ZMP
CHL1 (1 of 2)
Ensembl ID:
Description:
cell adhesion molecule with homology to L1CAM (close homolog of L1) [Source:HGNC Symbol;Acc:1939]
Human Orthologue:
CHL1
Human Description:
cell adhesion molecule with homology to L1CAM (close homolog of L1) [Source:HGNC Symbol;Acc:1939]
Mouse Orthologue:
Chl1
Mouse Description:
cell adhesion molecule with homology to L1CAM Gene [Source:MGI Symbol;Acc:MGI:1098266]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa11246 | Nonsense | Available for shipment | Available now |
sa15944 | Essential Splice Site | Available for shipment | Available now |
sa33944 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa10607 | Nonsense | Available for shipment | Available now |
sa33945 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa33946 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa11246
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 |
---|---|---|---|---|---|
ENSDART00000111855 | Nonsense | 22 | 1253 | 1 | 28 |
Genomic Location (Zv9):
Chromosome 6 (position 44851051)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 44919291 |
GRCz11 | 6 | 44914926 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGAAAACCCTGCTTCTTTTGGCTGCTTGCCTYAATATGAKCAGCAGGTAT[C/T]AAACTAACGCCCTGGAAATTCCACTTGATGGTAAGTAGAAGAAATGGCTT
Long Flanking Sequence:
CTGCCACACATGCACTGACAAACAGTTTACAGAAATACAATTCACGTCTCCGGGGACTCGGTGATAGGGCGCTTTAATATGGAGATTCCTCTCACAGATGCATTTCAAGTAACTACAAGTTGGGTTAGACATTGAGGCGAGTTGCTCAGCAGGAGACATGCAGAATATGCAAGTCTTTGTGTCTGCGCAGGTGACAGGGTTGTTTTTTTCATATGAGATACCGCGGGCCGACTGTTAGCATATGGTTGCTGGGAAGTCTGGGTGTGCATGGCAGTGATTCTTGTTTGCCGTTGATGTCTGGTTGCCAATAAGATCTGTGTTGTGTTTGGTGCAGGTAGCGAGACCACAGCCTGGGTTGGAGTGAGATGCACTGACTCCTGGCAGACTGCAGATTTCCCTGTCATCCTCCGCTCTCGCCTCTGAAACTGTGGCCAGTCATGCGGTTGTTACGGAAAACCCTGCTTCTTTTGGCTGCTTGCCTTAATATGAGCAGCAGGTAT[C/T]AAACTAACGCCCTGGAAATTCCACTTGATGGTAAGTAGAAGAAATGGCTTCCTGTTTTATGCAGTATTAATCTTGCAATATATCTTAACTTTACATATCTGACCATTTTTAATGCTGTTTCAGTTTAATTGTTTCCCATGTGTTCAATTGTATGCTCTCTGGAATAACAATGAATTACAGAAGCCTGTTTTCACCTCTAGCCCATTTTTATAGTAAAGAAAAAATATTTTAAATAAGTCTCTGATATTCTTAAAGTGTGTATGAGAAGTTTCTGCTCAAAATATGACACAAATAATATTTTATAACACTTTGAATCTGCCCCTTTTAGGCTTTAATCCTAATCGTGCCATTTTGTGGGCTGTTGCATTAAATTAAAATTAGATTGTCTTATTTTCAAAAGAGGGCGGAGCTACAACTGCCTGTGCATCAGCATAGTAGCAGATTCAACAACAAGACTAATGTCCTATGCTAATGAGGGAGAGATCGTCACTAATAGGCGG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa15944
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000111855 | Essential Splice Site | 32 | 1253 | 1 | 28 |
Genomic Location (Zv9):
Chromosome 6 (position 44851083)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 44919323 |
GRCz11 | 6 | 44914958 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
AATRTGAKCAGCAGGTATYAAACTAACGCCCTGGAAATTCCACTTGATGG[T/G]AAGTAGAAGAAATGGCTTCCTGTTTYAWGCAGTATTAATCTWGCAATWTA
Long Flanking Sequence:
AAATACAATTCACGTCTCCGGGGACTCGGTGATAGGGCGCTTTAATATGGAGATTCCTCTCACAGATGCATTTCAAGTAACTACAAGTTGGGTTAGACATTGAGGCGAGTTGCTCAGCAGGAGACATGCAGAATATGCAAGTCTTTGTGTCTGCGCAGGTGACAGGGTTGTTTTTTTCATATGAGATACCGCGGGCCGACTGTTAGCATATGGTTGCTGGGAAGTCTGGGTGTGCATGGCAGTGATTCTTGTTTGCCGTTGATGTCTGGTTGCCAATAAGATCTGTGTTGTGTTTGGTGCAGGTAGCGAGACCACAGCCTGGGTTGGAGTGAGATGCACTGACTCCTGGCAGACTGCAGATTTCCCTGTCATCCTCCGCTCTCGCCTCTGAAACTGTGGCCAGTCATGCGGTTGTTACGGAAAACCCTGCTTCTTTTGGCTGCTTGCCTTAATATGAGCAGCAGGTATCAAACTAACGCCCTGGAAATTCCACTTGATGG[T/G]AAGTAGAAGAAATGGCTTCCTGTTTTATGCAGTATTAATCTTGCAATATATCTTAACTTTACATATCTGACCATTTTTAATGCTGTTTCAGTTTAATTGTTTCCCATGTGTTCAATTGTATGCTCTCTGGAATAACAATGAATTACAGAAGCCTGTTTTCACCTCTAGCCCATTTTTATAGTAAAGAAAAAATATTTTAAATAAGTCTCTGATATTCTTAAAGTGTGTATGAGAAGTTTCTGCTCAAAATATGACACAAATAATATTTTATAACACTTTGAATCTGCCCCTTTTAGGCTTTAATCCTAATCGTGCCATTTTGTGGGCTGTTGCATTAAATTAAAATTAGATTGTCTTATTTTCAAAAGAGGGCGGAGCTACAACTGCCTGTGCATCAGCATAGTAGCAGATTCAACAACAAGACTAATGTCCTATGCTAATGAGGGAGAGATCGTCACTAATAGGCGGAGTTTTCCCTCTGATGACACATACAAATGGAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33944
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 |
---|---|---|---|---|---|
ENSDART00000111855 | Nonsense | 379 | 1253 | 9 | 28 |
Genomic Location (Zv9):
Chromosome 6 (position 44867530)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 44935680 |
GRCz11 | 6 | 44931128 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTATTGATCAAGTGTGTCGTGAAAGGAAATCCTCAACCTACTGTAGGATG[G/A]AGAGTTAACGGGCGGCCACTGAACGGTAGATACATGTTTCTTACAATCTT
Long Flanking Sequence:
AAATAAAAGCACAAGATATTCAGGAAAAAAGCTGGAAATATGTAACTATTGACCTCCATACTAAGCAAAACAAATACAATGGAAGTCAATGGTTTCCACTTTTCGTCAAAATGTCTACTTTTGTGTTCAACAGAGGAAAGAAAGTCATAAAGGTTTGGAACCAATTGAGGGTCAGTAAATAATAAGTAAATTTTCATTTCAGGAGAACTATCCCTTTAACACAAAAAAATAAAAAAAAAATAAAATCAAGGCTTTGAGGCATAGATATACTATTAATTTTGTCTATATTTTAAAAGCGTTTGCAAAAAAGAAAGCACTAGACTGACTCTGCTGTTAATACTGTGATTTGCATTTATCTTGTCATGTGTATAATATAATGTTTTATGTAACTCAGAGCCTCCTGAGTTTGAGATTGAACCTCAAAGCCAACTGGTGACGATTGGAGCTGATGTATTGATCAAGTGTGTCGTGAAAGGAAATCCTCAACCTACTGTAGGATG[G/A]AGAGTTAACGGGCGGCCACTGAACGGTAGATACATGTTTCTTACAATCTTACAGTAACAGTTTTATGTTTTATTTTAGTTTTTTATTTATTATATTAAATAATAATAATTAAAAAAAAACTTGAATTAAATTAAGAAAAAAATTCTAGTTTCAGTTTCTGTCCTGTACAGTATTTAGGCTTGTATTTGGATTACATATAGTATACAATTGTGTTGAAAAAATCTTCTGTCCGTTAAGCAACATTTGGGAATTTATTTTAAAGAATTAAAATTTCACAGGAGGGCTAATAATATTGAATTCAACTGCATAAATACAGTCAAACCCGAAATTATACATACTCCATATGTATAAATGTCTGATAACCTTTATTGGCAAAAAATAAAATGAATTTGTCAAAGCAACACTTTTTTTTTTTTTTTTATCTGGTCAAATATTGCATTTGCATATTTGCACTGATGTTTTTTTTTTATTTTTTTTTATTTATTTTGTTGTTGTTGTTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10607
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 |
---|---|---|---|---|---|
ENSDART00000111855 | Nonsense | 795 | 1253 | 18 | 28 |
Genomic Location (Zv9):
Chromosome 6 (position 44884385)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45042770 |
GRCz11 | 6 | 44947776 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GTGAAGAGGCACTCATTTCTGGTCAAAAACACCCCGACGTTCGTCCTTTA[C/A]GARATCAAAATTCAGGCCAAGAACCACGCGGGCTGGGGTCCGGACCCTAA
Long Flanking Sequence:
TTAATATTTTTACATATTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAAAATTTAATATAATTTTTATTTTGTTTTAATAATTTTTTGCAATATGTATGTTGTTGTTTTTTTTACAAAATTATTCTTACTCTTATACATACATACAAAATCAGCCAGCCTAATTATAAATGTTTTAATGATTTAAAATCAGGCTAATAGATTTATAATCTATTAATACATTTTACCCAAAGTATTAGTATTTAGAACAAGAAAACAACTAAATGTTATTTTCTTTTGATTTACTCTTTCCTGTCTTCTAACCAAGCTCTTGTTTTTCCTGTCACAGCCGTTGTCACCTATTGAACACAACGGGCCTGGTCTGGAGTACAAAGTGAGCTACAGGAGACATGGCAGCGATGAAGACTGGACGGAGCGCATGGTGAAGAGGCACTCATTTCTGGTCAAAAACACCCCGACGTTCGTCCTTTA[C/A]GAGATCAAAATTCAGGCCAAGAACCACGCGGGCTGGGGTCCGGACCCTAAAATAATAACAGCGTACTCGGGAGAGGATTGTAAGTAGAAACAACCTCCATTGTGCCTGAGCCGTGAAGATGAGTGTGCATTCAAATAAGCCAATACCGTTGACATTTCACTCACTGTCAAGCATCGCGCGTCGTGCCTGTGAGAGCATACAAAGTAGCACATTCTGAAAGATGCATTGTGGTTTCTAACCTTTTCTTCATCTGTAAAGGCTCTTGTTACGCCGCAAATAAGCAATGGCTGTAAATGGAAACACACCCACCCCTCCCTGTAGCGAAAGTGCAGTACATGTGTGATGAGAATATCAACAAACCTGGAGGGCAGAGAACAATGATGAAATAGCATCTTTGCTTTAATACACAATCTCCAAACGGCAGCGACTTGTTTAGCCTTATTGAGAATATTAAATGGAACAAAGTGGGAATGATTCTCCTCACTCTGAGTTTTCGTACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33945
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 |
---|---|---|---|---|---|
ENSDART00000111855 | Nonsense | 1041 | 1253 | 23 | 28 |
Genomic Location (Zv9):
Chromosome 6 (position 44905198)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45061933 |
GRCz11 | 6 | 44967727 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTCTTCTCTCAGCGGTGTTGAATATTAGCACCTCAGTTAGTCACAACTA[T/A]GCAAATATCAGCTGGATTCCAGGCACAGAACAGACGGAGTCAGAGTTATA
Long Flanking Sequence:
CCTCTTGAATTCCCCGAATGGCAGATTTGTAGTTCTATATCGATCTTCGTGTTTACCAGCAATCTACAAGGATTAGCTTGCTGCTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATTGATACAACATAATGTTGCAATATTCCATCTTGTGGAGAAAGCTTTTGCACCAATCGAATGTCACCATGAGCATGAAAAGAACAATTTTGCACCTATAGTTAGAATAGTGTCTCCCATTTCATTTGTGCACATTTCATCTCCATCACAAATGAGAAAATATGTAACTACGCCACATTTCATTGAAGTACTCTCTTGGAACCTCCATATGTTACAGTGAATAGAAAAAAGACATTCTTTCCCTTTCAAGTCTAACAAGCAACCCTTTCTCATGTCATTTACAGTACTAACCCTCTGTCATTTCTCTCTTCTCTCAGCGGTGTTGAATATTAGCACCTCAGTTAGTCACAACTA[T/A]GCAAATATCAGCTGGATTCCAGGCACAGAACAGACGGAGTCAGAGTTATATGTTGCCTTTATGAACAACCGTAAGCTCTTCTTACTGTTCTCCATGCTTGTTCTTGTAAATAAAGCCTTGAGGTGCAGTATTATATCGAAATTCTCTGTAGTATTTGTTTAGTGTTTAAAGTGAATTTAACATAAGACAGTTAACAATTATTGATTTGATTAGTGTTTTCTTTACATTTATTAATAGATATTTTGATTTAAAATAAAATATGCTAAGTTGTTTCAGCTCAAACTTGGGTAAACTACAGACAATTTTACCCACATTTGAGTTGAAACTACCCAGCATTTTTTTAAGTTACGAATATTAAGACATATAAATATTAAAATTTGTATTATACATAATAATTTAGTATTCGTAGGGCTGGGTATTAATTTAGATATATTTCGATTCTGTTCGATTCAGTTTCATGAGCTTTTACTTTAAATAAATTAGATCCTTGATTTGGTTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33946
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 |
---|---|---|---|---|---|
ENSDART00000111855 | Nonsense | 1088 | 1253 | 24 | 28 |
Genomic Location (Zv9):
Chromosome 6 (position 44907535)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 6 | 45064270 |
GRCz11 | 6 | 44970064 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TATCCGACATGCTAAACTCTTCTAAGACTTTCCACATCATTGAAGGGCTC[G/T]AACCTGGAACCGAATACACAGTGCGTCTTATGACAAAAAGCTGGGTTGAT
Long Flanking Sequence:
ACACCAAAACCAAGTACCAAAAAAAAAAAAAACAAGTGGTTTGATGGCTAATGGCCAAGTATGAAGAATTGAAAAGAAAAGAAAAAAATTACTCTATATATGTTTATATTTATTGATATTTGAATACATTTTAGTGTATAAACTATCATTAGACTGAATGACATTTCATTTTTTGTCTTCGGGATATCAGATATCAATTAAAGAGGTCACATTTAAATGTAAGATAATAAATTATCTAAAGCTTGTTAAACAATTATTTAATCTATGTTTTGACATTTGGTACAGTACATGCATGTATGAATTATATGAATTACACATACAGTATGTAAAATCTCTTTTGTAAACTAAAACAAAATGTCTTTGACCCATATTTATTGTAGAGATTTTGTAGTCTACTAACACCCCTTCACCCACTATGTACATCCTGTGTAGGTGAAGGTAACTGGAAGATATCCGACATGCTAAACTCTTCTAAGACTTTCCACATCATTGAAGGGCTC[G/T]AACCTGGAACCGAATACACAGTGCGTCTTATGACAAAAAGCTGGGTTGATAATTCTAGTATTTTCGAAGACGTTATCAGGACCAGGGCCAAAGGTGAGGAGAACATATAGTCTCCGAGATGACAGACATACAAACTGAAATCTTCTTCTTGTCTCTTCTTTCTCATCAAGAGTGCAAACAGCATCCTGTGATCAAATTATCATGCGTGGTGTGCTTCGTGTCCATCCCAGAGCATGTGTTCGGTGGACTTTATAAAAGAATTATGCTTTATCAGCCTCTGCTGTCGATTAATTAGACATGCAGTCTGGCATTTTAATATTAATATGGGAACATTTCCATTTGAGAGTTTGCCTGGTATCTCTCATTTAGTGTCAGATGTTCTCGGTGGATGTCAACATTGAATCATTGAATGAAGTGTCAAATTAAGGGTTGATTTGTCTTTTACAGGTCTGGCCAGCATTCATGGAAGCATCTCAAACCAGGGATGGTTCATCGGACTC
Associated Phenotype:
Not determined