| RH Map | Genethon Map | Method | In Situ | Human Gene | Mouse Chr. | Mouse Gene | Mouse Locus | Cross | Homology Group |
|---|---|---|---|---|---|---|---|---|---|
| R | 16p13.3 | HBA1 | 11 |
Hba | 16.0 | 141 | |||
| R | 16p13.3 | MPG | 11 |
Mpg | 16.0 | 141 | |||
| 16p13.3 | CCNF | 17 |
Ccnf | 10.4 | c | 142 | |||
| 16p13.2 | ERV1 | 17 |
Erv1 | 10.0 | 142 | ||||
| R | 16p13.3 | TSC2 | 17 |
Tsc2 | 10.3 | c | 142 | ||
| 16 | TPS2 | 17 |
Mcpt7 | 10.4 | 142 | ||||
| R | 16p13.3 | PKD1 | 17 |
Pkd1 | 10.4 | 142 | |||
| R | 16p13.3 | D16S259 | 17 |
D17H16S259 | S | 142 | |||
| R | 16p | D16S666E | 17 |
D17Lon4 | 10.4 | 142 | |||
| 16p13.2-13.3 | CREBBP | 17 |
Crebbp | 11.0 | 142 | ||||
| 16p13.3 | HAGH | 17 |
Glo2 | 11.0 | 142 | ||||
| 16 | TPS1 | 17 |
Mcpt6 | 11.7 | 142 | ||||
| R | 16p13.13 | PRM1 | 16 |
Prm1 | 3.4 | a, b, c | 143 | ||
| R | 16p13.13 | PRM2 | 16 |
Prm2 | 3.4 | 143 | |||
| 16p13 | GRIN2A | 16 |
Grin2a | 3.4 | 143 | ||||
| R | 16p13.1 | GSPT1 | 16 |
Gspt1 | 10(g) | 143 | |||
| R | 16p13.13 | TNP2 | 16 |
Tnp2 | 3.4 | 143 | |||
| 16p13.13 | PXG | 16 |
Pxg | 3.4 | 143 | ||||
| 16q13.3 | DNL1 | 16 |
Dnl1 | 4.3 | 143 | ||||
| WI-17351 | 19-27 | R | 16p13.13-p13.12 | MYH11 | 16 |
Myh11 | 5.0 | 143 | |
| SHGC-12858 | 34-41 | R | 16p13.11 | UMOD | 17* |
Umod | S | 144 | |
| SHGC-11016 | 39-41 | R | 16p12 | CRYM | 17* |
Crym | S | 144 | |
| 16p12.1-p11.2 | SCNN1B | 7 |
Scnn1b | 56.0 | 145 | ||||
| L36592 | 31-41 | R | 16p12.1-p11.2 | SCNN1G | 7 |
Scnn1g | 56.0 | 145 | |
| R | 16p12 | PRKCB1 | 7 |
Pkcb | 60.0 | b | 145 | ||
| R | 16p12.1-p11.2 | STP1 | 7 |
Stp1 | 61.0 | c | 145 | ||
| SGC30149 | 45-50 | R | 16p12.1-p11.2 | IL4R | 7 |
Il4r | 62.0 | b | 145 |
| R | 16p11.2 | CD19 | 7 |
Cd19 | 59(g) | 145 | |||
| R | 16p13.1-p11 | ITGAL | 7 |
Itgal | 60(g) | 145 | |||
| R | 16p11.2 | SPN | 7 |
Spn | 62.0 | b | 145 | ||
| 16q12-q13 | ADCY7 | 8 |
Adcy7 | 40.0 | 146 | ||||
| stSG1404 | 65-72 | R | 16q13-q22.1 | CES1 | 8 |
Ces1 | 43.0 | 146 | |
| 16 | ESB3 | 8 |
Es6 | 43.2 | 146 | ||||
| R | 16q13 | MT3 | 8 |
Mt3 | 45.0 | 146 | |||
| WI-6072 | 72-75 | R | 16q13 | MT1A | 8 |
Mt1 | 45.0 | a, b | 146 |
| G | 16q13 | MT2A | 8 |
Mt2 | 45.0 | 146 | |||
| R | 16q12-q22 | GOT2 | 8 |
Got2 | 46.0 | 146 | |||
| 16q13 | GNAO1 | 8 |
Gnao | 46.0 | 146 | ||||
| 16q22.2 | PSMD7 | 8 |
Mov34 | 42(g) | 146 | ||||
| 16q22.1 | HAS3 | 8 |
Has3 | 50.0 | a | 146 | |||
| 16q22 | CBFB | 8 |
Cbfb | 51.0 | 146 | ||||
| 16q22.1 | CDH1 | 8 |
Cdh1 | 52.0 | 146 | ||||
| 16q22.1 | CDH3 | 8 |
Cdh3 | 52.0 | b | 146 | |||
| R | 16q22.1 | LCAT | 8 |
Lcat | 53.0 | 146 | |||
| WI-7891 | 84-88 | R | 16 | CTRA | 8 |
Ctra | 53.0 | 146 | |
| R | 16q23-q24 | MOV34 | 8 |
Mov34 | S | 146 | |||
| R,G | 16q22 | HP | 8 |
Hp | 55.0 | b | 146 | ||
| SHGC-11957 | 84-86 | R | 16q22.1 | TAT | 8 |
Tat | 55.0 | 146 | |
| G | 16q23-q24.1 | CTRB | 8 |
Ctrb | 55.0 | 146 | |||
| 16q24.1 | COX4 | 8 |
Cox4 | 60.0 | 146 | ||||
| R | 16q24.1 | PLCG2 | 8 |
Plcg2 | 62(g) | 146 | |||
| R | 16q22-q23 | MAF | 8 |
Maf | 61.0 | b | 146 | ||
| 16q22-q24 | MF1 | 8 |
Mf1 | 64.0 | 146 | ||||
| R | 16q24.1-qter | CDH3 | 8 |
Cdh3 | 67.0 | 146 | |||
| R,G | 16q24.2-qter | APRT | 8 |
Aprt | 67.0 | b | 146 | ||
| 16q24 | FKHL5 | 8 |
Hfh8 | 67.0 | 146 | ||||
| 16q22-q24 | FKHL6 | 8 |
Fkh6 | 72(g) | 146 | ||||
| R | 16q24.3 | MC1R | 8 |
Mc1r | 68(g) | 146 |
| Method | Description |
|---|---|
| C | High-resolution cytogenetic methods |
| G | Genetic linkage mapping |
| G* | Genetic mapping, with disagreements between genetic and physical map resolved in favor of physical map |
| L | Long-range restriction site mapping |
| P | Multiple physical methods, including YAC and cosmid contigs |
| R | Radiation hybrid mapping |
| X | Multiple sources of high-resolution data |
| Key | Description |
|---|---|
| a | Gene Bank Accession Number for Mouse EST |
| b | Gene order has been changed from that shown in the chromosome committee reports or online databases, as required by high-resolution human physical mapping data; these data also indicate a probable difference between human and mouse organization, e.g. a small inversion in one species |
| g | Mouse gene order has been changed slightly to conform with human gene order in the absence of conflicting high resolution data |
| y | Position has been changed from that reported in chromosome committee report or or Mouse Genome Database based on additional data or review of previous data |
| p | Different sources of high resolution mapping data give conflicting positions |
| r | Difference between position in inbred mice vs. Mus spretus |
| u | This is a UniGene designation, given since no gene symbol has been assigned. Note: some of these designations may be retired. |
a - Duke/Davis cross
b - Frederick cross
c - Jackson Lab cross
| Mouse Chr. | Mouse Chr. | Mouse Chr. | Mouse Chr. | Mouse Chr. | Mouse Chr. | ||||||
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The asterisk character ('*') is used to indicate a different region of homology on the same mouse chromosome.
A question mark ('?') indicates that the authors are uncertain that this region is truly homologous.