ZMP
rhcgl2
Ensembl ID:
ZFIN IDs:
Description:
Ammonium transporter Rh type C-like 2 [Source:UniProtKB/Swiss-Prot;Acc:Q8JI14]
Human Orthologue:
RHCG
Human Description:
Rh family, C glycoprotein [Source:HGNC Symbol;Acc:18140]
Mouse Orthologue:
Rhcg
Mouse Description:
Rhesus blood group-associated C glycoprotein Gene [Source:MGI Symbol;Acc:MGI:1888517]
Alleles
There are 5 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa16468 | Nonsense | Available for shipment | Available now |
sa44242 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa30208 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa44241 | Essential Splice Site, Missense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa16468
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 |
---|---|---|---|---|---|
ENSDART00000014573 | Nonsense | 145 | 329 | 3 | 12 |
ENSDART00000048028 | Nonsense | 145 | 488 | 3 | 11 |
ENSDART00000053518 | Nonsense | 145 | 488 | 3 | 11 |
Genomic Location (Zv9):
Chromosome 25 (position 8792484)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8516280 |
GRCz11 | 25 | 8593348 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
TCTGTCATGACTGTTTACKSTGTGTTCAGMTTGATCAATGCAGATTTCTG[T/A]GYGGCCRGTTGTCTAATCGCATACGGTGCGGTGCTGGGGAAGGTCAGTCC
Long Flanking Sequence:
AACCATCAAGATTTTTACACTCTGTTGAAGTTTGTGGAAAAAACTCAATGTGTTTTAAATGCAAAACTACTCTGCCAGCAGGAGGCGCTTGTGGAAAATCAGAAGTACTGTAGCTGTTTTCACAGTAGCAGTTGAAGTCTAAGCATTGAACTCTCATGGTATTTTGTTGGGATTGTAAAAAAGTATGAATAAAAATAATAAATTAAAACTTTTCAGAAAAGTTTTTGTAAGTATAATTTCATATGTGTACTTGTCTACTGTCTGTATTTTGTATACTTTATGAATTCAGACACTCTTGACTCATAATGTTTTTTCTTATAAAAGGCTTTATAGTGTGTAATTATCTGATTCTGATCACAAATTATTTCATGCATGTGAAACATGGTATAATATGACTATCATGAGACTTTAAAGTCAATTTTGAGCTTTAATAAAATCGTAAATGAAAATTCTGTCATGACTGTTTACTCTGTGTTCAGATTGATCAATGCAGATTTCTG[T/A]GTGGCCAGTTGTCTAATCGCATACGGTGCGGTGCTGGGGAAGGTCAGTCCGGTTCAGCTGCTGGTCATGACACTGTTTGGGATCACGCTGTATGCTGTGGAGGAGTTCATCATCTTAAGTGTCCTCAACGTGAGTCTGATCTCGCTTTCACTATGGCCATTTTAAAAATATTTTGCAGTAACTTAAGTGCATATCTATAGTCGCTAAATTACATTCTCCTTTCAAAAGATTTTCTAATATGAGTGTATTTTAATATGTTTAGGAAACAGTTGTAGTTTTAATGTTTGTTTTATTGTTGAGATCAGCAATTACATTTCAAGTTTGAAGTTTGGTAAATTAGTTGTGTAATTATTTTTTGTGCATGTTTATGTGTGTATGCACAATATTTTAGTATCATAGTTGTGTGTTTGTCAATGAGAATATAACAAAGTTCAAACTTTATTGTCTTAAATGCACTTTTATAGCTGACAAGTTGTATTCTGCTTTCTAAGAAAGGATTT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44242
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:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014573 | Nonsense | 238 | 329 | 4 | 12 |
ENSDART00000048028 | Nonsense | 238 | 488 | 4 | 11 |
ENSDART00000053518 | Nonsense | 238 | 488 | 4 | 11 |
Genomic Location (Zv9):
Chromosome 25 (position 8791280)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8515076 |
GRCz11 | 25 | 8592144 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GCAACCATATGAACGGGTCCGTCTACCACTCGGACGTATTCGCCATGATC[G/T]GTAAGAATAAAGCCATTACAAACAAACTTTCAAGCTCTACAGTGTTTATC
Long Flanking Sequence:
TAATTGTTTATTTTATATTTGTAACAATATTTTAATATGGTTTATAATAAATGTGTGTGTGTGTGTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATTCTAAAGTATATACTTTTTGAGTCATAATTACTTTTTATTTATTATTTATTTAAAATACCTTAAGTACTTCAAGGTAAACATAATGAAAAAAAAAACTGTTATTAAATGTCTGAAATAAAATGTTAGAGTACAATAACATACAGCTGAACTTGACTCTAAAGGCTTCATGCTACCTTCTTCACTCTCTTACAGGCCAAAGACGCTGGCGGCTCTATGGTCATCCATACTTTTGGAGCTTACTATGGTCTCTCCATCTCAAGGGTTTTATATCGGCCCAATCTGAATAAAAGCAACCATATGAACGGGTCCGTCTACCACTCGGACGTATTCGCCATGATC[G/T]GTAAGAATAAAGCCATTACAAACAAACTTTCAAGCTCTACAGTGTTTATCTTGTTGCTAAATGAATAGAAAAGTCCAACATAACAGTAATAATGTGATTAATTAAGGTGTGGACATGTCTATACAGCACTCCAATAATGAGACCAAAACAGACAAACATGTTCATTTGATTTGTGTTGACATCGTGTATGACTGTAGCCAGATTCATTGCATCAAAAATATAAGTGTGTTATCTTAATGGTGTGAATAATATCAGAATTCTGTTGTCCATGTTAACACTATGCTTGATATGGTTGATGTAAGACTCATAGACTGGGTTGTTGTTGTTGTTTTTTCAGGAACACTTTTCCTGTGGATGTTTTGGCCGAGTTTTAACTCTGCTATTTGTAATCATGGAGACGGTCAGCACAGAGCCGCCATAAACACATACCTGGCCCTCGCCTCCACCGTCCTCACTACTGTGGCTATTTCCAGCATGTTTGAGAAAACCGGAAAACTAGA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa30208
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 |
---|---|---|---|---|---|
ENSDART00000014573 | Nonsense | 243 | 329 | 5 | 12 |
ENSDART00000048028 | Nonsense | 243 | 488 | 5 | 11 |
ENSDART00000053518 | Nonsense | 243 | 488 | 5 | 11 |
Genomic Location (Zv9):
Chromosome 25 (position 8790926)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8514722 |
GRCz11 | 25 | 8591790 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
CTCATAGACTGGGTTGTTGTTGTTGTTTTTTCAGGAACACTTTTCCTGTG[G/A]ATGTTTTGGCCGAGTTTTAACTCTGCTATTTGTAATCATGGAGACGGTCA
Long Flanking Sequence:
CCAAAGACGCTGGCGGCTCTATGGTCATCCATACTTTTGGAGCTTACTATGGTCTCTCCATCTCAAGGGTTTTATATCGGCCCAATCTGAATAAAAGCAACCATATGAACGGGTCCGTCTACCACTCGGACGTATTCGCCATGATCGGTAAGAATAAAGCCATTACAAACAAACTTTCAAGCTCTACAGTGTTTATCTTGTTGCTAAATGAATAGAAAAGTCCAACATAACAGTAATAATGTGATTAATTAAGGTGTGGACATGTCTATACAGCACTCCAATAATGAGACCAAAACAGACAAACATGTTCATTTGATTTGTGTTGACATCGTGTATGACTGTAGCCAGATTCATTGCATCAAAAATATAAGTGTGTTATCTTAATGGTGTGAATAATATCAGAATTCTGTTGTCCATGTTAACACTATGCTTGATATGGTTGATGTAAGACTCATAGACTGGGTTGTTGTTGTTGTTTTTTCAGGAACACTTTTCCTGTG[G/A]ATGTTTTGGCCGAGTTTTAACTCTGCTATTTGTAATCATGGAGACGGTCAGCACAGAGCCGCCATAAACACATACCTGGCCCTCGCCTCCACCGTCCTCACTACTGTGGCTATTTCCAGCATGTTTGAGAAAACCGGAAAACTAGACATGGTGAGCAGATGCTATAAATGCCTAGTTGTGCATGGTATAGAAATTGTATATATAATATATATATGGTATATATATTATATATCATATATAATATAATATATATACTATATATGTATGGTGTATAAAATATACATCATATACAGTATTTAAAATGTGCTTATGCGTGCGTATGTGTGTGTGTGTGTGCATGCAAAAAATGACATAGCTGTAAAAAAGTGAAAAAATATTTTTAATAGTTACAATTATCATTGTTTATATATTGGAATAATAAAAAGGTGTTTTTTATAATGTGGATATAATAATGTTTTGATTCATATTTTAAAGTAAAGTTATATTATTAATTATATAAT
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa44241
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, Missense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000014573 | Essential Splice Site | 307 | 329 | 6 | 12 |
ENSDART00000048028 | Missense | 308 | 488 | 6 | 11 |
ENSDART00000053518 | Missense | 308 | 488 | 6 | 11 |
Genomic Location (Zv9):
Chromosome 25 (position 8789618)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 25 | 8513414 |
GRCz11 | 25 | 8590482 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TCTTTAGGTGCACATTCAGAACTCTACCCTGGCGGGTGGCGTGGCCGTGG[G/A]CACCGCAGCAGAGTTCATGCTGATGCCGTACGGCTCTTTGATCGTAGGCT
Long Flanking Sequence:
ATATAATAAATAGAGAGCTAATGTATTAGTCCTCCTCTGACATTTTTGTTCTTTATTAAAAAGATTTTCCATTGATGTTTAACAGCAGGACATTTTCTCCGAATTTCCTATATTTCTTTTTCTGAAAAACATTGTTTTTTCTTTTAGTTTGTTTTTATTTATGTGTGGATTTTGCAAGTACTCCCCGTGTTGACATGGGTTTCCTCCTGGTGCTCTGATTTCCCCTCACAGTCCAAACACATGCACTGTAGGTGAATTGAATCAACTAAATTGGCCACAGTGTATGTGTGTGAATGAGTGTGTATGGGTTAATTTTCCTTCAGCTTGGTCCCTTTATTAATCAGGGGTCGCCTCAGTGGAATGAACCATCAACTTATCCAGCATATATTTTACCCAGCAGATGCCCTTCCATGTGATTTGAAGCACTTTAAAGTGTTGTGTTTGTGTTTGTCTTTAGGTGCACATTCAGAACTCTACCCTGGCGGGTGGCGTGGCCGTGG[G/A]CACCGCAGCAGAGTTCATGCTGATGCCGTACGGCTCTTTGATCGTAGGCTTCTTCTGCGGTATCATCTCTACACTGGGATACATCTACCTCACTGTGAGCCATTACACACATCTACTGACAAAGTCAAAACTAATCGCCCTCCTGTGAATTCTTTTTCAAATATTTCCCAAATGATGTTTAACAGAGCAAGGAAATTTTCACAGTATATCCTATATAGTTTTTCCTTCTGGCGAAAGTCTTATTTGTTTAATTTTGGGCTAGAATAAAGCAGTTTTTAATTTAAGCCATTTTAAGTTCAATATTATTAGCCTGCTTAAGCTATATGTTTTTATTGTCGACAGAACAAACCACTGTTACACAATGACTTGTGTAACAAATTATAATTTAAATTAAATTTGCACGCATATCTACATTAATAATTTGTAACAAATTATAATGTAGATTAAAGTGCTCGCATATCTACACCATTATTACTGTAACAAATTTGCTCAAGGTTATT
Associated Phenotype:
Not determined