ZMP
zgc:103670
Ensembl ID:
ZFIN IDs:
Description:
hypothetical protein LOC447926 [Source:RefSeq peptide;Acc:NP_001004664]
Human Orthologues:
KIF2A, KIF2B
Human Descriptions:
kinesin family member 2B [Source:HGNC Symbol;Acc:29443]
kinesin heavy chain member 2A [Source:HGNC Symbol;Acc:6318]
kinesin heavy chain member 2A [Source:HGNC Symbol;Acc:6318]
Mouse Orthologues:
Kif2a, Kif2b
Mouse Descriptions:
kinesin family member 2A Gene [Source:MGI Symbol;Acc:MGI:108390]
kinesin family member 2B Gene [Source:MGI Symbol;Acc:MGI:1920720]
kinesin family member 2B Gene [Source:MGI Symbol;Acc:MGI:1920720]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27143 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa21217 | Nonsense | Available for shipment | Available now |
sa34339 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34340 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa27143
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 |
---|---|---|---|---|---|
ENSDART00000063976 | Nonsense | 98 | 143 | 5 | 6 |
ENSDART00000085377 | None | None | 704 | None | 22 |
ENSDART00000115405 | Nonsense | 98 | 143 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 13449321)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 12895015 |
GRCz11 | 8 | 12932720 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGCTTTGTTTTACAGTGGGCTCGACTCGGGCACGGCCAGCCCAACAACTA[C/T]AACAACAGCAGCAGCAGCAGCCACAGCCGCAGCCAGAATCAGCACCCCCT
Long Flanking Sequence:
TCTAGTGAACCAACAGACTTTTCTGTTGTAATATATCCTGGGTATAAGGTCTCCAATATAGTCACTGTGAAGTTTTTTTTTTTGTTTGTTTGGGTATACAATTAAGCTTCCTGCAATCAACTTTAAAAAGTGTTTTCGAGAATCTTTTTTTACTCAATGTAAATGATAATTTTGAAGAAAAGATCTGTTTGACAAATAATTGACAAAATAGTGTTTTCAAAAATCAAGATTTTGGAATGCTCAAACTAATAATTCAATGTTCTGAAAGTGCTTGAGTGTTTTATAAACAGTGACTGTTTTAGTACACATCATTTATTGTTGTCTCCGGATACTACACTGGCTGTGTCCCAAAATGTGTTGTATCAGGACTGTGAGAAAGCTCCAGTGATGCTGTGAAATTTTCAGTTATAGTCTCCATTTGTCTTGAGAGTAATTTTGCTGACTCTTATGTGCTTTGTTTTACAGTGGGCTCGACTCGGGCACGGCCAGCCCAACAACTA[C/T]AACAACAGCAGCAGCAGCAGCCACAGCCGCAGCCAGAATCAGCACCCCCTCCACCAGCACAACAACCCTCTCAGCCCACACAGAGCCAGACCCAAAGCCAGCTAACTCAGCAGCAACAACAAAACGGTAATATGACCCTCCAGTGCGTTTCAATCTGTTCCTGTCAACCCCCTTTTCCCCACAGGAAAATGCTGAAAGGCGGATTGAGGCCCCCTGCAGAGGATGTATGTCATGTATAAAGAGAAAGCATCCTTTTAAAGTTTAGACCCTTACTTATCGGTCCTTGTTTTGGCTCAAATATTGGTATGTGGTTTGGATACCTCAGCTACCCATCAATGAATGCCAAAACCTCCATGATTAATCCTCTAGCTTTGAATTTATGAAGCTTACCAGAGTGTCTGCTGAATTAATCTAGAATGAAAACTCCTCTGCTTTCTGTGTTTTGATGCAACGTGCACTCTTGGTTTGCTTGTTTATGGCAGGGATGGGGGGCAGAATTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21217
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 |
---|---|---|---|---|---|
ENSDART00000063976 | Nonsense | 118 | 143 | 5 | 6 |
ENSDART00000085377 | Nonsense | 123 | 704 | 6 | 22 |
ENSDART00000115405 | Nonsense | 118 | 143 | 5 | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 13449381)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 12895075 |
GRCz11 | 8 | 12932780 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGCAGCAGCAGCCACAGCCGCAGCCAGAATCAGCACCCCCTCCACCAGCA[C/T]AACAACCCTCTCAGCCCACACAGAGCCAGACCCAAAGCCAGCTAACTCAG
Long Flanking Sequence:
GTCACTGTGAAGTTTTTTTTTTTGTTTGTTTGGGTATACAATTAAGCTTCCTGCAATCAACTTTAAAAAGTGTTTTCGAGAATCTTTTTTTACTCAATGTAAATGATAATTTTGAAGAAAAGATCTGTTTGACAAATAATTGACAAAATAGTGTTTTCAAAAATCAAGATTTTGGAATGCTCAAACTAATAATTCAATGTTCTGAAAGTGCTTGAGTGTTTTATAAACAGTGACTGTTTTAGTACACATCATTTATTGTTGTCTCCGGATACTACACTGGCTGTGTCCCAAAATGTGTTGTATCAGGACTGTGAGAAAGCTCCAGTGATGCTGTGAAATTTTCAGTTATAGTCTCCATTTGTCTTGAGAGTAATTTTGCTGACTCTTATGTGCTTTGTTTTACAGTGGGCTCGACTCGGGCACGGCCAGCCCAACAACTACAACAACAGCAGCAGCAGCAGCCACAGCCGCAGCCAGAATCAGCACCCCCTCCACCAGCA[C/T]AACAACCCTCTCAGCCCACACAGAGCCAGACCCAAAGCCAGCTAACTCAGCAGCAACAACAAAACGGTAATATGACCCTCCAGTGCGTTTCAATCTGTTCCTGTCAACCCCCTTTTCCCCACAGGAAAATGCTGAAAGGCGGATTGAGGCCCCCTGCAGAGGATGTATGTCATGTATAAAGAGAAAGCATCCTTTTAAAGTTTAGACCCTTACTTATCGGTCCTTGTTTTGGCTCAAATATTGGTATGTGGTTTGGATACCTCAGCTACCCATCAATGAATGCCAAAACCTCCATGATTAATCCTCTAGCTTTGAATTTATGAAGCTTACCAGAGTGTCTGCTGAATTAATCTAGAATGAAAACTCCTCTGCTTTCTGTGTTTTGATGCAACGTGCACTCTTGGTTTGCTTGTTTATGGCAGGGATGGGGGGCAGAATTAATTCACTGATGCATTAGGACAAATAATATTGGATTGATGTATTAAAAATATATGAATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34339
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 |
---|---|---|---|---|---|
ENSDART00000063976 | None | None | 143 | None | 6 |
ENSDART00000085377 | Nonsense | 676 | 704 | 21 | 22 |
ENSDART00000115405 | None | None | 143 | None | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 13463946)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 12909635 |
GRCz11 | 8 | 12947340 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCAGCTTGAGCAAATTCTTGACCAGAAGATCGAGATCCTCATTGAACTC[C/T]GAGGTAAATGCTGAGAATGCTCTTTTACTTTTTTAATGTTCTCCCAATGG
Long Flanking Sequence:
CCCAGGTGTGTCTGATTGGGGTTGGAACTAAACTTTGCAGGACACCGGCCCTCCAGGACCGAATCTGGACATCCCTGCTCTAAACCATTAAGACTTCCTCCTGTAGATGGTCTAAAAGCTTTTATTTGAATGTTAACAGGAAGAGGAAGTCTCTCCTCAGCTTTTCACATTTCACGAAGTGGTGTCTCAGCTGGTGGACATGGAGGAGCAGGTTCTGGAGGACCACAGGGCTGTGTTTCAGGTCATTATGCTTTTCATTTTTACAATGCATCTTTGTGAAGTTGGTAGTTCAGTCCCAAATTAAAAGGAATTGCTAATTATTATTGTTTTTTTTTTTAATATTGACTATCATACTTTGTGTCAAACAGGAGTCTATCAGGTGGCTTGAGGACGAGAAGGTTCTCCTGGAGATGACTGAGGAGGTAGACTATGATGTGGACTCTTACTCCTCTCAGCTTGAGCAAATTCTTGACCAGAAGATCGAGATCCTCATTGAACTC[C/T]GAGGTAAATGCTGAGAATGCTCTTTTACTTTTTTAATGTTCTCCCAATGGAATGATGGCGCACTAATGGATGCGCGTCTGCTTGTATTATCAGATAAAGTGAGGTCATTCCGTTCTGCACTTCAAGAGGAGGAACAAGCCAGCAAGCAGATTAACCCCAAGCGGCCCCGTGCGCTGTAGCCTGGAACACACTCGCGGAGGAACGACCAACACAAAGAGTCCTGTAGGCTTCTCCATAGTATTCAGGAGTGTTCTGAAGAAACTCTTTCCTACTCTCCCTCTTTCTCTCACACTGCATATGCTTTTCTTACTTGGTGATTCTAGTCCAAATATCTGAAAAATCAATATTTGATTTAGGCAGATAAAAATGTTTTTTTTTATTATAATAATAATAATAAGTTAAAAAAAAAAAGTCGTTTTTTGCTTTAAAACAATTACAATAATAATATGTAAATAATCTCATTTCAGTTTAAAGAGATTATTTTACTTACACCAATGGCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34340
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 |
---|---|---|---|---|---|
ENSDART00000063976 | None | None | 143 | None | 6 |
ENSDART00000085377 | Nonsense | 691 | 704 | 22 | 22 |
ENSDART00000115405 | None | None | 143 | None | 6 |
Genomic Location (Zv9):
Chromosome 8 (position 13464081)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 12909770 |
GRCz11 | 8 | 12947475 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATTATCAGATAAAGTGAGGTCATTCCGTTCTGCACTTCAAGAGGAGGAA[C/T]AAGCCAGCAAGCAGATTAACCCCAAGCGGCCCCGTGCGCTGTAGCCTGGA
Long Flanking Sequence:
ACAGGAAGAGGAAGTCTCTCCTCAGCTTTTCACATTTCACGAAGTGGTGTCTCAGCTGGTGGACATGGAGGAGCAGGTTCTGGAGGACCACAGGGCTGTGTTTCAGGTCATTATGCTTTTCATTTTTACAATGCATCTTTGTGAAGTTGGTAGTTCAGTCCCAAATTAAAAGGAATTGCTAATTATTATTGTTTTTTTTTTTAATATTGACTATCATACTTTGTGTCAAACAGGAGTCTATCAGGTGGCTTGAGGACGAGAAGGTTCTCCTGGAGATGACTGAGGAGGTAGACTATGATGTGGACTCTTACTCCTCTCAGCTTGAGCAAATTCTTGACCAGAAGATCGAGATCCTCATTGAACTCCGAGGTAAATGCTGAGAATGCTCTTTTACTTTTTTAATGTTCTCCCAATGGAATGATGGCGCACTAATGGATGCGCGTCTGCTTGTATTATCAGATAAAGTGAGGTCATTCCGTTCTGCACTTCAAGAGGAGGAA[C/T]AAGCCAGCAAGCAGATTAACCCCAAGCGGCCCCGTGCGCTGTAGCCTGGAACACACTCGCGGAGGAACGACCAACACAAAGAGTCCTGTAGGCTTCTCCATAGTATTCAGGAGTGTTCTGAAGAAACTCTTTCCTACTCTCCCTCTTTCTCTCACACTGCATATGCTTTTCTTACTTGGTGATTCTAGTCCAAATATCTGAAAAATCAATATTTGATTTAGGCAGATAAAAATGTTTTTTTTTATTATAATAATAATAATAAGTTAAAAAAAAAAAGTCGTTTTTTGCTTTAAAACAATTACAATAATAATATGTAAATAATCTCATTTCAGTTTAAAGAGATTATTTTACTTACACCAATGGCAGATTTTTTAGCTTGTTTCAAGGAAAAACTCAGTTATTTTTGACTTAAAATAAGTCCAAAATTTTTTTTAATTCAGCTTTATTTTTTTATTTGTCTAGAAAATGCTTCTTAATTTCAGAAGTTTTAGATGTTTGGA
Associated Phenotype:
Not determined