ZMP
crim1
Ensembl ID:
ZFIN ID:
Description:
Cysteine-rich motor neuron 1 protein [Source:UniProtKB/Swiss-Prot;Acc:Q7T3Q2]
Human Orthologue:
CRIM1
Human Description:
cysteine rich transmembrane BMP regulator 1 (chordin-like) [Source:HGNC Symbol;Acc:2359]
Mouse Orthologue:
Crim1
Mouse Description:
cysteine rich transmembrane BMP regulator 1 (chordin like) Gene [Source:MGI Symbol;Acc:MGI:1354756]
Alleles
There are 4 alleles of this gene:
| Allele Name | Consequence | Status | Availability |
|---|---|---|---|
| sa23148 | Essential Splice Site | Available for shipment | Available now |
| sa42982 | Nonsense | Mutation detected in F1 DNA | Not yet available |
| sa23147 | Essential Splice Site | Available for shipment | Available now |
| sa23146 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa23148
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 |
|---|---|---|---|---|---|
| ENSDART00000050534 | Essential Splice Site | 325 | 1027 | 6 | 17 |
| ENSDART00000134243 | Essential Splice Site | 325 | 451 | 6 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 39163617)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 39048514 |
| GRCz11 | 17 | 38996099 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATACATGCGACAACCTCTAATGCACTGTGTCCTGATTACTGTGTTTTGCA[G/A]AGACAAAGCCAGCCTGCACTTTTAACGGAGTGGAGTACCATGATGGAGAC
Long Flanking Sequence:
TCAAAACTGAATAATTCATAATAAATGAGAAGACATGACAAGAACAAAAAAATAAATAAAATACTGCAGTTCGGTGTCCTTTGTAAAGGTGATAATTTTTTGTTAGAGGCTCCCATTCAAAGCACGTTATCTCTGAATACCATATTAACAGAAGTCATCAAGGTGCGAATATATGTACATAAATACATCATCATTAAGCTTCATTTTAGATAAAAAAGCAGCCTATTCCCATATACACAAGTGCAGGCATTGTAATGCATGAGCTGAAAGCAGAATTTGGTACCTAGCGGTTGCCATGACTACCATTGGGCATCAATTCCGTGGCTATCTGAAACTGAGCTGCTAAAAGCTCTCCCGGACACAAATGCACAACGTTTAGGTCCCTGCGTACCCCATAACTCTTCTTGGCCCTGTTATGAAGACCCTGTTTGTTTTGTTGTGCTGTCAGTCATACATGCGACAACCTCTAATGCACTGTGTCCTGATTACTGTGTTTTGCA[G/A]AGACAAAGCCAGCCTGCACTTTTAACGGAGTGGAGTACCATGATGGAGACATGTTCAGGATGGACGCCTGCCGCTTTTGCCGCTGTCAGGGTGGTGTATCTGTGTGCTTCACCGCCCAGTGTGGCGTCTTGCACTGCGAGCGCTACTATGTTCCGGATGGAGAGTGTTGTCCTGTCTGTGAAGGTAAGATGACCTTTGCATTTGCAAAAAAAGCAACCCAAGGACAACGTTATTTTGACGTCCAATAACGACATCAAATGACGTTGATATTTGGTTGATTTTAAGTTGTGTTGGAAATTAACCAGAATCCAAGGTCAACATCTTAAATAAACGTCATATTGAAATCAAATACTGACATTTATTCGTCAGGGATAGCAACCAAAACCCAACAACTGATAGACGTCAGAGTGTCAAACTGTAACAATATTATGCTATTTTCACAGACATGACACATGCTAATAAAAAGCATTATTTGCACGTAAATAGACATTTTTGAGTTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa42982
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 |
|---|---|---|---|---|---|
| ENSDART00000050534 | Nonsense | 410 | 1027 | 7 | 17 |
| ENSDART00000134243 | Nonsense | 410 | 451 | 7 | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 39156913)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 39041810 |
| GRCz11 | 17 | 38989395 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TTAGCTGGCTGCTATGTGAATGGGCAAATCTTGGCTCACGGTGACCATTG[G/A]CGCGAGGACGACTGCACCTTCTGCCAGTGTGTGAGTGGAGATGCCCGCTG
Long Flanking Sequence:
GTCTTTACTCATCAATAGCTAGTCTCTGTTTGGAATTAGCATGTCCGACTGATCAATAGTTAATTGAAATTATTAGTGGATGGCCTAGGCTGATCCGTAGCTAGTCCATGCTGAGTATTAGCTATAGGGGCCCAGACTGGTCATTAGCTGGTCTATTAGCCATTAAATGATCTAAGTTGGTCCATTAGCTGGTCCAAGCCGGTTGTTGGTTGGTGCAAACTTCCATATGGCCTTAAACTTATCAACAAACCAGCCACCTGTTAGTCGTAACCTAAGGTGGTCAAAAAACATCTGCCCTATTCTAAATCTGGCACATTTTAAAACATCTTAAACTGACTTTTTCAGCAGGGTACATTTTATGGGATATCAGAACTCTTTTGTGGTGGCTATCATTTTATCATTCATTGTTCTCCTAACTTTTTTATAGACCCCATCTACCCGGTGCTCAGTTTAGCTGGCTGCTATGTGAATGGGCAAATCTTGGCTCACGGTGACCATTG[G/A]CGCGAGGACGACTGCACCTTCTGCCAGTGTGTGAGTGGAGATGCCCGCTGTGTGGCAGCTGCCTGCGGCCACAGCTGCCTCAATCCTGTCACCGTGCCCGGAGAGTGCTGTCCCGTGTGTGAGGGTAAGAACAGATTAACTTTACGAATGCTGCTTGGAGATATATTCTGTTGAGTGTATAATTTTTGGACCTGAAACATTCTCTATTGAAGTATGCAAACAAACGTTTGTAATTATGTGATAGGAAATGTGTGTGATTGTAGTCATAATGCCATTTTAGTTTGAATTATGTTCTTTGAATTGCATTGCTGTAGCGAGGAACACTTAATTATTCTATAGTCATTTTTGTTTTTTGGTCATCCAATATTATAGTGAAGCTACAGTTTAAGTGTTGCTGTTATTTTTTTTACAAAAGTTGTTATGATTACTGTCTCCATAAAGTAGTCTATAAACTGGACAGAAATTTTTCTATAATTTATTATTTAGACATTTCTAGTTAC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23147
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 |
|---|---|---|---|---|---|
| ENSDART00000050534 | Essential Splice Site | 588 | 1027 | 10 | 17 |
| ENSDART00000134243 | None | None | 451 | None | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 39119546)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 39004443 |
| GRCz11 | 17 | 38952028 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGGATTCCAGCATGATGAATTGGGCTGTCTGATTTGTCAGTGTAGAGG[T/G]AAGTCTATATTTATTCATTTGTTAAGTATTTTATTTGATTTGGTCAGACT
Long Flanking Sequence:
AGTTTAGCTCTAACCAGCTCCAGCTCACACCTTGCTTAATAGTCTAGTAGTCTTGAACACCTTGATTAGTTGGATCAGCTGTGTTTGATTAGGGTTGGAGCAAAACTGTGCAGAGCTGTGGCCCTCCAGGAATCCAGTTTGAGACCTATGCTATAAACAGAAATATGGTAAACACAGTCAACCATGATCTAATTATTCTATGTATACACTAATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATTATTTGTTTAATTTATGATTTACTACAATATGCCTCTAAAGCTTTCTTCATCTTTCTCGTTTTCTCTTATCAGTAAGAACAAGCATGGATGTGATACCTGCCGTTGTAAAAAATGCCCTGAGTTGCCATGTGACAAGGCCTGTCCAATGGGATTCCAGCATGATGAATTGGGCTGTCTGATTTGTCAGTGTAGAGG[T/G]AAGTCTATATTTATTCATTTGTTAAGTATTTTATTTGATTTGGTCAGACTACAGAATGACTACTACGTTTCGTAATTAGTAATAAATGTAAATAAATTTATCTGAGTTTTAAATCTTACGTATCTTTTATATATTTGATGCAATTTGAACAGTAATGAGCAAGGGCAATGACAGCAAAAAAAAGACTATAATAAAATGAAAGACAGAACATTTTTAAAAGTAATTGGAAGTGACAGACCAATTTTCAAATGTAGGTGCAATATAGTAACATTTTATTTTAAAATATCTTAAAATAAGAAATATCTTTTCATTTTCTATCCTAACTCTTGTGTGCTGTTGGAGATGTTTTCATCCACTCTGGGGAGATTTTGAGGCATAATTTGGCCACAACTGTCTTTGTGTTTCAGCAAATGGAATGATTTTTGGTGAAAAATCTTATTTTGACACATATTTTATGAAAATCCTTTGGAATTTTTTTAAAAACTCAACAATACACTTTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa23146
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 |
|---|---|---|---|---|---|
| ENSDART00000050534 | Nonsense | 626 | 1027 | 11 | 17 |
| ENSDART00000134243 | None | None | 451 | None | 7 |
Genomic Location (Zv9):
Chromosome 17 (position 39114031)
Other Location(s):
| Assembly | Chromosome | Position |
|---|---|---|
| GRCz10 | 17 | 38998928 |
| GRCz11 | 17 | 38946513 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGGCATGAGAATGGGCAGAGCTGGCACGACGGATGCAGGGACTGTTACTG[C/A]CATGCTGGAAGAGAAATGTGTGCGCTTATTTCTTGCCCAGTGCCACCCTG
Long Flanking Sequence:
ATTATGTAGTATTAGGAAGCAGATTAAGATAATGCAGAATATGTACTTTAAACTGTATTGAGAACTTTGAACTGTATTAGTACACTGAGTACTAATAATACTAATAAACAGTCAATATCCTATAAGCAGGTAATACGCCTATGTTAATAGTGACTATTGGTGCTTACACAAAAGTGTTACCATTCTGTTTGGTTTCTAATTATGTATTAAATGTTCAAAAAATCATTTTAAATACAAATAAATCAATCAAGTTAAGAGTACCATGGATATGATGAGCTTGTACTGGTTTGTTGAAAGTAATGATCATGGTTGTACCGCAGTGTTATTTTAGTGCTGTAATGGCAGAAAGTGATCTGATCTGTCTGTTGTTTGTTTGTCTGTGCAGATCAGAGCTCGTCGTCTGTGACTCCAGCAGTGAAGCTGGGCTCTTGTCTGTCTATGGACGGCCGCAGGCATGAGAATGGGCAGAGCTGGCACGACGGATGCAGGGACTGTTACTG[C/A]CATGCTGGAAGAGAAATGTGTGCGCTTATTTCTTGCCCAGTGCCACCCTGTGATAATCCTACCATCCGCCCCGGACACTGTTGCCCCACATGCCCAGGTGATTCAGTGCAGCATATTTACTCACTGGCAGGCAAAGTTTCTTAAAGAGATAGTTTACTCAAACATTCAATTTTACTCATTGTTTTCACACCCTCAAGTGGTTCCAGACCTTTATGAGATTCTTTATTGTGTTGAATATGAAGATATAAAAAAAAACAAAGCAGAAGTCATTGACATCTATGGTAAAAAATAAACAAAAACTACAGATACTGTGGAAGTCAATGGCTTCCAGTTCCAAAAACTCTTGGAACTAAAAACTATAGCTATTCATACTCCTTGACACTTTAGATATGAAGCAAGGCTGCAATTTATTGATTAAAAATGTGCTAAAATGGTTTTATTGTGAAAGAATATTACACTTTAAAATAACATTTTCTGTACAGATATAGTTTAATGTATGC
Associated Phenotype:
Not determined