ZMP
NP_001121673.1
Ensembl ID:
Description:
microtubule-associated protein 1B [Source:RefSeq peptide;Acc:NP_001121673]
Human Orthologue:
MAP1B
Human Description:
microtubule-associated protein 1B [Source:HGNC Symbol;Acc:6836]
Mouse Orthologue:
Mtap1b
Mouse Description:
microtubule-associated protein 1B Gene [Source:MGI Symbol;Acc:MGI:1306778]
Alleles
There are 8 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa40489 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16322 | Nonsense | Available for shipment | Available now |
| sa17173 | Nonsense | Available for shipment | Available now |
| sa40488 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa16946 | Nonsense | Available for shipment | Available now |
| sa33650 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33649 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa40489
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 |
|---|---|---|---|---|---|
| ENSDART00000085142 | Nonsense | 130 | 2033 | 4 | 7 |
| ENSDART00000114399 | Nonsense | 130 | 1976 | 4 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 36898960)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 34680909 |
| GRCz11 | 5 | 35281062 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTACATAAATAGTATAAACTCTGTTTACACCTAGGTACGGCTAATGGTCT[C/A]AGACACAGCCCATCATAAGCTGCTTGTCCTGGCAGGACAGTGCTTTGAAA
Long Flanking Sequence:
GTCACAGTTGCAGGCAAACTTCTTAATGCACAACACGGTCAAACACCATAAAGCCGTGCTTGCACACTATGACTGCAGTTTGACTCTGCATTAATAATATGGTAGAGCACTGCAGGTCTGACCCTGGCCGGCTGCCCAGAACAGTCAATGGCAACAAATTGGAAAATGCTGGCATGGAGAGTGAACAAAAAAAAGAGAGGAAAAAGCAAAAAAAGAAAAGCAGAAGTACATTTGTAAATGAATGATTTTTAAAGTTAAAGTCACAGATAACTGCAAAAAGTTTAGCTGAGCTCATAGAAACAGGCATACTTTTGTTGGCCAGGTTTTTAGGAGTATGATTTCATCTTTTTGGTAACATCAAATTGGTAACATTTTGGTAACATCATTCATTTTTTGTAGATATTGCACTTACATGTTATACCTAAAAATAATCTGCAAATGTTTCTTGTAGTACATAAATAGTATAAACTCTGTTTACACCTAGGTACGGCTAATGGTCT[C/A]AGACACAGCCCATCATAAGCTGCTTGTCCTGGCAGGACAGTGCTTTGAAAATACAGGCGAGCTGATTCTTCAATCAGGCTCCTTTTCTCTCTCCAGTTTCATTGACATTTTTACAGATCAAGAGGTAAGTGACTGTTTTTCTTGGTGAAAACATGCACTTTACACTGTAACCTGACAATGTGACCCTGGACAACAAAGCTGATTTTATGTTGCATGGCTATATTTTTGGCTATAATATTGGCAATTTTTGTGTAAACGTTGTTGTGGCAATTTTTGGCAGGTTATGTGTAATGTGTATTGCAATGCACTTTGTGTAGACAACAAAGCTATTTTCTTTGTATTTAGATTTTAAACATATTTCAAACAGTTGTATTTTGCCCAAATATTGTTAAATCCTATTAAACCATAAATTAATGGAAAGCTTATTTATTCACCTTTCAGTTGATGTATAAATCCCAATTTTAAAAATTACATTACTGGCTAGTTTTGTGGTCCAGGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16322
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085142 | Nonsense | 505 | 2033 | 5 | 7 |
| ENSDART00000114399 | Nonsense | 505 | 1976 | 5 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 36897421)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 34679370 |
| GRCz11 | 5 | 35279523 |
KASP Assay ID:
2259-6146.1 (used for ordering genotyping assays)
KASP Sequence:
TCCTTTTTCCAGGCAATTCTACTCAGAATCATATTCTAGAAGGCCTAGAA[A/T]AACTTAAACACTTAGACTTCCTCAAATATCCTGTGATCACACAAAATGAG
Long Flanking Sequence:
AGGGGTCTACAGCTAACAGTGACTGGACAAAGAATATGATCTCACCTGATATTGGTGTTATGTTTGCCAACATGCCTCAGAACCTGGAAAATCTTGAACCCAACTACAGAATTAGAAGAAATGCAGAGGAGGCAGCCTTCACACTGCAGTACTTAAACAAGTTGTCTCTAAAACCTGAACCTCTGCATAGGAGTATAGGTAATACAGTAGAACCAATTATACTATTCCAGAAAATGGGGGTCGGAAAGCTTGAAATGTATGTTCTTAACCCAGCTAAGAACAGTAAGGAGTTGCAGTTTTTTCTGAAAGAATGGTCTGGTAGTGATAAAGACAAAGCGACCATCTTGTTACCAAATGGAAAAGAATCAGAACTCCCCGTGTCATATTTGTCCTCTATCTCATCGCTGATTGTGTGGCATCCTGCTAACCCATCAGAAAAGATTGTCCGCGTCCTTTTTCCAGGCAATTCTACTCAGAATCATATTCTAGAAGGCCTAGAA[A/T]AACTTAAACACTTAGACTTCCTCAAATATCCTGTGATCACACAAAATGAGCTCAATTTAAACTTAGCCCCGACACTGAAACAAGCAAAGATGAAACATAAGACAGACAGTAAAGAGAGTCTCAAGTCCACATCAAAACCATCCCCTACCAAAAATCTCCACAAAGAATCCAGGGAAGAAACCACTGAAAAACTAAAAACTGTAAGTAAAACTGAACCAGCAGAAAAACAGGAGCCAACACAAAAAATAGAGAAAAAGGAAAAAACACTTGTGAAAAAAGTGAAAGCAGGGGAAAAGGACATTAAAAGCAAGGTTGAGCAAACACACAAAACTGACACTCCAGAGAAAAAGAAAGTTGAAATTAAACCAAAAACTATAAAGAAGGAATCCAAAAAATCTGTGGAAAAGACTGAGACTGTTAAAACTGAAAAAAACGTACCCAAGAAAGAAGACAAGGTTAAAAAAGAAGACAAGGTAAAGAAAGAAGAAGTGAAAAAAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa17173
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085142 | Nonsense | 753 | 2033 | 5 | 7 |
| ENSDART00000114399 | Nonsense | 694 | 1976 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 36896677)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 34678626 |
| GRCz11 | 5 | 35278779 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCCTGGTAGCCCTGCCAGATCTAAAGACAAGGCCAAGTCCAAGCCCACC[A/T]AAAAAGATGCAGGAGAATCAGTGGCAGCACCTWCCGTCTCAGGAGCCACG
Long Flanking Sequence:
AAATAGAGAAAAAGGAAAAAACACTTGTGAAAAAAGTGAAAGCAGGGGAAAAGGACATTAAAAGCAAGGTTGAGCAAACACACAAAACTGACACTCCAGAGAAAAAGAAAGTTGAAATTAAACCAAAAACTATAAAGAAGGAATCCAAAAAATCTGTGGAAAAGACTGAGACTGTTAAAACTGAAAAAAACGTACCCAAGAAAGAAGACAAGGTTAAAAAAGAAGACAAGGTAAAGAAAGAAGAAGTGAAAAAAGAAATTAAAAGACGAGACGTCAGGAAAGACTCCCTATTAAAGGAGAGCAGAAAGGATGAAAAGAAAGAATCCCTAAAAGATTCAAAAGAGCCAATGAAAGATTTAAGGAAAACTGGTAGCTTGAAAAAGAATGCCCCTAGCACACCTGATGTGAAAAAACCTGCACCTAAACCAAAGGTTGCAGCACGTGGGAAGAGCCCTGGTAGCCCTGCCAGATCTAAAGACAAGGCCAAGTCCAAGCCCACC[A/T]AAAAAGATGCAGGAGAATCAGTGGCAGCACCTTCCGTCTCAGGAGCCACGGTTGAAGAGCCCACCGTGGAAGACAGTGCAACAGATGTACTTGAGGCAGAGAGATCACTTATGTCTTCTCCAGAGGACCTCACTAAAGATTTTGAGGCTTTGAAAGCAGAAGAGATGGCTGAAGATGATGAGGTCCTTTCTCAGACCAAAATAGACGATTCTAATCAAGAAGAAGTGATTAGACATGAAGAAATAACTCATTGCAAAGAGTCTCCAGAAGCAGCAGAGTCCCTGGATGAAGGAATAGCAACCACTGAAGCTGAGGAGGAATGTGGAGGTACTCCAGGGGAACTAGAACCCAATCAGAAAAGCAACGGTACCAGTGAAAAGTTTGAAGATGAAGGGACAGGGTTGGAAGAGTCCTCTGAGTTAGGGGACTATGAAGAAAAGGGAGAGACAGAGGAAGTGGATGAGCAGGACAGAGCAATATCTACATTAAAAGATGAACAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa40488
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 |
|---|---|---|---|---|---|
| ENSDART00000085142 | Nonsense | 1029 | 2033 | 5 | 7 |
| ENSDART00000114399 | Nonsense | 970 | 1976 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 36895849)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 34677798 |
| GRCz11 | 5 | 35277951 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAAATGTCAACTCCAAGAGATGTAATGAGTGATGAGACAACTAATGAT[G/T]AAAGCGATTCTCCTTCCCAAGATTTTGTCAGGTACGGTATAACTACAGAA
Long Flanking Sequence:
GTACTCCAGGGGAACTAGAACCCAATCAGAAAAGCAACGGTACCAGTGAAAAGTTTGAAGATGAAGGGACAGGGTTGGAAGAGTCCTCTGAGTTAGGGGACTATGAAGAAAAGGGAGAGACAGAGGAAGTGGATGAGCAGGACAGAGCAATATCTACATTAAAAGATGAACAGGCAGAGCTTGAAACCAAGGAAGGGGCAAATTATGGTACCGATGAACCAGAATATCTTGACAAAGAAACAAAGTTGCAATGTTTTGATGTAACCACACCACCAAAGCTCACTGCACCTTTGTCTCCTGCTGATTCAGTTCATGATGAAACCCTACCTGCAGGTTCAGAAAGTGAGGCTGCCTCTGATGATGAAAACCGAGATGAGCCTCCAGAAGAATACACAACATCTGGACACACTCAGTCTACGATTGAGATCTCAAGTGTCCCAACGCCTATGGATGAAATGTCAACTCCAAGAGATGTAATGAGTGATGAGACAACTAATGAT[G/T]AAAGCGATTCTCCTTCCCAAGATTTTGTCAGGTACGGTATAACTACAGAACATGAACGAAAGAAACTTTCACCTCTTCAAGATGTTCCTGAATTAGACCACTCCAAGAGTGATGCCACTGAGGGCCATGATTATCATGTGTCAGCTTCCACCATTTCACCACCATCTTCATTGGAGGAAGATAAATCTGTCAAGGATTTTTCAGTTAAAGACACATTCTCTTTTGATTCAAGCAGGCTCACTACTACTACAAATTTGCCTTTTGTCAGGTCACCTTCTGTTGACCAAAATGTAAACATTGACCTTGTGCATGCAGGTGTATCTTCACCTATTGAACTGGGAACCACACTAGCAGGTATATCAAAAGGTCTGGAATCATACAGTCCAGATGAGAAGACCTTAGAGGGCCCTTTATCTCCTCAATCCTCAGGACACACACCTTTCTACCAGTCGCCGGTTGAGGAGAAAGCTGGCACTCTACCATCTGAGAAAACATCTGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16946
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:
A > T
Consequence:
Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000085142 | Nonsense | 1248 | 2033 | 5 | 7 |
| ENSDART00000114399 | Nonsense | 1189 | 1976 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 36895192)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 34677141 |
| GRCz11 | 5 | 35277294 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATCACCAATTTATGAAGCACACTTRTCGACCAATTTTGAATTTGACAGC[A/T]AATTGCCAAGTCARACTGACAATAGTGATAAAAAAATWGCAACTGATGAC
Long Flanking Sequence:
CACCACCATCTTCATTGGAGGAAGATAAATCTGTCAAGGATTTTTCAGTTAAAGACACATTCTCTTTTGATTCAAGCAGGCTCACTACTACTACAAATTTGCCTTTTGTCAGGTCACCTTCTGTTGACCAAAATGTAAACATTGACCTTGTGCATGCAGGTGTATCTTCACCTATTGAACTGGGAACCACACTAGCAGGTATATCAAAAGGTCTGGAATCATACAGTCCAGATGAGAAGACCTTAGAGGGCCCTTTATCTCCTCAATCCTCAGGACACACACCTTTCTACCAGTCGCCGGTTGAGGAGAAAGCTGGCACTCTACCATCTGAGAAAACATCTGAGGCCCAGGGTCCTGTTATTGTTGACATCACAAGTGACAAGGAATACTCTCCCAGAGAGGCTAGTCCTATTGATGAAGCAGTGCCTGTTTCACAACCAGGAAAGAAACAATCACCAATTTATGAAGCACACTTATCGACCAATTTTGAATTTGACAGC[A/T]AATTGCCAAGTCAAACTGACAATAGTGATAAAAAAATAGCAACTGATGACAATTCATCAGTAATATCTGCCACATCATTGCCACCATCCAAAATAGAAAGTCTGTCTGAAACAAAGCATTTCACAACATTTAAAGAGGACAGTAAAATGTCCATATCTGAAGGGACAACATCTGATAAGTCTGGCACTCCAGTTGATGAAGTTGTTGCAGACGACACATTTTCTCACATTGCCTCTGCATCAACAGCCTCACTTGCAACAAGTTCTTTACCGGAACCGACAACAGATGATGTCTCTCCATCACTTCATGCTGAAGTGGGCTCCCCTCATTCCACAGAAGTGGATGATTCTTTTTCTGTCTCAGTTGTTCAGACTCCAACCACGATGCAGGAAGCAGAAGTCTCTCCATCTAAGGAGGACAGTCCCCGTCCTATGTCAATCTCTCCCGATGTTTCACCAAAGACAGCTAAACTAAGAATGCCAGAACAAGAAACAAAATCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33650
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 |
|---|---|---|---|---|---|
| ENSDART00000085142 | Nonsense | 1665 | 2033 | 5 | 7 |
| ENSDART00000114399 | Nonsense | 1606 | 1976 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 36893941)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 34675890 |
| GRCz11 | 5 | 35276043 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACACTCTAGATAAATTTTCCACCAGCTCTTCATCATATTCATACAGTTGT[C/T]AAAATGTAGAATCTACTCAAATCTGTGATGGTGGGTCCATTGGACCAGAA
Long Flanking Sequence:
CCTCCCCATCAGATGCATCTCAGTCTACCCCATCAGTTACAACACCCTGCCAAATTGCAGAGCCAAGAGAAGTTTCTCCAGATCTAGATAATTTATCAGAGTCAGTCACTCCAAAACAGTCACCTAGCAAACAGTCTCCTTTGTCTCTTGACTCATCCCTTGTTTTAGGCAGACCAAGTATCTCTCATGAAGAAGTAAACAAAGGTAAACTTAGTCCCAATTCATTTTATGAAGAGAGTGCTATGGATAAATCAGAGGACACACAAAATCTAGAGAGGACTCCTCCAAAGGCTAGTTCACCCTTATCTCCTACTGAATCATTGTGTTTTTCTCAAAAGACAGAAGAGCTTAAACTTGGCTCAGAAACTACTACCTTCACAGGTTCAAAATCCCCCACCAGCCCCAAAATGTCACCTCCAGCCCAACTTTCCCCTTCTTCCACTCAGACAGACACTCTAGATAAATTTTCCACCAGCTCTTCATCATATTCATACAGTTGT[C/T]AAAATGTAGAATCTACTCAAATCTGTGATGGTGGGTCCATTGGACCAGAAACCTCAAAAGCATGCCATTCTCAGTCACGAGCAGAAGTGGACTTGTGTTTGGTGACCTCCTGTGAATACAGACATCCAAAAACAGAGCTTTCTCCATCCTTTATAAACCCCAGTCCTCTTGAGTACTTCATGACTGAGGAACCTAATTTGGGGGAGGAAAAGCCTCTTGCTAAGTCAGGAGAAGGACCACCGCCACCTGAAGAGAAACAGCAGACCAAACAGTGTGAGGAAACTCCACCCACCTCTGTAAGTGAATCAGCGCCCTCTCAAACAGACTCTGATGTTCCTCCTGGCACAGAAGAGTGCCCATCAATAACTGCAGATGCAAATATTGACTCTGAAGATGACTCAGAAACACTTCCAACAGATAGGACGATCACTTATCGTCATGCAGACCCACCTCCAGTCACACCCAGAGACCCTGCTCCTACTCCTCCACATCCTGATGCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33649
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 |
|---|---|---|---|---|---|
| ENSDART00000085142 | Nonsense | 1691 | 2033 | 5 | 7 |
| ENSDART00000114399 | Nonsense | 1632 | 1976 | 7 | 9 |
Genomic Location (Zv9):
Chromosome 5 (position 36893863)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 34675812 |
| GRCz11 | 5 | 35275965 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTGGGTCCATTGGACCAGAAACCTCAAAAGCATGCCATTCTCAGTCA[C/T]GAGCAGAAGTGGACTTGTGTTTGGTGACCTCCTGTGAATACAGACATCCA
Long Flanking Sequence:
CAGATCTAGATAATTTATCAGAGTCAGTCACTCCAAAACAGTCACCTAGCAAACAGTCTCCTTTGTCTCTTGACTCATCCCTTGTTTTAGGCAGACCAAGTATCTCTCATGAAGAAGTAAACAAAGGTAAACTTAGTCCCAATTCATTTTATGAAGAGAGTGCTATGGATAAATCAGAGGACACACAAAATCTAGAGAGGACTCCTCCAAAGGCTAGTTCACCCTTATCTCCTACTGAATCATTGTGTTTTTCTCAAAAGACAGAAGAGCTTAAACTTGGCTCAGAAACTACTACCTTCACAGGTTCAAAATCCCCCACCAGCCCCAAAATGTCACCTCCAGCCCAACTTTCCCCTTCTTCCACTCAGACAGACACTCTAGATAAATTTTCCACCAGCTCTTCATCATATTCATACAGTTGTCAAAATGTAGAATCTACTCAAATCTGTGATGGTGGGTCCATTGGACCAGAAACCTCAAAAGCATGCCATTCTCAGTCA[C/T]GAGCAGAAGTGGACTTGTGTTTGGTGACCTCCTGTGAATACAGACATCCAAAAACAGAGCTTTCTCCATCCTTTATAAACCCCAGTCCTCTTGAGTACTTCATGACTGAGGAACCTAATTTGGGGGAGGAAAAGCCTCTTGCTAAGTCAGGAGAAGGACCACCGCCACCTGAAGAGAAACAGCAGACCAAACAGTGTGAGGAAACTCCACCCACCTCTGTAAGTGAATCAGCGCCCTCTCAAACAGACTCTGATGTTCCTCCTGGCACAGAAGAGTGCCCATCAATAACTGCAGATGCAAATATTGACTCTGAAGATGACTCAGAAACACTTCCAACAGATAGGACGATCACTTATCGTCATGCAGACCCACCTCCAGTCACACCCAGAGACCCTGCTCCTACTCCTCCACATCCTGATGCCTGCATGGTAGATCCTGAAGTCCTGAAGGCTGAGGAGGCATCCGGGAAACCGAAAAAGAACATCAGCAGCAAGACTAAG
Associated Phenotype:
Not determined