Busch Lab

ZMP

kif1b

Ensembl ID:
ENSDARG00000037020
ZFIN ID:
ZDB-GENE-030820-1
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]

Alleles

There are 9 alleles of this gene:

Allele Name Consequence Status Availability
sa44009 Nonsense Mutation detected in F1 DNA Not yet available
sa44008 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa24361 Nonsense Available for shipment Available now
sa16498 Essential Splice Site Available for shipment Available now
sa44007 Nonsense Mutation detected in F1 DNA Not yet available
sa37744 Essential Splice Site Mutation detected in F1 DNA Not yet available
sa8450 Essential Splice Site Mutation detected in F1 DNA Not yet available

Mutation Details

Allele Name:
sa44009
Status:
Mutation detected in F1 DNA
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
ENSDART00000005447 Nonsense 194 1782 5 47
ENSDART00000050915 Nonsense 229 1770 7 47
ENSDART00000053807 Nonsense 229 1161 6 21
ENSDART00000141075 Nonsense 229 1763 6 46
ENSDART00000146458 Nonsense 229 1161 7 22
Genomic Location (Zv9):
Chromosome 23 (position 29705972)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 29536539
GRCz11 23 29463080
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGTCGTTCTCACGCCGTCTTTACTATCGTTTTCACTCAGAGGAAGTA[C/A]GACAGCGAGACGGACCTCTCCACCGAGAAGGTTGGATATTTTACACCTAT
Long Flanking Sequence:
TTTAGAAATAGAAAGATAACACATTTAAATTCAAGCAAAAGATTGAAAAAGCAACATATATTTATTATATATTTTTTGTTCTTTTATACTTGGTTCTTTGTTGTTACATTTAAATTAGAGCTACCAGTTTTTGGACTGTTATTGTAAACTATTTTGTTAGATAAGCTCCAGATTTGGATTCAGAACTGGCTTTACAATATTATGTTTGTGCATATATATTAGTTAAGCATCCTATAGAAAATATCAATTTAAATGAAAGATTTGTTATGGGTGGACTTATATGCTGAGCACTGTACATAAACTACTGTAACAACCTAATATCTATTTCTGAGAAAAATCCTACTATTTGTTTTGCTATAATAATTATATGCATTTAGTATGACCCCTCTGACACTGATTTTATCCCTTGGTGTCCTCAGAACTGTCGCTGCAACCAACATGAACGAGACGAGCAGTCGTTCTCACGCCGTCTTTACTATCGTTTTCACTCAGAGGAAGTA[C/A]GACAGCGAGACGGACCTCTCCACCGAGAAGGTTGGATATTTTACACCTATCCACAGCCCATTATGACATTTCACAGAGCTCAGATTAGTCCTGCAGCACAAAGTCAGCAAATCCTGTACCAAGCGGAAAGGAAAACTAAGAGAAAGAGAGCCGTCCCACTCATCCTGCGTTTGTGGGGCTCATTGTGTAATCGCTGCGGGCACAAAGACGGCTCTGTGAGGTTCACGGACACAATGGCTATTGTACAGAGCTACTACATTAGATTCACTACACAGGTCGCGCTCTAATATTACTCATGCAGTTTGGCAGTGGGACCGCTGGCCCAAAATCAAGCATGGCAAAAAGAAAAGATTACCCAAGCGTTCTTTAGTGCAATTTGTTTAGCATCCATGCAACAATGATTTTACTACAGCACTCTGAAATGATTGGACGATTGAATTGTTTAGTTTAATGACTAATGGAATTTACAGATTCTGAATCAGTGTGATAGGATCTTTAGA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa44008
Status:
Mutation detected in F1 DNA
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
ENSDART00000005447 Essential Splice Site 283 1782 9 47
ENSDART00000050915 Essential Splice Site 312 1770 10 47
ENSDART00000053807 Essential Splice Site 312 1161 9 21
ENSDART00000141075 Essential Splice Site 312 1763 9 46
ENSDART00000146458 Essential Splice Site 312 1161 10 22
Genomic Location (Zv9):
Chromosome 23 (position 29702674)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 29533241
GRCz11 23 29459782
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CATTCCTTACCGAGACTCAGTGTTGACATGGCTGCTAAGAGAGAATTTAG[G/A]TATGGATGACAATCCATAATGGCTGTTAATGATTAATCACATGGAGATAG
Long Flanking Sequence:
TGTTCTTTTTGTGCTTCTTAGGAGGGAGCAAACATCAATAAATCTTTAACTACACTAGGAAAGGTGATTTCTGCCCTGGCTGAGGTGGTGAGTATTATTCGTTTAATTGTTCTCTTCCTGTGCCTGCCTGTCTTCAGTACTATAACTCTGTGTGCCGTGTGTCTTTCTCCTGGCAATGCTTCCCTACCCAGGATAACTGTACCAGCAAGGTAATCTTTCCCTGTGTACGATCAATAACCACTGAAACCTCTCGATCTAATCCTATTCGCCATTTTCCATGTAATCTTTTGTCCTAATAATCTGTCTTGTGCTCATCTTGATGTCTCATACATCAAGTTATTTCCACTTCCCCTTTTTAATCGTTACTGCCGTAGTTGTATTGACATACTGATTCTAACATGCTTCACTGGCTGTTTTGAAACAGAGCAAGAAGAAAAAGAAGACCGACTTCATTCCTTACCGAGACTCAGTGTTGACATGGCTGCTAAGAGAGAATTTAG[G/A]TATGGATGACAATCCATAATGGCTGTTAATGATTAATCACATGGAGATAGAACTGTTTGAATTTAGTTTAGCTTGGCTTTATCTTTGTGTTTTAAATTAGAATTTGCTTTTGATTTGTTTTGTTTTTTTGTTTTTTGTTTTTTGGCTTTGTTTTTGTTTTGTGTGTGTTTTTTTTTGGCTTTGTTTTTGTTTTGTGTGTTGCTTTTGCTTGCTTTTTGTGTTTTGTTAAGTAAATTATTTTGTTTGTGCTTTGCTTTGTTTTGTGTTTTTTATTTTGTTTGTGCTTGGCAGACCCAGTCTTTAAGCCACAGTCACATTAAGTATAAGGGTGCTTTCACACCTAGACTTTTGTTTCGAAACCTGTCGTGTTTCCCCAGTTAGCGCTGTTTGTTTGGCATATGCGAATCCAGCAATCATGTTCAGATCTGCGCCAAAACAATTGGTCCGAGATCGCCTGAATGAGGTGGCCTCTGCTCGATTTCAACGAACTCTGAGGCAGA
Associated Phenotype:
Not determined

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.
Availability:
Order Allele From ZIRC
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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

Mutation Details

Allele Name:
sa44007
Status:
Mutation detected in F1 DNA
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
ENSDART00000005447 Nonsense 1171 1782 31 47
ENSDART00000050915 Nonsense 1159 1770 31 47
ENSDART00000053807 None None 1161 None 21
ENSDART00000141075 Nonsense 1159 1763 30 46
ENSDART00000146458 None None 1161 None 22
Genomic Location (Zv9):
Chromosome 23 (position 29662686)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 29493253
GRCz11 23 29419794
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTTGAAGTGTTTGGCCATTACCAGCAACACCCACTGCACATTCATGGA[C/T]AGGATGTGGTCAGGTAACATCCTGCTATCAGTGTTGTCCAGTGTTACAGA
Long Flanking Sequence:
ATTGGGATGTAGTTGGAGGCTTATTTGATTTCCATTGCAGCAGAATATGATGCCTACCTAATAATGAGGTAAAAGCCAAAACAACAAGTTGTTTAGAATTGAACTGGGACCAAATCTTTGGAACCCCAAAAATGGCAACATCATGGGATGGGTCTATATTTACCTGCAACACCTTAGACATAATTGTAAAATAATTAATCCAATAATTCTGTAACAGAAGGCACATCATATTCATTATTTATCATATTTGTTATTCATTTTCTGGAAAAAAAAATCTAAATTATAAAAACAATATTTGCATAATTGATTTGGATACAATATTGTACATGTTCTTACAGGCAATACAGGAAATGTGAATGTTTTTGTGGATTTATTTTTTCACTTTTCTTATCCAGATCTCAGTGGAGGTGACAGAGTCCTTCATTGAGTACATAAAGACCAAGCCAATTGTATTTGAAGTGTTTGGCCATTACCAGCAACACCCACTGCACATTCATGGA[C/T]AGGATGTGGTCAGGTAACATCCTGCTATCAGTGTTGTCCAGTGTTACAGATTTGATCAACTTTATCATGCATGTCACAAAATATTTTTTGTTTTAGTCATATTTTTATTTATATAATATTATAGTATGTAGTAATATTTTAAATTAGATTTTTTTGTCATATTCTATTGATGTCATTTTTTTACTTAAATTTACATTTTCATTTTATGAATTATCATATACTGTTTTACTTTTATTTCTTGTTCAGTTTATTTGAATACCATTAGACAAAATTTTTATAAGGAGAGTACTTTGGATATTTTTTTAAAAAGTACCACCAGGAGGAATCTTAAATTATTTATCAAAAATTGAACTGAAAAATCATATTTAACCTTAAATATATTTTTGTGTAAATTATATTTATTTATATTTTATATATGTCTAAGTATCTTTTTATTGTAATATGAATTTGTTTTTATCATGTAATATTTTGTTGTATATCCAGTTTGCCATGAAATAATA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa37744
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000005447 Essential Splice Site 1549 1782 41 47
ENSDART00000050915 Essential Splice Site 1537 1770 41 47
ENSDART00000053807 None None 1161 None 21
ENSDART00000141075 Essential Splice Site 1537 1763 40 46
ENSDART00000146458 None None 1161 None 22
Genomic Location (Zv9):
Chromosome 23 (position 29648536)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 29479103
GRCz11 23 29405644
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACGGACATCGAGAGCTTGGTGGATCGAGAGAAGGAGCTGGCCACTAAGG[T/C]AAGTGCCACTTATTATTCTCCTCTGACATCAGCAAAACATGTTCACTCAC
Long Flanking Sequence:
GTGGCTGTTTGTTGTCAGGTATGCAGCGGCGCAGACGGAAGGTTCTGGACACGTCAGTGGCATATGTGCGTGGAGAGGAGAATCTGGCCGGCTGGAGACCCCGAGGAGACAGTCTGATCCTGGAGCACCAGTGGGAGCTGGACAAAATGGAGCAGCTGCATGAGGTGAGGACACTAGAAAAGAAAACCAAGCTCTAGGCTGCCTGTGCTTATCTGTAATCTCCAGACCCTCATCTCCATGTGCGTGTGTTTGCCAGGTGGAAAAGACGCGTCACTTGCTTCTGCTGCGTGAGAAGCTGGGAGAAACACCTCCACCTAAATCTCTGAGCGAGTCTCTGTCCCCCAGCCTGAGCAGCGGGACCCTCAGCACCTCCACCAGCATCTCCTCCCAGATCTCCTCCACAACTTTCGAGAGTGCCATCACCCCCAGCGAAAGCAGCGGCTATGACTCCACGGACATCGAGAGCTTGGTGGATCGAGAGAAGGAGCTGGCCACTAAGG[T/C]AAGTGCCACTTATTATTCTCCTCTGACATCAGCAAAACATGTTCACTCACAGAAATGATGCTCGCTGGAGATTTTCTCTTCTTCTGGCCACTCTCTGTAAAACACTAGAGATGGCTATTTATGAACATCCAGACTGATCAGCAGTTTCTGGAACACTCAGACCAGCCTGTTTGACACCAGCAACAATCACCTTTCTTATTCATTCTGATGCTCAGTTTGAACTGCAGTATCATCTTGACTGTCTTCATGCTTCAATGCATCACGTTGCTGTCATGTGATTGGCTGATTAGATATAGCCGAGTAGATTTTTCTGATACAGTGGCCTGTAAATGTAATCATTTCAGTCCAGTGTCATTAGAGGATATTTCATCAGCATAAGTGTTCTAATCAATGGAATCCAATGATTCATTTAGTTTGCTTAAAAATCTATATTTCTCATTTTCGTTGTATATTTTGCTGGATTTTACCATGTTTGTGATGCCACAAAGCCACAAAATCTC
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa8450
Status:
Mutation detected in F1 DNA
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
ENSDART00000005447 None 1607 1782 43 47
ENSDART00000050915 None 1595 1770 43 47
ENSDART00000053807 None None 1161 None 21
ENSDART00000141075 Essential Splice Site 1595 1763 42 46
ENSDART00000146458 None None 1161 None 22
Genomic Location (Zv9):
Chromosome 23 (position 29646308)
Other Location(s):
Assembly Chromosome Position
GRCz10 23 29476875
GRCz11 23 29403416
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGTGCCACCCTCACACCCTCCTCCACCTGYCCCTCGCTCTCAGACTCCAG[G/A]TACACACTTCACACGCAAAAGCACTATTACTTCAAATTACAAGCTTCAAA
Long Flanking Sequence:
CTGATGTGTTTATGACATTTTGAATGCAGTGTAACATTTTGAAGGAAATGTGAGGCATTTTGCATTTTGTGTGTGCAGTTTTGAGAATTGTGTGTAGAGTTTTGTAAAAAAGGGGACACTGTTTTGAAAACATGTGAAAGCAGTTGAAAATAACTGTAACTCTTATTGAAGATAAGTATACTTACAGTTTTGTGAAAACCATGACATGCATATGTGTGTTAATTCTTTTACAGTGCCTCCGTCTCCTGACACACACTTTCAACAGTGAATACAACCAAATGTGCAACAGCATTAGTGACTGCAAGGTAACTTGGACTAAAACAATATAAAAAATGCAGTTTTGTTTGAATTGGAACATATCAGCTTTGATAATCTTGAATAAAACGGTGTGTGTATCAGTTTTCAGATATCTCTCCTATGGGTCGGGATCCATCAGTCAGTAGTTTCAGCAGTGCCACCCTCACACCCTCCTCCACCTGCCCCTCGCTCTCAGACTCCAG[G/A]TACACACTTCACACGCAAAAGCACTATTACTTCAAATTACAAGCTTCAAAAAGTCAAATATTCTACAATCCTCTGTTTTATCCAGGACCCCTGAAGCAAACTCTCGTGCAACCAGCCCCTCAGGCTCAGACTATGAGAACTTCCCCATGGTGCCCATTCTGGAGACGTCCTACCTGGCCCGCGCCGGCAAACACGAGTTCCTCAACCTTGTGCCTAACATAGAGGAAATGAGGCCTGGGTGAGGGTTTGGATATTTTTGGATTTAGTATTGTGTTTAAGGCAAGACACTGCAGGTGTTTTGTAAAAACAAAAGAACTAGTTGTCGACAGTCTTCCCTAGATTAATAGTTTACATATCGGTGATTTCTTGCAAGTTTTTTACAATTTTATATGTAATATGCAAATGAGGCATTCATTTGCATACATTACTTGCACAGATGTCAGAATTTTTGTTTTTCAGAATTTTTTTCTCACATTAGACTTCCAAGGTTTTTACAGTAT
Associated Phenotype:
Not determined