATATTTTCAAAATAAACAATAGTAATGGATGTTCAAATGTTTTCGAGCACAAAACTTCAGAACACTTTTCATAAATTATTAAATATAATTCATAAAACAAAATAATATTGTACACAATTGTCTTATTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10588
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 |
---|---|---|---|---|---|
ENSDART00000135768 | Nonsense | 902 | 1629 | 20 | 35 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 14552620)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14383527 |
GRCz11 | 22 | 14408102 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCTCCGTCTGCCAGTGCAAAGAAGGCTTTCAGAGGAACCAKAAGAACAGG[C/T]AATGTGAAGGTGGGAAACTGTATATTACTGCAATATAAAGTTGCACTCAT
Long Flanking Sequence:
TTCTCAGTGAAACAGTCAAAAGTCACAATAAAATTAAAGTCTTTGGAAAAGATGGGTAAGAAACTACAGACAAGAAATGGCAATTGATGTTTTTTTCAAACTTCTTATTTAAATTGAATAGAAACAACATAATTCTTGAGTTGTTTATTAATTGTTTTATGTTCAGTCCACTTAGATTTGTAAAAATTCATAAATTAACTTAATTCCTTCATGTTGTCCTAATACAAATCCATCGTGTGAGACACAGCATTTTTTTACAGTGCAGGACAACGCATAATTTCAATAAGCACATTTTTGTGAGTTCTGAATGTATCGGTGTGTATGAGATATGCTCATTTGTGGAGTGTATCCTTTGAAACGTGTGTGTTTTTATCACAGATGTGGACGGAGCATGTCGAGGACGGCCAGACTTGTGTGGAGACGACGCTTTCTGTAATCATAACAAAACTCCCTCCGTCTGCCAGTGCAAAGAAGGCTTTCAGAGGAACCAGAAGAACAGG[C/T]AATGTGAAGGTGGGAAACTGTATATTACTGCAATATAAAGTTGCACTCATATATAATTCATTATTATACTGTTTTAAATTGCATGTTGTTTCTTTATTATAACATTTAAAATCAGCAATAAACAATAAATAATATAAATGTAAATAATATAAATGTTTTTGTTTGTTTGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTTGGTTGGTTTGGTGGATTTGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTTGGTGGATTTGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTTGGTGGATTTGTTGGTTGGTTGGTTGGTTGGTTGGTTTGGTGGATTTGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTGGTTTGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17465
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 |
---|---|---|---|---|---|
ENSDART00000135768 | Essential Splice Site | 1175 | 1629 | None | 35 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 14543229)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14374136 |
GRCz11 | 22 | 14398711 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCRAATGAACGACGGAAAMAGTTTAGTCTGGGTCTGGTTTGCTTTCTTTC[A/T]GGCATCTCTCAGCCCTTCCGYATCGACCTGTTTGAGGACTACATYTACGG
Long Flanking Sequence:
TTTTAGCCTATTTTATTATTCATTTTATGAAATGTCTTTAGAGTCGTTAGTTTGTTCAACTCACTTGCTATCTTGGATGAGCTTTTTTTCATCAAGATTGTTGATTTCTGGGATTGCTAATTCGCAAATATGAAGTTATAATTGTAATGATATTATTGTGTTTTAACCTATTTTATGAATAATTTGTCCTTTTGATCAACTTGTCTGTCATCCTGGTTTAAATGTATCCATTAAGATTATCTAATTTTGCAGGGTTGTAAGCATGACTAAAAATGCTGTCTACATAGGGCACTCACTAGATTTCACAACAGAATATTTCAGATAGAGGTAAACAAACTGAAATATTCTGGGCATGTATTGCATTTTTCTTCTCGCTGACATTTCTCCTCTTTTGTTTTACATTATTGAATCTCCATTTGCCCTCAGACTCGCACATGGATCATATTAATTGCAAATGAACGACGGAAACAGTTTAGTCTGGGTCTGGTTTGCTTTCTTTC[A/T]GGCATCTCTCAGCCCTTCCGTATCGACCTGTTTGAGGACTACATCTACGGGGTGAGCATGAAACACGACATCTTCAGGGTTCATAAATACGGGAAGCTGCCCGCCGAGAGGCTCAGTCTAGGAGTGGAGAGATCATCCAGTGTCCTGGTTTTCCATCGATACAAACAGCAGGAAGGTGAGTCTCACAAAAAAAAAAAAAGCAACAGAGGAGGCTTTTGTCATCCTTCATTCACCATTTTCTACATTAGGTAAGACACTTCAGGTACATAGAGTAAAAAATAGTAACTATCATCATTTTTTCCAAGGTGATTGATTACATTAGTTGACTGTTAATTAATAGTTTCTATATTTTGAATTTTCTGTTTATTTACCTCTGTGAATTGCATTATGAGATCTTGATTTCTGCTTCGTCGACTTTTGATGCTGAAAATTCAATTCAACAGTGACTTTTATTAACATTTTAGTAAATGAAATAATACTGTATATTGTATAAGAAACAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12543
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 |
---|---|---|---|---|---|
ENSDART00000135768 | Nonsense | 1293 | 1629 | 28 | 35 |
ENSDART00000135768 | Nonsense | 1293 | 1629 | 28 | 35 |
The following genes are also affected by this mutation:
Genomic Location (Zv9):
Chromosome 22 (position 14534644)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 14365551 |
GRCz11 | 22 | 14390126 |
KASP Assay ID:
2261-6565.1 (used for ordering genotyping assays)
KASP Sequence:
ATCTGTGTCGTCCTGCCTGTGAGAMTGGAGGTCGRTGTATCACTAATGAA[C/T]GAGGGGAATCCCGCTGTTTTTGTTGGCCAAATTACTCTGGTGAACGCTGT
Long Flanking Sequence:
CTTTTTACTTTAAGGCAATAGCTTTAGTACTGTAGTACTAAATATCCAATTTACAACAAGGCACATAAATAAATTACATCCTGATCTTTTTTTATTATTATTATAATTGTTGTTTTCTTGTGCATTTAAAGAAGAACAATCTTTCATTTATTGATGGGTTTTGTTAATTAAAATGAAATGTATAAATCACTAATTGTTAAACAGATAGGACAAAAAACAATATTAGCTTATTTTCTTCCCTCAACTCTCTGATTGGTGGAATATCTGCACAGCATCATGGGTAATGTAGTTTTCACCACAAATTCACCTGTTAACCACTTTGACGAAGCAAACAAATTCTCTGCGCTGACAGCAGGTTTTGTCTTTACATATTAATGCTTCATCCTTAAAGTTGTAATTTAATTTGTAGAATATGATGGAATTGAACAGGTTTTACTTGTGTTTTAGGAGATCTGTGTCGTCCTGCCTGTGAGAATGGAGGTCGGTGTATCACTAATGAA[C/T]GAGGGGAATCCCGCTGTTTTTGTTGGCCAAATTACTCTGGTGAACGCTGTGAAATCAGCCACTGTAAAGACTTCTGTCTTAATGGAGGAACCTGCACTGGATCTCCACTAGGTTGGCACTGTTTTTTTGTTTATTCACCGTCTATAAATGGGTTAATTCATTCATTCATTTTCTTTTTTGGCTTAGTTCCTTTATTAATCTGCACAGCCGAGGCTCGAACTAGCGACCTTCTTGCTGTGAGGTGACAGCACTACCTACTGCACCACCGTGTCACCCCAATGTGTTAATTTCAAATGTAAAAGAGGCCAGAAACACCATTTTGAATTCTGCTCCAAAGGAGCCGTACACAAACATGTTTTATTTACTCGCATGTACTCATATTTTTCACTGTAAGAAAATCAAGGAGTTTAAAATATAACTCAATACTTTAGATCTCCATGCACATTCTGCTGAAAGGTTGGAAAAGTCCTTGACCTTGAAATACTGTAGATTTCAGTATC
Associated Phenotype:
Not determined