ZMP
MAP1A (1 of 2)
Ensembl ID:
Description:
microtubule-associated protein 1A [Source:HGNC Symbol;Acc:6835]
Human Orthologue:
MAP1A
Human Description:
microtubule-associated protein 1A [Source:HGNC Symbol;Acc:6835]
Mouse Orthologue:
Mtap1a
Mouse Description:
microtubule-associated protein 1 A Gene [Source:MGI Symbol;Acc:MGI:1306776]
Alleles
There are 10 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa24659 | Nonsense | Available for shipment | Available now |
| sa44280 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa10906 | Nonsense | Available for shipment | Available now |
| sa19362 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa45851 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa1846 | Nonsense | Available for shipment | Available now |
| sa6130 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
| sa38058 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa31110 | Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa24659
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 |
|---|---|---|---|---|---|
| ENSDART00000067321 | Nonsense | 475 | 2253 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 19863104)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 19275081 |
| GRCz11 | 25 | 19373032 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGCCTTCTAAGAAAGAAACAGACGAGCATGAGGATGTATCTGTAGTC[G/T]AAACAAAGAGTGACTCTGTCAAAGAGAACAAGGTTGAGAAAAAAGAAGAA
Long Flanking Sequence:
CCATCGAGCCCATCACTCTTTTCCACAAGATGGGTGTGGGAAGGTTAGACATGTTTGTCTTGAACCCTGTGAAGGACAGTAAGGAAATGCAGTTCCTCATGCAAAAGTGGGCAGGTAACAGCAAGGCCAAGACAGGGATAATTCTTCCCAATGGAAAAGAAGGAGAAATATCTGTACCATATTTGACATCTATTACTGCTCTCGTTGTATGGCTCCCTGCCAGTCCCACAGAGAAAATCGTAAGGGTTTTATTTCCTGGAAATGCACCACAAAACAAAATACTTGAAGGGCTCGAAAAGTTAAAGCACCTTGATTTCTTGCGGTATCCAGTAGCCACACAAAAAGACATAAATTCTGGTGTTTCACCTTCAGCAGTAAAACAAACAAAACTAAAGCAAAGGACTGACAGCAAAGAAAGTCTAAAGTCATCTCCCAAGACTCACACACCAGCCAAGCCTTCTAAGAAAGAAACAGACGAGCATGAGGATGTATCTGTAGTC[G/T]AAACAAAGAGTGACTCTGTCAAAGAGAACAAGGTTGAGAAAAAAGAAGAAAAGAAACACACCAAGTCATTGAAACCAAAAGCAGAAGTAACAGAAAAGAAAAAGTTATTGAAGGAAAAACCACTAAAAAAACACCCGAAGGAAAGGTTGTCCAAAATGGATGAAAAGAAAGACAAAGAAAAGAGGGAGATTAAGAAAGAAAAACGTGTAATTAAACAAGATGATTCAGTGAAAAAAGATGAGAAAAAAATGAAAGCCAAGGACAGTTCTAAACCTGAATTGAGGAAAATAACTAAACCTGAACTGAAACCTTTCACACCAGAGGTCAGAAAGACCCTCCATAAGGCCAAAACCCAAGGGAAACCCAAATCAATAAAGAAAAAACCTACAACTGCCAAGGCAGAGATTGCAGAGATTACAGCAGAACCTGTGGCCGAAAAGACTGAACCTGAGAAGCAGGAGAATGGGACTGTAGAAGATATATCTGCTCCGGAAGATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44280
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000067321 | Essential Splice Site | 504 | 2253 | 3 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 19863013)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 19274990 |
| GRCz11 | 25 | 19372941 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAAGAAGAAAAGAAACACACCAAGTCATTGAAACCAAAAGCAGAAGTAA[C/T]AGAAAAGAAAAAGTTATTGAAGGAAAAACCACTAAAAAAACACCCGAAGG
Long Flanking Sequence:
GTTCCTCATGCAAAAGTGGGCAGGTAACAGCAAGGCCAAGACAGGGATAATTCTTCCCAATGGAAAAGAAGGAGAAATATCTGTACCATATTTGACATCTATTACTGCTCTCGTTGTATGGCTCCCTGCCAGTCCCACAGAGAAAATCGTAAGGGTTTTATTTCCTGGAAATGCACCACAAAACAAAATACTTGAAGGGCTCGAAAAGTTAAAGCACCTTGATTTCTTGCGGTATCCAGTAGCCACACAAAAAGACATAAATTCTGGTGTTTCACCTTCAGCAGTAAAACAAACAAAACTAAAGCAAAGGACTGACAGCAAAGAAAGTCTAAAGTCATCTCCCAAGACTCACACACCAGCCAAGCCTTCTAAGAAAGAAACAGACGAGCATGAGGATGTATCTGTAGTCGAAACAAAGAGTGACTCTGTCAAAGAGAACAAGGTTGAGAAAAAAGAAGAAAAGAAACACACCAAGTCATTGAAACCAAAAGCAGAAGTAA[C/T]AGAAAAGAAAAAGTTATTGAAGGAAAAACCACTAAAAAAACACCCGAAGGAAAGGTTGTCCAAAATGGATGAAAAGAAAGACAAAGAAAAGAGGGAGATTAAGAAAGAAAAACGTGTAATTAAACAAGATGATTCAGTGAAAAAAGATGAGAAAAAAATGAAAGCCAAGGACAGTTCTAAACCTGAATTGAGGAAAATAACTAAACCTGAACTGAAACCTTTCACACCAGAGGTCAGAAAGACCCTCCATAAGGCCAAAACCCAAGGGAAACCCAAATCAATAAAGAAAAAACCTACAACTGCCAAGGCAGAGATTGCAGAGATTACAGCAGAACCTGTGGCCGAAAAGACTGAACCTGAGAAGCAGGAGAATGGGACTGTAGAAGATATATCTGCTCCGGAAGATTTAACAAAAGACTTAAATAAAATCAAACCCACTGAAGTGACATATCAGTCAGAATCCCCCAAAAGTGACCTTACTGTCTCTGAATTACCAGCTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10906
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 |
|---|---|---|---|---|---|
| ENSDART00000067321 | Nonsense | 774 | 2253 | 5 | 22 |
| ENSDART00000067321 | Nonsense | 774 | 2253 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 19862063)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 19274040 |
| GRCz11 | 25 | 19371991 |
KASP Assay ID:
554-6229.1 (used for ordering genotyping assays)
KASP Sequence:
AGCAGTTTGAAGAAGAGGACGTGATTGAAAAAGCTGAGCTGGAGGAGGCT[G/T]AAGATTTAGATGCCATTGCAGATGAAGAAATTAAAGAGCTCTCTCCTGAG
Long Flanking Sequence:
ATCAGTCAGAATCCCCCAAAAGTGACCTTACTGTCTCTGAATTACCAGCTGAGAAAGATATTGAACCCTCAAAGTCTGCAGAGGACAAAGTTGGAGAAACCGATATGGTGGAACAGAAAACTAAAGTGGAAGAAGTATCTGCATCAGCAGGAATTAAAGAAGTGTCATCAGCTGCTGTGAAAGAAAAAGATGAGTCCCAAACTTCAGAAATTGAGAAATTTGAGGATGAGGGTGCTGCAATTGAAGATGAAGATGAGGAAGAGATTGATATACAGCCTGTTAAGAAAAAGACTGACGATGAGGAGGAGGAAGATATGGGAATTGGAGATGAAGAGGATGAAGGGCCAGCAAAAGAAACTAAAGACCTGGAGGGAGTGGACAGAAAACATGAAGTTGAGGAAATGGAGAAGCAAAAACAAGTGGAGGAAAGAAGGATTGAAGCTGAAGACGAGCAGTTTGAAGAAGAGGACGTGATTGAAAAAGCTGAGCTGGAGGAGGCT[G/T]AAGATTTAGATGCCATTGCAGATGAAGAAATTAAAGAGCTCTCTCCTGAGAAAGTCAAAGACGAAGAGGATGCATACATGTCAAATGTTGGAGGTGTCACAGCTGGCATTACCTCTACAGCGCAAGGCGCTGCTGCAGCAGAAAACCTATCATACATCCAGGATGAAACCATCCCAGGTTACTCTGAGACTGAGCAGACAATTTCAGATGAGGAGATCCATGAAGAAGCAGAGGACAGGATACCACACCTTCAGTATGAAGTTGGAAGCTATGACGTCTCTGTCCCAGACCAACCAGGCTCATTTGATGCCATGCATGGAATGAGAGAAATGCAAGCTGCTGCAATGGGCAATGGAACCAGCAAAGTATTCATGGGTGCACAGGAACCAGCGATTTCTATCTACACCAGCATTCTTGCAGCTCCATTAGCTGAAGAAGAACATGTTTCTTCAGCGACATCCATAACAGAGTATGACAAACTGTCTTCTCTACCCACTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19362
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 |
|---|---|---|---|---|---|
| ENSDART00000067321 | Nonsense | 774 | 2253 | 5 | 22 |
| ENSDART00000067321 | Nonsense | 774 | 2253 | 5 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 19862063)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 19274040 |
| GRCz11 | 25 | 19371991 |
KASP Assay ID:
554-6229.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGTTTGAAGAAGAGGACGTGATTGAAAAAGCTGAGCTGGAGGAGGCT[G/T]AAGATTTAGATGCCATTGCAGATGAAGAAATTAAAGAGCTCTCTCCTGAG
Long Flanking Sequence:
ATCAGTCAGAATCCCCCAAAAGTGACCTTACTGTCTCTGAATTACCAGCTGAGAAAGATATTGAACCCTCAAAGTCTGCAGAGGACAAAGTTGGAGAAACCGATATGGTGGAACAGAAAACTAAAGTGGAAGAAGTATCTGCATCAGCAGGAATTAAAGAAGTGTCATCAGCTGCTGTGAAAGAAAAAGATGAGTCCCAAACTTCAGAAATTGAGAAATTTGAGGATGAGGGTGCTGCAATTGAAGATGAAGATGAGGAAGAGATTGATATACAGCCTGTTAAGAAAAAGACTGACGATGAGGAGGAGGAAGATATGGGAATTGGAGATGAAGAGGATGAAGGGCCAGCAAAAGAAACTAAAGACCTGGAGGGAGTGGACAGAAAACATGAAGTTGAGGAAATGGAGAAGCAAAAACAAGTGGAGGAAAGAAGGATTGAAGCTGAAGACGAGCAGTTTGAAGAAGAGGACGTGATTGAAAAAGCTGAGCTGGAGGAGGCT[G/T]AAGATTTAGATGCCATTGCAGATGAAGAAATTAAAGAGCTCTCTCCTGAGAAAGTCAAAGACGAAGAGGATGCATACATGTCAAATGTTGGAGGTGTCACAGCTGGCATTACCTCTACAGCGCAAGGCGCTGCTGCAGCAGAAAACCTATCATACATCCAGGATGAAACCATCCCAGGTTACTCTGAGACTGAGCAGACAATTTCAGATGAGGAGATCCATGAAGAAGCAGAGGACAGGATACCACACCTTCAGTATGAAGTTGGAAGCTATGACGTCTCTGTCCCAGACCAACCAGGCTCATTTGATGCCATGCATGGAATGAGAGAAATGCAAGCTGCTGCAATGGGCAATGGAACCAGCAAAGTATTCATGGGTGCACAGGAACCAGCGATTTCTATCTACACCAGCATTCTTGCAGCTCCATTAGCTGAAGAAGAACATGTTTCTTCAGCGACATCCATAACAGAGTATGACAAACTGTCTTCTCTACCCACTTCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45851
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 |
|---|---|---|---|---|---|
| ENSDART00000067321 | Nonsense | 1065 | 2253 | 6 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 19861076)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 19273053 |
| GRCz11 | 25 | 19371004 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGAAAAGGCATCGGTAGCATCTCCTAAGGAGGATATGTCTTTTAAAGAA[C/T]AAGCAATTCTCTCTTCCTCATCTCACAGTGTTTCTAAGCTTCCTGTTTCT
Long Flanking Sequence:
CTCTACCCACTTCCATTGCAGAAGATCAGTCAGTGGCATCAGTCACAGCACCTCAGACTGAAGACACAGGAAAAAGCTCCCTGGTCTTGGACACTGTTCAACCAATTACACAGACTGAGGCAACCCAAGGGAAAGACTACTTACATTCAGCTGGAACCATCTCACCAACATCCTCCTTGGAGGAAGACAAGTGCTTCAAGTCCTCTCCCTCTGATGAATCCCCTCCACTTCCCTTAGAAGGCAAAACTGAGGGAATTGAGATGGCTGCCCATTACGATGATGAAGAAGAGGATGAATATGATCAAACGCCAAATGTTGACATTTCACTTGAAAAGTTACAAGAAGGATATGCCTCACCAGATAAACTTGAACACAAGGACAAAGAAATGGACAAACCCAAAAGTCCTGTGCCCTTAGCTCCTGATATGTCAAAATCCTCTATTCCTGAGTCAGAAAAGGCATCGGTAGCATCTCCTAAGGAGGATATGTCTTTTAAAGAA[C/T]AAGCAATTCTCTCTTCCTCATCTCACAGTGTTTCTAAGCTTCCTGTTTCTGAAGCTAGTGTTTATCCAGAGGTAGAAGACCGGTGCGTTAGCCCTGATGACAGCACTGTAAAAATGGCATCTCCTACACATTCTGGACCACCTAGTGCTTCTCACTCTCCCCTTAGAATGTCACCGGTGGAAGGAAAGGATAAAGTGCTCCTTAAAGACACTCATCAAGAACAAGGAGTGCCAATTAGCCCTACTGAATTTAAATTTGAAAAGAAAAATGAAAAACAAGAATCTGACATTTTAGATGAGAAGGAAAAACCTCAAGCAGAGAAAGAAGAAAAAATTATTATTCAGAAAGCAGTCACTGCACCATCCCCACTAGTTGATGACTTCTTGGCTAAAAAGGAAAGTGAGTCAGTTCCACCACCAAAAGATGTAAGTGATACGAAGGAAATACCAGATCCAAGTGTTGAAAAGAAAGTTGAAGTTAAAGAGGGCTTAAAAGAAGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1846
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 |
|---|---|---|---|---|---|
| ENSDART00000067321 | Nonsense | 1780 | 2253 | 15 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 19855936)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 19267913 |
| GRCz11 | 25 | 19365864 |
KASP Assay ID:
554-1837.1 (used for ordering genotyping assays)
KASP Sequence:
TCTTCAAGATCAAATATCTTCGGCAGAGGAAAAATCWGAGGAAGATATGT[C/A]AAGCATTAAATCTGACAAAGATCATGTCTCTGATCCTAAGCATGTAGAAC
Long Flanking Sequence:
GAAAGAAGATACTAGTTCAGTCCAATCTGAGACATCCAAACCCAGCGATGACAAACATGAACCACAGAGAACTGATAAAAAGCCTGAAGTGTCTGAATCCCTAACTGCCACTCAAGCGCCCATGTCTGATGGAACTTACTCATCATCTTCATCTATTAGTTACTCTTCTTCAACATCTGCATCATATTCTACTGGCCAACATATAGGAGATGGGCTAGATACACATATTAATGTTCCTAGTTTTCAACTAAGGTCAGATGGGGACACTGTATCATATGAATACTCTTCCCTAAAAGAGGAAGAGTCACCCACTATGGATTTACCATGTTTAAAAAAGGACGAATACATGGAAGTCTCGGATCGAATGACACATGCTACGACAACAGCTGAATCAATATCTAGTCTTGCTAGGTTTTCTCCTCTCAGTCCCCTGGAGGAATCCAAATCATTTCTTCAAGATCAAATATCTTCGGCAGAGGAAAAATCAGAGGAAGATATGT[C/A]AAGCATTAAATCTGACAAAGATCATGTCTCTGATCCTAAGCATGTAGAACCACCTTTCTCAAAAATGCCAGAATCGGAAACTTCTAAGCATGCAGCTCAAACAACTGAGGTGGCATCTACAACATCTCTCAAGTTTGAGATAGCGCCTTTGGAGAAAGCTGACTCCAAGGAAAAACACTCAGAAGAAAAGTCCTCTGATGATGAGCCTGAGAATAATAAAAGCGATTTTGAGGAAGGAACACTGCCTTGCAGAATTGAGTGTGACAAATCATCTTCATCTGAGCAACACACTGATGCAAATGTACTCTCAACCAAAACATTGCATTCATTTGAGCTGAAATGCAGCTCTGAACCAACAGAAATGGCAAGTTCTCAAAACGTGCCAGTCATGGCATGTGGGACTCTGAGTACAAGCACACTAAGTGAACAAATCGTGAAGCAAGAATGGGAAGAGATGTCTGAAAAAATTAAAGACTTGCCTGAGAAAGTAGAAGAGAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa6130
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 |
|---|---|---|---|---|---|
| ENSDART00000067321 | Essential Splice Site | 1817 | 2253 | 16 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 19855152)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 19267129 |
| GRCz11 | 25 | 19365080 |
KASP Assay ID:
554-3709.1 (used for ordering genotyping assays)
KASP Sequence:
GAAAGCAAAGAAAARGACAAAGAGAGTAAAAAACAAACTGAAGAAATTAT[T/A]ATGGAAAAATATAGCAAAAAYGTACCYGAGTCTAGCCAGCATACTGCCAT
Long Flanking Sequence:
CAACACACTGATGCAAATGTACTCTCAACCAAAACATTGCATTCATTTGAGCTGAAATGCAGCTCTGAACCAACAGAAATGGCAAGTTCTCAAAACGTGCCAGTCATGGCATGTGGGACTCTGAGTACAAGCACACTAAGTGAACAAATCGTGAAGCAAGAATGGGAAGAGATGTCTGAAAAAATTAAAGACTTGCCTGAGAAAGTAGAAGAGAGATTTGACATGAAAGAAGAAACGTTGAGCCAGGCAAAATGTGAAGAAGTGATAGTAAAGCATAAAGAAATAGAGGATGAACAGATACATCCTGAAAAGAAGTGTGATGTGAGGTCAGAAAAGATGGGAGAGATCCTAGATGGCAAGAAATCAGAGAATAAGAGTGAAAGTGAAGGAAAACCCAAAGAGTCAGAAGAAAAAGAAGAGGTAAAACAAGCTGAAATCGTAGTAGAAAAGGAAAGCAAAGAAAAAGACAAAGAGAGTAAAAAACAAACTGAAGAAATTAT[T/A]ATGGAAAAATATAGCAAAAACGTACCCGAGTCTAGCCAGCATACTGCCATTTCTTCCACAATGGAACATGAAGATATTGTATGTCTAAAGGCTCCCCCTGGCTATGGGGAAGATGTTTATGAAGATATAGACAGGGAAGAATCGGATGAAGAGAGGGAAGTGAAGTATGATTCTAAAGAACGTCCATCAAGTCCACCATCAGGAGCGCAGGCTTGTTACGCTGAAGTCTCCAAGAAAGCAGATGAGGGATTCACTCGACCTTCTGACCTCAGTATGGAGGCCACGTCCTCTCATTCACCTTCACTTTTTAAACATCGTAAAGGGGATATTTCCCCATCCTTTATTAATCCAAGCCCACATGATCTGTCAAGTGAGGAGGGAGACGATGATGCCAGAAGTGATCATTCAAGAGATGATGATGGTGATGAGCGTGAGCAGCACTCTGTCAAAAGGAGATCCCACAAGCAACAACATCATCATCAGCAAAGTCGTCAGGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38058
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 |
|---|---|---|---|---|---|
| ENSDART00000067321 | Nonsense | 1820 | 2253 | 16 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 19855140)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 19267117 |
| GRCz11 | 25 | 19365068 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAAGACAAAGAGAGTAAAAAACAAACTGAAGAAATTATTATGGAAAAATA[T/A]AGCAAAAACGTACCCGAGTCTAGCCAGCATACTGCCATTTCTTCCACAAT
Long Flanking Sequence:
GCAAATGTACTCTCAACCAAAACATTGCATTCATTTGAGCTGAAATGCAGCTCTGAACCAACAGAAATGGCAAGTTCTCAAAACGTGCCAGTCATGGCATGTGGGACTCTGAGTACAAGCACACTAAGTGAACAAATCGTGAAGCAAGAATGGGAAGAGATGTCTGAAAAAATTAAAGACTTGCCTGAGAAAGTAGAAGAGAGATTTGACATGAAAGAAGAAACGTTGAGCCAGGCAAAATGTGAAGAAGTGATAGTAAAGCATAAAGAAATAGAGGATGAACAGATACATCCTGAAAAGAAGTGTGATGTGAGGTCAGAAAAGATGGGAGAGATCCTAGATGGCAAGAAATCAGAGAATAAGAGTGAAAGTGAAGGAAAACCCAAAGAGTCAGAAGAAAAAGAAGAGGTAAAACAAGCTGAAATCGTAGTAGAAAAGGAAAGCAAAGAAAAAGACAAAGAGAGTAAAAAACAAACTGAAGAAATTATTATGGAAAAATA[T/A]AGCAAAAACGTACCCGAGTCTAGCCAGCATACTGCCATTTCTTCCACAATGGAACATGAAGATATTGTATGTCTAAAGGCTCCCCCTGGCTATGGGGAAGATGTTTATGAAGATATAGACAGGGAAGAATCGGATGAAGAGAGGGAAGTGAAGTATGATTCTAAAGAACGTCCATCAAGTCCACCATCAGGAGCGCAGGCTTGTTACGCTGAAGTCTCCAAGAAAGCAGATGAGGGATTCACTCGACCTTCTGACCTCAGTATGGAGGCCACGTCCTCTCATTCACCTTCACTTTTTAAACATCGTAAAGGGGATATTTCCCCATCCTTTATTAATCCAAGCCCACATGATCTGTCAAGTGAGGAGGGAGACGATGATGCCAGAAGTGATCATTCAAGAGATGATGATGGTGATGAGCGTGAGCAGCACTCTGTCAAAAGGAGATCCCACAAGCAACAACATCATCATCAGCAAAGTCGTCAGGAGGAAGGCAAAGAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31110
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 > A
Consequence:
Missense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000067321 | Missense | 2114 | 2253 | 19 | 22 |
Genomic Location (Zv9):
Chromosome 25 (position 19854016)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 25 | 19265993 |
| GRCz11 | 25 | 19363944 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGGGGAGACTCAGGAAGAGGGCTGGTCAATGGCGTTAAGAGTAATGCAG[G/A]TACAAATTAAGTTATCAGATTTTATAGAGATGATAGAGCCTTGTCTTTGC
Long Flanking Sequence:
GACTGAGGAATGTCCATCAATTACAGCAGAAGGAAACCTTGACTCTGATGAAGATGCAGAACATCTTCCAGTGGACAAAATGTCTGCAGCTGGCGGCAGTGGAGGAAGCCATCATTCCTCCTCCCCGAGGAGCCACGATCCCCCTCCCATTCCAATGAAAGACCCACTTCCACATCCACCACACCCTGATGTGTGCATGATTGACCCAGAAGCACTTCTTAATGGTCAGATCCAAACAGAAAGACCAGTCAAGAAAGACCATAAAACAAATAGAGGTTTGAGGAAGACACTAGGAAAATCTGCTTCGCCAGCACGTAAGGGAGATGCAAAAACCAGAAGATCTACTACCCCAGTGAAACAGACATCCAAAGACTCCTCACCTCATACTCTCAAAAGAAAAGATTCAGAAAAGACATTTCGTTTGACAAAAATGTCTGAGACAGAGGGATCCAGGGGAGACTCAGGAAGAGGGCTGGTCAATGGCGTTAAGAGTAATGCAG[G/A]TACAAATTAAGTTATCAGATTTTATAGAGATGATAGAGCCTTGTCTTTGCTGACAAGTAAACCTTTTAATTTGAATTCATGCCGTACATTAAGTTATAATTCCTAAGTTCACTTGTAGCACTGATTTTAGTTTTTAATTTATTCATTTACTACTGCAATTTGATCCATTTAACAGTGAATAACAATAACAAACAAATAATATCTTGACTGCACAGCAATGGTATTGCATACTGTTGATATTAATCAATGTTATTTAACCAATGTTATTATTTTAGCTTCCAACCTGAAATCCAATGCTGGGACTCCACCAGGACCACCCATCTATGTCGACCTAGCTTACATTCCCAACCACTGCAGTGCTAAAAATGTAGATCAAGAGTTCTTCAAGCGAGTGCGAGCAGCATACTACGTTGTCAGTGGAAATGATCCAGGGAGTGGTGAACCCAGCCGTGCAGTTCTAGATGCACTCCTAGAAGGGAAAGCACAATGGGGCACTAATC
Associated Phenotype:
Not determined