ZMP
CC2D2A
Ensembl ID:
Description:
coiled-coil and C2 domain containing 2A [Source:HGNC Symbol;Acc:29253]
Human Orthologue:
CC2D2A
Human Description:
coiled-coil and C2 domain containing 2A [Source:HGNC Symbol;Acc:29253]
Mouse Orthologue:
Cc2d2a
Mouse Description:
coiled-coil and C2 domain containing 2A Gene [Source:MGI Symbol;Acc:MGI:1924487]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa29863 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
e50 | Nonsense | Available for shipment | Available now |
sa16835 | Nonsense | Available for shipment | Available now |
sa10580 | Essential Splice Site | Available for shipment | Available now |
sa32422 | Nonsense | Available for shipment | Available now |
sa24244 | Essential Splice Site | Available for shipment | Available now |
sa13219 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa29863
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 |
---|---|---|---|---|---|
ENSDART00000126768 | Essential Splice Site | 30 | 1666 | 2 | 38 |
Genomic Location (Zv9):
Chromosome 23 (position 2209835)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2256898 |
GRCz11 | 23 | 2192576 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGAGGAGAGAACTGCAGGAGTCTTTAGGAAAAGTCAGGGATGATAAACAG[G/A]TAACAACAGAGTGCGGTATTTCAATGTTAAATATACTTACACTCACTGGC
Long Flanking Sequence:
TGGAATAATTCTGAAATCTGGAAAGTTTCTCTTTTGTCTTTTGCGCAGAATAATGTTTATTTCATGCATCGAGCGACTACAGTCTGCTGTTAATAAGAGATTTCGGCTAACGTCACTTTATAAAAGGCTGTTGCTAACTTTAACTTTACTGAACTAAGGCTTTATCCCTCCATTATGAGTGTTTTATTAACGAACCTTTTCATCCAGGAGCTGCTGTGAGGTCCACACTGAAGATCTGAGATGTAACGTATTGGGAAGATTTCTGTCGTCAGTAAATGCATAACGTTAGAGCACAATGTCATCGCCAGGGTAACTGTTAACATTAATCTGGTTTTATTTTTTACTATACGTTAACTTGAGTATAAGCTTAGAGCAAGTCTGTTTTACGGCTGTTTCTAAGTTTAAGTTGTCCTGTTGTCCTCAGTGATGTACGAGAGAAAATAAAGAAGAAGAGGAGAGAACTGCAGGAGTCTTTAGGAAAAGTCAGGGATGATAAACAG[G/A]TAACAACAGAGTGCGGTATTTCAATGTTAAATATACTTACACTCACTGGCCACTTCATTAGGTACACCTTACTAGTATCGGGTTGGCTTCAGAACTGCTTTAATCCTTCGTGGCGTAGATTCAACAAGGTACTGCAAATATTCCTCAGAGATTTTGCTCCATATTGACATGATAGCATCACACAGTTGCTGCAGATTTGTCGGCTGCACATCCATGATGCCAATCTCCTGTTCCACCACATCCCAAAGCTGCTCTATTGGATTGAGTTCTGGTGACTGTGGAGGCCATTTGAGTAAAGTGAACTCATTGTCATGTTCAAGACACCAGTCTGAGATGATTCATGCTTTATTACATGGTGTGTTATCCTGCTGGAAGTAGCCATCAGAAGATGGAGACACTGTGCTCATAAAGAGATGGACATGGTCAGCAACAATACTCAGGTCGGCTGTGGCGTTGAAATGATGCTCAATTTGTACTATTGGGCCCAAAGTGTGCCAAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
e50
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 |
---|---|---|---|---|---|
ENSDART00000126768 | Nonsense | 223 | 1666 | 9 | 38 |
Genomic Location (Zv9):
Chromosome 23 (position 2220817)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2267880 |
GRCz11 | 23 | 2203558 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTGTCTGCTGATCAGGTTGAGGCTGGTTTGCCGACCGCCGAAGAGGCCTA[C/A]AACTTCTTCACCTTCAACTTTGACCCGGAGCCTGAACAGCAGCGCCAGAA
Long Flanking Sequence:
CCACTTTAAATCCCAATATGCACTGGGATTCTATATGAATGAGCTGAAAACGCTCGCTGAAATGTGCTAGCGAGAATACGTCGTTTCTCTTCTGCGTCAGATAGAGGTTCGGCATTCAGCAGCTTCTGGAAGACAGTGATTTAAATGTATAATTAAAAAAAATATTTGAAATATCCCTGTTACAAAAACACAAAACCACGTTTATAATATGTGTGTTAAACACCTGGTGGCATATAGTTTGCTCCCAGATTGCTGAACTTTTGAAAGCTTAAAAAAAAAGTGCCACAACCAAACACTATTACACAGCATGAAGATCCAGAATAAATGGTAAAACTACTCCGACTGTGTTCATCTGACAGAAGACAATCATTTACACCCGGGGGAGTAAATAATGTGGGGATTTTCATTGTTTGTGTGACCTCATCCTGAGATCCTGACACTGAAGTGTGTCTGTCTGCTGATCAGGTTGAGGCTGGTTTGCCGACCGCCGAAGAGGCCTA[C/A]AACTTCTTCACCTTCAACTTTGACCCGGAGCCTGAACAGCAGCGCCAGAAGAAGAAAAGACGCTCCAGGAGAAGAGAGGCAGAGGAGGAAGAAGAGGGAGACTCAGAAGGAGAAGTAGAAGGGGAGGATGAAGAAGGGGAGGAAGTAGGAGAGCTGGAGAGACAGAATGAAGGAGAGGAAGAGTCTGAAGCCAGGGTGACTTATCGTGCTTATTTGTTTTTAAGCCCTACACTGCAAAAAACTGCTTTTCTTACTTAGATTTTTTTTGTCTTGTTTCTAATCCAAATATCTAAAAGTTCTTAAATCAAGAAGCATTTTCTACACAAGCAAAACATATTGTCTTGTTTTAAAAAAAAATATGCCAAAATGAAGTGAGTTTTTCCTTAAATCAAGCTAAATAATCTGCCAATAGGGTGAGCAAAATAATCTTATCACAAATCGAAAAACACGATTATTTTGCTCACCCCATTGGCAAATTGTTTTGCTTGAAAATTGATATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa16835
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 |
---|---|---|---|---|---|
ENSDART00000126768 | Nonsense | 440 | 1666 | 13 | 38 |
Genomic Location (Zv9):
Chromosome 23 (position 2230216)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2277279 |
GRCz11 | 23 | 2212957 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
CTGTTGTTCGCTCTGTCTCAGGCTCTGAAGTCGAAGCATGTGAACCTCTA[T/A]ATAGCTGGAATGGGGGATCMTCAGGCAGACTACCARCTGGATGTAGATGT
Long Flanking Sequence:
TTCCAGGTATAGTTGGTTAATTTAAAGTAAAGTATGGATTTCAAGCTTCATGTAGATATATTTCTCATGCCTGTGAAGCAAGTGTTCTCTGAGGGTGCTTTCACACTAGCACTTTTGGTCCGCACCCGGGTTCGTTTGACATCGTAGTACGGTACGTTTAGCTAGTGTAAACGTGTCTTTCGAACTCGGGTGCGCACCCGTGAACCGTACCCGAGTCCGCCTGAAAGAGGTGGTCTGGGGTAGGGTTCATGCAAACTCTTGTACGGCCAACTGTACAACAAACTATCGTTTGATGTACCGAGAGCTCCTCACAAAGCCCAGATTGCAATTTGTAGCCTTTGGGCAGCTTGTCTCCATGGACCAGGATCTCTAATATCCTTGTAGCAGGTATCTTGAGGGAATGTGGAAATCCATAAAGCAACATGCTGACTTGATGATGAGGTGTTTCCACTGTTGTTCGCTCTGTCTCAGGCTCTGAAGTCGAAGCATGTGAACCTCTA[T/A]ATAGCTGGAATGGGGGATCATCAGGCAGACTACCAACTGGATGTAGATGTGTCTGGCCTCATCTTCTCCCATCATCCTCTGTTCAGCCGTGAACATGTGCTGGGAGCCCGTCTCGCGCAACTGTATGACCAACACCTGACCAGACTACACAAGAACCTCACACAGCTCCTGACTGACAAGGTAATCCAGAAGAGCCACATCTAGACCAACATTCCAGTCCTCAAGCTCTCGCTTTTGAAACTCAGTCTGAATGTGTGTGTGTAGTTGAACAGCTTGAGGAACACGATTCATAACATGCTGGAGCTGCACAGAGGAGAGGCTCTGAGTCAGGTGTCCCAGCAGAGGATAGCGGAGTACAAACAGGAAGTGAGGTAAGACAATAACAGTCACCTCTACCTTCAGTATTATATGATAGACAGTCATTGAATCGTGGGTTTTGCAATGAGAGAACTGATCTTGTCATGTAATAACCATGGCTGATAACAATTAGCTTGTAAGGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa10580
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 |
---|---|---|---|---|---|
ENSDART00000126768 | Essential Splice Site | 501 | 1666 | 14 | 38 |
Genomic Location (Zv9):
Chromosome 23 (position 2230480)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2277543 |
GRCz11 | 23 | 2213221 |
KASP Assay ID:
2261-7255.1 (used for ordering genotyping assays)
KASP Sequence:
CCAGTCCTCAAGCTCTCGCTYTTGAAACTCAGTCTGAATGTGTGTGTGTA[G/A]TTGAACAGCTTGAGGAACACGATTCATARCATGCTGGAGCTGCACAGAGG
Long Flanking Sequence:
GGCCAACTGTACAACAAACTATCGTTTGATGTACCGAGAGCTCCTCACAAAGCCCAGATTGCAATTTGTAGCCTTTGGGCAGCTTGTCTCCATGGACCAGGATCTCTAATATCCTTGTAGCAGGTATCTTGAGGGAATGTGGAAATCCATAAAGCAACATGCTGACTTGATGATGAGGTGTTTCCACTGTTGTTCGCTCTGTCTCAGGCTCTGAAGTCGAAGCATGTGAACCTCTATATAGCTGGAATGGGGGATCATCAGGCAGACTACCAACTGGATGTAGATGTGTCTGGCCTCATCTTCTCCCATCATCCTCTGTTCAGCCGTGAACATGTGCTGGGAGCCCGTCTCGCGCAACTGTATGACCAACACCTGACCAGACTACACAAGAACCTCACACAGCTCCTGACTGACAAGGTAATCCAGAAGAGCCACATCTAGACCAACATTCCAGTCCTCAAGCTCTCGCTTTTGAAACTCAGTCTGAATGTGTGTGTGTA[G/A]TTGAACAGCTTGAGGAACACGATTCATAACATGCTGGAGCTGCACAGAGGAGAGGCTCTGAGTCAGGTGTCCCAGCAGAGGATAGCGGAGTACAAACAGGAAGTGAGGTAAGACAATAACAGTCACCTCTACCTTCAGTATTATATGATAGACAGTCATTGAATCGTGGGTTTTGCAATGAGAGAACTGATCTTGTCATGTAATAACCATGGCTGATAACAATTAGCTTGTAAGGACATTTTTAAGAGATTTAAAAGAAATTATAATAAAGTTTATTAAATGTTAGTATCAGTATGTTAGTCTTAAGGATATCCATAAGCTATTGTGCACCAAAACCGTGACAAAATTCACATTTAGGAGGGAAAAAAACGTGCAGTTTGTCACGTATCCATGGCTGTCTGGGATACTAAATTCTGATTGGTCAGTTTCAACATTCCAAGGTATGGTATTCCCGGATAACAACCGCTAAACTGGGAACTTCGAATCACCTTGATCATCAG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa32422
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126768 | Nonsense | 628 | 1666 | 16 | 38 |
Genomic Location (Zv9):
Chromosome 23 (position 2233633)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2280696 |
GRCz11 | 23 | 2216374 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAGGAATATCAGAGGAAGATGAATGAATACAGGAGACTGCATGAGGAATG[G/A]AAATCCTGGAAAAGAAAACAGGTACGGCTATGCAGACGAAGCAGTGGGGT
Long Flanking Sequence:
TTTTCCAGTTGTCTTTTGTTTTTAACAGAAGAAAGAAACACTTAAAGGTTTGATCCGAGTAATGGGTGAGTAAATGATGACCAAATACATTTTTTGTGTGTGAACTCTCCCTTTAATTCAGCCTGTCATCTCCTCCTGTATTGTCAGACACACTCGACAGTTGCGTGATGTGGAGCAGGAGAAGGATAGAGCTCTCCTCAAAAACATCATCCGACTGTGGAAGGAGCTGAAAGCACTGAGAGACTTCCAGAGATTCACCAACACACCTTACAAACTCTTCATCAGGAGGTATGTCTTCTTGCGTGTGTGTTTGAATGATTGATTGTGTGCTTTGTTTTACGAGACTCTCGGCTGTTCCTACACAGGGAAAAGGTGGAGAGACTGCAGGACGAGCAGGAGTTTGAGAGCGACATCATGGCGGAGGTGTCAGAGCTGCAGGCGGAGACGGAGGAGGAATATCAGAGGAAGATGAATGAATACAGGAGACTGCATGAGGAATG[G/A]AAATCCTGGAAAAGAAAACAGGTACGGCTATGCAGACGAAGCAGTGGGGTATATGCACAGCTAGTGTTTTTAGCCAACGATAAACGTCCAGTGAAAGGTTTACATGACTATTTTCAATTTTATAAGGTGCCTTTTACAACATCGATGTTGTAATGTCATTAAAGAAGATGCCCACTAATACCCACGCACACTGGATTAATTAGGGCTGAGGCTATTAACTCCTGGCCGTTCACATATTGCGTCTTTTGCTCGCACAAATTCATTATTTTCAATGGAGGCGCACGACTTGCACATGCATATTAGGATCGAAAGCGCACTATCCACTCACGCTTTCCAGGCGCACCTAGTTGAAAGATTGTTGAAAGCGCACTACAAGTCATGTGACCAGAACTGACTTCACAGAAAAAAAAATACAAAGAGAAAGCACCAAGCACCAAATTTTCTAATATAGTTGATCTAAAGTGCCTTTCAGACAGAGGTTCAGCAGCCTTTCACTACAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa24244
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 > C
Consequence:
Essential Splice Site
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000126768 | Essential Splice Site | 827 | 1666 | 19 | 38 |
Genomic Location (Zv9):
Chromosome 23 (position 2238198)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2285261 |
GRCz11 | 23 | 2220939 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTCAGCAGCAACCAGAGAGTCACATTCAATCACGAGGGGGTCGGCAGTGG[T/C]GAGAGCTCTTTTTAAATATATACAAATAAAATGTTTTTCAGTGCACAGTC
Long Flanking Sequence:
CTATATATGTTTTCTATTGTCTACAGAACTTGCCTTATTACCCTAGTCAAGCCTTTAAATGTCACTTTAAGCTGTATAGAAGTGTCTTGAAAATATCCAGTCAAATATTATGTGCTGTCATCATGGCAAAAATAAAAGAAATCTATCATTAGAAATGAGTCATTAAAACTATTACGATTAGAAATGTGTTGAAAAAAAATTAATCTTTCTGTTTTTTTGACATTTCTATTTTTGTTCAGTTCAGAAACAGTACTTAAGACTTAACATTTCATTCAGCATTTAGCATTACAGTACTATTGGTGTTGGTCAGCATGTGTGTGAGCTGCTCTGGATGTTTTCCCGCAGGTGTTTGAGAGCGTGGGCTCATCCTCCACCCAGCTGACTGAAGTGTGTGTGCCGGTTCCCGAATCTTCTGTCCTGACCGGCAGCGCACCGTCAGAAGAGATGGAGTTCAGCAGCAACCAGAGAGTCACATTCAATCACGAGGGGGTCGGCAGTGG[T/C]GAGAGCTCTTTTTAAATATATACAAATAAAATGTTTTTCAGTGCACAGTCGTGTCTCCTGAGGGTCATTTTCAAAGACAGGAAGTGTAATGATGCTTTTGGTTAGGGCTGTGCAAATCAACGAAATTCGGTTTTGGCCTCTAACTACTATAAAAAAACTGGATATGTGTCCAATCCCACATCCCCCTTCCAGCGTTCTGTATTTCCTATATAAAGCTGTTTTTTTTTATTGTTATTATTATCTTTTTTCCTGAATAGTATTACACTTACATCAGGTACTTATTAGAGATTATACATCTAAACACACTCATGGATATAAGCACACATACATCCACTTTCTTTTTCAGCCATATACAGTGCTCAGCATAAACAAGTACACCCCCTTTTGAAAATAAACATTTGTATTCATTTCTCAGTGAATATAGCCAATAAACACTCATCCGGCCACTTTATTAGGTACACCTTACTAGTACCCCTTTTGCCTTCATAACTGCTTTAATC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa13219
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 |
---|---|---|---|---|---|
ENSDART00000126768 | Nonsense | 1368 | 1666 | 31 | 38 |
Genomic Location (Zv9):
Chromosome 23 (position 2263934)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 23 | 2310997 |
GRCz11 | 23 | 2246675 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCCCTCTRAAYCCACCACAGGAGCTGCTGGAYGCTTCYCCCAACGGCACA[C/T]AGGACAGCACGGTTCGCCCTCCACTGACAGACACTYTTMTGTCWCTCAGT
Long Flanking Sequence:
AGCTGCGTAAAACATATGCTGGATAAGTTGGCGGTTCATTCCCCTGTGGCGACCCCGGCTTAATAAAGGGACTAAGCAGAAAAGAAAATGCATGAATGAATACTGTGAAAAATTCCTCGTTCTGTTAAATATCATCTGGGAAATATCTAAAACAGAAATTCAGAGGAGGGCGAATAAATTTGGCTTCAACTGTTTATGCTATATATAATCTTACTGACCCCACACTTTTGATCCTATATGTGTGTGTGTGCTTTATGTGTGTGTATTGTGCACGCTCTCTGTGTGTTAAATGGTGTCCATCCTCTCAGTTTGATTCTCAGGAAGTTGAGCGTGTGTTATTGGCCAGTGAAGTGTTTGAGAAGGAGGCGAGTCGGCGTTTCTCAGACCGGCCCTGCATCACCACCGTCATCGACATCAACGGCAAAACGGTGTTCGTCACGCGCTTCATTCGCCCTCTAAACCCACCACAGGAGCTGCTGGATGCTTCCCCCAACGGCACA[C/T]AGGACAGCACGGTTCGCCCTCCACTGACAGACACTTTTCTGTCACTCAGTGTTCGTTGTCTCACACACTCTTCTGTCTCTCAGTATTTGTGTCTCACACACTCTTCTGTCACTCAGTGTTTGTGTCTCACACTCTTTTGTTTGTCTCTCTCTGCAGGAGTTAGTGGCGCGGTATGTCTCCCTCATCCCTTCTCTTCCAGACAGTGTGTCTTTTGCTGGAGTTTGTGACCTGTGGAGCACGTGTGACGTGAGGACTTTTACTCTGTTTGTTTCTGCTAAGGGCTGCACTATATATTGTTTCATTATCGACATCACAGTGTGCACGTCCAAATTCAAATCAAAATTCATTTAATTCAAATTTTATTTGTCACACACACACACACACACGGTCATAAGGTGCGTCCCAAATCACACACTCATGCACTATTATTATAGTGTCAGTAGAGCGTTCACACTGAAAACTCAAAAAATACTAAGTGCACTTTAAATAGCTGGATGATG
Associated Phenotype:
Not determined