Busch Lab

ZMP

rhcgl2

Ensembl ID:
ENSDARG00000029066
ZFIN IDs:
ZDB-GENE-040426-2595, ZDB-GENE-040426-2595
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.
Availability:
Order Allele From ZIRC
Order Allele From EZRC
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.
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.
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.
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