ZMP
kif1ab
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate kinesin family member 1 family [Source:UniProtKB/TrEMBL;Acc:B0S7
Human Orthologue:
KIF1A
Human Description:
kinesin family member 1A [Source:HGNC Symbol;Acc:888]
Mouse Orthologues:
Gm1305, Kif1a
Mouse Descriptions:
kinesin family member 1A Gene [Source:MGI Symbol;Acc:MGI:108391]
predicted gene 1305 Gene [Source:MGI Symbol;Acc:MGI:2686151]
predicted gene 1305 Gene [Source:MGI Symbol;Acc:MGI:2686151]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9755 | Nonsense | Available for shipment | Available now |
sa2037 | Nonsense | F2 line generated | Not yet available |
sa32904 | Nonsense | Available for shipment | Available now |
sa12082 | Nonsense | Available for shipment | Available now |
sa19735 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9755
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 |
---|---|---|---|---|---|
ENSDART00000089012 | Nonsense | 18 | 1770 | 1 | 48 |
ENSDART00000139196 | Nonsense | 18 | 1785 | 2 | 46 |
Genomic Location (Zv9):
Chromosome 2 (position 22160183)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23046888 |
GRCz11 | 2 | 22702539 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TGGCAGGAGCCTCGGTSAAAGTAGCCGTGAGGGTCCGACCCTTYAACTCA[C/T]GAGAGATCGGCAAAGACAGCAAGTGTAWCATCCAGATRTCCGGCAACACC
Long Flanking Sequence:
GACACCAATCAGCTTGAGTGTGGTGTGCAGTCTGGCGCATTACAGCTGCTGTCGCGTCATCCAGGACAGGTGAACGCTTCACACAGGTGGTGGATGAGGAGATTTCCCCTACCAAAAGCACTTTCAATGTCCAAAAAAGAAAAATATAAATGGGAGGAATTATTATTATTTACATTTGATTATTTTATTTCTGTACCTGAATAATTCGTTCTCACACAGCTTGTTCTCCAGTTCATACTCGGCCCAGAAAACTGTAAACTATTCAAGCTATTCACACCATCTGGTGAAATTCTGTTCAAAATATGAACAAAACATCCCAATGTCAGTTTTTTCCAATATCATGACAACAGTGTCTTTCTTTCCAGGTGGCAGACGGCCTCTGATTCCAGGCTGGGCTTCGGTCCATAAGATCCTGTGTAGTAGCAGATCCCCAGCACTCAGATTTCACCATGGCAGGAGCCTCGGTCAAAGTAGCCGTGAGGGTCCGACCCTTCAACTCA[C/T]GAGAGATCGGCAAAGACAGCAAGTGTATCATCCAGATGTCCGGCAACACCACCAGTGAGTTCTCTTTCAAAACATCCTGTTTCACTATCCATCATTTTTCCTACACCTGTTCCGGATCTCATTTAAGTCGGAGATGATTGACAGCACACTCTATAATAATTCATGCTTGTGATGAAATATTCATTTTCAGAGTCTCTCATTAGCAGCACCCCAATGAGAGAAAATATTAGCGCATACAGGTTTGAAAATGAAATGTTAAAGGTGACGGGTTCTTGTTTTATTTTTTGGTCAAGGTTTGTTTTAATTGGTTAGATGTGCTGTCAATAACCTAATCAGATGCAGTGTTTTATGTTTATTTCCTAAAAACAGAATATTTCTTTTTGTACTTATATCTTAACCATATTTGTTGATTTAAAATTTTATGTTTGGATCTTAATAACAAAATACTTTTTTAGTAGATGTGCAAAAAATGAATTTTAGCAACAACTATAAAACTGTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2037
Status:
F2 line generated
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 |
---|---|---|---|---|---|
ENSDART00000089012 | Nonsense | 645 | 1770 | 19 | 48 |
ENSDART00000139196 | Nonsense | 653 | 1785 | 18 | 46 |
Genomic Location (Zv9):
Chromosome 2 (position 22176871)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23063576 |
GRCz11 | 2 | 22719227 |
KASP Assay ID:
554-2664.1 (used for ordering genotyping assays)
KASP Sequence:
GGGCCTTTGCTCAGAGAGAACTACTGGAGAAACAAGGCATTGACATGAAG[C/T]AAGAGATGGATCAGAGGTAGCWCTTCTGTTCRTGGYACTTTTGTGCTYYT
Long Flanking Sequence:
TCAAAATGAACAAAAGAGCATGCTTGGGTTTTATTATTAAGTGCTGTGACAAGACGTTTACCTCTGCAGGGTCGGTCGTGAGGATGCCAGCAGTCGGCAGGACATTGTGTTAAGTGGCCACTTCATCAAAGACGAACACTGTATCTTCACAAGTACCACAAATGCCATTGGAGAGGGTACGGTGGTCCTAGAGCCTTGTGAGGGAGCAGAGACTTATGTTAATGGCAAGAGAGTTACAGAGCCCACAGTTCTCAAATCAGGTAGCTTATCTGTTTCCAGTCTCATTCTATCAAACAATTTTTTGGATGTCTTAACCCCCTCTGTTATTTTTATTAGGTAACCGTATCATTATGGGCAAAAGCCACGTGTTCCGCTTCAATGACCCAGAGCAAGCAAGGCAAGACAGAGAGAGGACTCCATGTGCGGACACACCAGTGGAGCCGGTGGACTGGGCCTTTGCTCAGAGAGAACTACTGGAGAAACAAGGCATTGACATGAAG[C/T]AAGAGATGGATCAGAGGTAGCACTTCTGTTCGTGGCACTTTTGTGCTTCTAAACTAGTATACATTTTTCATAGTATTTCCTATAATATTTTTTCATGTGGAGAAAGTAGTTTTATTTCAGCTAGAATAAAAGCAGTTTAAGAAATTAAGAAAAAAATAAAACAGTTAAAGGTGGTCAATATTATTAGCCTTCTCAAGCAATATTTTTCTGATTGTCTACAGAACGAACTATAAAACAATGACTTGTCTAATTACTATATCGTGCCTAATAAACCTACTTAAGCTTTTAAATTGCACTTTAAGCTAAATAATAGTATATTGAAAATATCTAGTAAAATAGCACGCACTGTCATCATAGCAAAGATAAAAGAGATATTTAGAGTTATTAGAAATTAGTTATTAAAACTGTTATGTTTAGAAATGTGTTGAAAGTAATATATCTTCTTTCTGTCAAACAGAAATTGGGGAAAATATACAGGGGGGCTAATAATTTAGGAGGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32904
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 |
---|---|---|---|---|---|
ENSDART00000089012 | Nonsense | 1083 | 1770 | 30 | 48 |
ENSDART00000139196 | Nonsense | 1098 | 1785 | 28 | 46 |
Genomic Location (Zv9):
Chromosome 2 (position 22191386)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23078091 |
GRCz11 | 2 | 22733742 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTTATCTAGTCTCTCCAGATATTTCTGACAGTCCTCTGAAGGGTGTTCTA[G/T]AATGTCCTCTAGATGTGACTCAAGACAAATCGCTTCAGCACTTAAAAATT
Long Flanking Sequence:
AAGATTTCATTTGAGGATCAGGCGTTTGAAAAGGTTGGTTGTGCCTCTCATTTTATTTTTACAATTATCTTTTTAGTAGTTTGGCCTTGCAGGCATTACATCGTTTTTCTAGATGATACAAGAATTGTTTTTTTCTTCTGCTCAGTTTCAGACAGAAGCATGCACCAGTGGGATGTCTCAAACACACACATCTGAAGAGGAGCTGCGCATTGTTGAAGGAGAAGGACAAAACTCAGAGTTGGGACTCAGTGCAGATGAGGTCAACAACAACACCTGCTTAGGTAATGAGTTATGTCGTATGCACAATGTCGTATAACAAATTTATGCATTGCCAAAGATAAAATAACACGCCCAATTACCATTTCACTTTCGAAGCAGTAGTATGTGTGTAAACAGATAAGAGTCAGCTATTATTTGTATTCTAATCAGATCTGTTTTCTCATGCACTGCTTTATCTAGTCTCTCCAGATATTTCTGACAGTCCTCTGAAGGGTGTTCTA[G/T]AATGTCCTCTAGATGTGACTCAAGACAAATCGCTTCAGCACTTAAAAATTGGCAGCAACTTCACCTTTAGAGTCACAGTGCTTCAGGCTTCCAGCATCTCTGCTGAGTATGCAGATATCTTCTGCCAATTCAAGTAAGTAGATCTACCCCTAGTAAGTTGTATTTATCCATTCATTCATTTTCTTTTTGCCTTAGTCCCTTAATTAATCAGGGGTCACCACAGCGGAATGTACAGCCAACTTTTCCGGCATATGTTTTATGCAGCGTATGCCCTTCCAGCTGCAACCCATCGCTGGGAAACACCCACACACTCTCATTCACACTCATACACTACGGACAATTTAACTCACCCAATTCACCTATAGTGCATGTCTTTGGACTTGTGGGGGAAACCGGAGCACCCGGAGGAAACCCACACGAACACGGGGAGAACATGCAAACTTCACACAGAAACGCCAACTGACCCAGCCGAGGCTCAAACCAGCAACCTACTTTCTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12082
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 |
---|---|---|---|---|---|
ENSDART00000089012 | Nonsense | 1186 | 1770 | 32 | 48 |
ENSDART00000139196 | Nonsense | 1201 | 1785 | 30 | 46 |
Genomic Location (Zv9):
Chromosome 2 (position 22192868)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23079573 |
GRCz11 | 2 | 22735224 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACAKCAAAAGTCAGCCAATCGTTTTTGAAGTWTTCGGCCACTACCAGAAA[C/T]AACCCTTYCCTCCTCTTTGCAARGACTTAATTAGGTAGGTTTTAGATTAC
Long Flanking Sequence:
ATCAAACTTTTTCCAGTCTTGCTTTAAATGAGCTGCTGAATCTGTGCTGTTTAATTTTCACATTTTCAGTAGATCTGCAGAATGCTACAAATTTGAAACATTTTATATAGATATTTTGAAAGTTGCCATTCAAAAACATCATGAAAAAAAGGAAATCATAGTTTTACATACACTAATCCAAGATCATCTGATGCAATATTAACTCATCCCCCCTGTGTTTTCCCATCAGTTTTATTCACAGGCATGACGAGGCATTTTCCACTGAGCCATTAAAGAATACTGGTCGAGGGCCTCCTCTGGGATTCTACCACGTTCAAAATGTAATCACAACCTTTATGTTATTTACTAAAAAAGCAATTAATTCAAATATGAAATAAATCAAGCATACATTCATATGTGCTTTGCTATTATTGCAGATAACTGTGGAGGTCACCAAGTCCTTTGTGGAATACATCAAAAGTCAGCCAATCGTTTTTGAAGTATTCGGCCACTACCAGAAA[C/T]AACCCTTCCCTCCTCTTTGCAAGGACTTAATTAGGTAGGTTTTAGATTACTTTATAAAAATGTTTTTTAGTCACCATAAAAGGTTGTTATGTTATGTTTTAAAGTCTCTGTGGTTTGAATAGAGCTAGGAAAAAAAGAGATTTGAATATAAAGCTGAGTTGACTTGGATTCATTTACTTTAATCTTAAATCTGACTGTGCTTCTGTTATGAAATGAGTGCCATAAAGTGCATTGATTCAATAAGTTATATTGTTCTCTGATATCTACATGGTAGGTATGTGGCTTGGGTAAGTGCAAAAATCTTGTTCATTTATAAACAAATGAATTACTATAAGCTCCATTTTGACCATATTTCTAGTCAAAAGTCAAAGTAAGATATTTAGTGTGAGAAGGTATTTGGAACGGTTGTGAATATTAATGATCTCTGCTCTGATGCTACTTCATTTAAACAGACCTTATGCCTCTTCAGGGTAGCACTAAATAAATGTATAATCAGTGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa19735
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089012 | Nonsense | 1294 | 1770 | 36 | 48 |
ENSDART00000139196 | Nonsense | 1309 | 1785 | 34 | 46 |
Genomic Location (Zv9):
Chromosome 2 (position 22202497)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 2 | 23089202 |
GRCz11 | 2 | 22744853 |
KASP Assay ID:
2259-1909.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGAGAATTACAGTCACTATCGCCCATGAAACCGGCAATGATATTGAGTG[G/A]AAAGAAGTTAAAGAACTTGTCATAGGTTAGATTTTCTTCCTCTCTTTCTC
Long Flanking Sequence:
CATACACAATATTTAGTGATATGTTTCAGGATTGTTGTAAAGGATTTTTTGATTAATTAATTCAAATTAAATTTTTTCTAAAATATTTACCAGTTTTGATTTAATTTTCATTTTATTCAGCAGCTTTCCTCCTTTTTATCTAGTTAGTTATCTAGTTAGGGTGTTTCTTTTGTCACTTAGTATTTTTTTTTTATCTGTTCTGTTTGTCATCATCATTTGTAATGTTTTTGCTATTCACTGTTACATTATCCTGCTACGGTCTTTGGACACTGATTTATTAGCTGCTATAACATTAATCTTTCTTCCTAGTATTCTTGTGTGAGCATACCGAAACAATAATACATGTTTTTACTCTCACTTTACATATACTTTAAACAGGCTTTGTGAGCAAAAGTATTCCTTTCTGTCGAAAAAAGTGAGTTAACCTTATTTTTTCCATAGGGCATCCAAAGGAGAATTACAGTCACTATCGCCCATGAAACCGGCAATGATATTGAGTG[G/A]AAAGAAGTTAAAGAACTTGTCATAGGTTAGATTTTCTTCCTCTCTTTCTCTCTCAAAGCTTATCAGAAGCTCAGAGGACAAAAGGAGATGTAATGACAAATATTCAGGTAGAGTTTCAGCTGACTTAGCATTACTTCCATTTTTTAGGGCGCATCCGTAACACACCCGAGGCGGATGAGACTATCATCGACCCCAACATCCTGTCCCTCAACATCCTGTCTTCAAACTACATACGGCCGACTTATGATGATAGGTACACCTCTGAAATGTTAAGAAAGATCTGTCATGTTTATGTTTTAATTTTGTGATAATTTTTAAAATATTGCTAATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATATTGTACTAATTACAATGTGGTTAAAACATAAATATTTTAATCCATTTTTGCATAGATGGGGTTACATTACAGTATTTAAATAAACTGCTGTAT
Associated Phenotype:
Not determined