ZMP
crb2l
Ensembl ID:
ZFIN ID:
Description:
crumbs homolog 2, like [Source:RefSeq peptide;Acc:NP_001038627]
Human Orthologue:
CRB2
Human Description:
crumbs homolog 2 (Drosophila) [Source:HGNC Symbol;Acc:18688]
Mouse Orthologue:
Crb2
Mouse Description:
crumbs homolog 2 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2679260]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa18042 | Nonsense | Available for shipment | Available now |
sa41102 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21177 | Nonsense | Available for shipment | Available now |
sa21178 | Nonsense | Available for shipment | Available now |
sa30898 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41103 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41104 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa18042
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 |
---|---|---|---|---|---|
ENSDART00000084305 | Nonsense | 10 | 1458 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 2992133)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 2768128 |
GRCz11 | 8 | 2826887 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCTCGAGAATCACCGCAGGACATGGATTTTGGACGGATGTGTTTACAGTA[T/G]AAAAGAGCRGTTCTGCTGTCATTGATGTTCAAGCTGGGTAGRACATCTTT
Long Flanking Sequence:
TATTGAAAAAGAAAACACAATATACCTGTACAAAAAAATCTATAAAAGTCATACCTGCCAAAATTTGTCTCTGAAAATCCGGGAGATAATAAACTAAACGGGAGGGTCGCGGGAGATGGGTCTAAAATACGGATAACAACCTGTTAAAACGGGAGTGTTGGCAGGTGTGCTTAAAGTTACATACAAACATGTACCGTTTGAATGAAGAGAGAGAGAGGGAGCGAGGCAGATTAACACAGGGTGAGGATTGGAAGAGAGAGAGTGACAGACAGCAAACCGAGCTTTGACCGAGCAGGATAATCAAAGAAATCCTCCCGCAAACTTCCGACTCCTCTCCGTGTTTTCCGCCAGACCGCCAGACAGTCCCGAAGCGACTCAACTCTACACGCGGGGATGCGGTGACTCTGAAGCGGGCAGAGTTCGGCGAGCGTCCGATGATTTACAGGCTGAGCTCGAGAATCACCGCAGGACATGGATTTTGGACGGATGTGTTTACAGTA[T/G]AAAAGAGCAGTTCTGCTGTCATTGATGTTCAAGCTGGGTAGGACATCTTTATCTTCATGACTTTTTGTACAACGTGAAAACAATACTATAGTAATTTACACTAGTGTTTAGTACTTGTGTTTAGTTGTGTTCTACAATATAGTACGTGTAGTGATTCTATGATTGCTATAGTAATATGCTACTATAACTATATTAATATAAACAAATTACCCAATACTGCAGTTTTCTAAAACAATATGATGTTATTGCTACTACAAAATACCAACGTTTACTATAGTATAAACAAATGCATACTACATTATTGATTACAGCTTATCAGTTCAGTATTTTTAGTATGCTGTAGTGTTCATTAACAAACAGTTGTGAAAGCTTTAATATACAGTGTTTACGTCCCGATTTATATTTATATCAATTTACCAGTGAATATAGTTAATATACATTGGTGAATTTGAACTAAACAGATTTAATAAACAGATATATTTATTAAAATAATATTTTAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41102
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 |
---|---|---|---|---|---|
ENSDART00000084305 | Essential Splice Site | 465 | 1458 | 7 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 3038377)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 2813140 |
GRCz11 | 8 | 2871899 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGAAGATCTCGTCAATGCTTTTCAATGCTCATGTCCCCCAGGGTTCGCAG[G/T]TATGTAAATATACTCTGTATATTGGAAGTTTAAAGAGGGGCTAATAAGGT
Long Flanking Sequence:
TTACAAGAGCAAACCGTTTTTGGTAACACTTTATAATAACCACACACTATAAACCATTTATTAAGCATTAGCATTAGAGTAAAAGTACACGTTTAAATGTACTCAAAAAGTACTCGTTACCCAATAATTTTACTCAAGTAGATGTAACGAAGTAAATGTAACTCGTTACTACCCACCTCTGTACATTTGTAATATATTTAAGAGCACTACTTTTTCACCCGGGCTTTCACCTTTCTTTTAAACACAAAAGAAGACATTTTAAAGTAAGCCGAAAACCCGAAACTATTGACGACTACTGTATTTTTGAAGGGCAATGCTTACTGGTTTTCAGCTTTCTTTAAAATATCTTCTTCAGTGTTTACATTTCTCCATCTTCTGCTTCACAGGTGAAAACTGCTCAGTGAATGTGAATGAATGCGAATCTGCGCCATGTGAGAACGGAGGATCTTGTGAAGATCTCGTCAATGCTTTTCAATGCTCATGTCCCCCAGGGTTCGCAG[G/T]TATGTAAATATACTCTGTATATTGGAAGTTTAAAGAGGGGCTAATAAGGTTTTTTAAAGGGCACATAGTTTACCCCTTTTTATGATTTAATATTATTATTATGGTTGTTCTAAGTGTGCCAGTTTAGGATCAGTTCAACACACAGTTCAGATGTTTTTATTATGTGTTTAAAAGTGTCATGTTGTGGGCGTGTACACAGCTCGCTGTTTTAGGGGCGTGTTGCTTCACATGAAAACTAGTTTCGGCTTCCCGCCTATAGTAACAAGGGGGCAGAGCCAAGAGCTCCCACGTTCTGTGTTTGCAACAGACAGGCAGACAGAGAGAAGCTAAGCTAGGATCAGCATTCAGCCGCACATCCAAGCGCAGACCAAGCAGAGAGCACACAATCATTTGTTTTACAGCCAACTGTGTGCTAGTTTAAAGTTTCGAGCTTGTACACTGAGGCTAATAGCCACGCACACTGAATGAACTTGATGTGCCGCTCAAAGCCGTGACATGGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21177
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 |
---|---|---|---|---|---|
ENSDART00000084305 | Nonsense | 935 | 1458 | 9 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 3061810)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 2836573 |
GRCz11 | 8 | 2895332 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGACGACACACAACTGTTCATGTACTCCGGCAGCATCAGCCAGAAGCCA[C/T]AACACGCTAATTACTTACCCAGAAACTCATCCAATGTGCTGGAGGGCTGC
Long Flanking Sequence:
GGCTGGGTTTCTCCACAGAGCACACTTCATGGACGTTCAGTCACGAGCGCAACAGAAGCTTCGCTGCGTTTCCCATCATGCAGAATCACAGCCGTGACGTTACGGTGTCTTTATGGCTCAGATCACGCCACTTAAACGGCCTGGTCCTCCAGCTCCAGCACGACAATCAACCCTACCTCACTTTATTTCTGAAAAACGGCTCACTGTATATATCAATATACAGCTCCATCAGAAGAGCCTCTGACTTCCTGACCAATGGGGAGAAGCTCTTCATGTCCATTAAAACAGAGCCGGGAGTTATATTATTTAACCAAACGCAGCGGATTCCTATGATCTACAGTGGCTTCGAGGTGCAAGTGGGAGATGTTGTGTATCTCGGTGGTCTTCCTGAAGGAGAGAACTCTGCGCTGTGGGGAGGATATTTCAAAGGCTGTTTGCAGGACGTCCGAATCGACGACACACAACTGTTCATGTACTCCGGCAGCATCAGCCAGAAGCCA[C/T]AACACGCTAATTACTTACCCAGAAACTCATCCAATGTGCTGGAGGGCTGCGTGGGGGACCAGACGTGCAAGGTCAGACTGATGGAAGTATTAGACAAATACAGTAAAAAGTGATTAGCTGACTTTACATTTAGAAATAACGAGTAAACATTTTGCTTTTGAACTGATTAGTTGACTTCAGCAACGTAAGTAAACCTTCATGATTGCTTTGCAAAGTTTTGCTTTTTTGCAAAAGTTGCCTTTAAAGCATTTAGCAGACTTTAACAAAGTGAATAAAACCTTTGCTTTGAAGTAATTAGTTGATTTAAAAAAAAAAAGAAAGTAAACCTGTTGCTTTTAAAGCGATTAGTTAACTTAAAGTGAGTAAACTTGTTGCTTTTAAAGCGATTAGTTGACTTAATAAAGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTAATAAAGTGAGTAAACCTGTTGCTTTTAAAGCGATTAGTTGACTTAATAAAGTGAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21178
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 |
---|---|---|---|---|---|
ENSDART00000084305 | Nonsense | 1132 | 1458 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 3065539)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 2840302 |
GRCz11 | 8 | 2899061 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCACATGTCAATTGATGGAAATCCTGCAGGATTCAGTCTCTCTCCTGCT[G/T]GAAATGTAGACTTTTTTAACTCCTCCACTGTGATGCTGGCAGAAAACTAC
Long Flanking Sequence:
CTGACCTCAGACTTTTAAATTGATTTCTTCTGCCGAACACATCTCTGCCTAGCGTCTGCAGTCTTAAAACTCTGCTGTATTCACATTCAGTTTTTGACAGAGCAAATGACTACACTAGCTAAATCCAATGTTTTGTGTTCACTCCAGGTTTAGCCAACGCCACATTTGAAAACAACGCCCTGAAGTTCAGCGCAAACGGCTCATTTTTTGAGCCTGTGATGAGAATTTCAATGGATCTGCGGACGCGAGAAGAAAACGGGACCATTTTACGCTCCTCCAATGGAATCGAGTTCTTCTGCATGGGGCTACTAAACTCCTCCATCATCGTGAAGTTTCGTGATAGTAATAGTCTTGAAGTTCACGCTTTCATCAGCGACGTCACCGTTTCTGATGGAGAATGGCATAAAGTGGAGCTCTATGCATCCAGCTCGAGAATATCAGCGTTTCGTTGGCACATGTCAATTGATGGAAATCCTGCAGGATTCAGTCTCTCTCCTGCT[G/T]GAAATGTAGACTTTTTTAACTCCTCCACTGTGATGCTGGCAGAAAACTACACTGGGTGTTTGGGCGAAGTGCGCATCGGTGGAGTTCACCTATCATTTTTCGGACCTCTAAATGAAGAGGCGCCACAAAAAACTCAATTCATCCGAATCGGTGGGATGCTGGAGCCTCATTTAGGATGCATTGGATCTCCTTTATGTCTTTCCGAGCCCTGCCTGAATAATGGCACGTGCACGGATCTCTTTAATCTTGCCGTGTGTAAATGTGCTCCAGGATGGACCGGCGAGCGCTGCCAGGAGAATATTGACGAATGTGGAGAGCAGCCCTGTGTTCAGGGGTCCTGTCAGGATCTGCTGGGGGATTATGAGTGCCGGTGTCCGGTTGGATTTGGTGGGAAGAACTGTGATGTGGAGGTGGACCAGTGCAAGGATCATCAATGCGAGAATGGAGGGTCATGTGTGGCTACTGTCAGCGGATACACGTGTGTTTGTTTGCCTGGACAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30898
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 |
---|---|---|---|---|---|
ENSDART00000084305 | Nonsense | 1174 | 1458 | 11 | 14 |
ENSDART00000084305 | Nonsense | 1174 | 1458 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 3065665)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 2840428 |
GRCz11 | 8 | 2899187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGGTGGAGTTCACCTATCATTTTTCGGACCTCTAAATGAAGAGGCGCCA[C/T]AAAAAACTCAATTCATCCGAATCGGTGGGATGCTGGAGCCTCATTTAGGA
Long Flanking Sequence:
AATGTTTTGTGTTCACTCCAGGTTTAGCCAACGCCACATTTGAAAACAACGCCCTGAAGTTCAGCGCAAACGGCTCATTTTTTGAGCCTGTGATGAGAATTTCAATGGATCTGCGGACGCGAGAAGAAAACGGGACCATTTTACGCTCCTCCAATGGAATCGAGTTCTTCTGCATGGGGCTACTAAACTCCTCCATCATCGTGAAGTTTCGTGATAGTAATAGTCTTGAAGTTCACGCTTTCATCAGCGACGTCACCGTTTCTGATGGAGAATGGCATAAAGTGGAGCTCTATGCATCCAGCTCGAGAATATCAGCGTTTCGTTGGCACATGTCAATTGATGGAAATCCTGCAGGATTCAGTCTCTCTCCTGCTGGAAATGTAGACTTTTTTAACTCCTCCACTGTGATGCTGGCAGAAAACTACACTGGGTGTTTGGGCGAAGTGCGCATCGGTGGAGTTCACCTATCATTTTTCGGACCTCTAAATGAAGAGGCGCCA[C/T]AAAAAACTCAATTCATCCGAATCGGTGGGATGCTGGAGCCTCATTTAGGATGCATTGGATCTCCTTTATGTCTTTCCGAGCCCTGCCTGAATAATGGCACGTGCACGGATCTCTTTAATCTTGCCGTGTGTAAATGTGCTCCAGGATGGACCGGCGAGCGCTGCCAGGAGAATATTGACGAATGTGGAGAGCAGCCCTGTGTTCAGGGGTCCTGTCAGGATCTGCTGGGGGATTATGAGTGCCGGTGTCCGGTTGGATTTGGTGGGAAGAACTGTGATGTGGAGGTGGACCAGTGCAAGGATCATCAATGCGAGAATGGAGGGTCATGTGTGGCTACTGTCAGCGGATACACGTGTGTTTGTTTGCCTGGACACACAGGGCCATACTGCCGGTGAGTCTGAACAATGACTAAAGATATACAATTAAAGTCAGTTGGGTTATTAACCCTCCTGAATCATTAGCCCCCTGTATATTTTACTATATTTATACTATACAATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41103
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 |
---|---|---|---|---|---|
ENSDART00000084305 | Nonsense | 1174 | 1458 | 11 | 14 |
ENSDART00000084305 | Nonsense | 1174 | 1458 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 3065665)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 2840428 |
GRCz11 | 8 | 2899187 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCGGTGGAGTTCACCTATCATTTTTCGGACCTCTAAATGAAGAGGCGCCA[C/T]AAAAAACTCAATTCATCCGAATCGGTGGGATGCTGGAGCCTCATTTAGGA
Long Flanking Sequence:
AATGTTTTGTGTTCACTCCAGGTTTAGCCAACGCCACATTTGAAAACAACGCCCTGAAGTTCAGCGCAAACGGCTCATTTTTTGAGCCTGTGATGAGAATTTCAATGGATCTGCGGACGCGAGAAGAAAACGGGACCATTTTACGCTCCTCCAATGGAATCGAGTTCTTCTGCATGGGGCTACTAAACTCCTCCATCATCGTGAAGTTTCGTGATAGTAATAGTCTTGAAGTTCACGCTTTCATCAGCGACGTCACCGTTTCTGATGGAGAATGGCATAAAGTGGAGCTCTATGCATCCAGCTCGAGAATATCAGCGTTTCGTTGGCACATGTCAATTGATGGAAATCCTGCAGGATTCAGTCTCTCTCCTGCTGGAAATGTAGACTTTTTTAACTCCTCCACTGTGATGCTGGCAGAAAACTACACTGGGTGTTTGGGCGAAGTGCGCATCGGTGGAGTTCACCTATCATTTTTCGGACCTCTAAATGAAGAGGCGCCA[C/T]AAAAAACTCAATTCATCCGAATCGGTGGGATGCTGGAGCCTCATTTAGGATGCATTGGATCTCCTTTATGTCTTTCCGAGCCCTGCCTGAATAATGGCACGTGCACGGATCTCTTTAATCTTGCCGTGTGTAAATGTGCTCCAGGATGGACCGGCGAGCGCTGCCAGGAGAATATTGACGAATGTGGAGAGCAGCCCTGTGTTCAGGGGTCCTGTCAGGATCTGCTGGGGGATTATGAGTGCCGGTGTCCGGTTGGATTTGGTGGGAAGAACTGTGATGTGGAGGTGGACCAGTGCAAGGATCATCAATGCGAGAATGGAGGGTCATGTGTGGCTACTGTCAGCGGATACACGTGTGTTTGTTTGCCTGGACACACAGGGCCATACTGCCGGTGAGTCTGAACAATGACTAAAGATATACAATTAAAGTCAGTTGGGTTATTAACCCTCCTGAATCATTAGCCCCCTGTATATTTTACTATATTTATACTATACAATTTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41104
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000084305 | Nonsense | 1305 | 1458 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 8 (position 3068041)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 8 | 2842804 |
GRCz11 | 8 | 2901563 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAACACAACTCCCATGATTCCACACTCATCCACTGTCCTCCGTCAGATG[G/A]CGGTTTCCTCCTCGTGAGTGTGATGTGGATCTGCAGTGTGAGAATGGAGG
Long Flanking Sequence:
TAATAGCTTAGCTCACTACATTTGTCAAGTAGCTTGCCCAACACTGCTCATTCATAATAACTGATTTATTTTATTTTTGCCATGATGACAGTAAATAATATTTGACTAGATATTTTCAAAATACTTGTACTTGGCTTAAAATGACATTTAAAGGCTTAACTAGGTTAAGTATGCAGGTTAGGGTAATTAGGCAAGTCATTGTATAACAGTGGTTTGTTCTGTAGACTATCCAAAACAAATATTGCTCAAGGGGGGCTAATAATATTGACCTTAAAATGGTTTTAAAGGTTTTAAATGGTTTTTGGAAATTTTTACAAAATGCTGTCAAAAATGCCAAAGATCGTTTGGGAAACATTTAAAAAGAAAAAAATAAATAAATTCACAAGAGGCCGAATAATTTAGTGTGAAATTTTCAGGACTTTGCACTTAGAAACACCCTTAAAAGTAAATGAAACACAACTCCCATGATTCCACACTCATCCACTGTCCTCCGTCAGATG[G/A]CGGTTTCCTCCTCGTGAGTGTGATGTGGATCTGCAGTGTGAGAATGGAGGCGTTTGCAGTGAAGGATCATGGGGAGCCAACTGTACCTGCAGACCAGGATTCACTGGAGTCAGGTGACATCACATGACCACATCACAACCCCACTCTTCAAGAAAAATATCCATCATTTAGCAGTTTTCTGTATTTCGGCATTGATGTTTTTATTTTTATATATTCTTTTTTGTTTTGAAGGGGGCGGGGTCTTGTCTACCTTCTTTTTTGTCCTCGGCTGATGATATGCCTGAATCTGCATTTATTTATTTAAAATTTCCATTGCACTGCAATTTTTCCACCATTAAATCTATCTAGACATTTCCTATTAATGATGTCACACGTCTAATTTCATTTAGAAATTCAATTTTTATCTGTTTTAACTTGTTTTTGTATTGTTTAAATGGTTAAAATTGCAATACTGTATGGTATTGTTAAGGTTTTAACACTATTACTGCTTTTATCGATAC
Associated Phenotype:
Not determined