ZMP
cngb1a
Ensembl ID:
ZFIN ID:
Description:
Novel protein similar to vertebrate cyclic nucleotide gated channel beta 1 (CNGB1) [Source:UniProtKB
Mouse Orthologue:
Cngb1
Mouse Description:
cyclic nucleotide gated channel beta 1 Gene [Source:MGI Symbol;Acc:MGI:2664102]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa10125 | Nonsense | Available for shipment | Available now |
sa43167 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa2970 | Nonsense | F2 line generated | Not yet available |
sa39216 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa36727 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa12618 | Nonsense | Available for shipment | Available now |
sa13410 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa10125
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 |
---|---|---|---|---|---|
ENSDART00000098585 | Nonsense | 99 | 708 | 3 | 16 |
ENSDART00000140089 | Nonsense | 87 | 613 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 43920366)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45509421 |
GRCz11 | 18 | 45506375 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AGAAGAAAGAGSCTGAAGAGAAGCCTGTGGAGGAGGAAGAGGAGGARGTG[C/T]AGATCTAYGARTTCATGGGCTACAAGATCCCAGTTCCCCAATTCAAAATC
Long Flanking Sequence:
TTAAAAATATATAAAAAAAACTGTTTTTATTCTGAAATAACACAAATAAGACTTTCTCTAGAAGAAAAAAATATTATAGGAGATACTGTGAAAAAAATTCTTTGCTCTGTTAAACATCATTTGGGAAATATTTATAAAAAAGAAAGAAAAATTCACAGGAGGGCAAATAATTCAATAAAATAAAAAGGGCTAATTAAAATTCAACTGAACATGTGTAACATAAGACATAAGGTCACATATAATGATAAGAAAATACCAATTTGCTAAATAAATCAAATGTATGGTTAAAATGGAAATGAATGAGTCTAGACGTCTGAACACATTCAGGTTAAAATCAAATAAGGGGGATAAATTGGGACGAAGCTCTAGTTTCATCACCTTTTATATTTGAACTTGTAGCTCCAGCCAAGAAGCCTGGCGAAGCGCCGCCTCCACCACCTCCACCAGAGCAGAAGAAAGAGGCTGAAGAGAAGCCTGTGGAGGAGGAAGAGGAGGAAGTG[C/T]AGATCTATGAGTTCATGGGCTACAAGATCCCAGTTCCCCAATTCAAAATCCCCCAGATGCCTGAGTGGCTGAGAGCCATTCTGGCATACCGCTTCCCCTCCAGCATTGACCCTTACACTGGTGAGATCTACTGATGCACAGCAAATGCTCGAAGTGACTAAGGGACTGGTCTAAAACTACTTTAGAAAAAAGGTTCATTCAGTCTTTGCTAATGTTAGGTTCAGAAACAAGGCAATTGCAATATGTAAAATATGTTACAGATTGGCGGGTGGAGCTAAACATCAATAGGCAGTTATGTAGAAACAGTGGGTGGAGCTAAACAGGCAATTGGTGTAGAAGCAGTGGGTGAAGCTAAACAGGCATAAGTGTAGAAGTAGAGGGTCGAGCTAAACAGACAGTGATGTAGAAGCAGTGGGTGTAACTAAACAGACAGTGATTTAGGAGCAGGGGCGGAGCTAAACAGGCAGTTTTGTAGAAGCAGTGGGTGGAGCTAAACAAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa43167
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098585 | Essential Splice Site | 139 | 708 | 3 | 16 |
ENSDART00000140089 | Essential Splice Site | 127 | 613 | 2 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 43920488)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45509543 |
GRCz11 | 18 | 45506497 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGCCATTCTGGCATACCGCTTCCCCTCCAGCATTGACCCTTACACTGG[T/A]GAGATCTACTGATGCACAGCAAATGCTCGAAGTGACTAAGGGACTGGTCT
Long Flanking Sequence:
GGGAAATATTTATAAAAAAGAAAGAAAAATTCACAGGAGGGCAAATAATTCAATAAAATAAAAAGGGCTAATTAAAATTCAACTGAACATGTGTAACATAAGACATAAGGTCACATATAATGATAAGAAAATACCAATTTGCTAAATAAATCAAATGTATGGTTAAAATGGAAATGAATGAGTCTAGACGTCTGAACACATTCAGGTTAAAATCAAATAAGGGGGATAAATTGGGACGAAGCTCTAGTTTCATCACCTTTTATATTTGAACTTGTAGCTCCAGCCAAGAAGCCTGGCGAAGCGCCGCCTCCACCACCTCCACCAGAGCAGAAGAAAGAGGCTGAAGAGAAGCCTGTGGAGGAGGAAGAGGAGGAAGTGCAGATCTATGAGTTCATGGGCTACAAGATCCCAGTTCCCCAATTCAAAATCCCCCAGATGCCTGAGTGGCTGAGAGCCATTCTGGCATACCGCTTCCCCTCCAGCATTGACCCTTACACTGG[T/A]GAGATCTACTGATGCACAGCAAATGCTCGAAGTGACTAAGGGACTGGTCTAAAACTACTTTAGAAAAAAGGTTCATTCAGTCTTTGCTAATGTTAGGTTCAGAAACAAGGCAATTGCAATATGTAAAATATGTTACAGATTGGCGGGTGGAGCTAAACATCAATAGGCAGTTATGTAGAAACAGTGGGTGGAGCTAAACAGGCAATTGGTGTAGAAGCAGTGGGTGAAGCTAAACAGGCATAAGTGTAGAAGTAGAGGGTCGAGCTAAACAGACAGTGATGTAGAAGCAGTGGGTGTAACTAAACAGACAGTGATTTAGGAGCAGGGGCGGAGCTAAACAGGCAGTTTTGTAGAAGCAGTGGGTGGAGCTAAACAAGCTTTAATGTAGAAGCAGTGAGCGGGGCTAAACAGGCAGTGATGTAGAAGCAGTGGGTGTAACTAAACAGGCAGTGATGTAGAAGCAGTGGGTGTAACTAAACAGGCAGTGATTTAGAAGCAGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa2970
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:
G > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098585 | Nonsense | 145 | 708 | 4 | 16 |
ENSDART00000140089 | Nonsense | 133 | 613 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 43921679)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45510734 |
GRCz11 | 18 | 45507688 |
KASP Assay ID:
554-3090.1 (used for ordering genotyping assays)
KASP Sequence:
AGTCATACACACACTGGTTTCTTCTTGCTCAGATCTGATCTACGTGGTGT[G/A]GCTGTTCTTCGTGACGTTTGCGTGGAACTGGAATGTTTGGCTGATTCCTG
Long Flanking Sequence:
GCAGTGATGTAGAATCAGTGGGTAAAGCTAAACAGGCGGAGCCTTATAAGCAGGGGCGGAGCTAAACAGGCAGTAATGTAGAAGCAGTGGTTGAAGCTTAACAGGCGGAGCTATAGAAGCAGGGGCGGAGCTAAACAGGCATTTATGTAAAAACAATGGGTGGAGCTAAACAAGCGGTTATGTAGAAACTGTGAGTGGAGCTAAACAGATTTGTAGAAGCAGCAGGTGGAGTTAAACAGGCAGTGATGTAGAAGTAGTCTCTGATTAGCTTCTGTAGAGGCAGAGTTTAGCCACGTTATTAAATAATAAAGTTTACATAGTAAATCTGGCAGATTGGTGTTAAAATGACTGACAAGAAAGTTTTCTGAAATGTTTTTAACATTTTGATTTAAATAGATTTGATTTCGCAGTTCATAAGCCCTTTAAAGTAATAATAACTTGTGATCCTGAAGTCATACACACACTGGTTTCTTCTTGCTCAGATCTGATCTACGTGGTGT[G/A]GCTGTTCTTCGTGACGTTTGCGTGGAACTGGAATGTTTGGCTGATTCCTGTGCGCTGCACTTTCCCCTATCAGACGCCTGACAACATTCACTGGTGGCTGCTGATGGACTACTTCTGTGACTCCATCTACATCATGGACATCTTCGTGGTTCAGCCACGACTGCAGTTCGTCAGAGGAGGAGACATTGTGGTGAGCAAGAGTTACAGTTAAAGTCTGAATTATTAACCCTCCTGAAATATTAGCCCCCTGTATATTTTTCCCCAATTTGTGTTTAACGGAGAGCAGATTTTTTCAATACCTTTCTAAACACAATAGTTTTAATAACTCATTTCTAATAACTGATTTATTTTATCTTTGCCATGATGACAGTAAATAATATTTGACTAGATATTTTTTCAAGACACTAGTAATCAGCTTAAAGTGACATTTAAAGGCTTAACTAGGTTAATTAGGTTAACTATGCAGGTTAGGGTAATTAGGCAAGTTATTGTATAACAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa39216
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:
A > G
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098585 | Essential Splice Site | 209 | 708 | 5 | 16 |
ENSDART00000140089 | Essential Splice Site | 197 | 613 | 4 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 43922877)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45511932 |
GRCz11 | 18 | 45508886 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CACCACTGTTTGTTTTATTTTATTGAAATCTATTGATGTTTATTTGTTTC[A/G]GTGCGACAAAAACGACATGAGAGAGAACTACAGGCAAACAGAGCGATTTA
Long Flanking Sequence:
ATTTAAAAAAGAAAAACAATTCAAAGGGGGGCTAATAATTCTGACTTCAACTGTACATAGTGATCATCTTTAGTGGTCTTTAGTAGTGAAACGAGAGTGTTTATAAAGTTTTATCGTTACAATTCTCACAAATTGGTTTTTGGATGATGGTTTTCTTTAAATTCTGCTCGCGCTGTCTTTTCTTTACTCATTCATTCATTTTCCTTCGGCTTAGTCCTTTATCAGTGGTCGCCACAGCAGAATAACCCTCCAACTATTCCAGCATATGTTTTACGCAGTGGATGCCCTTCCAGCTGCAACTCAGAACTGGGAAACACCCACACACTCTCACATTCACACATGCACTCATACAGTACGGCCAATTTAGTTCATCCTAATTCACCTAAATCACACTCTGCCGCCCTTTTCTGTATAATAAATGTCTAACAAAATGCAATGATATGTACACGCCACCACTGTTTGTTTTATTTTATTGAAATCTATTGATGTTTATTTGTTTC[A/G]GTGCGACAAAAACGACATGAGAGAGAACTACAGGCAAACAGAGCGATTTAAGGTAAAACTTTTGTACTGAGCATACATGCATTTACACTGAGCAAACACTTTCAGTGTTATTAAAACTGTATTATAACCTTAAGTGTGTTGAATGTAGGGTCAATATAGTTAGCTTATTTTAAAGTCATACAACTAAAATAATTCTTAGTGATTTGAAATAAACTACAATTAAATAAAACCAACAAAAAACATATTTAATGTTTTACTAAATGTATAAAATATTTGTATTCTCATCATTTGATTTGCTTAACTGATATGGAAAATATTTTAATATATAATAAATAATAATAAAAATGTATATATGTATGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAATTTCAGCTATTTATTCATTCAATCATTTTTTAATTCAATCATTTTTTAATTTTTAATCTGGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa36727
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098585 | Nonsense | 273 | 708 | 7 | 16 |
ENSDART00000140089 | Nonsense | 261 | 613 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 43924387)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45513442 |
GRCz11 | 18 | 45510396 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCGTTCTTCGAGTTTAATGATCGTCTGGAGGCTTGGATGAGCAAAGCCTA[C/A]ATTTACAGGTAAGAACAGACGCCACCACTAGAGGACGCTAGAACACAAAT
Long Flanking Sequence:
TCAGGGGCGTAGTGGACATTTTAAAAGTGGGGGGGATAGCTCCATGAAATCCAAAAGTTTACATTCCTAATCATCTGTTTCTAAATGGTCTGTCTCTTAAAGTGAGGGGGACGTATCCCCCCTGTCCCACCTGCTTGCTACTCCCCTGGTGCTACTCACTGCGACACCGTGACGCCCATTCTACAAACCTTCAAATTGAAATGAAAATTTGATTTATAAATAAAAATAATAGTTAGTGATGCTAAGATGTCTCCTTGTGTCTCAGATGGATGTGATCAGTCTCTTTCCACTGGATGTCCTCTATGTCTTCACTGGTGTCAAATCTCTCTTACGGTTTCCTCGTCTTCTAAAGGTATAAAACTCACTGTTGCTAATGTTTTCTCTCTGACACAAACGCACACACACAGACAACACAGACACACTTATTCTGTTTTCTACTTGCAGTACAACGCGTTCTTCGAGTTTAATGATCGTCTGGAGGCTTGGATGAGCAAAGCCTA[C/A]ATTTACAGGTAAGAACAGACGCCACCACTAGAGGACGCTAGAACACAAATGTAAACACATTAGACACTGAAAAGCCCCAAATCTCAGTTTCTGCTGGCAGGGTCTCACTATAAAGTCATCATAAATGCATCATAAATTTACCCTTAAATGCAGCTGTTATTCACTGACTGCTGTGTGGTTTCAGGGTGATCCGTACAAGTGCGTATCTGCTGTACTCTCTGCACTGCAATGCCTGTATTTTCTATTGGGGCTCGGACTATGAGGGACTGGGCTCCACCAAATGGGTTTATAATGGCAAAGGGAACAGGTGAGCTTGTGTGTGTCAGTGCTTTACTCTATGGTCTAGTGTTGATAATGTGATATAAAGAGTGTGTGTTTGTGTTGTGCAGTTACATCCGCTGCTATTACTTCGCTGTCAAGACTCTGATCACCATCGGAGGTTTGCCGGACCCCACCACTGTCTTTGAAATTGTCTTTCAGCTGGTTAACTACTTCGTGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa12618
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 > G
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098585 | Nonsense | 378 | 708 | 10 | 16 |
ENSDART00000140089 | Nonsense | 366 | 613 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 43925211)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45514266 |
GRCz11 | 18 | 45511220 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGTTCAGATGAGAGACGTGATCGGAGCYGCTACAGCAGGAGAAGCGTA[T/G]TATAGACACTCTGTGGACAGCACTGTCAAATACATGACCTCCTACAGGAT
Long Flanking Sequence:
CAGTGCTTTACTCTATGGTCTAGTGTTGATAATGTGATATAAAGAGTGTGTGTTTGTGTTGTGCAGTTACATCCGCTGCTATTACTTCGCTGTCAAGACTCTGATCACCATCGGAGGTTTGCCGGACCCCACCACTGTCTTTGAAATTGTCTTTCAGCTGGTTAACTACTTCGTGGGGGTCTTCGCTTTCTCCATTATGATCGGTCAGGTGAGGGGGGAAACATGTTTGGGTGAATCTCAGATCAGAGGGATTTTCAACTCTCACCTTTTTATGTATTCATCATTTTTTGTTTGTTTTGAATCGTGTATTTATCCTATTATGTCAAATTGTTGTCCAATAAAATCTGTCCTGAAGTCTTTTGAGAGCCAAAGTGGCAGTGTGCCGATTCTTACTTTTCTTATTCACCTGATATCCCCATTGCGCTCTGGTAAAGTGTTGTTTTTGTGTGTTCTGTTCAGATGAGAGACGTGATCGGAGCCGCTACAGCAGGAGAAGCGTA[T/G]TATAGACACTCTGTGGACAGCACTGTCAAATACATGACCTCCTACAGGATCCCCCGCGACGTCCAGAACCGCATTAAGACTTGGTATGACTACACCTGGAAGTCTCAGGGCATGCTGGGTAAGCAGAATGTGGTGGACGGCTTGCGTGGAGTGTGTTTGAACTGCGTTTAATGGTATGTCTGTATACAGATGAACAGGAGCTGCTCATACAACTGCCAGATAAGATGCGTTTGGACATCGCTGCTGATGTCAACTACAGCATCGTCAGTAAGGTGGCGCTCTTTCAGGTGACTCTTTCAGTCTTTTTTTTTTAATGAATAAAAAATAATGATTTACCTGTGCTGGAGCGTTCCAGTTTAAAGGGATAGTTCACCCTGATATTTGAAAATGAACATTTGCTCGTCATTTATTCACGTTATATCCTCATTTATTCAAGAGATTATGTCAGAACTCTGAGAAATAAAGTTGCAGTTCTGAGTTATAAAGTCCGAATTCTGACT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13410
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000098585 | Essential Splice Site | 625 | 708 | 15 | 16 |
ENSDART00000140089 | None | 613 | 613 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 18 (position 43931663)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 18 | 45520718 |
GRCz11 | 18 | 45517672 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GACARACGTTTTCMCGGCTGAAGGAGGCTTATAAGGGAGCAACYCTAGAG[G/A]TATTTATTTATAGCCTGCTGTCGTGATGCCTTAGGCCAAAAGCATGTTCT
Long Flanking Sequence:
CTAGTGCTAGCGATTAGCCTTGTTTACCAAACATCTTGTGTTTTCCTCTCATGTAGTATCTCTTTTCATTTGTATCTTTCTCTTCTCCACCTCCACCAATGAGAAACTCAGTGTTTGTTAGTTTATTACAGAAAAAGGTAATCGTAGTCACATGATGTTTACCGATGGGATCAATTTACTGTGTCTGTGTGTGTGATGAATGATGTTATGTAAGTGTTTAAGTGTCGCCTCAAATCTCAAAATCCTGTTACGGTCTCAGCGACGTACATGTTTGTTTAAAACACAACCTCCTGTCTTCTTAATGAGTTTGTCTTTTTTTCTGTAGGAAGATGTTGACCAAAGATAAGAAGCCTGCAGAAGCGAAGGGCGAGGTTAAAGACACGGGTGAGGTTATTCCTCAGCGGCCCGAGACTCCCAAACTCTACAAGGCAGCCCTAGAGGTCGCCACAGGACAGACGTTTTCCCGGCTGAAGGAGGCTTATAAGGGAGCAACTCTAGAG[G/A]TATTTATTTATAGCCTGCTGTCGTGATGCCTTAGGCCAAAAGCATGTTCTGAAAGCCAAAAGCAATGGGTGACCATCAAAACAACTGATCATTAAAGGTCCCATGGAGTGCTTTGAAATATGCATTTTTATTCAGTGTTTGACATAATCTTTACTGAAACATAAAGAGAGGGTGGGACTTAGAGTAGCTCCTCCCTTTTTTTTAAAAACACCCAATAGTCTTGTGTTTTGTTTTATCACCGCTCTGCCAGTGAGAACACTTGAGCTCAAGTGCATCAAATGAAAAACAGCGTCTTGATAGGGGGCAGGGCATGTCAGATGGAGAGTGTTTGATTGGTCAAAAGATTTGATGAGAAAATGAAGTATGAAGTGACGAGAATAAACTGTTTATGCGAAAGTGACAAACTACAATCTTTACATGTTTATATCAGTTCAGTTTTACATGTTTATATCAGTTTTATATCTTCCAAACATGAATTTTGTCACTGTTTTGGAGCACAC
Associated Phenotype:
Not determined