ZMP
MAPT (2 of 2)
Ensembl ID:
Description:
microtubule-associated protein tau [Source:HGNC Symbol;Acc:6893]
Human Orthologue:
MAPT
Human Description:
microtubule-associated protein tau [Source:HGNC Symbol;Acc:6893]
Mouse Orthologue:
Mapt
Mouse Description:
microtubule-associated protein tau Gene [Source:MGI Symbol;Acc:MGI:97180]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa33151 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa30832 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa40055 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa33151
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130546 | Essential Splice Site | 618 | 752 | 8 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 22385729)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 22042120 |
GRCz11 | 3 | 22172668 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCAAGATCGGCTCCACTGAGAACCTCAAACACCAACCTGGAGGCGGGAAG[G/A]TAGTTATGTCATGCATGTCAGAAAATTGGGACACAATTAATCTAAAGCTG
Long Flanking Sequence:
CTTACATCACTAAAAAGATGGAAAGCTTATTTATTTAGCTTTTATCTGATGTATTAATCTCAATAATCATAAAAAAATAAACATTTATGTACAAACAAGTACATTTATGAATTGTTTTGTGGTTAATAAAATGACACGGAAGCTTGTAAATACTATCATGCCAATGGTAGGCTAGAAGGCCTTTTATAGGACAATAAACTATAGTGTAATAAAAAAAAGCAAAAACAGAAGAAAACATTGTGGTCTTCTGCTGTTTCTCATTGTCAGCCGACTCACCTAAAACCCCAGACCGCAGTGGTTGCAGCAGCCCCGCCAGTCGGTCCTCCACTCCCGGGCAACAGGTGAAGAAGGTAGCGGTTGTACGCACCCCACCCAAATCACCTGGCTCGCTGAGATCCCGCGCTCAGATTGCTCCTGTGGCACCCATGCCTGACTTGAAGAACGTCAAGTCCAAGATCGGCTCCACTGAGAACCTCAAACACCAACCTGGAGGCGGGAAG[G/A]TAGTTATGTCATGCATGTCAGAAAATTGGGACACAATTAATCTAAAGCTGCAGTGTTTAGTGCAGTAAACTGTAAGAGTCAGTTTTGACCTCATGCAATGTTCACAGGCCAGTCAATTCATCCTTTTTGAGTGTATATTGGGATTCTGTATGAGACTAGCATCATTTCTAAGAAGCCATTACTCAAGCTCACACAGAAAATATTTGAATACAAAGAAAAAATAATGCTTGCCAAGCTAATCTAATGTCTTTAAGAAGAAAACAAACCCCTTTGCAGAGCCGGGGAGCCGCAGTTCGGCTCAAAGCACCTGGTTAACACTCTTGACTCTCCTTTTCCAGGTGACTATTGTTCATAAGAAGATCGACTTGACTAATGTTAAGTCTAGATGTGGATCCAAAGACAATATGCAGCATGTTCCTGGTGGTGGTAATGTGAGTAACCAGTAGGGTTAGAAATCCTCACTTAAGTGCAGTTAATACTAGACATATATTATAAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30832
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130546 | Nonsense | 633 | 752 | 9 | 11 |
ENSDART00000130546 | Nonsense | 633 | 752 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 22381674)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 22038065 |
GRCz11 | 3 | 22168613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCAGATTCAGATTGTGCACAAAAAGATCGACCTAAGCAACGTCCAGT[C/A]AAAGTGCGGCTCCAAGGCCAACATTCATCACAAACCGGGTGAGATTTCAA
Long Flanking Sequence:
CTCACAAGTGCTGCTTTTGCCTTCAGAAACCTAGTTTTATCTGAAACCAAAAATAAGATACAACTTTTTTTTCCATTACAGTCTCCTCCTTTTGCACAACATTGAGCGAATCTCTTTCTGACTTTCCATGGCTTAAATCTTATTTAAAAGGGTATATATTTAAAAAAGTGTAATAGCCAAGTAAGGTTCTTTGAGAAAGAATCTGAACATGAATACAATCTGGTATAAATGCCATGTTCACTTTTTTCCACATTGAAATACGCCTCTCATTGAATTTGCATGAAGCATGGGCACAGCAAATGGAATTTATATCAATTTTGAGGTAGCTCTCAGTGGCAGCAAGATCCTACGAACCCTGTTGTTGTGATTAATGGTCATCTTCCTACAACCAATCATCAGCTCCAAAAGCATTTTCTTTTTGGCTGATGACTGATGATATTTGCTTCTTATGCTTCAGATTCAGATTGTGCACAAAAAGATCGACCTAAGCAACGTCCAGT[C/A]AAAGTGCGGCTCCAAGGCCAACATTCATCACAAACCGGGTGAGATTTCAATCAGATCATATAAGAAAACTGAATTTAAAATGAAAGTTAGACGGATTAGGCTTAAACCCTTTCAAAAAAAGTCAGTGTATCCACCTTACCTCACTTGACTAATTGTGAATTTTTACACTTTTACATGTATTTTAGGGGGTGGAAATGTCGAGATCAAATCTGAGAAGTTGGATTTCAAAGCCCAGTCAAAGGTTGGATCTCTGGAAAACATTGGACATGTCCCTGGGGGTGGACAGAGGAGGGTATGGATTTTACGTTATTAAACAAAAGCATTGATATTTGAGTTTCAAAAGTGCAATACTGTGTTGCATTAATTGCGTTGGATTACTTAAAAAAATAGTTCACCTAAAAATGAAAATGTACTCACTATTTTACTTACCCTCAAGTGCTTCCAGACTTTGAGTTTCTTTCTTATGTAGAACACAAAAGATCTTTTAAAGAAAGCCTGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40055
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130546 | Nonsense | 633 | 752 | 9 | 11 |
ENSDART00000130546 | Nonsense | 633 | 752 | 9 | 11 |
Genomic Location (Zv9):
Chromosome 3 (position 22381674)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 3 | 22038065 |
GRCz11 | 3 | 22168613 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCTTCAGATTCAGATTGTGCACAAAAAGATCGACCTAAGCAACGTCCAGT[C/A]AAAGTGCGGCTCCAAGGCCAACATTCATCACAAACCGGGTGAGATTTCAA
Long Flanking Sequence:
CTCACAAGTGCTGCTTTTGCCTTCAGAAACCTAGTTTTATCTGAAACCAAAAATAAGATACAACTTTTTTTTCCATTACAGTCTCCTCCTTTTGCACAACATTGAGCGAATCTCTTTCTGACTTTCCATGGCTTAAATCTTATTTAAAAGGGTATATATTTAAAAAAGTGTAATAGCCAAGTAAGGTTCTTTGAGAAAGAATCTGAACATGAATACAATCTGGTATAAATGCCATGTTCACTTTTTTCCACATTGAAATACGCCTCTCATTGAATTTGCATGAAGCATGGGCACAGCAAATGGAATTTATATCAATTTTGAGGTAGCTCTCAGTGGCAGCAAGATCCTACGAACCCTGTTGTTGTGATTAATGGTCATCTTCCTACAACCAATCATCAGCTCCAAAAGCATTTTCTTTTTGGCTGATGACTGATGATATTTGCTTCTTATGCTTCAGATTCAGATTGTGCACAAAAAGATCGACCTAAGCAACGTCCAGT[C/A]AAAGTGCGGCTCCAAGGCCAACATTCATCACAAACCGGGTGAGATTTCAATCAGATCATATAAGAAAACTGAATTTAAAATGAAAGTTAGACGGATTAGGCTTAAACCCTTTCAAAAAAAGTCAGTGTATCCACCTTACCTCACTTGACTAATTGTGAATTTTTACACTTTTACATGTATTTTAGGGGGTGGAAATGTCGAGATCAAATCTGAGAAGTTGGATTTCAAAGCCCAGTCAAAGGTTGGATCTCTGGAAAACATTGGACATGTCCCTGGGGGTGGACAGAGGAGGGTATGGATTTTACGTTATTAAACAAAAGCATTGATATTTGAGTTTCAAAAGTGCAATACTGTGTTGCATTAATTGCGTTGGATTACTTAAAAAAATAGTTCACCTAAAAATGAAAATGTACTCACTATTTTACTTACCCTCAAGTGCTTCCAGACTTTGAGTTTCTTTCTTATGTAGAACACAAAAGATCTTTTAAAGAAAGCCTGTA
Associated Phenotype:
Not determined