ZMP
si:dkeyp-34f6.1
Ensembl ID:
ZFIN ID:
Description:
zinc finger and BTB domain-containing protein 10 [Source:RefSeq peptide;Acc:NP_001122011]
Human Orthologue:
ZBTB10
Human Description:
zinc finger and BTB domain containing 10 [Source:HGNC Symbol;Acc:30953]
Mouse Orthologue:
Zbtb10
Mouse Description:
zinc finger and BTB domain containing 10 Gene [Source:MGI Symbol;Acc:MGI:2139883]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa36868 | Nonsense | Available for shipment | Available now |
sa18611 | Nonsense | Available for shipment | Available now |
sa16074 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa36868
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 |
---|---|---|---|---|---|
ENSDART00000113797 | Nonsense | 192 | 580 | 2 | 4 |
The following transcripts of ENSDARG00000077101 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 33136853)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 32304660 |
GRCz11 | 19 | 31891973 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGTCGCCGGGAGCCGCTACTTCAAGACCCTTTACTGTCTGACAAAGAGC[G/T]AGAGCTGTGACCAAACTACCATTACACACCTGGATGTGGCAGCCGTGCAG
Long Flanking Sequence:
TGTGAGAGCAGATGATGGAGATTGATGGCGGATGGGATAATGGCCAAATATTTCTCTTCTTAAAGAGCATTAACAAGGGCAGAGTGCGTGCATCCTGAGAGCAGGGGGGTTTATCGGCGCACAGCGCTATAGTTTCCACAGTACTGCAGCTTTCCAGGCTGTTAAACCAGTTCTCTTGTCAGAGTTGTCACTGTACACCTGCCCTTCACTTTGTGTTTACACTGTATACTAATGCTGATTGTCATTTTTGTTTGTTGTCACTCCACCAGGAGATGGAAAGGCCAGAGGACGCGGAAAGCCCGGAGGTGGAGGACTACCGGAACAAGCCCAACGAGAACTCGTACTGCTACCAATTGCTGCAGGAGCTGGACAAACAGCGCAAGAGTGGCATCCTCTGTGATGTCAACATCGTAGTGAGCGGTCAGGTGTTCAGAGCACACAAGAACATCCTGGTCGCCGGGAGCCGCTACTTCAAGACCCTTTACTGTCTGACAAAGAGC[G/T]AGAGCTGTGACCAAACTACCATTACACACCTGGATGTGGCAGCCGTGCAGGGCTTCTCTGTCATCTTGGACTTCCTTTACTCTGGCAACCTCTTGCTCACTAGTCAGAATGCCATCGAGGTGATGTCTGTGGCAAGTTACCTCCAGATGACCGAGGTGGTCCAGTCCTGTCGCGCCTTTATCAAAGACGCCCTTAATATTAGCATCAAGCAGGAAGCCCCCGATTCTGTGGTGGTTGACTATAATAAGAGGCGGACTGTGGCAAAAGATTGTCAGGGTGCCGACAAGAAGCCTAGCAATTTCTGGGCCACCAGCATCCTGTCTAAGCTATCCATCAAGGCCAGTGTCCAAGGCCAAGTGAAGGATGAACCCAGCGATGTGGAAGTGTCTGGGGGAGAAGGCTGTGCGCTGGGAAGCTCTGGTTGGGGTGGGGAGAACTCGTCCGAGTCCACAGAGACGGAGCCACAGGGACCGGGTCCGGTGTTTGTCTGGAACCCAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18611
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 |
---|---|---|---|---|---|
ENSDART00000113797 | Nonsense | 440 | 580 | 3 | 4 |
The following transcripts of ENSDARG00000077101 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 33127039)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 32294846 |
GRCz11 | 19 | 31882159 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GAAGCKCCGGAAAACGCCCTCAATAAGCTGAAGTGTCCCCACTGTAACTA[C/A]ATTGCCAAGCACCGGCGAACACTAAAGAGGCACCTGATCATCCAYTCAGG
Long Flanking Sequence:
CCCATGGGAAATTGAGTGAGTCTTCACTAGCAAAAAAGCAGAGATTGCAGTTTTGTCCGCACTGTAGTTTAACCCAGATAAACAATCAGGCTGTTTTCTTGAATGTTAGTTCAGGAGAACGGCGACTGGAAGGAAAGAGATCTTGCTTTTTATGCAGCTTGTTTACAAGTAGAAAATTGCATTAGACTAATATAGTTATGGCCTCCGGCATGAAGTTTCTATGGCAACTGGCACACTTTCACTTCATGTTTATAGTTTTTTGTTTTATGCGAGGATGACACTGAGGGTTCATGCAGACATTTATTTTCTCTATCTATCACATTAAGCCACTTGCTGTATTTCTGCTAAGCTGTCAATTAAAGTTGATAAAGTGAATGGAGAAAACTTGCATCTCAGAAACCGGTGTGAAAACTGCTGAGAACCTGTTTGTTTGTGTGGTTTCTCCAAGGCGAAGCGCCGGAAAACGCCCTCAATAAGCTGAAGTGTCCCCACTGTAACTA[C/A]ATTGCCAAGCACCGGCGAACACTAAAGAGGCACCTGATCATCCACTCAGGCGTGCGTTCATTCAGCTGCGACATCTGCGGGAAGCTCTTCACTCGCAGAGAACACGTCAAGAGACATTCCCTGGTAAGACACAAGATCAATTGTTGTTGGAGGGTAAATCACATTAAAAACATTTCAAGTAACATCTAAAGAAAAGTTATTTAGAAGATTTTTTTTTCCTTACATTTTTTTCAAACAGTGAAAATCACTAAATGAAATACCTTAGTTTAACTCGTCATTTTTTACAAAGTTACTTTGACTTAATAAAAAAGAGTTTTGTAACTCAACCTGATTATAATAAGCAGAACAGAAGCTGAATGAGTTATGAATCAATTAATTACTTGTGCAATACCAAACCATTTGAGTAGCTATATAGTTGTTTGGACTCAATTTATTATGTTAACTGAACTTTAAATTTGTTACTAATACTCTAAACGATTTATCTATATAAACACAAATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16074
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 |
---|---|---|---|---|---|
ENSDART00000113797 | Nonsense | 552 | 580 | 4 | 4 |
The following transcripts of ENSDARG00000077101 do not overlap with this mutation:
Genomic Location (Zv9):
Chromosome 19 (position 33123874)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 19 | 32291681 |
GRCz11 | 19 | 31878994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACCTGGAGTTYGCCCGCGATGAAGACTTYGACGAAGCCGGAGAAGGGGAC[G/T]AGGACATGGAGGCAGAAGGGGAGGAGCCCAATGAGATTGACCAATCCCAC
Long Flanking Sequence:
ACAATTTTTATTTATGCCATACAATCTAGATATACAAATAGGTGTTTCTTAGTCAAATATAGTCCGATTCTAACAAATGGAATGTTTGTCCAATGGAAAGCTTGTTTATTCGGTTTTCAGTTGATGTAAATTTGTTCATATGATGGTTTTGTGAAATTGAGCCATATGAGTTTTTTTTTGTTCAAGGGTCACAAACACGCGACAGAGATTCTTGCTGATTCATTTCACTCATAATACCAATGCGTCTTGCATCACTCACCAATCTCCCCATTTATGACTTTCACTTTTAGGTGCACAAAAAGGATAAGAAATACAAATGTATGGTATGCAAGAAGATCTTCATGCTGGCGGCCAGCGTGGGCATACGGCACGGCTCGCGACGCTACGGCGTTTGTGTGGAGTGTGCCGATTCTCACCAGGGCACGCAGGAGGGTCTGGAGGGCATGCAGGACCTGGAGTTCGCCCGCGATGAAGACTTCGACGAAGCCGGAGAAGGGGAC[G/T]AGGACATGGAGGCAGAAGGGGAGGAGCCCAATGAGATTGACCAATCCCACTGCGAGGGTGATGCTGGTGCCACCCCCGTGAAGGACTAATGTAGACATAACCTGGTAGAAACACGAATCAAAATGCAAAGTAAAAAAAATATAGCTGGGAAACAATCAACAATTCCAAAGTGCTATCAAACCTCTTTGTTGCACGTGAAGTTATGTCAAAGAGATCTATAGCTTTGTTAGAGAGGGACTCCAATATTTAAAGATTGTTCTGTGTGTCAGAGAAAGAGGTATAATGATATATATATAACAAAAAAAAATCAGGTTTTTCTGTGATGTATTTTGTTTTTCTTTTGTAGGGGATGAGGGTGTACAGAGTTTAGTTTTTTTGAGTTAGGCCAATCATATTAAAAGAAATATTAATTATTTAATTTATGAAGAAAGATATTATGGTCTTATGAAACAGTAGAATTAGTTTTTTGTTTTCTTTTCTTTTTAAATGTACATCTGCTT
Associated Phenotype:
Not determined