ZMP
LOC555987
Ensembl ID:
Human Orthologue:
JAKMIP1
Human Description:
janus kinase and microtubule interacting protein 1 [Source:HGNC Symbol;Acc:26460]
Mouse Orthologue:
Jakmip1
Mouse Description:
janus kinase and microtubule interacting protein 1 Gene [Source:MGI Symbol;Acc:MGI:1923321]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa42365 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa35659 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28282 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa28281 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa22443 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa42365
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 |
---|---|---|---|---|---|
ENSDART00000111315 | Nonsense | 167 | 824 | 2 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 15114181)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16976167 |
GRCz11 | 14 | 17281820 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCTGAGAAACTCAGACTGACGCAGGAGCTTCAGGAGGCCAAGACGTCA[C/T]GAAGGCAGGCAGAAGAGGCACTGGCCCATGCTGTACAGGCGGACCGGGCC
Long Flanking Sequence:
AAGCCACATACCTTCTATTTAGATTTTAGAACAATTTAACATATTGGATCAATGCATTCTATGGCACTTTAATTATGAAATGCTAATGTCACCTTGTTTTGTAGTGAGACCAGTAAGTGCACTTATCTTGTCTGTCATTTGTGTAGATGACCAAATTACGGGAGCGTTTCCAGGAGTTACGGGCCCAGCGTGAAACTGAGCAGCACAAGCACTCGGTGGCGCTTAGTGAACTCCGTGTCAAACTCCATGAGGAGAAGCAGCGCGAGGTGGCGGCCGCACGAGAGAGCCTGTCCCGACAGCATGAGGCTGAGCTGGCCCGGTCTGCACGTGTCCGCGAGACAGAACTGGCCCGGCTGCAGGCGCTGGTGTGCGTTTTACGGGACGGGGCCAGCAGCGAGCTACGAAATGCTCTGAAAGAGGAGGCAAGAGAGGAGGCCCGCAGGAGCTACGAGGCTGAGAAACTCAGACTGACGCAGGAGCTTCAGGAGGCCAAGACGTCA[C/T]GAAGGCAGGCAGAAGAGGCACTGGCCCATGCTGTACAGGCGGACCGGGCCAAAGCGGCTGATCTCAGAGTAGCCCATCAGGCTCATCAAGATGAGATCCAGAGAATCAAACGCGAGAGTGAGAGAGAAATACGGAGGCTGGTAAGATTGATATATTAAATACATACATATATGTCACCAAAATGGAAACATGAAAGATAGTCTGTTTTCAGTCAGTGTGTTTGCTTTAAATAAACAAACACAATGTTTATATGTTTATTAGGGGTGTGACAAGATTTTGCAAGATTAAATCGCAACAAGATATCTCGTTGAGGTGAAATGTTGTCTCTTGAGTTGTGATGTTATGATGGAGCATGAGAGTGAAATTAGCATTACATATTGGAGGTAGGATTGGATTTTAACTGCAAATGAAGTGCTTTGCACACACCTGACAACTCAAGCTTTGTGTCACGTGTCACTTGGTTGCTTGGGTGAGAAGCCAGTCAGTAGAGTTTATAGCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35659
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 |
---|---|---|---|---|---|
ENSDART00000111315 | Essential Splice Site | 543 | 824 | 10 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 15083747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16945733 |
GRCz11 | 14 | 17251386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGGCACGGATTGCCGACCTGGAGCGGAGCTTGGCAGAGAAGGGGCAG[G/A]TAAATGAGAAAGAGGGCGGGGAGAAGAAACCCCTGACTCCAGTCACATTG
Long Flanking Sequence:
ATCCCTCCACCACCCCAACTCCACACCATTAAACCCGATACTTACTTAAATCTGAGAGGGGAGTGTTCTGGAGCTGGGCTAGACACTGCACTCAAACCCTATCTTTTTCTATCCTGATTGGGGGAATAACCTAGTTAGGGTGTCTTTCCGAGCTCAGAGCCCTCTCCCCGGACAGCACGCCATATAAGCATATTCTATTCAGTCAAATATCTGTGAGTGTGAACTTGTCAACTCTGACTATAACATGAAAGGAATATTCTTAAAGCAACTCAAATAAACAATTTAACCATAATATTGTCTTATTCTGAATAAGGTAAATAGTGAAATGACTGATGTCCATGTAAACGTACCCATCATGCGTACTGTAGGTATGCCCCAGGCTGGCTCTTTTATTAGCTCTGTGCTCTGTCCGTCAGACGCGGGAGCAGCTGCAGACGGAGCTGATTGGCTGTCAGGCACGGATTGCCGACCTGGAGCGGAGCTTGGCAGAGAAGGGGCAG[G/A]TAAATGAGAAAGAGGGCGGGGAGAAGAAACCCCTGACTCCAGTCACATTGGCTTTGCTGCTTGTCTTTCTGACAGCCATGCTTGTGTGCTGGCGCTACACAGAGAGGATATGGCTCCAAATCATGTGACTTCACCCTCAGGATCAGTCATACTGTGTTGTTTTCTCAGAGTGTTTGTTCTTTACTTCTTCTTTGCTTGACTGATGCATGTTTCTTGTATAATTGTCGATCGATCATACCTGTCGCACAGCTTTTGTACTAAATGTGGTCAGTACTACAGTTTTTCTCAACTGCTTAGGCTCAATTCTCGATTTAAATTTGTATTTTTCAAAACATGATGTTTAGATCTCTGAACATTTAGCTCATTTGTCACTTCATAGTGGCATTTAAGCAAATTGCCAATGCTTTGGCACATGTACAGTAAGTACAATTGTCTGTAGTTTGGACAAACACTAATTGCATATGGCTTGTTGATCAAAACTGATGAGTCGATTTTCTCTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28282
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 |
---|---|---|---|---|---|
ENSDART00000111315 | Essential Splice Site | 564 | 824 | 11 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 15077587)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16939573 |
GRCz11 | 14 | 17245226 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAAGAAAAACAAAATCTCATCAGGATAAACCAGGAGCTCAGAGAAAAG[G/A]TACAGCCTTTATCTTTAAATATCCTAAAACAGGCCTCAACATATACTCCA
Long Flanking Sequence:
AAATATTTGGAAAATATTTTAGAAATGGATTTAGAAGCATCCAATGAAGGAGAGGTCCTAATCCAAATAAAAAAAAGAAAGAAAAAACTTTTTACGACAGGTTATATAGTGTCAATAACTTTAGACAATATATTTATTTGAATTTAATTTGCATCAAATGATATCAATCCATTACAGAATAAAATAAATATACACATTTAACTCAAGCCCACACAGTTTATCACAAAATCCAGTACATCAAGAGAAACTGAGGATTTTGTAAAAGTCTCTTCATTTTTTCCACAGCTGTATATATTTTGTTAATATTTTGCACTGATTGTTTGTGACGCGACTGAATGAGAGTGTGGATGTGATTAGTAGTGATCAACAGGAAAGTTCTTGTAGTGTAATGTGTAGTGGTGTGTGTGTGTGTGTGTGTTTGGGTTTGTGTGACGCAGGACTCAAAGTGGGTGGAAGAAAAACAAAATCTCATCAGGATAAACCAGGAGCTCAGAGAAAAG[G/A]TACAGCCTTTATCTTTAAATATCCTAAAACAGGCCTCAACATATACTCCACACATTCACGATTCTTCTACTGTGTGTTTCTGTTTGTGTGTGTGTGTGTGTGGTAGATAGTATCGCTGGAGCAGTGTGAGATCCGATTGCGCTCAGAAGTTCGAGACACTCTGGATCAGAACGAACTACTTGAATTCCGCATTCTAGAACTGGAAGTAAGAGAATCTGTTTTGGTTCCACAGCAGCAAACAATGGCGGCAAAACCCGGTCCACATCTGCACAAGTTACACACATGAACCCATTTCACCCCTTTTACATGCACTGTTTTTGTGTTCATGTTATGTTAAAACTATTTTCATACGCATTTTAAATGTATTTCTATTTTAATAACTGTATATTTATACCACTGTTGTTTTGTTAGATATACATTTGGCTGGAATAAAATGTATTTGAATGAAACTCCTCATCAATCTTTTGGTTTTGACTGCACCTCCCGCATGTTGTGGTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28281
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 |
---|---|---|---|---|---|
ENSDART00000111315 | Essential Splice Site | 647 | 824 | 14 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 15071747)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16933733 |
GRCz11 | 14 | 17239386 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATCATTCCTGACCTCATGAAAAAGCTTGACATTCTTGGGGATAATGGGG[T/A]AAGAATTGTACATTTCGGCTGTTGTCTACTCGTTTGTCTTGTATCTCACA
Long Flanking Sequence:
TCTTATGAAATGTTTACATTGCAAAAATTGTTTGATTACCTGTCAACTACAGTATGTTATTGTGATATTTCATTCACTTTATTAAAAGCAATATGAAAAATGCGTAAAATTCAGTTTTAGAGATGTCATGTGGTATCTAGCTTGAGGTTAGCATCTTGAGCTACAGCACAAAATGGTGAAACATGCTGTAGTTTAAGAAGTTTAACAATAATGTCAACAGTAATTAGTAACTGAATCAAATGTTTTACATCATATTTAAGCATTTTACATGATTTTACATTAATAATTTGTAAATTACACATTTGTTGGACAGTATATCAATCCAGTTCAAGGAAAATGAATGGAATATTCTTGAAATGTATACTCGCAATTCTGGTGGTCATACATGTGCTGTGCGATAACAAATCATTTATTGTTTGTTAACCTTCACATGTGTTTGGTTTAGGATGTCATCATTCCTGACCTCATGAAAAAGCTTGACATTCTTGGGGATAATGGGG[T/A]AAGAATTGTACATTTCGGCTGTTGTCTACTCGTTTGTCTTGTATCTCACAATGGAGAAATTCACTTTTCTCCTTTACCTGACAGAACCTGCGAAACGAAGAGCAGGTGACGGTGATTCAGGCGGGCACTGTGCTGTCTTTATGTGAAAAGGTATCTTCTCCTTCATTCTCTAAAGATAAGATTTGTCTATTATGTTGGCAGTAGTTTTGTTTTATTGTTTTGGTGTGTGAGCGCAGTGGCTGAAGCAGATCGACAGCACTGAAGCGGCGCTGACACAGAAGATGATTGATCTGGAGAACGAGAAGGTGAGAACATCTGCTTCTGCCATCTGAGATCAATGTGCTGAACTGTTTGTTCTCACAGCCTGTCTAGTGAAAGATGAGGCCTGATGACAGTCGATTAAAAATGTATCATTAGTGTGTTCTGCTGGCGTTGACCTCGGTGTACTGATGTTATCAACAGGAGCTGTTCAGTAAACAGAAAGGCTTCTTGGAAGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa22443
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111315 | Essential Splice Site | 669 | 824 | 15 | 20 |
Genomic Location (Zv9):
Chromosome 14 (position 15071596)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 14 | 16933582 |
GRCz11 | 14 | 17239235 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGGTGACGGTGATTCAGGCGGGCACTGTGCTGTCTTTATGTGAAAAG[G/A]TATCTTCTCCTTCATTCTCTAAAGATAAGATTTGTCTATTATGTTGGCAG
Long Flanking Sequence:
CATCTTGAGCTACAGCACAAAATGGTGAAACATGCTGTAGTTTAAGAAGTTTAACAATAATGTCAACAGTAATTAGTAACTGAATCAAATGTTTTACATCATATTTAAGCATTTTACATGATTTTACATTAATAATTTGTAAATTACACATTTGTTGGACAGTATATCAATCCAGTTCAAGGAAAATGAATGGAATATTCTTGAAATGTATACTCGCAATTCTGGTGGTCATACATGTGCTGTGCGATAACAAATCATTTATTGTTTGTTAACCTTCACATGTGTTTGGTTTAGGATGTCATCATTCCTGACCTCATGAAAAAGCTTGACATTCTTGGGGATAATGGGGTAAGAATTGTACATTTCGGCTGTTGTCTACTCGTTTGTCTTGTATCTCACAATGGAGAAATTCACTTTTCTCCTTTACCTGACAGAACCTGCGAAACGAAGAGCAGGTGACGGTGATTCAGGCGGGCACTGTGCTGTCTTTATGTGAAAAG[G/A]TATCTTCTCCTTCATTCTCTAAAGATAAGATTTGTCTATTATGTTGGCAGTAGTTTTGTTTTATTGTTTTGGTGTGTGAGCGCAGTGGCTGAAGCAGATCGACAGCACTGAAGCGGCGCTGACACAGAAGATGATTGATCTGGAGAACGAGAAGGTGAGAACATCTGCTTCTGCCATCTGAGATCAATGTGCTGAACTGTTTGTTCTCACAGCCTGTCTAGTGAAAGATGAGGCCTGATGACAGTCGATTAAAAATGTATCATTAGTGTGTTCTGCTGGCGTTGACCTCGGTGTACTGATGTTATCAACAGGAGCTGTTCAGTAAACAGAAAGGCTTCTTGGAAGAGGAACTTGACTACAGAAAGCAAGCGTTGGATCATGCCCAACTGGTAGGACCATATGCATGGTAGCAGTGTAACTATTGGATATTTATAACCAGAGGAGAAGCATTAGTGGTACAAAAACATTATGCTATATTATGAATTAACTTCCATGTAACA
Associated Phenotype:
Not determined