ZMP
BAHCC1
Ensembl ID:
Description:
BAH domain and coiled-coil containing 1 [Source:HGNC Symbol;Acc:29279]
Human Orthologue:
BAHCC1
Human Description:
BAH domain and coiled-coil containing 1 [Source:HGNC Symbol;Acc:29279]
Mouse Orthologue:
Bahcc1
Mouse Description:
BAH domain and coiled-coil containing 1 Gene [Source:MGI Symbol;Acc:MGI:2679272]
Alleles
There are 10 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24918 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa45472 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45473 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa15411 | Nonsense | Available for shipment | Available now |
sa35350 | Nonsense | Available for shipment | Available now |
sa42078 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa42079 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa35351 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa874 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24918
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 |
---|---|---|---|---|---|
ENSDART00000110615 | Essential Splice Site | 101 | 2554 | 3 | 37 |
Genomic Location (Zv9):
Chromosome 12 (position 36705984)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 34516441 |
GRCz11 | 12 | 34617504 |
KASP Assay ID:
554-7446.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTACAAAACTTAGACATGCAAAACTATGTCTAAATTTGATTTCTTTCC[T/C]TAGATTTCTATCTACGAAGCCTCCCATCGCAGCCCCACCTTCTCTCTGCA
Long Flanking Sequence:
GAAGAAATAAAAGTTTCTACATAAACAAACATGTAAAACATACATATTTCTAACAAGGTGTTAAATTATTGTAAACAGAAGTTCTGAAAGCTCTTGTTTAGTTAAGCTACTCATAAATGTCGGGTAAAGAACTGAACTTGTTTGTGCAGGGGTTTCTGGGAAAGGTTGTACCGTGCTTTAGGGCTTCATGAACCTGAGTCCAGCCACAGCAAAAGGCCAAAACTGTCACTCTCTTTTGTTACATTTGTTTATCCTGACAATGTTCTCTCTCCATTCTCTCTCTCTCTCTCTCTCAGCCCCAGGGTATCCCCGCTTTTCAGGGAGTCTAGCCCCCACCTTCCTGCCCATGAGCCCCCTGGATCACCATGGCAACAGCAGCGTACTTTATGGACAGCACCGTTTCTATGACACTCAGAAAGGTGAGTGAGGTTCAGTTTCTTTTGTCAAGCAGCCTACAAAACTTAGACATGCAAAACTATGTCTAAATTTGATTTCTTTCC[T/C]TAGATTTCTATCTACGAAGCCTCCCATCGCAGCCCCACCTTCTCTCTGCAAATCACAGCCTCCCACCGCTTTCTAGAACTGCTCCTGCCCACCCGCTGGACTCCTGCAGTCGTGAGAGGGAACCTGGAAGCACAGTTTCCCAGAAGAGCTCCAAAGAGACAGGTGTAGCGGAGCGAAGAGTAGGACCCGGAGGAAAAGAAAAAGAAAAGAGTAAACAAGAATCTAAGCAGGATCGTCATCATGGTCCTCCCACCCTTCATCACCACCACCAGCATCATCCACAGCATCATCCCCAAGGCCTAGAAGATGACTTTCGGCACAAAGATGACCCCAAGCACCTTAGCTCCTGCCTGCTTAGCACTAAGACGCAGAATGGCTCTGATCCAGGGGCGGCCACCAGGGGCTCTTTACCCAGTTGTGTGGGTCCTGGAGCCTCCAGTCTGGGGACTGGCCGGCAGACAAGTGGAGACAGTCACTGTTGCAAGGAAGGGGTCAGTGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45472
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 |
---|---|---|---|---|---|
ENSDART00000110615 | Nonsense | 224 | 2554 | 3 | 37 |
Genomic Location (Zv9):
Chromosome 12 (position 36706353)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 34516072 |
GRCz11 | 12 | 34617135 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACAAAGATGACCCCAAGCACCTTAGCTCCTGCCTGCTTAGCACTAAGACG[C/T]AGAATGGCTCTGATCCAGGGGCGGCCACCAGGGGCTCTTTACCCAGTTGT
Long Flanking Sequence:
CAACAGCAGCGTACTTTATGGACAGCACCGTTTCTATGACACTCAGAAAGGTGAGTGAGGTTCAGTTTCTTTTGTCAAGCAGCCTACAAAACTTAGACATGCAAAACTATGTCTAAATTTGATTTCTTTCCTTAGATTTCTATCTACGAAGCCTCCCATCGCAGCCCCACCTTCTCTCTGCAAATCACAGCCTCCCACCGCTTTCTAGAACTGCTCCTGCCCACCCGCTGGACTCCTGCAGTCGTGAGAGGGAACCTGGAAGCACAGTTTCCCAGAAGAGCTCCAAAGAGACAGGTGTAGCGGAGCGAAGAGTAGGACCCGGAGGAAAAGAAAAAGAAAAGAGTAAACAAGAATCTAAGCAGGATCGTCATCATGGTCCTCCCACCCTTCATCACCACCACCAGCATCATCCACAGCATCATCCCCAAGGCCTAGAAGATGACTTTCGGCACAAAGATGACCCCAAGCACCTTAGCTCCTGCCTGCTTAGCACTAAGACG[C/T]AGAATGGCTCTGATCCAGGGGCGGCCACCAGGGGCTCTTTACCCAGTTGTGTGGGTCCTGGAGCCTCCAGTCTGGGGACTGGCCGGCAGACAAGTGGAGACAGTCACTGTTGCAAGGAAGGGGTCAGTGGAGAAATGCGAATTAGCGAGCCAGCCTCAGACTGCCTTCGTCACAGTGCCATGCTGGGCCATGCCCACCCAATGCCCTACTCCATGCCCCCACCTCTGGGCCTAGGCTCTGCAGTGGGAGGATCCTGGCTGCATCCGAATCATCCACACCATCACCATCCTCATCATCCCCATGCAGAGCTCTTTTGTCCACCTCCCCCTGCTCCACTGACCATGCCCACTGCTCAGGAAAAGAGCCTTGGCAGAGACTCTGAGGTTACAGGGCCCACCTTTGTGCCCTCTGTGGGGCCACTGGGAGATAAAATCAGTGGACCATTCCAGCTGGGGAACCATCACTGTCGAGGTGTGGGAGGTGGTATGATTGCAGTTGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45473
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 |
---|---|---|---|---|---|
ENSDART00000110615 | Essential Splice Site | 425 | 2554 | 5 | 37 |
Genomic Location (Zv9):
Chromosome 12 (position 36707060)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 34515365 |
GRCz11 | 12 | 34616428 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTTACGCACAAACGAGGTTCAGCACAGTCAGAATCAGCATACCCACTC[A/G]GCACGTTCATGTAGCTTGGACAGCAGTGAGGAATCTGATGCCTTTCGTCC
Long Flanking Sequence:
TACTCCATGCCCCCACCTCTGGGCCTAGGCTCTGCAGTGGGAGGATCCTGGCTGCATCCGAATCATCCACACCATCACCATCCTCATCATCCCCATGCAGAGCTCTTTTGTCCACCTCCCCCTGCTCCACTGACCATGCCCACTGCTCAGGAAAAGAGCCTTGGCAGAGACTCTGAGGTTACAGGGCCCACCTTTGTGCCCTCTGTGGGGCCACTGGGAGATAAAATCAGTGGACCATTCCAGCTGGGGAACCATCACTGTCGAGGTGTGGGAGGTGGTATGATTGCAGTTGGTGGCAGTGCAGGGAAAGAAACGAAAACTCCTGAGAGGAGTAGCAGTGGAAGTCGAGCAGCTAACCTACTGCCTCAGAATAGCTGCCAAAGAAAATCTTCCCAGCAGCAACATGCATATGGTAAAGCAGACAAGAGTCCAGACTGGCCCCCCGGCCCCCATTTACGCACAAACGAGGTTCAGCACAGTCAGAATCAGCATACCCACTC[A/G]GCACGTTCATGTAGCTTGGACAGCAGTGAGGAATCTGATGCCTTTCGTCCCTCTCTGCCACAGGGGACGAAGGGTGGCCACCAAGCTAAGAGTAGCATTTATGCCAGCACTCCACCTTTCCGGGACTGTTCTCACTCAGGTCCGTCAAACAGGGCATCGTCCGAAGGTAAAGGAGCCACGGAGGTTGAGTGTACTCAGAAAAGCAGCCAGAGGGTTGCACGAATACGTCATCAGCAGCACAGGGCTAGCACTGGTGGACAGGGTCCAGAGATGGAGCCTAACAGTACCACACAAGACAAGAGGAAAATGGACATGGAGTCAGCATCACAAGGATACGGCGGGAATCGGACCGGAACTCATCCCTCCTGGGAAGTGCGAGGACCCCAGCCTCGGCCAGATGAAGAACCACACAAGGCTTACAACTCTTTGGGTGCTGCTTCCCAGACTTCACGTGTGGACCAAGGGCCTCTTCCCCCTCTAACAGCCCCGCAGGAGGCCAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15411
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 |
---|---|---|---|---|---|
ENSDART00000110615 | Nonsense | 498 | 2554 | 5 | 37 |
Genomic Location (Zv9):
Chromosome 12 (position 36707280)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 34515145 |
GRCz11 | 12 | 34616208 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAGGAGCCACRGAGGTTGAGTGTACTCAGAAAAGCAGCCAGAGGGTTGCA[C/T]GAATACGTCATCAGCAGCACAGGGCTAGCACTGGTGGACAGGGTCCAGAG
Long Flanking Sequence:
ATAAAATCAGTGGACCATTCCAGCTGGGGAACCATCACTGTCGAGGTGTGGGAGGTGGTATGATTGCAGTTGGTGGCAGTGCAGGGAAAGAAACGAAAACTCCTGAGAGGAGTAGCAGTGGAAGTCGAGCAGCTAACCTACTGCCTCAGAATAGCTGCCAAAGAAAATCTTCCCAGCAGCAACATGCATATGGTAAAGCAGACAAGAGTCCAGACTGGCCCCCCGGCCCCCATTTACGCACAAACGAGGTTCAGCACAGTCAGAATCAGCATACCCACTCAGCACGTTCATGTAGCTTGGACAGCAGTGAGGAATCTGATGCCTTTCGTCCCTCTCTGCCACAGGGGACGAAGGGTGGCCACCAAGCTAAGAGTAGCATTTATGCCAGCACTCCACCTTTCCGGGACTGTTCTCACTCAGGTCCGTCAAACAGGGCATCGTCCGAAGGTAAAGGAGCCACGGAGGTTGAGTGTACTCAGAAAAGCAGCCAGAGGGTTGCA[C/T]GAATACGTCATCAGCAGCACAGGGCTAGCACTGGTGGACAGGGTCCAGAGATGGAGCCTAACAGTACCACACAAGACAAGAGGAAAATGGACATGGAGTCAGCATCACAAGGATACGGCGGGAATCGGACCGGAACTCATCCCTCCTGGGAAGTGCGAGGACCCCAGCCTCGGCCAGATGAAGAACCACACAAGGCTTACAACTCTTTGGGTGCTGCTTCCCAGACTTCACGTGTGGACCAAGGGCCTCTTCCCCCTCTAACAGCCCCGCAGGAGGCCACACTGGGCCCTCAGGGACCTGAAAGCAATGCCATGAGGAATCTGATGAAGTACAGTAGCCAGCAACCACTGCTGTTCACTCAGAAGAGCCCATTTGGTGGTCTGGGCTGCCTCAAGCAGGGAGCAGTAGCTGGGGAGAGAAGTGAGAGGAACGAAAGAAGCGACAAAAGTGGAAATGGTTCGAGCTGTGCTCTCCAGGAGGGAAAGCAGACCCTGCCCCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35350
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 |
---|---|---|---|---|---|
ENSDART00000110615 | Nonsense | 890 | 2554 | 10 | 37 |
Genomic Location (Zv9):
Chromosome 12 (position 36713440)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 34508985 |
GRCz11 | 12 | 34610048 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTTTACGGAGCCCGAGGGCCCACCTCACACATGCAGCATCCCGCAGTCTA[T/A]TCCCGCTCCCAGTTTCTACGGCAACAGGAACTCTACGCGCTGCAGCAACA
Long Flanking Sequence:
TCTTGACTGGCACTGCGGCTTTCATGAGCCAGAGATCAGGCTAGTGTAGCTGGTGAGCTCACTGGTGACCATCGTTTTGCGTTAATCCACTGAGGTATGGCCAGACGAGCTGTGAGTGCATGGGGCAGACGATGATAAAAGGAAGTTTGCATTCACTCTCTGCCCACGGGTTGAGTGCACAACATGATGAGGAAAGAGATGTGGAAATGTGAGGGTTTTTTACCCTTGGGACTGAGGATGACTTTTGCAAAGAAAAAAGAGAGTGAAAAAAGAGGGACGGAAAAGGGGTGGAATCTTATAGCCGTAAATCAATAGGCCTTCAGAGCGATAAGTGAGACTTGCCTTGAGGCGAAAGAAAAACCTTTGTTCATACTTTTCTCATTCCTGTATCTTTCTCTCTCTCGCTTTCTCTCTGTAGATGTAATGGAGCAGCAGGGACTGTGGCCCCCTGTTTACGGAGCCCGAGGGCCCACCTCACACATGCAGCATCCCGCAGTCTA[T/A]TCCCGCTCCCAGTTTCTACGGCAACAGGAACTCTACGCGCTGCAGCAACATCAGCACCAGCAGCACCGTGCAGCACAGGCTATGGAGTTGGCGCACAGACACAGTCACTCACAGGTAACACATGGAGGAGGATTTGTACACACGGTTAGCCCTGCTTCCTCATACACCTCAAGGTGATTTCCCAGCAGCTATTTCTCTGCGTCTTTCAGCAGACCTACCCAGGACGCCCGAGGTTGCGAAAGGCCTGTTATTCCTGCTCTCAGAAATTCATAGCAGTTTTAGCCAAAAGAATGGCCAGCTTTCATTTTCAAAGTGCATTTTAATGTTGGACATTTTGAAAGAGTGGGATTCTTCTCAGGAACGGGGCCGGTTTCTGCTTTTATCTGACTTCTTTTGTACAAAGAAGCAGAGCAGAATGCAAGTGAACAGTGGATCATTAGCACCCATTGTACTGCATCCCTGGTGGATGTCCTTACGTAAGAAACCTGAGACGACTGAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42078
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 |
---|---|---|---|---|---|
ENSDART00000110615 | Essential Splice Site | 1577 | 2554 | 23 | 37 |
Genomic Location (Zv9):
Chromosome 12 (position 36745516)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 34476909 |
GRCz11 | 12 | 34577972 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTAGTCCAGTCAAGATGTCAATGCATTCAATCGATCCATCATTTTCACA[G/T]AGGAGGAAGATGACGGCATCTACGACAGCGAGGAAGGGGCAGAGGGCATC
Long Flanking Sequence:
GCTGTGCATGTGTTGTTCATGATTAGTTCATGTTAGTAAATGCATTAACTAATGAACCTTATTGTAAAGTGTTACCGGCACTTCTATGTTAAGCTGTTTTGAGACAATCTACATTGTAAAAGCGCTATAGAAATATACATGAAATTAATTTAATTGAATGAATTTTATAATGTGTATTTTAAAGAGCAGTGTTGGTGCGGTCTCAGATTTGTAATGGTAATGTATTTGCAGCTGAATCAGGAGCTTGAATCAGTCACTAGGTCTGACACTTGATGGTCAAACCTGCCAGTGACTAGACTTCTCTGACTGCTAAAGTTCCTGTGAACGCTGACAGTCACAGCCACATTTGGCACCCGTTTCATGAACTTTGCTAAATATCGAACAAACCGCGCAGTGAGAGAAATCGGCAGGCTGCGTTCGCCATGACCGATTCAGACGCCTGCTGTGAACTGTAGTCCAGTCAAGATGTCAATGCATTCAATCGATCCATCATTTTCACA[G/T]AGGAGGAAGATGACGGCATCTACGACAGCGAGGAAGGGGCAGAGGGCATCAAGAATCTATCATCTAAAGAGCAGCTGTCTGGAGCCGGCCGTCCTTCACAGTGCTCCATCGTGAAGCTTGAGGCTAATCAGAAAGCCAAGAACAAAACTGAAAGACAAGGATTCGGTAAATGTTACATCTTTGCTTAATTAGACAGCATGGATTGACAGATATCACCTTAGTTCACAAACACTCATCTTTCACTGTCATTCTTACCATTTTTTTTTCTGATTCCCTCCAGGGTCTATGAATGTGTCCGTCACTAAAGAAGAGATGAAGAGAAGGAAGGCCCCCTGTAGGCCAGCCCAGGTCTGTGCTGACCATAACCACTCAGAACTAGATGAGGACAGGAGATTGACTGGCCCGAAGTGGAGAGAGGGCTCAAGGGAGAACACCTTTGACCACACTAGGGTTCTCAAAACCTCACCTACTCCACGAGAAAGGACCACCAGGAAGAGCGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42079
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 |
---|---|---|---|---|---|
ENSDART00000110615 | Essential Splice Site | 1851 | 2554 | 29 | 37 |
Genomic Location (Zv9):
Chromosome 12 (position 36749397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 34473028 |
GRCz11 | 12 | 34574091 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGAGTTACTGTATGCTGCTTATGTACATACATTGGACCTGCCTGATATG[T/A]AAGAGAACCAGACCTGCATTATGGATGGATGGATGTATAAGTAGCTGGAT
Long Flanking Sequence:
GTGTGTGTGTGTGCGTGTGCGTGTGCGTGTGTGTGTGCGTGCGTGTTTGTGTGCGTGTTTGTGTGTGTGTGTGGAAGAATGAGACTCACATGCTGTTTCGTGACTGTTAGCAGGCAAAGGGACGAGCAGTCAGTCGTTTGCTGGAGAGCTTTGCTGCCGATGAAGGTTTCCAGATAGACGATGACAGCAGCTTCTCAGAGGGAGAGGAAGAAGAGGAGGAGGAAGAGGAGGAACCAGAGCTGATGGGCAGTGCTTTGCCAGGTACAAAATATGCAAACAGACTGGCATGATTGAAATGTAACTGTGTTCATATCAACATAGAATGTGCTCGTGGTCAAAAGAGAATGACCTCTACCTTTAATCTGTCTTTGTCTCAACCAGCCCTGCCCAACTGCATTCTCACCAAAGAAATCCTGAGGGATGGGCTGAAAGTATTGATCTCGAAAGAGGACGAGTTACTGTATGCTGCTTATGTACATACATTGGACCTGCCTGATATG[T/A]AAGAGAACCAGACCTGCATTATGGATGGATGGATGTATAAGTAGCTGGATGAATTGGTGGATGGATGGATGGATGGATGAATGGATGGATGGATGGATAAGTGGATGGATGGATGGATGGATAAGTGGATGGATGGATGGATAGATGGATGGGTTGTTGGGTAGGTGGATGGATAGAAAGGTTAATAGAATGAATGACATAATAGATAGATAGAACAATGAAATGACGTATGGATGGATGGATGGATGGATGGATGGATGGATGGATAAGTGGATGGATGGATGGATGGATGGATGAATGGATGGATGGATGGATGGATGGATAAGTAGATTGGTGGATGGATGGATGGATGGATGGGTGGGTGGGTGTGTAGGTGGAGGGATAGAAAGATGAATAGAAAGAATGACATAATAGATAGAACAATTAAATGATGGATGGAGAAGTAGATGGATGGATGGATGGATGGATGGATGGATGAATGGAAAAATGAATGGAATGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35351
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 |
---|---|---|---|---|---|
ENSDART00000110615 | Nonsense | 2165 | 2554 | 34 | 37 |
Genomic Location (Zv9):
Chromosome 12 (position 36756795)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 34465630 |
GRCz11 | 12 | 34566693 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTAAGACTAAAAATGGAAAAGCATTGTTGCTTCTTGGGAACCCAGAGCTA[C/T]AAAGAAGTGGACGAATGGAAAAGGGCTTTGGAGCCAAAGGTATTGGAGAG
Long Flanking Sequence:
CTGAGTCCCCTTAGCAATACCTTTGTTTATCTCCATCAACAGGAAGGCCAAAATCTGTCAATGCATCATCAAAGAGCGGTGCATCTGAGAATGTGACCGAAACTGCTTCCCCTCTTCTCAGCTGGCCAGTTGCCACCATGTCCAGGAGGAAACCCTCCATGGATTTGTTCCAGTTTAATGGGTTAACAAAGAAAGCTCTTAAGGGAAAGGAGTCAGACATGTTCCCCCTACTTAGCTCCACTATGACCACTCCAGCCAAAGGCATCTTCAGCACTTCCTTTGAGGTGGACTCTTTCAGCAGCATTGCAAATGGTTGCACTTCCTTTGGAAATCAACAGTTGGCACCAGGCCTGCCTCCTAGTCACAAGGTTGTCCCTGGGTCACGGTGTAGAAAGATAGGAGACAGGAAGGAATTTCTGGTCAAACTGGACCATGAAGGGGTAACATCCCCTAAGACTAAAAATGGAAAAGCATTGTTGCTTCTTGGGAACCCAGAGCTA[C/T]AAAGAAGTGGACGAATGGAAAAGGGCTTTGGAGCCAAAGGTATTGGAGAGCTGACCTCAACAATGGGCTATTCCCAGTCTGTTCTTCTTGTCAAAGATGCCAAAAGGAACAGTTGCCATCTTCTCAAAGGTTCCTCTGACATGCGAAAGCACCCTCAGGGTCTCGGGCTTAGTGAATATACAGATTATGGGCCAAATTGCCACAGCGACTGCCTAAGCTCTTATTCAGACATGGATGAAGATGAAGATGAGGAGGAAGATGCCAGAAGGGCGGCAATGCGCACCACTGGACGTTTTTTGTCTCGTCTTTCTGTTTCATCGTCATCCTCAGGATCCTCCAGTGCATCTAGCTCAGGCTCATTGTCCAGTTCCAGCGTCTGCTCGTCTGACAATGATTCGTCCTACAGTTCAGATGAAGAAGAGGCATCTCGGCTTCTGCTCCAGGGTTGCCTTTCTTCTCATCACACATTGCTCCAACAACAGCAGCATTCAGACCCTCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa874
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 |
---|---|---|---|---|---|
ENSDART00000110615 | Nonsense | 2188 | 2554 | 34 | 37 |
Genomic Location (Zv9):
Chromosome 12 (position 36756866)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 12 | 34465559 |
GRCz11 | 12 | 34566622 |
KASP Assay ID:
554-0776.1 (used for ordering genotyping assays)
KASP Sequence:
AAGGGCTTTGGAGCCAAAGGTATTGGAGAGCTGACCTCAACAATGGGCTA[T/A]TCCCAGTCTGTTCTTCTTGTCAAAGATGCCAAAAGGAACAGTTGCCATCT
Long Flanking Sequence:
AAGAGCGGTGCATCTGAGAATGTGACCGAAACTGCTTCCCCTCTTCTCAGCTGGCCAGTTGCCACCATGTCCAGGAGGAAACCCTCCATGGATTTGTTCCAGTTTAATGGGTTAACAAAGAAAGCTCTTAAGGGAAAGGAGTCAGACATGTTCCCCCTACTTAGCTCCACTATGACCACTCCAGCCAAAGGCATCTTCAGCACTTCCTTTGAGGTGGACTCTTTCAGCAGCATTGCAAATGGTTGCACTTCCTTTGGAAATCAACAGTTGGCACCAGGCCTGCCTCCTAGTCACAAGGTTGTCCCTGGGTCACGGTGTAGAAAGATAGGAGACAGGAAGGAATTTCTGGTCAAACTGGACCATGAAGGGGTAACATCCCCTAAGACTAAAAATGGAAAAGCATTGTTGCTTCTTGGGAACCCAGAGCTACAAAGAAGTGGACGAATGGAAAAGGGCTTTGGAGCCAAAGGTATTGGAGAGCTGACCTCAACAATGGGCTA[T/A]TCCCAGTCTGTTCTTCTTGTCAAAGATGCCAAAAGGAACAGTTGCCATCTTCTCAAAGGTTCCTCTGACATGCGAAAGCACCCTCAGGGTCTCGGGCTTAGTGAATATACAGATTATGGGCCAAATTGCCACAGCGACTGCCTAAGCTCTTATTCAGACATGGATGAAGATGAAGATGAGGAGGAAGATGCCAGAAGGGCGGCAATGCGCACCACTGGACGTTTTTTGTCTCGTCTTTCTGTTTCATCGTCATCCTCAGGATCCTCCAGTGCATCTAGCTCAGGCTCATTGTCCAGTTCCAGCGTCTGCTCGTCTGACAATGATTCGTCCTACAGTTCAGATGAAGAAGAGGCATCTCGGCTTCTGCTCCAGGGTTGCCTTTCTTCTCATCACACATTGCTCCAACAACAGCAGCATTCAGACCCTCCCACCGCCCCACCACGACACACTTTTGGAGCCAAAACTATGAGTATCTCTAATTCAAAGGCTGCAGTAAATAG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |