ZMP
KIF13A
Ensembl ID:
Description:
kinesin family member 13A [Source:HGNC Symbol;Acc:14566]
Human Orthologue:
KIF13A
Human Description:
kinesin family member 13A [Source:HGNC Symbol;Acc:14566]
Mouse Orthologue:
Kif13a
Mouse Description:
kinesin family member 13A Gene [Source:MGI Symbol;Acc:MGI:1098264]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32112 | Nonsense | Available for shipment | Available now |
sa36271 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12480 | Splice Site, Nonsense | Available for shipment | Available now |
sa9913 | Nonsense | Available for shipment | Available now |
sa36272 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa28758 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32112
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 |
---|---|---|---|---|---|
ENSDART00000101404 | Nonsense | 51 | 1932 | 3 | 40 |
Genomic Location (Zv9):
Chromosome 16 (position 56897397)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 53479962 |
GRCz11 | 16 | 53366789 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTCTTTTGTCTTATGTTTGCTGCTGTCGTCTGTTTCACTCTCAGGAAA[C/T]AACCAAAGGTAAGACATGTTTCACTCATATTTACCTTAGAGCGCAGTATT
Long Flanking Sequence:
GCTTTAAGTTATTCAAGGTGTTTTTTGTCACGCGTTTAGTCTGCATTATTGCATTCAGTGTAAACCTGCACAACTGATCACTGAAAGATCCGGATCTCAATTCAGTTGGCATTTCTGTGTGGAGTTTGCATGTTTTCCCCTTGTTGGCATGGGTTTCCTTCAAGTGCTCCAGTTTCCCCCAATCTCCAAACCCATATGCTATAGGGGATTTGATGAACTAAATTGGCTGTAGTGTACGAGTGTTAATGAGAGTGTGTGGGTGTTTCCCAGTGTTGGATTGCAGCTGGAAGGGCATTCGATGTGTAAACATATGCTGGTGGTAAGTTGGTGGTTCATTCCGCTGTGGCGATCCCAGATAAATAAAGGGACTAAGCGGAAAAGAGCCTGTAGCACTGTGTTTTCATGTAAAGCGTGTGATGAGTGTGAGGATGCTGACCGACTCTTCTCTTCTCTTCTTTTGTCTTATGTTTGCTGCTGTCGTCTGTTTCACTCTCAGGAAA[C/T]AACCAAAGGTAAGACATGTTTCACTCATATTTACCTTAGAGCGCAGTATTACTCGCCCTCCTGTGAGATTTGTATTGTGCGTGATTCATGCTCAGCAGGCACAGGATGTCAACATGACGTCAGATTGATTGATGTTGTACACCAATGTCATAGGGACGTTGCAGTTTGTTTGTAAATGAAAATTGTGTTGATGTCAGAACTCAACGTCAATGTCAAACCTAAAATCAACCAAATATCAACATCTAATGATGTTACAGCTTGATGTTGTGTGGACGTTACCACTATAACGTCGATCAGACGTTGGATTTTGGTTGCCATACCTGACGAATAAATGTCAGCATTTGACATCCAGTAGGGATTATAGATTTTGGTTGCACGATTATAGTCTGAGGATTAATCACAGTTTCACGGTTATTATGTATTCATTCATTTGATTTCAGAACACTACTAGTTTAGAAAAATCACATGAAAACTCCTTATATTGTAGTGTTCTTTAACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36271
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 |
---|---|---|---|---|---|
ENSDART00000101404 | Nonsense | 197 | 1932 | 8 | 40 |
Genomic Location (Zv9):
Chromosome 16 (position 56921366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 53503931 |
GRCz11 | 16 | 53390758 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCAGTTTATGTGGTTTATGAGTGTGTTTTCTGTGCTTCATCAGGATATC[G/T]AGTCTCTGATGTCGGAGGGCAATAAATCTCGAACCGTCGCCGCTACAAAC
Long Flanking Sequence:
CTGTAAAAGTTATCTAAAAGTAATCCAAAAGTTGTCAGATTACATTACTGTAAAAGTAATCTAAATGTAGTCAGATTACAATACTGTAAAAGTAATCTAAATGTAATACAATAGTAGTCAGATTACATTACTGTAAAAGTAATCTAAATGTAGTCAGATTACAATACTGTAAAAGTAATCTAAATGTAATTCAACAGTAGTCAGATTACATTACTGTAAAAGTAATCTAAATGTAATCCCAAAGTAGTCAGATTACGTTACTGTAAAAGTAACCTAAATGTAATCCAAAAGTAGTCCGTTTACGTTGCTGTAAAAGATATCTAAAAGTAATCCAAAAGTAGTCAGATTACATTACTGTAAAAGTAATCTAAATGTACTCAGATTACAATACTGTAAAAGTAATCCAAAAGTAGTCAGATTACGTTACTATAAAAGTTTTCGCATGTGTGTTGCAGTTTATGTGGTTTATGAGTGTGTTTTCTGTGCTTCATCAGGATATC[G/T]AGTCTCTGATGTCGGAGGGCAATAAATCTCGAACCGTCGCCGCTACAAACATGAATGAAGAAAGCAGTCGATCCCACGCCGTCTTCAGTGTTATCCTCACACAGACGCTGTACGACCTGCAGTCCGGGGTCAGAACTAATAAAACAACATTATTCTTTCCATACTCAGTGGATGCATTCATCTTTATTTTTTTATTACATAGTTTTTTTTTACTTGTTTGTGACATGCAACAAAACACATTTTCTTTTCAAACATATATATAATATATATAATGGATAATACAGTTTGTAAAGTAGTGTTTCCCGTCTTTTAGTGGATATATGAGATGATTACTTGGTTACTTTGGCCCAATCCCAATTCTATTTTTGTACCCCTTCCCCTTCCCCATTTTCCCTTGAAACCGAGGGGAAGGGCTTCAAAATTTACCCCTACGAATTGGAACAGCACTTCAGTACCTGCACACGTCATCATATGTCATCGCGACCTCTTGCTATGATGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12480
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:
Splice Site, Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101404 | Splice Site, Nonsense | 1024 | 1932 | 24 | 40 |
Genomic Location (Zv9):
Chromosome 16 (position 56939615)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 53522180 |
GRCz11 | 16 | 53409007 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGCTGCACAACACTAAAGACTCCAGCACTGGAGGAGTGTTTCAGCTGCGC[C/T]AGGTACCACACACACTCCTGCTACACACAGACTCACGGATGAGAAACACA
Long Flanking Sequence:
CTCTGGGAATGTGTGTGTGTGTGTTGCAGGATTTCGTGGTGCAGGTGACGGAGGAGTTTCTGGAGTTCATCTCTGACGGGGCTCTCGCTATAGAGGTGTGGGGTCACAGATACACCGGCAACGGACGCTCCGTCTGGGAGACGCACACACTGCAGGCCAAGAAGCGGACACTTAGAGACCGGTGCGTGTGTGTGTGTGTGTGTATCTGTGTGTTTGTGAGAGAGAAAGATGTGTGTGTAGGAGGTAGAATGAGAGCGAGTGTGTATATGTTCTGTTTCCTGTGTTCGTTTTTCATATTTGTACTGTGTGTGCATGTGCATGCGTACTCTTATGTGTCTATGAGACTGTGTGTCTATGTCGATGTGTGCAGCTGGAGTGAGGTGTCCCGCAGTATCGAGCTGTGGGTCTCCATCCAGGAGCTGAATGAGCAGGGCGAGTACTCGTCTGTGGAGCTGCACAACACTAAAGACTCCAGCACTGGAGGAGTGTTTCAGCTGCGC[C/T]AGGTACCACACACACTCCTGCTACACACAGACTCACGGATGAGAAACACACACAAAACACTCTACTCAGGCCCGTAGCCAGCCTGGTGTAAGGCAGACCCGGCGCTACGGGGGGGCAAAGGGGGGCATTTCCCCCTCAGAAAGAATTTGTGCCCCCCCAGTTTTTATAAAGGATTGTTCACTCAAAACGGAAAATTCTTTCTGTCATTAATTATTAACACTCCTGTCGTTCCAACCTTCAGAACACACATTTAAATATTTTAAAATATATGACATAGCAATTGAATTATGAAAATTGTGAGATTAAAGCTAGTCCTATAGTCCAGAGATCCGGTCCCCGCGTTAGGTCAGGTGCGCCGCAAATAAAACACGCACACGGCGATGGAGGCGCACTCAACTCACAAGTGAGAAAAGTGGGTGACATGATAGGAGCAGCTTAATTCATTACATGTTTTGGTCAACTAATTCTTTAAACACAACTCTCTTGAGCTCTAAAAGGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9913
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 |
---|---|---|---|---|---|
ENSDART00000101404 | Nonsense | 1390 | 1932 | 35 | 40 |
Genomic Location (Zv9):
Chromosome 16 (position 56969569)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 53552134 |
GRCz11 | 16 | 53438961 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TTTTTTTTTACTTTAACATGCTCATATATGTTTTTCTAGAGCTCTAGTTG[T/A]AAATCAGACGGCCGGACGGGTTGTGAGGWTGAAGATGTGAAGGTCAGTGA
Long Flanking Sequence:
TCATTCAAATAAGGGCGGCACAGTGGCTCGTTGGGCTGGCTCACAGCAAGAAGGTCGCTGGTTCGAGCCTCGGCTGGGTCAGTTGGCATCTCAGTGTGTAGTTAGCATGTTCTCCCTGCGTTCCCGTGGGTTTCCTCCGGGTGCTCCGGTTTCCCCCACAGTCCAAACACATGCGGTACAGGTGAATTAGTTGGGCTAAATTAGTAGTGTATGAGTGTGAATGAAGTGTATGGATGTTTTCCAGTATTGGGTTGCAGCTGGAAGGGCATCTGCTGCGTGAAACATGTGCTGGATAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCTGATTAATAAAGGGACTAAGCCAAAAAGAAAATTACATTTGAAAATAAATATAAATAATTTGAATAAAATATTGCACATTTTCATATTTATTATTGCACTTTTTTTTTAGTTTTCCTTTACATTTTTTTTTTTACTTTAACATGCTCATATATGTTTTTCTAGAGCTCTAGTTG[T/A]AAATCAGACGGCCGGACGGGTTGTGAGGATGAAGATGTGAAGGTCAGTGAACAGACGGTTTGTATAAAGGCTTTATACTTCTCCATGAAGCGCACGTGTATGTTCCGGCCAAGCGGCAACCTCCCGCTCTCTCTCAGGAAGCCAATACTGAAGTAACTAAAACTGCAATTCATCCGAAATTCCGCTAGTCCTGGCCGCTCCTGCTCCAAAACAGAGCAAATTTCAATTGAGCCCACTGTTAGAATGGCCAACTTTACAGCAGAAAAAAAGGTGTTTACAGCCTGGTACAAAAAAAGATTTTGGTTAATACAGCTAATATTACCCTTCATGACAACTGTGAGGGGGGTGAATTTATTTACAACTCATCCGTTTCCTTTATATTAAGTTATATTAAGTTTGCATAATTAAGGGCGTGGCCACTTGAGTGACAGCTAGATCTCGTTGGTCGTCGTCACGTCACCTCAGCTGAATCCTGCAGATCAGCCACTGAACTCGGCATA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36272
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 |
---|---|---|---|---|---|
ENSDART00000101404 | Nonsense | 1575 | 1932 | 39 | 40 |
Genomic Location (Zv9):
Chromosome 16 (position 56980386)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 53562951 |
GRCz11 | 16 | 53449778 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTTTGAGATCTACAATGCGAGCCTCGAGACCCAAGAAGGAGCTTTATG[T/A]GCACGCAGTGAATTGACCTCCGGGATTGGGATGTTATCAGGAACTCGAGC
Long Flanking Sequence:
AATAGTCAAGGGTGTTTAACTGATTGTATTTCAATTACATTACAACGTCGATGCTCTAAAAGGAATCTTATCAGATTGAAAATAGCCACATAAAGCTTTCACTGGAAAATGATCATTAGCCGAAAAACACTGGCTGTGCATATAGCCCAATAAATTAAATAATGGGTTTTTTGGAAACTCTGATTTAGGTTCCAGTCAAGACACAATGTTGTAAACACATAGACTGAATAAAATAAGCAAAAGATATGCTTTAAAATTCCACAAGAGGGCGATAGAGCACTTCCTAATCACTGCATTGCTGTTTTTTTCCTATTTGTTCATTGCTGATTTGTCCAGGATTCAGAGGAGGATGATCCAGGCATGGATTCAGCCTTCACCTGTTCCAATGTTCCAGCCCTCGGCTCTCTGGAGCTCCAAAACTTCAAGCCTTACATCCCGGAGGAATTTGCCAACTTTGAGATCTACAATGCGAGCCTCGAGACCCAAGAAGGAGCTTTATG[T/A]GCACGCAGTGAATTGACCTCCGGGATTGGGATGTTATCAGGAACTCGAGCTGCAGAAAAGGAAGTTTCCCGTAGTCCCACTGCCAGCAGCTGCACTAGTGGCTACTTCTCCCATAGTGCCTCAAACGCCACTCTATCTGATGTGCTCTTCAGTGGTAGTGATAGTTGTGACCAGCTCAACATTAGAGAACCAACAGATTCTCAGGAGCACGGAAAAGGCTGCCATTCTTCCAGAAGTGCCTCGGGATTTTGTCCAGCTCAGATTATTCCTTCCCAGCCTTATTCCCATTACTTGACTGACCGGGATTGTTCCCCTTCACCTCCCCGTAAAAGTATGCTGAGCATCAGTCAGGAATTCACAGACTTTAAAGGTGCAGATGATGGTGTAGAAGAGGATGCTCTAGGTCATTTTGGCTGTAAGGCAGAATCAGCTTCTCAAGATAAAACGCAAAACAAGAGTTCTCCTTCCAAGTGTCGTCTTCAAAATGGAAAAGACGAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa28758
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000101404 | Nonsense | 1715 | 1932 | 39 | 40 |
Genomic Location (Zv9):
Chromosome 16 (position 56980804)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 16 | 53563369 |
GRCz11 | 16 | 53450196 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGGTGCAGATGATGGTGTAGAAGAGGATGCTCTAGGTCATTTTGGCTGT[A/T]AGGCAGAATCAGCTTCTCAAGATAAAACGCAAAACAAGAGTTCTCCTTCC
Long Flanking Sequence:
ACTTCAAGCCTTACATCCCGGAGGAATTTGCCAACTTTGAGATCTACAATGCGAGCCTCGAGACCCAAGAAGGAGCTTTATGTGCACGCAGTGAATTGACCTCCGGGATTGGGATGTTATCAGGAACTCGAGCTGCAGAAAAGGAAGTTTCCCGTAGTCCCACTGCCAGCAGCTGCACTAGTGGCTACTTCTCCCATAGTGCCTCAAACGCCACTCTATCTGATGTGCTCTTCAGTGGTAGTGATAGTTGTGACCAGCTCAACATTAGAGAACCAACAGATTCTCAGGAGCACGGAAAAGGCTGCCATTCTTCCAGAAGTGCCTCGGGATTTTGTCCAGCTCAGATTATTCCTTCCCAGCCTTATTCCCATTACTTGACTGACCGGGATTGTTCCCCTTCACCTCCCCGTAAAAGTATGCTGAGCATCAGTCAGGAATTCACAGACTTTAAAGGTGCAGATGATGGTGTAGAAGAGGATGCTCTAGGTCATTTTGGCTGT[A/T]AGGCAGAATCAGCTTCTCAAGATAAAACGCAAAACAAGAGTTCTCCTTCCAAGTGTCGTCTTCAAAATGGAAAAGACGAGGATTCTGTACCTCATGTGCCACCAGAAGCAACTCGGGAGATTGAGTCCCTTGAGGATCCAGAACTCTTTAAAGGTGCAGATGATGGTCTAGTAGAGGATGGTCTTGGTAGCTTTGGCTGTAAGGCAGAATCAGTTCCTCAAGCTAAAATCCAAGACAGGAGTTCTCCCTCGCAGTGTCATCTTCATAATGGAAAGCAGTTCTCTGGGGATTCTGTACCTCATGTGCAACCGGAAGCAACTCAAGAGATTGAGTCCTTTGAGGATCCAGAACTCTTGGAGGACTCTAGTGAAGATGAAAATGCACCGGTTGCTCAGTTGCCTGACTGGATGGCCCCTGGGGAACAGGTTTGGGTGGGCAAACAGAGCGGGATGGTGCATTATGTTGGAGGGGTGGAGTTTGCCAAAGGCATCTGGGTTGGA
Associated Phenotype:
Not determined