ZMP
si:dkey-217m5.3
Ensembl ID:
ZFIN ID:
Description:
hypothetical protein LOC794050 [Source:RefSeq peptide;Acc:NP_001076365]
Human Orthologues:
CCL11, CCL13, CCL15, CCL16, CCL2, CCL23, CCL24, CCL26, CCL7, CCL8
Human Descriptions:
chemokine (C-C motif) ligand 11 [Source:HGNC Symbol;Acc:10610]
chemokine (C-C motif) ligand 13 [Source:HGNC Symbol;Acc:10611]
chemokine (C-C motif) ligand 15 [Source:HGNC Symbol;Acc:10613]
chemokine (C-C motif) ligand 16 [Source:HGNC Symbol;Acc:10614]
chemokine (C-C motif) ligand 2 [Source:HGNC Symbol;Acc:10618]
chemokine (C-C motif) ligand 23 [Source:HGNC Symbol;Acc:10622]
chemokine (C-C motif) ligand 24 [Source:HGNC Symbol;Acc:10623]
chemokine (C-C motif) ligand 26 [Source:HGNC Symbol;Acc:10625]
chemokine (C-C motif) ligand 7 [Source:HGNC Symbol;Acc:10634]
chemokine (C-C motif) ligand 8 [Source:HGNC Symbol;Acc:10635]
chemokine (C-C motif) ligand 13 [Source:HGNC Symbol;Acc:10611]
chemokine (C-C motif) ligand 15 [Source:HGNC Symbol;Acc:10613]
chemokine (C-C motif) ligand 16 [Source:HGNC Symbol;Acc:10614]
chemokine (C-C motif) ligand 2 [Source:HGNC Symbol;Acc:10618]
chemokine (C-C motif) ligand 23 [Source:HGNC Symbol;Acc:10622]
chemokine (C-C motif) ligand 24 [Source:HGNC Symbol;Acc:10623]
chemokine (C-C motif) ligand 26 [Source:HGNC Symbol;Acc:10625]
chemokine (C-C motif) ligand 7 [Source:HGNC Symbol;Acc:10634]
chemokine (C-C motif) ligand 8 [Source:HGNC Symbol;Acc:10635]
Mouse Orthologues:
Ccl11, Ccl12, Ccl2, Ccl24, Ccl26, Ccl6, Ccl7, Ccl8, Ccl9
Mouse Descriptions:
chemokine (C-C motif) ligand 11 Gene [Source:MGI Symbol;Acc:MGI:103576]
chemokine (C-C motif) ligand 12 Gene [Source:MGI Symbol;Acc:MGI:108224]
chemokine (C-C motif) ligand 2 Gene [Source:MGI Symbol;Acc:MGI:98259]
chemokine (C-C motif) ligand 24 Gene [Source:MGI Symbol;Acc:MGI:1928953]
chemokine (C-C motif) ligand 26 Gene [Source:MGI Symbol;Acc:MGI:3589281]
chemokine (C-C motif) ligand 6 Gene [Source:MGI Symbol;Acc:MGI:98263]
chemokine (C-C motif) ligand 7 Gene [Source:MGI Symbol;Acc:MGI:99512]
chemokine (C-C motif) ligand 8 Gene [Source:MGI Symbol;Acc:MGI:101878]
chemokine (C-C motif) ligand 9 Gene [Source:MGI Symbol;Acc:MGI:104533]
chemokine (C-C motif) ligand 12 Gene [Source:MGI Symbol;Acc:MGI:108224]
chemokine (C-C motif) ligand 2 Gene [Source:MGI Symbol;Acc:MGI:98259]
chemokine (C-C motif) ligand 24 Gene [Source:MGI Symbol;Acc:MGI:1928953]
chemokine (C-C motif) ligand 26 Gene [Source:MGI Symbol;Acc:MGI:3589281]
chemokine (C-C motif) ligand 6 Gene [Source:MGI Symbol;Acc:MGI:98263]
chemokine (C-C motif) ligand 7 Gene [Source:MGI Symbol;Acc:MGI:99512]
chemokine (C-C motif) ligand 8 Gene [Source:MGI Symbol;Acc:MGI:101878]
chemokine (C-C motif) ligand 9 Gene [Source:MGI Symbol;Acc:MGI:104533]
Alleles
There are 2 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa44948 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa43506 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa44948
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 |
---|---|---|---|---|---|
ENSDART00000061434 | Nonsense | 59 | 136 | 3 | 4 |
ENSDART00000142164 | Nonsense | 26 | 103 | 2 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 39357828)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 39430240 |
GRCz11 | 20 | 39333119 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTTGCAGGTATATTAACAAAAGTTTTACATTTATTTTTCTGCAGGGTCA[C/T]AGGGTCCTGAAAAGTGCTGCTTTTCTTTTACCAATGCAAGAATTCCATTA
Long Flanking Sequence:
TGTCGCTTTCTGCTCAGTTGTTGGAAGTGATTGTACGTCCTTTTTTTATTTCTGCTTTTTTTGTAAGCAAGCAATAGACTATGTACTCTTTTTCCTAAAAATGTATTTCATAGATTGATTTGTATTAGGAATTGATTTCTTTTTCTGCAGGGTCCCAATGTAAGTGCTGCTTTTCCTTTTCCAATGCAAGACTTCCAGTACAGCAGGTTGAGAGTTGTCATACTACAAATCTTCTGTGCAACATGAATGGTGTTATACAAGTATTTTTTGACAGTTTCTATCAATTTAAAGTATTGTGATATGGTTTTAACACTAAGTATTTTTTTAATTTTCATTTTTCTGTAATATATTACATTTTTTTGTTTTGTTTTGTGAAATAATGAAAAATATTTTCCTTTGAAAATGCTAAATTTATGTATATTTGTTATAGATAATGTATTTTATACATTAACTTGCAGGTATATTAACAAAAGTTTTACATTTATTTTTCTGCAGGGTCA[C/T]AGGGTCCTGAAAAGTGCTGCTTTTCTTTTACCAATGCAAGAATTCCATTAAAGCAGATTGAGAGTTATTATACTACGCATCTTCAGTGCAACATGAATGCTGTTATGTAAGTATTTTTGACAGTTTCTTTACATTTAAAGGGTTGTGATTTGGTTTTGTGAAATAAAGAAAAATCTTTTCTTTTGAAAATGCAGTTTCATCATAAGGGCTCAAAGGGAGATCTGCACTAATCCAACTGAGAAATGGGTTCGGAGACTGATGAAGATGGTGGACAATCAAAACATGAAGCAGATGACAGAGGCTGGCTCTGTGGACAGCGCCTAAGATGAGAACGCTCTTCTTTTTTCTGAATATTGCACTGAATCGTTTCTCAACTGTGTTTAAGCTTTACTTTTATAAGCACCTGACTATACTGTTACTCTGCTTTGATTATTGTATATCTATATATTTTTGCAAATTATATTCATGCTAGAACTGTAATGTGAATCTGTCTGTATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43506
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000061434 | Essential Splice Site | 94 | 136 | 4 | 4 |
ENSDART00000142164 | Essential Splice Site | 61 | 103 | 3 | 3 |
Genomic Location (Zv9):
Chromosome 20 (position 39357634)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 39430046 |
GRCz11 | 20 | 39332925 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTGATTTGGTTTTGTGAAATAAAGAAAAATCTTTTCTTTTGAAAATGCA[G/T]TTTCATCATAAGGGCTCAAAGGGAGATCTGCACTAATCCAACTGAGAAAT
Long Flanking Sequence:
CCAGTACAGCAGGTTGAGAGTTGTCATACTACAAATCTTCTGTGCAACATGAATGGTGTTATACAAGTATTTTTTGACAGTTTCTATCAATTTAAAGTATTGTGATATGGTTTTAACACTAAGTATTTTTTTAATTTTCATTTTTCTGTAATATATTACATTTTTTTGTTTTGTTTTGTGAAATAATGAAAAATATTTTCCTTTGAAAATGCTAAATTTATGTATATTTGTTATAGATAATGTATTTTATACATTAACTTGCAGGTATATTAACAAAAGTTTTACATTTATTTTTCTGCAGGGTCACAGGGTCCTGAAAAGTGCTGCTTTTCTTTTACCAATGCAAGAATTCCATTAAAGCAGATTGAGAGTTATTATACTACGCATCTTCAGTGCAACATGAATGCTGTTATGTAAGTATTTTTGACAGTTTCTTTACATTTAAAGGGTTGTGATTTGGTTTTGTGAAATAAAGAAAAATCTTTTCTTTTGAAAATGCA[G/T]TTTCATCATAAGGGCTCAAAGGGAGATCTGCACTAATCCAACTGAGAAATGGGTTCGGAGACTGATGAAGATGGTGGACAATCAAAACATGAAGCAGATGACAGAGGCTGGCTCTGTGGACAGCGCCTAAGATGAGAACGCTCTTCTTTTTTCTGAATATTGCACTGAATCGTTTCTCAACTGTGTTTAAGCTTTACTTTTATAAGCACCTGACTATACTGTTACTCTGCTTTGATTATTGTATATCTATATATTTTTGCAAATTATATTCATGCTAGAACTGTAATGTGAATCTGTCTGTATTGTTACATAACTATATGAAAATAAACAACAGGCAGAGCATTTGGATTTTGGTCTGTTTTTTTTGTGTTAGTTTAGTGCATTAAATAATGTTAACAGTTTTACTTTTAATACTATATTAGCAAATATTGAGTTAACTAATTAAATGATTTTGCAGTGTTTGCGATAATAATGCCAACAGGAACATTGATACAGCGAAT
Associated Phenotype:
Not determined