ZMP
cdhr1
Ensembl ID:
ZFIN ID:
Description:
Cadherin-related family member 1 [Source:UniProtKB/Swiss-Prot;Acc:Q6B3P0]
Human Orthologues:
CDH23, CDHR1
Human Descriptions:
cadherin-related 23 [Source:HGNC Symbol;Acc:13733]
cadherin-related family member 1 [Source:HGNC Symbol;Acc:14550]
cadherin-related family member 1 [Source:HGNC Symbol;Acc:14550]
Mouse Orthologue:
Cdhr1
Mouse Description:
cadherin-related family member 1 Gene [Source:MGI Symbol;Acc:MGI:2157782]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9596 | Essential Splice Site | Available for shipment | Available now |
sa35513 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa15425 | Nonsense | Available for shipment | Available now |
sa1445 | Nonsense | F2 line generated | Not yet available |
sa9583 | Nonsense | Available for shipment | Available now |
sa35512 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa9596
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 |
---|---|---|---|---|---|
ENSDART00000026679 | Essential Splice Site | 119 | 856 | 4 | 17 |
ENSDART00000110005 | Essential Splice Site | 120 | 857 | 5 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 29726158)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29372106 |
GRCz11 | 13 | 29502556 |
KASP Assay ID:
2260-6529.1 (used for ordering genotyping assays)
KASP Sequence:
CACAAGATGAGATTGAAGTCTTTGTCAGCATCTCTGATAGCCTTAATAAA[G/A]TAAGTATTACGACTGRKTAAGGACTCGTATATCAGTACCAGAGATGTGAT
Long Flanking Sequence:
TTCTTAAAGGATAATAATAAAAAAATGACAAATGTTTAAAATGAAATGACATATTCATTTTAATAGTTAAAAAAAGTCTAGAAAGCTGGAGTCTGGGGCCAACAGTATGACTAAAAATAATGTAATATACTGCAAAACATCAAAATGTCATCTTGACTTGTGTGAATGCTAAAAGTACAGAACTATTTTCTTAAATCTGTATATTACAGGAACACAGATATATGTTCTTAATGGAACTGACCCAGAAGGCCAGCCAGTAAAGTATGGAATTACCTTTGAACCCGGATCCAAAGAGTTTTTTCGTGTTCATCCCAAATCTGGAGTAGTAACATTAATAGAGGACCTTGACAGAGAGGTACAGTGCACAGTTTTATTTATAATTAGTTTCAAGTGTTAAAATTTGAATGCTGAGAAAACGTTTATAACACTATGTTTATTTATTATCACAGGCACAAGATGAGATTGAAGTCTTTGTCAGCATCTCTGATAGCCTTAATAAA[G/A]TAAGTATTACGACTGATTAAGGACTCGTATATCAGTACCAGAGATGTGATCATTCTAATACTTTGATGTATTGTCAGGTAGTTGAAAAGGTTTCAGTTTTTATCATGGATGCCAATGATGAGAGACCACAGTTTCAAAACATGCCTTCCATCGTAGATGTGCCAGAGGTGAGGAGTCTAGTCTCAGAGAATCTGTCATTATATTATTCATTCAGGCTCCTGTAGAATGTATTTTGGAAGATACCTGGCCAGTAAACATTTTTGATTAAAGTGATTTGACTCTGTGTGTGTTTGAACATAGAACACAACGTCTGGAAGTAGCATCTATAAGGTGCAGGCAGTGGACAGGGACACCGGCTCAGGAGGATCAGTCACTTACTTCCTTCAGGTAACATCTAAGCATATGCAGATATTCAATATAAATATAATTCAATATATTGTGATAATGAACATTCACAATATTAATATTGTATGTGTTACAATATTGTAAATAGTTATTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35513
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 |
---|---|---|---|---|---|
ENSDART00000026679 | Nonsense | 134 | 856 | 5 | 17 |
ENSDART00000110005 | Nonsense | 135 | 857 | 6 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 29726038)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29371986 |
GRCz11 | 13 | 29502436 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATTGTCAGGTAGTTGAAAAGGTTTCAGTTTTTATCATGGATGCCAATGAT[G/T]AGAGACCACAGTTTCAAAACATGCCTTCCATCGTAGATGTGCCAGAGGTG
Long Flanking Sequence:
TGTAATATACTGCAAAACATCAAAATGTCATCTTGACTTGTGTGAATGCTAAAAGTACAGAACTATTTTCTTAAATCTGTATATTACAGGAACACAGATATATGTTCTTAATGGAACTGACCCAGAAGGCCAGCCAGTAAAGTATGGAATTACCTTTGAACCCGGATCCAAAGAGTTTTTTCGTGTTCATCCCAAATCTGGAGTAGTAACATTAATAGAGGACCTTGACAGAGAGGTACAGTGCACAGTTTTATTTATAATTAGTTTCAAGTGTTAAAATTTGAATGCTGAGAAAACGTTTATAACACTATGTTTATTTATTATCACAGGCACAAGATGAGATTGAAGTCTTTGTCAGCATCTCTGATAGCCTTAATAAAGTAAGTATTACGACTGATTAAGGACTCGTATATCAGTACCAGAGATGTGATCATTCTAATACTTTGATGTATTGTCAGGTAGTTGAAAAGGTTTCAGTTTTTATCATGGATGCCAATGAT[G/T]AGAGACCACAGTTTCAAAACATGCCTTCCATCGTAGATGTGCCAGAGGTGAGGAGTCTAGTCTCAGAGAATCTGTCATTATATTATTCATTCAGGCTCCTGTAGAATGTATTTTGGAAGATACCTGGCCAGTAAACATTTTTGATTAAAGTGATTTGACTCTGTGTGTGTTTGAACATAGAACACAACGTCTGGAAGTAGCATCTATAAGGTGCAGGCAGTGGACAGGGACACCGGCTCAGGAGGATCAGTCACTTACTTCCTTCAGGTAACATCTAAGCATATGCAGATATTCAATATAAATATAATTCAATATATTGTGATAATGAACATTCACAATATTAATATTGTATGTGTTACAATATTGTAAATAGTTATTTATTTATTTTATACTTTGAGTACTTTTTAAGAACATTAATTTTCTGCATTATCAGTGGTGATCATAACAGCATCAAATGAAGACTTAATAGGTGATTGGTTTTCATTTATTATTCATATTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15425
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 |
---|---|---|---|---|---|
ENSDART00000026679 | Nonsense | 229 | 856 | 8 | 17 |
ENSDART00000110005 | Nonsense | 230 | 857 | 9 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 29722989)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29368937 |
GRCz11 | 13 | 29499387 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AWAAATTATTKYGTTTTTAGGATGGAGGAGGCATTTACAAGGGCAAGCAA[C/T]AAGTGATGTCATCATCTGCTACTTTGACCATAAATGTGATCGACACTCAA
Long Flanking Sequence:
AAGGAGAATGCGTTAATCTCAGCTTTAGGAAGGTGTAGTCAGTGATGTTATCCTGATTAAATAAAAGTTAATTGTTTACCTGTATAAATCATGATCAGTGTGAATTGTAAAGCAGGATAAGGCCTGCCTCAGGATTCTGTATTCTTGAGGATTGAAATGATCCAGTGTCAAAGATTTCTGTTTTAAAAGCAAACCCTGCTATTGTAACTCAAAGGATGTCTCTGTTTGTTCTTAAATCCAGAGCAGTGAGCAAAGCCCAAAGTTTGCCATTGACCATCATAGCGGCGTGCTGCGGATAAAACCTGGAGAATCCCTCGATTATGAAAAATCGCGGACGCATTTCATCACTGTGGTGGCAAAGGTGAGAGTTAGTCATTTAGTTCTTGTTATTTTACAAGGTCAAGCATTTGTTCATCTATTTCCAGCTATTATTTTTCTTCCTGCATCACAATAAATTATTTTGTTTTTAGGATGGAGGAGGCATTTACAAGGGCAAGCAA[C/T]AAGTGATGTCATCATCTGCTACTTTGACCATAAATGTGATCGACACTCAAGATTCTCCCCCGATTTTTATTGGAACTCCTTACTTTGGTTATGTCTATGAAGTCTCTTCGCCAGTGAGTATCATAACACTCCACAATAATTTTCCTGCATGGTTTCTTACCAGTATATGCTTCTGTTGATTTAAAAATGAATCTTCTACCTGCTAAATGTTTTTTTTTTTTTTAATGCATATAATGAATGGAAAATGGGACTATACATAGACACAACCATTCAAAGAACATGGTTGGTTACAATTTGTTCTGTCACTGTGGTACACCGACCAAAGCTGTATTTGTTTATTAAAAATATTGTAAAATACGCATGTTTAAATCTTTTTCTATTATTAAATCTTTTAAAATGCAATTTGTTTTTCTGCTGACTGAAGAGAAATCAGAAATGTTTAACATCATTTATCCTGTCTTCAATGTTTTGTGATTCTTCAGAAATTACTAATAAATTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa1445
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:
A > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000026679 | Nonsense | 276 | 856 | 9 | 17 |
ENSDART00000110005 | Nonsense | 277 | 857 | 10 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 29721308)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29367256 |
GRCz11 | 13 | 29497706 |
KASP Assay ID:
554-1371.1 (used for ordering genotyping assays)
KASP Sequence:
TTAAGATCTAATTTTGTCTACAGGGATCTGAGATATTTACAGTTTCTGCC[A/T]AAGATGGAGACATGGATAATCCAAATACGATCATATATTCATTGGACTCT
Long Flanking Sequence:
CTGAATGTTCTGCAAGAACGCTTTCTTTGCCATTTCAGATGACTTTATTAATAAGTTATTTGAATTATTGCAGAGATGTATGGATGCAGTCGTCCAAGCTCATGGGAGTCATAAACAATATAAATTCTTTTTCCACTCGAAATGACTTTATATTCTATTCTGTACACTATTTCTGTCAAGTGACAAGACATTTGTCTTAGCAAAGTCAAACCTTACTGTCCTAATGAAATAATTAAAAATCAAGGCATGATCATATTTTATTTGGGTAAAATAAGTGTAATTTAGAAACCTTTACCTTTCATATAAGCCACTTCTGATACCAATTGATCAACTAGAAGTCAGGTTGTTATTTATTGCTAAAACATGGATAGGCGACAAGACTTTTGTTAGGTAGTGTAGATGGCTCTTCTATACAAACAGCATGTGGCTTAAATCAGCCGGAAAAGACCTTTAAGATCTAATTTTGTCTACAGGGATCTGAGATATTTACAGTTTCTGCC[A/T]AAGATGGAGACATGGATAATCCAAATACGATCATATATTCATTGGACTCTGGTATGTTGTATTGGTTATTATTTTGCACGTTGATTGATGGCTAGAAAGTAATTTAATAATGACTTTTCACATCACAATGCTGAATCAATGCATCAATGTATTCAGGAGCAGATGGGTCCTTTTCCATTAATAAAACCAGTGGAGTCATCACTCTGAATTTGTACCCAGCAGACCTGAGGAGGGAAGTTTTTAATATTAAAGTCAAGGTACACTTTTTTGTGTGTGTGTGTGTTTTGTGTATTTTTTGTTTAGCATTGTTTTTAGATTGATTTCTGTTCGGTGTTGTTTTGTTTTTATCTTTTGTTTTAGTTTAGTTTATAGTTTTGTTTTGCTTCCTTTGTTTTGTTTTGTTTCATTCCATTAGTTTTGCCTATTTTTTTGTTTTGTTTTCTGGTATCAGATGTATTTAGCAACATCTCTTTTATACGTATGTCCTTGTTGCATTTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9583
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 |
---|---|---|---|---|---|
ENSDART00000026679 | Nonsense | 439 | 856 | 12 | 17 |
ENSDART00000110005 | Nonsense | 440 | 857 | 13 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 29719878)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29365826 |
GRCz11 | 13 | 29496276 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCAAGTCACYGTCCTAGTGGAGGATTCTGCWGCAATGGATTTTGAGAAAT[C/A]ACAGTTCCTGACTTTTAAGGTAGAAKTTTTTTYGTTTCACAGCTGTTAGT
Long Flanking Sequence:
TGTAGTGCAAAAAAAGTGATATTATTTAAAAATAGGAGATAAGACACCATTAGTTTAATGCGCTACTTCCATGTTTTTTAGGAGTGATTTTCAATCATAATAAAACATTGTCATTTATGTTACGTAAATGCACCCAAACAAGCAGGTGGTCCCTTTTAAGCTTTTGTCATATTATGCAATAATGTTTTCAGTTATTTAGCACTTAGTCACATTCAGATTCATCTGAAAAACAAGATCACATGGATCAGCACAGTTGTTGATACAATGTTTTACATACATTTTGATTAACTTTGACATATTCCAGCTCTGTGTTTTAATGGCTTACTATGAAATTTTGTAATCAAAAGTGCTACGTATTTGTTTTTAGGGATCAAATGCAAAATTCAACCTCAGACTAGTGGGCCCGGGCCGCATGTTAAGAGTGGTTCCTCAAACTGTTCTGAATGAAGCCCAAGTCACTGTCCTAGTGGAGGATTCTGCTGCAATGGATTTTGAGAAAT[C/A]ACAGTTCCTGACTTTTAAGGTAGAATTTTTTTTGTTTCACAGCTGTTAGTCTTTTTTTCTGAACCAAAATGGTTATCACTATTCACAAATAATAATACAATTTAACCTTGATTTACAGAACACACTATGAAGTCATTCAGTGTAACAGTGTTTTATATACCAACGGTCTTGTCAGGAATGTTTTGAGAAAAAGTAATACAAAATAATGACATAATAAGAATTATTAAATAATAATAAAATACTTTATGAAGGGATAGCAGTCATGAAATGCTATAAAATAATAACCAAAATTATTGTTTGTATTTTTATTTATTATATTTTAACACTATCCTTCAAATCAAAACTATTTCACTCATTTGCCAGCCAATTTGAATAGTATCACTCAATTGAATGGACATTATCTGTGGTTATCAGCTGATAGATATAGGCCAGTAGAGGTCTTCTGCGATTACTAGTAGGCTCAGAAGGCGGTTATCATCCATCCACATGGTTAGTCAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa35512
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 |
---|---|---|---|---|---|
ENSDART00000026679 | Nonsense | 552 | 856 | 15 | 17 |
ENSDART00000110005 | Nonsense | 553 | 857 | 16 | 18 |
Genomic Location (Zv9):
Chromosome 13 (position 29709493)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 13 | 29355441 |
GRCz11 | 13 | 29485891 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CAGCCTTGGGCCAGTCTGGATGCTGAGGTCAAATCCAAGTATAACTTCTA[C/A]GTGAAAGCCGAAGACCCTGAAGGAAAATACAGCCTCGCGGAAGTCTTTGT
Long Flanking Sequence:
GGCTGTGAATACTCATGTACATGTGATTTTTCAGTTTTTTTTTTTTTTTTTAATTTTGCAACTATTAATTTTAATTAATTAATTATTAATTAATATTGTGTGTTGAATTTTGAGGACATAAATGAATTTAATTCATTTTGGGAATAAGGCTGTAAAAAAAAAAAAATGTGGAAAAGTGAAGCGCTATGAATTCTTTCCAGATGCACTGTATATACATGCAGACATGATGCCAATATTAACTTACAATGGAGTGAATTCAGTAAACTATATAGGCATGATGTTTTGTTATGTTGATTCCTTTCCACTGTGTTCTCAAAGCTTTAAATCATGTTAACATGTCCCTGTACAACTACCGCTTTCTAATCCCGATTTTCCCTATAAAACTAATTTCCTGTCCTATATCTTTTCCGCAGCTTTCTCATTCAGGCTGATTCTGGAATCATCTACACTCAGCCTTGGGCCAGTCTGGATGCTGAGGTCAAATCCAAGTATAACTTCTA[C/A]GTGAAAGCCGAAGACCCTGAAGGAAAATACAGCCTCGCGGAAGTCTTTGTCACCATTACTGACCTCAATGACCATCCACCAGCGTTTAATGAAAACTCTTTGGAGCAGACCATGGTGATTGGTGCACCTGTCAAAATAGAGGTATGTTGTTTTTTTACTTTTTGAAATTTTGGTTTATCTGACTGGTGAAAGTATAAGTTGACTGAGATTGATGATTTGTAGGCGATTGATGAAGATGCAGAGGAGCCCAACAATCTCATTGAATACTCCATAATGAAAGCCGATCCAGACAACATATTTGACATTAATGCAGACACGGGAGAAATAAAGCTGAAGCCGTACATCAAGTCAATGGACATTGTCCAGAATATCACCAATCAGAGAGACTGTACCTGGTCTGTTGTTGTTCAGGCTAAAGACAGAGGTTCACCATCCTTTAGCACAACCACAGTGGTAAAGATTGACATCACAGAAGCGGTAAGTGTATATTAGTGTTTAAT
Associated Phenotype:
Not determined