ZMP
ccr6a
Ensembl ID:
ZFIN ID:
Description:
chemokine receptor 6a [Source:RefSeq peptide;Acc:NP_001093461]
Human Orthologue:
CCR6
Human Description:
chemokine (C-C motif) receptor 6 [Source:HGNC Symbol;Acc:1607]
Mouse Orthologue:
Ccr6
Mouse Description:
chemokine (C-C motif) receptor 6 Gene [Source:MGI Symbol;Acc:MGI:1333797]
Alleles
There are 4 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa37065 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa13724 | Nonsense | Available for shipment | Available now |
sa37066 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa45705 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa37065
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 |
---|---|---|---|---|---|
ENSDART00000122256 | Nonsense | 28 | 375 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 30639381)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30710594 |
GRCz11 | 20 | 30613473 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACGGTGATTATTATGAAGGAGCTGTGGAGCCGTGTTCTGTGGAGAGCAGG[C/T]AGAAGCTTGAGAACTTCCTCCGCTTGTTTATTCATCCAATCATTTGTGTG
Long Flanking Sequence:
CCTGAAGGGTCCTTATTGATAACTTAAAGCAGGGGTCACCAATCCTGTTCCTAGAGATCTACCTTCCTGCAGGTTTCAGTTGCAACCCTGACCAAACACACCTGTCTGTAATTATCAAGAGCTTCTTCATGTCCTAATTAATTGGTTCAGGTGTGTTTAATCAGGGATGGAGCTGAATTCTGCAGAAAGGTAACTCTCCAGGAACAGGGTTGGTGACCCCTTTAACTTAAAGGAACATACTAGTAAAGTACAAACATGAAAAGTACAACCCTAGTGACAACTTTTGTACCTTTATTTCTGGAAGTGTTGAATAAACTTTGCTCTGCTTTAGATTTCAGTTAGTCCTCTTCATCTTGACTTGAACTCTGCCTTTCAAGTAATAATCTTACTGATGTTCCTGTTCTTTCTTTATAGAGAAAATGATTAATGATTCCTCTGAAAACTACAACTACGGTGATTATTATGAAGGAGCTGTGGAGCCGTGTTCTGTGGAGAGCAGG[C/T]AGAAGCTTGAGAACTTCCTCCGCTTGTTTATTCATCCAATCATTTGTGTGGCTGGTTTCATCGGCAACAGTCTTGTGATTGTAACGTACGCCCTCTACAAGCGAACCAAGTCCATGACTGACGTGTATCTGCTGAATGTGGCCATCGCTGACATCCTGTTTGTGGTGGCTCTGCCTTTAATCATCTACAGCGAGCAGCACAGTTGGGCCATGGGGAACATGTCCTGCAAGCTTCTGCGTGGCATCTATAGCGTCAATCTGTACAGCGGGATGTTACTTCTGGCTTGCATCAGTGGAGATCGATACCTTGCCATTGTGCAAGCCCGTCGCTCGTTCCGGCTGCGTTCAAGCACTCTTCTTTACAGCCATTTAGTTTGTGCAGCCGTCTGGTTGCTGGCCTTGCTTCTGTCCCTTCCCACCTTCATCTTTTATGAGCGTTACGAAAATGGTCTGACTGAATCTACCTTCCTATTCAACAATAATACCATCATGGAAGAAATT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13724
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 |
---|---|---|---|---|---|
ENSDART00000122256 | Nonsense | 70 | 375 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 30639509)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30710722 |
GRCz11 | 20 | 30613601 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ATTGTAACGTACGCCCTCTACAAGCGAACCAAGTCCATGACTGACGTGTA[T/A]CTGCTGAATGTGGCCATCGCTGACATCCTGTTTGTGGTGGCTCTGCCTTT
Long Flanking Sequence:
ATGTCCTAATTAATTGGTTCAGGTGTGTTTAATCAGGGATGGAGCTGAATTCTGCAGAAAGGTAACTCTCCAGGAACAGGGTTGGTGACCCCTTTAACTTAAAGGAACATACTAGTAAAGTACAAACATGAAAAGTACAACCCTAGTGACAACTTTTGTACCTTTATTTCTGGAAGTGTTGAATAAACTTTGCTCTGCTTTAGATTTCAGTTAGTCCTCTTCATCTTGACTTGAACTCTGCCTTTCAAGTAATAATCTTACTGATGTTCCTGTTCTTTCTTTATAGAGAAAATGATTAATGATTCCTCTGAAAACTACAACTACGGTGATTATTATGAAGGAGCTGTGGAGCCGTGTTCTGTGGAGAGCAGGCAGAAGCTTGAGAACTTCCTCCGCTTGTTTATTCATCCAATCATTTGTGTGGCTGGTTTCATCGGCAACAGTCTTGTGATTGTAACGTACGCCCTCTACAAGCGAACCAAGTCCATGACTGACGTGTA[T/A]CTGCTGAATGTGGCCATCGCTGACATCCTGTTTGTGGTGGCTCTGCCTTTAATCATCTACAGCGAGCAGCACAGTTGGGCCATGGGGAACATGTCCTGCAAGCTTCTGCGTGGCATCTATAGCGTCAATCTGTACAGCGGGATGTTACTTCTGGCTTGCATCAGTGGAGATCGATACCTTGCCATTGTGCAAGCCCGTCGCTCGTTCCGGCTGCGTTCAAGCACTCTTCTTTACAGCCATTTAGTTTGTGCAGCCGTCTGGTTGCTGGCCTTGCTTCTGTCCCTTCCCACCTTCATCTTTTATGAGCGTTACGAAAATGGTCTGACTGAATCTACCTTCCTATTCAACAATAATACCATCATGGAAGAAATTCAGTATGTCTGCTCTTTCAAGTTTGAGTCGAATGAAACAGCGCGTATGATGAAAACCATCGTGCCCAGCTCTCAGGTGGCAGTGGGTTTCTTTTTGCCTTTGCTCATAATGGGATTCTGTTACTCCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37066
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 |
---|---|---|---|---|---|
ENSDART00000122256 | Nonsense | 284 | 375 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 30640149)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30711362 |
GRCz11 | 20 | 30614241 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCATATGCCTTATAACCTTGTGCTGTTGTACCATACCATCAATTTATTT[G/T]AACAGCAGGAATGCAGCCATGAGGAGGCCGTCGCGTTGACCATGACCATC
Long Flanking Sequence:
GGATGTTACTTCTGGCTTGCATCAGTGGAGATCGATACCTTGCCATTGTGCAAGCCCGTCGCTCGTTCCGGCTGCGTTCAAGCACTCTTCTTTACAGCCATTTAGTTTGTGCAGCCGTCTGGTTGCTGGCCTTGCTTCTGTCCCTTCCCACCTTCATCTTTTATGAGCGTTACGAAAATGGTCTGACTGAATCTACCTTCCTATTCAACAATAATACCATCATGGAAGAAATTCAGTATGTCTGCTCTTTCAAGTTTGAGTCGAATGAAACAGCGCGTATGATGAAAACCATCGTGCCCAGCTCTCAGGTGGCAGTGGGTTTCTTTTTGCCTTTGCTCATAATGGGATTCTGTTACTCCAGCGTCATTGTCACCCTTCTTCGGGCCAAGAACTTTCAGAGGCACAAAGCAGTGCGTGTAGTGCTCACCGTGGTCCTTGTGTTTGTGGTCTGCCATATGCCTTATAACCTTGTGCTGTTGTACCATACCATCAATTTATTT[G/T]AACAGCAGGAATGCAGCCATGAGGAGGCCGTCGCGTTGACCATGACCATCACAGAAAGTTTGGCATACCTGCACTCTTGCCTCAATCCTCTGCTGTATGCCTTCATCGGGGTCAATTTCAGAAACCACTTCCGGAAGATCCTACGGGACATTTGGTGTTTGGGGAAGAACTATATGTCGGCAAGGCGGTCATCACGTGTTACCACTGAAATGTACCTTTCGACGCGGCGCTCTATGGATTATTCCAACAATGAAAATGGCACGTCGTTTACCATGTGATTGGATGCCTTTTAATTGACTGAATAACAACGGCTCAGTCATTATTTACTCACCTTCATGCTGGGTCAAATTAGGTCAATTGTTTTGATTGAAATAATATGAGAGGAATTCCCCAGTACTGGGTTGTGGCTAAAAGGGTATCCGCTGCGTAAAACATATCCCAGAGTAGATGGCGGTTCATTCAACTGTGGTGACCCTTAATAAATCAGGGACTAAGCCGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45705
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:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000122256 | Nonsense | 341 | 375 | 2 | 2 |
Genomic Location (Zv9):
Chromosome 20 (position 30640322)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 20 | 30711535 |
GRCz11 | 20 | 30614414 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACCACTTCCGGAAGATCCTACGGGACATTTGGTGTTTGGGGAAGAACTA[T/A]ATGTCGGCAAGGCGGTCATCACGTGTTACCACTGAAATGTACCTTTCGAC
Long Flanking Sequence:
GAAAATGGTCTGACTGAATCTACCTTCCTATTCAACAATAATACCATCATGGAAGAAATTCAGTATGTCTGCTCTTTCAAGTTTGAGTCGAATGAAACAGCGCGTATGATGAAAACCATCGTGCCCAGCTCTCAGGTGGCAGTGGGTTTCTTTTTGCCTTTGCTCATAATGGGATTCTGTTACTCCAGCGTCATTGTCACCCTTCTTCGGGCCAAGAACTTTCAGAGGCACAAAGCAGTGCGTGTAGTGCTCACCGTGGTCCTTGTGTTTGTGGTCTGCCATATGCCTTATAACCTTGTGCTGTTGTACCATACCATCAATTTATTTGAACAGCAGGAATGCAGCCATGAGGAGGCCGTCGCGTTGACCATGACCATCACAGAAAGTTTGGCATACCTGCACTCTTGCCTCAATCCTCTGCTGTATGCCTTCATCGGGGTCAATTTCAGAAACCACTTCCGGAAGATCCTACGGGACATTTGGTGTTTGGGGAAGAACTA[T/A]ATGTCGGCAAGGCGGTCATCACGTGTTACCACTGAAATGTACCTTTCGACGCGGCGCTCTATGGATTATTCCAACAATGAAAATGGCACGTCGTTTACCATGTGATTGGATGCCTTTTAATTGACTGAATAACAACGGCTCAGTCATTATTTACTCACCTTCATGCTGGGTCAAATTAGGTCAATTGTTTTGATTGAAATAATATGAGAGGAATTCCCCAGTACTGGGTTGTGGCTAAAAGGGTATCCGCTGCGTAAAACATATCCCAGAGTAGATGGCGGTTCATTCAACTGTGGTGACCCTTAATAAATCAGGGACTAAGCCGAAGGAAAATGAATGAATGAGTATGAAAGTAAGTAAATGATGGCTTCTTTTATTGGACGCATGAATTTGAAGGAAACACACGAGTAACGGACCAACAAGGGAAAGTGAAGATCGCATGAACTATTTACAGATGATATCAGTGAGATCTTTTCTTGTATATGTTGTGTTAACCTCTT
Associated Phenotype:
Not determined