ZMP
crb1
Ensembl ID:
Description:
crumbs homolog 1 [Source:RefSeq peptide;Acc:NP_001038408]
Human Orthologue:
CRB1
Human Description:
crumbs homolog 1 (Drosophila) [Source:HGNC Symbol;Acc:2343]
Mouse Orthologue:
Crb1
Mouse Description:
crumbs homolog 1 (Drosophila) Gene [Source:MGI Symbol;Acc:MGI:2136343]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa14330 | Nonsense | Available for shipment | Available now |
sa29788 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa1482 | Nonsense | Available for shipment | Available now |
sa12558 | Nonsense | Available for shipment | Available now |
sa159 | Essential Splice Site | Confirmed mutation in F2 line | Not yet available |
sa24173 | Nonsense | Available for shipment | Available now |
sa24174 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa14330
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 > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089774 | Nonsense | 155 | 1428 | 2 | 13 |
ENSDART00000141006 | Nonsense | 155 | 1428 | 2 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 24368195)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23504549 |
GRCz11 | 22 | 23531113 |
KASP Assay ID:
2261-6861.1 (used for ordering genotyping assays)
KASP Sequence:
ARYCCAGGGTACGCATGCATCTGTCAGGAGGGTTACACTGGRAGATCTTG[C/A]GARAAAGAGGTGGACCACTGCTCTCCTAACCCCTGCMGAAACCGCGCCAT
Long Flanking Sequence:
AAGAATGTTCATTTTTGGGTGAACTTTCCCTTTAAGAGTATAACTATGCTGCATGCTCTTCCTTTTTATGGGAGCAGAATGTTAAACAAATGTCTAAATGTCCATGTTTTTATCCTTGTAGGTGTAACACTACTCAAGACCTCAACACTCTGCCTGGACAACCCTTGCCAACACCAGTCAGAGTGCAGGGAAGCCCTGTCTGATTTCCTGTGCCAGTGTCAGACGACTGTGCCAGTCTTTCCCAGCACGCGTTGTGATTCTTCCAGTACGTTCTGCCAACTGTCCATCTGCCAGGGCAATGTGACATGTCAACCCACCGGCGCCCACCCAGGGGAACTAGTTTGCCAGTGTGACTCCGGCTTGCTGGGGCAGGACTGTCTTTCCAGTGCCCAGCTCTGCGCTCAGGGGCATTGTGGGGACAGTGCCCACTGTCTGGCAGTGCGAGACCAGAGCCCAGGGTACGCATGCATCTGTCAGGAGGGTTACACTGGAAGATCTTG[C/A]GAAAAAGAGGTGGACCACTGCTCTCCTAACCCCTGCAGAAACCGCGCCATCTGCCGCAGCAGAAGGAATGGGCCCACTTGCTTCTGCGTGCCAGGATTCCAGGGCCAGCTCTGCGAGATTGAGGTGAATGAATGTGTGTCGAGGCCCTGTAGAAACGGAGCCACCTGTGTGGACAAGATCGGGCACTACATCTGTCTCTGCAGGCCTGGATACATGGGTAGGTGAAGTGAGGGAGAGAGAGAAAAGGGGGGTCTCATGCTTTGCTGCCAAGTGCCACTCACCTGTTTGACCAGACGTGTCAAACTGCACTGCTGAGTTTGGGCCACAGTCCAACAGAGTTTAGTTCCAACCCTTCTCCAACATGTACACATTTTCAAATAAGTCTGAAGGTCTTTATTAGGTGGATCGGGTGCTTCAACTTTTTTGGAAATAGATTCGTTAGTTGCCTCTGATTATTGCCAAATTTTAATCCATTCAGTGATTTAAAATATTTGTTTATG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa29788
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 |
---|---|---|---|---|---|
ENSDART00000089774 | Essential Splice Site | 340 | 1428 | 4 | 13 |
ENSDART00000141006 | Essential Splice Site | 340 | 1428 | 4 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 24375394)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23497350 |
GRCz11 | 22 | 23523914 |
KASP Assay ID:
2261-6862.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGCCCTCTGTGAGAATCAACAGGAGAACTACACCTGCAACTGCTGGCCAG[G/T]TGACTCGCAGAATGACTTGTATATCAAGTTAAAGTATGATTTTGCATTAA
Long Flanking Sequence:
CTCTGATAACTAATTTCTTTAGTCTTTACCATAATAATAGTACATAATATATTTCTAATAATTTTGCAAGGTACTAGTTTTCAGCTTAGTGCCGTTTTAAGGCCTTAACTAGGTTAACTACAAGTTAGATCAGTTAGTCACTGTTCAGTAGCCAACCAGTGCTTAACACACTGCTTAAATAAACTGCAGTAACCATCTTAATGATTCTAAAATAGGTTAATTCATATAGTGTTTTTCATTGCTGGAATGTGTTCTCATTAGCTTCACCTATTGTAATATAATAACACAGCAAATGTAAGATAATTTTGGTAGTGAAATATGCATGCATGTATAAATAGTATAGCCTATATGTTGTAGCTACCGCTGTGACTGCTCACAGACTGCTAACTTCACTGGTGTTGACTGTGAGATCCCGCCTCCGCCCTGCTGGTCTCAACCCTGCCTCAACAGCGCCCTCTGTGAGAATCAACAGGAGAACTACACCTGCAACTGCTGGCCAG[G/T]TGACTCGCAGAATGACTTGTATATCAAGTTAAAGTATGATTTTGCATTAAACGGAATTGATGGATTGGATTTGGAAATGTATCTGGTAACATCTGATTAAAAATGTTTATGTAGGCTAATATCCTCCTGAGACCCATTTTTTTCTGTGATTCCCTACATCCTTTGGCTTAAAAAAAGTTTTATTTAGAGTTTTTACATTTTGTTTTTATTTTTAATTTTACAGCATGCCCACTGTAGTGGACCACGGGACCATTTTAGTTTGAAACGACCGCCAAACTCAGACAACAAAGCTGTCCAGGATGTGGCTGTAAAGGGATATTAATCCAATATTAATGTAACAAAAATTAAACAAAAGCCATTTTTTCCTTTTATTTTTAATTTCCTGAAACAGCTTAGTCTGAGAGAGCCAAAAAAAAAGAAGAAGTGATGTTAATTCAAAATAAATTTAAAATAAAAGTGATTTAAAACTGATTGTCATTCACTAATTGTCTCTAATTCTC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1482
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 |
---|---|---|---|---|---|
ENSDART00000089774 | Nonsense | 355 | 1428 | 5 | 13 |
ENSDART00000141006 | Nonsense | 355 | 1428 | 5 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 24377070)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23495674 |
GRCz11 | 22 | 23522238 |
KASP Assay ID:
554-1407.1 (used for ordering genotyping assays)
KASP Sequence:
TTGTTCCAGGGTTTGAAGGGCGTAACTGTGAGGTAGACGTCAGTGAATGT[G/T]AAAGCAATCCCTGTGTGAATGAAGGCATTTGCATGGAGCTTTCTTGGAAA
Long Flanking Sequence:
ATTTTTGAACAACTTAATTGTTTTATGTTCAATCCACTTACATTTATAAAAATAATTAAGGTAACTTAATCGATTTTATTGGTACAACATGAAAGAATTAAATTAACTTATTAGTTTTTACAAATTTTAGTCAATTACACATAAAACAATTAAGTTGTCCCCAAAAAAACTTAAGAACTGTGTTGTTTCAGCTCATTTAAAATGAGTAGTTTGAACAAACATCCTTTTTAGTGTGTAGAAGGAATACTGCTCTGGCTCAAAGTTAACAAGAATTATTTATATTATACATTAAATGATTCATTACATTGTGTTTTATTAACATCTATACCCCTAGCCTAAACCTATCTTCACATTAATGTAAAAACAGTAATCATTGTTGTAGTGTCACAAAAATTGTGTATATTGATGTGCGTATACCACAGCATCATGAGGCTTTCTGTCATATTTGTGTTGTTCCAGGGTTTGAAGGGCGTAACTGTGAGGTAGACGTCAGTGAATGT[G/T]AAAGCAATCCCTGTGTGAATGAAGGCATTTGCATGGAGCTTTCTTGGAAAACACTTTACGGTACTGAGCCCCTGTTTACAGCTAGATACAATCCCAGACTTGCTTCCGGGTTCATCTGCAAGTGTCCGCCAGGATTCTCAGGTACCTGCAGACTTACAAACTCATTTATTTACACATACATTAACAAAAGCATTCTAAATAAAGCAGGATGGGTATCATTGTAAAACTTTGTGGACAAACTCTAGTGGAAACATTTATGTTCACTCTATATTGCAATTTCATTTAATAAAAGACCAAGCTCCTTCTGCAGAAAACATCACTCAAATCTTGTCTCTTCACGTCCATGTTTTAATTCTTTACCTAGTTTGGGTTAAGTTTTTTCTTTGTTTGAGGACAAAAATTATGTTTTCCTGTCGGACCCAATTAAATTAAACTTTCTGTTTTTTGTCCGCGCAACATGCTCCTTTCAAGACTTTCTGCTGATGAAAGGTGGTCACTGT
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa12558
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 |
---|---|---|---|---|---|
ENSDART00000089774 | Nonsense | 509 | 1428 | 6 | 13 |
ENSDART00000141006 | Nonsense | 509 | 1428 | 6 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 24380974)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23491770 |
GRCz11 | 22 | 23518334 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AAACGCTCACTGTGTTCTCCTTTGAGACAAGCAGAGCATTCTTGCACCTG[C/T]AGACCCCRCTGCTGGGTGCAGAAACWTAYTTCAATATCACGCTAAGCTTT
Long Flanking Sequence:
TTTGTTACAAACTCTTCTCTGACATTGGCACAGATGCAACAAATAGTTGTAAGGATAAACTCTTGCAGAACCTGGCTTACAATTTCAGTAAGAACAGTTTATCCTAAGGCAACAATCCTTGCTAAGTGCGTATTTGTCAGGACCTTTGACTGAACTCTACTCTTGTTTTTCCTCTTCCAGGTGCCTTGTGCGAGCAAAACACAACTGCCTGTACCACCAGCCCATGTCATAATGGAGCCACATGTGAAGACTTCCTAGGCAGCTACAAGTGCATCTGCCCTTCTGAAAGCCAAGATGGAGTCCTCTACGGTGGTCGAAACTGTAGCGAGCCTCTTACAGGTTGCGAAGGTCACGAGTGCCAGAACGGAGCGTCCTGCATCCCATTCCTCAGCGAAGGTGTACATGGATACAGTTGCATCTGTCAGCCTGGCTACACCGGCTCTTACTGCCAAACGCTCACTGTGTTCTCCTTTGAGACAAGCAGAGCATTCTTGCACCTG[C/T]AGACCCCGCTGCTGGGTGCAGAAACATATTTCAATATCACGCTAAGCTTTCGTACAGTCCTGGAGAACACAGTGCTCTTCCAAAGGGGCAGCGGAGGGGTCACACTCAGCCTGGAGATACAGGAGACACACCTGATTCTTGATCTTAAGACTGACCCTCAGCCAAACGCAACCAGCTGGACTCTGATGTTGCCTCAGGTTGTATCTGATGGTGAATGGCACACAGTAGAAGCCGTACTTGGAGAGGGTACCCTGCTGCTGCAGCTGCTGGAGCCATGCCAGGGTGGACAAAACTGTGGTACAACAGCCCAAGTAAAGATCGGCGCCCTTGAGCTGGAGTCAGCCCTACTAAGCACCTTTGTTGGAGGATTGGATGAGGGAGGGAGCTCCAGATCATTCATCGGCTGCATGAGGGACTTGCTCGTGGACTCGCAGCTGATGATACCGGAGGACTGGTTGAGCAGCTCAGCTGTAAATGTTGTGCAGGGCTGTAGCCATCAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa159
Status:
Confirmed mutation in F2 line
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089774 | Essential Splice Site | 896 | 1428 | 7 | 13 |
ENSDART00000141006 | Essential Splice Site | 896 | 1428 | 7 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 24383929)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23488815 |
GRCz11 | 22 | 23515379 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATCGCGTTGTGAAAGTTACTGCAGGCTGCACCAGTGATGACACTTGCTCA[G/C]TAAGTTACAATGAGAAGTCTCATGAGATTTCAACTGCAACTGTACAACGA
Long Flanking Sequence:
CCATCAATGACGAACCTGACTCGGAAACACTTCATCTGTCCATGTTCTTGCGTACTCGAAAAGACTCTGGTCTTTTGGTGCTGCTGGCCAACAGCACCTCTGACTACTTGCAGATGTGGCTGGAAAAGGGAAAACTGACAGTTCAAGTCAACAACTTGAAGACTGTGACTGGTGAAAGGGTGCTTAATGATGGTGAGAGACATTTTGTCAGTGTCACCATCGAGGATGGCATGATGACTCTGCAGGACTCGGATCATGAATTCGAAGCAACATATGTTCAACCTGTTTCCATTCAGTTTGGGGATACGATCAATGTCGGTGGCCTGTTTGATGTACAAGCCTTAACTGCGTTTGGTGGACATTTTAAAGGTTGTCTACAAGACTTGCAGCTTAATGAGAAGAAGCTTGAGTTTTTCCCAATTGATACTTCTGCGATGTCGTACAAACCCGATCGCGTTGTGAAAGTTACTGCAGGCTGCACCAGTGATGACACTTGCTCA[G/C]TAAGTTACAATGAGAAGTCTCATGAGATTTCAACTGCAACTGTACAACGATTAGATAACACCAGATCTGGCAGCTACTGTATCTGGAAAAAAAGATCAGCTTATCTCATTTGGCTCTCGGTTGTCATGCTTAAATCCTTACATTCATGACATAAGAAACTAATCTAAATAACAGAAGGCAACAGAAATTGTTATGATTTGATTGAACGTTTTTAAGTGAGTACATAAAAAATGCTATAATCAAATAAGCTAAGCTTTTATATATTTATTTATAGATATATAAGTAAAGTTTCCACTAACCATGCCTCAATGTAGTTAGAAAACTTGTTCTAAGTGGTTGTTAGGTAGGCAGTTGCTAAGGCATTGCTAGGGTGTTGCTAGGCAGTTGCTAAGACATTGCTTAGAGGTAGCTAGAGTTTTCTGAGTGATTGTTAGGGTTTTCTTGTTGGTTGGCATGGTGTTCTGAGTGGTTGCTAGGTGGGTGCTAAGGCATTGCTAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24173
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000089774 | Nonsense | 987 | 1428 | 9 | 13 |
ENSDART00000141006 | Nonsense | 987 | 1428 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 24386577)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23486167 |
GRCz11 | 22 | 23512731 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGCTGATATCCCGCCATCTGACCAGTATTGTCTTTAATATCCGTACACGT[A/T]AGCGCAATGCCATAGTGTTGCATGCAGAGAGTGGATCAGAGTTTGTAACT
Long Flanking Sequence:
AATAATCATTTTAATATTAACTTAATAATAATCTTTTCATTACAGAAAAATCCTTGCCAAAATGGTGGCATCTGCTTTTCTTCATGGGATGATTTTACTTGCAACTGCCCTCCTAACACATCAGGACAACACTGTGAGGAGGTGAGCTGGTGTGACCTCAACCCGTGCCCACCACAAGCAATATGCCGGGCCCTAAACCAGGGCTATGAATGTGAGTATTTTATGACACCTAATCTCATGTGTATGGAACTCGACTTCTTAATTCAAGTCAAGGGCTATAAATTGTAGCAAATTTGCTGAAAACGTGTTGTAAGCCTCAAATGAGATTGTATTGCAAATAGTTATCTTCATCCAAGAAGTTACATCTAAACTATTTCTGCCTTTATTTCTATGCAGGCATTTCAAACGTGACTTTCCAGGAGAACACCACACTTGTATACCAAGGCAATGGGCTGATATCCCGCCATCTGACCAGTATTGTCTTTAATATCCGTACACGT[A/T]AGCGCAATGCCATAGTGTTGCATGCAGAGAGTGGATCAGAGTTTGTAACTGTATCTCTTCAAGATGGATTTCTGGTTCTTGAGCTTCTAAGTGGACCTACTACTTCATCCTCATTGTCACCAGTAACCCTGCACAGCCCAAGGGTAGTCGCTGATGGGGAATGGCATGTTATAGAGCTGTTAATGGCCACTCCAGGGTCTAACAGCTCCCACTGGATTATGGTCCCCCTAGATGAAAAAGATGAGCCTACTAAATCAGACTCTATGACCGGAAATCTAGACTTCCTCAGAGAGAGCGTGTACATCATGCTAGGAGGACTAGGCCCTGATTCTGGCTCCAATCTCATTGGTTGCTTGAGTAATGTTGAGATTGGTGGAATCGTGCTTCCGTATTATGGACAGACTGAGGTGAGATTTCCACGCACACAGGAAGAAATGTTCAATAAGATATCCGAGGAGCCTGTTCAAACCGGCTGTTTCGGGGAGGTGGTGTGTGAGCCC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24174
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 |
---|---|---|---|---|---|
ENSDART00000089774 | Nonsense | 993 | 1428 | 9 | 13 |
ENSDART00000141006 | Nonsense | 993 | 1428 | 9 | 13 |
Genomic Location (Zv9):
Chromosome 22 (position 24386596)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 22 | 23486148 |
GRCz11 | 22 | 23512712 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GACCAGTATTGTCTTTAATATCCGTACACGTAAGCGCAATGCCATAGTGT[T/A]GCATGCAGAGAGTGGATCAGAGTTTGTAACTGTATCTCTTCAAGATGGAT
Long Flanking Sequence:
ACTTAATAATAATCTTTTCATTACAGAAAAATCCTTGCCAAAATGGTGGCATCTGCTTTTCTTCATGGGATGATTTTACTTGCAACTGCCCTCCTAACACATCAGGACAACACTGTGAGGAGGTGAGCTGGTGTGACCTCAACCCGTGCCCACCACAAGCAATATGCCGGGCCCTAAACCAGGGCTATGAATGTGAGTATTTTATGACACCTAATCTCATGTGTATGGAACTCGACTTCTTAATTCAAGTCAAGGGCTATAAATTGTAGCAAATTTGCTGAAAACGTGTTGTAAGCCTCAAATGAGATTGTATTGCAAATAGTTATCTTCATCCAAGAAGTTACATCTAAACTATTTCTGCCTTTATTTCTATGCAGGCATTTCAAACGTGACTTTCCAGGAGAACACCACACTTGTATACCAAGGCAATGGGCTGATATCCCGCCATCTGACCAGTATTGTCTTTAATATCCGTACACGTAAGCGCAATGCCATAGTGT[T/A]GCATGCAGAGAGTGGATCAGAGTTTGTAACTGTATCTCTTCAAGATGGATTTCTGGTTCTTGAGCTTCTAAGTGGACCTACTACTTCATCCTCATTGTCACCAGTAACCCTGCACAGCCCAAGGGTAGTCGCTGATGGGGAATGGCATGTTATAGAGCTGTTAATGGCCACTCCAGGGTCTAACAGCTCCCACTGGATTATGGTCCCCCTAGATGAAAAAGATGAGCCTACTAAATCAGACTCTATGACCGGAAATCTAGACTTCCTCAGAGAGAGCGTGTACATCATGCTAGGAGGACTAGGCCCTGATTCTGGCTCCAATCTCATTGGTTGCTTGAGTAATGTTGAGATTGGTGGAATCGTGCTTCCGTATTATGGACAGACTGAGGTGAGATTTCCACGCACACAGGAAGAAATGTTCAATAAGATATCCGAGGAGCCTGTTCAAACCGGCTGTTTCGGGGAGGTGGTGTGTGAGCCCAATCCCTGCCTGCATGGAG
Associated Phenotype:
Not determined