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 |
sa12480 | Splice Site, Nonsense | Available for shipment | Available now |
sa9913 | Nonsense | Available for shipment | Available now |
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:
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