ZMP
LOC100333692
Ensembl ID:
Human Orthologue:
COL2A1
Human Description:
collagen, type II, alpha 1 [Source:HGNC Symbol;Acc:2200]
Mouse Orthologue:
Col2a1
Mouse Description:
collagen, type II, alpha 1 Gene [Source:MGI Symbol;Acc:MGI:88452]
Alleles
There are 6 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa9187 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa34995 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa13949 | Essential Splice Site | Available for shipment | Available now |
sa9455 | Nonsense | Available for shipment | Available now |
sa16061 | Essential Splice Site | Available for shipment | Available now |
sa31809 | Essential Splice Site | Available for shipment | Available now |
Mutation Details
Allele Name:
sa9187
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 |
---|---|---|---|---|---|
ENSDART00000047844 | Essential Splice Site | 158 | 1257 | 11 | 47 |
Genomic Location (Zv9):
Chromosome 11 (position 114051)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 46546 |
GRCz11 | 11 | 46546 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CCGTTGGTACAGCAGGATCTCCCGGGTTCCCAGGATCCCCCGGTGCAAAG[G/A]TGTGACCTCTCTTGATTCCTCTATCAATGATCCCTCATGTCTCTGCTGCA
Long Flanking Sequence:
AACTCTTCTGCTGTGCAGGATACTCATGTTCACTGCAGACACACCACTGGGAGAAAATGAGCAGAATAGTCTGTGTGTAGTCTTGTAGAGAGTGTGGATCAGCGGCGCAGTGATGTCCAGAAGTGTAGTAATGCTGTGTAGAGGATGGGGTTAGGTTATAGTCTTTATATGCTGTGTGATATGCACACGTGTGTGCACATGATGACGACGATGATGATGACGCACAGCACTGAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTATCAGGGTGCTCGTGGTAATGACGGTCTGCCTGGCGGTGCTGGTCCACCGGTGGGTTTGAGGATCCTTCATTTCTTCAGTCGCTGTGAATCGTGTCTTTATTTGCAGATCAGCAGCTCATCGCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGGGTCCCGTTGGTACAGCAGGATCTCCCGGGTTCCCAGGATCCCCCGGTGCAAAG[G/A]TGTGACCTCTCTTGATTCCTCTATCAATGATCCCTCATGTCTCTGCTGCATCACAGTCACTATTCACACCTGTACAGCAGAACACACACCTGTACACCTGACACTGACTCAATAGAACACACACCTGTACCACAGAACACACACCTGTACCACAGAACACACCCCTGTACCACAGAACACACACCTGTACCACAGAACACACACCTGTACCACAGAACACACACCTGTACACCTGTGTTGCTCCAGCAGATGAACACTCGTAGCTCCACACACACACACACTGAGGTGTCTCAGATGTTGCTGATGGAGGTTTACTGACGGTGTGTGTCTCTCAGGGTGAAGCGGGACCAACCGGAGCCCGAGGGCCTGAGGGAGCACAGGGGCCCCGTGGAGAGTCTGGTGTTCCTGGAGCCTCGGGACCCTCTGGAGTCTCTGTGAGTATTAAACAGCAGGGCAGGGGACGCGGGTACGGATGGAGATCAGGGTTAGCTGGAGGAGAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa34995
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047844 | Essential Splice Site | 158 | 1257 | 11 | 47 |
Genomic Location (Zv9):
Chromosome 11 (position 114050)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 46545 |
GRCz11 | 11 | 46545 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CGTTGGTACAGCAGGATCTCCCGGGTTCCCAGGATCCCCCGGTGCAAAGG[T/C]GTGACCTCTCTTGATTCCTCTATCAATGATCCCTCATGTCTCTGCTGCAT
Long Flanking Sequence:
ACTCTTCTGCTGTGCAGGATACTCATGTTCACTGCAGACACACCACTGGGAGAAAATGAGCAGAATAGTCTGTGTGTAGTCTTGTAGAGAGTGTGGATCAGCGGCGCAGTGATGTCCAGAAGTGTAGTAATGCTGTGTAGAGGATGGGGTTAGGTTATAGTCTTTATATGCTGTGTGATATGCACACGTGTGTGCACATGATGACGACGATGATGATGACGCACAGCACTGAGGTGTGTGTGTGTGTGTGTGTGTGTGTGTTTTATCAGGGTGCTCGTGGTAATGACGGTCTGCCTGGCGGTGCTGGTCCACCGGTGGGTTTGAGGATCCTTCATTTCTTCAGTCGCTGTGAATCGTGTCTTTATTTGCAGATCAGCAGCTCATCGCATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTTCAGGGTCCCGTTGGTACAGCAGGATCTCCCGGGTTCCCAGGATCCCCCGGTGCAAAGG[T/C]GTGACCTCTCTTGATTCCTCTATCAATGATCCCTCATGTCTCTGCTGCATCACAGTCACTATTCACACCTGTACAGCAGAACACACACCTGTACACCTGACACTGACTCAATAGAACACACACCTGTACCACAGAACACACACCTGTACCACAGAACACACCCCTGTACCACAGAACACACACCTGTACCACAGAACACACACCTGTACCACAGAACACACACCTGTACACCTGTGTTGCTCCAGCAGATGAACACTCGTAGCTCCACACACACACACACTGAGGTGTCTCAGATGTTGCTGATGGAGGTTTACTGACGGTGTGTGTCTCTCAGGGTGAAGCGGGACCAACCGGAGCCCGAGGGCCTGAGGGAGCACAGGGGCCCCGTGGAGAGTCTGGTGTTCCTGGAGCCTCGGGACCCTCTGGAGTCTCTGTGAGTATTAAACAGCAGGGCAGGGGACGCGGGTACGGATGGAGATCAGGGTTAGCTGGAGGAGAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13949
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047844 | Essential Splice Site | 411 | 1257 | 21 | 47 |
Genomic Location (Zv9):
Chromosome 11 (position 109945)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 42440 |
GRCz11 | 11 | 42440 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GGCTKGAAAGGCTGGAGAGAAGGGACTCGCTGGAGCTCCGGGTCTGCGTG[T/A]AAGTGTTGATTTGCAGCTTCATAAACTCMGAGAAACGAGCGGACACACAA
Long Flanking Sequence:
TAGAGCAATGCAGTAATGCAACATTAGAAGGAGCGCTTAGGCTGTTGAAGGACGACTCTGTTTCTGCAACATTATTAATCTATATAGGTAATATTCTAACATCAATGCAATGCTGCTCCGTCACTTCCTGTTTCCTGTCACATGACTTCAATCTTACAGAAGAACACACACATTAAATACATGTTCAGATGTGTTGTGTCTTCATTTACCGTGTGTTTTGTTGAGGGTGTAGGGCGCTCCGGGTGAAGACGGTCGTCCGGGACCCCCGGGGCCTCAGGGTGTTCGCGGTCAGCCAGGAGTCATGGGATTCCCGGGACCCAAGGGTGGAAATGTAAAAACCAACACTCTTCTTAGTCCATGTCTGTCTGTCTGTGCGTGTTATTATTGCTCTGTTGTGTCAATATTCAATCATAACCCTTTTATGTGCATCTGTGTCTCGCTGCAGGGTGAGGCTGGAAAGGCTGGAGAGAAGGGACTCGCTGGAGCTCCGGGTCTGCGTG[T/A]AAGTGTTGATTTGCAGCTTCATAAACTCAGAGAAACGAGCGGACACACAACAGACGGATCTCCAGAGTCTGAAACACTGCTGAGAGCCTCTTCTAGAGCTAAAACTCTGACCTGGTCTAGGAAAACTCGACATTTGGATGTGCTTCGTGGTTTTCGTCTCTATTTCAGTCAGCTTCAGCAGTTTCTAAGCAGATATTTTAGTAAATGATCATTTACAAAGTGAAAATAGTGAGNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNGATCATAGTAGAGCATCTAAATATCAGAGTCTGACATAAACCACACGCCTGGATCAGGTTCACAGCTGCTCTTGCTGAAATGACCACCACCATAGTGAAGAACACATTAAACAGTGTGCGCACATGCACTGATAATGCTGATCATCGCTCTCCAGGAGTGTTTGTGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa9455
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 |
---|---|---|---|---|---|
ENSDART00000047844 | Nonsense | 674 | 1257 | 34 | 47 |
Genomic Location (Zv9):
Chromosome 11 (position 106131)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 38626 |
GRCz11 | 11 | 38626 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CATTTTTAAAATGTTTGCAGGGTGCCACGGGTTTCCCCGGAGCCGCTRGA[A/T]GAGTTGGACCTCCTGGTCCTAATGTAAGAAAAGCAATAGAAAGCAAAACA
Long Flanking Sequence:
GCAAATGCTTTGATAGTCACACACATGAGAGTTTCCTGATATCTGCCTACAGTGAAGGCCTCAGAGCTGCTGTATAATGTGTCATTCAGAAACTCTGCTTTGCTCTGTATGTATTAGGGTGCAGATGGACAGCCGGGAGTGAAAGGAGAGCAGGGTGAAGGTGGACAGAAGGGTGATGCTGGAGCCCCGGGCCCTCAGGGGCCCTCTGGAGCTCCGGGCCCGCAGGTAACATCAGCGTAATTGTTCTGTTTCTGAACCGTGATGTGAAATGGTGATGTTTACCCTAAAGCAGTTCTGTAGTTCTTAATACTGGACTCCTCTTTTTCTTAAAGGGACCAACCGGTGTGTCTGGACCAAAAGGGGCTCGTGGTGCTCAAGGCCCTCCTGTAAGTACAAGATCAAGTAGACACAGGACATGCAGATAAATTAATGTGTTGATAAGTAAATGCTCATTTTTAAAATGTTTGCAGGGTGCCACGGGTTTCCCCGGAGCCGCTGGA[A/T]GAGTTGGACCTCCTGGTCCTAATGTAAGAAAAGCAATAGAAAGCAAAACACATCTATAGTGTGGAGTAAAACATCTGATGAGTATGAGCAACGTTCTGACAGACATTCATGAGGGCGATCAGAGAAACCTCTGTGTGTTCTTCACTGGGTCCGCCATCATGTTTCTAATTTTCTTATTCTCAGGGTAACCCTGGTCCAGCCGGTCCTGCTGGTCCTCCTGGTAAAGATGGGCCAAAGGGTGTCAGAGGAGACGGTGGTCCTCCTGGAAGACCTGGAGACGCTGGTTTACGGGGTTCGGCTGGTCCTGCAGGAGAGAAGGGAGATCCTGGTGAAGACGGTCCTCACGTACGTACTGCAGGATCTCAGTAAACATGATTCTGACTGTAAAAGCAGATAATAAAGACGCTAACAGTGAAAGCAATGGATGAAAACCTGCTAATTAAATGAAAAGTGCACAGATATGAGCAGCTGAGTGTAAACTACTGAGTGCCCTTGAGCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16061
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 |
---|---|---|---|---|---|
ENSDART00000047844 | Essential Splice Site | 861 | 1257 | 39 | 47 |
Genomic Location (Zv9):
Chromosome 11 (position 104207)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36702 |
GRCz11 | 11 | 36702 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTCCTGGTCCAGTMGGACCCACTGGTAAWCAGGGAGACAGAGGRGAGGCR[G/A]TAAGTACAGATTTTTACAGCTCTTCATGACGTGTAGAATAAAATGTATGT
Long Flanking Sequence:
GAGATAGACTTAAAGCTGAATAAATATGTGTCCGATTATTATTCTAATAATATCAGGTGTGTAAAATAATGAATGACTGAACCGTAAGTGTTCACTTCCTGTGTTCATCAATGCTCCTGGAGAACTCTTACACTGCCAGAAGCTTAAACACTAGAGTAGAACCAAATAGATGAAGACATTCACACACACTGCACATACATGAGCTGGATTAATGCAAGATTCATGTCGCGTAAATCGTTTGCAGGGCAATCCTGGATCTGATGGTCCTCCTGGTCGAGATGGTTCTGCTGGAATAAAGGTAGGGAGGATATGTAGACCTGGTTTCACTAACTGTAATGACCATGGTGTAGTCTGAGTTCTGCTTGCTGACGATCGGTCTGTGTTCTGTTCAGGGAGACCGAGGTGACACGGGTCCAGCTGGAGCTCCTGGTGCTCCAGGGGGTCCTGGTGCTCCTGGTCCAGTCGGACCCACTGGTAAACAGGGAGACAGAGGAGAGGCG[G/A]TAAGTACAGATTTTTACAGCTCTTCATGACGTGTAGAATAAAATGTATGTATTAGTGATGTTATGGTAGAATTATCAAGAATGATCACTGTTCTCATTCAAACAACAACTAAAAACCCACCACCAACCAAACACTTGAGCACAATGGAACAATGTCTCAGAAAATGGCATGACAGAAAAGAGGACTTATTCTTTCCAAAAGATTATTCTAATCGTAATGAGAAGTCTAATGATGACATTTAATGAGGAAGGCACATGACACACTCATTCCTTTCAACTGCAGGGTCCCCATGGGCCTTCTGGACCTCCAGGGCCTGCTGGAGCTCGGGGAATGCCTGTGAGTACCTATCATGTCAGAAATTAATAGCATTCTGGCGTAATTACAGCATTTTTCTTCATTATCAAGTCTGTTTGTTAAAACTCAAATTCTGCTTTTAGCAGTCCATTTGTCAATATACACTCCTAATTCAGTGTAGACCTTCAGAATTAATGTGTAAGCCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31809
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:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000047844 | Essential Splice Site | 915 | 1257 | 41 | 47 |
Genomic Location (Zv9):
Chromosome 11 (position 103582)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 11 | 36077 |
GRCz11 | 11 | 36077 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAAAGGACACAGAGGCTTCACTGGTCTCCAAGGTCTGCCTGGGTCTCCT[G/T]TAAGTGCCTACATCGCTCATATTTGCACTCATTTTGTGTAAATGACGTAC
Long Flanking Sequence:
AACCAAACACTTGAGCACAATGGAACAATGTCTCAGAAAATGGCATGACAGAAAAGAGGACTTATTCTTTCCAAAAGATTATTCTAATCGTAATGAGAAGTCTAATGATGACATTTAATGAGGAAGGCACATGACACACTCATTCCTTTCAACTGCAGGGTCCCCATGGGCCTTCTGGACCTCCAGGGCCTGCTGGAGCTCGGGGAATGCCTGTGAGTACCTATCATGTCAGAAATTAATAGCATTCTGGCGTAATTACAGCATTTTTCTTCATTATCAAGTCTGTTTGTTAAAACTCAAATTCTGCTTTTAGCAGTCCATTTGTCAATATACACTCCTAATTCAGTGTAGACCTTCAGAATTAATGTGTAAGCCATGTTCATTAATCACAGGGACCACAAGGACCGCGTGGAGATAAAGGAGAAGCTGGGGATTCGGGAGATAGAGGACAGAAAGGACACAGAGGCTTCACTGGTCTCCAAGGTCTGCCTGGGTCTCCT[G/T]TAAGTGCCTACATCGCTCATATTTGCACTCATTTTGTGTAAATGACGTACAAATGTAAGATGTAATGTGATTACTCAAAGGCATGTTTACACTCCAAACACAGGGTCAACCTGGTGATCAAGGTGCTTCTGGACCCTCTGGACCTGGTGGAGCAAGAGTATGTATATTAATGATAAGTCTGCATGAGGACTGATTTTTGCAGGGTGTGCTCTGCAGTGTTAAGGTCCAGTGTTAACCTTTCAACAACTTTTAGGGACCCCCAGGCCCTGTCGGTCCAGCTGGAAAAGATGGAGCAAACGGTTTACCTGGACCCATTGGACCCCCGGGACCCCGTGGTCGTTCTGGGGAGACTGGTCCATCAGTAAGTACCAAAAAAAAAACACCTTTCACACCTCTACTTTGGAAAAGTCAGGAAAGTGGGCGTGTCCAGCTCTGTTTAGGAGGGAGTGTCAGAGGAGCAAAAGAGGGAGGGTCTGTAAAAATTTTGCATAAAAATGGGA
Associated Phenotype:
Not determined