ZMP
Q1RLV8_DANRE
Ensembl ID:
Description:
LOC573743 protein [Source:UniProtKB/TrEMBL;Acc:Q1RLV8]
Human Orthologue:
ZBTB41
Human Description:
zinc finger and BTB domain containing 41 [Source:HGNC Symbol;Acc:24819]
Mouse Orthologue:
Zbtb41
Mouse Description:
zinc finger and BTB domain containing 41 homolog Gene [Source:MGI Symbol;Acc:MGI:2444487]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25102 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa9876 | Nonsense | Available for shipment | Available now |
sa14303 | Essential Splice Site | Available for shipment | Available now |
sa16227 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa25102
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089618 | Essential Splice Site | 357 | 733 | 4 | 10 |
ENSDART00000108841 | Essential Splice Site | 457 | 833 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 2 (position 13597103)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 14081762 |
GRCz11 | 2 | 13764679 |
KASP Assay ID:
554-7691.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTAAGTCACGGTTTGCCAGGCTAAAGCACCAAGAAAAGTTCCATTTAGG[T/A]AAAGTTTTCCTAAAACCATTTTTCTGAATGTGTTGTTTTTCTTGTTTCAT
Long Flanking Sequence:
TAATTTAATGCATTTACTTGCTGCAGTTCACAATATATATTCAGGCTTGTTTTTTGGCTTTGGAATTCTTTATTGTTTAAGCATGAAACATGTTGTCTGCTAACAGATTTCATCCTGACCACCTGCAGGAGTTTCTCACTCAGAAGAAGAAGAGTGAAGTGTGGAAATGTGATGTGAGTCATATGCCTTATTTATTCTTTGTTATTTTATATGCATTTTTAACATGTTATTAATATATGCCAATTGCCACAGAATGCCATAAAGTTTTAACTAAATTCTGTTTGTGAACACTTTTCATTTGTCTGCAGTTAGTCTAAATTTGTCATTTTGTTTTTGTTGCATCTTTTGCAGATCTGTCACAAGTCCTTCAGCCGTCGCCCCCACCTGGAGGAGCACATGATCTTACATTCACAGGATAAACCCTTTAAGTGTGCCTACTGTGATGACTACTTTAAGTCACGGTTTGCCAGGCTAAAGCACCAAGAAAAGTTCCATTTAGG[T/A]AAAGTTTTCCTAAAACCATTTTTCTGAATGTGTTGTTTTTCTTGTTTCATCTCTGTTCTGTGGTGTGAATGCACCAAAAAGTTGAAGTCTTATTCAGCTCAAAACATTCTTTTAATGTTCACAAAATGTCCATAATTCAGGACCATTCCCTTGTGACATCTGTGGTCGTCAGTTTAATGACACAGGCAACCGCAAACGTCATATAGAGTGCACACATGGGGGAAAGAGGAAATGGACCTGTTTTCTGTGCGGCAAATCAGTTCGAGAGAGGTGAGAGAAGTTGCTTTTATTCTCAATCTTTAGTCATGTTTCCATCCAAAGATGCAAACGTTTTATGTGAATATATCTAATTTGTATCTAAAGCACCATTTCCATTACCATTTTGTTTCATTTTAGAATGATCTAAACAACATTTCAGACGTTGTGCTATGTGGGTCCGTCCACTGGTTTGTCCATAAATGCCATCCCATTGTGCATATTTTTGTTATCACATGGTCTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9876
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 |
---|---|---|---|---|---|
ENSDART00000089618 | Nonsense | 384 | 733 | 5 | 10 |
ENSDART00000108841 | Nonsense | 484 | 833 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 2 (position 13597324)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 14081983 |
GRCz11 | 2 | 13764900 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTTTAAWGACACAGGCAACCGCAAACGTCATATAGAGTGCACACATGGG[G/T]GAAAGAGGAAATGGACCTGTTTTCTGTGCGGCAAATCAGTTCGAGAGAGG
Long Flanking Sequence:
ACATGTTATTAATATATGCCAATTGCCACAGAATGCCATAAAGTTTTAACTAAATTCTGTTTGTGAACACTTTTCATTTGTCTGCAGTTAGTCTAAATTTGTCATTTTGTTTTTGTTGCATCTTTTGCAGATCTGTCACAAGTCCTTCAGCCGTCGCCCCCACCTGGAGGAGCACATGATCTTACATTCACAGGATAAACCCTTTAAGTGTGCCTACTGTGATGACTACTTTAAGTCACGGTTTGCCAGGCTAAAGCACCAAGAAAAGTTCCATTTAGGTAAAGTTTTCCTAAAACCATTTTTCTGAATGTGTTGTTTTTCTTGTTTCATCTCTGTTCTGTGGTGTGAATGCACCAAAAAGTTGAAGTCTTATTCAGCTCAAAACATTCTTTTAATGTTCACAAAATGTCCATAATTCAGGACCATTCCCTTGTGACATCTGTGGTCGTCAGTTTAATGACACAGGCAACCGCAAACGTCATATAGAGTGCACACATGGG[G/T]GAAAGAGGAAATGGACCTGTTTTCTGTGCGGCAAATCAGTTCGAGAGAGGTGAGAGAAGTTGCTTTTATTCTCAATCTTTAGTCATGTTTCCATCCAAAGATGCAAACGTTTTATGTGAATATATCTAATTTGTATCTAAAGCACCATTTCCATTACCATTTTGTTTCATTTTAGAATGATCTAAACAACATTTCAGACGTTGTGCTATGTGGGTCCGTCCACTGGTTTGTCCATAAATGCCATCCCATTGTGCATATTTTTGTTATCACATGGTCTTAAAAAACGTTTTTCTTTTTGTTTTGTTTTTATGTGCATGCAGGAATTTATTTGATAAATGTGTTTCGTTGTTGTTCATGCACATTTTTTCTTGTTTCGTATTTTTTTCTTAGGTTTATCTAACTCAGTTGTGTGCAAACGTTGTTTTATTATGTGCATTTTTTTATTTAATGTGCATCTTGGCATTTCTATTGAAAATATTTCAAAGTGTGCATAAAAAATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14303
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 |
---|---|---|---|---|---|
ENSDART00000089618 | Essential Splice Site | 400 | 733 | 5 | 10 |
ENSDART00000108841 | Essential Splice Site | 500 | 833 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 2 (position 13597375)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 14082034 |
GRCz11 | 2 | 13764951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAAGAGGAAATGGACCTGTTTTCTGTGCGGCAAATCAGTWCGAGAGAGG[T/A]GAGAGAAGTTGCTTTTATTCTCAATCTTTAGTCATGYTTCCATCCAAAGA
Long Flanking Sequence:
AAATTCTGTTTGTGAACACTTTTCATTTGTCTGCAGTTAGTCTAAATTTGTCATTTTGTTTTTGTTGCATCTTTTGCAGATCTGTCACAAGTCCTTCAGCCGTCGCCCCCACCTGGAGGAGCACATGATCTTACATTCACAGGATAAACCCTTTAAGTGTGCCTACTGTGATGACTACTTTAAGTCACGGTTTGCCAGGCTAAAGCACCAAGAAAAGTTCCATTTAGGTAAAGTTTTCCTAAAACCATTTTTCTGAATGTGTTGTTTTTCTTGTTTCATCTCTGTTCTGTGGTGTGAATGCACCAAAAAGTTGAAGTCTTATTCAGCTCAAAACATTCTTTTAATGTTCACAAAATGTCCATAATTCAGGACCATTCCCTTGTGACATCTGTGGTCGTCAGTTTAATGACACAGGCAACCGCAAACGTCATATAGAGTGCACACATGGGGGAAAGAGGAAATGGACCTGTTTTCTGTGCGGCAAATCAGTTCGAGAGAGG[T/A]GAGAGAAGTTGCTTTTATTCTCAATCTTTAGTCATGTTTCCATCCAAAGATGCAAACGTTTTATGTGAATATATCTAATTTGTATCTAAAGCACCATTTCCATTACCATTTTGTTTCATTTTAGAATGATCTAAACAACATTTCAGACGTTGTGCTATGTGGGTCCGTCCACTGGTTTGTCCATAAATGCCATCCCATTGTGCATATTTTTGTTATCACATGGTCTTAAAAAACGTTTTTCTTTTTGTTTTGTTTTTATGTGCATGCAGGAATTTATTTGATAAATGTGTTTCGTTGTTGTTCATGCACATTTTTTCTTGTTTCGTATTTTTTTCTTAGGTTTATCTAACTCAGTTGTGTGCAAACGTTGTTTTATTATGTGCATTTTTTTATTTAATGTGCATCTTGGCATTTCTATTGAAAATATTTCAAAGTGTGCATAAAAAATAGGTGGATGGAAGCATAATTGCATAATTATATAAACTGTTTGCAAATGTTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16227
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089618 | Nonsense | 577 | 733 | 10 | 10 |
ENSDART00000108841 | Nonsense | 677 | 833 | 11 | 11 |
Genomic Location (Zv9):
Chromosome 2 (position 13632733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 14117206 |
GRCz11 | 2 | 13800123 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGATGTACGTCCTTTCAACTGCCCACACTGCAGTGCTACCTTCAAGCGT[A/T]AGRACAAGCTCAARTATCACRTTGATCATGTGCACAGTGTTCRTCTGCTT
Long Flanking Sequence:
CTCTTGCCCCCCCATAGCACCAGGCCTGTGTATGAATGAGCTTAACAGAGGAGAAAAGTCAGAGTTTAGCAGCTGTTGAACATGTGCACCTGCACTACAGAGAAAGGAAGGCTTTGACAACTTTCATTCTTAGTTGTTATGGTTACTACTAATGTTTGCAGTTATTTAAAATTGATCAAAACTGACTGGAACTACATGTACATTTCAGCAAATTTAATGCATGGCCTTCAGCCAGAATTTCAATAGACCCTGATTGTAATTGTAATGACAATTGAGAGATGTACAGTGTCTCAAAAATCCTGATGTATCGTATTTTAAACATTTTAACATGATTTTTCTTTTTCTGATTGAATATTTTGTTCTCCTTAGGTGAGAAACCCCACAAGTGTGTGATCTGTAACCAGACGTTCAGCATCAAGAAAACTTTGACCAAACACATGGTTATTCATTCAGATGTACGTCCTTTCAACTGCCCACACTGCAGTGCTACCTTCAAGCGT[A/T]AGGACAAGCTCAAGTATCACGTTGATCATGTGCACAGTGTTCGTCTGCTTGACCAGCAGCAGAATCAGCCTGCCAGCCCTGCTAACAAGTTAATCGACCCATCACTGTCAAATAAAAATTCCAAACCATGTCAAAATGCATCTAAGACTGTGCTGCAGAGTGTGGCAGCTGATGTTTGTGTTCCTGTGACACTCATTCCTGTACAGATGACTGAGGAAGCTGATCTTGCTGTTCATGGAGTGCCACATGGCATTCTTCCTGCTTTAAGCCAGCCACAGCAGAGCTACCAGTCTGCCACTGACTTAGTATTCTTGGAAAAATACACTCTCACACCTCAGCCAACCAATATAGTGCATCCAGTGCGAGTAGAACAAATGCTGGACCCTCGAGAGCAGTCTTACCTAGGCACACTTCTGGGACTGGACTCAGCTACACCTGTACAAAACACGTCTAGTGCTGAACATACTCAATAAATTGTCATATGCATGTCTTTGTGTGAT
Associated Phenotype:
Not determined