ZMP
mrc1a
Ensembl ID:
ZFIN ID:
Description:
Mannose receptor C1-like protein [Source:UniProtKB/TrEMBL;Acc:C1J0C7]
Human Orthologues:
MRC1, MRC1L1
Human Descriptions:
mannose receptor, C type 1 [Source:HGNC Symbol;Acc:7228]
mannose receptor, C type 1-like 1 [Source:HGNC Symbol;Acc:23403]
mannose receptor, C type 1-like 1 [Source:HGNC Symbol;Acc:23403]
Mouse Orthologue:
Mrc1
Mouse Description:
mannose receptor, C type 1 Gene [Source:MGI Symbol;Acc:MGI:97142]
Alleles
There are 9 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa27081 | Essential Splice Site | Mutation detected in F1 DNA | Not yet available |
sa21118 | Nonsense | Available for shipment | Available now |
sa38650 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa31612 | Essential Splice Site | Available for shipment | Available now |
sa21117 | Nonsense | Available for shipment | Available now |
Mutation Details
Allele Name:
sa27081
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 |
---|---|---|---|---|---|
ENSDART00000112544 | Essential Splice Site | 216 | 1440 | 3 | 30 |
Genomic Location (Zv9):
Chromosome 7 (position 65454743)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58636483 |
GRCz11 | 7 | 58938913 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AGACACAGACTATGACACAGACAAAAAGTGGGGCTTTTGTCCAACTAAAA[G/A]TGAGTAATTCTGCCCTATGAAAACATTTTAGATACTTCTCACAAAATAAT
Long Flanking Sequence:
GAAATCAAGGTGCACTCAAAAAATATTTTTTTTACTTGTTTAAGCTACTTATTTAAAATGAGCTGAAAAACAATTCTTGAGATTTCATTGGGACAGCTTACTTTTTTTGTTCAATCCACATAAATATGTTAAAAGTGTTAAGTTAACTTAATTGATTTATTTTGGGACAGCATGAATGAACCCCAGCCATTATAAATTTGCAAAAATGCTAATAATGTAATATTTTTTTAAGCTAGGGCAAGTACTTTCTCAATTTTTAATTGTTTAGATCTAATATAAAATATATCTCTTGCTTTCCCTTTATTTTGTTTATAAATTTTCTGCAGAGATCTATACAATAGGTGGAAATTCATTTGGGAAACCATGTCAGTTCCCATTTAAATTTGCTGACAAGTTGTATGCGGAATGTACTACGGAGGGAAGATCAGATGGCCAGCTTTGGTGTTCCACAGACACAGACTATGACACAGACAAAAAGTGGGGCTTTTGTCCAACTAAAA[G/A]TGAGTAATTCTGCCCTATGAAAACATTTTAGATACTTCTCACAAAATAATATCTTGGACAAGTTTTTTTTGTTTTTTTTTACTTTTGCAATTCAGTTAAAAAAGAACTTCGTTATATACTAGATTCAATGCACTAGATTTACAGAAAATTGTTTCTTTCATTAAATAGTTAATTAACAGTTTAGGAAAATTCAAACTTCAAAACACAACTTTCAGATTTAAGATTATTTAAATTATTTGGTATAAAAATACGTTCCGGTTTCCCCCACAGTCCAAAGACAGGCAGTACAGGTGAATTTGGTTGGCTAAATTGTCCGTAGTGTATGAGTGTGTATGTGAATGTGTGTGTGTGTATGTTTACCAGAGAGGGTTGCGGCTGGAAGAACATCCTCTGCGAAAAAGTTGGCGGTTCATTCCGCTGTGGCGACCCCGAATTAATAAAGGGATTAAGCCGACTAGAAAATGAATGAATGAATGAATGGTATAAAAATACTAGATACA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21118
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 |
---|---|---|---|---|---|
ENSDART00000112544 | Nonsense | 374 | 1440 | 7 | 30 |
Genomic Location (Zv9):
Chromosome 7 (position 65448755)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58630495 |
GRCz11 | 7 | 58932925 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CCCAACTTCTGTCCTGCTGCATGGGTGCCATATGCTGGTAATTGCTATTA[T/A]CTGCAGCGCACCAAGAAAATGTGGAATGATGCATTAGCAGCATGTCACAG
Long Flanking Sequence:
CTAACAGTTATTAATGTAGAGTTAATGCTTAACAAATAATGAATTCACTAGATGCTATTGCTTAGAGTGCAGTCATTATAAAATGTTACCGACACTTCTATACAGCTTAAAGTGAGATTTAAAGGCTTAACTAGGCAAGTTAGGTTAATTAGTCAAGTTGTTGTATAACAGTGGTTTGCTCTGTAGACTATCCTGCTTTTATTCTAGCTGAAATAAAACAAATAAGACTTTCTCCAAAAAAAAAAAAAAGTATTATCAGACACTATGAAAATGCTCCACCTCTGTTAAACATCATTTGGGAAATATAAAAGAAAATAATAATAAATCACAGGATGGTGACTTCAAATATATATATATATATATATATACACACTATATTAAATAATTCATCTATTAAAACATGACATGGCAAGGTTTTACAAAGATATTTTTCTTGCAGGTAAAGATCAGCCCAACTTCTGTCCTGCTGCATGGGTGCCATATGCTGGTAATTGCTATTA[T/A]CTGCAGCGCACCAAGAAAATGTGGAATGATGCATTAGCAGCATGTCACAGGGAAGGAGCAAACTTGGCCAGTATACACAACATAGAAGAGCACAGTTTCATTATATCACAGAGTGGATACTGTAAGTATGTGCAGACTTATAGACTAAAGCAACACATACATATAAAAAAAACCCTTCATATTTATTTTTACTAACAACTGATACAAATTGGAATGTTTGTTATTTAGTGCCTACAGATGAACTTTGGATTGGGCTTAATGATCAGAAGACTCAGAATCTGTTTGAATGGTCAGACAGAACTCATGTCACTTTTACGACGTGGCTAGTAGGAGAACCTTCACATTTCATAAATCGCTTGGAGGATTGTGTCCTCATCAAGGGAAAGGTAAGTCTGTTTTCTTTCTTTCTTTTTTTCTGGAAAACAAGCCTGCATTGTGTATAGATGATAACAGCCTTCTGAGCCTACCAGTAGGTGCAGAAGGCCCCTACTGGCAAATAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa38650
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 |
---|---|---|---|---|---|
ENSDART00000112544 | Nonsense | 507 | 1440 | 10 | 30 |
Genomic Location (Zv9):
Chromosome 7 (position 65445916)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58627656 |
GRCz11 | 7 | 58930086 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GAAGAATTGTCAATGTGACTAAATTATATGTCTTTTGTTCCCATAGGGCT[G/A]GGTTAGATATGGCTCATACTGCTATATGAGTGCCATTGAAAGCAAGACCT
Long Flanking Sequence:
TTTATACATAAACTTTAAACAGAGAAAAAACAATACCTATAATTAGAAATAATATATTAATAATAAATATAATAATAATAGTATAACATCGAATTACTACATTTGTTTTATTAATATTTTCATTATCTATTCACAATTAAAATGTACAAAATAAATAACAGTTTGACGTGCTTCAATCTTCTGCTAACTTAAAATATGGGTGCTTGATGGATCTTTATGCTAACACTTTATAACAAGATCGCATTTAATAAGATTAGTTAACTTTAATCTTAGTTCCTTTCAACATTTGCTACTTTTATTAAAAGTTGCAATTGTTAACATTGATAAAGGTACAGTGATTAACATGAATGAACAATTAACATAGCATATTTTATTAGATTTGATTTGCTAAGATTAGTAAAGGTTGAGCTTAAAAATAGGTCTGGCTTATTTGTATTGGTAAAGATGTGTGAAGAATTGTCAATGTGACTAAATTATATGTCTTTTGTTCCCATAGGGCT[G/A]GGTTAGATATGGCTCATACTGCTATATGAGTGCCATTGAAAGCAAGACCTTTAATGAAGCCAAACAGATTTGTGAGCAGACAGGAGCCAATTTGGTTGATGTTGCCAGCAGGTAATGCATATAATATATGTTGATGGTTATACTGTATACAATACACTCTCAGAAATAAAGGTACACAAGCTGTCACTGGGTAGTACCTTTTCAAAAGGTAAAAATTTGTACCTTAATGGTCCATTTTATTACCTCAAGGGTGCACATTAGTACCTAAAAAGTATACAAGTGTTTCTCTTAAAATGCTTTGGGACTAATATACACTTTTACGGTACTAATATGGACCCTACAAGTACAAATGTGTACCTGTTGAAAAGATACCACCCCAGTGACAGCTCGCATGCCTTTATTTCTTAGAGTGTAGATACATGATTTGTCTTGTTTAAAAATTATATAAACTAAACAAATTAATTTCAAGATTTATATTTAAAGGAAAAAGACCTACTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa31612
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 |
---|---|---|---|---|---|
ENSDART00000112544 | Essential Splice Site | 544 | 1440 | 10 | 30 |
Genomic Location (Zv9):
Chromosome 7 (position 65445804)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58627544 |
GRCz11 | 7 | 58929974 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AAACAGATTTGTGAGCAGACAGGAGCCAATTTGGTTGATGTTGCCAGCAG[G/A]TAATGCATATAATATATGTTGATGGTTATACTGTATACAATACACTCTCA
Long Flanking Sequence:
AATATTTTCATTATCTATTCACAATTAAAATGTACAAAATAAATAACAGTTTGACGTGCTTCAATCTTCTGCTAACTTAAAATATGGGTGCTTGATGGATCTTTATGCTAACACTTTATAACAAGATCGCATTTAATAAGATTAGTTAACTTTAATCTTAGTTCCTTTCAACATTTGCTACTTTTATTAAAAGTTGCAATTGTTAACATTGATAAAGGTACAGTGATTAACATGAATGAACAATTAACATAGCATATTTTATTAGATTTGATTTGCTAAGATTAGTAAAGGTTGAGCTTAAAAATAGGTCTGGCTTATTTGTATTGGTAAAGATGTGTGAAGAATTGTCAATGTGACTAAATTATATGTCTTTTGTTCCCATAGGGCTGGGTTAGATATGGCTCATACTGCTATATGAGTGCCATTGAAAGCAAGACCTTTAATGAAGCCAAACAGATTTGTGAGCAGACAGGAGCCAATTTGGTTGATGTTGCCAGCAG[G/A]TAATGCATATAATATATGTTGATGGTTATACTGTATACAATACACTCTCAGAAATAAAGGTACACAAGCTGTCACTGGGTAGTACCTTTTCAAAAGGTAAAAATTTGTACCTTAATGGTCCATTTTATTACCTCAAGGGTGCACATTAGTACCTAAAAAGTATACAAGTGTTTCTCTTAAAATGCTTTGGGACTAATATACACTTTTACGGTACTAATATGGACCCTACAAGTACAAATGTGTACCTGTTGAAAAGATACCACCCCAGTGACAGCTCGCATGCCTTTATTTCTTAGAGTGTAGATACATGATTTGTCTTGTTTAAAAATTATATAAACTAAACAAATTAATTTCAAGATTTATATTTAAAGGAAAAAGACCTACTAGAATTAAACTCTACAGTTCTCAAAAGAAAATGGGAATGTTCACTCATTTGCAAGATTATGCAACACAGATTAAGTCGGGTGTGTTTATGTAACCCATAATCCATAGATCTAGGT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa21117
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 |
---|---|---|---|---|---|
ENSDART00000112544 | Nonsense | 820 | 1440 | 17 | 30 |
Genomic Location (Zv9):
Chromosome 7 (position 65431421)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 7 | 58613161 |
GRCz11 | 7 | 58915591 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TACTTCATCAACGAAGAGTCCCTACCTATGGAAGATGCTCGCTCGTTCTG[C/A]AAAAAGAATAATGGGGATCTTGTTGTCATTACTGGACAAACAGAGAGGAA
Long Flanking Sequence:
AAGGCTTAACTAGGTTTGTTTGGTTACCTAGGCTTGGGTTGGGTAATTAGGTAATTACTTAGGCTTGGGTTGGGTTGGGTAATTAGGTAAGTTATTGTATAACGATGGTTTGTTCTGTAGACAATGAAAAAAAAAATCTAGCTTAAAGAGGCTAACAATTTTGACCTTAAAATGGCTTTTAAAAAATTTAAAACTGCTTTTATTCTAGTTGACAAAACAAATAAGACTTTCTTTAAAAAATATTATCAGACTTAAAGTGAAAAGTTCTTTGCTCTGTTAAAAATAATTTGCAAAATATTTAAAAAAGAAAAAAAAATCAAAGGGGGGCTAATAATTCTGACTTCAACTGTGTGTATATATATATATTTATATATATATTAATATTTTGTTATTTCTGCAGTGGAATATAACAAGACATCTGATGGTTGGATTCAGTACAACGATAGCCAGTACTTCATCAACGAAGAGTCCCTACCTATGGAAGATGCTCGCTCGTTCTG[C/A]AAAAAGAATAATGGGGATCTTGTTGTCATTACTGGACAAACAGAGAGGAAGTTTGTATGGAAGCAGGTAAATCAGACTATTAAGTGAATTATGACAGATAATCACATACTTTTTTGCTTTCATTGTTGTTGTTGCGGACAGAAATCTAGAAAGTTGGGGCATTTATATACATACCTGTCAACATTGTGATATTAAAATAAGGGATATGCCCACCATTACAAGGGATTGTGTGTACAGAATCCATTTGGGAAACAGCGTCTATTTATCACTATGAAGCGCGTCAGCTGACAATCATGCACCGCTACATGACTGTTTTGAGGATTGCATATGAAGGGGAGATGGCACCTGTAATGAAAAAGAAAGGGAATCCCACCGTTTTTATATTTATTTCAAAGTGTTTTCATGCCTAAACAAAGCAAAAGCACAGAACAGGCTCATGTTTTAAGAGCAAGGGGTGGCCCCTTGTGGTTCGGCACTAAGGGTTGCGTAAAGGGAGGATC
Associated Phenotype:
Not determined