ZMP
kdm5ba
Ensembl ID:
ZFIN ID:
Description:
lysine (K)-specific demethylase 5Ba [Source:RefSeq peptide;Acc:NP_001121799]
Human Orthologue:
KDM5B
Human Description:
lysine (K)-specific demethylase 5B [Source:HGNC Symbol;Acc:18039]
Mouse Orthologue:
Kdm5b
Mouse Description:
lysine (K)-specific demethylase 5B Gene [Source:MGI Symbol;Acc:MGI:1922855]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa7348 | Missense | Mutation detected in F1 DNA | Not yet available |
sa27786 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16159 | Nonsense | Available for shipment | Available now |
sa31828 | Nonsense | Available for shipment | Available now |
sa38842 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35081 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35082 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa14585 | Nonsense | Available for shipment | Available now |
sa21908 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa7348
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 > G
Consequence:
Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058729 | Missense | 113 | 1483 | 4 | 29 |
ENSDART00000135443 | Missense | 120 | 1477 | 5 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 25757471)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24586296 |
GRCz11 | 11 | 24823912 |
KASP Assay ID:
554-4114.1 (used for ordering genotyping assays)
KASP Sequence:
ATCAAACATGGAAGTAAACGCGTCCTTTGGTGTCCTCTGTTTCTAGCTGG[T/G]CAAAGAGGAYGGAGGCTTTGATGTGGTCTGTAAAGAGCGGAGATGGACCC
Long Flanking Sequence:
CATAAAGTAGTTTTCTTTATGAAGAATTCAGATATTCTAATTATTAGCTACATCAGTGCCTGTTAAGTTAACTTGGTGCTTGTGCCCACAAGCATAACGTGAAAGAAGCTGAATGGGATTCAGTGCCCTGATGTGATGATAATGTTGTTGTTGTTTTTCGACGCATAGTTGTACAAGTTTAAAAATTACTTTTCTTCAAATATACTAAACATCATAAGCATTCATTTTATGTGTCATAGACATAAACAGGCTCTTAGGAGCTTATGGACCACTTGGGATGTCCAGGAAAGATCAAATTTTTTTGGTACAAATTGTTCACCCGCTAGCAAAAAAAACAGCAAATATTACAAATACTTGAACCTAAACCCTGTTATTGTTTACAGTTTGCAAGTAGTGTCGAATTCTAGAGTTGAAAATGCTGTCATAGACATTCTCGGTGACATTTTAAAAATCAAACATGGAAGTAAACGCGTCCTTTGGTGTCCTCTGTTTCTAGCTGG[T/G]CAAAGAGGACGGAGGCTTTGATGTGGTCTGTAAAGAGCGGAGATGGACCCAGATCGCATTGAAGATGGGCTTTGCTCCCGGCAAAGCTATTGGCTCTCACCTCCGTGCTCACTATGAGAGGATTCTCTACCCATACTATCTGTTCCAGACAGGAGCTAATCTTATGGTGAGGCCGCTAAAGCGATTGTGTAACATCCCCTTTTCATCCTTACATCATCCATTTTCCATCCCTTTTTCCTAATAAATGTTCTTTGTTCTGATGATGCACACATGACAGTCATTGTCCCTGATTATGTTTTGGCAGAGGACTCATCTGTATGTGAACAGAAAGGGTGCCCTAGTTTATTAACAATTGTTGATAAAGCGCCCTAGTTTATATATGTTTTGATTAGAGACAGTAGTTTGGGATAAGTAACACTGCAAACATAAACAAACTACTACTAATGCCCTATAAAACATACACAGAAACAAGTTTAAGTAGCGTCTGGCAGGCTGTCCGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa27786
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 > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058729 | Essential Splice Site | 212 | 1483 | None | 29 |
ENSDART00000135443 | Essential Splice Site | 219 | 1477 | None | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 25759084)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24587909 |
GRCz11 | 11 | 24825525 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAAGCTATATGATAATCGTGAAACTCTGACATTTACCTTTTTTCCCCAA[A/G]GGGCCGCTGTTTTAAATCAGAACCGGGTGAGGTGTGTGAAAACAAACCCA
Long Flanking Sequence:
ACCTGTCTAGTTAACTTAATTAACCCAGTTAAGTCTTTAAATGTCACTGTAAGCTGTATAAAAGTGTCTTAATAAAACATCTAGTAAAATATTATTTACTGTCCTCATGGCAAAGATAGAATAAATCAGTTACTTGAAATTGGTTATTAAAACTTATGTTTAGAAATGTGTTGAAAAAATGTTCTCTCCGTTAAACAGAAATTGGGGGGAAAATAAATCTGACTTCAAATATATATATATATATATATATATATTTACTGACAGCAGTGAATCTCTCTTTAGCAGAACTCTCAAAAACCAACTCTGACAAATGACACCAAAGACAAGGAGTATAAACCCCATGACCTGCCTCAGCGTCAGTCGGTGCAACCAGTGGAAACCTGCACTATTGCTCGCAGAGCTAAACGTACAGAGGTAAAGTTCCTAAAAAATGAAAATATTTATATTGGCTTAAGCTATATGATAATCGTGAAACTCTGACATTTACCTTTTTTCCCCAA[A/G]GGGCCGCTGTTTTAAATCAGAACCGGGTGAGGTGTGTGAAAACAAACCCAACCTGAGGAGGAGAATGGGCTCCTATGTGGCAAAACCAGAACCGGGTACATGTAAGTATTTTTTAAATTTCAGCAATTACTTGTGAGAATCATTTTCAGTATATAAAACGTCATCATGGCTTGGTTTTAGCATCCATCTGTAATACTGTTCATTAAGTCACACTTTTTTTATTCAGGTTGCATTAAATTGATCAAAAGTGACTGCGTTATCATGATAAATGTATAGTTACATATTTAGTAGGGATGCTCTGATCGATCGGCTGGGGATCGGTGTCGGCCGATAATCACATTTAATGACTTGATCAGTACTCGCTGATCTGGCCGATCTCATGAACCGATCGCAAGCGTTTGTTTATTAGTTTACAAGCAGAGGAAGAAGCACATAAAACATACATCCTGGATTATACATACAGCAGCTACAACACGTGAAGATAATGAATGATATGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16159
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 |
---|---|---|---|---|---|
ENSDART00000058729 | Nonsense | 647 | 1483 | 15 | 29 |
ENSDART00000135443 | Nonsense | 647 | 1477 | 16 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 25769573)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24598398 |
GRCz11 | 11 | 24836014 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTRATCCCATTGTGTTTGTGCTGTTCTCCAGGGTATGTGGCACTCCCAG[C/T]AGGTTGACTATGATATACTGCCAGATGAGGAAAGGCAGTGTGCTAAATGC
Long Flanking Sequence:
TTTTAATGCTGGATTGGTATAAACAATACATTAGAACAATCGTGAACCAAACCCCTGGATTTCTTGTCTTTCAGTTGCCTCTTGGTCGACAGTGTGTGGAGCACTACCGATCCCTCTACAGATACTGTGTTTTCTCCCATGATGAGATGGCCTGTAACATTGCCGCCAAGGCAGACAGTCTAGAGTTGGAACTGGCATGCGCTGTCCAGAAGGACATGAACGCTATGATTCAGGAGGAGAAGATACTCAGAGAAAAAGCCTATAAGCTGGTGGGTGGCTATTTTAAAGGCAGCGAGTTGGTTTAAGCTTCTGTAACTTGCACTTGCTGACCCAGTTGGTTAAGTAACCTGTCTAATAAGTTCTGTGTATCTATAATTGTATATATTTTATAAACAATTAAACCTTTATAGCTGTTGCGCCTACTCGCTTTGTTTTGTCTGCCTATTTCTAATTGATCCCATTGTGTTTGTGCTGTTCTCCAGGGTATGTGGCACTCCCAG[C/T]AGGTTGACTATGATATACTGCCAGATGAGGAAAGGCAGTGTGCTAAATGCCGGACCACCTGTTACCTGTCTGCCATCACCTGTCCCTGTAGCCCTGAACAGGTGGTCTGTCTCCACCACACCCAGGACCTCTGCTCTTGCCCTGCTAGAAACTACACGCTCAAGTACGTGTTTGCTAAAGCGAGACATTACCGCATGCCATGGGGTTTAATATTTGGCACTGCTGATCAAATGTTAAGCAGTTGTTGCTTTTATTCCTCATTTATCTTTTTTTTTTTTGGCTTTTTACTTTCAACAGCTATAAATACACACTTGCCGAGCTCAAGACATTTTTCCAGGCTTTGACGGCTCGTGCTGAGTCCTATGATGACTGGGCTTCTAAAGTTAACAAGATTCTGAAAGCCGATCAAGACAATAAAAGTGGTGAGTTGTTGTTGTTGCAGTGTGTTTGTTTTATTTTAAAATATATATCCATCTTGTATTACTTTAGAAAGTAGGGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31828
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 |
---|---|---|---|---|---|
ENSDART00000058729 | Nonsense | 761 | 1483 | 17 | 29 |
ENSDART00000135443 | Nonsense | 761 | 1477 | 18 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 25774095)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24602920 |
GRCz11 | 11 | 24840536 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGAGCTCCGCTGTTTGTTGGCAGAAGCAGAGAAGAAAATGTACCCC[G/T]AGACCGACCTGCTAAATGACATGCGTCAGGTCATCCAGAATGCAGATAGA
Long Flanking Sequence:
ATTAGTTATTAAAAACATTTTAACAAATTTTCCTTTTTTTAAATACTAAGAATTTTAATACTACTACAGTAAAGTCAACAGTTTATCAAAACATTTTTAAAATTAGTTTTAAAACAAGAATAGATGTTTTTCAGTAGTTTTATGACAATTGATCAAAGGTTTTGATCCACTTAGTGCATGCGTGCGTGACACAATCTCCTTGTAATAGCAGTGAGATCAGAGAACAGTGTCTGATTTATGTAGGTAGAAAAATATGGAAATGTATTATCAATAAGTAGGTGCCATTTAAGAGTACTTTGAGTTCTTCTCATCAAAACAGTTCTGTTCCGATAAATGACAGCTACAGTAATGTGTAATTTCACTCATTTGAACTTCAGGTATTATTCAAGTACTTGGCTCAATCATTGCATTTATTTCTTTAAAGTTTTAAATATTTTTTTATGTTAGATTTGGAGGAGCTCCGCTGTTTGTTGGCAGAAGCAGAGAAGAAAATGTACCCC[G/T]AGACCGACCTGCTAAATGACATGCGTCAGGTCATCCAGAATGCAGATAGATGTACCATAATGGCCCAACAACTCCTCAATGGCAAGAGACAGACCAGGTACATTTATTGCCTTCTCTGATATGTAAATCTATCCACAGATCTTGCAGAACGTGCTTTAAACTAATGCAAAACTGTAATCCTATACTCATCTTGGTGAACAGGTATCGCTCCGGTGGGGGAAAGTCTCAGAACCAGCTCACAGTAGAGGAACTGAGGGCATTCATCAATAAGCTATATGACCTTCCCTGTACCATCCGACAGGCTCCTTTTTTGAAGGTATTAAAATTTAAAACATCTTGCGTAATTCTCACAGTCCCCAGATTTCTTTTTTTAGTGTTCATTGTAAATGTTAATTTGAGTACAATCATAGTATTTCAAATTACATTTGGTCCACAGAATGTGATCTTTAATGATCTTACAATATAAAGACTATGTTCATGTGGCAGGTTTGACTATACGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38842
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 |
---|---|---|---|---|---|
ENSDART00000058729 | Nonsense | 826 | 1483 | 18 | 29 |
ENSDART00000135443 | Nonsense | 826 | 1477 | 19 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 25774394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24603219 |
GRCz11 | 11 | 24840835 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTGAGGGCATTCATCAATAAGCTATATGACCTTCCCTGTACCATCCGA[C/T]AGGCTCCTTTTTTGAAGGTATTAAAATTTAAAACATCTTGCGTAATTCTC
Long Flanking Sequence:
AGTTCTTCTCATCAAAACAGTTCTGTTCCGATAAATGACAGCTACAGTAATGTGTAATTTCACTCATTTGAACTTCAGGTATTATTCAAGTACTTGGCTCAATCATTGCATTTATTTCTTTAAAGTTTTAAATATTTTTTTATGTTAGATTTGGAGGAGCTCCGCTGTTTGTTGGCAGAAGCAGAGAAGAAAATGTACCCCGAGACCGACCTGCTAAATGACATGCGTCAGGTCATCCAGAATGCAGATAGATGTACCATAATGGCCCAACAACTCCTCAATGGCAAGAGACAGACCAGGTACATTTATTGCCTTCTCTGATATGTAAATCTATCCACAGATCTTGCAGAACGTGCTTTAAACTAATGCAAAACTGTAATCCTATACTCATCTTGGTGAACAGGTATCGCTCCGGTGGGGGAAAGTCTCAGAACCAGCTCACAGTAGAGGAACTGAGGGCATTCATCAATAAGCTATATGACCTTCCCTGTACCATCCGA[C/T]AGGCTCCTTTTTTGAAGGTATTAAAATTTAAAACATCTTGCGTAATTCTCACAGTCCCCAGATTTCTTTTTTTAGTGTTCATTGTAAATGTTAATTTGAGTACAATCATAGTATTTCAAATTACATTTGGTCCACAGAATGTGATCTTTAATGATCTTACAATATAAAGACTATGTTCATGTGGCAGGTTTGACTATACGTTATACTTAAATAATTTATAAAAAGAAAAGAAACCGAAAGGAAGCACTATTGACCAATGTGAGAACATGCGTCTTAATACAATTCCCTTCTGAAATATTTCAAATTACCTTCATAATGCATATATTTATTAGACAATACATGCATATTTGTAGATGTATATATTAATGTACTTAAATATACGTAAACATATGTATATTTTTCTATGAATTGATCATTCTCAGGGCTCGCAAAATCCCATAACCTGGCGTCCCCAGGCTATTAATTTTTTTGTCGGGCTATCAAAATCTATCTACACCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35081
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 |
---|---|---|---|---|---|
ENSDART00000058729 | Nonsense | 1067 | 1483 | 22 | 29 |
ENSDART00000135443 | Nonsense | 1067 | 1477 | 23 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 25779151)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24607976 |
GRCz11 | 11 | 24845592 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTCTGTGTTTGTCTTGAAGGTTTTGTGTCCTAGGTGTGAGACGGGATCG[C/T]AGAAGTCCAAGTCTAAAAAGGCGAAGGAAGGCTTGGTACCATGCAAGAAA
Long Flanking Sequence:
TCCCAGCATACTTGCCCAGCTGTCTTCAGCTCAAAGACTGTGTAAGCAGAGCCAGAGAGTGGATAATGGAAGCAGATGCTCTTCAGGTACGTTTCCCATGTTTCTGTAGTGCTCCATTATTCAAGACTCTATGATTGGATACATGGAACCCTGTGTAAGTGGCTCTCGGTCCATTTAAACATTTATTGCTACAGGCTGGAGGGCGTATTCCTGGTCTGGTCACCCTTTCTGAACTAGTGTCAAGAGCCAAAGGTATTCCCGTAATGTTGGAGGCACTCACTCGACTGGAAAGCTTAATATCTGAGGTTCAAGCTTGGAAGGAAAGTGCAGCTAAAACATTCCTGTTGAGGAACTCATCCCTCTCTCTCCTTGAGGTAGATGCTCGATTTATTAAAATACCTATTTTGTGTGGTAACATAATTTTTAGGTGGGTAAATTCATTGTTATTGACTTCTGTGTTTGTCTTGAAGGTTTTGTGTCCTAGGTGTGAGACGGGATCG[C/T]AGAAGTCCAAGTCTAAAAAGGCGAAGGAAGGCTTGGTACCATGCAAGAAAGCTGATGTAAAACTGGACTCCCTTTTTGATGTGGAAAAAGTGCTTTCTACGAGCAAAGATACAGCTTCAGCGGTAGGCCACTTTTTGGTGCAGAACAAAATGAAGGTTTTGTTTTGTACTGGCAACCCTTGTAAATTTTTTGCAAGACTCAAAAGAAAGAGTTTCTGAAGGTTTTAAAATTTGTTCAACCAAATTTAATACCTTAATTATCTTAAATCATATAGTAAAAAAAAAAGCCTTGGCTATAATTTTAAAGGGAAAATTAAAATTTGACAATGGAAAAAGCGAAATCAAAAGTGTCTCAATGTAAATATTAAACATTGAATTTCTATCGTTATATTAAAATAACAGCACTGCTGTTTTACACTCAATACTGTGATTCAATTGCTTATTCTAATGCTTAAAGCATGAGATAAAACATTTTCATGATTCATCAAAATTAGATTATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35082
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 |
---|---|---|---|---|---|
ENSDART00000058729 | Nonsense | 1206 | 1483 | 23 | 29 |
ENSDART00000135443 | Nonsense | 1206 | 1477 | 24 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 25781554)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24610379 |
GRCz11 | 11 | 24847995 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTCTGAGAAGCCACCCCTGGATAAGGTGCTTCCTCTGCTCGCATCCTTA[C/T]AGCGGATTCGGGTACGGCTTCCTGAGGGCGATGCTCTGCGATATGTGATT
Long Flanking Sequence:
ATGGTGTTGTGTAAACTGCTTTTAGATGCATATTAGTATAGCTTAAATATTTATGTGCATTAACAAGTCTGAAATATGACTTTGAAAACTCTTAAATGCTATGACTGCTAAAACCTTATATTTACCTTTGTTATTTGTTTGTTCTTGAGTCCTGACTGCTCAGGTCTGTGTTATACACTCATATTGGTTTGCTCTCCTCCAAACAGATGGCCACTCTCAGTGACGTACATCAGAAAGAGCTGGACAGCCTGTCCATGTTGAGGACCTCAAATGAGTCAAAGTTCCAGTCTTCGCCCAGCTGTTTGGCCCCCACAGTGTGCTTGTGTCACACCGTCCCTGCGGGCCCCATGCTCCAATGTGAACTCTGCAGAGACGCCTACCACAGCGGCTGCGTGCCAGGCTTCAAAGACATCCAGATAGGGCAACCCTGGTTATGCCCACTCTGCAAGCGTTCTGAGAAGCCACCCCTGGATAAGGTGCTTCCTCTGCTCGCATCCTTA[C/T]AGCGGATTCGGGTACGGCTTCCTGAGGGCGATGCTCTGCGATATGTGATTGAGAGAACGGTGCGCTGGCAACACAAAGTGCAGCAGGTTTCTCTTCCTACACTGCATCCAAACGGAAAGGTGAGAATTTTGTGCTCCAATATAAACAGCTCGTAAGATAAATGCTTTGATTTAATTTGAGGATGTTTCAATTTATTTATTCGATGCAGGCAAGGCACATTTCTGGTTTTACATCATCTCAGACACTGGAAGGGAGCAACAGTTCTTTCTACATGCTGCAGCCGTGTATTCCTCTCAGTGGTGAGTCGGTGACCTCTGATGTTTTAATAAATCTCACAGAGTGCTTGTAAACGTCTGGATGTGAACAGCTGGGAACCTGTGGTGTGTTCTAGAGCTCAGTGCTGAGTTGGAGGAGCTGCTGGTGGAAGGGCTTCTCCTGCAGGTGACTTTGCCGGAGCTCCAGCAGCTTTATAGCAGCCTGATCAACAGGTTTTCACCATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa14585
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 |
---|---|---|---|---|---|
ENSDART00000058729 | Nonsense | 1451 | 1483 | 28 | 29 |
ENSDART00000135443 | Nonsense | 1447 | 1477 | 28 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 25784159)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24612984 |
GRCz11 | 11 | 24850600 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCGTCCTCTCAGGTAAACTGGGTCCAGTGTGACGGCAGCTGTAACCAGTG[G/A]TTCCACCAGGTCTGTGTGGGAGTGTCTGCTGAGCAGGCYGAAAACGAGGA
Long Flanking Sequence:
AAATCTAATTTTTTATCACAAAAGCTGAAGTATAAGACTTCTAACTGATTTTGAATGGCTTTTGTTGCATCTAGGATGCAGTTCCAGAAATCAAAAAGGAACACGAAAAGCTGGAGAAGAACAGCAAACGGCGCCTAGAAAAGGAAATCACAGAGGGCCAGTACAGAGACAAGATAAAGAAGCCTAAAAAAAAGAAGCCTAAAATGATTAAAGAGAGGAGAAGAGAGGAAAAACGAACCACCTCCCCCTCCAACTCCCTTTCTGACCCATCAAATTCAGACGACTCTGAGGAGGACTGGTCTGTGTGCTCGGCAAAGCGATGCCAGCAACCAGAAGGAAACGAGGTTAGTTCTAGCACAACTGAAATGTTTTTGTTGCTAAAGCAGTGCATCATTCTTGCTTGCGTAATTGGTTTATTTTAAGGCTCATGAATAATTAACACACTTTTCCTCGTCCTCTCAGGTAAACTGGGTCCAGTGTGACGGCAGCTGTAACCAGTG[G/A]TTCCACCAGGTCTGTGTGGGAGTGTCTGCTGAGCAGGCCGAAAACGAGGACTACATCTGCGTCAGCTGCGCAATAAACGATTTGTCAGAATAAGGACCAAAATCATGTTTTTTTCGAAGGATAGTCAAAAAGGCTCCCCGTTTTGCACATAAGTTACAGCACCAAGAATGCACCAGATATCATCCTCTTACTGAATCCCGCCCTCCTCGCTCCCTTGGTGCTACTGCCTTCTTGATAGGACTGTTAACAAGAAAAAAATCTGTATGATTCTTCAGCTTTTTGTTTTGTATTTTTGAAGATTTCCTTCTATAACACTTTTCTTTTCCTTCTCTAGAGAACGTGATGCATAGATGTACCTCAGGGGTTTCCATCCCATAAATGCAAAACAAAGGGGAACTTCGGCATCCCCAAAATGTATTTTTGTTCATATTTATTATTTTATTTCTTTCCCCAATCGCCTTGAGAATTTCTTAACATGAATTTGTCGATCTGGGCTATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21908
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 |
---|---|---|---|---|---|
ENSDART00000058729 | Nonsense | 1463 | 1483 | 28 | 29 |
ENSDART00000135443 | Nonsense | 1459 | 1477 | 28 | 28 |
Genomic Location (Zv9):
Chromosome 11 (position 25784193)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 24613018 |
GRCz11 | 11 | 24850634 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAGCTGTAACCAGTGGTTCCACCAGGTCTGTGTGGGAGTGTCTGCTGAG[C/T]AGGCCGAAAACGAGGACTACATCTGCGTCAGCTGCGCAATAAACGATTTG
Long Flanking Sequence:
AGACTTCTAACTGATTTTGAATGGCTTTTGTTGCATCTAGGATGCAGTTCCAGAAATCAAAAAGGAACACGAAAAGCTGGAGAAGAACAGCAAACGGCGCCTAGAAAAGGAAATCACAGAGGGCCAGTACAGAGACAAGATAAAGAAGCCTAAAAAAAAGAAGCCTAAAATGATTAAAGAGAGGAGAAGAGAGGAAAAACGAACCACCTCCCCCTCCAACTCCCTTTCTGACCCATCAAATTCAGACGACTCTGAGGAGGACTGGTCTGTGTGCTCGGCAAAGCGATGCCAGCAACCAGAAGGAAACGAGGTTAGTTCTAGCACAACTGAAATGTTTTTGTTGCTAAAGCAGTGCATCATTCTTGCTTGCGTAATTGGTTTATTTTAAGGCTCATGAATAATTAACACACTTTTCCTCGTCCTCTCAGGTAAACTGGGTCCAGTGTGACGGCAGCTGTAACCAGTGGTTCCACCAGGTCTGTGTGGGAGTGTCTGCTGAG[C/T]AGGCCGAAAACGAGGACTACATCTGCGTCAGCTGCGCAATAAACGATTTGTCAGAATAAGGACCAAAATCATGTTTTTTTCGAAGGATAGTCAAAAAGGCTCCCCGTTTTGCACATAAGTTACAGCACCAAGAATGCACCAGATATCATCCTCTTACTGAATCCCGCCCTCCTCGCTCCCTTGGTGCTACTGCCTTCTTGATAGGACTGTTAACAAGAAAAAAATCTGTATGATTCTTCAGCTTTTTGTTTTGTATTTTTGAAGATTTCCTTCTATAACACTTTTCTTTTCCTTCTCTAGAGAACGTGATGCATAGATGTACCTCAGGGGTTTCCATCCCATAAATGCAAAACAAAGGGGAACTTCGGCATCCCCAAAATGTATTTTTGTTCATATTTATTATTTTATTTCTTTCCCCAATCGCCTTGAGAATTTCTTAACATGAATTTGTCGATCTGGGCTATTTACACCAAATAATATTAATTGGACTAATCAAAATG
Associated Phenotype:
Not determined