ZMP
zbtb4
Ensembl ID:
ZFIN ID:
Description:
KAISO-like zinc finger protein [Source:UniProtKB/TrEMBL;Acc:Q06Z31]
Human Orthologue:
ZBTB4
Human Description:
zinc finger and BTB domain containing 4 [Source:HGNC Symbol;Acc:23847]
Mouse Orthologue:
Zbtb4
Mouse Description:
zinc finger and BTB domain containing 4 Gene [Source:MGI Symbol;Acc:MGI:1922830]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa12821 | Nonsense | Available for shipment | Available now |
sa12483 | Nonsense | Available for shipment | Available now |
sa1477 | Nonsense | Available for shipment | Available now |
sa35289 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44762 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa22094 | Nonsense | Available for shipment | Available now |
sa35288 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa17032 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa12821
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 |
---|---|---|---|---|---|
ENSDART00000073962 | Nonsense | 122 | 1529 | 1 | 2 |
ENSDART00000088650 | Nonsense | 122 | 913 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 23892470)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22415620 |
GRCz11 | 12 | 22536839 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTAAGAACTGCAAGTCATCTCTGTCAGTTTCTGTTGATGGTAGTGRTTCC[A/T]GATACCCMGCATCTCCTTTACAAYACTCTAATAAAATGGACAGTCCAAAG
Long Flanking Sequence:
AGATAAAACAGACACTCAGAGTCTTGAATTTTCCAGGATCTTGTTGGACAACAGAAAGACCCTTTGAATGTCTAGTGCTCTGATTTAGACCAACTGTAGCCTTGGAGAGCATCTCAGAGGATTTGAACAAGGATCCAATGAAACACAGAAATAAGCACATTAGAGGAGACAGGATGGGAGAGGGCACAGAGGAGGCAAATAGTGCCAAAACAACAAGGATATCACTTAGTTTTCCCCTTAGTGCAGGATTGCCTGGCTTTTCTGCACAGAAGCACTGTTCCTCATCCCCCCCCACTTCCTCTTCTGACGTCCATAGCAAAGATGGCTTAGATGGCACGGCATGGATGGAGGAAACATATAGAGACAAACAGTTATCCAAAACGTCATCAAAAACTGACCGTCTGCCATGCTCTTCCTCCTCCTTCCCTGTCGATCTAACTGCTCCAGTCAGTAAGAACTGCAAGTCATCTCTGTCAGTTTCTGTTGATGGTAGTGGTTCC[A/T]GATACCCAGCATCTCCTTTACAACACTCTAATAAAATGGACAGTCCAAAGGAAACAGCTGGGGTCAGTCTCAATAATGGATACAAAGAGCATTCAACAACAGAAACAGCACATATCCTTTTCAACCTTAGTGCAAGAGCCTACCAGGACCAAGGTGTAAAGGACCCAGAGAATTCAAAAGGCAAAAAACGCAAAGCAAACAGCCTTCATGTTGAACTGAGCCTTCCTCTCCCCAGCATCAACCCTCACTCTTCCTCATCAACTCCTCCTCCTCATTCGCCCTCGTCTGTCTCTCTAACTTCCTCCCCCTTGACTCACCCCACAGCATCTTTCCATGACTCCTTTAGGGCAGTGCCGAAGCCAGAACTACTGTGTGGGGTGTGTCACCGTCTGTTCAGCACTGCATCGTCCCTCACTGTCCACATGCGTCTCCATCGGGGGGGACGAGTACTCAGCTGCCGACACTGTGGCAAAGCCTTCATCCATAATAAAAGACTGCAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12483
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 |
---|---|---|---|---|---|
ENSDART00000073962 | Nonsense | 403 | 1529 | 1 | 2 |
ENSDART00000088650 | Nonsense | 403 | 913 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 23891625)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22414775 |
GRCz11 | 12 | 22535994 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTGTCCAGCCTGMAGCGACACTCCARTGTGCATTCCTGGCGCCGGAAGTA[C/A]CCCTGTCACTTCTGTGACAAGGTTTTTGCTCTGGCTGAATATCGTACTAA
Long Flanking Sequence:
AGGGCAGTGCCGAAGCCAGAACTACTGTGTGGGGTGTGTCACCGTCTGTTCAGCACTGCATCGTCCCTCACTGTCCACATGCGTCTCCATCGGGGGGGACGAGTACTCAGCTGCCGACACTGTGGCAAAGCCTTCATCCATAATAAAAGACTGCAATCCCACGAGGCCACCTGCAGGCAAGGACTGCCAGCTTTTCCAGTGCCACCCAAAGAAGAGCCCCTGGAGGAGGGTGAAGTGGAGGGGGAGAGAACAGATGAGGCTGCAGAGCCAGAACAGCTTGGACAAGAAACAAGGCCTGGCCAACCCACAAAGAAAGTGCGAGACCTTACAGCCCGTCATGCTGAAGCACTGACATGCGGGGATACCCTGGGGGATGACGATCACTTTGTTAAAGTGGTGGATGGACATATTATTTACTTTTGCTCAGTGTGTGAGCGCTCTTACATGACATTGTCCAGCCTGAAGCGACACTCCAATGTGCATTCCTGGCGCCGGAAGTA[C/A]CCCTGTCACTTCTGTGACAAGGTTTTTGCTCTGGCTGAATATCGTACTAAACATGAGGTGTGGCACACTGGTGAGCGACGCTACCAATGCATCTTTTGCTGGGAGGCATTTCCTACCTACTACAACCTTAAAACACACCAAAAGGCTTTCCATGGCATAAATCCAGGCTTGATCTCAAGTGAAAAAACAGCTAATGGTGGCTACAAGCAGAAGGTCAATGCCCTTAAACTTTACCGCCTGCTGCCCATGCGATCCCTAAAACGACCTTACAAAACCTATAGTCAGCCAATGGCTGATGGACTACTAACTTCTGACTCAACTGATAACCTGCATTTGTCTGTAGATGGCAGCCTTCCACAACCCTTGGACACAAAGAAATTGGAGTCTTTCCTGAAAGATCTTCAAAACCAAGACATCAAGGCTGAGGCTGAGGGATTCCCCATCAGGATGGACATAGAGCAGGGTACAGAAATAGCATCTCCACAAACAGATATGGCACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1477
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 |
---|---|---|---|---|---|
ENSDART00000073962 | Nonsense | 628 | 1529 | 1 | 2 |
ENSDART00000088650 | Nonsense | 628 | 913 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 23890952)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22414102 |
GRCz11 | 12 | 22535321 |
KASP Assay ID:
554-1402.1 (used for ordering genotyping assays)
KASP Sequence:
CCTCAGTCATCATGCACAGCACTGCAGTTTCTTCCTCTGTCATTGTTCAC[A/T]GAAATAAGACAGACTCTGAAGAGAGAAAAAGAAGTCCAGAAAAGCATCAA
Long Flanking Sequence:
TCTCAAGTGAAAAAACAGCTAATGGTGGCTACAAGCAGAAGGTCAATGCCCTTAAACTTTACCGCCTGCTGCCCATGCGATCCCTAAAACGACCTTACAAAACCTATAGTCAGCCAATGGCTGATGGACTACTAACTTCTGACTCAACTGATAACCTGCATTTGTCTGTAGATGGCAGCCTTCCACAACCCTTGGACACAAAGAAATTGGAGTCTTTCCTGAAAGATCTTCAAAACCAAGACATCAAGGCTGAGGCTGAGGGATTCCCCATCAGGATGGACATAGAGCAGGGTACAGAAATAGCATCTCCACAAACAGATATGGCACTAGAAGCAGGACAGGTAGAGGATTCAGATTTGTGGCCATCAGGTAATAACAACGACAAAGGCCAAACTCCAAAGTGCCCAGAAAGAGCTGTGTCTTCAGTCATAGCATTTGCACGCAGTAAACCCTCAGTCATCATGCACAGCACTGCAGTTTCTTCCTCTGTCATTGTTCAC[A/T]GAAATAAGACAGACTCTGAAGAGAGAAAAAGAAGTCCAGAAAAGCATCAACTGGCAAAGACAGATCAAAAAACAATAAAAAAGCATAGCCAGAAAGAGCACACAGAGGCATACAGGGAGTGGAATGCTGTCGGTTCAGACCCAGAGATCTCAAAAATCAGACATCCAACGGAGAAACTTCACAAGGGACGAAAAGTTCACCATAAAACAGACTCAAGTAAAACAATACCTTTAGCGGTGGGATCAGAAGTCAAAGGGAGTGGTCCACTTTGTCAGATAACTGTGCGCATAGGGGAGGAGGCAATTGTCAAAAGGAGCATTTCAGAAACAGATCTAAGAAGAGACAAAAGCCCTACACGAAGCAAACCTAAAAAAAGTAACCTCTTACAAGACAAACAGAGAGAGCAAAGACACACCCATCATCACCAACGTAAACATCGCAACTCCAATCAGGAAGGAAAGGAGAGGGAGCCCAAAAGGAAAAGCTCTAAAGTGAAAACC
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:
sa35289
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073962 | Nonsense | 701 | 1529 | 1 | 2 |
ENSDART00000088650 | Nonsense | 701 | 913 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 23890733)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22413895 |
GRCz11 | 12 | 22535114 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGGAGAAACTTCACAAGGGACGAAAAGTTCACCATAAAACAGACTCAAGT[A/T]AAACAATACCTTTAGCGGTGGGATCAGAAGTCAAAGGGAGTGGTCCACTT
Long Flanking Sequence:
TGAAAGATCTTCAAAACCAAGACATCAAGGCTGAGGCTGAGGGATTCCCCATCAGGATGGACATAGAGCAGGGTACAGAAATAGCATCTCCACAAACAGATATGGCACTAGAAGCAGGACAGGTAGAGGATTCAGATTTGTGGCCATCAGGTAATAACAACGACAAAGGCCAAACTCCAAAGTGCCCAGAAAGAGCTGTGTCTTCAGTCATAGCATTTGCACGCAGTAAACCCTCAGTCATCATGCACAGCACTGCAGTTTCTTCCTCTGTCATTGTTCACAGAAATAAGACAGACTCTGAAGAGAGAAAAAGAAGTCCAGAAAAGCATCAACTGGCAAAGACAGATCAAAAAACAATAAAAAAGCATAGCCAGAAAGAGCACACAGAGGCATACAGGGAGTGGAATGCTGTCGGTTCAGACCCAGAGATCTCAAAAATCAGACATCCAACGGAGAAACTTCACAAGGGACGAAAAGTTCACCATAAAACAGACTCAAGT[A/T]AAACAATACCTTTAGCGGTGGGATCAGAAGTCAAAGGGAGTGGTCCACTTTGTCAGATAACTGTGCGCATAGGGGAGGAGGCAATTGTCAAAAGGAGCATTTCAGAAACAGATCTAAGAAGAGACAAAAGCCCTACACGAAGCAAACCTAAAAAAAGTAACCTCTTACAAGACAAACAGAGAGAGCAAAGACACACCCATCATCACCAACGTAAACATCGCAACTCCAATCAGGAAGGAAAGGAGAGGGAGCCCAAAAGGAAAAGCTCTAAAGTGAAAACCAAAGTGAGGAAATACTTCTTCCGGCAGGAAGTCAGGGAAGACAGAAATGACCATGATGTAGAGGACAACCTTTGGAGGCCTTATTATTCTTACAAACCTAAGCGAAAGGCTCTTCATATACAAGGAGCTAAAGCCTGGAAACGCAAAATGCACTACAAACGATCCCTGAGGCCTATGAGGAGAGCTGAAAGACTCATGAAAAATCATCTGAATAAAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44762
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073962 | Nonsense | 1034 | 1529 | 2 | 2 |
ENSDART00000088650 | None | None | 913 | None | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 23889599)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22412761 |
GRCz11 | 12 | 22533980 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AATGTGATAAGGTCTGCAAAACCTCTGCTGCACTTAACTGCCACCTCAAG[C/T]GACATGAGTTAGGGAGTTTAACAGAGGTTGAAGATGCACATGAAAAGCAA
Long Flanking Sequence:
AACAGAAGGAAAAAGAAAAGGGAACAAATGGAAAGCCTAATCTCCCTCTCCCTTCAACTGTTCCTCAGGCTACACCTAATCCAACACACACAGCATCCTCTATCATCAAGCAACGATGGTCAGAAGATCAAGCCTCTGAGTGTGGAACATGTGGGCGCTGGTTCTCTAGCCCAAGGAAACGAGACAAACATGAAATGACACATCTGTTTGAGTTTGTATGCATGCATTGCAGAGCTCCATTCCCCTCACAGTTTAAGCTAGAGGAACATCAGAGAAGTCAGCATCCCAAAAACAAGCCCTTGTCTGCCCCCACTTTCTACACTTCACAGTCATCAAAAGGTGAGGTGGAAATGAAAGTGGCTGATGATGATGGAGTGAATGGACGGTCCATTGAGAAAGGCAGCCCAGTTCGCTTGGGCAGGAGACCTTTAATTAGATACACATGCTCAAAATGTGATAAGGTCTGCAAAACCTCTGCTGCACTTAACTGCCACCTCAAG[C/T]GACATGAGTTAGGGAGTTTAACAGAGGTTGAAGATGCACATGAAAAGCAAGACATGCCAAGTTACACACCTCCTGCAGTGGACACTATACCAAGCTTAGGTTTAGACACCAACTGTGAGCAAGTACAGCCAGTGTCTGTCATATATTATTCCAAACCAGAATGTCAAAACACCGATAACGAACTGGGTGAGAAGATGGAAGAACACCAAAGAGTCAGAGATTGTGAAAGCCCTAAGGTGACAAAGAATGAAAAAGTTCACAGTCCACGGTGTGCACAGTTTTCCCAAGTTATTCACAGCCCCACTTTAGAAAGATTTAACGTCATTTCTCCAAACCTCCCTAGTGTTTTGGTAATGAATGGTGCAGAGTGCCTAGACTACAGGACACCAGAAAAGCAAAATTTAGAAAAACTAGATCAGCAGAAAAGAAGCCAGACACCAAGTAACAGACAAATCCAAGTTTCTCAAATGCTGACAGAGCCTCAGATTAGAAGAGAAACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22094
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 |
---|---|---|---|---|---|
ENSDART00000073962 | Nonsense | 1184 | 1529 | 2 | 2 |
ENSDART00000088650 | None | None | 913 | None | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 23889149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22412311 |
GRCz11 | 12 | 22533530 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTTAGAAAAACTAGATCAGCAGAAAAGAAGCCAGACACCAAGTAACAGA[C/T]AAATCCAAGTTTCTCAAATGCTGACAGAGCCTCAGATTAGAAGAGAAACA
Long Flanking Sequence:
AATGTGATAAGGTCTGCAAAACCTCTGCTGCACTTAACTGCCACCTCAAGCGACATGAGTTAGGGAGTTTAACAGAGGTTGAAGATGCACATGAAAAGCAAGACATGCCAAGTTACACACCTCCTGCAGTGGACACTATACCAAGCTTAGGTTTAGACACCAACTGTGAGCAAGTACAGCCAGTGTCTGTCATATATTATTCCAAACCAGAATGTCAAAACACCGATAACGAACTGGGTGAGAAGATGGAAGAACACCAAAGAGTCAGAGATTGTGAAAGCCCTAAGGTGACAAAGAATGAAAAAGTTCACAGTCCACGGTGTGCACAGTTTTCCCAAGTTATTCACAGCCCCACTTTAGAAAGATTTAACGTCATTTCTCCAAACCTCCCTAGTGTTTTGGTAATGAATGGTGCAGAGTGCCTAGACTACAGGACACCAGAAAAGCAAAATTTAGAAAAACTAGATCAGCAGAAAAGAAGCCAGACACCAAGTAACAGA[C/T]AAATCCAAGTTTCTCAAATGCTGACAGAGCCTCAGATTAGAAGAGAAACAACTCCATCTGTACCAATATCACTAAAAACAGGCAGAGGTTATGCATTTACAGACTGTGACAAAAATCCAAATCAAGATTTCAGTGATTTACAAGATGCTCAGGATCTAAGAATCTTTCCTCAATCTAGCAGCCAAGCCCAAGACTTATCCATGCCAACAACACTGGCAAAAAAGAGGGAGCTTGATGAACAGATTAAACATCCATCCAACATCTTAAAAGCCCAGTCTTGTAATGAGGAGGTGTCATTGCTAGTGCCCAAAGAGGAACCACTCAGTCCTATTCCATCTCCCACATGCTCTGTCATTCAAACCACTCCTAAAGGTCTTTCTCAAAGGTATTCAAAGTCAACGTGTCACTCTCCAGAACCTCTGGACCTACAGTTGCGACCACAGTTGGATCATAACCAATCACACAGAGGAAGACACAACTCAGAAAAACAGGGTCTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35288
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000073962 | Nonsense | 1400 | 1529 | 2 | 2 |
ENSDART00000088650 | None | None | 913 | None | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 23888499)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22411661 |
GRCz11 | 12 | 22532880 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTACTCATACAGAACACCACAGGGTCTCGGGCTACCCTGTGCAGGAGTA[T/A]TCTCTTCCAATGGTTATTCCTGGAGGGTACTGTTCTGGTAAGAATCAGGA
Long Flanking Sequence:
CAGGATCTAAGAATCTTTCCTCAATCTAGCAGCCAAGCCCAAGACTTATCCATGCCAACAACACTGGCAAAAAAGAGGGAGCTTGATGAACAGATTAAACATCCATCCAACATCTTAAAAGCCCAGTCTTGTAATGAGGAGGTGTCATTGCTAGTGCCCAAAGAGGAACCACTCAGTCCTATTCCATCTCCCACATGCTCTGTCATTCAAACCACTCCTAAAGGTCTTTCTCAAAGGTATTCAAAGTCAACGTGTCACTCTCCAGAACCTCTGGACCTACAGTTGCGACCACAGTTGGATCATAACCAATCACACAGAGGAAGACACAACTCAGAAAAACAGGGTCTTATGTTGCCAGCAAATTCAGCTGGGATAATCGATCCTTCTTCCCCCGCCCTGCTAAATCCTCAAGTGCCCGCAGCAGAGCCTGAATTAAAAGACATCACCTCTGGTACTCATACAGAACACCACAGGGTCTCGGGCTACCCTGTGCAGGAGTA[T/A]TCTCTTCCAATGGTTATTCCTGGAGGGTACTGTTCTGGTAAGAATCAGGAGGAGCAGATCCTGATGTCTTACCCTGCTGGACCCCTACCATTTCCTCCACTTGGGAAAATGGTACCCCATGCTGACTCCACTAAACTGCCCTTTTACCCCGACCCTTATCACCTACTGTATGGCCCACAGCTACTGCCATACCCTTATAACCTTGCTGCCCTTCCAATGGCTCTAAATATGATGGCATCAGGGGACAAAGAGCCCTTGCCCTTCTTGCCTTTTTTTAATTATGCCGCCGCAGCTGCCCCTTTAACAGGCACATTGCCCCATCCTTTAGTGATGAACCCCAGCCTATACAACAGTGGCGGCAGCAGTAGCACAAAGCAGGACAACCCATAAGTTAGTAAACAATGGCAGCAAGGGAATACTGTATAAGAGCAGAGAAGGCCATTAAGGGTGGAGATTATGTTTTTTTTCTGTTTGTTAACCAAACACTCTTGCACAGCTCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17032
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 |
---|---|---|---|---|---|
ENSDART00000073962 | Nonsense | 1445 | 1529 | 2 | 2 |
ENSDART00000088650 | None | None | 913 | None | 2 |
Genomic Location (Zv9):
Chromosome 12 (position 23888366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 22411528 |
GRCz11 | 12 | 22532747 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCCTRCCATTTCCTCCACTTGGGAAAATGGTACCCCATGCTGACTCCACT[A/T]AACTGCCCTTTTACCCCGACCCTTATCACCTACTGTRTGGCCCACAGCTA
Long Flanking Sequence:
ATGAGGAGGTGTCATTGCTAGTGCCCAAAGAGGAACCACTCAGTCCTATTCCATCTCCCACATGCTCTGTCATTCAAACCACTCCTAAAGGTCTTTCTCAAAGGTATTCAAAGTCAACGTGTCACTCTCCAGAACCTCTGGACCTACAGTTGCGACCACAGTTGGATCATAACCAATCACACAGAGGAAGACACAACTCAGAAAAACAGGGTCTTATGTTGCCAGCAAATTCAGCTGGGATAATCGATCCTTCTTCCCCCGCCCTGCTAAATCCTCAAGTGCCCGCAGCAGAGCCTGAATTAAAAGACATCACCTCTGGTACTCATACAGAACACCACAGGGTCTCGGGCTACCCTGTGCAGGAGTATTCTCTTCCAATGGTTATTCCTGGAGGGTACTGTTCTGGTAAGAATCAGGAGGAGCAGATCCTGATGTCTTACCCTGCTGGACCCCTACCATTTCCTCCACTTGGGAAAATGGTACCCCATGCTGACTCCACT[A/T]AACTGCCCTTTTACCCCGACCCTTATCACCTACTGTATGGCCCACAGCTACTGCCATACCCTTATAACCTTGCTGCCCTTCCAATGGCTCTAAATATGATGGCATCAGGGGACAAAGAGCCCTTGCCCTTCTTGCCTTTTTTTAATTATGCCGCCGCAGCTGCCCCTTTAACAGGCACATTGCCCCATCCTTTAGTGATGAACCCCAGCCTATACAACAGTGGCGGCAGCAGTAGCACAAAGCAGGACAACCCATAAGTTAGTAAACAATGGCAGCAAGGGAATACTGTATAAGAGCAGAGAAGGCCATTAAGGGTGGAGATTATGTTTTTTTTCTGTTTGTTAACCAAACACTCTTGCACAGCTCTTGTGTCTTTTTTGTAAAGCAGCAAATGTATGGAGATTCATAGGAATCAGATGTGGTGGAATGATGGAGAGTGTCTTGAAGACAAAGAAGAAAGGATATGAGGGGGTGAAGAACAAATAATATAACGCCCCCTT
Associated Phenotype:
Not determined