ZMP
cacna1ba
Ensembl ID:
ZFIN ID:
Description:
voltage-dependent N-type calcium channel subunit alpha-1B [Source:RefSeq peptide;Acc:NP_001108020]
Mouse Orthologue:
Cacna1b
Mouse Description:
calcium channel, voltage-dependent, N type, alpha 1B subunit Gene [Source:MGI Symbol;Acc:MGI:88296]
Alleles
There are 13 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa1562 | Nonsense | F2 line generated | Not yet available |
sa26487 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa31446 | Nonsense | Available for shipment | Available now |
sa20443 | Essential Splice Site | Available for shipment | Available now |
sa20442 | Nonsense | Available for shipment | Available now |
sa40452 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa40451 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45208 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40450 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33622 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa33621 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa1562
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000047719 | Nonsense | 370 | 2312 | 8 | 48 |
ENSDART00000141154 | Nonsense | 370 | 2270 | 8 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 31016641)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28777998 |
GRCz11 | 5 | 29378151 |
KASP Assay ID:
554-1505.1 (used for ordering genotyping assays)
KASP Sequence:
CAAAGGAGCGAGAGCGTGTGGAGAAAAGACAGGAGTTCTTAAAGCTGCGC[A/T]GACAACAGCAGATCGAAAGAGAGTTAACCGGATAYCTGGAGTGGATCTGC
Long Flanking Sequence:
TATATTTTTAACATACAGAATAACAATACCTTACTTATCTATATTGAGTTGAGCTTGAGGTGAAAGCATTTCAACATTTCAAACCAAATTGCACACTTCAGCTTTAAGTGAGGTATAAACTGTAGCCTTTTAGTTCTTTTCTATTGATTCTCAAACATTGATTTTTTTCACAGCTCTTGCAAATGTGGACACCACACCTTTTTTTTCTTCTAAATCTACGATTTCTTTTGCATTTCTTTTATTCAGTTTTGTTTCTCATTCAGTCTTATGAATAGGGGCATTTGTTTTTGTGGATGCACCACTTTATTACAAGATTCACAATTTTAAAAACACACATGAATGCTTTCACACACAGCCTGTGCTATAAAGCAGGTCTCCCCTGATTCCCGTGTGCAGTACAGTGTGTTCATGGATGTGTCTGCATTTGCTTCTGTGCCCACAGGGAGTTTGCAAAGGAGCGAGAGCGTGTGGAGAAAAGACAGGAGTTCTTAAAGCTGCGC[A/T]GACAACAGCAGATCGAAAGAGAGTTAACCGGATACCTGGAGTGGATCTGCAAGGCAGGTCAGTCTCCCAAATGTGTCTCTCATCTACATTAAAAGATGATCTATAATGCAAAGAGGTGTTTGAACACAGACGTGTGTCCACAGTGTGTTTAAATGACCAGATAATAATTATAAAAATCCAGTCACTCTTCTATTTTAATAATCCCCCTAAATCATAAACAGTCTCTCCAAATGCACATTTTAGATATTTCACTTAAGGCGAGTATATTTCCATGTAAAGTCCATATGGTAGGTCAGGCTTGCCATCGCACACCATTTGCCTTACCCTTAATCGAACCCTGATACACACCTTTAAAAAATTTAACTACACATCATAAGAATGTGGAGTACTAGAACTGTGATTGGCCAGCTTGGTAATGACATAATGTGTGGGTGGGGCCGAGAGCTTTGTAAGCGGAGCCTGGCTGATGATGGAAGTTATTTTGAGTCCTCACACTGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa26487
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047719 | Essential Splice Site | 417 | 2312 | 9 | 48 |
ENSDART00000141154 | Essential Splice Site | 417 | 2270 | 9 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 31011027)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28772384 |
GRCz11 | 5 | 29372537 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGACAAGGATGATGTTGCCTGGTACAAGAGGAAATGCAACAACCCAGG[T/C]AACTCTTGAAAAATTACATTTATTAATTAAAAGTGCAGAATATCTTAAGT
Long Flanking Sequence:
CCGTGGGGATTTAATTGGCTTAGAGAGGTGATTTCCCAAAGTCCTCCATGGTGGCACAGCTTTGAAGTTTTAACACAGTAAATCATTATGGAATTAACTGCTTACAGGTGCTTTGACTTCTTCAGATATCTCGCTACCGCCATTATGGATTTCACTGCACTGTAGTGATTGAATTCCCATGCATCACTTCAGGCTACCTTTTACCTTGTAGTGGTTTCTATTTTCCGTGCAACCACCTATAAACACACTGGCAATCACATAACAATGCACTTTAACAACCACTTAGAATAGCTGTACCACTTACTGTAATAACCAAACACAAGAGAGCAAAACCTGTTCATTGTCATAAAAATAAACATGACTTAAATTGCAAACCTGTGTGAGTAGTAAAATGTTGTTGTTGTTGTTTTTTCAGAGGAAGTAATGCTTGCTGAAGAAGATAAAAATGCAGAGGACAAGGATGATGTTGCCTGGTACAAGAGGAAATGCAACAACCCAGG[T/C]AACTCTTGAAAAATTACATTTATTAATTAAAAGTGCAGAATATCTTAAGTCTTTTAATAATTACAGCCAATGATAGTAATAAATAAAGGTTCCACATGTGCACATGCACTAAATAAAGTCATTACATGAACTAGGTAGTTACAAGGTACTCTCCTAAAACTAATCTTAACCCATGTAAAGGGTTGCCTGGTCCAAATAAATATTCCAACCCAATGATAACTTAAAACCCACCCAAAAGGACAGAAAACATCCAGATTTTTGAGAGAGTGAATTAATGGATTGCCAAACTGGGAAAGATTTATCGTGTTTTCTCTGATATTTTGTGGTACACGTACTTGTAGATACAGTATGCTGACTTTTAGAACACCGAACAACACTTACAAGTACCTTAATCAGACAGAGATGTAACTGACATTCTGCTCATTTTATATGTGACGTGCCATAAGGTGGTTTTACTCGCTCACTTGGAGCAGACTTTGGGTTGCCAGGTATGTATTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31446
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 |
---|---|---|---|---|---|
ENSDART00000047719 | Nonsense | 1060 | 2312 | 21 | 48 |
ENSDART00000141154 | Nonsense | 1039 | 2270 | 20 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 30984156)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28745513 |
GRCz11 | 5 | 29345666 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGATATGGGAGGAGATTCAATGGCTGTAAACCCCCATCAACCTTCAGTT[G/T]GAAGCCGGTGGTGTCTTGAGAAACCAGAAGATTCGGACAACAAACGAAAT
Long Flanking Sequence:
GATTGCCCTGTTTCTGAGTTCTTCTTGGTCTACTGCTTTGGAAATGACACTGATGAGCAGCGCTGCACATTGAAGTTGAAGTTCTTTTAATTTAATTCGCCATCTTACATTACACAGCACTCATGGGCATGGTGGTTTTGAGTGTAATGATCTTACATGATTATCAATGTTGGAAAACAATAGAAAAGTAGTGCATTGGAAAGGGCAAGCGTGTTCTGTGTAAATGGCCCATTATTTGTCAGTTAGCAACTCCTCATTTATAAATGCAATTCAAGTTTAATTTGTTGTCAAGTCATACCAACTATTTTAAGGCCTTTTTATTTGGTAGATTGAGTCAATTGAATGCTATGACACATGAATCAGTGTGTTATATTTTAGTGATTTGTTCACTTAAAAAGCAAAAGCATTCACAAGAAAAACTGTAATCTGAGTTTGTCTGCTTCAGGCACATGGATATGGGAGGAGATTCAATGGCTGTAAACCCCCATCAACCTTCAGTT[G/T]GAAGCCGGTGGTGTCTTGAGAAACCAGAAGATTCGGACAACAAACGAAATATTGGTCAGACTGGAGGAATGAGCACCCATATACCCGTGACTGTCACTTCTCCCCCGGGAGAAACAACCCTTATTCCCAGTTAGTATTTCTCGTTTTAGGGCATGATAAACTTTTCCATTTTTATAGTCTGCATGTTTGGCCCCAAGGTTGTTAACATTAAAAGCTGACATAAGTTTGGTAAATTCAAACATTACCTCTGTTTGTTTTCTCAGTGAACAGTATAGACAGCGAGACAGTGCCCATGACTGAGAAGAATCTAGAAGATCTAAATCAAAGCAGCATTCGTCCCATCCTCCCCTTCAGCTCCATGTTCATTTTCAACCCAACTAATCCGTGAGTGTGTGTGGTACAGTATTTCTGGGAAAATGTTGTAAATGTTTAAAACTGTGTGCTTTGAACAACTATTACAGAACAATGCCATTGATAGTGTTGTTTAAAAAAAACAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20443
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 |
---|---|---|---|---|---|
ENSDART00000047719 | Essential Splice Site | 1186 | 2312 | 23 | 48 |
ENSDART00000141154 | Essential Splice Site | 1165 | 2270 | 22 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 30982235)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28743592 |
GRCz11 | 5 | 29343745 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCCCTGGCTGCAGAAGACCCGGTCCAAGCCAATGCACCTCGGAACAATG[T/C]GAGCTGTTTTATCTGTGCTAAACGGGATGTCAGATTTTGACCTCATTTTC
Long Flanking Sequence:
TGTGTGTGTGTGTAAGATAAACGTTTTAAGATCTTTAAGTCTAAAAGCCATCCACTCACATAAACCTCCACATAAAGCTCTGTATTAATAGGCAATTTCCAAATGCATCTGTCCATCTTGGCTCTGTTGGTGTAACAGTATAGGATTACTTCTATTTTATTATACTGTATATTAATGTCACACAAGTGCATTGTTGACTTGACCATGCCTACCAGACACTTTCTCTAAGATATGCGCTATTACTTAAACTTAAAGACTTGCCTGTGGCTTGCATGAACATATTAATTATCGGTGGTTAAATAAATCAGTATCGACTTCTGTGTGCAATTGCCTTAAGCCTAATTCTCATAGTTTGTGTTTTTTATTCAGGGTGAGACGTTTATGCCACTACATTGTGAGTCTGCGCTATTTTGAGATGTGTATCCTGGTGGTCATTGCCATGAGCAGTATAGCCCTGGCTGCAGAAGACCCGGTCCAAGCCAATGCACCTCGGAACAATG[T/C]GAGCTGTTTTATCTGTGCTAAACGGGATGTCAGATTTTGACCTCATTTTCCATTAAGTCCCAGATGAGTGATGCTAACTGAAGACCATTTTATTTTTCGCTTCACAGGTCCTGAAGTATTTGGACTATGTCTTCACTGGTGTTTTCACATTCGAGATGGTCATTAAGGTAATTTTGTGGTAAATTGCTGAAGTTAATTGCATATCTCTTTGGAGACATGATCCTGCAGTCCTTTCTTAACCTGAGATGAGGATATTTGGCGTCCGTGTCTCTATTTGTAGCACATTTTAATATCATAGATGTGAAAAAATGACACAATTTTATTGCGAATAATTCAGCTAGTTGGTCAATTTAAAGGGTTAGTTCACCAAAAAATGAAAAATTACTCACCATTTATTTAATTTACCCTCAAGTGGTTCCAAATCTGAATTTCTTTATTCTGTTGAACACAAAAGAAGACTCGAAATCATTGACATTCATGACAACTTGTTTTTCAGAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20442
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047719 | Nonsense | 1191 | 2312 | 24 | 48 |
ENSDART00000141154 | Nonsense | 1170 | 2270 | 23 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 30982114)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28743471 |
GRCz11 | 5 | 29343624 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGCTAACTGAAGACCATTTTATTTTTCGCTTCACAGGTCCTGAAGTATT[T/A]GGACTATGTCTTCACTGGTGTTTTCACATTCGAGATGGTCATTAAGGTAA
Long Flanking Sequence:
CTCTGTTGGTGTAACAGTATAGGATTACTTCTATTTTATTATACTGTATATTAATGTCACACAAGTGCATTGTTGACTTGACCATGCCTACCAGACACTTTCTCTAAGATATGCGCTATTACTTAAACTTAAAGACTTGCCTGTGGCTTGCATGAACATATTAATTATCGGTGGTTAAATAAATCAGTATCGACTTCTGTGTGCAATTGCCTTAAGCCTAATTCTCATAGTTTGTGTTTTTTATTCAGGGTGAGACGTTTATGCCACTACATTGTGAGTCTGCGCTATTTTGAGATGTGTATCCTGGTGGTCATTGCCATGAGCAGTATAGCCCTGGCTGCAGAAGACCCGGTCCAAGCCAATGCACCTCGGAACAATGTGAGCTGTTTTATCTGTGCTAAACGGGATGTCAGATTTTGACCTCATTTTCCATTAAGTCCCAGATGAGTGATGCTAACTGAAGACCATTTTATTTTTCGCTTCACAGGTCCTGAAGTATT[T/A]GGACTATGTCTTCACTGGTGTTTTCACATTCGAGATGGTCATTAAGGTAATTTTGTGGTAAATTGCTGAAGTTAATTGCATATCTCTTTGGAGACATGATCCTGCAGTCCTTTCTTAACCTGAGATGAGGATATTTGGCGTCCGTGTCTCTATTTGTAGCACATTTTAATATCATAGATGTGAAAAAATGACACAATTTTATTGCGAATAATTCAGCTAGTTGGTCAATTTAAAGGGTTAGTTCACCAAAAAATGAAAAATTACTCACCATTTATTTAATTTACCCTCAAGTGGTTCCAAATCTGAATTTCTTTATTCTGTTGAACACAAAAGAAGACTCGAAATCATTGACATTCATGACAACTTGTTTTTCAGAGCTTGCACAGTTATTCTTTTGTCCTTTAGTGACTGACATACTTCAAATAAATTGACTAAATAATAATAACCTTTCATTTTATATTACTCTTCTGAAATACTTCTCTTGTAAGACTACTGTATAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40452
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047719 | Essential Splice Site | 1207 | 2312 | 25 | 48 |
ENSDART00000141154 | Essential Splice Site | 1186 | 2270 | 24 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 30981455)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28742812 |
GRCz11 | 5 | 29342965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TAAGATTTTATCCTGATTAATCTTTCATATTTATGCTTTTCCTTTGACAA[G/T]ATGGTGGATTTAGGTTTAATTCTGCATCCTGGTTCCTACTTTCGAGATCT
Long Flanking Sequence:
GCACATTTTAATATCATAGATGTGAAAAAATGACACAATTTTATTGCGAATAATTCAGCTAGTTGGTCAATTTAAAGGGTTAGTTCACCAAAAAATGAAAAATTACTCACCATTTATTTAATTTACCCTCAAGTGGTTCCAAATCTGAATTTCTTTATTCTGTTGAACACAAAAGAAGACTCGAAATCATTGACATTCATGACAACTTGTTTTTCAGAGCTTGCACAGTTATTCTTTTGTCCTTTAGTGACTGACATACTTCAAATAAATTGACTAAATAATAATAACCTTTCATTTTATATTACTCTTCTGAAATACTTCTCTTGTAAGACTACTGTATAATAATGGGACATAGCTCAGAGCAAGCGATATAAAGTCTGTCAGTAATTGTCTTGAAATTGATAGTTAAATGAACTGAATTGGTTAGAAAAATGCCGCTGTAAATGATGTTAAGATTTTATCCTGATTAATCTTTCATATTTATGCTTTTCCTTTGACAA[G/T]ATGGTGGATTTAGGTTTAATTCTGCATCCTGGTTCCTACTTTCGAGATCTATGGAATATTTTGGACTTCATTGTGGTCAGTGGTGCACTGGTGGCATTCGCATTCTCGTAAGTTGCCTTCATTTGCCTTACCTACAGAAACTCCCGTAACTAAAACCCGTACTTAAGAGTGTGACTTTTATCACTGAACTTAACAACAAAATACCCCATACAGTAATTTGAGACCCCTATTAGTGCAAGTTCTTGCCCGTATCCTTTTTATTTTATTTTAAAGGTTTTATCCACAGTGTAACAAAAGTGTCTTTGTGTATCTTCGTTGTTCCTACTAAAAGCTGGACATTTAATATATATTTAATTCATGCCATTCATTATGCTGCAAGGAAACTTAGCTTTGATTAAGATGTTTGCCAGATCCCACTGATCTGTTGTTTCCTTTCTGTCCTTCTTCGGAGGTGTGGGAGAGTTGACATCACTTTAATGAACTTTTGAGAATGTAGTCCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40451
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:
G > T
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047719 | Essential Splice Site | 1274 | 2312 | 26 | 48 |
ENSDART00000141154 | Essential Splice Site | 1253 | 2270 | 25 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 30975673)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28737030 |
GRCz11 | 5 | 29337183 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCGAGTCTTGCGACCTCTGAAGACCATCAAACGTCTACCAAAACTGAAG[G/T]TAAATATTCTGTTGCATTGCAATAGTTGAGCAGAAATTGGCAAAATATTG
Long Flanking Sequence:
AAGGATCATTTAATAACAGAGTGACATCTCTTGTAGAACCCATTTAGTGCATAAGTATATACAGTATATGCATGCAATAGAGAATTGTGTATTTCATACTCTTTCACCAGAGCATGTGCTTTTGTGAAATAACACAATCCATTGCTGGAGTGATTAAAAGCTGTGGCACTGAAAGATGCTCATTTGTAAGTTGATTTAAGTTGTCTGTATGAAAGGTGAGTATGTTTAGTCTAGTTAGTGCCCCATTATTGATTTTTACCAAAGGAAACATTTACATAATGTTTACTCACATTCTCGTGTGTTTTGTCTGGATTTATGTGAATCCTTTGATGAAGCCTGACTACAGCATGTGTTTGATCCTATTCTGAATCTGCTGACCTCTTTGTTCTTTTGACTGGTGTAGAGGAACCAAGGGCAAAGACATCAGCACTATCAAGTCACTGAGGGTGTTGCGAGTCTTGCGACCTCTGAAGACCATCAAACGTCTACCAAAACTGAAG[G/T]TAAATATTCTGTTGCATTGCAATAGTTGAGCAGAAATTGGCAAAATATTGGTTACATAATTAAAAAGATGTTATGTAGATAAGGATATAAATAAAGATAACTATGCTAAAATATTTCTTATTGTTTTTAATGTTCAAAACAGTTGTGCTGGTTAATATTTGGAGGAACCCAAGTTTTTTTCTCAGAATTAAAAAAAAAACAGCGTAAGGCAGAAATATTTCAAATGTTTTGTATTATGATGATTATCTGTGTTATACGTCTACAGCAATTTCATTAATCTTTCAGATCCTAGGCATTAAATGCAGTTTTTTTCCATAGAACAATAGTTATACAAAAGAATAAAAACCCTGTCTGGCACATTTAGAACAAGAGTATTTGTTTACATATGACAAGGATTGATTTGAAGATCATAGCCCCAAATTATAAATTAAATATTATTAAAATGTTTGCTTTTTCACAATACATCAAATCTTAATTTTACCCAGTTGTTTGATAATGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45208
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047719 | Nonsense | 1471 | 2312 | 31 | 48 |
ENSDART00000141154 | Nonsense | 1450 | 2270 | 30 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 30965686)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28727043 |
GRCz11 | 5 | 29327196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTCCTCTTGCCTTCTTATGCTTGCAGTTCCATGGGGCGCCTGACTTTTA[T/G]GAGGCAATGCTTAAGTATCTCAACATTGTCTTCACTGTTCTCTTTTCACT
Long Flanking Sequence:
TTAGTTTTCCCAAATATGAAAGTTCTGTTATCTTTTTTGTTATCCCCCAAACCTGTTTGAATTTTCTTCCTCTATTGCACACAAAAGATGATTTTCTGAAGATTATTAGAAACTGGCAGCCATTGTATTTATTTATTTTTCCTACTATGGATGTCAATGGACGCCAGTTTCTAACATTCCTCAAAATATCTTCTGTTGTGTGTAACAGAAAACAGAAACTGAAAAGGCTTTAGAACCACTTGAGAGCAAATAAAGACAACATTTTTCTGTTTGTGTGAATTATCCCTGTGAATATTTTAGTAATTAAACTGTTTTTACTCTTTTGTGTTTTTGATCACCAAATTAGCATATTAGAATGATTTCTGAAGAATCATGAGACACATATTTGATATAAAGTTTGTTTTTTACTTTAATATGATGAAAATAACTTGATTTCATATTGAATTTCATATTCCTCTTGCCTTCTTATGCTTGCAGTTCCATGGGGCGCCTGACTTTTA[T/G]GAGGCAATGCTTAAGTATCTCAACATTGTCTTCACTGTTCTCTTTTCACTGGAGTGTATTCTCAAGATTATTGCTTTCGGCCCCTTGGTGAGTATCATGCTTATAAACACCACCTAAATGTCACAGGTTACTCAAAAACCAAGTATATGTTAAAACCAATTGACAGCTTTCTTTAGAAATATTCTGACTGAAAATGATGGTAGCTTTAGTCGCCAGCTGCTTTGATTGTATGGAAAAGATCTGCTTGAACATTCTGCTAAAAATCTTTTTTTTTTTTTTTTTGACAATGAAAAAATCTTAAAAGTTTGGAATGACATGAAGAACACAATTTTGCCCTAATTCTTCAATCCCAGGCTGCATTCAAAATTGCATACTTCCATATAGTATGCTAAAATCAGTGTGCGAACCAAGTAGTATGTCCAAATTCATAGAATTCCAAAAACAGAATGCGAGAATTATGGAAATGACCTACTACTTCTAGTGAGATTCTGAAGTGTGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40450
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047719 | Nonsense | 1472 | 2312 | 31 | 48 |
ENSDART00000141154 | Nonsense | 1451 | 2270 | 30 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 30965685)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28727042 |
GRCz11 | 5 | 29327195 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCCTCTTGCCTTCTTATGCTTGCAGTTCCATGGGGCGCCTGACTTTTAT[G/T]AGGCAATGCTTAAGTATCTCAACATTGTCTTCACTGTTCTCTTTTCACTG
Long Flanking Sequence:
TAGTTTTCCCAAATATGAAAGTTCTGTTATCTTTTTTGTTATCCCCCAAACCTGTTTGAATTTTCTTCCTCTATTGCACACAAAAGATGATTTTCTGAAGATTATTAGAAACTGGCAGCCATTGTATTTATTTATTTTTCCTACTATGGATGTCAATGGACGCCAGTTTCTAACATTCCTCAAAATATCTTCTGTTGTGTGTAACAGAAAACAGAAACTGAAAAGGCTTTAGAACCACTTGAGAGCAAATAAAGACAACATTTTTCTGTTTGTGTGAATTATCCCTGTGAATATTTTAGTAATTAAACTGTTTTTACTCTTTTGTGTTTTTGATCACCAAATTAGCATATTAGAATGATTTCTGAAGAATCATGAGACACATATTTGATATAAAGTTTGTTTTTTACTTTAATATGATGAAAATAACTTGATTTCATATTGAATTTCATATTCCTCTTGCCTTCTTATGCTTGCAGTTCCATGGGGCGCCTGACTTTTAT[G/T]AGGCAATGCTTAAGTATCTCAACATTGTCTTCACTGTTCTCTTTTCACTGGAGTGTATTCTCAAGATTATTGCTTTCGGCCCCTTGGTGAGTATCATGCTTATAAACACCACCTAAATGTCACAGGTTACTCAAAAACCAAGTATATGTTAAAACCAATTGACAGCTTTCTTTAGAAATATTCTGACTGAAAATGATGGTAGCTTTAGTCGCCAGCTGCTTTGATTGTATGGAAAAGATCTGCTTGAACATTCTGCTAAAAATCTTTTTTTTTTTTTTTTTGACAATGAAAAAATCTTAAAAGTTTGGAATGACATGAAGAACACAATTTTGCCCTAATTCTTCAATCCCAGGCTGCATTCAAAATTGCATACTTCCATATAGTATGCTAAAATCAGTGTGCGAACCAAGTAGTATGTCCAAATTCATAGAATTCCAAAAACAGAATGCGAGAATTATGGAAATGACCTACTACTTCTAGTGAGATTCTGAAGTGTGCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33622
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047719 | Essential Splice Site | 1528 | 2312 | 32 | 48 |
ENSDART00000141154 | Essential Splice Site | 1507 | 2270 | 31 | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 30964035)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28725392 |
GRCz11 | 5 | 29325545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGACTGTGCTGGGCAGCATCACTGACATTTTAGTCACTGAGATTAACG[T/G]AAGTGAGCTCTGCATTTTTGCATAATTGAAGTAGTTTCAGAGCCTAAAAG
Long Flanking Sequence:
AGCCTTTAAATGTCACTTTAAGCTGCATAGAAGTGTCTTAAAAAATATCTAGTCAGATATTATTTACTGTCATCATAGCAAAGATACAATAAATCAGTTATTAGAGATGAGTTATTAAAGCTATTATGTTTAGAAATGTGTACAATTTTTTTTTTTCTCTTTTAAAGAGAAATTGGGGTGGGGGGTATGAACGGGGGCTTATAATTCTGACTTCAGCTGTATATTTAAATGCCTGCAGACATTAATTCTTCAATGCGGTTGTCTGCTGTTGCCATCTTTAACAGTGTATTGTTTTTACTTTGTGCCACACAGACCACAAGCACAGTAAACTGAAGTATACTTTCATTCGGGAAATATAGTGAGCTTCTTCAGCTTGTCTCTGAATAATCTCACTAATTCTTTTTTTTTTTTACAGAATTACCTGAAAGATGCCTGGAATGTGTTTGACTTTGTGACTGTGCTGGGCAGCATCACTGACATTTTAGTCACTGAGATTAACG[T/G]AAGTGAGCTCTGCATTTTTGCATAATTGAAGTAGTTTCAGAGCCTAAAAGTGTGTAATAACAAACAGCAGAGACTGGCTGTGAGGGAAAGCCTAGACATACATGATGTTGACAAACCAGCTCATTAGAAATATGTGCTTCAGCCTACATTTTTGCAAAACGAAAGTCAAGTTGCTCCTGACACATTTCAATGCACGTTTTAGATGACACATCCACTAGAGGGCAAAGTTAACATTATTGTAAGTCTGAAATATGGTATATAAAGTATGCTTTATGCTTCAAATATATGTCCTTCTTGTGTACGTCCATGAAAAGGTGCCGCTTGTCACGCAGCAAACCACTGATCTAAACCCTTCCCTACATCCAAAAATAATGTTTTGAAAAGCAAACCTAAAAGATAAGTGAACTGCGACCATTTAGTTTTATCTTAATGTTACATTACTCCACCAAACTCAAATCTGAGCACTCTGCTTTACAAGTATAACACCAGAAAAAGTGAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33621
Status:
Available for shipment
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For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047719 | Nonsense | 1571 | 2312 | 34 | 48 |
ENSDART00000141154 | None | None | 2270 | None | 46 |
Genomic Location (Zv9):
Chromosome 5 (position 30958337)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 5 | 28719694 |
GRCz11 | 5 | 29319847 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTACAAGAAGTTATAATATATTCATTTTTATTTCCAGGCACTGCCTTA[T/A]GTTTGCCTTCTAATCGCCATGCTGTTTTTCATCTACGCCATTATTGGGAT
Long Flanking Sequence:
CAGAAACGCACCCAAGTTTGTTTCTCTTTAGCAAGAGAATATTTTCTTAAAAATGTCCTTTAGAATATCTTAAATCAATATTGCTTACCAGTTTGCAAACTAAGACAAAGTACATTTTTAGGACTTTTCAAACATTTGAGCTTTGGTAAAATACTGTCATGGGTGTTTAAGGATTTGGAAATACAAACTTGATGTTGTCAAGAGATATGAGAATTAAATTCAAGACAGCTGAAGGAGAAAATGAGAAGAAAATAACTTTCGCATTGACAAAGTTCGTGTTCCCACAGGAGCGTCAGCTGAACTTCAGTTTCCTGAGGCTCTTTAGAGCAGCCCGACTCATCAAGCTCCTCCGGCAGGGATACACCATTCGCATCCTGCTCTGGACATTTGTCCAGTCTTTTAAGGTAACTCTAGTTAGACTGTTTTGATGCTCATTGCTGGAGATTGTTTTGTTACAAGAAGTTATAATATATTCATTTTTATTTCCAGGCACTGCCTTA[T/A]GTTTGCCTTCTAATCGCCATGCTGTTTTTCATCTACGCCATTATTGGGATGCAGGTAGATATATACAATAATCTCAGAGCTTCAGTGACTGTAATTACCAGTTAAAGGTCATTGCAGTGTTGGAGTGCATCTTATTATAAGTGAATAAAGCAGGAAATAGGAAAATGTGTTCTGCCTGAAGGTTATTCGATGGTTTCAAAACATGCATTTATTTGATATACCATTGTGATTGCAGGTGTTTGGAAACATTGATTTGAATGATGACACGGCAATCAACCGTCACAACAACTTCCGCACTTTCCTCCAAGCTCTTATGCTTTTGTTCAGGTCTGCACAGTTCTTATATTCCTCAACTACTGCAGTCAAAAACATCTAAATATTAAAGAAAATCTTACAAAGGCTTCTGGGGATGCACTACAGAGTCAGAATCGAAAAGTCAATTTCTAAACTGGCCCTGAACACTATATTTAGCCTGATCACTATATTTAGATTTGACGGAT
Associated Phenotype:
Not determined