ZMP
CDHR5 (2 of 2)
Ensembl ID:
Description:
cadherin-related family member 5 [Source:HGNC Symbol;Acc:7521]
Human Orthologue:
CDHR5
Human Description:
cadherin-related family member 5 [Source:HGNC Symbol;Acc:7521]
Mouse Orthologue:
Cdhr5
Mouse Description:
cadherin-related family member 5 Gene [Source:MGI Symbol;Acc:MGI:1919290]
Alleles
There are 7 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa25373 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25372 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa41048 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa18896 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa34204 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa41047 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa25373
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 |
---|---|---|---|---|---|
ENSDART00000130122 | Nonsense | 8 | 728 | 1 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 58623722)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57076331 |
GRCz11 | 7 | 57378771 |
KASP Assay ID:
554-7347.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGACTCCCACTCAACGGGCAGCACAGTCAATGCTTTATGTGAAGAAGTAC[C/T]AGCTGGTGACACGGTCTCATAGTCCTCCATGGTTATTTGTGTGTATTAGA
Long Flanking Sequence:
AATTATTCGAAATGAGTTATTAAAACTAATGTTTAGAAATGTGTTGGGAAAAAAAAATCTTTCCGTTAAACAAAAATTGGCAGGAAAAAAGTACAGGGAGGCTAATGATTCAAAAGGGCTAATAATTCTGACTTCAACTGCATATAATAAGTATGTGTGTGACTATATATTATTTTAATTTGACTTTATGTCACAGCTCATTTATTTTGATATATCCAGTGCTGCATTAATTTGATGGTCATTATTTACACTGTCAAAAGCTTTTCGGCACATTTCTCATGCCCAGGTTTCACACAGCCTCCCAAACAGCAGTGGAAAACTTGCACTAAAGCAAAATGAGCCCTGAAAAACAGATGCAAGTATTCGGGTGGGAGGGAGCAGTGCACTGCTGGCAGGCTCTTTAGGCAATATATGACCGTCAGATGAAGTCACAAACATTGCGACTGGAGTTGACTCCCACTCAACGGGCAGCACAGTCAATGCTTTATGTGAAGAAGTAC[C/T]AGCTGGTGACACGGTCTCATAGTCCTCCATGGTTATTTGTGTGTATTAGAATCTGGGAAATGGACATGACATTTAGCCATAAAACCATAATTATCATCTTTGGCTGTTTATTTGCGTCATTCCTTCCAAAAATCTGCTCTACTGATAAAAGTAAGTAATTTTTTTCTCACGCTGGTGGAGGTTTTGTCGACAGCAATGTTATTATGTGTCAGTCTCTCTTATTGGGTTTTTTATATGCTGTCAGTTATTTCAGCTCAGACAGTGACAATAGGAACGCCATGTCTGTTTGTTGTCATTGTCAAAAGACCACCTCAAGAATGTAGAGCTTCAAAATAATCTAGATGCTTAAAATGCTTTCCTACACAAACTGTCGTAACTCCAAATTCACTTTTAATGTGCTGGAAAATCTATACAGTGTCATAAACTACATGGATAAAATATCTGTTAATTAACAGTTTCCGTATTTTGTGCTTCACAAGTGTTTTCCATTTATTTACTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25372
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130122 | Essential Splice Site | 137 | 728 | 3 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 58616572)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57069181 |
GRCz11 | 7 | 57371621 |
KASP Assay ID:
554-7517.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGAAGAGCTGACTGTCCAAGTCCGATGTAATAAAACTGGCTACAGAAGC[G/A]TAAGTTGAGTCAATTTACAGTTCAGTAAATTCTGCTCAGATGATTGTACA
Long Flanking Sequence:
TTCTGTGATTGATCCTGTGCTCTCAACAAATGCCGCTAATGTGTGCTTATCCTTGTTATCTACACCGGGCTTGACATATCGGCTAATTCTCATCCTAGATAAGCAAACATGCAACAGTCTGAGGACCCGATTAAACAAGGTCAAGCTGCACTTTTTCTATTATCCTGCCTTTCTTGATTCCACTTTTGTGCAATACTCCTCTGGTGATGACTAAATTTAACCAGGATCAAACTATCTGCCATCTTGACCATCTTAAAGGGATAGTTTACCCAAAAAAATTTATTCTGTCTTCAATTACTCGTTATTTTGGGTGAACCATCCTTTTAAACTGATTTACTGGTTTGATTTAAGCTGACTTAGGTTTAACACTAGATTACTGATGCACATTCACAATAACAGATTACAGCAGTTTGATTCTTACTTTTACCATTTCCCAGACACTTTTAGGTCATGAAGAGCTGACTGTCCAAGTCCGATGTAATAAAACTGGCTACAGAAGC[G/A]TAAGTTGAGTCAATTTACAGTTCAGTAAATTCTGCTCAGATGATTGTACATTTAGCAATTCTCAAAAATATCACCGTTTTAGATCAAATATACTAAAGGAATCTTTCAGGCAAAGCATTTTACACATAAGCAATTAATCATTTGCTTTTTAAAGAGTTATAATTTTTTTTTTTCAAGATGATTTTTAAAAACCTTTAACACCACTTTACTTAATAAAAGTGAGTAAACATGTTGCCCTAAAATTGTTTAGTAAATCAACTATGTGCATAGTTATAAAAATTGAGTTAAGTGAACTTAATAGTTCCAAGTTACAATGGGTAAAAAAAAAAAAAAAAGAGTAATATGTTTCCACAACAGAAATAAAAAGCTTGGCTGGCATTTTTGAAGTGTTTCTTTACTAAGACAATAAGACAAAAACAAAAGCCAAATAAAATAAAATAAACAAGTAAAACAGGGTGAGAATGTGGTAAATCTGAACATGTGGTAAAAATCAGGCAGCT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41048
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 |
---|---|---|---|---|---|
ENSDART00000130122 | Nonsense | 206 | 728 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 58609991)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57062600 |
GRCz11 | 7 | 57365040 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACATGACGGATTCTTTACAGAACAGATACTTCAGACTTAAGACCATGTA[T/A]ACACCAAACATCCTTGTCAACAAGGTTTTAGATTATGATGTCATCCAGCA
Long Flanking Sequence:
TTCATTTCTTCACCTTTAATTACTTATAGTCTTATAGATTCAAGATGTGTTATATAATGTCGACCTGCCAATCTCTTTTGTGTTTAATAGATGTTTTGTAGATATGTAAACAAAGACTAAGACAATATTATGTTGAGGTGTCAGTGGAAATCTAATAGACATCTCATAATAGTCAATATTTATAATGAAACAGACAGATTAAATAGACTTCATGTAGTGCTTCATTACTGTTTCCTTGACTAGTCTATTTTGGACCATTGTTAGATGTCTATTAGATTTAGCCTTGTTTTATACAAGATATCTATGTTTAGATGTCTATTTAGACTTTTTTAAACAATGATTGTTAAGAATGATAAGTTTTTTGGCTTTTATTTATGTGATCAGTGGCAGCATCTTCAGAAACCAATACGTGTGAATGACAATTCTCATATTTGCTTGATCTTCTCTTATAACATGACGGATTCTTTACAGAACAGATACTTCAGACTTAAGACCATGTA[T/A]ACACCAAACATCCTTGTCAACAAGGTTTTAGATTATGATGTCATCCAGCAGGTGAAGCTGATCTTGTATGTGCAGGTATGTGAAACAGTTTTCTTTGAATTTTTAGAAATGTTAGACTATCTCGCTCATGTGTAACTTAAAGAAGTTTCACCTCTAACAGGATACTCCACTCCAGTCACAACCTGGTGAGCGTTCCTTCACAGCTACAACAACCATCACTGTCAATATTAAAGACATTGACAACCGTCCTCCTTGGTTTCAACCGTGCACAAAAGTAACGGTTGGCAGTGCCAAAATCTGCCTGAGCCTAGGGTACAGGGGAAGGGTAAACCTAACAGAGAAACAGGTACAATACATGGTTTCTTTATCACCTTTTAAATAATGAATATACCTAATACTGCATATGCTGTTCTGTTCTTGTGTTTAATTGTACATGCTCTCCATAATTAAGTACAGCCCATTTTGAAAATTAATATATTTCTCTATTTCTCAGTGAGTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa18896
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 |
---|---|---|---|---|---|
ENSDART00000130122 | Nonsense | 218 | 728 | 6 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 58609955)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57062564 |
GRCz11 | 7 | 57365004 |
KASP Assay ID:
554-6159.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTTAAGACCATGTATACACCAAACATCCTTGTCAACAAGGTTTTAGATTA[T/A]GATGTCATCCAGCAGGTGAAGCTGATCTTGTATGTGCAGGTATGTGAAAC
Long Flanking Sequence:
GATTCAAGATGTGTTATATAATGTCGACCTGCCAATCTCTTTTGTGTTTAATAGATGTTTTGTAGATATGTAAACAAAGACTAAGACAATATTATGTTGAGGTGTCAGTGGAAATCTAATAGACATCTCATAATAGTCAATATTTATAATGAAACAGACAGATTAAATAGACTTCATGTAGTGCTTCATTACTGTTTCCTTGACTAGTCTATTTTGGACCATTGTTAGATGTCTATTAGATTTAGCCTTGTTTTATACAAGATATCTATGTTTAGATGTCTATTTAGACTTTTTTAAACAATGATTGTTAAGAATGATAAGTTTTTTGGCTTTTATTTATGTGATCAGTGGCAGCATCTTCAGAAACCAATACGTGTGAATGACAATTCTCATATTTGCTTGATCTTCTCTTATAACATGACGGATTCTTTACAGAACAGATACTTCAGACTTAAGACCATGTATACACCAAACATCCTTGTCAACAAGGTTTTAGATTA[T/A]GATGTCATCCAGCAGGTGAAGCTGATCTTGTATGTGCAGGTATGTGAAACAGTTTTCTTTGAATTTTTAGAAATGTTAGACTATCTCGCTCATGTGTAACTTAAAGAAGTTTCACCTCTAACAGGATACTCCACTCCAGTCACAACCTGGTGAGCGTTCCTTCACAGCTACAACAACCATCACTGTCAATATTAAAGACATTGACAACCGTCCTCCTTGGTTTCAACCGTGCACAAAAGTAACGGTTGGCAGTGCCAAAATCTGCCTGAGCCTAGGGTACAGGGGAAGGGTAAACCTAACAGAGAAACAGGTACAATACATGGTTTCTTTATCACCTTTTAAATAATGAATATACCTAATACTGCATATGCTGTTCTGTTCTTGTGTTTAATTGTACATGCTCTCCATAATTAAGTACAGCCCATTTTGAAAATTAATATATTTCTCTATTTCTCAGTGAGTATTGGCAATGTATTTTGGTTGATTTAAACAAAACAGAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34204
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 |
---|---|---|---|---|---|
ENSDART00000130122 | Nonsense | 437 | 728 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 58604293)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57056902 |
GRCz11 | 7 | 57359342 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCCTTTGTTTTTCAGGGAATCAATCCTGACATTAAATATGAAGTGCAGTA[T/A]AGCAGCTACGTTAATATCACTACAGATGGGTTTATACTTTTAAAAAAAGC
Long Flanking Sequence:
GCCAACTGACCCAACTTAGGCTTGAACCAGCGACCCAGCGACCTTCTTGCTGTGAGGCAACAGCACTACCTACTGCACCACTGCGTCGCCTGGCACACTCAGAAGAATCAGAAGAATCATAATATTAATATTATATCTTAAAAAAGGGGTAAACTAGGTGCCCTTTAACATCCCACATGGCAAAATAATGGAGAGGGGTCTGGATGCAGACCTGGTGCAGTGCAATCTGGGCTGCAACCAATGCTTTTTAATGTGCTCACCTAACCCTACCACTAACCCTACCCATCACAGTGATGTCACTGGCTCCATTTGAGTGCATTGTGTCTGACATTGCATCGCTGAGTGATACAATCTCAGCTTGCATCATAAAGGCTGCATTCAGATATTATTGGAGAAATGGACACCCAAAAATATTGAATACTGTACATCTGAGATTAAATGCCTGCTTCTGCCTTTGTTTTTCAGGGAATCAATCCTGACATTAAATATGAAGTGCAGTA[T/A]AGCAGCTACGTTAATATCACTACAGATGGGTTTATACTTTTAAAAAAAGCAGTTCGGACTGATGCCTTCGCATTGCAGGCAAGTTAATATATTTTATTGATGAGAATATTTTATACACTCACTAGACACTTTATTAAGTACACCTTACTAGTACTGGGTTGGACCTCCTTTTGCTCTAAACATTGCCTTAATCTTTCGTGGCATAGATTCAACAAAGTACTGGAAACATTCCTCAGAGATTTTGGTCAATACTGACATGATAGCATCACACAGTTGCTGCAAGTTTGTTGGCTGCATATCCATGATGCGAATCTCCTGTTCCACCTGTCCCAAAGGTGCTCTAATGGATTAAGTTATGGTGACTGTGGAGGCCATTTGAGTACACTGAACTAATTATCATGCTCAAGAAACCAGTCTGAGATTATTTGCACTTTATGACATGGTGCATTATCCTGCTGGAAGTAGCTACCAGAAAATGGGTACACTGTGGTCATAAAGGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa41047
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 > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000130122 | Nonsense | 535 | 728 | 13 | 14 |
Genomic Location (Zv9):
Chromosome 7 (position 58599731)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 57052340 |
GRCz11 | 7 | 57354780 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGATCGGCTATCTGATATCCCGTGTCAAGAAGGGGAATTCTGACGCATTC[A/T]AGTTGTCTGAGGTCAGCATCTTCCCATCAAAGCTCAGTGAGTCCAGCTCT
Long Flanking Sequence:
CTCAAACTCCCCTCTTGCCCTTCTAATGGGAGGGAGCCCCAGGCTCGAGGATTTTACGAGCTCAGAGCTCACTCCCAGGACAGCATGCCAATTACGCTTTATTGATCATCAGCTAAGTATGAACTCTTGAAATGGAAACTGCGCAGAGCTGGTGGTCCTTAATGAATGTGGTTGAGAACCACTGACCTAAAAATATCTTTGTTTCATTTCTGAAGATAAACAAAGATCTTGAAACAAGGTGAGGGTGAGTACTTAACAAAAGTTAGATTTTTTGTTTGAACTAACCCTGTTGGAGTTCTAATATCTTTTCAGCATTCAGTATAATTAATATCCCTCTACATGTCTGCCATCCAGCAGTGGGCATCCAGTCACAAGACGAGAGCTATCGCGCAGGAGACATGGCTTTGCTGGGCTTTGTAATGGCCGCTTTACTAGTGCTCTGCCTCATTGTGATCGGCTATCTGATATCCCGTGTCAAGAAGGGGAATTCTGACGCATTC[A/T]AGTTGTCTGAGGTCAGCATCTTCCCATCAAAGCTCAGTGAGTCCAGCTCTGAGTGTCCCCTTTGTAAAAGAACTGACGATTAAAAAAAAAAAACATTCCCTAAGAATAACCATGTACTTCAGCAGGTAATGTGCAGCTTATGAAATTTTAAGATTAACCCTCTGCCCCTCATTCAGTGTTTAGGGCCATGCTTGAAGTTTACTCAGCCCCCTAACAGGCCAAGAGATAGCATGCAGTTCACCAATGATGGTTTCTTGAATGAAGGGGACACAGGGAGGTCCAGATCCAGGCGTGCAGACCTGAGGGAACAGAGGCTCGATGCGGTTCAAGGGGCGAGGGTTCGAGTGATTCCTCGCGAGAGACAGAGGCACTGCAGCTCCTGCGGATTCCAGGTGCACGCCAACCATTCACACTACAGTCCTGGCCTCCCGGTCAAAGAAAAGCCCAGTAAGCAAAGGGTCAAATCTATTCTGGCAAAGGAGAGGAGGAAGGATGACAAA
Associated Phenotype:
Not determined