ZMP
LOC556406
Ensembl ID:
Human Orthologue:
CLIP2
Human Description:
CAP-GLY domain containing linker protein 2 [Source:HGNC Symbol;Acc:2586]
Mouse Orthologue:
Clip2
Mouse Description:
CAP-GLY domain containing linker protein 2 Gene [Source:MGI Symbol;Acc:MGI:1313136]
Alleles
There are 9 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa15415 | Nonsense | Available for shipment | Available now |
| sa38514 | Splice Site, Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33734 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa20554 | Essential Splice Site | Available for shipment | Available now |
| sa45229 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa33735 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa15415
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 |
|---|---|---|---|---|---|
| ENSDART00000082983 | Nonsense | 115 | 992 | 1 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 61118486)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58750613 |
| GRCz11 | 5 | 59420322 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
GCGATGAGCAGCAGAACGCRCAGCTCCAAGGTGGAGCAGGAGCYTCCGGM[C/T]AGCGCGTGGTCATGCCGCTCAGAGAAGGCATKCTWAACAGCTCYGTCAAA
Long Flanking Sequence:
CATAGACCTCCTCTGTTAGTCTGTTATAGTATAAACTATCTTTATTTGCTTTAACAAAGTCCGAGGCGGTTCTTTGGCAACCTGGCATGGATTATATTGATAAAGCTTTGCTAAATCTGTCCACAGGTTGCCCCTACAAGCAGACGACTCCCACCCCAAGCAGCAATGCCTCAGACAAGTCCAGCTCCAAAGCCTCTGAGGTTGGCGACGAGGTGGCCGGCGACTTTGTAGTCGGTGAACGTGTCTGGGTGAACGGAGTCAAGCCGGGAGTCATTGCCTACCTTGGAGAGACCCAGTTTTCCCCGGGACAGTGGGCGGGAGTGGTGCTGAATGATCTGGTTGGAAAAAACGATGGCTCTGTCAATGGCGTGCGCTACTTCGAGTGCCAGGCTTTGCAGGGCATCTTCACGAGGCCTTCTAAGCTCACACGCCAACCCATTGGAGACGGGAGCGATGAGCAGCAGAACGCACAGCTCCAAGGTGGAGCAGGAGCTTCCGGA[C/T]AGCGCGTGGTCATGCCGCTCAGAGAAGGCATGCTTAACAGCTCTGTCAAAACCGGCAACGAGTCCGGATCCAACATGTCTGACAGTGGATCGGTGAAGAAAGGTGGAGAGAAGGACCTAAAAGTTGGAGATCGTGTGCTGGTGAGTGTTAACGTTTTCCCACAGTCAGTACGTTTACTTTAAACGTAATTTTAGACAATACTCTGATTGAGAGTCTACTATGTAAACAGCGATTTTTGATGACCTTAATCCAACTAAAGTCATAATCAAACTAAGCAGAAATCAAATTAAGATGTGGAGTATTCTAAATCTTTATTCACAGAGCTTACAGTGTACAATTATTTTATTACTTTTATAAGTTTAATATATATTTTTAACAATACAAATAAAATAAAGTACATATTAACAATAACAAGAAAAACAGAAAGATATTGCACATAGGTATGTCACATTTATACTGAATATTGTACTCAGCAAAAATACATATGTCAGTGGTTCTCA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38514
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:
Splice Site, Nonsense
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000082983 | Splice Site, Nonsense | 341 | 992 | 5 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 61148176)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58780303 |
| GRCz11 | 5 | 59450012 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGTTTGAATTTCTGAAGCACAAATGACCTTTTATTTGATCTCATTTAGTA[T/A]GCAACAGAGACGGAGAGCAACCTACAGCAAGTCCGAGCAATGCTGGCCAG
Long Flanking Sequence:
GCGCCGTGCTGAAACTAGCAAAAAACACTTGCTTCAAACCTGGTGCCACATTGTGCTGGGTGTCCAATAGGGCCCCAATTCTTTATCGCATCAATTTGTATTTTCTTTGACCTAAGATTTATGAAGTACATTTTTTTGACTTTATTACTAATAGTTGACAGAGACGTCATCGAGGTATGCGCGGAAGATCTCGGGAACCACGGCTTTGCAGGAAGCCCTGAAGGAGAAACAGCAGCACATCGAGCAGCTCCTGGCCGAGAGAGACCTGGAGCGGGCTGAAGTCGCGAAGGCCACCAGCCATATCTGCGAGGTGGAAAAGGAGCTGGCGGCGCTGAAGGCGCGACATCTGCAGGTGTGACTCGAACACACAAACACAGTACTGTTCATATATGTCCATTTACTATATTAACTGACAAATGCAAACCTAAACATGCCGTTTAGCATTGCATTTGTTTGAATTTCTGAAGCACAAATGACCTTTTATTTGATCTCATTTAGTA[T/A]GCAACAGAGACGGAGAGCAACCTACAGCAAGTCCGAGCAATGCTGGCCAGCACACAGAAAGACAAAATGGAGCTGGCCAATCAGCTTGAAGAAGAAAAAAGGTAAATGTTTTCCTGTAACTACATATGTTGCACAGTTTTATGCTGACATTTCTTTGCCATGGTGTTTTTAATTAAACTTTTATCATGTTAATAAGTTACTTATTGAAGAGCATGACATTGGAATAAGCTAGGGCATGTCTGTCAAAGGTTTTGATTCACTTCAAATGTTGACTAAATAGATATATAGATACTTTCTGAAAACAATTATAAAACAAAGAGCATATAAAAATAAAACATTTCTTATTAATAATACAATTTTGCCATCAGCAATTTAGGCAGCTTATATGGGCCTGGTCTATATAATACACCTGTACAAATAGTTGAAAAATATTGACTATAATTATTATAAAATAAATTAATAACTTTCAATATTTTAATTAAATGTCATTTATTATAAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33734
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 |
|---|---|---|---|---|---|
| ENSDART00000082983 | Nonsense | 545 | 992 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 61160919)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58793046 |
| GRCz11 | 5 | 59462755 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GTCAGGGTCAAGAGATTTCTGACCTGAAGCAAAGACTCCAGCAGGCCACT[C/T]GAGAAAACATGGAGATGATGGACAGCTGGAAAGCCAAACTGGACGCTCTT
Long Flanking Sequence:
AACTCAAAGGAAGGGGAAAAACGTCCTGCGAATAAACTAGAGAGAGTATCATTGTACCATTGCCCTAATTCTTTGAGAGTTGCCCCAGAGCAAAAAGGAGGATTTGACGTATAAATGATGGGAAATGCAGGATTCATGACCCTTTCTTTGTCCTCTAGCAAACTACCGTGGAGGAGAAGACTCGTGTTATGCAGCTTGAAGAGGAACTGGCCTTGCGCAAGGCTGAGGTCGAGGAGCTCCAGGTTCGATTTCAGAGAGGCTCCTCTGGTTCGGCCACAGATGCTGAAGATGGAGAACCAGGCATAACCTCCGAAACTCTGGTCTTGCGGGAACAGCTTCTCTCGGTGGGCCGTGAACGCCGCGAAGAGAGCAGCCAGCTGCGCGAGAGGTACGAGGCATCTCTGAGCACCAGCCAGAAAGAAATCGAACGCCTTAAAGCCATTACAGAACGTCAGGGTCAAGAGATTTCTGACCTGAAGCAAAGACTCCAGCAGGCCACT[C/T]GAGAAAACATGGAGATGATGGACAGCTGGAAAGCCAAACTGGACGCTCTTGTTGGAGACCATCAACGTGCTCTTGAAGAACTGAAAGCCTCGTTAACAACAGATTGTGGGTCTGGTGAGATCAATGGAGGAGAAGGTGAAGGAAGCTTGCCTGAGATGAGAGCAGCTCTTGAGGGCTTAAAGATGGAGCACCAACTGGAGTTGGAGAACTTGAAGGCCAAACATGAGATTGATGCTGCAGTGATGGCCAAAGAGCGTGAAGACTTACGCAGCCGGCTTCAGGAGCTACGGGACCAGCTTGAGGACAGCGAGGAGAACTGGAAGATCCAGGTGGAGACCAAGAGCAACCAGCACACGCTGGAAATCAAAGAGGTTTCAGAGAAGCTTCAAAAGGCTGAGCTGAGGATCGTAGATCTGGATAAGTCTCAGGAAGAGCGTGAAAAGGTCAACCAACTTCTTAAAGAGCAGCTAATGCTGGCTGAGAAGAAGATGGTAGATTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa20554
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 |
|---|---|---|---|---|---|
| ENSDART00000082983 | Essential Splice Site | 752 | 992 | 8 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 61161544)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58793671 |
| GRCz11 | 5 | 59463380 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAACCGACTGCAGGCTGTAGAGGCAGATCACACCACTCAGGATGTTAATG[T/C]TAGTGACCTTTGATTCAGTAAATGATTCAATTATTTACAAAAGTTTAGGA
Long Flanking Sequence:
TGGAGGAGAAGGTGAAGGAAGCTTGCCTGAGATGAGAGCAGCTCTTGAGGGCTTAAAGATGGAGCACCAACTGGAGTTGGAGAACTTGAAGGCCAAACATGAGATTGATGCTGCAGTGATGGCCAAAGAGCGTGAAGACTTACGCAGCCGGCTTCAGGAGCTACGGGACCAGCTTGAGGACAGCGAGGAGAACTGGAAGATCCAGGTGGAGACCAAGAGCAACCAGCACACGCTGGAAATCAAAGAGGTTTCAGAGAAGCTTCAAAAGGCTGAGCTGAGGATCGTAGATCTGGATAAGTCTCAGGAAGAGCGTGAAAAGGTCAACCAACTTCTTAAAGAGCAGCTAATGCTGGCTGAGAAGAAGATGGTAGATTATGAGGCCCTGCAGAAGGCTGAAGCTCAGAGCCGAGCTGAAATCCTCTCTCTGCAGGAGAAGCTCAGAGTCACAGAGAACCGACTGCAGGCTGTAGAGGCAGATCACACCACTCAGGATGTTAATG[T/C]TAGTGACCTTTGATTCAGTAAATGATTCAATTATTTACAAAAGTTTAGGAGGCTACCCAGTAGGCACAGGATGTCAACATGGCATCAGATTGACGTTATACCACTATGTTGTGGGACGTTGCATTTGGTTTCGAAATCAGGTTGACATCAATGTCCCACTCGGACAGATGTTGCATTTTAATTACTTTCCAATGCAACCTAAAAACAAATTATTAGCAACTAATGATGTTACAGCTTGGCGTTGTGTGGATGTAATCAATATGATGTCTATCAGACGTTAGATTTTGTTTGCCATACTTGACGAATAAATGTCAGTATTTGACAAAAATATGACGTTGGTTTAAGATGTTGGCTCAATGTAAGGTTTTTGGTCACTTTCCAACACAACCTAAAATCACCAAAATATCGACGTCATTTTATGTCATTTTTGGACATCAAAATAACGTCCTTAGACGATGGTGACATAAATATAACCTAATATTAATGTATTAACGTTTTAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa45229
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 |
|---|---|---|---|---|---|
| ENSDART00000082983 | Nonsense | 839 | 992 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 61165382)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58797509 |
| GRCz11 | 5 | 59467218 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGAGGCAGAGCTGGAGACCATGACTAAGAAATCCCATGATGCATCAGGC[C/T]AGCTAGTCAATATTAGCCAGGAGCTTCTGAAAAAAGAAAGGTAAAGAGGC
Long Flanking Sequence:
TAAATCAGAAATTATACAATACTATTTAAAAAAGTATACAATTCAAACAAAACACAGGCAGTATGGTTCTCTCTCTTAAACATAAACATGTTTCCCTATTTCAGTATATGAAATATGTTCTTTAACCATGAATGTGTCTTATTAGAAACTCTGGAGAAACTCACGAAAAGGGAAAAGGAAGTGTCCACTCTAACAACCCAAGTAGATGCCCTAAAGACCCAAATAACTGGTAATTTTTCACTTCTCTGCCAATCACACGACCCTTTTTGTAAAACAACAAACATAGGTACTGTATACACTGTGTATATGTAATATAACATGTGATGATGCTAGTAATACTTTGTGATATACGTAACAATAAACTTCACTGCATCTTGTCTGCAGCCTTGGAGGAAAAGGTTCGTCTTGGAGAAAAAACGGCAGATGGACTCATTAAGGAGAAGACCCGTTTGGAGGCAGAGCTGGAGACCATGACTAAGAAATCCCATGATGCATCAGGC[C/T]AGCTAGTCAATATTAGCCAGGAGCTTCTGAAAAAAGAAAGGTAAAGAGGCGAGCATTGTGATTTATGACTGGTGTAATTGACTGGTTTTAATGGTGGGAATGACATCATGTGCTTTTGGAAATTGACCACATATTGGTTCAGTCAATGAAGTACTTTTAAAGATACTTTGATCTTGCACTTGATTCTCTCAGCTTTATTTTATAGAAAACCTTTTTCTGGATTATATTGATTTCCAAAACACTAGGATGAATCATTTCCCAATCTGCCATTGCTGATTATAATAGACTCCCATTTGAGCTAATGAAGACAATTAAACTGATTAAAACTGTGGCCAAAACATCATTAAGCCTTTTCAATCAATCAATGCTGACAGTGATTACCTGTTGTGTTCTGTCTAGATATTTTGGATGAATGACAGAGGAAGGGTAGGGATTTAATGGTATTTTCAATACAGGCCTTTCAGTTTGGCACATGTACTGAGCAAATGCAGTGTTAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa33735
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:
Essential Splice Site
Transcripts:
| Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
|---|---|---|---|---|---|
| ENSDART00000082983 | Essential Splice Site | 852 | 992 | 11 | 15 |
Genomic Location (Zv9):
Chromosome 5 (position 61165423)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 5 | 58797550 |
| GRCz11 | 5 | 59467259 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCATCAGGCCAGCTAGTCAATATTAGCCAGGAGCTTCTGAAAAAAGAAAG[G/T]TAAAGAGGCGAGCATTGTGATTTATGACTGGTGTAATTGACTGGTTTTAA
Long Flanking Sequence:
TTCAAACAAAACACAGGCAGTATGGTTCTCTCTCTTAAACATAAACATGTTTCCCTATTTCAGTATATGAAATATGTTCTTTAACCATGAATGTGTCTTATTAGAAACTCTGGAGAAACTCACGAAAAGGGAAAAGGAAGTGTCCACTCTAACAACCCAAGTAGATGCCCTAAAGACCCAAATAACTGGTAATTTTTCACTTCTCTGCCAATCACACGACCCTTTTTGTAAAACAACAAACATAGGTACTGTATACACTGTGTATATGTAATATAACATGTGATGATGCTAGTAATACTTTGTGATATACGTAACAATAAACTTCACTGCATCTTGTCTGCAGCCTTGGAGGAAAAGGTTCGTCTTGGAGAAAAAACGGCAGATGGACTCATTAAGGAGAAGACCCGTTTGGAGGCAGAGCTGGAGACCATGACTAAGAAATCCCATGATGCATCAGGCCAGCTAGTCAATATTAGCCAGGAGCTTCTGAAAAAAGAAAG[G/T]TAAAGAGGCGAGCATTGTGATTTATGACTGGTGTAATTGACTGGTTTTAATGGTGGGAATGACATCATGTGCTTTTGGAAATTGACCACATATTGGTTCAGTCAATGAAGTACTTTTAAAGATACTTTGATCTTGCACTTGATTCTCTCAGCTTTATTTTATAGAAAACCTTTTTCTGGATTATATTGATTTCCAAAACACTAGGATGAATCATTTCCCAATCTGCCATTGCTGATTATAATAGACTCCCATTTGAGCTAATGAAGACAATTAAACTGATTAAAACTGTGGCCAAAACATCATTAAGCCTTTTCAATCAATCAATGCTGACAGTGATTACCTGTTGTGTTCTGTCTAGATATTTTGGATGAATGACAGAGGAAGGGTAGGGATTTAATGGTATTTTCAATACAGGCCTTTCAGTTTGGCACATGTACTGAGCAAATGCAGTGTTAATATTAATAACAATAATGATAGTAATAATATCAGGCAGCACGGTG
Associated Phenotype:
Not determined