ZMP
zgc:66125
Ensembl ID:
ZFIN ID:
Description:
kinesin family member 4 [Source:RefSeq peptide;Acc:NP_957117]
Human Orthologues:
KIF4A, KIF4B
Human Descriptions:
kinesin family member 4A [Source:HGNC Symbol;Acc:13339]
kinesin family member 4B [Source:HGNC Symbol;Acc:6322]
kinesin family member 4B [Source:HGNC Symbol;Acc:6322]
Mouse Orthologues:
AC122507.1, Kif4
Mouse Descriptions:
kinesin family member 4 Gene [Source:MGI Symbol;Acc:MGI:108389]
kinesin family member 4B (Kif4b), non-coding RNA [Source:RefSeq DNA;Acc:NR_033653]
kinesin family member 4B (Kif4b), non-coding RNA [Source:RefSeq DNA;Acc:NR_033653]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10251 | Nonsense | Available for shipment | Available now |
sa37382 | Nonsense | Available for shipment | Available now |
sa12877 | Nonsense | Available for shipment | Available now |
sa43726 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa10251
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 |
---|---|---|---|---|---|
ENSDART00000026178 | Nonsense | 32 | 1248 | 2 | 31 |
Genomic Location (Zv9):
Chromosome 21 (position 43307213)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 44746871 |
GRCz11 | 21 | 44771117 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGATGCAGACCTCTGGTGCCCAAAGAGATCAAWGAGGGATGCCAGTGCTG[T/A]CTTAATTTTGTACCCAGTGAACCTCAGGTCTGTGTGTGTCAGRTCATTSC
Long Flanking Sequence:
TATTTTTTTATTTGCTAAAAAACATTTGTGAAACTGTTGTCGATGTTGAAACATTTCATCCACTTTCCCCCTCTATCTCCATAACAGCTGACACAGAGCAGTTTACTTGTTTTAACACACATTATTTATAATTTGGCTAGAAAATCTCAATTTGTATTTATTGATTTTTTTTTTTTAATCCAGTAATATCGTTTCCACTGGCCCATTACAATAAATCCTTAGCGTTTAGCCCTGTACACCTTTGACATTTAATCTATAATGGTGGTAAAAAGGTCTCAAGTCTCAAATTTGACTTGGTGAAACCTGCAGAAACTCTCTAATGGGCTCGTCTTGCTCTGTGCGCACTGTCTTTGTTAGACGATATGTGATTGTAATTTGTAATTCAACATCATGTGCTTTTCCAGAATGACCAAGGAGGACGAGAAGGCCATTCCCGTGAGGGTTGCATTGAGATGCAGACCTCTGGTGCCCAAAGAGATCAATGAGGGATGCCAGTGCTG[T/A]CTTAATTTTGTACCCAGTGAACCTCAGGTCTGTGTGTGTCAGGTCATTCCTTTAACACTTGTGCATCATGTCATGCTGTTAAATCCTAATAGTCATTTTTTTTTCTCCTTTTATTTCAGGTGATTGTTGGCAACGACAAGGCGTTCACTTTTGATTATGTGTTTGACCCCACAACAGAACAGGAGGAAGTTTTCAACACTGCGGTGTCTCCTTTATTATCTGGACTTTTTAAAGGTTTGTAAGGCCATGTCCACACTAATGCGTTTTCATTTGAAAACGCATATTTTTGTCTCCGTTTTGCCCTTCCATCCACACTGAGACGCGTTTTTAGGAAACAAAAACGTATCTTTTTGAAAACGCTCTCCAAAGTGGATAAATTTGAAAACGACTTTTTCGTGTCGTAGTGTAGACTGTGAAAACGGAGTCTTTCGAAAACGATGACGCGTTTTTTGTCATGTGACACTCAGTCATGTTACTAATTCGTTTACTTTATTTTCGTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37382
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 |
---|---|---|---|---|---|
ENSDART00000026178 | Nonsense | 76 | 1248 | 3 | 31 |
Genomic Location (Zv9):
Chromosome 21 (position 43306991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 44746649 |
GRCz11 | 21 | 44770895 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAACAGAACAGGAGGAAGTTTTCAACACTGCGGTGTCTCCTTTATTATCT[G/T]GACTTTTTAAAGGTTTGTAAGGCCATGTCCACACTAATGCGTTTTCATTT
Long Flanking Sequence:
CGTTTAGCCCTGTACACCTTTGACATTTAATCTATAATGGTGGTAAAAAGGTCTCAAGTCTCAAATTTGACTTGGTGAAACCTGCAGAAACTCTCTAATGGGCTCGTCTTGCTCTGTGCGCACTGTCTTTGTTAGACGATATGTGATTGTAATTTGTAATTCAACATCATGTGCTTTTCCAGAATGACCAAGGAGGACGAGAAGGCCATTCCCGTGAGGGTTGCATTGAGATGCAGACCTCTGGTGCCCAAAGAGATCAATGAGGGATGCCAGTGCTGTCTTAATTTTGTACCCAGTGAACCTCAGGTCTGTGTGTGTCAGGTCATTCCTTTAACACTTGTGCATCATGTCATGCTGTTAAATCCTAATAGTCATTTTTTTTTCTCCTTTTATTTCAGGTGATTGTTGGCAACGACAAGGCGTTCACTTTTGATTATGTGTTTGACCCCACAACAGAACAGGAGGAAGTTTTCAACACTGCGGTGTCTCCTTTATTATCT[G/T]GACTTTTTAAAGGTTTGTAAGGCCATGTCCACACTAATGCGTTTTCATTTGAAAACGCATATTTTTGTCTCCGTTTTGCCCTTCCATCCACACTGAGACGCGTTTTTAGGAAACAAAAACGTATCTTTTTGAAAACGCTCTCCAAAGTGGATAAATTTGAAAACGACTTTTTCGTGTCGTAGTGTAGACTGTGAAAACGGAGTCTTTCGAAAACGATGACGCGTTTTTTGTCATGTGACACTCAGTCATGTTACTAATTCGTTTACTTTATTTTCGTTGTGATTATGATTTTAGTGATGTCGTCCTTACTGTGAGGGTAAGCAGCGTCATCAGCAGGATACTGTTCTTCAAAGCGGTCCAGTATATCGGCATATTTGTTTTGGCACGTCTCCCAGTCTACATTTCCACTCTCTTTTGCAACTTTGTATTCATGTGTTACTCGAAGCAGCAACTCTACTTCATTGTCAGTCCATTTAAAAAACTCTGTGCTTTTCCTTGAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12877
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 |
---|---|---|---|---|---|
ENSDART00000026178 | Nonsense | 103 | 1248 | 4 | 31 |
Genomic Location (Zv9):
Chromosome 21 (position 43305421)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 44745079 |
GRCz11 | 21 | 44769325 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCTATGGGCAGACGGGRTCAGGCAAGACGTTCTCTATGGGCGGCACTTA[C/A]ACRTCCGAACAGGAGAACGAGCCCACGGTCGGGGTGATCCCGMGAGTGAT
Long Flanking Sequence:
CGATGACACTGGAATACCCTGTCTAGTGGCTGGGAATGAGCTTTCCACAGTGTGTGCTGTAATGTTAATGTTGTTTTCGTGTGTTTACATAAATGAATATGGCCACTGTTTGAATGCACAGTAGTGTTACGAGCTTATTGCCATATTATATCATTATGATAATAAGATATAATTGCCTTCAGTTATTTCCTAAAGCTAAATACCCCAAAAAACTGGAATAACTACAGCAGGTCTCGTATGAAGAGCTCATAATGACATGTGAAGTGTGCTTGTGTTGAAGTACTGTCCCACTTCATAGGGGTAAATTTGAAGCCCTTCGCACTTTAAGGGCCAAGGGAAAGGGGTTTAAAATGGGATTGGGCCTTATTTTTCATGCATAAGGGGTAAATCTGCAGTATGTAATGGATATGTTCATTGTTTGTACTTGCAGGTTATCACGCCACTGTTCTGGCCTATGGGCAGACGGGGTCAGGCAAGACGTTCTCTATGGGCGGCACTTA[C/A]ACATCCGAACAGGAGAACGAGCCCACGGTCGGGGTGATCCCGCGAGTGATACGACGAATCTTCCAGGAGAAAGCTAAACGCACAGACTGTGAATTTGTGCTAGCTGTATCTTACCTCGAGGTATAGATGCGTGTGTTGTTTGGTGTTAATGGTTGTGTGCTGTTGGGATGTTTTCATCCACTCTCTGGGCTGATTTTGAGTCTTAATTTGCTCACATTTTTTCTGTTTCAGCTAATAGAATGATTTTTGGTGACTAATCTTATTTTGACACATTTTGTGAAAATGGTTTGGAGTTTTTCAAAAACTCAACAAACTCTGGGCAAATTTACTCTTGTTGTGTTAGTGGCTGTTTTCACCTATTGACTTGCCATGGCAGCATATAATCATGCATTCTTGATTGTTGCTGGTTTTGCCTGTTGGGAAGAGAAACAATTGGTCGTTTTTGCTGTTGATCATCAGATGCAGTGCAAAAACAACGTAGTTTCTGACCTTTATATGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43726
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 |
---|---|---|---|---|---|
ENSDART00000026178 | Nonsense | 406 | 1248 | 11 | 31 |
Genomic Location (Zv9):
Chromosome 21 (position 43297538)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 21 | 44737196 |
GRCz11 | 21 | 44761442 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGTCCTGGAGCAGAACCGCAGTCTGCAGGATCAGAACAGCAAACTGAGC[C/T]GAGAGCTGAGCGAGTCTGTGGGACAGACGGCTGCCATGTTTGAAAGGATG
Long Flanking Sequence:
TGATCCTGTCTACTGTCCCAAGCATCTTTCATGCTGGCCCCGGGCTATCGGGCAGTCCTTACTGTTGAGCCCTGTGTTATGATAAGCACTTGAAGATGCATCATATAACTCATGTCATTTAAACTGCAACTCATAGTTTACTGTTTATTAATGCATGATCAAAATTAAAATGGTTAATATTAGTTAATGCACTGAGTTTACCTGAACAAACAATTAATTAATTTTTCCCAATAGTACTATTAACAAGCATTAATAAATACTGTAGTAACTGTGTTGTTCTTTGTTTGTTCATTTTCATAAACACATTAACTAAAACAACCTTAGTGTTACCGCCTGCTTTAACACATGCGTTTTGATCTTTAAAGGAAGTGGTTACCTTTCAAAGCAGTTTCTCTAATCAGCTCATGTCTGATTTGTTCTGCAGGTCTGAGCCAGCGGAGAACGTGTCGAAGGTCCTGGAGCAGAACCGCAGTCTGCAGGATCAGAACAGCAAACTGAGC[C/T]GAGAGCTGAGCGAGTCTGTGGGACAGACGGCTGCCATGTTTGAAAGGATGCTAATGGTACATTTTATTTATTTATTTAAGTCTGCATCTGTGCCGAGGAGAAGCCAGCATTCTTTTTAGACAGAGCAACAAATGATGATAATATTTAATGCTTCTGTTTACAGTTATTAAAGTTCCAGCAGTTTACAGGTGGCTCGCAGTAATAGCTTTCAAAATATGAACTCTTCCCCACCATGTTTGTTTATTTATTTTTTAGTTAAAAAAAAGTTGCCACTCACTGCCAGCATTTTTTATTTATTTTATTTTATTTTTTACCAAAATTTTTACCTAAATTATATATATATATATATATATATATATATATATATATATGTGTGTGTATGTGTATGTATATGTATATATATATATATATATATATATATATATATATATATATATATATATGTGTGTGTGTATATATATGTATATATATATGTATGTATGTATATATATATATATGTA
Associated Phenotype:
Not determined