Busch Lab

ZMP

kif7

Ensembl ID:
ENSDARG00000033099
ZFIN ID:
ZDB-GENE-050307-1
Description:
Kinesin-like protein kif7 [Source:UniProtKB/Swiss-Prot;Acc:Q58G59]
Human Orthologue:
KIF7
Human Description:
kinesin family member 7 [Source:HGNC Symbol;Acc:30497]
Mouse Orthologue:
Kif7
Mouse Description:
kinesin family member 7 Gene [Source:MGI Symbol;Acc:MGI:1098239]

Alleles

There are 7 alleles of this gene:

Allele Name Consequence Status Availability
sa20875 Nonsense Available for shipment Available now
sa16261 Nonsense Available for shipment Available now

Mutation Details

Allele Name:
sa20875
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:
G > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041577 Nonsense 366 1363 4 18
Genomic Location (Zv9):
Chromosome 7 (position 15308365)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 14185533
GRCz11 7 14430996
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACCGGGCTACAGTCAACTGCCGGGGGGAACCAGATCGCATTGAGGGCCTT[G/T]AACTCCAGATCAAAGCGCTGAGACGAGCCCTTGAAAACCGCCAGCGCTCT
Long Flanking Sequence:
CTGAAGAACTTATGTGAAATTTCAGTTGCTGTCTGAGCTTTCACCGCCTTCCTTTTTTCATGTGTTCAATGCTTTTTCCCTGCATCGATTTATTTAATTATGCATAACTTAATTTCTAAACTAATTTTGTTTCCTTTTCATATATTAATTTCTTTGATTGTTACCAACATCTGGTGAAAATTTCAAGTCAATAGCACCATTAGAAATATGTTTCCTGAGAAAAATGGTGTCATTTCAATACTCATTTCCCTGACAGTATAACATTGCATTGGCATCTTCAAAACTGCAAGCCTTTGTATTGTAAATCTGTGTGTTTTGCCAGGATCTTAAAAGACTCTCTTGGAGGCAACGCCAAAACCCTGATGATTGCCTGCATTAGCCCTTCGTCCTCCGACTTTGATGAGAGCCTAAACACACTCAACTACGCCAAGCGTGCTCGTAACATACAAAACCGGGCTACAGTCAACTGCCGGGGGGAACCAGATCGCATTGAGGGCCTT[G/T]AACTCCAGATCAAAGCGCTGAGACGAGCCCTTGAAAACCGCCAGCGCTCTGAAACCCGCATTATTGCACGATCTGACCCTGAGAAGAGACTTCGGCCGTTTGAAGTGGATGTAAGGAAGCTGCAAGCTGAGAGCGCCCACTATAGGACGTGCACCGACTCTGCCTACAGGCTTTTAACAGAGCTGCAGGGCGAAGGAACTCTTAATGCGGGGCAAATCCTGCGGGTTAAAGAGTGGCTGTGTGGTGTTGAGGAGGAACGCAGCGGTTTGACCTCAGCGTCAGGACTCGACAGCGGCATTGAAAGCAGCTCTACTGAGGACAGCACTGCGCTCAAAAGGAGACAAGCCGTGCTGAACAACCAGGTTGGCTTCAGGCATATCCATTTTCAAATATGAATATTTTATAATCAACAATTCATCATGAAAAGGCAATTATGTATCTGTAGTCAGGTCATTATTTCTAGAGCATTAATTACACATATGGGCAAATGTCTTGCGGTA
Associated Phenotype:
Not determined

Mutation Details

Allele Name:
sa16261
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID Consequence Amino Acid Affected Amino Acid Total Exon Affected Exon Total
ENSDART00000041577 Nonsense 774 1363 10 18
Genomic Location (Zv9):
Chromosome 7 (position 15297478)
Other Location(s):
Assembly Chromosome Position
GRCz10 7 14174646
GRCz11 7 14420109
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CAGAGCTGGAGGCCGAGGCAGAGCAGGCCCGAGTGGAGCTCACAGAGGCA[C/T]AAAAGCAGCTGCAGGAGCTGGAGGTTCAGGGCGGCCGTGATGCCGCTGAC
Long Flanking Sequence:
GTATATATATAAAATGCCACTTTTAAGATCTGACTTCTTTAAAAATCTGTGATCTTCACTCTCTGACTGATATAAAATATAAAGTGCTTATCATGTCTTTAAAATATGAAGAAAGTATTTTGCCCCAGTATTTTCAATAGAGTTTCAATGCTAGTCTGCTACTACTGACGGCATCTTGTTTTACGCTATAACAACTAATTGAATGCTTAAGTCTATTTAACTGATTGTATTTTAATTACATTGAAACATTGATGTTGTTAAAAGAACCCTATGAAATTAAAAATAGTCACATAAACCTTTCTCCGGAAGTTTATCATTGGCTGAAAACATCAGCTGTGCATATATCCCATTTATATAAATGCAAAAAAACTAATTATAATAATCATGTTTTCTCTTTCTGCATAGGGAAAGACGCTCAGGCCATGAACAGGCAGTACAGTCGTAAGATCTCAGAGCTGGAGGCCGAGGCAGAGCAGGCCCGAGTGGAGCTCACAGAGGCA[C/T]AAAAGCAGCTGCAGGAGCTGGAGGTTCAGGGCGGCCGTGATGCCGCTGACCGCTCTAAAGCTCAGGAGTGCAGGAGGAAAATCGCAGCTGCGCAGAGCAAAGTTCAGGTCTGTGTCTGGCAGCTTTAGATCGCCGAAAGCCATCATTATGGAAATCCTGTTTGAGTGATGTTTGTCTTTAAAGATTTTAGGGTACCAATATTTCAGGATTTTAAAACCACAGTAAAATATAAAGCAATACAATAAAAAAAAACAATATTTGCAGCATCTACAACCAAATTTCCTGTTAACATTAGGAAGTTAAAATGAGTTTAAGATAAAATGATTTAAGTGAGTACATGTTGATATTACTTTCATGTATTTTGTAATACAATTGAAGGCAAAATTAATAGCCCCCTTCTGTAAATTTTTTATTCTTTTTCAAATATATCTAAAAAAAAAAAATGTAGTGATGTTTAACAGCAAGAACATTTTCCCAGTATTTACCCTTGCTCTTTTGGA
Associated Phenotype:
Not determined