ZMP
kif7
Ensembl ID:
ZFIN ID:
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 |
---|---|---|---|
sa8588 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa20875 | Nonsense | Available for shipment | Available now |
sa38596 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa16261 | Nonsense | Available for shipment | Available now |
sa34018 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa8588
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 |
---|---|---|---|---|---|
ENSDART00000041577 | Nonsense | 85 | 1363 | 1 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 15319530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 14196698 |
GRCz11 | 7 | 14442161 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGGAGGTGTACACTAACTGCGTTCAACCACTTATCGAGGCCTTCTTTCAT[G/T]GATTTAATGCTACYGTGTTTGCCTATGGGCAGACAGGCTCAGGCAAAACY
Long Flanking Sequence:
AAAATCATTATAAAGACATAGGTTTTAAAAACACATGCAGATGATAAATTATAATACAGACTCAACATTGTGTATCCTGCAATGTGACTACTGCACATAATCACATTGCAATATCAATGTTGAAACAATATATTGTGAAGCCTCACTATATGTTTATGTGCTTTGTTCTCTGTTATTTATTTCAGTGCCCATAATAAGGATTATCACAGACCCACAGTAGTAATGAGGGACCGCTAATCAGCTCAGCTATGTCTCCAAAAGGAGTCGGCCACAGTAAGGTGGAAGAAAGTGCTGTACAGGTGGCCGTCCGCGTGCGTCCGTTGCTTCCCAAAGAGATTTTGCACAGCCATGAGAGCTGCATCACTTCAGACCCAGAGGAGCGGAGGGTCACCCTGGGCAATGACCGCCACTTCCACTGTGACTTTGTGTTTGAGGACGGCTCTACCCAGGAGGAGGTGTACACTAACTGCGTTCAACCACTTATCGAGGCCTTCTTTCAT[G/T]GATTTAATGCTACCGTGTTTGCCTATGGGCAGACAGGCTCAGGCAAAACCTACACCATTGGGGAAGCCAGCATTTGTGAGTATTTTAAATAAATGTCAAATTACGTTTTGGGGGTGAACGTTAGGGGTAATTTGCTAACATTGTTTAACATGAACTATATTCCTAAAAGTCCCGTAAAATTTAAATAATGTTTTTTAGATGTTAGTAAGAGTAATATAAAGCCGACTTTCCACTGCACATGACAGACGACAAGTGACAGACTGGAAGTCATTCATTTTCAGTGGAGAGTAGGGCTGTGCAATTAATTGCAAATCCCGTTTTGATTTCGATTTTGTCTTCTGATTATGAAAAACCATTTATCGAGATTAACGATTATTCCATCATTCACCGCTCCCTTTCCAGTTTTCCACATTTGTTGCTCTGCAAGGCTCAGTTCCATGTCAAAATGACTAAAAACATGTAATGTGATATAACTTCTGCAGCACGGGATTCGCATCATT
Associated Phenotype:
Not determined
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.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
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:
sa38596
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 > A
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041577 | Essential Splice Site | 595 | 1363 | 6 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 15303392)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 14180560 |
GRCz11 | 7 | 14426023 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTCACTCCTCCCTGCGACTCTGATGTGGGCAGAAGCCTCGCCAGACAG[G/A]TAATTGATATGTTTTGATTTGTCTCACAGCATCCCCGACCGCAAACACAA
Long Flanking Sequence:
TCTTAAACCTAAGCTAAACTAAAATGAAAACCTAATATTCATTTATTCATATTTCTTTAGTTCAGTCTATAATTATCATTGGTCATGACAGCAAATTTTTTCGGCATAAACACAGCGGACGTCCTTCCAGCTGAAACCCAGTACTGGGAAAAATCTAAATATTTAACAAATATATAAAAAAATGTATCTTTTATCTGTAAATTCTGAAAGATCTACATCTATAAAGTTATGTTTATTACCCTTAAAACAGCAATATCACATGTTTTCCCACAAGGCTCTAACCGTATATTATTTTTATTTTGTTTTTATAGAGCGATAAGCTACAGGAGCAGCAGGATCTAATAGCGGAGCTTCACAGTCTGTTAGCTCAGCCTGGAGGAGCGGGGTTTCTCCACCTGAAACAGAGACCTCACACTGCTCCTATCAACTCACTACTGCAGACTCCAGACCGCCTCACTCCTCCCTGCGACTCTGATGTGGGCAGAAGCCTCGCCAGACAG[G/A]TAATTGATATGTTTTGATTTGTCTCACAGCATCCCCGACCGCAAACACAACATCGGCTTTTATTCGAGATACCATCCACAGCTGCCGCCACCTGGGCTAAGCTGTTAGTCGCGCACAAACATCTTCAGACATTCGCCACACACGCTGTGTAATTCTGTGTTTCGACTTCACCCACGTGCTTTCAGATGCAAACAGTTTGGCAAAGTAGCACTGCAAAGTCTTGACAGTCAATTATACAATTGGTCCCTTAACATCAATATAAAGTGACACTCAACTAAAATTTTTAAACCTAAAGATTAAAATAAAAATGATTATATATAGTTGACGTCAAAATGATTAAACCTCTTGTAAATTTTTTTTGTTATTTAAAAATTTCCCAACAGATGTTTAACAGAGCAAGGAATTTTTCACAGTATTTCCAATAATATTTCTTCTTCTGGAGAAAGTCTTATTTGTTTTATTTCGGTTAGAATAAAAGCAGTTTTTCATTGTTTTTTTTT
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.
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 |
---|---|---|---|---|---|
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
Mutation Details
Allele Name:
sa34018
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:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000041577 | Nonsense | 884 | 1363 | 12 | 18 |
Genomic Location (Zv9):
Chromosome 7 (position 15291210)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 14168378 |
GRCz11 | 7 | 14413841 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAGCAGTCTCTTTCTCTTTCTCAAAGGAGCTGGAGATAAAGAACGAACAA[C/T]AGCAGAAAATTCTGAGGATTAAGACGGAGGAAATCGCAGCCTTCCAGCGG
Long Flanking Sequence:
TGCTACAAGGATTCTCAGATTTTTCACTGCTATTTAAACATTGATTTCCTACTATGGATCTCAGTGACTACCGGATTTCAGCATTCTTCAAAATATCTTCTTCTGTTCAACAGAAAACTGAACTATTTTAGTTTTAAATAGTAGTGTATACAATACAAAACTTACCAAGCAGATTTTCTATCGTAAATATATAAGAATTAAGGTATTTTTCTGTCTCTGGTGCTACTGATTACTCCTCTTTCCTTGAATGGTACTGTTACTACATTTTGCAGTCTACTTTTTTCTTTTTGTAGTGTTCATCACAGATTTTTATTTTATAAAACCATGTTCTGTTCTGTTGTGTAAGGGCCAGCATTAGTCATCTTCTTTTCTCTGTTGTGAACAATAATAATCTACAGAGAAACCGCAGCCTCTCGGTTATTCTCGTGGTTCAATAGAGAATCATTCACCAAGCAGTCTCTTTCTCTTTCTCAAAGGAGCTGGAGATAAAGAACGAACAA[C/T]AGCAGAAAATTCTGAGGATTAAGACGGAGGAAATCGCAGCCTTCCAGCGGCAAAGGAGAAGTGGAAGTAACGGCTCGGTCGTATCACTAGAGGAACAGCAGGTGGGTTCAGACAGAGAAGCCAAATTGTGCTTCTTTTCATCGAACCCTTCCCGCAGCTATTACCCAGCATTATTTTTAGATCTGTTTACTCAGTGTTTAATAGTTTGACTGACGTTTGAAGGAATTTTATTATTCTCACCTTGAGGAAAAGGGTACATTTCAGTAGCTTGTTTCAACACGTATGATTTGTTGCCTAAATTTCCTCTTAGCCTGGTATTGGCATGCGATTTATGTTATTGATTCTAGAATAGATTCTATAATACACTTGCTGTTTCCAAGGACATGGTTGTGAATTTGATTCCCAATGGAATCCCAATTTGATTCGTTTTTGAATTTTAAAATAAAAATAAATAAAAAAAACTGCTATTTTTTATTTTTTTTTTATTTTTTGCAATATGC
Associated Phenotype:
Not determined