ZMP
kif1b
Ensembl ID:
ZFIN ID:
Description:
kinesin-like protein KIF1B [Source:RefSeq peptide;Acc:NP_919363]
Human Orthologue:
KIF1B
Human Description:
kinesin family member 1B [Source:HGNC Symbol;Acc:16636]
Mouse Orthologues:
Gm1305, Kif1b
Mouse Descriptions:
kinesin family member 1B Gene [Source:MGI Symbol;Acc:MGI:108426]
predicted gene 1305 Gene [Source:MGI Symbol;Acc:MGI:2686151]
predicted gene 1305 Gene [Source:MGI Symbol;Acc:MGI:2686151]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa24361 | Nonsense | Available for shipment | Available now |
sa16498 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa24361
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000005447 | None | None | 1782 | None | 47 |
ENSDART00000050915 | None | None | 1770 | None | 47 |
ENSDART00000053807 | Nonsense | 1074 | 1161 | 21 | 21 |
ENSDART00000141075 | None | None | 1763 | None | 46 |
ENSDART00000146458 | Nonsense | 1074 | 1161 | 22 | 22 |
Genomic Location (Zv9):
Chromosome 23 (position 29683219)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 29513786 |
GRCz11 | 23 | 29440327 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCACGAACGAGGTCGTAGTAACTCCTTTAACAGCAGCCAGCGAGCCT[C/A]GGACTCTACAGAGACCTTCAATTCTGGAAACCGGAAGCCCCCTCACCCCC
Long Flanking Sequence:
CGAACAGTCAGATGATCAGATGTGCAAGATGGTAGACGACGATTCTTCGTTTCGACGTGGGCGCATGAGGTGGATGCGACAAGAACAAGTGCGCCTCAAGAACCTCCAGCAACAGGAAATTTCCAAGCAACTCAGAAGGCAAACTGGACCTCACAGATTCATCCCACCTGAAGACCGCAAGCTGCGCTTCCCCTTTAAGAGTAACCCTAAACATCGCAACTCCTGGACTCCTGGCACCCATATTATTATCACCGATGAACAGGTGATTGAATTAAAAGTTCCCAAAGAAGCAGTCCAAGAAGAGAACGATGACACCGAAGAGTCTGTAGAGCCCAGACCACAAGTGGTCCCCACTATCCAGACATATCCCCCTCTTCCTAGTCCCATGGGTCAACGTAAAAGCAAAGATCTAGAGCAAGGTGTGAGTCATAGACCTAATCAAAGCCAGAAACTCCACGAACGAGGTCGTAGTAACTCCTTTAACAGCAGCCAGCGAGCCT[C/A]GGACTCTACAGAGACCTTCAATTCTGGAAACCGGAAGCCCCCTCACCCCCAACAGGCCTTTTACCAGCCACGCTACAACCAAAACCAGCATTATTATCCACCACAACCGCATCCACAGTTCTTTCATTACAATACTGATGCCGGCTACCAGCAATACCCACCCAATCAGCAGCACAGTCACCACAACAATTTTAACACGCCACCCCGTATGCGTAGGCAATTGTCTGCCCCCAATTTGAAGGGCAGTCGAGAAACCGCAGTGTGACATTGAAAGCAGGGCTATAGGTTCATGTACAAAACTAGCTGACGCTACAAATCACACATTACAGACTCATCACAGCATTGGACAGCTTGTCCCCATCAAGTCAAACTGTTATGTGGCACTTGTTAAAAATGATTGAATGTTTTTGTTGTCATTAATCCAAATTGTAATGGTCTACCTGAGAAATAGCTTCGTGAGCACCTTGCAACATTTTTATCCCCAATTTATGTTAACTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16498
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 |
---|---|---|---|---|---|
ENSDART00000005447 | Essential Splice Site | 944 | 1782 | 25 | 47 |
ENSDART00000050915 | Essential Splice Site | 933 | 1770 | 25 | 47 |
ENSDART00000053807 | None | None | 1161 | None | 21 |
ENSDART00000141075 | Essential Splice Site | 933 | 1763 | 24 | 46 |
ENSDART00000146458 | None | None | 1161 | None | 22 |
Genomic Location (Zv9):
Chromosome 23 (position 29674806)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 29505373 |
GRCz11 | 23 | 29431914 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCCAGGACCCCTTCTATGATCGTTCTCCATGGTTCATCCTGGTGGGCAG[G/A]TTGGTGGTGACCACTGCTCAGGAGAAACCTAATAGATGAGGGCAGGAGAG
Long Flanking Sequence:
ACATTGTAAACATTTTCCAATTCACTTTGTGATTTTTGTTTTTCCTCCATGTTTTTTTTCATATATTTTTCATGTTCTAATATTTAGAAACCTTGAATGTGTATTGCAGTAAAAATGTCCAATTATTCACGTACATGCAATGTGTATTGTCTGTTATATGTATAAAGTCACAAGCCTTGAATGTGGGTTATATAAATAATCCAGTACTCTTACTTGTGCCTGCATCATACCCACACACCTTTTTTTAGCTCACCTATTTTTCATGGCTGTGTGAACGAGCGTCTGGCCGACCGCACACCATCGCCCACCTTCTCCACCACCGATTCGGAGATCACTGAGCTGGCCGACGAGCGACAGAGCGAGATGGAGGACTTTATGGATGACGAGGCTTTCGTGGATGACACCAGCTCAGATGCTGGAACCGAGGAGGGCTCGGACATCTTCAGTGATGGCCAGGACCCCTTCTATGATCGTTCTCCATGGTTCATCCTGGTGGGCAG[G/A]TTGGTGGTGACCACTGCTCAGGAGAAACCTAATAGATGAGGGCAGGAGAGAGAGAGAATGAGTAATAGAGTTGTGTGGCTGTTCATCTAGCTTCATGTCCCAAAGATTATTTAGGTATAATATTAAAGGGGTTCTTTTATGTTATTGTATCCTATTTCACATACATTTATAGCATAATGTTGCTGTTTGAGCATCAAAGAGTTACAAAGTCCATTTAGAAAGGCGCAGTAAACACTGTTTCTGGACTCACTCAAAAATCTCAACTGTAATCCTGAGTTTCCTTCCATCACAAATTTGAAAAATAAAGCAATACAAGTGTGGTTTTGACATAATCTTTGTCAAATATGTTTATTAAACAGCTGATGCTAAATAAATTTGTAAAAATTGCATGATGTTTTAAAATGCAAAGCTTTAAAAAGCATTCAGATGTTGTTTGTTGTTGTCGGAGTATCGAAAGCACACTGGCCGCTTTTACAAAAGGGCTGGGGAAGCAGCTCATT
Associated Phenotype:
Not determined